U.S. patent application number 10/105311 was filed with the patent office on 2002-10-03 for method and apparatus for producing probe carrier.
Invention is credited to Kameyama, Makoto, Okamoto, Tadashi, Okamura, Nobuyuki.
Application Number | 20020142341 10/105311 |
Document ID | / |
Family ID | 26612442 |
Filed Date | 2002-10-03 |
United States Patent
Application |
20020142341 |
Kind Code |
A1 |
Kameyama, Makoto ; et
al. |
October 3, 2002 |
Method and apparatus for producing probe carrier
Abstract
Ambient humidity for a plurality of nozzles of a liquid ejection
device for ejecting droplets of solutions containing probes to the
surface of a carrier is controlled to 50% or more, preferably 60%
or more. Part of solution supply passages to the plurality of
nozzles are constructed from gas permeable membranes permitting
gas-liquid separation under reduced pressure. These gas permeable
membrane portions are gathered and altogether placed under reduced
pressure to remove air bubbles from the respective solutions
supplied to the plural nozzles and decrease the amount of a
dissolved gas causing air bubble generation.
Inventors: |
Kameyama, Makoto; (Chiba,
JP) ; Okamura, Nobuyuki; (Kanagawa, JP) ;
Okamoto, Tadashi; (Kanagawa, JP) |
Correspondence
Address: |
FITZPATRICK CELLA HARPER & SCINTO
30 ROCKEFELLER PLAZA
NEW YORK
NY
10112
US
|
Family ID: |
26612442 |
Appl. No.: |
10/105311 |
Filed: |
March 26, 2002 |
Current U.S.
Class: |
435/6.11 ;
427/2.11; 435/287.2 |
Current CPC
Class: |
B01J 2219/00725
20130101; C40B 40/06 20130101; B01J 2219/00659 20130101; B01J
2219/0074 20130101; B01J 2219/00605 20130101; B01L 2200/142
20130101; B01J 2219/00527 20130101; B01L 2200/0684 20130101; B01J
19/0046 20130101; B01J 2219/00385 20130101; B01L 3/0268 20130101;
C40B 40/10 20130101; B01J 2219/00698 20130101; B01J 2219/0072
20130101; B01J 2219/00722 20130101; B01J 2219/00378 20130101; C40B
60/14 20130101; B01J 2219/0036 20130101 |
Class at
Publication: |
435/6 ;
435/287.2; 427/2.11 |
International
Class: |
C12Q 001/68; C12M
001/34; B05D 003/00 |
Foreign Application Data
Date |
Code |
Application Number |
Mar 28, 2001 |
JP |
094340/2001 |
Mar 28, 2001 |
JP |
094111/2001 |
Claims
What is claimed is:
1. A method for producing a probe carrier comprising: scanning a
liquid ejection head having a plurality of liquid ejection nozzles
relative to a support device supporting a carrier thereon to impart
a plurality of solutions to predetermined positions on the carrier,
the plurality of solutions containing plural types of probes
capable of specifically binding to target substances, thereby
obtaining the probe carrier, wherein at least the support device
and the liquid ejection head are installed in an environment where
humidity can be maintained at 50% or more.
2. A method for producing a probe carrier as claimed in claim 1,
wherein part of solution supply passages between a plurality of
probe solution reservoirs for supplying plural types of probe
solutions to said plurality of nozzles of said liquid ejection head
and said respective nozzles are constructed from hollow yarns
permitting gas-liquid separation under reduced pressure, and an
exterior of said hollow yarn supply passage portions is reduced in
pressure, whereby air bubbles infiltrating the probe solutions
supplied to said respective nozzles are removed, and an amount of
dissolved oxygen in the solution is decreased.
3. A method for producing a probe carrier as claimed in claim 1,
wherein said humidity is maintained at 60% or more.
4. A method for producing a probe carrier as claimed in claim 1,
wherein said liquid ejection has a thermal energy generator which
gives thermal energy for ejection to a liquid in said nozzle.
5. A method for producing a probe carrier as claimed in claim 1,
wherein said probe is any of DNA, RNA, CDNA (complementary DNA),
PNA, oligonucleotide, polynucleotide, other nucleic acid,
oligopeptide, polypeptide, protein, enzyme, substrate for enzyme,
antibody, epitope for antibody, antigen, hormone, hormone receptor,
ligand, ligand receptor, oligosaccharide, and polysaccharide.
6. An apparatus for producing a probe carrier, comprising: a
support device for supporting a carrier; a liquid ejection head for
imparting a plurality of solutions to predetermined positions on
said carrier, said plurality of solutions containing probes capable
of specifically binding to target substances; and a scan device for
scanning said liquid ejection head relative to said support device,
and wherein said liquid ejection head includes a plurality of
reservoirs accommodating a plurality of probe solutions containing
the plural types of probes specifically binding to the target
substances, and a plurality of liquid ejection nozzles for
receiving supply of the probe solutions from said plurality of
reservoirs and imparting droplets of the probe solutions onto the
predetermined positions on said carrier, and at least said support
device and said liquid ejection head are installed in an
environment where humidity can be maintained at 50% or more.
7. An apparatus for producing a probe carrier as claimed in claim
6, wherein part of solution supply passages between said plurality
of probe solution reservoirs and said respective nozzles are
constructed from hollow yarns comprising gas permeable membranes
permitting gas-liquid separation under reduced pressure, and said
hollow yarn supply passage portions are passed into a vacuum
chamber.
