U.S. patent application number 11/740650 was filed with the patent office on 2008-02-14 for sample vessels.
Invention is credited to Shuqi Chen.
Application Number | 20080038813 11/740650 |
Document ID | / |
Family ID | 27557382 |
Filed Date | 2008-02-14 |
United States Patent
Application |
20080038813 |
Kind Code |
A1 |
Chen; Shuqi |
February 14, 2008 |
SAMPLE VESSELS
Abstract
A device for processing a biological sample includes a
processing unit having at least one opening to receive a sample
vessel and a plurality of processing stations positioned along the
opening. The processing stations each have a compression member
adapted to compress the sample vessel within the opening and
thereby move a substance within the sample vessel among the
processing stations. An energy transfer element can be coupled to
one or more of the processing stations for transferring thermal
energy to the content at a processing station.
Inventors: |
Chen; Shuqi; (Framingham,
MA) |
Correspondence
Address: |
FOLEY HOAG, LLP;PATENT GROUP, WORLD TRADE CENTER WEST
155 SEAPORT BLVD
BOSTON
MA
02110
US
|
Family ID: |
27557382 |
Appl. No.: |
11/740650 |
Filed: |
April 26, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10241816 |
Sep 11, 2002 |
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11740650 |
Apr 26, 2007 |
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09782732 |
Feb 13, 2001 |
6780617 |
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10241816 |
Sep 11, 2002 |
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09910233 |
Jul 20, 2001 |
6748332 |
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10241816 |
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09339056 |
Jun 23, 1999 |
6318191 |
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09910233 |
Jul 20, 2001 |
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60259025 |
Dec 29, 2000 |
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60090471 |
Jun 24, 1998 |
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60318768 |
Sep 11, 2001 |
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Current U.S.
Class: |
435/287.2 |
Current CPC
Class: |
A61B 5/150755 20130101;
B01L 2400/0655 20130101; B01L 2400/0481 20130101; B01L 2300/044
20130101; A61B 5/150221 20130101; G01N 35/1002 20130101; B01L 7/52
20130101; B01L 7/525 20130101; B01L 2300/1805 20130101; B01L
2300/0832 20130101; A61B 5/15003 20130101; A61B 5/150786 20130101;
B01L 3/505 20130101; B01L 2400/0683 20130101; B01L 3/50825
20130101; B01L 3/502 20130101; B01L 3/5027 20130101; G01N 35/00009
20130101; A61B 5/150351 20130101; A61B 5/150022 20130101; B01L
2300/0636 20130101; A61B 5/150343 20130101; B01L 2300/0816
20130101 |
Class at
Publication: |
435/287.2 |
International
Class: |
C12M 1/00 20060101
C12M001/00 |
Goverment Interests
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
[0002] Portions of the disclosed subject matter were made with
government support under grant numbers 1R43HL65768, 1R43HL65867 and
1R43HL67568 awarded by the National Institutes of Health. The
government has certain rights in those portions.
Claims
1. A flexible vessel for thermal cycling a sample, the flexible
vessel comprising: a soft-sided reaction vessel comprising: a
receptacle for receiving the sample, and a flexible body coupled to
the receptacle, the flexible body having first and second portions
coupled together and in fluid communication with each other,
wherein the flexible body is configured for insertion into a
thermal cycler such that the first portion is received into a first
temperature zone and the second portion is received into a second
temperature zone of the thermal cycler.
2. The vessel of claim 1, wherein the flexible body is formed from
two faces of plastic sheeting that are sealed together to form
sealed sides.
3. The vessel of claim 2, further comprising a plurality of
additional soft-sided reaction vessels, each having a receptacle
and a flexible body coupled to the receptacle, wherein the
plurality of additional bodies are formed from the two faces of
plastic sheeting and each has sealed sides.
4. The vessel of claim 3, wherein the two faces of plastic sheeting
are sealed together such that each flexible body is separated from
its adjacent flexible body by a sealed side.
5. The vessel of claim 1, wherein the flexible body contains dried
PCR reagents.
6. A flexible vessel for thermal cycling a sample, the flexible
vessel comprising two faces of flexible material that are sealed
together to form a plurality of flexible bodies, each flexible body
separated from its adjacent flexible body by a sealed side, and
each flexible body having a first portion and a second portion, the
first and second portions coupled together and in fluid
communication with each other, wherein the flexible bodies are
configured for insertion into a thermal cycling apparatus such that
the first portion of each flexible body is received into a first
temperature zone and the second portion of each flexible body is
received into a second temperature zone of the thermal cycler.
7. The vessel of claim 6, further comprising a plurality of
receptacles, each receptacle fluidly coupled to its respective
flexible body.
8. The vessel of claim 6, wherein the flexible material is a thin
plastic film.
9. The vessel of claim 8, wherein the thin plastic film comprises
aluminum lamination.
10. The vessel of claim 8, wherein the thin plastic film is
selected from the group consisting of polyethylene, polyurethane
and alloys thereof.
11. The vessel of claim 8, wherein the thin plastic film transmits
about 80% to about 90% of incident light.
12. The vessel of claim 6, wherein the vessel body has a
coefficient of heat transfer of about 0.02 to about 20
W/m*degK.
13. The vessel of claim 6, wherein each flexible body contains
dried PCR reagents.
14. A thermal cycling system comprising the reaction vessel of
claim 6 received into the thermal cycler, wherein the first
temperature zone of the thermal cycler is configured for receiving
the first portion of the reaction vessel, the first temperature
zone comprising a first heater, the first temperature zone movable
between an open orientation in which the first heater affects the
temperature of the reaction mixture contained within the first
portion, and a closed orientation in which the reaction mixture is
forced from the first portion and the first heater does not
substantially affect the temperature of the reaction mixture, and
the second temperature zone of the thermal cycler is configured for
receiving the second portion of the reaction vessel, the second
temperature zone comprising a second heater, the second temperature
zone movable between an open orientation in which the second heater
affects the temperature of the reaction mixture contained within
the second portion, and a closed orientation in which the reaction
mixture is forced from the second portion and the second heater
does not substantially affect the temperature of reaction
mixture.
15. The thermal cycling system of claim 14, wherein each flexible
body contains a PCR reaction mixture.
16. The thermal cycling system of claim 15, wherein the PCR
reaction mixture is sealed within each flexible body.
17. The thermal cycling system of claim 16, wherein each flexible
body is heat-sealed to seal the reaction mixture within each
flexible body.
18. The thermal cycling system of claim 16, wherein the first
portion of each flexible body is coupled to a fitting, and closure
of the fitting seals the reaction mixture within its respective
flexible body.
19. The vessel of claim 1, wherein the flexible body comprises a
thin plastic film.
20. The vessel of claim 19, wherein the flexible body further
comprises aluminum lamination.
21. The vessel of claim 19, wherein the thin plastic film is
selected from the group consisting of polyethylene, polyolefin,
polyurethane and alloys thereof.
22. The vessel of claim 19, wherein the thin plastic film transmits
about 80% to about 90% of incident light.
23. The vessel of claim 1, wherein the vessel body has a
coefficient of heat transfer of about 0.02 to about 20
W/m*degK.
24. The vessel of claim 1, wherein the flexible body is formed from
two walls of plastic and has a flattenable cross-sectional
profile.
25. The vessel of claim 24, further comprising a plurality of
additional soft-sided reaction vessels, each having a receptacle
and a flexible body coupled to the receptacle, wherein the
plurality of additional bodies are each formed from two walls of
plastic and has a flattenable cross-sectional profile.
26. A flexible vessel for thermal cycling a sample, the flexible
vessel comprising a plurality of flexible bodies, each flexible
body separated from its adjacent flexible body, and each flexible
body having a first portion and a second portion, the first and
second portions coupled together and in fluid communication with
each other, wherein the flexible bodies are configured for
insertion into a thermal cycling apparatus such that the first
portion of each flexible body is received into a first temperature
zone and the second portion of each flexible body is received into
a second temperature zone of the thermal cycler.
27. A thermal cycling system comprising the reaction vessel of
claim 26 received into the thermal cycler, wherein a first
temperature zone of the thermal cycler is configured for receiving
the first portions of the flexible bodies of the reaction vessel,
the first temperature zone comprising a first heater, the first
temperature zone movable between an open orientation in which the
first heater affects the temperature of reaction mixtures contained
within the respective first portions, and a closed orientation in
which the reaction mixtures are forced from the respective first
portions and the first heater does not substantially affect
temperatures of the reaction mixtures, and a second temperature
zone of the thermal cycler is configured for receiving the second
portions of the flexible bodies of the reaction vessel, the second
temperature zone comprising a second heater, the second temperature
zone movable between an open orientation in which the second heater
affects temperatures of the reaction mixtures contained within the
respective second portion, and a closed orientation in which the
reaction mixtures are forced from the respective second portions
and the second heater does not substantially affect temperatures of
the reaction mixtures.
28. The thermal cycling system of claim 27, wherein each flexible
body is sealed to seal the reaction mixture within each flexible
body.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. application Ser.
No. 10/241,816, filed Sep. 11, 2001, which is a
continuation-in-part of U.S. patent application Ser. No.
09/782,732, filed Feb. 13, 2001, now U.S. Pat. No. 6,780,617, which
claims the benefit of U.S. Provisional Patent Application Ser. No.
60/259,025, filed Dec. 29, 2000. application Ser. No. 10/241,816 is
also a continuation-in-part of U.S. patent application Ser. No.
09/910,233, filed Jul. 20, 2001, now U.S. Pat. No. 6,748,332, which
is a continuation of U.S. patent application Ser. No. 09/339,056,
filed Jun. 23, 1999, now U.S. Pat. No. 6,318,191, which claims the
benefit of U.S. Provisional Patent Application Ser. No. 60/090,471,
filed Jun. 24, 1998. application Ser. No. 10/241,816 further claims
the benefit of U.S. Provisional Patent Application Ser. No.
60/318,768, filed Sep. 11, 2001. Each of the aforementioned patent
applications and patents is incorporated herein by reference.
BACKGROUND
[0003] As result of the Human Genome Project and other genetic
research, a tremendous amount of genomic and biomarker information
is presently available to healthcare providers. Using molecular
diagnostic testing, genomic and biomarker information can provide a
resource to healthcare providers to assist in the rapid and
accurate diagnosis of illness. However, the development of
diagnostic testing systems allowing the use of such genetic
information, particularly in the clinical setting, has failed to
match pace with the genetic research providing the information.
Current diagnostic testing systems are mainly limited to large
medical testing centers or research labs due to the high costs
associated with acquiring and operating the systems and the
complexity of the molecular diagnostic assays being employed. These
current systems require a large initial capital investment and
incur high costs for reagents, disposables, operation, maintenance,
service and training.
[0004] Sample preparation and handling generally includes sample
collection and any preprocessing required for subsequent biological
and chemical assays. Sample collection and handling is an important
part of in vitro diagnostic (IVD) testing, and is an important
factor in determining the feasibility of test automation. With the
advancement of medicine, the number of possible assays available to
perform is continually increasing. In parallel, sample collection
methods have evolved over the last several decades. In the case of
blood sample collection, for example, disposable plastic syringes
first replaced glass syringes to improve safety. Later developments
had vacuum tubes replacing the traditional syringes to simplify the
blood collection process. However, a vacuum tube is generally not
suitable for use as an IVD test reaction chamber. Thus, a
re-sampling process is necessary for delivery of the sample to
distinct assay containers for each of a variety of IVD tests.
Automation of these processes is a daunting task. Indeed, in large
clinical testing centers giant automation testing systems costing
several million dollars are currently used. The major automated
task in these machines is liquid handling, which entails the
pipetting of the sample from sample tubes to 96-well plates, the
addition of the reagent(s) to the wells, as well as moving reaction
mixtures from well to well.
[0005] Recently, nanotechnology has emerged to revolutionize
automation and testing formats. In this direction, by using
silicone micro-fabrication and etching technology, the
lab-on-a-chip platform was developed in an attempt to integrate and
miniaturize certain parts of the automation process into a chip
with dimensions less than 2 mm by 2 mm. Liquid processing rates for
certain lab-on-a-chip platforms can be on the scale of nanoliters
per second. However, it is often difficult for users to interface
with this type of platform to, for example, deliver the sample to
the chip.
[0006] Another concern of current sample handling devices is the
large sample volume routinely drawn from a patient for IVD testing.
In the case of blood sample collection, for example, a small vacuum
tube may take close to 5 ml whole blood. When multiple samples are
required in the testing of various assays, several tubes of blood
are frequently ordered. However, only a small amount is needed for
each assay. The drawing of a large volume of blood for multiple
tests is a concern for pediatric patients as it can lead to iron
deficiency anemia. It is even more critical for patients with
pre-existing anemia or a bleeding disorder.
SUMMARY
[0007] The present invention provides sample processing devices and
methods that facilitate the rapid analysis of biological samples,
such as blood, saliva, or urine, in an efficient and cost effective
manner with minimal, if any, exposure to biohazards. The sample
processing devices and methods of the present invention are
particularly suited to the clinical setting, allowing the clinician
to readily proceed from acquisition of a test sample to analysis of
the test results, with minimal human intervention. The sample
processing devices of the present invention may be implemented as a
hand-held system suitable for the processing of a single sample or
as a larger, bench top unit suitable for the simultaneous
processing of multiple samples. The present invention may be
valuable in all diagnostic and therapeutic monitoring areas,
including in the point-of-care or clinical setting, in
high-throughput screening, and in biological warfare detection. In
addition, the present invention provides a sample vessel for
holding a biological sample throughout the processing of the
sample.
[0008] In accordance with one embodiment of the present invention,
a device for processing a sample includes a processing unit having
an opening to receive a sample vessel and at least one processing
station positioned along the opening. The processing station
includes a compression member adapted to compress the sample vessel
within the opening and thereby displace a content of the sample
vessel within the sample vessel. The content displaced by the
compression member can be, for example, the sample, a reagent, or a
mixture of the content and a reagent
[0009] In accordance with another aspect, the processing station
may include an energy transfer element for transferring energy to
or from the content within the sample vessel and a control system
coupled to the energy transfer element to control the energy
transferred to or from the content. The energy transfer element can
be, for example, an electronic heat element, a microwave source, a
light source, an ultrasonic source or a cooling element.
[0010] In accordance with a further aspect, the energy transfer
element transfers thermal energy to or from the content within the
sample vessel. An energy insulator may be positioned adjacent the
processing station. The energy insulator can be, for example, an
energy shielding layer, an energy absorption layer, an energy
refraction layer, or a thermal insulator, depending on the type of
energy transfer element employed. A temperature sensor may be
coupled to the control system to monitor temperature at the
processing station. Alternatively, the processing station may
include a heat sink to dissipate thermal energy from the processing
station.
[0011] In accordance with another aspect, the processing station
may include a stationary member opposing the compression member
across the opening. The compression member can operate to compress
the sample vessel against the stationary member within the
opening.
[0012] In accordance with a further aspect, a driver may be coupled
to the compression member to selectively move the compression
member and thereby compress the sample vessel within the opening.
The driver can be, for example, a motor coupled to the compression
member by a cam. Alternatively, the driver can be an
electromagnetic actuating mechanism.
[0013] In accordance with another aspect, the processing device can
include a sensor for detecting a signal from the content within the
sample vessel. An energy source can optionally be provided for
applying energy to the content within the sample vessel to generate
a signal from the content. In one embodiment, the processing device
can include an electrophoresis system comprising a pair of
electrodes adapted to have a predetermined voltage difference and
an electrode actuator for inserting the electrodes into the sample
vessel.
[0014] In accordance with a further aspect, the processing device
may include a reagent injector cartridge actuator adapted to
receive a reagent injector cartridge having at least one needle in
fluid communication with a reagent reservoir. The reagent injector
cartridge actuator can be operable to move the reagent injector
cartridge to inject a quantity of reagent into the sample
vessel.
[0015] In accordance with another embodiment of the invention, a
sample vessel for holding a sample includes a sample containing
portion for holding the sample and a handling portion for handling
the sample vessel. The sample containing portion can have a wall
constructed of a flexible material permitting substantial
flattening of a selected segment of the sample containing portion.
The handling portion can be coupled to the sample containing
portion and preferably has a generally rigid construction to
facilitate handling of the sample vessel.
[0016] In accordance with another aspect, the sample containing
portion of the sample vessel can be a tubule.
