U.S. patent application number 11/701049 was filed with the patent office on 2007-06-14 for method and apparatus for controlling reactions.
Invention is credited to Carol T. Schembri.
Application Number | 20070134799 11/701049 |
Document ID | / |
Family ID | 22457020 |
Filed Date | 2007-06-14 |
United States Patent
Application |
20070134799 |
Kind Code |
A1 |
Schembri; Carol T. |
June 14, 2007 |
Method and apparatus for controlling reactions
Abstract
The invention relates to a method and an apparatus for
performing an assay on chemical, biochemical, or biological fluids.
The apparatus includes an assay chamber for fluid reactions and a
centrifugal force activated-valve for controlling fluid movement
through the assay chamber. An active surface can be positioned in
the assay chamber to react with fluids passed through the assay
chamber. The active surface may contain biomolecular probes. The
biomolecular probes can be DNA, DNA fragments, RNA, RNA fragments,
reagents, protein, protein fragments, lipids, and lipid fragments.
The apparatus is particularly useful when multiple reactions,
dilutions, or washing steps are required to determine a final
answer. The centrifugal force activated-valve provides positive
control over fluid in the assay chamber and allows for repeated use
of the same chamber for multiple reaction steps. The apparatus can
be disposed of after an assay to eliminate potential contamination
from reuse of the same apparatus. Fluids passed through the assay
chamber may be recovered for subsequent analysis, processing, or
reactions.
Inventors: |
Schembri; Carol T.; (San
Mateo, CA) |
Correspondence
Address: |
AGILENT TECHNOLOGIES INC.
INTELLECTUAL PROPERTY ADMINISTRATION,LEGAL DEPT.
MS BLDG. E P.O. BOX 7599
LOVELAND
CO
80537
US
|
Family ID: |
22457020 |
Appl. No.: |
11/701049 |
Filed: |
January 31, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10146402 |
May 14, 2002 |
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11701049 |
Jan 31, 2007 |
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09695008 |
Oct 23, 2000 |
6395553 |
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10146402 |
May 14, 2002 |
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09133102 |
Aug 12, 1998 |
6162400 |
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09695008 |
Oct 23, 2000 |
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Current U.S.
Class: |
436/36 |
Current CPC
Class: |
Y10T 436/111666
20150115; B01L 2400/0409 20130101; B01L 2400/0633 20130101; B01L
3/502 20130101; G01N 35/1097 20130101; B01L 2300/0877 20130101;
Y10T 436/2575 20150115; G01N 33/491 20130101; Y10T 137/108
20150401; B01L 2300/0636 20130101 |
Class at
Publication: |
436/036 |
International
Class: |
G01N 33/00 20060101
G01N033/00 |
Claims
1. A method for performing an assay on a sample using an analytical
device having a reusable centrifugal valve and an active surface,
the method comprising: introducing a sample into a reaction chamber
of the analytical device; spinning the analytical device at a
rotational speed to actuate the centrifugal valve from a stationary
closed position to an open actuated position, the open actuated
position opening the valve, thereby allowing the sample to exit
from the reaction chamber through the valve; introducing a wash
fluid into the reaction chamber; and spinning the analytical device
at a rotational speed to actuate the valve from the stationary
closed position to the open actuated position, the open actuated
position opening the valve and allowing the wash fluid to exit from
the reaction chamber through the valve.
2. The method of claim 1, further comprising after the step of
introducing the wash fluid: spinning the analytical device at the
first rotational speed to generate a radially outward flow of the
wash fluid; then spinning the analytical device at the rotational
speed to actuate the valve from the stationary closed position to
the open actuated position and allowing the wash fluid to exit from
the reaction chamber through the valve.
3. The method of claim 2, further comprising after spinning to
allow the wash fluid to exit: optically scanning the active surface
to assay the active surface.
4. The method of claim 1 wherein the active surface is not attached
to the reaction chamber.
5. The method of claim 1 wherein the active surface is attached to
the reaction chamber.
6. The device of claim 1, wherein the active surface comprises
biomolecular probes.
7. The device of claim 1, wherein the biomolecular probes are
selected from the group consisting of DNA, DNA fragments, RNA, RNA
fragments, reagents, protein, protein fragments, lipids, and lipid
fragments.
8. A method for performing an assay on a sample using an analytical
device having a reusable centrifugal valve and an active surface,
the method comprising: introducing a sample into an assay chamber
of the analytical device; and spinning the analytical device at a
rotational speed sufficient to actuate the centrifugal valve from a
stationary closed position to an open actuated position and
allowing the sample to exit from the assay chamber through the
centrifugal valve.
9. The method of claim 8, further comprising: distributing the
sample to a chamber radially outward from the valve, the chamber
operative to contain the sample for further processing.
10. The method of claim 9, further comprising: scanning an
optically transparent portion of the analytical device with an
optical detection means to assay the active surface.