8. An apparatus for producing a probe carrier as claimed in claim
6, wherein said humidity is 60% or more.
9. An apparatus for producing a probe carrier as claimed in claim
6, wherein said liquid ejection head is equipped with a thermal
energy generator which gives thermal energy for ejection to a
liquid in said nozzle.
10. An apparatus for producing a probe carrier as claimed in claim
6, wherein said probe is any of DNA, RNA, cDNA (complementary DNA),
PNA, oligonucleotide, polynucleotide, other nucleic acid,
oligopeptide, polypeptide, protein, enzyme, substrate for enzyme,
antibody, epitope for antibody, antigen, hormone, hormone receptor,
ligand, ligand receptor, oligosaccharide, and polysaccharide.
11. An apparatus for producing a probe carrier, comprising: a
plurality of probe imparting chambers each including a support
device for supporting a carrier, a liquid ejection head for
imparting plural types of probe solutions, capable of specifically
binding to target substances, to predetermined positions on said
carrier, and a scan device for scanning said liquid ejection head
relative to said support device; and means for transporting said
carrier, and wherein the other of the plurality of chambers are
arranged around said transport means as a center, and the transport
means transports the carrier for insert and taking out the carrier
onto and from the chambers.
12. An apparatus for producing a probe carrier as claimed in claim
11, wherein the apparatus further comprises testing chamber for
testing a probe impartment state on a surface of said carrier.
13. An apparatus for producing a probe carrier as claimed in claim
11, wherein at least ambient humidity for said liquid ejection head
constituting said plurality of probe imparting chambers is
maintained at 50% or more.
14. An apparatus for producing a probe carrier as claimed in claim
11, wherein part of solution supply passages between a plurality of
probe solution reservoirs and respective nozzles of said liquid
ejection head are constructed from hollow yarns permitting
gas-liquid separation under reduced pressure, and said hollow yarn
supply passage portions are passed into a vacuum chamber.
15. An apparatus for producing a probe carrier as claimed in claim
11, wherein ambient humidity for said liquid ejection head is 60%
or more.
16. An apparatus for producing a probe carrier as claimed in claim
11, wherein said liquid ejection head is equipped with a thermal
energy generator which gives thermal energy for ejection to a
liquid in said nozzle.
17. An apparatus for producing a probe carrier as claimed in claim
11, wherein said probe is any of DNA, RNA, cDNA (complementary
DNA), PNA, oligonucleotide, polynucleotide, other nucleic acid,
oligopeptide, polypeptide, protein, enzyme, substrate for enzyme,
antibody, epitope for antibody, antigen, hormone, hormone receptor,
ligand, ligand receptor, oligosaccharide, and polysaccharide.
Description
[0001] This application is based on Japanese Patent Application
Nos. 2001-094340 filed Mar. 28, 2001 and 2001-094111 filed Mar. 28,
2001, the contents of which are incorporated hereinto by
reference.
BACKGROUND OF THE INVENTION
[0002] 1. Field of the Invention
[0003] This invention relates to a method and apparatus for
producing a probe carrier. More specifically, the invention relates
to a method and apparatus for producing a probe carrier which
comprises probes fixed in a two-dimensional array arrangement onto
a carrier.
[0004] 2. Description of the Related Art
[0005] In analyzing the base sequence of gene DNA, or in making
genetic diagnosis simultaneously for many items with high
reliability, it is necessary to screen DNA having the desired base
sequence with the use of plural types of probes. DNA microchips
have attracted attention as means of providing the plural types of
probes used in this screening procedure. High throughput screening
or combinatorial chemistry for drugs, etc. also requires that many
solutions of candidate proteins or drugs (for example, 96 types,
384 types or 1,536 types) be arranged, and subjected to orderly
screening. For these purposes, methods for arranging many types of
drugs, screening techniques automated in the arranged state,
dedicated devices, and software for controlling a series of
screening operations or processing the results statistically are
under development.
[0006] These parallel screening operations basically use so-called
probe carriers, each of which comprises many known probes, as
screening means, arranged for a substance to be evaluated, thereby
detecting the presence or absence of actions on or reactions with
the probes under the same conditions. Generally, what actions on or
reactions with probes should be utilized is determined beforehand.
Thus, the probes loaded on one probe carrier belong to one type of
substance, if classified roughly, such as a group of DNA probes
with different base sequences. That is, substances utilized as one
group of probes include, for example, DNA's, proteins, and
synthetic chemicals (drugs). In many cases, a probe carrier
comprising plural types of probes forming a group is used.
Depending on the nature of the screening operation, an arrayed form
in which DNA's having the same base sequence, proteins having the
same amino acid sequence, or the same chemicals are arranged at
many points may be used as probes. Such an array is used mainly for
drug screening.
[0007] Concretely, a probe carrier comprising plural types of
probes forming a group often takes a form in which plural types
constituting a group of DNA's having different base sequences, a
group of proteins having different amino acid sequences, or a group
of different chemicals are arranged in an array on a carrier or the
like according to a predetermined order of arrangement. Of these
probe carriers, the DNA probe carrier is used in analyzing the base
sequence of gene DNA or in conducting simultaneous, highly reliable
genetic diagnosis of many items.
[0008] One of the problems with the probe carrier comprising plural
types of probes forming a group is how to place as many types of
probes as possible, e.g., DNA probes having many types of base
sequences, on one carrier. In other words, the problem is how to
arrange the probes in an arrayed form at a high density.