[0017] In accordance with a further aspect, the sample vessel can
include at least one pressure gate disposed within the sample
containing portion to divide the sample containing portion into a
plurality of segments. At least one of the segments of the sample
vessel can have a filter contained therein that is structured to
separate selected components of a sample material from other
components of the sample material. Additionally, at least one of
the segments of the sample vessel can contain a reagent. The
reagent can be, for example, an anticoagulant, a cell lyses
reagent, a nucleotide, an enzyme, a DNA polymerase, a template DNA,
an oligonucleotide, a primer, an antigen, an antibody, a dye, a
marker, a molecular probe, a buffer, or a detection material. The
sample containing portion also can include an electrophoresis
segment containing a gel for electrophoresis. The electrophoresis
segment can include a pair of electrodes adapted to maintain a
predetermined voltage difference therebetween. Additionally, one of
the segments can contain multilayer membranes or a micro-array
bio-chip for analyzing the sample.
[0018] In accordance with another aspect, the sample containing
portion can include a self-sealing injection channel formed
therein. The self sealing injection channel is preferably normally
substantially free of sample material and capable of fluid
communication with the sample material in the sample containing
portion.
[0019] In accordance with another aspect, the sample vessel can
include an instrument for obtaining a sample coupled to the sample
vessel.
[0020] In accordance with a further aspect, the handling portion of
the sample vessel includes an opening for receiving a sample. The
sample vessel also can include a closure for selective closing the
opening. Preferably, the closure seats against the handling portion
to close the opening. In addition, the instrument for obtaining a
sample can be coupled to the closure of the sample vessel.
[0021] In accordance with another aspect, the handling portion has
a wall thickness greater than a thickness of the wall of the sample
containing portion. Preferably, the thickness of the wall of the
sample containing portion is less than or equal to 0.3 mm. In one
embodiment, the handling portion can include a cylindrical sleeve
sized and shaped to fit over a portion of the sample containing
portion. The handling portion is preferably positioned
longitudinally adjacent the sample containing portion.
[0022] In accordance with another embodiment, a sample vessel for
holding a sample includes a sample containing portion having at
least one pressure gate disposed within the sample containing
portion to divide the sample containing portion into a plurality of
segments. Preferably, at least one segment of the sample containing
portion has a wall constructed of a flexible material permitting
substantial flattening of the segment of the sample containing
portion.
[0023] In accordance with another embodiment, a method of
processing a sample within a sample vessel includes the steps of
introducing the sample vessel into a device for processing the
sample and compressing the sample vessel to move the sample within
the sample vessel from a first segment to a second segment of the
sample vessel.
[0024] In accordance with another aspect, the method of processing
a sample can include the step of introducing a reagent to the
sample within a segment of the sample vessel.
[0025] In accordance with a further aspect, the method of
processing a sample can include the step of heating the sample in
the first segment to a first temperature. The method can also
include the step of heating the sample to a second temperature in
the second segment. In one embodiment, the first temperature can be
effective to denature the sample and the second temperature is one
at which nucleic acid annealing and nucleic acid synthesis can
occur. The method of processing a sample can further include the
steps of compressing the sample vessel to move the sample within
the sample vessel from the second segment to the first segment of
the sample vessel and heating the sample to the first temperature
in the first segment.
[0026] In accordance with another aspect, the method of processing
the sample can include the step of analyzing the sample by
detecting a signal from the sample within a segment of the sample
vessel and analyzing the detected signal to determine a condition
of the sample. The analyzing step can include applying an
excitation energy to the sample within the segment of the sample
vessel. Additionally, the analyzing step can include conducting
electrophoresis analysis of the sample by applying a selective
voltage to the sample within a segment of the sample vessel,
detecting light emitted from the sample, and analyzing the detected
light to determine a condition of the sample.
[0027] Alternatively, the analyzing step can include applying an
excitation energy to a bio-array member contained within a segment
of the sample vessel, detecting light emitted from the bio-array
member, and analyzing the detected light to determine a condition
of the sample. The bio-array member can be, for example, a
multi-layer membrane or a micro-array bio-chip.
[0028] In accordance with a further aspect, the method of
processing a sample can include the step of agitating the sample
within a segment of the sample vessel.
[0029] In accordance with another embodiment, a method of treating
a sample within a sample vessel can include the steps of
introducing the sample vessel into a device for processing the
sample within the sample vessel and compressing one of the segments
to mix the reagent with the sample within the sample vessel.
Preferably, the sample vessel has a plurality of segments including
a segment for containing a reagent and a segment for containing the
sample.
[0030] In accordance with another aspect, the method of processing
the sample can include the step of introducing the reagent into a
reagent segment of the sample after the step of introducing the
sample vessel into the device for processing the sample.
[0031] In accordance with another embodiment, a thermal cycler
includes a processing unit having an opening to receive a sample
vessel containing a sample. The processing unit can have a first
processing station, a second processing station, and a third
processing station positioned along the opening. The first
processing station can include a first compression member adapted
to compress the sample vessel within the opening and a first energy
transfer element for transferring energy to the sample at the first
processing station. The second processing station can include a
second compression member adapted to compress the sample vessel
within the opening and a second energy transfer element for
transferring energy to the sample at the second processing station.
The third processing station can include a third compression member
adapted to compress the sample vessel within the opening and a
third energy transfer element for transferring energy to the sample
at the third processing station. Compression of the sample vessel
by of one of the compression members can displace the sample within
the sample vessel between the processing stations.
[0032] The present disclosure is also directed to sample vessels
that can permit the collection and the processing of biological and
chemical samples, such as, for example, blood, saliva, tissue, or
urine, in a closed system. Sample devices disclosed herein may
provide a uniform sample handling system that simplifies the sample
collection process and reduces exposure to biohazards. One or more
of the sample vessels disclosed herein can accommodate multiple
fluid samples and a plurality of assays of different types, while
concomitantly reducing the volume of sample necessary for
testing.
[0033] In accordance with one exemplary embodiment, a sample vessel
may comprise a tubule having an opening for receiving a sample
material and at least one compressible section, a generally rigid
container receiving at least a portion of the tubule, and an
interface in fluid communication with the opening in the tubule.
The at least one compressible section may have a wall constructed
at least partially from a material having sufficient flexibility to
permit compression of opposed sections of the wall into contact.
The interface may facilitate delivery of a sample material to the
tubule through the opening.
[0034] In accordance with another exemplary embodiment, a sample
vessel may comprise a tubule having a plurality of lumens and a
wall constructed at least partially from a material having
sufficient flexibility to permit compression of opposed sections of
the wall into contact with one another, and a pressure gate
connecting at least two lumens of the plurality of lumens. The
pressure gate may permit selective fluid flow between the at least
two lumens.
[0035] In accordance with another exemplary embodiment, a sample
vessel may comprise a tubule having a wall that forms a lumen when
the tubule is in an open configuration. The wall may have a
plurality of sections including at least a first section of the
wall having sufficient flexibility to permit compression of a
portion of the tubule and at least a second section of the wall
having sufficient rigidity to support a flow channel within the
tubule during compression of the tubule.
[0036] In accordance with another exemplary embodiment, an
apparatus for drawing a sample into a sample vessel may comprise a
cylindrical housing having an opening for receiving the sample
vessel, first means for compressing a first portion of the sample
vessel, and second means for compressing a second portion of the
sample vessel. The first compression means may be positioned at a
proximal end of the housing and the second compression means may be
positioned at a distal end of the housing.
BRIEF DESCRIPTION OF THE DRAWINGS
[0037] These and other features and advantages of the sample
vessels and processing devices and methods disclosed herein will be
more fully understood by reference to the following detailed
description in conjunction with the attached drawings in which like
reference numerals refer to like elements through the different
views. The drawings illustrate principles of the sample vessels and
methods disclosed herein and, although not to scale, show relative
dimensions.
[0038] FIG. 1 is a schematic diagram of a device for processing a
sample according to the present invention;
[0039] FIG. 2 is a schematic diagram of the device of FIG. 1,
illustrating a compression member of a processing station of the
device compressing the sample vessel;
[0040] FIG. 3 is a schematic diagram of an alternative embodiment
of a device for processing a sample according to the present
invention;
[0041] FIG. 4 is a schematic diagram of an alternative embodiment
of a device for processing a sample according to the present
invention;
[0042] FIG. 5 is a perspective view of an embodiment of a hand held
device for processing a sample according to the present
invention;
[0043] FIG. 6 is a perspective view of an embodiment of a bench top
device for processing a sample according to the present
invention;
[0044] FIG. 7 is a perspective view of the device of FIG. 6,
illustrating the device with the top cover removed;
[0045] FIG. 8 is a perspective view of an embodiment of a thermal
cycling processing unit according to the present invention;
[0046] FIG. 9 is a perspective view of the processing unit of FIG.
8;
[0047] FIG. 10 is a partially exploded, perspective view of a
processing station of the processing unit of FIG. 8, illustrating a
heat block unit and an insulator block unit of the processing
station;
[0048] FIG. 11 is a partially exploded, perspective view of the
processing unit of FIG. 8, illustrating a plurality of heating
block units and insulator block units;
[0049] FIG. 12 is a partially exploded, perspective view of a
processing station of an alternative embodiment of a processing
unit according to the present invention;
[0050] FIGS. 13A-13G are side elevational views, in cross-section,
of a processing unit of the present invention, illustrating the
operation of the processing unit;
[0051] FIG. 14 is a side elevational view, in cross section, of a
gel electrophoresis analysis unit of the present invention;
[0052] FIGS. 15A-15B are side elevational views, in cross-section,
of embodiments of a sample vessel according to the present
invention;
[0053] FIG. 16 is a side elevation view, in cross section, of a
portion of a sample vessel according to the present invention,
illustrating an injection channel formed in the sample vessel;
[0054] FIG. 17 is a side elevational view of a reagent cartridge
according to the present invention;
[0055] FIG. 18 is a side elevational view, in cross-section, of a
sample vessel according to the present invention;
[0056] FIGS. 19A-19C illustrate an alternative embodiment of a
processing unit of the present invention.
[0057] FIG. 20A is a perspective view of an exemplary embodiment of
a sample vessel;
[0058] FIG. 20B is a side-elevational view in cross-section of the
sample vessel of FIG. 20A;
[0059] FIG. 20C is an exploded view of the sample vessel of FIG.
20A, illustrating the tubule and collar removed from the
container;
[0060] FIG. 21A is a perspective view of an exemplary embodiment of
a sample vessel;
[0061] FIG. 21B is a side-elevational view in cross-section of the
sample vessel of FIG. 21A;
[0062] FIG. 21C is an exploded view of the sample vessel of FIG.
21A, illustrating the tubule and collar removed from the
container;
[0063] FIGS. 22A-22B are side-elevational views in cross-section of
an exemplary embodiment of a sample vessel having a pair of lumens
separated by a pressure gate;
[0064] FIG. 23 is a side-elevational view in cross-section of an
exemplary embodiment of a sample vessel having three lumens
separated by a pair of pressure gates;
[0065] FIG. 24 is a side-elevational view in cross-section of
another exemplary embodiment of a sample vessel having three lumens
separated by a pair of pressure gates, illustrating a self-sealing,
reinforced wall section for facilitating injection by a needle;
[0066] FIG. 25A is a perspective view of an exemplary embodiment of
a sample vessel having a pair of lumens connected by a
micro-fluidic channel;
[0067] FIGS. 25B-25C are digital photographs of the sample vessel
of FIG. 25A illustrating fluid flow through the lumens of the
sample vessel;
[0068] FIG. 26A is a perspective view of an exemplary embodiment of
a segmented sample vessel having a plurality of lumens;
[0069] FIGS. 26B and 26C are cross-sectional views of the sample
vessel of FIG. 26A;
[0070] FIG. 27 a perspective view of another exemplary embodiment
of a segmented sample vessel having a plurality of lumens,
illustrating a hinged cover for the sample vessel;
[0071] FIG. 28 a perspective view of an exemplary embodiment of a
segmented sample vessel having a plurality of lumens, illustrating
alternative interfaces for the sample vessel;
[0072] FIG. 29A is a side elevational view in partial cross-section
of an exemplary embodiment of a sample vessel, illustrating the
compression of the sample vessel;
[0073] FIG. 29B is a cross-sectional view of the sample vessel of
FIG. 29A taken along a line transverse to the longitudinal axis of
the tubule 1200;
[0074] FIGS. 30A-30C are side elevational views in cross-section of
an exemplary embodiment of a sample vessel, illustrating
compression of the sample vessel into a plurality of
configurations;
[0075] FIG. 31 is a side elevational view in cross-section of an
exemplary embodiment of a sample vessel having a composite
cross-section and a micro-fluidic flow channel;
[0076] FIGS. 32A-32B are side elevational views in cross-section of
another exemplary embodiment of a sample vessel having a composite
cross-section and a micro-fluidic flow channel, illustrating the
sample vessel in a open configuration (FIG. 32A) and a compressed
configuration (FIG. 32B);
[0077] FIG. 33A is a side elevational view in cross-section of an
exemplary embodiment of a sample vessel having a plurality
micro-fluidic flow channels interconnecting a plurality of
depressions formed on an interior wall surface of the sample
vessel;
[0078] FIG. 33B is a top view of an interior wall surface of the
sample vessel of FIG. 33A;
[0079] FIGS. 34A and 34B are side elevational views in
cross-section of an exemplary embodiment of a sample vessel having
a composite cross-section including opposed planar wall sections,
illustrating the sample vessel in an open configuration (FIG. 34A)
and a compressed configuration (FIG. 34B);
[0080] FIG. 35A is a perspective view of an exemplary embodiment of
a sample vessel having an adapter for facilitating handling of the
sample vessel and/or connecting of the sample vessel to an external
device;
[0081] FIGS. 35B-35E are side elevational views in cross-section of
a plurality of exemplary embodiments of an adapter connected to the
sample vessel illustrated in FIG. 35A;
[0082] FIGS. 36A-36E are perspective views of an apparatus for
drawing a sample into a sample vessel, illustrating the operation
of the apparatus; and
[0083] FIG. 37 is a perspective view of another exemplary
embodiment of a sample vessel, illustrating the sample vessel with
a portion of the wall removed to show a microarray on an interior
surface of the wall of the sample vessel.
DETAILED DESCRIPTION
[0084] To provide an overall understanding, certain exemplary
embodiments will now be described; however, it will be understood
by one of ordinary skill in the art that the sample vessels and
methods described herein can be adapted and modified to provide
devices and methods for other suitable applications and that other
additions and modifications can be made without departing from the
scope of the present disclosure.
[0085] Unless otherwise specified, the exemplary embodiments
described below can be understood as providing exemplary features
of varying detail of certain embodiments, and therefore, unless
otherwise specified, features, components, modules, and/or aspects
of the exemplary embodiments can be otherwise combined, separated,
interchanged, and/or rearranged without departing from the scope of
the present disclosure. Additionally, the shapes and sizes of
components are also exemplary and unless otherwise specified, can
be altered without affecting the disclosed devices or methods.
[0086] The present disclosure provides devices and methods for
processing a sample. The term "processing" as used herein generally
refers to the preparation, treatment, analysis, and/or the
performance of other testing protocols or assays on a content of
the sample vessel in one or more steps. Exemplary processing steps
include, for example: displacing a content, e.g., the sample or a
reagent, of the sample vessel within the sample vessel to, for
example, adjust the volume of the content, separate content
components, mix contents within the sample vessel; effecting a
chemical or biological reaction within a segment of the sample
vessel by, for example, introducing a reagent to the sample,
agitating the sample, transferring thermal energy to or from the
sample, incubating the sample at a specified temperature,
amplifying components of the sample, separating and/or isolating
components of the sample; or analyzing the sample to determine a
characteristic of the sample, such as, for example, the quantity,
volume, mass, concentration, sequence, or nucleic acid size or
other analyte size, of the sample. One skilled in the art will
appreciate that the forgoing exemplary processing steps are
described herein for illustrative purposes only. Other processing
steps may be employed without departing from the scope of the
present invention.
[0087] A device for processing a sample according to the present
invention can integrate one or more processing units into a single
system depending on the process being employed. The processing
units can include one or more processing stations at which one or
more processing steps can be performed on the sample within the
sample vessel. Sample materials that can be processed according to
the present invention are generally biological samples or samples
containing biological substance and include, for example, blood,
urine, saliva, cell suspensions, biofluids, a piece of tissue, soil
or other samples. A sample processing device of the present
invention is particularly suited for nucleic acid amplification,
such as polymerase chain reaction (PCR) or ligase chain reaction
(LCR) amplification, and can include, for example, a sample
pretreatment unit for extracting nucleic acid from sample, a
thermal cycling reaction unit for amplification of the nucleic acid
or signal, and (optionally) an analysis or detection unit for
analyzing the amplified product. The sample processing device of
the present invention can also be used for isothermal reaction of
nucleic acid or signal amplifications, such as strand displacement
amplification (SDA), rolling circle amplification (RCA), and
transcription-mediated amplification (TMA). Other exemplary
processes to be performed on samples can include clinical
diagnosis, therapeutic monitoring, and screening of chemical
compounds for discovery of new drugs. The following description
primarily focuses on PCR amplification for illustration. However,
one skilled in the art will appreciate that the devices and methods
of the present invention are not limited to PCR amplification, as
the devices and methods described below can be employed in other
sample processing.