11. The method of claim 8, further comprising the steps of: washing
the active surface by introducing a wash fluid into the assay
chamber after spinning the analytical device to remove the sample
from the assay chamber; spinning the analytical device at a first
rotational speed to generate a radially outward flow of the wash
fluid, the first rotational speed being below a rotational speed
necessary to actuate the centrifugal valve from the stationary
closed position to the open actuated position, the wash fluid
operative to remove un-reacted sample from the active surface and
the assay chamber; and spinning the analytical device at a
rotational speed greater than the first rotational speed to actuate
the centrifugal valve from the stationary closed position to the
open actuated position and allow the wash fluid to exit from the
assay chamber through the centrifugal valve.
12. The method of claim 11, further comprising: scanning an
optically transparent portion of the analytical device using the
optical detection means to assay the active surface.
13. The method of claim 12, further comprising: adding fluid to the
assay chamber and spinning the analytical device below the first
rotational speed to distribute the fluid; and scanning an optically
transparent portion of the analytical device using the optical
detection means to assay the active surface.
14. The method of claim 8 wherein the active surface is not
attached to the reaction chamber.
15. The method of claim 8 wherein the active surface is attached to
the reaction chamber.
16. The method of claim 8, wherein the active surface comprises
biomolecular probes.
17. The method of claim 8, wherein the biomolecular probes are
selected from the group consisting of DNA, DNA fragments, RNA, RNA
fragments, reagents, protein, protein fragments, lipids, and lipid
fragments.
18-24. (canceled)
25. An analytical device for controlling reactions, comprising: a
housing enclosure defining an assay chamber and a fluid discharge
port positioned radially outward from the assay chamber and in
fluid communication with the assay chamber, the housing enclosure
adapted for rotation about an axis; an active surface in the
chamber; means for introducing fluid into the assay chamber; and a
centrifugally-operated valve in fluid communication with the fluid
discharge port, the valve repetitively operable between a
stationary position and an actuated position, the valve operative
to transition from the stationary position to the actuated position
when a centrifugal force generated by rotating the housing
enclosure exceeds a predetermined limit, and to transition from the
actuated position to the stationary position when the centrifugal
force does not exceed the predetermined limit.
26. The device of claim 25, wherein the active surface comprises
biomolecular probes.
27. The device of claim 26, wherein the biomolecular probes are
selected from the group consisting of DNA, DNA fragments, RNA, RNA
fragments, reagents, protein, protein fragments, lipids, and lipid
fragments.
28-30. (canceled)
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation application of
application Ser. No. 09/695,008 filed Oct. 23, 2000, which is a
divisional of application Ser. No. 09/133,102 filed Aug. 12, 1998
(now U.S. Pat. No. 6,162,400). Priority is claimed under 35 U.S.C.
120 from both of the foregoing applications, which are incorporated
herein by reference.
BACKGROUND OF THE INVENTION
[0002] The present invention relates generally to analytical
devices for performing assays and more particularly to an
analytical device that includes a centrifugal force actuated valve
to control fluid and a method of utilizing the analytical device to
perform an assay.
[0003] There are many analytical methods that require one or more
reactions or analytical steps to determine a final answer. Examples
are heterogeneous immunochemistry reactions, hybridization of DNA
to DNA, and hybridization of DNA to RNA. In order to determine the
concentration or presence of an analyte, such analytical methods
require multiple, serial reactions either with or without washing
steps or a single reaction with a washing step. Other assays, such
as clinical chemistry assays, often require precise dilutions prior
to mixing with other chemicals.
[0004] It would be desirable to reduce the cost of conducting the
reactions in an assay by automating the reaction steps rather than
using expensive manual labor to perform the steps. Additionally, it
would be advantageous to use centrifugal force in the automation
process to minimize variations due to surface tension and capillary
action and to move and control fluid.
[0005] Centrifugally driven analytical devices have employed
several methods for controlling fluid movement, such as
differential flow, stop junctions, siphons, and complex, two-axis
mechanisms.
[0006] Differential flow allows fluid to enter a chamber quickly
but exit slowly. As the fluid enters and exits the chamber there is
a finite residence time in which most of the fluid can be
manipulated. However, the disadvantage of differential flow is that
the entire volume of fluid is never completely controlled.
[0007] Stop junctions employ the pressure created by a capillary to
stand off fluid flow until the centrifugal force generated by
rotation overcomes capillary back pressure. Stop junctions are
sensitive to the exact geometry and surface properties of the
junction and to fluid properties of the sample.
[0008] Siphons allow fluid movement into a chamber under the action
of centrifugal force and prevent the fluid from exiting the chamber
until the siphon is primed or the siphon level is high enough. The
disadvantage with siphons is that some of the fluid is lost in the
entrance of the siphon and that great care must be taken to prevent
the siphon from priming prematurely or from losing prime
prematurely.