[0009] As one method for fixing plural types of probes in an
arrayed form on a carrier, there can be named a method described in
U.S. Pat. No. 5,424,186, the method for preparing DNA probes having
different base sequences in an arrayed form by sequential
elongation reaction of DNA on a solid phase carrier with the use of
photodegradable protective groups and photolithography. The use of
this method makes it possible to produce, for example, a DNA probe
carrier loaded with more than 10,000 types, per cm.sup.2, of DNA's
different in sequence. With this method, when DNA is to be
synthesized by sequential elongation reaction, a photolithography
step is performed using dedicated photomasks for four types of
bases (A, T, C, G) to elongate any of the bases selectively at a
predetermined location in the array, thereby synthesizing plural
types of DNA's having desired base sequences in a predetermined
arrangement on a carrier. As DNA strand lengthens, therefore, the
cost required for production becomes high, and a long time is
needed. In addition, the efficiency of nucleotide synthesis at each
elongation stage is not 100%, so that the proportion of DNA's
undergoing a deficiency in the designed base sequence is not low.
Furthermore, the use of the photodegradable protective group during
synthesis results in a low efficiency of synthesis, in comparison
with the use of an ordinary acid-degradable protective group. Thus,
an array obtained finally shows a low proportion of DNA's having
the designed base sequences.
[0010] Moreover, the product directly synthesized on the solid
phase carrier is used unchanged. Thus, it is, of course, impossible
to remove DNA having a defective base sequence from DNA's having
the designed base sequences by purification and separation. Another
possible problem is that the base sequences of DNA's synthesized on
the carrier cannot be confirmed in the resulting array. This
problem means the following facts: Assume that little elongation of
a predetermined base takes place during a certain elongation stage
because of a mistake in the process or the like, leading to the
appearance of a completely defective product. Screening using this
defective probe carrier gives erroneous results, but this fault
cannot be prevented at all. This inability to confirm the base
sequence is a major and essential problem with the above-described
method.
[0011] Another method proposed for producing a probe carrier
comprises synthesizing and purifying DNA's for probes beforehand,
confirming their base lengths if desired, and supplying the
respective DNA's onto a carrier by a device such as a
microdispenser. PCT International Patent Application Laid-open No.
WO 95/35505 describes a method of supplying DNA's onto a membrane
by use of a capillary. The application of this method, in
principle, enables an array of about 1,000 DNA's/cm.sup.2 to be
produced. Basically, this method involves supplying a probe
solution to a predetermined position on a carrier by a single
capillary-shaped dispense device for each probe, and repeating this
procedure, thereby producing a probe carrier. No problem is posed
if dedicated capillaries are used for the respective probes.
However, if a small number of capillaries are used to perform the
same procedure, the capillaries need to be washed thoroughly in
changing the types of the probes in order to prevent mutual
contamination. The position of supply should also be controlled for
each procedure. Thus, the method is not said to be suitable for
producing an array having many types of probes arranged at a high
density. Besides, the supply of the probe solution to the carrier
is carried out by tapping the front end of the capillary on the
carrier. Thus, neither reproducibility nor reliability is
complete.
[0012] As another method, a proposal has been made for a method in
which when solid phase synthesis of DNA is performed on a carrier,
a solution of a substance necessary for synthesis is supplied onto
the carrier by the ink-jet method at each elongation stage. For
example, European Patent Publication No. EP 0 703 825B1 describes a
method for solid phase synthesis of plural types of DNA's having
predetermined base sequences by supplying nucleotide monomers and
activators, which are utilized in solid phase synthesis of DNA, by
different piezo jet nozzles. The supply (coating) by this ink-jet
method, as contrasted with the supply (coating) of a solution using
the capillary, is high in reliability, as seen from reproducibility
of the amount of supply, and permits microfabrication of the
structure of the nozzle. Thus, this method has features suitable
for achieving a high density probe carrier. However, this method
also basically utilizes sequential elongation reaction of DNA on
the carrier, and thus still entails problems, such as the
aforementioned major problem with the method described in U.S. Pat.
No. 5,424,186, i.e., the problem that the base sequences of DNA's
synthesized on the carrier cannot be confirmed. This method
dissolves the tiresome procedure of performing a photolithography
step using a dedicated mask at each elongation stage, but remains
slightly problematical in terms of the requirement indispensable to
the probe carrier that the predetermined probes be fixed at
respective points. The aforementioned publication EP 0 703 825B1
describes only a method using a plurality of individually formed
piezo-jet nozzles. The method using the small number of the
nozzles, like the aforementioned method using capillaries, is not
necessarily suitable for producing a high density probe
carrier.
[0013] Japanese Patent Application Laid-open No. 11-187900 (1999)
discloses a method for forming spots containing probes on a solid
phase by adhering liquids containing the probes, as droplets, to
the solid phase by a thermal ink jet head. However, the ink jet
head used is an ordinary printer head, and thus does not have an
optimal structure for producing a probe carrier. Detailed reasons
for this will be described below.
[0014] The conventional ink jet head is a method developed for
printing of characters or images. Thus, the solution used for it is
ink of a single color (black) in the case of monochromatic
(generally black) printing, or generally comprises inks of three
primary colors, i.e., yellow (Y), cyan (C) and magenta (M) in the
case of color printing. In color printing, variable density inks of
black or Y, M and C may be used where necessary, but more than ten
types of inks, at most, are not used.
[0015] A large amount of ink is used for printing on a paper face.