[0088] An exemplary embodiment of a device for processing a sample
is illustrated in FIG. 1. The processing device 10 illustrated in
FIG. 1 includes a processing unit 12 having an opening 14 to
receive a sample vessel 16. The opening 14 can be a tubular shaped
opening, an open-faced slot or other structure for receiving the
sample vessel 16 in a removable and replaceable manner. The
processing unit 12 includes a first processing station 18 and a
second processing station 20, each positioned along the length of
the opening 14. The first processing station 18 includes a
compression member 22 adapted to compress the sample vessel 16
within the opening 14 and thereby displace a content of the sample
vessel within the sample vessel 16. The content of the sample
vessel can be, for example, the sample, a reagent contained within
the sample vessel, or a mixture of the sample and the reagent. A
driver 24 is coupled to the compression member 22 to selectively
move the compression member 22 and thereby compress the sample
vessel 16 within the opening 14. The driver 24 can be, for example,
an electromagnetic actuating mechanism, a motor, a solenoid, or any
other device for imparting motion, preferably reciprocal motion, to
the compression member 22, as described in further detail
below.
[0089] Preferably, the compression member 22 is constructed from a
rigid material such as a rigid plastic or a metal. The compression
member can be constructed in any shape sufficient to impart a
compressive force on the sample vessel. For example, the
compression member 22 can be a block having a rectilinear, planar
surface for engaging the sample vessel 16, as illustrated in FIG.
1. Alternatively, the compression member can have a curved,
angular, or non-planar surface for engaging the sample vessel
16.
[0090] Moreover, the compression member 22 alternatively can be an
inflatable membrane that can be inflated by a fluid, e.g., air,
nitrogen, saline, or water, to impart a compressive force on the
sample vessel. In this embodiment, the amount of compression of the
sample vessel may be controlled by the adjusting the inflation
pressure of the membrane.
[0091] The first processing station 18 can optionally include a
stationary member 26 positioned opposite the compression member 22
across the opening 14. The compression member 22, thus, can
compress a portion of the sample vessel 16 within the opening 14
against the stationary member 26, as illustrated in FIG. 2. One
skilled in the art will appreciate that the stationary member 26
may be replaced with a second compression member, such that the
processing station includes two compression members that move
together to compress the sample vessel therebetween. In addition, a
stationary member or second compression member may be omitted by
securing the sample vessel 16 within the opening on either side of
the compression member.
[0092] In the illustrated embodiment, the sample vessel 16 is a
closed tubule flow-chamber for holding the sample. Preferably, one
or more segments of the sample vessel 16 are constructed of a
flexible, compressible material, such as, for example, polyethylene
or polyurethane, to allow selective compression, and preferably
flattening, of the sample vessel to move the sample, or other
contents of the sample vessel, within the sample vessel, preferably
while the sample vessel 16 remains in the device 10. In one
preferred embodiment, the sample vessel 16 includes a plurality of
segments separated by an integral, internal structure, such as a
micro-fluidic pressure gate, as described in more detail below.
Alternatively, the sample vessel 16 can be constructed without
internal, integral structures to form segments and the device 10
can be utilized to segment the sample vessel by compressing
selective portions of the sample vessel. One skilled in the art
will appreciate that other types of sample vessels suitable for
containing a sample may be used with the device 10 without
departing from the scope of the present invention.
[0093] The second processing station 20 can include a sensor 28 for
detecting a signal from the content, e.g., the sample or a reagent,
of the sample vessel 16. For example, the sensor 28 can be an
optical sensor for measuring light, for example fluorescent light,
emitted from the sample or from fluorescent probes within the
sample. In addition, multiple sensors or a spectrum sensor can be
used when detection of multiple wavelength light is required. The
detected signal can be sent to a CPU 30 to analyze the detected
signal and determine a characteristic of the sample.
[0094] In operation, a sample can be introduced to a first segment
A of the sample vessel 16 by injecting the sample through the walls
of the sample vessel 16 or by introducing the sample through an
opening formed in the sample vessel 16, as described in more detail
below. In the present exemplary embodiment illustrated in FIGS. 1
and 2, the sample vessel 16 includes a pressure gate 32 that
divides the sample vessel 16 into a first segment A and a second
segment B. The sample vessel 14 can be inserted into the opening 14
of the device 10 such that the first segment A of the sample vessel
16 is aligned with the first processing station 18 and the second
segment B is aligned with the second processing station 20, as
illustrated in FIG. 1.
[0095] The driver 24 can operate to move the compression member 22
into contact with the sample vessel 16 such that the first segment
A of the sample vessel 16 is compressed within the opening 14
between the compression member 22 and the stationary member 26. As
the first segment A of the sample vessel 16 is compressed, a
quantity of sample is displaced from the first segment A to the
second segment B through the pressure gate 32. The volume of sample
displaced is proportional to the amount of compression of the first
segment A by the compression member 22. Thus, the compression
member 22 of the first processing station 18 can be used to
displace a specific quantity of sample into the second segment B of
the sample vessel 16 for analysis at the second processing station
20. Substantially all of the sample can be displaced from the first
segment A of the sample vessel 16 by completely flattening the
first segment A of the sample vessel 16, as illustrated in FIG. 2.
The sample can be analyzed in the second segment B of the sample
vessel 16 at the second processing station 20.
[0096] An alternative embodiment of a device for processing a
sample is illustrated in FIG. 3. The device 38 includes a
processing unit 40 having three processing stations positioned
along the opening 14, namely, a first process station 42, a second
processing station 44 adjacent the first processing station 42, and
a third processing station 46 adjacent the second processing
station 44.
[0097] The first processing station 42 includes a compression
member 22 coupled to a driver 24 and adapted to compress a segment
of the sample vessel 16 against a stationary member 26 within the
opening 16. The first processing station 42 can operate to displace
a selective quantity of the sample from a first segment A of the
sample vessel into other segments of the sample vessel.
[0098] The second processing station 44 includes a compression
member 22 coupled to a driver 24 and adapted to compress a second
segment B of the sample vessel 16 against a stationary member 26
within the opening 16. The second processing station 44 includes an
energy transfer element 48 for transferring energy to or from the
contents of the sample vessel 16. The energy transfer element 48
can be, for example, an electronic heat element, a microwave
source, a light source, an ultrasonic source, a cooling element, or
any other device for transferring energy. In one embodiment, the
energy transfer element 48 transfers thermal energy to or from the
sample within the sample vessel. The energy transfer element 48 can
be embedded in or otherwise coupled to the compression member 22,
as illustrated in FIG. 3. Alternatively, the energy transfer
element 48 can be coupled to the stationary member 26 or can be
positioned within the processing station independent of the
compression member or the stationary member. The energy transfer
element 48 can be coupled to a control system that controls the
energy transferred to or from the sample vessel 16 by the energy
transfer element 48. The control system can be a component system
of the CPU 30 or can be an independent system. The control system
can also include a temperature sensor 50 to monitor the temperature
of the energy transfer element.
[0099] The second processing station 44 also can include a sensor
52 for detecting a signal from the content of the sample vessel,
particularly during processing in the second processing station.
For example, the sensor 52 can be an optical sensor for measuring
light, for example fluorescent light, emitted from the sample or
from fluorescent probes within the sample. The sensor 52 can be
coupled to the CPU 30 for analysis of the detected signal to
determine a characteristic of the sample.
[0100] The third processing station 46 can include a sensor 28 for
detecting a signal from the content, e.g., the sample or a reagent,
of the sample vessel 16. For example, the sensor 28 can be an
optical sensor for measuring light, for example fluorescent light,
emitted from the sample or from fluorescent probes within the
sample. In addition, multiple sensors or a spectrum sensor can be
used when detection of multiple wavelength light is required. The
detected signal can be sent to a CPU 30 to analyze the detected
signal and determine a characteristic of the sample.
[0101] In operation, a sample can be introduced into a first
segment A of the sample vessel 16 and the sample vessel 16 can be
introduced into the opening 14 of the device 10. In the embodiment
illustrated in FIG. 3, the sample vessel 16 includes two pressure
gates 32 that divide the sample vessel 16 into three segments,
namely, the first segment A, a second segment B, and a third
segment C. The first processing station 42 can operate to displace
a selective amount of the sample into the second segment B of the
sample vessel 16 for processing at the second processing station
44.
[0102] At the second processing station 44, energy can be
transferred to or from the sample within the second segment B. In
this manner, a biological or chemical reaction involving the sample
may be carried out in the second segment B. The sensor 52 can be
used to monitor the reaction during the reaction process.
[0103] Upon completion of the reaction, the sample can be moved
into the third segment C of the sample vessel 16 by compressing the
sample vessel 16 within the opening at the second processing
station 44. Preferably, the compression member 22 of the first
processing station 42 substantially flattens the first segment A of
the sample vessel 16 to inhibit the sample from entering the first
segment A. The sample can be analyzed in the third segment C of the
sample vessel 16 at the third processing station 46.
[0104] A further embodiment of a device for processing a sample is
illustrated in FIG. 4. The device 56 includes a processing unit 58
having a processing station 60 positioned along the opening 14. The
processing station 60 includes a compression member 22 coupled to a
driver 24 and adapted to compress a segment of the sample vessel 16
against a stationary member 26 within the opening 16. In the
embodiment illustrated in FIG. 4, the sample vessel 16 includes a
pressure gate 32 that divides the sample vessel 16 into two
segments, namely, a first segment A and a second segment B. The
processing station 60 can operate to displace a selective quantity
of the content from the second segment B of the sample vessel into
the first segment A of the sample vessel. For example, a reagent
can be introduced into the second segment B of the sample vessel
16. A quantity of reagent can be displaced from the second segment
B into the first segment A of the sample vessel 16 to mix with the
sample in the first segment A. Alternatively, the reagent can be
introduced into the first segment A of the sample vessel 16 and a
quantity of the sample can be displaced from the second segment B
into the first segment A by the processing station 60. Thus, the
first segment A of the sample vessel 16 can act as a reaction
mixture chamber for the sample and the reagent. The reagent can be
pre-packaged in the sample vessel 16 or can be introduced to the
sample vessel 16 after the sample is introduced to the sample
vessel 16. For example, the reagent can be introduced using a
reagent injector cartridge, described below, that is included with
the device.
[0105] Referring to FIG. 5, another embodiment of device for
processing a sample is illustrated. The illustrated device 100 is a
hand held system for processing a nucleic acid sample, preferably
in an "insert and test" format in which a sample vessel containing
a nucleic acid sample is inserted into the device 100 and
processing results are produced by the device with minimal human
intervention. The device 100 can include a housing 112 having an
opening 114 for receiving a sample vessel 116 containing a sample
for processing by the device 100. The opening 114 can be a tubular
shaped opening, as illustrated in FIG. 5, or can be an open-faced
slot or other structure for receiving the sample vessel in a
removable and replaceable manner. A control panel 118 is located on
the top of the housing 112 for inputting information to the device
100 and a monitor 120 is provided for displaying operating
information, such as the results of processing. An external
communication port 121 can be located on the housing 112 for
receiving information or outputting information, such as the
results of processing and remote diagnosing of the system, to a
remote system, such as a computer network. A battery 123 (FIG. 7)
can be located within the housing to provide electrical power to
the components of the device 100.
[0106] A multi-sample device 200 for processing multiple samples is
illustrated in FIG. 6. The device 200 is a bench top thermal
cycling system for processing up to 96 nucleic acid samples
simultaneously. The sample processing device 200 operates on the
same principals as the sample processing device 100 illustrated in
FIG. 5, except that the multi-sample device 200 provides increased
capacity and throughput. The multi-sample processing device 200 can
include a housing 202 having a plurality of wells or openings 204,
with each well being capable of receiving a sample vessel 206
containing a sample for processing by the device. The exemplary
multi-sample device 200 illustrated in FIG. 6 has ninety-six wells
for treating up to 96 samples simultaneously. One skilled in the
art will appreciate that a multi-sample processing device according
to the present invention may be designed with any number of wells,
depending on the sample being tested and the processes being
employed, without departing from the scope of the present
invention. A control panel 208 is located on the top of the housing
202 for inputting information to the multi-sample processing device
200 and a monitor 210 is provided for displaying operating
information, such as the results of testing.
[0107] FIG. 7 illustrates the general components of the sample
processing device 100 illustrated in FIG. 5. The illustrated device
100 includes three primary processing units for processing a sample
within the sample vessel, namely, a pretreatment unit 122 for
pretreating the sample, a reaction unit 124 for amplifying certain
components of the sample, and an analysis unit 126 for analyzing
the sample. The sample vessel can be loaded into the device 100
through the opening 114. The processing units of the device are
preferably arranged along the axis of elongation of the opening
114. This arrangement allows the sample to be moved within the
sample vessel between the processing units of the device 100 in a
manner described in detail below. Preferably, the processing units
are arranged linearly as illustrated in FIG. 7, however, other
arrangement are possible so long as the sample vessel can be
positioned adjacent one or more of the processing units of the
device 100.
[0108] Continuing to refer to FIG. 7, a pair of sample vessel
loading wheels 128 is located at the entrance 130 of the sample
vessel opening 114. The entrance 130 is preferably tapered to
facilitate loading of the sample vessel into the opening 114 of the
device 100. The loading wheels 128 further facilitate loading of
the sample vessel by guiding the sample vessel into the opening
114. A sample collection unit 132 can be positioned proximate the
entrance 130 of the opening 114 to allow a selective volume of the
sample to dispense into the next processing unit or units within
the sample vessel. The sample collection unit 132 can include a
compression member 22 opposed to a stationary member 26 across the
width of the opening 114. A linear motor 138 is coupled to the
compression member 22. The linear motor 138 can operate to move the
compression member 22 toward or away from the stationary member 26
to selectively open and close the opening 114 therebetween. When
the sample vessel is positioned within the opening 114, the linear
motor 138 can operate to compress the sample vessel between the
compression member 22 and the stationary member 26. As a result, a
selective volume of the sample can be moved to the next processing
unit within the sample vessel. Preferably, the sample vessel
remains compressed between the compression member 22 and the
stationary member 26 of the sample collection unit 132 during
processing of the sample by the other processing units to prevent
the sample from exiting the processing unit area during
processing.
[0109] The pretreatment unit 122 is positioned adjacent the initial
sample collection unit 132. Depending on the process being
implemented, the sample may require pretreatment or preparation
before proceeding with additional processing steps. Pretreatment
can include, for example, adding a reagent or other material to the
sample and incubating the mixture for certain time period. The
pretreatment unit 122 of the device 100 allows for any of such
pretreatment steps to be implemented. For PCR testing, the sample
pretreatment unit 122 can provide for nucleic acid extraction from
a biological sample, such as blood. Any known methods for
extracting nucleic acid can be utilized in the pretreatment unit,
including using a cell lysis reagent, boiling the nucleic acid
sample, GITC, or formamide for solubilization. Alternatively,
filters can be used within the sample vessel to separate nucleic
acid from unwanted cellular debris.
[0110] The pretreatment unit 122 can include a compression member
22 and a stationary member 26 opposed to the compression member 26
across the opening 114. The compression member 22 and/or the
stationary member 26 can optionally include an energy transfer
element for transferring energy, e.g. thermal energy, to the sample
within the sample vessel. The energy transfer element can be, for
example, an electronic heat element (such as Kapton heater, a Nomex
heater, a Mica heater, or a silicone rubber heater), a microwave
generator, a light source, an electronic cooling element (such as
Peltier element), an ultrasonic energy transfer element, or any
another device suitable for transferring thermal energy. A driver
24, for example an electromagnetic actuator such as linear stepper
actuator, a relay actuator, or a solenoid, is coupled to the
compression member 22 and operates as a driver. During operation of
the pretreatment unit 122, the driver 24, moves the compression
member 22 to open the opening 114 between the compression member 22
and the stationary member 26 of the pretreatment unit 122 to allow
receipt of a sample vessel. After a sample vessel is loaded, the
driver 24 drives the compression member 22 toward the stationary
member 26, resulting in good surface contact between the sample
vessel and the compression member and the stationary member and
thus improved pretreatment. Once the pretreatment is completed, the
driver 24 moves the compression member 22 of the pretreatment unit
122 to further compress the pretreatment segment of the sample
vessel to move a selective amount of pretreated sample within the
sample vessel to the next processing unit.