[0009] Two-axis mechanisms provide better fluid control, but at
substantial instrumentation cost, complexity, and size. Two-axis
mechanisms are typically mounted on a large turntable. The
turntable has two positions, each position having a local center of
rotation.
[0010] U.S. Pat. No. 5,171,533 to Fine et al. discloses single use
centrifugal valves for performing a biological assay. Sealant
materials are used to provide a counteracting force to the
centrifugal force of rotation. The sealants are designed to yield
at predetermined levels of centrifugal force. The valves in the
Fine et al. patent require that the fluid move through different
chambers.
[0011] From the foregoing it will be apparent that there is a need
for a simple, easy to automate, and economical means for performing
an assay or a reaction. Further, it will be apparent that a
disposable analytical device is desirable for preventing
contamination resulting from repeated use of the same analytical
device.
SUMMARY OF THE INVENTION
[0012] The invention provides an analytical device incorporating a
centrifugal force-activated valve for controlling reactions and for
moving fluid within the analytical device. The centrifugal
force-activated valve allows for several fluids to be passed
through the analytical device and allows the analytical device to
be used for multiple serial reactions. The centrifugal
force-activated valve provides simple and reliable control over
fluid movement and can be tuned to open or close over a wide range
of rotational speeds.
[0013] An analytical device embodying the invention is economical,
easy to use, injection moldable from a variety of plastics, readily
adaptable to automation, capable of repeated reaction, mixing, and
washing steps, disposable to prevent contamination, and may be
transparent to allow an assay by optical detection means.
[0014] In a preferred embodiment of an analytical device according
to the present invention, a housing enclosure adapted for rotation
about an axis includes an assay chamber, a fluid discharge port in
fluid communication with the assay chamber, means for introducing
fluid into the assay chamber, and a centrifugal force-activated
valve in fluid communication with the fluid discharge port.
Preferably, the fluid introducing means is self sealing. Fluid
entering the valve through the fluid discharge port may exit the
valve through a fluid drain. The fluid drain is in fluid
communication with the valve and an exterior portion of the housing
enclosure. Chemical, biological, or biochemical fluids may be
introduced into the assay chamber.
[0015] Additionally, an active surface can be positioned on an
interior surface of the assay chamber. The active surface may
contain biomolecular probes. The biomolecular probes can be DNA,
DNA fragments, RNA, RNA fragments, reagents, protein, protein
fragments, lipids, and lipid fragments. Additionally, the active
surface can be disposed on a structure positioned on an interior
surface of the assay chamber. For example, the structure can be in
the shape of balls or beads. The structure can be attached to an
interior surface of the assay chamber or can be loosely contained
in the assay chamber. Typically, the active surface is arranged in
an array pattern positioned on a surface of the assay chamber.
[0016] An analytical substrate can be positioned in an opening in
the housing enclosure. The active surface can be disposed on an
interior surface of the analytical substrate and in opposing
relation to the assay chamber.
[0017] The analytical substrate can be made transparent to optical
detection means external to the housing enclosure. A transparent
analytical substrate allows for an assay of the active surface by
scanning the active surface through the analytical substrate using
the optical detection means.
[0018] The analytical device may also include a reservoir chamber
disposed radially outward from the centrifugal valve and in fluid
communication with the valve. Fluid exiting the centrifugal valve
is stored in the reservoir chamber. Optionally, fluid contained in
the reservoir chamber can be extracted through fluid extracting
means in fluid communication with the reservoir chamber.
Preferably, the fluid extraction means is self sealing.
[0019] In another embodiment, the housing enclosure includes a
portion defining a valve chamber for containing the centrifugal
force-activated valve. A fluid discharge port is positioned at a
radially inward end of the valve chamber and is in fluid
communication with the valve chamber and the assay chamber. A valve
seat is disposed in the valve chamber and is disposed radially
outward from the fluid discharge port. The valve seat is in fluid
communication with the fluid discharge port and the valve chamber.
An actuator is movably disposed in the valve chamber and is biased
to a stationary position relative to the valve seat by a counter
acting force provided by bias means positioned in the valve chamber
and disposed radially outward from the actuator. The actuator moves
radially outward from the stationary position to an actuated
position when the housing enclosure is rotated and the centrifugal
force acting on the actuator exceeds the counteracting force of the
bias means. When the centrifugal force drops below the
counteracting force, the actuator moves radially inward from the
actuated position to the stationary position.
[0020] A method according to the present invention includes
injecting a sample into the assay chamber through the fluid
introducing means. The analytical device is then spun at a first
rotational speed lower than that required to actuate the
centrifugal force-activated valve. The first rotational speed needs
to be sufficient to distribute the sample across the active
surface. The sample is allowed to react with the active surface. At
the conclusion of the reaction period, the analytical device is
spun at a second rotational speed to actuate the centrifugal
force-activated valve and empty the sample from the assay chamber.