Thus, the conventional head for ink jet printing is equipped with a
full capacity tank (reservoir) to be filled with ink, a channel for
guiding the ink to a nozzle, and the nozzle for ejecting the
ink.
[0016] A liquid ejection head for production of a probe carrier, on
the other hand, is required to eject as many types of liquids as
possible, as explained earlier. If the head has a plurality of
nozzles, the head is desirably one having the same number of
solution reservoirs as the number of the plural nozzles, the
solution reservoirs corresponding one-to-one to the plurality of
nozzles.
[0017] With a liquid ejection device for production of a probe
carrier, moreover, the consumption of the liquid is small compared
with printing on the paper face, so that the reservoir with a
relatively small capacity is sufficient.
[0018] With the conventional ordinary head for ink jet printing,
furthermore, desired ink needs to be ejected at a desired position
on the paper face in order to form characters or images. Thus, the
head is configured to be capable of selecting respective nozzles
independently with arbitrary timings. Powered transistors and
logical circuits, necessary for ejecting ink (liquid) from the
desired nozzles, may be provided outside or inside the head.
[0019] Ink jet systems are classified into a thermal jet system for
ejecting the liquid by thermal energy generated by a heater, and a
piezo-ink jet system for ejecting the liquid by deformation of a
piezoelectric element caused when a voltage is applied to the
piezoelectric element. Of these systems, the thermal jet system is
simple in structure as compared with the piezo-ink jet system, and
is suitable for a downsized head and a multi-nozzle head.
[0020] As described above, the method of producing a probe carrier
by means of a liquid ejection device is excellent in that minute
amounts of probe solutions to be imparted are arranged at a high
density on a solid phase carrier. The minimum ejection amount of
the liquid ejected at a time from an ejection orifice of the liquid
ejection device can be decreased to the range of 0.1 pl to 50 pl.
Even when many wells are placed on the carrier and minute amounts
of the probe solutions are supplied into the respective wells, the
sizes of the wells can be made small to achieve an even higher
density.
SUMMARY OF THE INVENTION
[0021] Various advantages can be obtained by using the
above-mentioned liquid ejection device in producing a probe
carrier. However, new problems to be solved surface when a probe
carrier producing method and apparatus using the liquid ejection
device are put into practice.
[0022] To produce a relatively large scale probe array having not
less than 1,000 types of solutions, the efficiency is better when
spotting the solutions in a plurality of steps using a plurality of
relatively small scale liquid ejection devices, than when
performing production in one step with the use of a single upsized
liquid ejection device having an increased number of nozzles.
Development of an apparatus preferred for use in such a case is
necessary. In response to this need, the inventors of the present
application propose a configuration employing a so-called single
wafer processing device in which transport means, such as a carrier
transport robot, is provided at the center, and plurality of probe
imparting means are arranged around the transport means. In this
case, testing means and drying means in charge of related steps are
also arranged around the central transport means.
[0023] Not only the use of the single wafer processing device, but
also the completion of all spotting procedure in one step poses the
problem that the first ejection of the solution may fail, or that
subsequent ejection may also be impeded. When checking by the
testing means shows the necessity for performing spotting again,
the dots formed by the previous spotting are already dry. Such a
problem becomes more striking particularly in the single wafer
processing in which the carrier is needed to transport from one of
the means to another of the means.
[0024] The single wafer processing, as well as the one-step method,
thus poses the common problem, for which two causes are
conceivable.
[0025] One of the causes is that a front end portion of the nozzle
of the liquid ejection head is prone to dry, thereby increasing the
viscosity of the solution in the nozzle, leading to unsuccessful
ejection of the probe solution, or disordering the direction of
ejection.
[0026] To produce the probe carrier means to use a number of types
of solutions, use the corresponding number of nozzles, and impart
desired probes accurately from the respective nozzles to many
wells. This means that unlike the ink jet head for printing, the
using frequency of each nozzle for ejection is extremely low; the
head for printing can be capped to prevent drying of its nozzle
front end portion during standby; whereas the liquid ejection head
for production of a probe array cannot be capped for preventing
drying of the nozzle front end portion, because some of the many
nozzles are always in use. This is one of the causes for the
tendency toward drying of the nozzle front end portion of the
liquid ejection head built into the probe carrier production
apparatus.
[0027] The other cause for non-ejection is air bubbles infiltrated
into or generated in the probe solution. That is, air bubbles
infiltrate or are generated in the solution somewhere in a solution
supply passage leading from the probe solution reservoir to the
front end portion of each nozzle. When these air bubbles arrive at
the front end of the nozzle, the state of absence of the solution
in the nozzle occurs, resulting in non-ejection. In the absence of
the solution in the nozzle, the interior of the nozzle at the front
end of the nozzle is directly exposed to the outside air, with the
result that the front end portion of the nozzle is rapidly dried.
If air bubbles are present in the solution within the nozzle,
moreover, the air bubbles induce a drop in the ejection pressure,
directly causing the failure of ejection of the probe solution.
[0028] Therefor, a first object of the present invention is to
provide a method and an apparatus for producing a probe carrier,
which can always prevent drying of a front end portion of a nozzle
for ejection of a probe solution, and in which no inconvenience
occurs to the ejection of the probe solution.
[0029] A second object of the present invention is to provide a
single wafer processing apparatus capable of imparting a vast
variety of probes efficiently onto a probe carrier.