[0111] The reaction unit 124 can include a plurality of processing
stations 150A-150C and is preferably positioned adjacent the
pretreatment unit 122. The reaction unit 124 can effect thermal
cycling of the sample by selectively moving the sample, with the
sample vessel, between the processing stations 150A-150C. The
phrase "thermal cycling" as used herein refers to a process of
heating and/or cooling a sample in two or more steps, with each
step preferably occurring at a different temperature range from the
previous step. Each of the processing stations 150A-150C can be
maintained at a pre-selected temperature range controlled by a
temperature control system 152 and a CPU 174. Although the
exemplary embodiment includes three thermal cycling processing
stations 150A-150C, the reaction unit 124 can include any number of
processing stations 150, depending on the thermal cycling process
employed. Alternatively, the reaction unit 124 can incubate a
sample at a selective temperature for an isothermal reaction such
as for TMA or SDA process.
[0112] In PCR based testing, thermal cycling can be used to
denature, anneal, elongate and thereby amplify the nucleic acid
sample. The PCR thermal cycling steps each occur at specified
temperature ranges. Denaturing occurs at approximately 92.degree.
C.-96.degree. C.; elongation occurs at approximately 70.degree.
C.-76.degree. C.; and annealing occurs at approximately 48.degree.
C.-68.degree. C. Each of the PCR thermal cycling steps, i.e.
denaturing, annealing, and elongation, can be carried out
independently at a separate processing station of the reaction unit
124 by maintaining the processing stations at the temperature
ranges effective for carrying out each of the PCR thermal cycling
steps. For example, the denaturing step can be carried out at
processing station 150A, the elongation step at processing station
150B, and the annealing step at processing station 150C.
Alternatively, one or more of the PCR thermal cycling steps can be
combined and carried out at the same processing station, thereby
reducing the number of processing stations required. For example,
denaturing can be carried out at processing station 150A and
elongation and annealing can be carried out at processing station
150B, thus, eliminating the need for a third processing
station.
[0113] Moreover, a processing station can be provided within the
reaction unit 122 for cooling of the sample by using a thermal
energy element, a Peltier thermal electric element for example, to
transfer thermal energy from the processing station. In PCR
processing, for example, a processing station can be provided to
preserve the nucleic acid sample between process steps by cooling
the sample to a refrigeration temperature, e.g., 4.degree. C.
Additionally, a processing station can optionally be provided to
cool the sample between thermal cycling steps to decrease the
temperature down ramping time between successive thermal cycling
steps. For example, as denaturing generally occurs at 92.degree.
C.-96.degree. C. and annealing generally occurs at a significantly
lower temperature, e.g., 48.degree. C.-68.degree. C., the sample
can be cooled after denaturing in a cooling processing station,
preferably at a temperature lower than the annealing temperature,
to bring the sample temperature more quickly into the annealing
temperature range. A thermal cycling processing station can
optionally include a heat sink 166 coupled to either the
compression member 22 or the stationary member 26 to conduct heat
away from the station and radiate the heat to the environment.
[0114] Each of the illustrated processing stations of the reaction
unit 124 includes a compression member 22 and a stationary member
26. The compression member 22 of each thermal cycling processing
unit can be coupled to a driver 24 for selectively moving the
compression member 22 toward and away from the stationary member
26. As discussed above, the drivers 24 can be any device capable of
imparting motion, preferably reciprocal motion, to the compression
members. A driver control system 160 is coupled to the drivers 24
to control the operation of the drivers 24. In one preferred
embodiment illustrated in FIG. 7, the drivers 24 are
electromagnetic actuators coupled to the driver control system 160,
which can be, for example, a control system for controlling the
reciprocal motion of the actuators. Alternative drivers,
compression members and stationary members are described below in
connection with FIGS. 8-12. The driver control system 160 is
coupled to the CPU 174 such that the sample incubation time period,
the pressure and the sample moving speed within the sample vessel
can be controlled and coordinated by the CPU 174 to achieve the
best reaction results.
[0115] Each of the thermal cycling processing station 150A-150C can
optionally include an energy transfer element for transferring
energy, such as thermal energy, to the sample within the sample
vessel. The energy transfer elements can be, for example, an
electronic heat element, a microwave generator, a light source, an
electronic cooling element, or any another device suitable for
applying thermal energy. Each of the energy transfer elements is
coupled to the temperature control system 152 to maintain the
associated processing station within a selected temperature range.
One or more temperature sensors, coupled to the temperature control
system 152, can be positioned proximate the processing stations
150A-150C to monitor the temperature of the stations.
[0116] Between two adjacent processing units or two adjacent
processing stations, at least one layer of energy insulator 146 can
optionally be provided to insulate the processing unit or the
processing station from adjacent units or stations. An energy
insulator layer can also be formed on the boundary of a processing
station to prevent energy transfer to or from the environment. The
energy insulator 146 can be, for example, an energy shielding
layer, an energy absorption layer, an energy refraction layer, or a
thermal insulator, depending on the type of energy transfer element
employed. A thermal insulator can be constructed from a low thermal
conductivity material such as certain ceramics or plastics. In one
embodiment, the thermal insulator can be attached to the
compression members and the stationary members. Alternatively, the
thermal insulators can be separate from the compression members and
stationary members and can be controlled independently by a driver
to open and close the opening 114. In this embodiment, all the
compression members and insulators can open initially to allow
loading of the sample vessel, and then, the thermal insulators can
compress the sample vessel within the opening to close the vessel
and form separate segments within the sample vessel. Additionally,
a spring element or other biasing mechanism can be optionally
utilized to bias each thermal insulator. Through the spring
element, a driver associated with one of the thermal insulators can
apply sufficient pressure on the thermal insulator to minimize the
quantity of sample remaining in the junction between adjacent
processing stations during an incubation period, while still
allowing sample flow through the thermal insulator when a higher
pressure is applied to the sample in an adjacent processing
station. This design simplifies the operation of multiple thermal
insulators.
[0117] In an alternative embodiment, the processing stations can be
spaced apart to inhibit conductive heat transfer between adjacent
processing stations and, thereby, eliminate the need for insulators
between the stations.
[0118] Operation of the thermal cycling reaction unit 124 will be
generally described with reference to FIGS. 13A-13G. The thermal
cycling process begins by opening each of the processing stations,
e.g. first processing station 150A, second processing station 150B,
and third processing station 150C, to receive the sample vessel
within the opening 114, as illustrated in FIG. 13A. After the
sample vessel is loaded with pretreated sample material, or the
pretreated sample is dispensed from pretreatment unit 122 into the
reaction unit 124, the second processing station 150B and the third
processing station 150C are closed by moving the compression member
22B and the compression member 22C of each station toward the
respective stationary member 26B and 26C, as illustrated in FIG.
13B. As the second processing station 150B and the third processing
station 150C are closed, the sample vessel is compressed between
the compression member and the stationary member, displacing the
sample within the sample vessel into a segment of the sample vessel
adjacent the first processing station 150A.
[0119] Next, the compression member 22A and the insulator 146A can
compress the sample vessel to adjust the sample volume contained
within the segment of the sample vessel adjacent the first
processing station 150A, as well as the surface area to volume
ratio of the segment. The insulator 146A can then be closed to seal
the sample in the first processing station 150A, as illustrated in
FIG. 13C. Alternatively, if the device 100 is provided with a
sample pretreatment unit, the sample pretreatment unit can function
to close the sample vessel within the first processing station
150A. Other alternatives include pre-sealing the sample vessel
after loading a sample, or providing the sample vessel with
pressure gates, discussed below, formed between adjacent reaction
zones. Once the sample is sealed within the first processing
station 150A, the sample can be heated or cooled by the first
processing station 150A. In PCR thermal cycling, for example, the
sample can be heated to a temperature effective to denature the
nucleic acid sample. Preferably, the sample vessel is pressed into
contact with the compression member 22A and the stationary member
26A by the compression member 22A to flatten the sample vessel and
to ensure good thermal contact between the sample vessel and the
compression member 22A and the stationary member 26A. The
compression member 22A can also optionally periodically squeeze the
sample vessel to agitate the sample and to generate sample flow in
the segment of the sample vessel during the reaction period to
speed up the reaction.
[0120] After a predetermined period, the second processing station
150B can be opened to allow the sample to move into the second
processing station 150B, as illustrated in FIG. 13D. Next, the
first processing station 150A closes, compressing the sample vessel
and moving the entire sample, within the vessel 16, into a segment
of the sample vessel adjacent the second processing station 150B,
as illustrated in FIG. 13E. The third processing station 150C can
then open to allow the sample to move into the segment of the
sample vessel adjacent the third processing station 150C, as
illustrated in FIG. 13F. The second processing station 150B closes,
compressing the sample vessel and moving the sample completely into
the segment of the sample vessel adjacent the third processing
station 150C, as illustrated in FIG. 13G. The sample can then be
heated or cooled by the third processing station 150C for a set
time period. In PCR thermal cycling for example, the sample can be
heated to a temperature effective to anneal the nucleic acid sample
in the third processing station 150C. The heat sink 166 can
facilitate the temperature transition from the denaturing
temperature of the first processing station 150A to the annealing
temperature of the third processing station 150C by dissipating
excess heat to the environment. Thus, the sample can be moved from
the denaturing step at the first processing station to the
annealing step at the third processing station.
[0121] After a predetermined time period, the second processing
station 150B opens to allow the sample to move into the second
processing station, as illustrated in FIG. 13F. The third
processing station 150C then closes, compressing the sample vessel
16 and moving the sample entirely into the segment of the sample
vessel adjacent the second processing station 150B, as illustrated
in FIG. 13E. The sample can then be heated or cooled by the second
processing station 150B for a set time period. In PCR thermal
cycling for example, the sample can be heated to a temperature
effective to elongate the nucleic acid sample. Upon conclusion of
the elongation step, the sample can be returned to the segment of
the sample vessel adjacent the first processing station 150A to
repeat the cycle, i.e., denaturing and annealing and elongating or,
the sample can be moved to a segment of the sample vessel adjacent
the sample detection unit 126 if PCR thermal cycling is
completed.
[0122] The illustrated thermal cycling reaction unit 124 provides
denaturing in the first processing station 150A, annealing in the
third processing station 150C, and elongation in the second
processing station 150B, as this arrangement is deemed
thermodynamically efficient. One skilled in the art will
appreciate, however, that the PCR thermal cycling steps can occur
in any of the processing stations without departing from the scope
of the present invention.
[0123] Sample thermal cycling using the reaction unit 124 of the
present invention results in faster thermal cycling times and lower
energy consumption compared to conventional thermal cycling
devices. Sample vessel shape alteration, i.e. flattening, by the
reaction unit 124 results in significant increases in the
surface/volume ratio and sample vessel contact with the members of
the reaction unit. This allows the processing stations of the
reaction unit 124 to heat the sample more directly, increasing the
sample temperature ramping rate and avoiding unnecessary
temperature ramping of the members and thus decreasing the amount
of energy consumed. Equally important is that sample vessel shape
alteration provides for the uniform transfer of thermal energy to
the sample, dramatically reducing reaction mixture temperature
gradients. The reaction unit 124 further allows the use of fluid
flow to mix the sample as the sample is moved from one processing
station to another.
[0124] Moreover, the reaction unit 124 allows the use of a
disposable, single-use sample vessel that minimizes contamination
of the sample, contamination of the reaction unit and exposure of
the operator to biohazards. Additionally, the reaction unit 124
does not require a fluid handling system, as the sample can be
moved within the sample vessel during processing.
[0125] Referring again to FIG. 7, the reaction unit 124 can
optionally include a reaction sensor 168 for monitoring the
reaction in real-time within the reaction unit 124 by analyzing the
sample, including any reaction products from the reaction with the
sample. The reaction sensor 168 can include an integral light
source 169 for applying excitation energy to the sample within the
sample vessel. Alternatively, a light source, or other source of
excitation energy, can be provided separate from the reaction
sensor 168. The reaction sensor 168 can be an optical sensor for
measuring light, for example fluorescent light, emitted from the
sample or from fluorescent probes within the sample. In the case of
PCR, any known real-time PCR detection system can be employed,
including, for example, using fluorescent dyes, such as ethidium
bromide, intercalating into the DNA molecule, using a dual labeled
probe tagged with a reported dye and a quenching dye, or using
hybridization probes, which will result in Fluorescence Resonance
Energy Transfer (FRET) only when the two probes are hybridized and
in close proximity. In each of these approaches, the fluorescence
signal is substantially proportional to the amount of specific DNA
product amplified. The reaction detection sensor 168 is placed to
monitor the fluorescence from the sample, preferably in the
annealing processing station, or other processing stations of the
reaction unit, dependent on the assay selected. Multiple sensors or
a spectrum sensor can be used when detection of multiple wavelength
light is required. The detected signal is then sent to the CPU 174
for further analyzing the amount of product.
[0126] Continuing to refer to FIG. 7, the sample detection or
analysis unit 126 of the device 100 is provided to analyze the
sample after processing by the reaction unit 124. The analysis unit
126 is preferably positioned proximate the reaction unit 124. In
one embodiment of the invention, a source of excitation energy, for
example a light source, can apply excitation energy to the sample
and a signal detector, for example an optical sensor, can detect
light emitted from the sample in response to illumination by the
excitation light. Specific illustrative practices, include
detecting the transmission of light through the sample, detecting
reflected light, detecting scattering light, and detecting emitted
light. The detected light, in the form of the signal output from
the sensor, can be analyzed by a CPU 174 provided in the device
through known signal processing algorithms. Suitable sample
analysis systems, employing a light source and an optical sensor or
sensors, detects signals including light intensity at a given
wavelength, phase or spectrum of the light, as well as location of
the signal. For example, the flow induced testing system described
in U.S. Pat. No. 6,318,191 and the multi-layer testing system
described in U.S. Pat. App. Pub. No. US 2004/0105782 A1, both of
which are incorporated herein by reference, describe suitable
sample analysis systems.
[0127] In the case of a PCR based assay, gel electrophoresis or
capillary electrophoresis can be employed to analyze the nucleic
acid sample, as illustrated in FIGS. 7 and 14. Suitable nucleic
acid sizing gels include agarose and polyacrylamide. The gel 184
can be introduced to the sample vessel 16 during processing or,
preferably, is pre-loaded into an analysis segment 210 of the
sample vessel, as discussed in more detail below. The exemplary
analysis unit 126 includes a light source 170 for illuminating the
nucleic acid sample and the gel and an optical sensor 172 in the
form of linear charge coupled device (CCD). Electrode activators
176 operate to insert a positive electrode 180 and a negative
electrode 182 into the sample vessel 16. The positive electrode 180
and the negative electrode 182 are electrically connected to a
voltage source, which creates a voltage difference between the
electrodes. As nucleic acid products are negatively charged, the
nucleic acid products within the sample will move through the gel
184 toward the positive electrode 180. The gel separates the sample
components by size, allowing smaller components, such as nucleic
acid products, to travel faster, and thus, further, than larger
components. A suitable dye or fluorescent tag can be introduced to
gel to identify the nucleic acid products. Light from the light
source 170 can illuminate the dyed or tagged nucleic acid products
in the gel and the optical sensor 172 can then identify the
illuminated nucleic acid products. The output signal of the optical
sensor 172 can be analyzed by CPU 174 according to known signal
processing method to determine the presence, absence, quantity or
other condition of the nucleic acid sample.
[0128] Alternatively, the nucleic acid sample can be analyzed in
accordance with conventional nucleic acid analysis methods, such
as, for example, chemiluminescence, fluorescently labeled primers,
antibody capture, DNA chip, and/or magnetic bead detection
methods.
[0129] One skilled in the art will appreciate that the processing
units and the processing stations of the above-described exemplary
embodiments of the sample processing device of the present
invention can be arranged in any order depending on the sample
being processed and the process being utilized. The sample
processing device of the present invention may include any
combination of the processing units and processing stations
described herein, as well as additional processing units and
processing stations that will be apparent to those skilled in the
art upon reading this disclosure. Moreover, the sample processing
device may include only a single processing unit, such as, for
example, a reaction unit for thermal cycling a sample, or may
include a only a single processing station, such as, for example, a
processing station for displacing a specified volume of reagent or
sample.
[0130] FIGS. 8-12 illustrate alternative embodiments of a reaction
unit 250 for thermal cycling a sample according to the present
invention. The reaction unit 250 can include one or more openings
252 for receiving one or more sample vessels 16. The embodiments
illustrated in FIGS. 8-12 have three openings 252, permitting the
simultaneous thermal cycling of up to three samples. The reaction
unit 250 comprises three processing stations: a first processing
station 254, a second processing station 256, and a third
processing station 258. Thermal insulators 260A-260D are positioned
between the processing stations and at the top of the first
processing station 254 and the bottom of the third processing
station 258.