Spinning at the second rotational speed is stopped when the assay
chamber is empty. Wash fluids are injected into the assay chamber
and the analytical device is spun at the first rotational speed to
distribute the wash fluids. The analytical device is then spun at
the second rotational speed to empty the wash fluids. The washing
step can be repeated as necessary to effect complete washing of the
assay chamber and the active surface. After the washing step, the
active surface can be scanned to detect the presence of an
analyte.
[0021] Other aspects and advantages of the present invention will
become apparent from the following detailed description, taken in
conjunction with the accompanying drawings, illustrating by way of
example the principles of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
[0022] FIG. 1 is a cross section of an analytical device according
to the present invention.
[0023] FIG. 2a is a cross section of a centrifugal force-activated
valve with a valve chamber cap according to the present
invention.
[0024] FIG. 2b is a cross section of a centrifugal force-activated
valve with a valve chamber cap having fluid extraction means
according to the present invention.
[0025] FIG. 2c is a cross section of a centrifugal force-activated
valve with a valve chamber cap having a fluid drain according to
the present invention.
[0026] FIG. 3a is a cross section of a normally closed centrifugal
force-activated valve in the stationary position according to the
present invention.
[0027] FIG. 3b is a cross section of a normally closed centrifugal
force-activated valve in the actuated position according to the
present invention.
[0028] FIG. 4a is a cross section of a normally open centrifugal
force-activated valve in the stationary position according to the
present invention.
[0029] FIG. 4b is a cross section of a normally open centrifugal
force-activated valve in the actuated position according to the
present invention.
[0030] FIG. 5a is a cross section of a valve seat with compliant
material according to the present invention.
[0031] FIG. 5b is a cross section of an actuator with elastomeric
material according to the present invention.
[0032] FIG. 6 is a cross section of an analytical device having a
substrate disposed in the housing enclosure according to the
present invention.
DETAILED DESCRIPTION
[0033] In the following detailed description and in the several
figures of the drawings, like elements are identified with like
reference numerals.
[0034] As shown in the drawings for purposes of illustration, the
invention is embodied in an analytical device having an assay
chamber for fluid reactions and at least one centrifugal
force-activated valve in fluid communication with the assay
chamber. The valve provides positive control of fluid contained in
the assay chamber and allows for multiple, fluid reaction steps,
mixing steps, and washing steps to occur in the assay chamber. The
analytical device of the present invention is easy to use, can be
manufactured at low cost, is adaptable to automation, provides
predictable fluid control that can be tuned over a wide range of
rotational speeds, and can be disposed of after use to prevent
contamination from repeated use of the same analytical device.
Previous apparatus for controlling reactions have incorporated
complex fluid control methods, such as, siphons, stop junctions,
two-axis rotation, differential flow, and single use centrifugal
valves. The analytical device of the present invention provides
positive fluid control with less complexity and greater flexibility
than the previous apparatus.
[0035] Referring to FIG. 1, there is provided in accordance with
the present invention an analytical device generally designated as
1. The analytical device includes a housing enclosure 3 defining an
assay chamber 5, and a centrifugal force-activated valve 7a
disposed radially outward of the assay chamber 5. The housing
enclosure 3 is adapted for rotation 6 about a rotational axis 4.
Fluid is communicated from the assay chamber 5 to the valve 7a, as
shown by arrow 19, thru a fluid discharge port 9 positioned
intermediate to the assay chamber 5 and the valve 7a. An active
surface 13 can be positioned on an interior surface of the assay
chamber 5. Fluid is introduced into the assay chamber 5, as shown
by arrow 17, using fluid introducing means 11. Fluid introducing
means 11 is in fluid communication with the assay chamber 5. Fluid
introducing means 11 can be an opening positioned in the housing
enclosure 3 near the rotational axis 4. Preferably, fluid
introducing means 11 is self sealing, for example, a diaphragm or a
septum. If the reaction is fast or the volumes of fluid large
enough that evaporation is not an issue, the fluid introducing
means 11 need not be sealed. Rotation 6 of the housing enclosure 3
generates a radially outward flow of fluid contained in the assay
chamber 5, thereby urging the fluid into contact with the fluid
discharge port 9. Additionally, it is desirable to position the
active surface 13 at a radially outward portion of the assay
chamber 5 to allow fluid to react with the active surface 13 when
the housing enclosure 3 is rotated and the fluid is urged radially
outward. When the centrifugal force from rotation 6 of the housing
enclosure exceeds the force necessary to actuate the valve 7a, the
valve opens, and fluid enters the valve 7a through the fluid
discharge port 9. In a typical application, chemical, biochemical,
or biological fluids are reacted in the assay chamber.