[0030] To attain the foregoing objects, the present inventors
conducted in-depth studies and obtained the following findings:
[0031] (i) If ambient humidity at the front end portion of the
nozzle is maintained at not less than 50%, drying of the nozzle
front end portion over time can be prevented. The set humidity is
preferably 60% or more. A concrete constitution for setting and
maintaining such ambient humidity is preferably a constitution in
which the liquid ejection nozzle for imparting the probe solution
onto the supported carrier is installed in an environment where
humidity can be maintained at 50% or more, preferably 60% or
more.
[0032] (ii) Part of solution supply passages between the plurality
of probe solution reservoirs and the respective nozzles are
constructed from hollow yarns comprising gas permeable membranes
permitting gas-liquid separation under reduced pressure, hollow
yarn portions of the supply passages are bundled, the bundled
hollow yarn supply passage portions are passed into a vacuum
chamber, and the exterior of the bundled hollow yarn supply passage
portions is reduced in pressure. By so doing, the infiltrating air
bubbles can be removed, and the amount of dissolved oxygen in the
solution, the cause of air bubble generation, can be decreased
efficiently.
[0033] The present invention has been accomplished based on the
above findings.
[0034] A first apparatus for producing a probe carrier according to
the present invention is an apparatus comprising: a support device
for supporting a carrier; a liquid ejection head for imparting a
plurality of solutions to predetermined positions on the carrier,
the plurality of solutions containing plural types of probes
capable of specifically binding to target substances; and a scan
device for scanning the liquid ejection head relative to the
support device,
[0035] and wherein the liquid ejection head includes a plurality of
reservoirs accommodating a plurality of probe solutions containing
the plural types of probes specifically binding to the target
substances, and a plurality of liquid ejection nozzles for
receiving the supply of the probe solutions from the plurality of
reservoirs and imparting droplets of the probe solutions onto the
predetermined positions on the carrier,
[0036] and at least the support device and the liquid ejection head
are installed in an environment where humidity can be maintained at
50% or more.
[0037] In this apparatus, it is desired that part of solution
supply passages between the plurality of probe solution reservoirs
and the respective nozzles are constructed from hollow yarns
comprising gas permeable membranes permitting gas-liquid separation
under reduced pressure, hollow yarn portions of the supply passages
are bundled, and the bundled hollow yarn supply passage portions
are passed into a vacuum chamber. According to this configuration,
the exterior of the bundled hollow yarn supply passage portions can
be reduced in pressure. As a result, air bubbles infiltrating the
probe solutions supplied to the respective nozzles can be removed,
and the amount of dissolved oxygen in the solution, the cause of
air bubble generation, can be decreased efficiently.
[0038] A first method for producing a probe carrier according to
the present invention is a method comprising:
[0039] scanning a liquid ejection head having a plurality of liquid
ejection nozzles relative to a support device supporting a carrier
thereon to impart a plurality of solutions to predetermined
positions on the carrier, the plurality of solutions containing
plural types of probes capable of specifically binding to target
substances, thereby obtaining the probe carrier,
[0040] wherein at least the support device and the liquid ejection
head are installed in an environment where humidity can be
maintained at 50% or more.
[0041] In this method, it is preferred that part of solution supply
passages between a plurality of probe solution reservoirs for
supplying plural types of probe solutions to the plurality of
nozzles of the liquid ejection head and the respective nozzles are
constructed from hollow yarns comprising gas permeable membranes
permitting gas-liquid separation under reduced pressure, hollow
yarn portions of the supply passages are bundled, the bundled
hollow yarn supply passage portions are passed into a vacuum
chamber, and the exterior of the bundled hollow yarn supply passage
portions is reduced in pressure, whereby air bubbles infiltrating
the probe solutions supplied to the respective nozzles are removed,
and the amount of dissolved oxygen in the solution, the cause of
air bubble generation, is decreased efficiently.
[0042] By this method, no air bubbles are generated in the probe
solution supplied, whereby a single wafer processing type method
and apparatus for producing a probe carrier can be provided, in
which no inconvenience occurs to the ejection of the probe solution
even when the probe carriers continue to be produced.
[0043] A second apparatus for producing a probe carrier according
to the present invention is an apparatus comprising: a plurality of
probe imparting chambers each including a support device for
supporting a carrier, a liquid ejection head for imparting plural
types of probe solutions, capable of specifically binding to target
substances, to predetermined positions on the carrier, and a scan
device for scanning the liquid ejection head relative to the
support device; and means for transporting the carrier, and wherein
the other of the plurality of chambers are arranged around the
transport means as the center, and the transport means transports
the carrier for inserting and taking out the carrier into and from
each of the chambers.
[0044] In the production apparatus of this constitution, it is
desired that at least ambient humidity for the liquid ejection head
constituting the plurality of probe imparting means is maintained
at 50% or more.
[0045] In this apparatus, it is also desired that part of solution
supply passages between a plurality of probe solution reservoirs
and respective nozzles of the liquid ejection head are constructed
from hollow yarns comprising gas permeable membranes permitting
gas-liquid separation under reduced pressure, hollow yarn portions
of the supply passages are bundled, and the bundled hollow yarn
supply passage portions are passed into a vacuum chamber. According
to this configuration, the exterior of the bundled hollow yarn
supply passage portions can be reduced in pressure. As a result,
air bubbles infiltrating the probe solutions supplied to the
respective nozzles can be removed, and the amount of dissolved
oxygen in the solution, the cause of air bubble generation, can be
decreased efficiently.