[0131] Referring specifically to FIGS. 8 and 10, the first
processing station 254, as well as the second and third processing
stations 256 and 258, includes an embedded heat element 262 for
transferring thermal energy to the sample vessel when the sample
vessel is positioned within an opening 252. The heat element 262
can be a Kapton heater, a Nomex heater, a Mica heater, a silicone
rubber heater or any other thermal energy transfer element suitable
for delivering thermal energy. The heat element 262 can be seated
in a recess 264 formed in the processing station 254 and secured to
the processing station by an adhesive or other attachment means.
The heat element 262 of each of the processing stations is
preferably coupled to a temperature controller 266 for controlling
the temperature of the heat element. One or more temperature
sensors 268 can be positioned in the processing station 254 to
measure the temperature of the processing station 254. The
temperature sensor 268 can be coupled to the thermal controller 266
such that the temperature controller 266 can monitor and adjust the
temperature of the processing station in a feedback control
manner.
[0132] Referring to FIGS. 10 and 11, each processing station
comprises a stationary member 270 and a compression member 272
adapted to compress the sample vessel selectively within one or
more of the openings 252 and thereby move the sample within the
sample vessel. The compression member 272 is preferably
complimentary in shape to the stationary member 270 and includes a
plurality of finger-like closure elements or shutters 274 sized and
shaped to slide within the openings 252. Guide rails 276 are
positioned on either side of the compression member. The guide
rails 276 are preferably sized and shaped to fit within grooves 278
formed in the side walls of the stationary member 270. The
combination of the guide rails 276 and the grooves 280 allow the
compression member 272 to reciprocate relative to the stationary
member 270 to selectively open and close the openings 252.
[0133] Each thermal insulator 260 can be configured in a manner
analogous to the processing stations. For example, the thermal
insulator 260B comprises an insulator stationary member 280 and an
insulator compression member 282 adapted to compress a sample
vessel within one or more of the openings 252. The insulator
compression member 282 includes a plurality of finger-like closure
elements or shutters 284 sized and shape to slide within the
openings 252 to selectively open and close the openings 252.
[0134] Each compression member 272 and insulator compression member
282 is coupled to a driver, such as an electromagnetic driver
mechanism, as described above, or any other mechanism for imparting
motion, preferably reciprocating motion, to the compression
members. Each compression member can be coupled to an arm 286 for
providing a connection between the compression member and the
driver, as best illustrated in FIGS. 9-11. In one embodiment,
illustrated in FIG. 10, the arms 286 are hollow tubes that receive
coiled springs 288 and dowels 290. The springs 288 operate to bias
the compression members 272, 282 in a direction away from the
stationary member 270 and the insulator stationary member 280,
respectively. An elastic element, such as the coiled spring used
here, provides a simple mechanism for assisting the driver to
regulate the compressing pressure applied to the sample vessel. The
driver can be a motor 292 for driving a rotating shaft, as best
illustrated in FIG. 8. The rotary motion of the shaft can be
translated to reciprocating motion through cams 294 provided for
each of the compression members 272 and 282. The cams 294 are
coupled to the arms 286. The cams 294 can be configured to
selectively open and close the compression members 272 and 282 in
accordance with conventional cam design methods.
[0135] In one alternative embodiment of the reaction unit, the
compression members 272 and 282 of each of the processing stations
and insulators include holes 296 for receiving a cam 294 and a
linear spring element 298. Spring elements 298 each operate to bias
a respective compression member in a direction away from the
corresponding stationary member. The cams 294, in combination with
the springs 298, act to impart reciprocating motion to the
actuators and regulate the compressing pressure on the sample
vessel.
[0136] FIGS. 19A-19C illustrate a further embodiment of the
reaction unit of the present invention. The reaction unit 350
includes nine openings 352 for receiving up to nine sample vessels
simultaneously. The reaction unit 350 includes three processing
stations: a first processing station 354, a second processing
station 356, and a third processing station 358. Thermal insulators
360A-360D are positioned adjacent each of the processing stations
and at the top of the first processing station 354 and the bottom
of the third processing station. Top thermal insulator 360A and
bottom thermal insulator 360D are movable independent of the first
processing station 354 and the third processing station 358,
respectively. Intermediate thermal insulators 360B and 360C are
coupled to the first processing station 354 and the second
processing station 356, respectively.
[0137] Each processing station comprises a stationary member 370
and a complementary compression member 372 adapted to compress the
sample vessel selectively within one or more of the openings 352
and thereby move the sample within the sample vessel. Each
stationary member 370 has a projection 374 aligned with one of the
openings 352. The compression members 372 are each provided with a
projection 376, positioned on an opposite side of the opening 352.
When a compression member 372 is slid on the corresponding
stationary member 370, the projections 374 and 376 engage and close
the openings 352 therebetween.
[0138] Each compression member 372, as well as intermediate thermal
insulators 360B and 360C, include an arm 380 coupled by a cam 384
to a rotary shaft 382. A stationary insulator member 362 is
coupled, and aligned with an edge of each opening 352 on each
stationary member 370. Each stationary insulator member 362 is
inserted in each of the openings of a movable insulator compression
member 360 to react to compression and open or close the opening.
The shaft 382 is rotated by a stepper motor or a servo motor 386.
The cams 384 translate the rotation of the shaft 382 into linear
reciprocal motion, which is imparted to the arms 380 to effect
selective opening and closing of the openings 352 and compression
of the sample vessels therein.
[0139] Each arm 380 includes an inner shaft 390 received within an
outer sleeve 392. A spring 394 is interposed between the inner
shaft 390 and the respective compression member or thermal
insulator. A second spring 396 is positioned on an opposite side of
the respective compression member or thermal insulator. The spring
394 cooperates with the second spring 396 to allow the compression
member or thermal insulator to "float" along the axis of the arm
380. In this manner, the arm 380 can apply sufficient force to the
compression member or thermal insulator to compress the sample
vessel within an opening 352 and, thereby, displace substantially
all of the sample from the compressed portion of the sample vessel.
An increase of pressure within the sample vessel, for example, from
the compression of an adjacent portion of the sample vessel,
however, can cause the sample to displace within the sample vessel
through the compressed portion of the sample vessel, as the springs
394 and 396 will allow small axial movements of the compression
member or thermal insulator.
[0140] Each stationary member 370 and compression member 372 can be
provided with an embedded thermal energy transfer device 398 for
each opening 352 to apply thermal energy to the sample vessel
within the opening 352. In addition, the stationary member 370 and
compression member 372 can include temperature sensors 399
associated with each energy transfer device 398 to monitor the
temperature of the sample vessel.
[0141] FIGS. 15A and 15B illustrate embodiments of a sample vessel
16 according to the present invention. The illustrated sample
vessel 16 is a closed tubule system that provides a disposable,
single use container and reaction vessel for the sample. The sample
vessel 16 can be constructed of a resiliently compressible,
flexible, and ultra-high strength material, such as polyethylene or
polyurethane. The sample vessel 16 can have a seamless, flattenable
cross-sectional profile and thin-walled construction that is
optimized for fast and uniform heat transfer, for maximum surface
contact with the sample, and for high pressure resistance.
Preferably, the walls are constructed to converge when the sample
vessel is compressed in a direction perpendicular to the
longitudinal axis of the sample vessel such that the volume of the
compressed portion of the sample vessel decreases and the ratio of
the surface area to the volume of the compressed portion increases,
without fracturing of the sample vessel. In one illustrative
preferred practice, the walls of the sample vessel 16 have a wall
thickness of approximately 0.01 mm to 0.5 mm. Experimental results
indicate that constructing a sample vessel having a wall thickness
within this preferred range significantly increases the efficiency
of heat transfer to the sample. In an alternative embodiment, a
two-layer wall structure can be used, with the inner layer
providing bio-compatibility, using material such as polyethylene or
polyurethane, and the outer layer providing lower permeability,
using material such as high density polyethylene or aluminum foil.
In addition, the material selected to construct the portions of the
wall of the sample vessel, such as a detection segment of the
sample vessel 16, can be optically transmissive over a selected
wavelength range to facilitate optical analysis of the sample
within the sample vessel.
[0142] The sample vessel 16 can be divided into multiple segments
by one or more pressure gates 32. In the case of PCR testing, for
example, the sample vessel can be divided into a sample collection
segment 205, a sample pretreatment segment 206, a sample reaction
segment 208, and a sample analysis segment 210. The illustrated
pressure gates 32 are internal to the tubule structure of the
vessel 16 and provide a fluid tight seal between the segments of
the sample vessel 16, under normal operating conditions.
Preferably, the pressure gates 32 open upon the application of
pressure greater than a certain value, for example, approximately 3
atmospheres. When external pressure is provided to one segment, the
pressure gate 32 can open, allowing the sample to flow from the
high pressure compartment to the low pressure compartment.
[0143] The sample vessel 16 can include a handling portion having a
generally rigid construction to facilitate handling of the sample
vessel. The handling portion can be coupled to one or more of the
segments of the sample vessels used to contain the sample. For
example, the handling portion can be a cylindrical sleeve
constructed of a generally rigid material, such as a plastic or a
metal, that is sized and shaped to fit over one or more of the
segment of the sample vessel. In one embodiment, the cylindrical
sleeve can be removable and replaceable. Alternatively, the
handling portion can be a rigid segment, such as a rigid ring,
positioned at an end of the sample vessel or between two segments
of the sample vessel. In the embodiments illustrated FIGS. 15A and
15B, the handling portion is a segment of the sample vessel having
an increased wall thickness. For example, the sample collection
segment 205 and the sample pretreatment segment 206 have a wall
thickness greater than the wall thickness of the reaction segment
208. The increased wall thickness provides sufficient rigidity to
the sample collection segment 205 and the sample pretreatment
segment 206 to facilitate handling of the sample vessel 16. In one
embodiment, the wall thickness of the handling portion is greater
than 0.3 mm.
[0144] The sample vessel 16 can include an instrument, such as a
sampling pipette or a needle 107, for direct collection of the
sample to be treated and analyzed within the sample vessel 16, as
illustrated in FIG. 15A. The needle 207 can be positioned at one
end of the sample vessel 16 and can be connected to the sample
collection chamber 205 through a conduit 209 formed in the wall of
the sample vessel 16. A needle cover 211 can be provided to secure
the needle 207 prior to and after use. The needle cover 211 can be,
for example, a penetrable rubber cover or a removable plastic
cover.
[0145] In another embodiment, illustrated in FIG. 15B, a sampling
instrument 214, such as a pipette, a stick, or a tweezer, can be
coupled to a cover 212 that selectively closes the conduit or
opening 209 formed in the wall of the sample vessel. The cover 212
can include a reservoir 216 for containing a reagent and a sample
during sampling. For sampling, the cover 212 can be removed from
the sample vessel to expose the sampling instrument 214. The
sampling instrument 214 can be used to collect the sample, by
pipetting, swabbing, or gathering the sample, for example, and then
the sampling instrument 214 can be inserted into the sample
collection segment 205 through the conduit 209. The sample can then
be introduced to the sample collection segment 205 by compressing
the cover 216 to displace the sample from the reservoir 216.
Alternatively, the sample can be introduced to the sample
collection segment 205 or to another segment of the sample vessel,
depending of the segments present in the sample vessel, after
collection by a separate instrument.
[0146] Sample vessel 16 can be particularly suited for PCR testing
using the sample processing device of the present invention, as
described above. For example, nucleic acid extraction can be
performed within the sample pretreatment segment 206 of such a
sample vessel 16. A cell lyses reagent, for example,
GENERELEASER.RTM. from Bioventures, Release-IT.TM. from CPG
Biotech, or Lyse-N-Go.TM. from Pierce, or other extraction reagents
can be introduced to the pretreatment segment 206 to extract
nucleic acid from the initial sample. Extraction reagents can be
stored within the pretreatment segment 206 or can be delivered to
the segment. Additionally, one or more filters can be positioned
within the pretreatment segment 206 of the sample vessel to
separate nucleic acid from unwanted cellular debris.
[0147] After incubation of the sample for certain time period, a
portion of pretreated sample can be moved into the reaction segment
208. For a reaction sample volume of approximately 5 .mu.l-25
.mu.l, a PCR reaction segment 208 of the sample vessel 16 according
to one illustrative practice of the invention has a wall thickness,
indicated by reference character t in FIG. 15A, of approximately
0.01 mm-0.3 mm, a diameter of less than approximately 6 mm, and a
length of less than approximately 30 mm. PCR reagents, such as
nucleotides, oligonucleotides, primers and enzymes, can be
pre-packaged in the reaction segment or reaction segments 206, or
can be delivered, for example, through the walls of the sample
vessel using a needle, using for example, a reagent injector
cartridge described below, before moving the sample into the
segment.
[0148] A pre-packaged reagent storage segment 214 can be used to
stored a pre-packaged reagent. Such a reagent storage segment can
be formed between any two adjacent processing segments and may
store any reagent needed for a reaction. For example, the reagent
storage section 214 can store PCR reagents, while reagent storage
sections 236 and 244, described below, may include detection
reagents. If the reagent storage segment 214 is utilized, the
sample vessel 16 can be compressed at the reagent storage segment
214 to displace the reagent into the pretreatment segment 206.
Alternatively, the sample can be moved from the pretreatment
segment 206, through the reagent storage segment 214 where mixing
with the reagent, to the reaction segment 208.
[0149] A self-sealing injection channel 218 can be formed in the
sample vessel to facilitate delivery of reagent or other materials
to the sample vessel, as illustrated in FIG. 16. The illustrated
self sealing injection channel 218 is normally substantially free
of fluidic material and is capable of fluid communication with the
adjacent segment in the vessel. An injection of reagent through an
injection channel occurs preferably prior to moving any sample into
the segment to avoid contamination. In addition, the sample
treatment devices of the invention can utilize a reaction cartridge
220 with a single or multiple needles 222 in fluid communication
with one or more reservoirs, as illustrated in FIG. 17. The
reaction cartridge 220 can be used to inject or deposit reagent or
other materials, simultaneously, or sequentially into multiple
segments of the sample vessel. Suitable self-sealing injection
channels and reagent cartridges are described in U.S. Pat. No.
6,318,191, incorporated herein by reference.
[0150] One skilled in the art will appreciate that while it may be
preferable for the wall of the sample vessel to be uniform along
the circumference and the longitudinal axis of the vessel, only a
portion of the wall along the circumference and/or the longitudinal
axis of the vessel need be resilient and compressible and have the
preferred thickness to affect flattening of the sample vessel.
Thus, the sample vessel need not have a uniform axial or
circumferential cross-section.
[0151] PCR thermal cycling can be performed in the reaction segment
208 of the sample vessel 16. The thin walled, compressible
construction of the sample vessel 16 greatly improves the rate and
efficiency of thermal cycling. The construction of the sample
vessel allows the vessel to deform or flatten readily, increasing
thermal contact with the reaction unit of the device 10 and
increasing surface/volume ratio of the sample within the sample
vessel. As a result, the reaction mixture ramping rate is increased
and thermal energy is more uniformly transferred to the sample.
[0152] PCR analysis can be performed in the sample vessel 16. For
example, real-time detection methods can be used within the
reaction segment 208; gel electrophoresis or other nucleic acid
detection methods can be used within the analysis segment 210 to
analyze the sample. In the case of gel electrophoresis, a gel can
be introduced to the analysis segment 210 to facilitate gel
electrophoresis, as described above in connection with FIG. 14.
[0153] In one preferred embodiment, illustrated in FIG. 15A, the
analysis segment 210 is divided into two electrophoresis
capillaries, namely, a sample capillary 230 and a control capillary
232, by a diametrically-central divider 234. Pressure gates 32 at
either end of the capillaries control the movement of the sample
and the reagents into both capillaries. Each capillary is filled
with an electrophoresis gel such that gel electrophoresis can be
performed simultaneously in both capillaries. A pair of electrodes
240, for both capillary 230 and 232, can be positioned within the
walls of the sample vessel. A reagent storage segment 236 can be
provided at the proximal end of the sample capillary 230 for
storing reagent within the sample vessel prior to the sample
entering the sample capillary 230. A control material can be stored
in a control storage segment 242 positioned at the proximal end of
the control capillary 232. A reagent can be stored in a reagent
segment 244 positioned at the distal end of the capillaries and in
communication with both the sample capillary 230 and the control
capillary 232 for detection or display signal. The presence of the
control capillary 232 facilitates detection and analysis of the
sample by providing a basis of comparison for the sample
analysis.