[0036] The centrifugal force-activated valve 7a, includes a valve
chamber 23, a valve seat 25 positioned radially outward of the
fluid discharge port 9, an actuator 27 movably positioned in the
valve chamber 23, and bias means 29 positioned in the valve chamber
23 and radially outward of the actuator 27. The bias means 29
provides a counteracting force to urge the actuator 27 into a
stationary position relative to the valve seat 25. As will be
further described below with respects to FIGS. 3a, 3b, 4a, and 4b,
the valve seat may be positioned radially inward or radially
outward of the actuator. Additionally, a fluid drain 15 can be
positioned in the valve chamber 23. The fluid drain 15 allows fluid
entering the valve chamber 23 as shown by arrow 19, to exit the
valve 7a through the exterior of the housing enclosure 3, as shown
by arrow 21.
[0037] In a typical embodiment of the present invention, housing
enclosure 3 can be made from almost any structural material.
Obvious choices include metals, ceramics, plastics, fused silica,
and glasses. The housing enclosure 3 can be machined from metal,
for example, steel, aluminum, and copper. The housing enclosure 3
can also be machined or injection molded from plastic. Stainless
steel is a preferred metal since it won't generally react with the
chemical analysis occurring in the analytical device 1. More
preferred, especially for a disposable analytical device, is
injection molded plastics. Possible choices for injection molded
plastics include acrylic (polymethyl methacrylate), polyethylene,
polypropylene, polystyrene, ABS, polycarbonate, and the like.
Selection of the material for the housing enclosure 3 is dependent
on the specific requirements for the assay. For example,
polypropylene is desirable because of its higher temperature limits
and inertness; however, the inertness of polypropylene make it
difficult to label and difficult to glue in subsequent
manufacturing assembly steps. Typically, the valve chamber 23 and
the valve seat 25 are made of the same material as the housing
enclosure 3.
[0038] The actuator 27 can also be made of the same materials as
the housing enclosure 3. Preferably, the actuator 27 is made from a
dense, inert material, such as, a stainless steel ball. Stainless
steel balls are easily obtained and the material is dense and
inert. The shape and material properties of the actuator 27 should
be compatible with motion of the actuator 27 in the valve chamber
23. Actuator 27 should move back and forth in the valve chamber 23
with minimal friction, and should be properly shaped and sized to
prevent binding in the valve chamber 23. Suitable shapes for
actuator 27 include a ball, a machined shape, and a molded
shape.
[0039] Referring to FIG. 1, bias means 29 provides a counteracting
force to urge the actuator 27 to a stationary position relative to
the valve seat 25. Rotation 6 of the housing enclosure 3 generates
centrifugal forces that urge the actuator 27 to move radially
outward in opposition to the counteracting force of bias means 29.
The magnitude of the centrifugal force acting on actuator 27 is
proportional to the product of the mass of the actuator 27 and the
square of the rotational velocity of the housing enclosure 3
divided by the radial distance of the actuator 27 from the
rotational axis 4. The counteracting force of bias means 29 can be
provided by a compression spring, a compressible material, a coil
spring, a leaf spring, or a diaphragm. For purposes of
illustration, FIG. 1 shows a coil spring. The centrifugal
force-activated valve of the present invention can be tuned to
actuate at a predetermined rotational speed by selecting the mass
of the actuator 27 and the counteracting force of bias means
29.
[0040] In a preferred embodiment of the present invention, valve
seat 25 is integral to the valve chamber 23 and is made of the same
material as the housing enclosure 3. Valve seat 25 operates to
prevent fluid communication between the fluid discharge port 9 and
the valve chamber 23 when the actuator 27. is forcefully engaged
with the valve seat 25. Centrifugal force-activated valve 7a
operates as a normally closed valve when the valve seat 25 is
positioned radially inward of the actuator 27. For a normally open
valve, valve seat 25 is positioned radially outward of the actuator
27.
[0041] Referring to FIGS. 3a and 3b, there is provided an
illustration of a normally closed centrifugal force-activated valve
7 according to the present invention. FIG. 3a shows actuator 27
biased into a stationary position by bias means 29. In the
stationary position, actuator 27 is forcefully engaged with the
valve seat 25 and fluid communication between the fluid discharge
port 9 and the valve chamber 23 is prevented, as shown, by arrow
53. Actuator 27, moves radially outward from the stationary
position to an actuated position when the housing enclosure 3 is
rotated and the centrifugal force acting on actuator 27 exceeds the
counteracting force of bias means 29. In the actuated position, as
shown in FIG. 3b, actuator 27 is disengaged from valve seat 25
allowing fluid communication between the fluid discharge port 9 and
the valve chamber 23, as shown by arrow 55.
[0042] Referring to FIGS. 4a and 4b, there is provided an
illustration of a normally open centrifugal force-activated valve 7
according to the present invention. FIG. 4a shows actuator 97
biased into a stationary position by bias means 99. In the
stationary position, actuator 97 is forcefully disengaged from the
valve seat 95 allowing fluid communication between the fluid
discharge port 9 and the valve chamber 93, as shown, by arrow 55.