[0046] The present invention can provide a single wafer processing
type method and apparatus for producing a probe carrier, in which
when very many probes to be imparted onto a carrier are to be
imparted by the single wafer processing type apparatus dividedly in
a plurality of steps, drying of a front end portion of a nozzle for
ejection of a probe solution can be always prevented, which are
free from generation of air bubbles in the probe solution supplied,
and in which solutions on dots on the carrier can be prevented from
drying before completion of the impartment of all probes, whereby
first ejection of the probe solution can be reliably induced in the
production of the probe carrier having very many types of
solutions, in which no inconvenience occurs to the ejection of the
probe solution even when the probe carriers continue to be
produced, and in which the dot-shaped solutions on the surface of
the carrier before completion of probe impartment and during
movement between the steps do not dry before all the impartments
are completed.
[0047] A second method for producing a probe carrier according to
the present invention is a method comprising: using an apparatus
for producing a probe carrier comprising a plurality of probe
imparting means each including a support device for supporting a
carrier, a liquid ejection head for imparting plural types of probe
solutions, capable of specifically binding to target substances, to
predetermined positions on the carrier, and a scan device for
scanning the liquid ejection head relative to the support device,
testing means for testing a probe impartment state on a surface of
the carrier, and means for transporting the carrier, and wherein
other chambers are arranged around the transport means as the
center; supporting the carrier on the support device in each of the
probe imparting means; using the liquid ejection head having a
plurality of liquid ejection nozzles; and scanning the liquid
ejection head relative to the support device to impart the plural
types of probe solutions to predetermined positions on the carrier,
thereby obtaining the probe carrier.
[0048] In the production method of this constitution, it is desired
that at least ambient humidity for the liquid ejection head
constituting the plurality of probe imparting means is maintained
at 50% or more, whereby drying of front end portion of the liquid
ejection nozzle is relieved to prevent a failure in the ejection of
the nozzles, and even if testing of the carrier during processing
before completion of probe impartment shows the necessity for
corrected impartment, drying of the carrier surface in the course
of the process is prevented to make the corrected impartment
possible.
[0049] In this method, it is also preferred to construct part of
solution supply passages, which extend between a plurality of probe
solution reservoirs for supplying plural types of probe solutions
to the plurality of nozzles of the liquid ejection head and the
respective nozzles, from hollow yarns comprising gas permeable
membranes permitting gas-liquid separation under reduced pressure,
bundle hollow yarn portions of the supply passages, pass the
bundled hollow yarn supply passage portions into a vacuum chamber,
and bring the exterior of the bundled hollow yarn supply passage
portions to a reduced pressure, thereby removing air bubbles
infiltrating the probe solutions supplied to the respective
nozzles, and efficiently decreasing the amount of dissolved oxygen
in the solution, the cause of air bubble generation.
[0050] The above and other objects, effects, features and
advantages of the present invention will become more apparent from
the following description of embodiments thereof taken in
conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0051] FIG. 1 is a schematic perspective view showing an embodiment
of a first apparatus for producing a probe carrier according to the
present invention;
[0052] FIG. 2 is a sectional configuration drawing of a vacuum
degasification chamber, an essential part of the probe carrier
production apparatus according to the present invention;
[0053] FIG. 3 is a schematic configurational plan view showing an
embodiment of a single wafer processing type probe carrier
production apparatus, a second apparatus for producing a probe
carrier according to the present invention; and
[0054] FIG. 4 is a schematic perspective view of a probe imparting
chamber constituting the single wafer processing type probe carrier
production apparatus according to the present invention.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
[0055] In the present invention having the aforementioned features,
ambient humidity for the liquid ejection head constituting the
plurality of probe imparting means, or set humidity within an
environment control chamber is at least 50%, and preferably 60% or
more.
[0056] The liquid ejection device is desirably a device equipped
with a thermal energy generator which gives thermal energy for
ejection to the liquid in the nozzle.
[0057] Suitable as the probe is any of DNA, RNA, cDNA
(complementary DNA), PNA, oligonucleotide, polynucleotide, other
nucleic acid, oligopeptide, polypeptide, protein, enzyme, substrate
for enzyme, antibody, epitope for antibody, antigen, hormone,
hormone receptor, ligand, ligand receptor, oligosaccharide, and
polysaccharide.
[0058] Embodiment 1
[0059] FIG. 1 shows an embodiment of the present invention, in
which the numeral 1 denotes a carrier of probes. The carrier 1 is
fixed onto a support device 3 of a probe imparting device (means)
2, generally called an imaging device, so as to be spotted with
probes. The support device 3 may be stationary, or may be
horizontally scannable in order to change the position where the
probes are imparted.
[0060] Directly above the support device 3, a liquid ejection head
(liquid ejection device) 4 having a plurality of nozzles (not
shown) for ejecting a plurality of probe solutions is provided so
as to be vertically movable and horizontally scannable. The
vertical movement and horizontal scanning of the liquid ejection
head 4 are carried out by a scan device 5.
[0061] Liquid ejection nozzles, whose number corresponds to the
number of probes of plural types necessary for imparting probes,
are formed in the liquid ejection head 4. Each of the nozzles is
supplied with a solution containing the probe to be imparted, from
a probe solution reservoir (not shown) via a liquid channel.
Normally, each nozzle corresponds to one dot to be imparted onto
the surface of the carrier 1. The nozzles, solution supply
passages, and reservoirs are present in numbers corresponding to
the number of the dots.
[0062] A liquid ejection head of a thermal jet type, in which
ejection heaters are provided in the respective nozzles, is used as
the liquid ejection head of the present embodiment.