[0154] One skilled in the art will appreciate that the number of
segments within the sample vessel is dependent upon the sample
being processed and the processing methods being employed. For
example, in the case of PCR testing, the number of segments within
the sample vessel can be three or more. Alternatively, thermal
cycling and analysis may be performed in one segment, reducing the
number of segments to two. In certain cases, an isothermal nucleic
acid amplification method, for example, only one segment may be
necessary.
[0155] FIG. 18 illustrates a sample vessel 416 particularly suited
for use in a multi-opening sample processing device such as, for
example, the sample processing device illustrated in FIG. 6. The
sample vessel 416 includes an opening 420 for receiving the sample,
a cap or closure 424 for selectively closing and sealing the
opening 420, and a sample containing portion 426 within which the
sample can be treated. The opening 420 is formed in a handling
portion 428 that is preferably constructed of a generally rigid or
semi-rigid material, such as plastic or metal, to facilitate
handling of the sample vessel 416. The handling portion 428
includes a collar 430 against which the cap 424 seats. Sample
material can be introduced into the sample containing portion 426
of the sample vessel 416 through the opening 420. The collar 428
preferable tapers from a larger diameter to the smaller diameter of
the sample containing portion 426. The sample containing portion
426 is preferable constructed of a resiliently compressible,
flexible, and ultra-high strength material, such as polyethylene or
polyurethane. The sample containing portion 426 can have a
seamless, flattenable cross-section profile and thin-walled
construction that is optimized for fast and uniform heat transfer,
for maximum surface contact with the sample, and for high pressure
resistance. In accordance with one embodiment, the sample
containing portion 426 has a wall thickness of approximately 0.01
mm-0.3 mm. Preferably, the sample containing portion 426 of the
sample vessel 416 is in a flattened state prior to introduction of
the sample. Introduction of the sample to the sample containing
portion 426 will cause the walls of the sample containing portion
to separate and the volume of the sample containing portion to
increase. Compression of a selected portion of the sample
containing portion 426 can cause the sample to displace to another
portion within the sample containing portion along the length of
the sample vessel. The surface of the sample vessel can be
chemically treated to reduce a surface effect on the reaction.
[0156] The embodiments of the sample vessel described herein in
connection with FIGS. 14-16 and 18, are not limited to use with the
embodiments of the sample processing device described herein. The
sample vessel of the present invention may be used with any sample
testing or processing system. Likewise, the sample processing
device of the present invention is not limited to use with the
sample vessels described herein. Other sample vessels may be used
without departing from the scope of the present invention.
[0157] Certain changes may be made in the above constructions
without departing from the scope of the invention. It is intended
that all matter contained in the above description or shown in the
accompanying drawings be interpreted as illustrative and not in a
limiting sense.
[0158] The present disclosure is also directed to sample vessels
that may be utilized to collect and process one or more samples in
a closed system. Exemplary samples that may be collected,
processed, or otherwise contained by the sample vessels disclosed
herein include biological samples, such as blood, urine, saliva,
tissue, cell suspensions, microbial organisms, viruses, nucleic
acids, and oligonucleotides samples; soil; water; and any other
sample materials that may be assayed using known assays. The term
"collection" as used herein generally refers to the extraction or
gathering of the sample from a sample source, the subsequent
transfer of the sample into the sample vessel, or the combination
of extraction and subsequent transferring of the sample into the
sample vessel. Exemplary sample gathering may include pipetting,
biopsying, swabbing, drawing a fluid sample or other methods for
extracting a sample from a sample source. Exemplary sample sources
may include humans or other animals, plants, water sources, cell
cultures, food, other sample vessels, and chemical and biological
assays. Sample sources may also include interim storage media, for
example, test tubes, syringes, absorbent applicators and other
interim storage media for containing a sample of interest. The term
"processing" as used herein generally refers to the preparation,
treatment, analysis, and/or the performance of other testing
protocols or assays on a content of the sample vessel in one or
more steps. Exemplary processing steps include, for example:
displacing a content, e.g., the sample or a reagent, of the sample
vessel within the sample vessel to, for example, adjust the volume
of the content, separate content components, mix contents within
the sample vessel; effecting a chemical or biological reaction
within a segment of the sample vessel by, for example, introducing
a reagent to the sample, agitating the sample, transferring thermal
energy to or from the sample, incubating the sample at a specified
temperature, amplifying components of the sample, extracting,
separating and/or isolating components of the sample; or analyzing
the sample to determine a characteristic of the sample, such as,
for example, the quantity, count, volume, mass, concentration, or
expression level of a molecule, a target, a content, a marker or an
analyte, binding activity, nucleic acid sequence, or nucleic acid
size or other analyte size, of the sample. One skilled in the art
will appreciate that the forgoing exemplary processing steps are
described herein for illustrative purposes only. Other processing
steps may be employed without departing from the scope of the
present disclosure.
[0159] FIGS. 20A-20C illustrate an exemplary embodiment of a sample
vessel 1000 for collecting and processing one or more samples. The
illustrated sample vessel 1000 comprises a tubule 1200 that
provides a disposable, single use container and collection and
processing vessel for the sample. The tubule 1200 may be
constructed from any biocompatible material and may be manufactured
by injection molding, insert molding, dip molding, blow-molding,
extrusion, co-extrusion, lamination, assembling from a sheet
material, or other processes generally used to manufacture medical
devices and implants. The tubule 1200 may receive sample in solid
or liquid form and, in certain embodiments, may be sized to collect
and/or process sample volumes in the range of 2 microliters to 2000
microliters.
[0160] The tubule 1200 may be used with any known sample testing or
processing system, including, for example, the systems described in
U.S. Pat. No. 6,318,191, U.S. patent application Ser. No.
10/605,459, filed Sep. 30, 2003, which is a continuation of U.S.
patent application Ser. No. 09/339,055, abandoned, and U.S. Pat.
No. 6,780,617. Each of the aforementioned patents and patents
applications is incorporated herein by reference.
[0161] In the exemplary embodiment illustrated in FIGS. 20 and 21,
the tubule 1200 may include an opening 1400 for receiving a volume
of sample material. The tubule 1200 may include a compressible
segment 1600 having a wall 1800 constructed at least partially from
a material having sufficient flexibility to permit compression of
the opposed segments of the wall 1800 into contact. For example,
the wall 1800 may be constructed to converge when the compressible
segment 1600 of the tubule 1200 is compressed in a direction
perpendicular to the longitudinal axis of the tubule such that the
volume of the compressed segment 1600 of the tubule 1200 decreases,
without fracturing of the sample vessel. The walls 1800 of the
compressible segment 1600 may be constructed of a resiliently
compressible, flexible, and ultra-high strength material, such as
polyethylene, polyurethane, polyvinyl chloride, polypropylene, or
any other plastic material suitable for biomedical or chemical
assaying applications. In one illustrative embodiment, the walls
1800 of the compressible segment 1600 have a wall thickness of
approximately 0.01 mm to 0.5 mm. Experimental results indicate that
constructing a compressible segment of a tubule having a wall
thickness within this range significantly increases the efficiency
of sample processing, such as heat transfer to the sample and
sample transfer between the segments, and detection. In the
illustrated embodiment, the compressible segment 1600 of tubule
1200 extends the entire length of the tubule 1200. Alternatively,
as discussed below, the tubule 1200 may include one or more
discrete compressible segment 1600 spaced apart from one or more
segments having different (e.g., non-flexible) properties.
[0162] In other exemplary embodiments, the tubule 1200 may comprise
a multi-layer wall structure. For example, the tubule 1200 may
include an inner layer providing bio-compatibility, using material
such as polyethylene or polyurethane, and an outer layer providing
lower permeability, using material such as high density
polyethylene or a metal foil, such as aluminum foil or a metal
deposition. One skilled in the art will appreciate that one or more
additional layers may also be employed, depending on, for example,
the sample type, the reagent(s) employed, and the assay(s) being
performed.
[0163] The material selected to construct portions of the wall of
the tubule 1200, for example an optional detection segment of the
tubule 1200, can be optically transmissive over a selected
wavelength range to facilitate optical analysis of the sample
within the tubule 1200.
[0164] The sample vessel 1000 of the exemplary embodiment
illustrated in FIGS. 20A-20C may comprise a general rigid container
2000 for receiving all or at least a portion of the tubule 1200. In
the illustrated embodiment, the container 2000 is sized to receive
the complete length of the tubule 1200. The container 2000 may be
constructed of a material having increased rigidity compared to the
material of the tubule 1200 to facilitate handling of the tubule
1200. In certain embodiments, the container 2000 may be constructed
of a material having a lower permeability than the material of the
tubule 1200. In the illustrated embodiment, the container 2000 is a
glass vacuum tube. Suitable glass vacuum tubes are available under
the trademark VACUTAINER.RTM. from Becton-Dickenson. The sample
vessel 1000 can be used in a manner similar to a glass vacuum tube
to collect a sample, such as a blood sample. A container 2000 may
be optionally used with any of the tubule embodiments disclosed
herein.
[0165] The sample vessel 1000 may comprise an interface 3000 that
is in fluid communication with the opening 1400 in the tubule 1200.
The interface 3000 may permit collection of the sample within the
tubule 1200 by facilitating delivery of the sample material to the
tubule 1200 through the opening 1400. In certain exemplary
embodiments, the interface 3000 may include an instrument for
collecting the sample form a sample source. In the exemplary
embodiment illustrated in FIGS. 20A and 20B, the interface 3000 is
a stopper 3200 that may be coupled to the tubule 1200 and may
selectively seal the opening 1400 in the tubule 1200 to facilitate
collection of the sample from a separate instrument. In the
exemplary embodiment, the stopper 3200 is removably and replaceably
connected to the rigid container 2000 and seals an opening 2200 in
the container 2000. The stopper 3200 may include a first annular
portion 3400 having an opening 3600 sized and shaped to receive the
tubule 1200 in a fluid tight relationship. The first annular
portion 3400 is further sized and shaped to engage the walls of the
container in a fluid tight relationship. The stopper 3200 may
include a second annular portion 3800 that has a diameter greater
than the diameter of both the first annular portion 3400 and the
container 2000. The opening 3600 extends through the second annular
portion 38 to form an interface channel 3700. A penetrable,
self-sealing portion 4000, such as a self-sealing membrane, may be
provided to selectively seal the opening 3600 and, thus, permit
selective transfer of the sample (from, for example, the sample
collection instrument) through the interface channel 3700 into the
tubule 1200. The self-sealing portion 4000 may be constructed of
any biocompatible, resilient, self-sealing material that can be
penetrated by a needle or other sample collection instrument.
Suitable materials may include rubber and silicon. In certain
embodiments, the stopper 3200 may be constructed completely from a
biocompatible, resilient, self-sealing material such as rubber or
an elastomeric polymer. The interface channel 3700 may taper or
otherwise narrow through the cross-section of the stopper 3200 to
provide a guide for a needle or other instrument transferring the
sample to the tubule 1200.
[0166] Alternatively, the interface 3000 may include other
mechanisms for selectively sealing the opening 1400 in the tubule
1200. For example, the interface may include a self-sealing
elastomeric duckbill closure. Alternatively, the interface 3000 may
include a valve for selectively closing and opening the interface
channel 3700.
[0167] The sample vessel 1000 may include a clamp 5000 for
compressing the compressible segment 1800 of the tubule to adjust
the volume of the tubule 1200. The clamp 5000 may be configured to
compress opposing wall portions of the compressible section 1600
into contact thereby dividing the tubule 1200 into two segments,
1600A and 1600B, as best illustrated in FIG. 20B. When the clamp
5000 is employed, the segment 1600A remains in fluid communication
with the interface channel 3700 and segment 1600B is sealed from
segment 1600A by the clamp 5000. Once the sample is delivered to
the segment 1600A of the tubule 1200, the clamp 5000 may be
removed, providing additional volume in the tubule 1200 that may
permit future segmentation of the tubule and displacement of the
sample within the tubule 1200 by compression of the tubule
1200.
[0168] The clamp 5000 may be positioned at any location along the
longitudinal axis of the tubule 1200. Additional clamps may also be
employed to divide the tubule into additional segments. In
illustrated exemplary embodiment, the clamp 5000 is disk-shaped and
includes a radial slot 5200 that is sized to receive the tubule
1800 in a compressed state. One skilled in the art will appreciate
that other devices may used to compress and, thereby, divide the
tubule 1200.
[0169] In certain exemplary embodiments, the tubule 1200 may be
wholly or partially evacuated to place the lumen 4200 of the tubule
1200 under negative pressure, e.g., at a pressure less than
atmospheric pressure, to facilitate fluid flow into the tubule
1200. Negative pressure can be generated by, for example,
compressing the tubule 1200 to collapse the lumen 4200. An
apparatus suitable for compressing the tubule is illustrated in
FIGS. 36A-36C, described below. Alternatively the tubule 1200 may
be compressed by hand. The tubule 1200 may also be manufactured to
include a negative pressure.
[0170] In certain embodiments, the container 2000 may be wholly or
partially evacuated to a negative pressure. For example, the
container 2000 may be evacuated to inhibit loss of negative
pressure within the tubule 1200 and to hold the shape of the tubule
1200 during storage.
[0171] A reagent may be pre-packaged in the tubule 1200 or can be
introduced to the tubule 1200 after the sample is introduced to the
tubule 1200. For example, a reagent can be introduced using a
reagent injector cartridge associated with the sample processing
system, by a needle, or by another device capable of fluid
communication with the tubule 1200. The reagent can be, for
example, an anticoagulant, a cell lyses reagent, a nucleotide, an
enzyme, a DNA polymerase, a template DNA, an oligonucleotide, a
primer, an antigen, an antibody, a dye, a marker, a molecular
probe, a buffer, or a detection material. The reagent can be in
liquid or solid form. In the case of a solid reagent, the reagent
may be coated onto the walls of the tubule 1200.
[0172] In certain exemplary embodiments, the interface 3000 may
include one or more chambers 44 that are in fluid communication
with the tubule 1200 to selectively receive a volume of fluid, such
as the sample material or a reagent, from the tubule 1200. In
certain exemplary embodiments, the chamber 4400 may be evacuated or
constructed to have a substantially small initial volume and may be
expendable when receiving fluid. The chamber 4400 can be used as a
waste container to receive and store overflow sample, wash buffer,
or reaction mixture during the sample processing. For example,
compressing a segment of the tubule 1200 may move a portion of the
sample to the chamber 4400.
[0173] In the exemplary embodiment illustrated in FIGS. 21A-21C,
for example, the stopper 3200 includes an annular chamber 4400 that
is in fluid communication with the interface channel 3700 in the
stopper 3200, and, thus, the tubule 1200, through a pressure gate
4800. In certain embodiments described herein, one or more pressure
gates may be employed to selectively control the flow of fluid
between segments, lumens, and other portions of the tubule, as well
as between the tubule and external devices. For example, the
illustrated pressure gate 4800 provides a fluid tight seal between
the chamber 4400 and the interface channel 3700 under normal
operating conditions. The pressure gate 4800 may open upon the
application of a fluid pressure greater than a certain threshold
pressure, for example, approximately 3 atmospheres. When a fluid
pressure equal to or greater than the threshold pressure is applied
to the pressure gate 4800, the pressure gate 4800 can open,
allowing the sample or a reagent to flow from the high-pressure
compartment, e.g., from the tubule 1200 or from the chamber 4400,
to the low-pressure compartment. In certain embodiments, the
pressure gate may be reversible, i.e., the pressure gate may be
configured to re-close if the fluid pressure is reduced to value
less than the threshold pressure. In other embodiments, the
pressure gate may be irreversible, i.e., the pressure gate may be
initially closed and may remain open once opened. For example, once
a threshold pressure is exceeded the irreversible pressure gate
remains open, even if the pressure applied to the pressure gate is
reduced to below the threshold pressure. One example of an
irreversible pressure gate is the pressure gate described below in
connection with FIGS. 22A-22B.
[0174] In the illustrated embodiment of FIGS. 21A and 21B, the
pressure gate 4800 is a slit formed in the stopper 3200 between the
interface channel 3700 and the chamber 4400. The material forming
the stopper 3200 may be selected to be sufficiently flexible and
resilient to allow the slit to open at the threshold pressure and
to close at pressures lower than the threshold pressure.
[0175] A label 6000 identifying the sample within the sample vessel
1200 may be attached to the interface 3000, the container 2000, or
the tubule 1200. The label 6000 can be a bar code or other indicia
for identifying the sample.