Actuator 97 moves radially outward from the stationary position to
an actuated position when the housing enclosure 3 is rotated and
the centrifugal force acting on actuator 97 exceeds the
counteracting force of bias means 99. In the actuated position, as
shown in FIG. 4b, actuator 97 is forcefully engaged with the valve
seat 95 preventing fluid communication between the fluid discharge
port 9 and the valve chamber 93, as shown by arrow 53. Optionally,
it may be desirable to position actuator stops 57 in valve chamber
93 to prevent bias means 99 from urging the actuator 97 into a
fluid discharge port 9 blocking position when the actuator is in
the stationary position. The actuator stops 57 are disposed
radially inward of the actuator 97.
[0043] In another embodiment of the present invention, a compliant
material 59 is conformally disposed on the valve seat 58, as
illustrated in FIG. 5a. The compliant material 59 forms a tight
seal between the actuator 56 and the valve seat 58 when the
actuator 56 is forcefully engaged with the valve seat 58.
Alternatively, the valve seat 58 may be a compliant material
positioned in the valve chamber, for example, an o-ring or a
gasket.
[0044] Referring to FIG. 5b, in an alternative embodiment of the
present invention, an elastomeric material 61 is disposed on the
actuator 60. The elastomeric material 61 forms a tight seal between
the actuator 60 and the valve seat 62 when the actuator 60 is
forcefully engaged against the valve seat 62, preventing fluid
communication between the fluid discharge port 9 and the valve
chamber 23.
[0045] In another embodiment of the present invention, the valve
chamber 23 includes a valve chamber cap 41 disposed in valve
chamber opening 43, as shown in FIG. 2a. The valve chamber opening
43 is disposed radially outward of the valve chamber 23 and is in
fluid communication with the valve chamber 23. The valve chamber
cap 41 has an outer surface 45, and an inner surface 47. The inner
surface 47 is in fluid communication with the valve chamber 23. The
valve chamber cap 41 allows for the insertion of the actuator 27,
the bias means 29, and optionally the valve seat 25 into the valve
chamber 23. The valve chamber cap 41 can be permanently attached to
the valve chamber opening 43, by gluing, welding, fasteners, or the
like. The valve chamber cap 41 and the valve chamber opening 43 can
be adapted to permit the valve chamber cap 41 to be removably
attached to the valve chamber opening 43, for example, using
threads, bayonet mount, friction fit, or an o-ring.
[0046] One advantage of the removable valve chamber cap 41 is that
it allows for application specific selection of a bias means and an
actuator. For example, prior to performing an assay using the
analytical device 1, a user can select the mass of actuator 27 and
the counteracting force of bias means 29 to actuate the centrifugal
force-activated valve 7 at a predetermined rotational speed.
[0047] In another embodiment of the present invention, as
illustrated in FIG. 2b, a valve chamber cap 42 includes fluid
extraction means 49 contained in the valve chamber cap 42.
Preferably, the fluid extraction means 49 is self sealing, for
example, a diaphragm or a septum. The fluid extraction means 49 is
in fluid communication with the inner surface 47 and outer surface
45 of the valve chamber cap 42. In some assays, it may be desirable
to analyze fluids that have been passed through the assay chamber
5. To extract fluid from the valve chamber 23, a device such as a
syringe is inserted through the fluid extraction means 49 to
withdraw fluid remaining in the valve chamber 23. Optionally, a
radially outward portion of the valve chamber 23 can be sized to
capture a specific volume of fluid to be extracted from the valve
chamber 23.
[0048] FIG. 2c illustrates another embodiment of the present
invention. A fluid drain 51 is disposed in a valve chamber cap 44.
Fluid drain 51 is in fluid communication with the inner surface 47
and the outer surface 45 of the valve chamber cap 44. Fluid
entering the valve chamber 23 exits the valve chamber 23 through
the fluid drain 51. Fluid drain 51 in valve chamber cap 44 may
either supplement or replace fluid drain 15 in the valve chamber
23.
[0049] In an alternative embodiment of the present invention, as
illustrated in FIG. 1, housing enclosure 3 has a reservoir plate 31
having a recessed portion defining a reservoir chamber 33
positioned radially outward of the assay chamber 5 and disposed
below the valve chamber 23. Reservoir chamber 33 is in fluid
communication with fluid drain 15. Fluid exiting the valve chamber
23 through the fluid drain 15 enters the reservoir chamber 33, as
shown by arrow 21. Reservoir chamber 33 can be sized to accommodate
any volume, preferably about 3 milliliters. As the volume of the
reservoir chamber 33 is decreased the distance between the
reservoir chamber 33 and the fluid drain 15 may also decrease. If
the distance is such that fluid entry into the reservoir chamber is
restricted, a fluid channel 16 may be included to provide a clear
and unobstructed path for fluid exiting the fluid drain 15 to enter
the reservoir chamber 33. Fluid channel 16 is disposed below the
fluid drain 15 and is in fluid communication with the fluid drain
15 and the reservoir chamber 33. Fluid channel 16 has a first
channel wall 18 disposed opposite to and substantially parallel
with a second channel wall 20. Fluid channel 16 is substantially
wider than fluid drain 15 and is substantially symmetrical with
fluid drain 15.