[0063] The probe imparting device 2 is composed of, at least, the
aforementioned support device 3, liquid ejection head 4, and scan
device 5. The entire device 2 is installed within an environment
control chamber 6. The environment control chamber 6 has the
function of maintaining the humidity inside the chamber at a
constant high humidity of 50% or more. In the present embodiment,
the humidity is always set at 60%.
[0064] The aforementioned plural solution supply passages are
usually composed of thin tube members 10, called hollow yarns, as
shown in FIG. 2. In the present embodiment, part of the many hollow
yarns 10, which are the many solution supply passages, are
constructed of gas permeable membranes permitting gas-liquid
separation under reduced pressure. The many hollow yarns 20
comprising the gas permeable membranes are tied in a bundle, and
the bundled portions are placed inside a vacuum degasification
chamber 30. That is, the vacuum degasification chamber 30 is
mounted such that the many bundled solution supply passages (hollow
yarns) 10 pierce through the chamber 30 and the portions 20
comprising the gas permeable membranes among the many hollow yarns
are located within the vacuum degasification chamber 30. On the
side walls of the chamber 30, through which the many hollow yarns
pass, sealing 31 with molten resin is applied to ensure high air
tightness. Degasification of the chamber 30 is performed by a
vacuum pump 32 provided in the outside.
[0065] The probe carrier production apparatus constituted as above
was used to impart many types of probe solutions onto the carrier
1, thereby preparing a probe carrier. First, the carrier 1 was
carried from the outside into the environment control chamber 6 via
a carrier carry-in/carry-out gate 6a of the chamber 6, and was
fixed onto the support device 3. Then, the gate 6a was immediately
shut so that the humidity inside the chamber would not be
disturbed. Then, the liquid ejection head 4 was scanned and driven
according to a probe imparting program entered in the scan device 5
to complete a predetermined imparting operation. During the probe
imparting operation, the interior of the aforementioned vacuum
degasification chamber 30 was maintained at a predetermined degree
of vacuum, and its degasification was continued.
[0066] The carrier 1, whose probe impartment was completed, was
taken out of the gate 6a, brought into a testing chamber (not
shown), and observed for dots of the probe solutions adhering to
the surface of the carrier 1. As a result, dropouts due to
non-ejection from the nozzles, or deformed dots were not observed.
Then, probe impartment was performed sequentially for a plurality
of carriers, but neither dropouts of dots nor deformation of dots
was observed in any of the carriers.
[0067] With such a series of imparting operations, one nozzle
corresponds to one dot. Thus, if the imparting operations last for
a relatively long time, the front end portions of the nozzles are
exposed to the atmosphere in a wait state over such a lengthy time.
Nevertheless, no abnormalities occurred in the imparted dots, as
stated above. This is because the atmosphere surrounding the
nozzles was maintained at a high humidity at which the front end
portions of the nozzles did not dry. Another reason is that air
bubbles were removed from the probe solutions supplied to the
nozzles. It has been found that the amount of dissolved oxygen in
the probe solution can be decreased to at least 5 ppm (normally 0.5
ppm) or less by a continuous run of the vacuum degasification
chamber 30. The decrease in the amount of dissolved oxygen prevents
occurrence of air bubbles in the solution after passage through the
chamber 30.
[0068] In the present embodiment, the environmental humidity was
set at 60%, while it was set at 50% in other embodiments. Although
slight decreases in the yields tended to be observed in comparison
with the humidity of 60%, the performance of the resulting probe
carriers was sufficient, showing the productions to be fully
reliable.
[0069] When the environmental humidity was set below 50%, it had a
tendency to degrade yielding percentage in proportion to lowering
of the humidity, and deficiency in performance was coming out in
the produced probe carriers.
[0070] Embodiment 2
[0071] FIG. 3 shows a second embodiment of the present invention,
and is a schematic configurational plan view of a probe carrier
production apparatus according to the present invention. In the
drawing, the numeral 101 denotes a transport chamber provided with
a transport robot (transport means) 102 for transporting a carrier
(solid-phase substrate) S. A plurality of probe imparting means
(chambers) 103a, 103b and 103c, testing means (chamber) 104, drying
means (chamber) 105, and an in-and-out chamber 106 for bringing the
carrier S into and out of the transport chamber 101 are arranged
around the transport chamber 101 as a center. A carrier
carry-in/carry-out gate is provided between each of the chambers
and the central transport chamber 101.
[0072] The probe imparting chambers 103a, 103b and 103c each have a
structure as shown in FIG. 4. In the apparatus shown in FIG. 4, the
carrier S is supported on a support device 113 of a device 112,
generally called an imaging device, so as to undergo impartment of
probes. The support device 113 may be stationary, or may be
horizontally scannable in order to change the position of imparting
the probes.
[0073] Directly above the support device 113, a liquid ejection
head (liquid ejection device) 114 having a plurality of nozzles
(not shown) for ejecting a plurality of probe solutions is provided
so as to be vertically movable and horizontally scannable. The
vertical movement and horizontal scanning of the liquid ejection
head 114 are carried out by a scan device 115.
[0074] Liquid ejection nozzles, which are present in a number
allocated to each of the chambers and corresponding to the number
of probes of plural types necessary for imparting probes, are
formed in the liquid ejection head 114. Each of the nozzles is
supplied with a solution, which contains the probe and takes charge
of probe impartment, from a probe solution reservoir (not shown)
via a liquid channel. Normally, each nozzle corresponds to one dot
to be imparted onto the surface of the carrier S. The nozzles,
solution supply passages, and reservoirs are present in numbers
corresponding to the number of the dots.