[0176] FIGS. 22A and 22B illustrate another exemplary embodiment of
a sample vessel 10000. The sample vessel 10000 comprises a tubule
11200, which can be analogous in construction to the tubule 1200,
having a plurality of lumens 14200A and 14200B. The plurality of
lumens 14200A and 14200B can be separated by a pressure gate 148
that permits selective fluid flow between the lumens 14200A and
14200B. FIG. 22A illustrates the pressure gate 14800 in a closed
position and FIG. 22B illustrates the pressure gate in an open
position that permits fluid flow between the lumens.
[0177] In the exemplary embodiment, the lumens 14200A and 14200B
are parallel to each other and extend in a direction generally
parallel to the longitudinal axis of the tubule 1200. One skilled
in the art will appreciate that other lumen orientations are
possible. The lumens 14200A and 14200B may be uniform in size
(e.g., diameter, width, length) and shape or, alternatively, the
lumens 14200A and 14200B may be different in size and shape, as in
the illustrated embodiment. For example, in the illustrated
embodiment, the lumen 14200B has a smaller diameter than the lumen
14200A. Although two lumens are illustrated in the exemplary
embodiment, one skilled in the art will appreciate that the tubule
1200 may be constructed of any number of lumens.
[0178] The pressure gate 14800 in the present embodiment is
coextensive with the lumens 14200A and 14200B, i.e. the pressure
gate 14800 extends along the entire length of the lumens.
Alternatively, the pressure gate 14800 may extend along only a
portion or portions of the lumens, particularly in embodiments in
which the tubule 1200 is segmented into discrete longitudinally
extending segments, as in the case of the embodiment illustrated in
FIGS. 26A-26C. In such embodiments, one or more pressure gates may
be provided between adjacent lumens.
[0179] In the exemplary embodiment, the opposed portions of the
wall 11800 of the tubule 11200 are compressed into contact to form
a longitudinally extending seam 17000 that divides the tubule 11200
into two lumens, lumens 14200A and 14200B. In addition to dividing
the tubule 11200 into multiple lumens, the seam 17000 may further
provide an irreversible pressure gate, pressure gate 14800, between
the lumens 14200A and 14200B. The seam 17000 may be formed by
mechanically clamping or otherwise compressing a cylindrical tubule
or by applying vacuum pressure to the interior of a cylindrical
tubule. Alternatively, the seam 17000 may be formed during
manufacturing of the tubule by, for example, extrusion, molding, or
lamination processes. The opposed wall portions that are compressed
into contact to form the seam 17000, and the pressure gate 14800,
may be bonded together by mechanical or chemical bonding, by
heating sealing, for example, by bringing hot surfaces into contact
with the tubule wall immediately after extrusion, by ultrasonic
welding, by mechanical interlocking, or both other connection
mechanisms, to create the irreversible pressure gate 14800.
[0180] The pressure gate 14800 is initially in a closed
configuration that inhibits fluid flow between the lumens 14200A
and 14200B. The pressure gate 14800 may open by separating the
compressed opposed walls forming the pressure gate 14800. Applying
a threshold pressure to the pressure gate 14800, as described
above, may open the pressure gate 14800. Alternatively, energy may
be applied to the pressure gate 14800 to weaken the bond between
the compressed opposed walls. For example, thermal energy or light,
e.g., ultra-violet light, may be applied to the pressure gate 14800
or to selected portions or all of the tubule 11200. The threshold
pressure and/or the amount energy to open the pressure gate 14800
may vary depending on the type and strength of the bond.
Alternatively, the bond between the compressed opposed wall
portions may be weakened or broken by chemical reaction with
reagent or the sample.
[0181] In certain exemplary embodiments, one or more of the lumens
may include one or more reagents. Reagents may be provided to one
or more lumens prior to sample collection, e.g., one or more
reagents pre-packaged with the tubule, or after sample collection.
In the exemplary embodiment illustrated in FIGS. 22A and 22B, for
example, a reagent may be provided in lumen 14200B. Lumen 14200A
may be utilized for sample collection and processing. Sample
collection may occur with the pressure gate 14800 in a closed
configuration, as illustrated in FIG. 22A. Upon transfer of the
sample to lumen 14200A, the pressure gate 14800 may be opened
automatically due to release of pressure within the lumen 14200A,
or selectively by applying energy to the pressure gate and/or a
threshold fluid pressure. In other embodiments, the lumen 14200A or
14200B may be compress to provide the threshold pressure. Upon
opening the pressure gate 14800, the reagent(s) can mix with and
interact with the sample in the lumen 14200A, as illustrated in
FIG. 22B. Automatic release of the pressure gate 14800 and mixing
of the reagent with the sample may be beneficial in certain
applications, such as the mixing of an anticoagulant with a blood
sample.
[0182] FIG. 23 illustrates another embodiment of a multi-lumen
tubule 11200 that includes three lumens, namely a first lumen
14200A, a second lumen 14200B, and a third lumen 14200C. Each lumen
may be separated a pressure gate 14800, for example, an
irreversible pressure gate, as described above. Each of the lumens
14200A, 14200B, and 14200C may be provided with one or more
reagents and/or may be used for sample collection and processing.
For example, second lumen 14200B may be provided with one or more
prepackaged reagents and first lumen 14200A may be used for sample
collection and processing. Upon sample collection in first lumen
14200A, pressure gate 14800A may be opened allowing fluid
communication between the second lumen 14200B and the first lumen
14200B. FIG. 23 illustrates the pressure gate 14800A in an open
configuration. Lumen 14200C may be utilized as an injection channel
for receiving one or more reagents, typically, but not necessarily,
after sample collection in first lumen 14200A. The lumen 14200C may
be free of sample material until pressure gate 14800A is
transitioned to an open configuration. FIG. 23 illustrates pressure
gate 14800B in a closed configuration that inhibits fluid
communication between third lumen 14200C and first lumen 14200A.
Reagent may be delivered to the third lumen 14200C by a needle
19000, such as a needle from a reagent injection cartridge, or by
other instruments that can penetrate the lumen or otherwise provide
fluid communication between a reagent source and the lumen 14200C.
The lumen 14200C may be free of sample and reagent material until
reagent is injected to avoid cross contamination of the injection
needle 19000. The portion of the wall 11800C proximal the third
lumen 14200C may be constructed of a resilient, self-sealing
material to facilitate re-sealing of the wall 11800 after
penetration to deliver reagent.
[0183] One or more lumens of the tubule 11200 may include a
reinforced wall portion 17100, as illustrated in FIG. 24. The
reinforced wall portion 17100 may have an increased wall thickness
compared with the remainder of the tubule wall 11800 to facilitate
needle penetration and re-sealing. For example, the reinforced
portion may have a wall thickness of approximately 1 mm to 5 mm
greater than other portions of the wall. The reinforced portion
17100 may be constructed from a different material, having
increased strength and/or resiliency, for example, than the
remainder of the tubule wall 11800. Needle guides 17200 may be
provided to direct needle penetration and inhibit tearing of the
tubule wall 11800.
[0184] FIGS. 25A-25E illustrate another exemplary embodiment of a
multi-lumen tubule 11200 that includes a pair of parallel lumens,
namely first lumen 14200A and 14200B. In the illustrated
embodiment, the lumens 14200A and 14200B are connected parallely by
a thin layer fluid channel 17600 in the form of a slit opening that
extends the length of the tubule 11200. Although one fluid channel
is illustrated, additional fluid channels may be provided. The
fluid channel 17600 permits the sample to be moved between the
first lumen 14200A and the second lumen 14200B and to occupy both
lumens simultaneously. For example, during sample collection,
portions of the sample, or the entire sample, can be transferred
from the opening 11400 along the length of the first lumen 14200A,
through the fluid channel 17600, and along the length of the second
lumen 14200B. FIGS. 25B-25E illustrate the flow of a sample, in
fluid form, through the first lumen to the end of the first lumen
due to relatively low flow resistance of the lumen relative to the
fluid channel 17600 (FIG. 25B), through a portion 17400 of the
fluid channel 17600 distal to the opening in the first lumen 14200A
(FIG. 25C), along the fluid channel 17600 and through the second
lumen 14200B (FIG. 25D) to fill both lumens (FIG. 25D). In
embodiments in which a solid reagent is packed into the lumens
14200A and/or 14200B of the tubule 11200, flow of the sample
through the lumens via the fluid channel 17600 can facilitate
mixing of the solid reagent with the sample. For example, in the
case of blood samples, the inventors have determined that by
allowing the blood sample to flow through the first lumen 14200A
and the second lumen 14200B via the fluid channel 17600 can improve
mixing of the sample with an anticoagulant coated on the inner
walls of the two lumens.
[0185] FIGS. 26A-26C illustrate another exemplary embodiment of a
multi-lumen tubule 11200 having three parallel lumens, namely a
first lumen 14200A, a second lumen 14200B, and a third lumen
14200C. In the exemplary embodiment, each lumen of the tubule 11200
is divided into a plurality of longitudinally extending segments
18000. For example, the third lumen 14200C, illustrated in
cross-section in FIG. 26B, includes five segments 18000A-E. Each of
the segments 18000 can be used for one or more sample collection
and/or sample processing steps, including the processing steps
described above. In PCR (polymer chain reaction) testing, for
example, one segment may used for sample collection, one segment
may be used for sample pretreatment, e.g., nucleic acid extraction,
one or more segments may used for sample processing, e.g.,
thermocycling, and one or more segments may be used for sample
analysis. Any number of segments may be provided. In addition, one
or more segments may be used to store reagent or as an injection
channel for the delivery of reagent. The number of segments may be
varied depending of the sample being processed and the processing
steps selected.
[0186] Each of the segments 18000 may be separated by a seal 18200
that provides a temporary or permanent fluid seal between adjacent
segments 18000. A seal 18200 may be a pressure gate, such as the
reversible and irreversible pressure gates described above.
Alternatively, a seal 18200 may be formed by bonding or fusing of
compressed opposed wall sections of the tubule. The seal 18200 may
be formed by applying energy, such as thermal energy or RF energy,
by ultrasonic welding, or by using a bonding agent. A clamp may
also be applied to the exterior of the tubule to compress the wall
of the tubule and form a seal separating the segments in the
tubule. For example, the clamp may be an electro-mechanical
clamping mechanism as described below in connection with FIG. 29.
Any other mechanism for provided an external compressive force on
the tubule may be employed as the clamping mechanism. One or more
clamps may be provided as part of the sample processing system used
to process the sample within the tubule 11200. The segments may be
connected by one or more micro-fluidic flow channels that provide
selective fluid connection between the segments, as described
below. A seal 18200 may be a filter disposed within the tubule to
separate selected components of a fluid within the tubule from
other segment or components of the fluid within the tubule.
[0187] In the illustrated exemplary embodiment, the interface 3000
for facilitating delivery of the sample to the tubule 11200
includes a needle 18400 for direct collection of the sample to be
processed with the sample vessel 10000. The needle 18400 is
positioned a proximal end of the tubule and is fluid communication
with an opening in the tubule 11200. In the illustrated exemplary
embodiment, the needle 18400 is in fluid communication with an
opening in the first lumen 14200A, however, the needle 18400 may be
connected to any one or all of the lumens 14200 of the tubule
11200. A removable and replaceable needle cover 18600 may be
provided to secure the needle 18400 prior to and after use.
Alternatively, the needle cover 18600 may be connected by a hinge,
as shown in FIG. 27, or by another mechanism that allows to the
cover 18600 to be moved into and out of position about the needle
18400. A needle safety mechanism may be coupled to the needle and
the sample vessel.
[0188] FIG. 28 illustrates another embodiment of the cover 18600 in
which the sample collection instrument, e.g., the needle 18400, is
connected to the cover 18600. In the illustrated exemplary
embodiment, the proximal end 18400A of the needle 18400 may be used
for sample collection from a sample source and the distal end
18400B of the needle 18400 may be used to provide a fluid
connection with an opening in the tubule 11200 through interface
3000. For example, the distal end 18400B may be used to penetrate a
self-sealing membrane 4000 provided in the interface 3000. In
another embodiment, a cover 19000 may include a sample instrument
in the form of a needle 18400 and may have a compressible portion
in fluid communication with the needle to facilitate drawing a
fluid sample into the needle 18400 and transferring the sample to
the sample vessel 11000. Cover 19000 may be particularly useful as
a finger prick for collection a blood sample.
[0189] FIG. 29 illustrates a processing station 30000 of an
exemplary sample processing device, such as a sample processing
device described in U.S. Pat. No. 6,318,191 and U.S. patent
application Ser. No. 09/782,732, filed Feb. 13, 2001. The exemplary
processing station 30000 includes multiple compression members,
namely first compression member 30200A, second compression member
30200B, and third compression member 30200C. Each compression
member 30200 is adapted to compress a sample vessel, for example,
the tubule 1200 of sample vessel 1000 described above, and thereby
displace the contents of the sample vessel, e.g. reagent or sample,
within the sample vessel. Although the exemplary processing station
30000 is illustrated in connection with sample vessel 1000, one
skilled in the art will appreciate that any of the sample vessels
disclosed herein may be used in with the exemplary processing
station 30000. A plurality of compression members 30200 may be
oriented parallel to the longitudinal axis of the tubule 1200, as
illustrated in FIG. 29A. Alternatively, a plurality of compression
members 30200 may be oriented transverse to the longitudinal axis
of the tubule, i.e., oriented latitudinally, as illustrated in FIG.
34B described below, or in other orientations depending on the
compression configuration desired. A driver may be coupled to one
or more of the compression members 30200 to selectively move the
compression member into contact with the sample vessel. The driver
can be, for example, an electromagnetic actuating mechanism, a
motor, a solenoid, or any other device for imparting motion on the
compression members 30200. A stationary member 30400 or another
compression member may be provided opposite compression member
30200.
[0190] A compression member 30200 may be employed to compress a
portion of the wall 1800 of the tubule 1200 into contact with
another portion of the wall 11800 of the tubule 1200 to form a seal
in the tubule 1200 and thereby divide the tubule 1200 into multiple
segments. In alternative embodiments, a compression member 30200
may compress a portion of the wall 1800 of the tubule 1200 into
proximity with another portion of the wall 1800 of the tubule 1200
to form a micro-fluidic channel 30600 between segments of the
tubule 1200. For example, in the embodiment illustrated in FIG. 29,
compression member 30200B compresses a portion of wall 1800 into
proximity with another portion of the wall to create a
micro-fluidic channel 30600 that connects a first segment 18000A
and a second segment 18000B of the tubule 1200. The width of the
micro-fluid channel 30600 may be adjusted by displacing the
compression member 30200B towards or away from the tubule 1200.
Micro-fluid channels may be formed having a gap less than 200
microns, preferably 10 to 30 microns.
[0191] The compression members 30200 may be arranged in a variety
of orientations to compress the tubule 1200 into a variety of
configurations. For example, in FIG. 29B, the width of the
micro-fluidic channel 30600 extends across the entire width of the
tubule 1200. Such a compressed configuration may be formed by a
compression member 30200B having a planar compression surface 30800
for engaging the tubule 1200 that is sized to engage the entire
compressed wall surface of the tubule. In other embodiments, the
size or shape of the compression surface 30800 may be varied and
the number and orientation of compression members 30200B may be
varied. For example, FIG. 30A illustrates a compressed tubule 1200
having a centrally located flow channel 30600 that may be formed by
a compression member 30200 having a groove formed on the bottom
surface thereof or by three compression members 30200 aligned
transverse to the longitudinal axis of the tubule 1200. A centrally
positioned compression member may compress wall portion 1800A into
proximity with an opposed wall portion, while a pair of compression
members, one on either side of the central compression member, may
compress side wall portions 1800B and 1800C, respectively. FIG. 30B
illustrates a compressed tubule 1200 having a centrally located
lumen 30600 formed by compressing the tubule 1200 into a non-planar
configuration. In this illustrated embodiment, a triangular profile
flow channel is formed, which inherently forces a cell or particle
to flow through the central line of the channel, thus reducing the
need to regulate the tolerance in forming the flow channel. FIG.
30C illustrates a compressed tubule 1200 having a flow channel
30600 formed off-set from the center of the tubule 1200. In the
illustrated embodiment, the flow channel is formed on a lateral
edge of the tubule 1200.
[0192] At least a portion of the wall of the tubule 1200 may be
optically transparent to allow monitoring or detection of the
sample or reaction. The transparent portion of the wall may be
located in the flow channel section, thus allowing the monitoring
of sample or reaction under flow or through a thin layer of liquid,
for processes such as counting cells, reaction hybridization, or
detection, for example, microarray spots.