[0050] It may be desirable to recover fluids used in an assay for
subsequent analysis or reactions. Reservoir plate 31 may include
fluid extraction means 35 in fluid communication with the reservoir
chamber 33 and the exterior of the reservoir plate 31. Preferably,
the fluid extraction means 35 is self sealing, for example, a
diaphragm or a septum. Typically, a syringe or the like is inserted
through the fluid extraction means 35 and fluid is withdrawn from
the reservoir chamber 33.
[0051] FIG. 1 illustrates an alternative embodiment of the present
invention. Air or gas 39 displaced by fluid 21 entering the
reservoir chamber 33 from centrifugal force-activated valve 7a is
vented to the exterior of housing enclosure 3 through a vapor vent
37 of centrifugal force-activated valve 7b. Vapor vent 37 is in
fluid communication with the valve chamber 73 of centrifugal
force-activated valve 7b. Rotation 6 of the housing enclosure 3
above the rotational speed necessary to actuate valve 7b from the
stationary position to the actuated position, forces the actuator
77 to disengage from the valve seat 75. Air or gas 39 enters the
valve chamber 73 through the fluid drain 78 and exits the valve
chamber 73 through the valve seat 75 and enters the vapor vent 37.
Centrifugal force-activated valve 7a is in fluid communication with
the assay chamber 5. Fluid 21 entering fluid drain 15 of valve 7a,
displaces air or gas 39 in the reservoir chamber 33. Valve 7b is
not in fluid communication with the assay chamber 5. However, the
reservoir chamber 33 is common to both valve 7a and valve 7b;
therefore, fluid entering the reservoir chamber 33 from centrifugal
force-activated valve 7a displaces air or gas 39 through
centrifugal force-activated valve 7b.
[0052] In a most preferred embodiment, the housing enclosure 3 has
a portion defining an opening 63, as shown in FIG. 6. The opening
63 is positioned over the assay chamber. An analytical substrate 65
having an inner surface 67 and an outer surface 68 is disposed in
the opening 63. The inner surface 67 is positioned above and in
opposing relation to the assay chamber 5 and is in fluid
communication with the assay chamber 5. An active surface 13 may be
positioned on the inner surface 67 of the analytical substrate 65.
Additionally, the analytical substrate 65 can be made transparent
to optical detection means 69. The optical detection means 69 is
external to the analytical device 1. The optical detection means
69, scans through the analytical substrate 65 to assay the active
surface 13, as shown by arrow 71. Suitable materials for the
analytical substrate 65 include glass, plastics, fused silica, and
quartz. The analytical substrate 65 can be secured in the opening
63 using glue, adhesives, a weld, fasteners, or the like.
Preferably, the active surface 13 is positioned at a radially
outward portion of the inner surface 67, so that fluid directed
radially outward by rotation 6 of the housing enclosure 3 will be
urged into contact with the active surface 13.
[0053] In alternative preferred embodiments, the active surface 13
includes biochemical, chemical, or biological moieties. The active
surface 13 can be disposed on the surface of a structure attached
to the inner surface 67 of the analytical substrate 65, for
example, balls, beads, or other structure that can be fixedly
attached to the inner surface 67. The active surface 13 may
comprise an array or other orderly structure of biomolecular
probes. The biomolecular probes can be DNA, DNA fragments RNA, RNA
fragments, reagents, protein, protein fragments, lipids, and lipid
fragments. A dye, label, tag, or reagent may be attached or dried
onto to the active surface. Alternatively, fluid introduced into
the assay chamber 5 may contain a dye, label, tag, or reagent.
Preferably, the active surface 13 is disposed at a radially outward
position on the assay chamber 5 or the analytical substrate 65.
Rotation 6 of the analytical device 1, generates a radially outward
flow of the fluid, bringing the fluid into contact with the active
surface 13.
[0054] Additionally, the active surface 13 can be disposed on the
surface of a structure that is not attached to the analytical
substrate 65 or to the interior surface of the assay chamber 5. For
example, the active surface 13 can be disposed on balls or beads
loosely contained in the assay chamber 5. Further, after the
conclusion of a reaction, the balls or beads can be extracted from
fluid remaining in the valve chamber 23 via the fluid extraction
means 49 in valve chamber cap 42 as illustrated in FIG. 2b or from
fluid captured in the reservoir chamber 33 via the fluid extraction
means 35 in the reservoir plate 31 as illustrated in FIG. 1.
[0055] The best mode for making the analytical device 1 is to
injection mold the housing enclosure 3, preferably from plastic.