[0193] One skilled in the art will appreciate that while it may be
desirable in certain applications for the wall of the tubules
disclosed herein to be uniform along the circumference and the
longitudinal axis of the tubule, only a portion of the wall along
the circumference and/or longitudinal axis of the tubule need be
resilient and compressible. Thus, the tubule need not have a
uniform cross-section, either along the longitudinal axis or
transverse to the longitudinal axis. In certain exemplary
embodiments, for example, a section of the wall of the tubule may
be formed of a material selected to provide a property distinct
from a property of another section of the wall. Exemplary
properties that may be varied include permeability, flexibility,
hardness, resiliency, optical transparency, biocompatibility,
surface smoothness of the inner wall, and surface chemistry of the
inner wall, for example the hydrophobic or hydrophilic properties
of the inner wall surface. Surface properties may be rendered by
coating with a layer of material, such as a thermoset urethane
aired by UV energy or other cross linking methods.
[0194] FIGS. 34A and 34B illustrate an exemplary embodiment of a
sample vessel 1000 in the form of a tubule 1200 having wall
sections 1800A that are formed of a material selected to provide a
property distinct from a property of a plurality of other wall
sections 1800B of the tubule 1200. Wall sections 1800A may be
opposed to one another, as illustrated, or positioned at other
positions in the cross section of the tubule 1200. Wall sections
1800A may similar in size, shape and material properties, as
illustrated, or may vary in size, shape, and material properties
from one another. In the illustrated embodiment, wall sections
1800A are selected from a material having sufficient flexibility to
permit compression of the tubule 1200, as illustrated in FIG. 34B.
Wall sections 1800B are formed of a material having increased
rigidity compared to the material of wall sections 1800A. In the
illustrated embodiment, wall sections 1800B preferably have
sufficient rigidity to resist flexing during compression and
thereby maintain a planar configuration. Wall sections 1800B may be
opposed to one another, as illustrated, or positioned at other
positions in the cross section of the tubule 1200. Wall sections
1800B may be similar in size, shape and material properties, as
illustrated, or may vary in size, shape, and material properties
from one another. In the illustrated embodiment, the wall sections
1800A and 1800B are spaced latitudinally, i.e., about the
circumference of the tubule 1200 and transverse to the longitudinal
axis. Wall sections 1800A and 1800B are interposed between one
another in an alternating arrangement about the circumference of
the tubule 1200. Wall sections 1800A and 1800B may be formed from
the same material or a different material. For example, wall
sections 1800A may be formed of a relatively low durometer
polyurethane, for example, in the range of from 40 A to 90 A
depending on thickness, and wall sections 1800B may be formed of a
polyurethane having a relatively higher durometer, for example, in
the range of from 40 D to 90D depending on thickness. A tubule
having wall sections of varying properties may be manufactured by
conventional extrusion, co-extrusion, injection molding, insert
molding, dip molding, blow molding, transfer molding, or lamination
processes.
[0195] During compression of the tubule 1200 illustrated in FIGS.
34A and 34B, the wall sections 1800A flex allowing a first wall
section 1800B to be moved into proximity or contact with second
wall section 1800B'. Wall sections 1800B may provide improved
sealing surfaces due to the increased rigidity compared with wall
sections 1800A. In addition, walls sections 1800B permit the
formation of a precisely defined micro-fluid flow channel 30600, as
illustrated in FIG. 34B. The increased rigidity of the wall
sections 1800B allows for the formation of a smaller and more
uniform flow channel than more flexible wall sections. FIG. 34B
illustrates the formation of a micro-fluidic flow channel 30600
between segments 18000A and 18000B of the tubule 1200. In the
illustrated embodiment, the compression members 30200A-C are
oriented transverse to the longitudinal axis of the tubule to form
a flow channel 30600 that extends latitudinally, i.e., transverse
to the longitudinal axis, between first segment 18000A and second
segment 18000B.
[0196] In other exemplary embodiments, the number of wall sections
of differing properties may be varied. For example, a single wall
section 1800B having increased rigidity may be provided or three or
more wall sections having increased rigidity may be provided.
[0197] In certain exemplary embodiments, a flow channel 30600 may
be pre-formed in a section of the wall 1800 of the tubule as
illustrated in FIGS. 31 and 32A-B. The pre-formed flow channel
30600 may be a groove 31600 formed in a wall section of the tubule
1200. The groove 31600 may be formed by scoring or etching the wall
1800 of the tubule 1200 or may be formed during the extrusion or
molding of the tubule 1200. The groove 31600 in the illustrated
embodiments extends longitudinally, however, the groove 31600 may
be formed in any direction, including latitudinally. More than one
groove 31600 may be provided. The groove 31600 may have a variety
of cross-section shapes and sizes. In the embodiment illustrated in
FIG. 31, the groove 31600 has a triangular cross-section. In the
embodiment illustrated in FIGS. 32A-32B, the groove 31006 has a
rectangular cross-section. The cross-sectional size of the groove
31600 can be selected based on desired shear rate profile of the
flow channel 30600.
[0198] The groove 31600 may be formed in any section of the wall
1800 of the tubule 1200. For example, the groove 31600 may be
formed in a wall section 1800B having increased rigidity compared
to other wall sections of the tubule 1200, as is the case for the
illustrated embodiments of FIGS. 31 and 32A-B. During compression
of the tubule 1200, as illustrated in FIG. 32B, the wall section
1800B contacts wall section 1800B' to provide a fluid tight seal.
Groove 31600 provides a flow channel 30600 that extends
longitudinally through the fluid tight seal.
[0199] FIGS. 33A and 33B illustrate an exemplary embodiment of a
sample vessel 40000 comprising a tubule 41200 having a plurality of
flow channels 30600 and one or a plurality of depressions 40800
formed on an interior wall surface 41000 of the wall 41800 of the
tubule 41200. Each depression 40800 can form a micro-cup during
compression of the tubule 41200 that can hold a fixed volume of
sample or reagent. The volume of a depression forming a micro-cup
can be from 0.1 microliter to 10 microliter, preferably, from 0.5
microliter to 4 microliter. A pattern of one or more grooves 31600
and depressions 40800 may be formed on the interior wall surface
41000 of the tubule 41200 and may interconnect to provide a network
of micro-cups interconnected by micro-fluidic flow channels 30600,
as best illustrated in FIG. 33B. Such a network may be used to
perform a variety of processing steps within one or more micro-cups
and may permit the transport of small, precise volumes of sample
and reagent between the micro-cups via micro-fluid flow channels by
selectively compressing the tubule 41200. The network of grooves
and depressions may be formed using semi-conductor processing
techniques. For example, a mask pattern may be applied to an
interior wall surface of the tubule 1200 using conventional
photolithographic techniques. The grooves and depressions may then
be formed by etching or otherwise removing portions of the interior
wall surface based on the pattern imaged onto the interior wall
surface. It may be desirable to form the network of grooves and
depressions on a planar substrate 41800A constructed of a material
suitable for use in the tubule 41200, as illustrated in FIGS. 33A
and 33B. A second layer 41800B of material can be attached to the
planar substrate 41800A to form the wall 41800 of the tubule
41200.
[0200] Referring to FIGS. 33A and 33B, one or more sample or
reagent processing devices 41400 may be provided on the interior
wall surface 41000 of the tubule 41200. For example, a microarray
device may be embedded on the interior wall surface 41000 of the
tubule 41200. An exemplary microarray device 41400 may comprise a
plurality of reagent coated zones for simultaneous analysis of a
plurality of analytes within a sample. The processing device 41400
may also be a micro-fluid device or a lab-on-a-chip device, or any
other device for processing a sample. The processing device 41400
may be interconnected with one or more depressions 40800 or other
processing devices via flow channels 30600. Any number of
processing devices of any type may be provided in the tubule
41200.
[0201] Referring to FIG. 37, a sample vessel 70000 comprising a
tubule 71200 divided into multiple segments 78000A-C. Segment
78000B may be constructed of a rigid, generally non-flexible
material and may have a processing device, such as a microarray
71400, embedded on the interior wall thereof. The segment 78000B
may provide a pre-formed flow channel between two compressible
segments 78000A and 78000C. By alternately compressing the two
flexible segments 70800A and 78000C, the sample may flow through
the flow channel 70600 to facilitate high efficient hybridization
or binding of analytes to the reagent spots of the microarray
71400. A flow channel 706 having a small gap may also increase wash
efficiency as a laminar flow is formed.
[0202] FIGS. 35A-35E illustrates an exemplary embodiment of a
sample vessel 1000 comprising a tubule 1200 and an adapter 50000
that is connected to the tubule 1200 of the sample vessel 1000. The
adapter 50000 may be provided to facilitate handling of the sample
vessel 1000 and/or to facilitate connection of the tubule 1200 to
an external device, such as a micro-fluid device, a lab-on-a-chip
device, a microarray device, a reagent source, another sample
vessel, or any other device suitable for containing or processing a
sample. In the illustrated embodiments, the adapter 50000 is a
generally planar tab that is coextensive with the tubule 1200. One
skilled in the art will appreciate that the adapter 50000 need not
be coextensive with the tubule and may be constructed of varying
sizes and shapes depending upon the application. Moreover, more
than one adapter may be provided.
[0203] The adapter 50000 may be constructed of any material
suitable for use in construction the tubule 1200. For example, the
adapter may be constructed of polyurethane. The adapter 50000 may
be constructed of the same or a different material than the tubule
1200. To facilitate handling, the adapter 50000 may be constructed
of a material having increased rigidity compared to the material of
the tubule 1200, for example a high durometer polyurethane. In
certain embodiments, the adapter 50000 may be manufactured with the
tubule 1200 in, for example, a co-extrusion process or an injection
molding process. Alternatively, the adapter 50000 may be
manufactured independently and attached to the tubule 1200 in a
post-forming process by, for example, bonding.
[0204] The exemplary embodiment of FIGS. 35A-35E also includes a
container 2000 and an interface 3000, as described above. The
container 2000 removably and replaceably encloses the tubule 1200
to protect the sample tubule 1200 and when removed, may allow
direct manipulation of tubule 1200. A portion of adapter 50000 may
not be enclosed by container 2000. The exposed portion of the
adapter 50000 can be directly accessed by a user for labeling,
handling and other processing. The interface 3000 includes an
interface channel 3700 that communicates with an opening in the
tubule 1200 to facilitate delivery of a sample to the tubule 1200.
In the illustrated embodiment, a removable and replaceable cover
58600 is provided to selectively open and close the interface
channel 3700. The exemplary cover 58600 includes a sample
collection instrument in the form of a tissue swab 584 for
collecting tissue samples from a sample source.
[0205] FIGS. 35A-B illustrate an embodiment of the adapter 50000
that is constructed to facilitate handling of the sample vessel
1000.
[0206] FIG. 35C illustrates an embodiment of the adapter 50000C
that is designed to facilitate delivery of a reagent or a sample
from an external device, such as a needle 9000 from a reagent
injector cartridge. The adapter 50000C includes a reversible or
irreversible pressure gate 4800 that provides a fluid channel to
permit selective displacement of a fluid, e.g., a sample or
reagent, between the tubule 1200 and the external device, in the
present embodiment, needle 9000. The adapter 50000C may include a
self-sealing membrane 54000, valve, or other sealing mechanism to
facilitate selective communication with the external device. A
reservoir 50200 may be provide to contain a fluid delivered from
the external device or fluid from the tubule 1200. In use, the
needle 9000 may penetrate the self-sealing membrane 54000 to
deliver fluid to the reservoir 50200 or to withdraw fluid from the
reservoir 50200. Pressure gate 4800 may be opened in the manner
described above, e.g. by compressing the tubule 1200 or the
reservoir 50200, to withdraw fluid from the reservoir 50200 or to
deliver fluid to the reservoir 50200 from the tubule 1200. The
needle 9000 may be coupled with a sensor, such as an electrode, a
fiber optical sensor, for penetrating the self sealing membrane
54000 and measuring a sample property.
[0207] FIG. 35D illustrates an embodiment of the adapter 50000D
that comprises a compressible reservoir 50600 and a reversible or
irreversible pressure gate 4800 that provides a fluid channel to
permit selective displacement of a fluid, e.g., a sample or
reagent, to the tubule 1200 from the compressible reservoir 50600.
The compressible reservoir 50600 may contain a pre-packed reagent.
In certain embodiments, the compressible reservoir 50600 may be a
blister pack. Upon compression of the compressible reservoir 50600,
pressure gate 4800 may open and fluid with the compressible
reservoir 50600 can be displaced in to the tubule 1200.
[0208] FIG. 35E illustrates an embodiment of the adapter 50000E
that comprises a reservoir 50200, a first reversible or
irreversible pressure gate 4800A that provides a fluid channel to
permit selective displacement of a fluid, e.g., a sample or
reagent, between the tubule 1200 and the reservoir 50200, and a
second reversible or irreversible pressure gate 4800B that provides
a fluid channel to permit selective displacement of a fluid, e.g.,
a sample or reagent, between an external device 50800 and the
reservoir 50200. A connector 50900 may be provided to interface
with the external device 50800. Such device may be an Access.TM.
card for Micronics Inc., a LabChip.RTM. product from Caliper, Inc.
or a GeneChip.RTM. from Affymetrix, Inc.
[0209] FIGS. 36A-E illustrate another exemplary embodiment of a
sample vessel 60000 that comprises a tubule 1000 and an apparatus
60200 for drawing a sample into the tubule 1200 of the sample
vessel 1000. The apparatus 60200 includes a cylindrical housing
60400 having an opening 60600 for receiving the tubule 1200. The
opening 60200 extends from a proximal end 60800 to a distal end
61000 of the housing 60400. Both the housing 60400 and the opening
60600 can be sized and shaped to accommodate the size and shape of
the tubule 1200 or other sample vessels. For example, the housing
60400 and opening 60600 are cylindrical in shape and have a
circular cross-section analogous to that of the tubule 1200. The
adapter 60000 comprises first means 61200 for compressing a first
portion of the tubule 1200 and second means 61400 for compressing a
second portion of the tubule 1200. The first compression means
61200 may be spaced apart from the second compression means 61400.
For example, the first compression means 61200 may be positioned at
the proximal end 60800 of the housing 60200 and the second
compression means 61400 may be positioned at the distal end 61000
of the housing 60200. The spacing between the first and second
compression means may be selected based on the desired sample
collection volume in the tubule 1200.
[0210] The first compression means 61200 may comprise a first pair
of spaced apart rollers, 61600A and 61600B. At least one of the
rollers 61600A-B may be selectively movable into contact with the
other roller to compress the tubule 1200 between the rollers
61600A-B. A first activator 62000 may be coupled to the rollers
61600A, 61600B to effect separation or compression of the rollers.
The second compression means 61200 may comprise a second pair of
spaced apart rollers, 61800A and 61800B. At least one of the
rollers 61800A-B may be selectively movable into contact with the
other roller to compress the tubule 1200 between the rollers
61800A-B. A second activator 62200 may be coupled to the rollers
61800A, 61800B to effect separation or compression of the rollers.
In addition to rollers, or other compression mechanisms may be
employed for the first and second compression means, including the
compression members described above. Any structure suitable for
selective compression of the tubule 1200 may be employed. The first
and second compression means need not be the same structure.
[0211] In use, the tubule 1200 is inserted into the opening 60600
at the proximal end 60800 of the housing 60400 and drawn completely
through the opening 60600 to the distal end 61000 of the housing
60400. As the tubule 1200 is drawn through the housing 60400, the
tubule 1200 is flatten and compressed, as illustrated in FIG. 36B,
to evacuate the tubule 1200. At the time of sample collection, a
cover 68600 may be removed to expose a sample collection
instrument, such as a needle 68400, that is in fluid connection
with the tubule 1200. The needle 68400 can be inserted into the
sample source and the first compression means 61200 may be
separated to draw the sample into the tubule 1200, as illustrated
in FIG. 36C. The sample vessel 1000 may then be inserted into a
device 63000 for removing the needle 68400, or other sample
collection instrument, as illustrated in FIG. 36D. The device 63000
may also include a mechanism for sealing the proximal end of the
tubule 1200 after the needle 68400 is removed, by, for example,
compressing and heating the wall of the tubule 1200 at the proximal
end to bond or fuse the walls together. The second compression
means 61400 may separate and the adapter 60000 may be removed from
the tubule 1200, as illustrated in FIG. 36E.
[0212] While the sample vessels disclosed herein have been
particularly shown and described with references to exemplary
embodiments thereof, it will be understood by those skilled in the
art that various changes in form and details may be made therein
without departing from the spirit and scope of the disclosure.
Those skilled in the art will recognize or be able to ascertain
using no more than routine experimentation, many equivalents to the
exemplary embodiments described specifically herein. Such
equivalents are intended to be encompassed in the scope of the
present disclosure.
* * * * *