The bias means 29 is a coil spring and the actuator 27 is a
stainless steel ball. Preferentially, an o-ring is positioned on
the valve seat 25 between the actuator 27 and the valve seat 25, to
supply compliance. The coil spring holds the stainless steel ball
against the o-ring of the valve seat 25.
[0056] In a preferred embodiment of a method according to the
present invention, a fluid sample may be introduced into the assay
chamber 5 via fluid introducing means 11. The analytical device 1
is spun at a first rotational speed to generate a radially outward
flow of the sample, whereby the fluid reacts with the active
surface 13. The first rotational speed is below the threshold
rotational speed necessary to actuate the centrifugal
force-activated valve 7, from the stationary closed state to the
open actuated state. The closed valve 7 prevents the sample from
exiting the assay chamber 5 through the valve 7. Spinning at the
first rotational speed continues until a predetermined reaction
time has passed or the reaction has reached a desired state of
completion. After spinning at the first rotational speed, the
analytical device 1 is then spun at a second rotational speed
greater than the first rotational speed. The second rotational
speed exceeds the threshold rotational speed necessary to actuate
the valve to the open actuated state. The centrifugal
force-activated valve 7 opens and fluid exits the assay chamber 5
through the valve 7. The introducing step, the first rotational
speed step, and the second rotational speed step may be repeated as
necessary to complete the reaction.
[0057] In an alternate embodiment, after spinning the analytical
device 1 at the second rotational speed, a wash fluid may be
introduced into the assay chamber 5 via fluid introducing means 11.
The analytical device 1 is spun at a first rotational speed to
distribute the wash fluid. The wash fluid removes un-reacted sample
from the active surface 13 and the assay chamber 5. The analytical
device 1 is then spun at the second rotational speed to remove the
wash fluid from the assay chamber 5. The introducing step, the
first rotational speed step, and the second rotational speed step
may be repeated as necessary to ensure complete washing of the
active surface 13 and the assay chamber 5.
[0058] In another embodiment, the analytical device 1 is spun at
the second rotational speed to remove any sample remaining in the
assay chamber 5. The active surface 13 is assayed by scanning the
active surface 13 with optical detection means 69. The optical
detection means are external to the analytical device 1.
[0059] In the most preferred embodiment of a method according to
the present invention, the analytical device 1 includes an
analytical substrate 65 having an active surface 13 disposed on a
radially outward portion. A fluid sample is introduced into the
assay chamber 5 via fluid introducing means 11. The analytical
device 1 is agitated to mix the sample and to generate a radially
outward flow of the sample, whereby the sample reacts with the
active surface 13. The agitation can be accomplished, for example,
by reversing the direction of rotation 6 of the analytical device 1
multiple times. Mixing continues until a predetermined reaction
time has passed or the reaction has reached a desired state of
completion. The analytical device 1, is then spun at the second
rotational speed to empty the sample from the assay chamber 5. The
introducing step, the mixing step, and the second rotational speed
step may be repeated as necessary to complete the reaction.
[0060] In an alternate embodiment, after spinning the analytical
device 1 at the second rotational speed, a wash fluid may be
introduced into the assay chamber 5 via fluid introducing means 11.
The analytical device 1 is spun at a first rotational speed to
generate a radially outward flow of the wash fluid. The wash fluid
removes un-reacted sample from the active surface 13, the
analytical substrate 65, and the assay chamber 5. The analytical
device 1 is then spun at the second rotational speed to empty the
wash fluid from the assay chamber 5. The introducing step, the
first rotational speed step, and the second rotational speed step
may be repeated as necessary to ensure complete washing of the
active surface 13, the analytical substrate 65, and the assay
chamber 5.
[0061] In another embodiment, the housing enclosure 3 has a
reservoir plate 31 positioned radially outward of the assay chamber
5 and positioned below the centrifugal force-activated valve 7a.
Reservoir plate 31 includes a reservoir chamber 33. The analytical
device 1 is spun at the second rotational speed to remove fluid
from the assay chamber 5. Centrifugal force-activated valve 7a,
opens and fluid exits the assay chamber, enters the valve, and is
stored in the reservoir chamber 33. Optionally, fluid in the
reservoir chamber 33 may be removed via fluid extraction means 35.
A syringe or the like may be used to withdraw fluid from the
reservoir chamber for further analysis or other use.
[0062] In another embodiment, the analytical device 1 is spun at
the second rotational speed to remove any sample remaining in the
assay chamber 5. The analytical substrate 65 is transparent to
optical detection means 69. The active surface 13 is assayed by
scanning the active surface 13 through a transparent portion of the
analytical substrate 65 via the optical detection means 69. The
optical detection means are external to the analytical device
1.
[0063] Although several specific embodiments of the invention have
been described and illustrated, the invention is not limited to the
specific forms or arrangements of parts so described and
illustrated. The invention is only limited by the claims.
* * * * *