[0075] A liquid ejection head of a thermal jet type, in which
ejection heaters are provided in the respective nozzles, is used as
the liquid ejection head of the present embodiment.
[0076] The imaging device 112 is composed of, at least, the
aforementioned support device 113, liquid ejection head 114, and
scan device 115. The entire device 112 is installed within each of
the chambers 103a, 103b and 103c. These chambers 103a, 103b and
103c have the function of maintaining the humidity inside the
chamber at a constant high humidity of 50% or more. In the present
embodiment, the humidity was always set at 60%. In the present
invention, like the plurality of probe imparting chambers 103a,
103b and 103c, the testing chamber 104 and the transport chamber
101 are also set to have the same humidity.
[0077] The aforementioned plural solution supply passages have the
same structure as used in the apparatus of Embodiment 1. Each of
the solution supply passages is usually composed of thin tube
members 10, called hollow yarns, as shown in FIG. 2. In the present
embodiment, part of the many hollow yarns 10, which are the many
solution supply passages, are constructed of gas permeable
membranes permitting gas-liquid separation under reduced pressure.
The many hollow yarns 20 comprising the gas permeable membranes are
tied in a bundle, and the bundled portions are placed inside a
vacuum degasification chamber 30. That is, the chamber 30 is
mounted such that the many bundled solution supply passages (hollow
yarns) 10 pierce through the chamber 30 and the portions 20
comprising the gas permeable membranes among the many hollow yarns
are located within the vacuum degasification chamber 30. On the
side walls of the chamber 30, through which the many hollow yarns
pass, sealing 31 with molten resin is applied to ensure high air
tightness. Degasification of the chamber 30 is performed by a
vacuum pump 32 provided in the outside.
[0078] The probe carrier production apparatus constituted as above
was used to impart many types of probe solutions onto the carrier
S, thereby preparing a probe carrier. First, the carrier S was
carried from the transport chamber 101 into the chamber 103a via a
carrier carry-in/carry-out gate G of the chamber 103a, and the
carrier S was supported on the support device 113. After the gate G
was shut, the liquid ejection head 114 was scanned and driven
according to a probe imparting program entered in the scan device
115 to complete a predetermined imparting operation. During the
imparting operation, the interior of the aforementioned vacuum
degasification chamber 30 was maintained at a predetermined degree
of vacuum, and its degasification was continued. In this first
chamber 103a, 363 dots were formed on the carrier S, followed by
formation of 363 dots in the next chamber 103b and 363 dots further
in the next chamber in the same manner, whereby a total of 1,089
dots were formed on the carrier S.
[0079] The carrier S, whose probe impartment was completed, was
taken out of the gate G of the chamber 103c by the transport robot
102, and brought into the testing chamber 104, where the dots of
the solutions adhering to the surface of the carrier S were
observed. As a result, dot dropouts due to non-ejection from the
nozzles, or deformed dots were not observed. Then, probe impartment
was performed sequentially for a plurality of carriers, but neither
dropouts of dots nor deformation of dots was observed in any of the
carriers.
[0080] In another trial run, whenever probe impartment in each of
the chambers 103a, 103b and 103c was completed, the carrier S was
carried into the testing chamber 104, and the surface of the
carrier was tested. After each operation, drying of the carrier
surface was not observed.
[0081] With such a series of spotting operations, one nozzle
corresponds to one dot. Thus, if the probe imparting operations
last for a relatively long time, the front end portions of the
nozzles keep exposed to the atmosphere in a wait state over such a
lengthy time. Nevertheless, no abnormalities occurred in the
imparted dots, as stated above. This is because the atmosphere
surrounding the nozzles was maintained at a high humidity at which
the front end portions of the nozzles did not dry. Another reason
is that air bubbles were removed from the probe solutions supplied
to the nozzles. It has been found that the amount of dissolved
oxygen in the probe solution can be decreased to at least 5 ppm
(normally 0.5 ppm) or less by a continuous run of the vacuum
degasification chamber 30. The decrease in the amount of dissolved
oxygen prevents air bubbles from newly forming in the solution
after passage through the chamber 30.
[0082] In the present embodiment, the environmental humidity was
set at 60%, while it was set at 50% in other embodiments. Although
slight decreases in the yields tended to be observed in comparison
with the humidity of 60%, the performance of the resulting probe
carriers was sufficient, showing the productions to be fully
reliable.
[0083] When the environmental humidity was set below 50%, it had a
tendency to degrade yielding percentage in proportion to lowering
of the humidity, and deficiency in performance was coming out in
the produced probe carriers.
[0084] In the present embodiment, the transport means, the probe
imparting means, and the testing means were constituted as chambers
which were isolated from each other. However, they may be installed
in a single space without being isolated. In this case, the entire
ambient humidity may be controlled in a centralized manner.
Moreover, it is needless to control the humidity of the entire
space, or to control the ambient humidity of each chamber, but it
is sufficient that the surrounding atmosphere for the liquid
ejection head can be maintained at a predetermined high humidity.
Thus, it is permissible, for example, to cover the liquid ejection
head with a small-space chamber having an opening/closing window
for a probe imparting operation, and to perform humidity control of
only the surrounding atmosphere for the liquid ejection head.
[0085] Herein, the probe fixed onto the carrier (solid phase
substrate) can specifically bind to a particular target substance.
The probe includes an oligonucleotide, a polynucleotide, or other
polymer which can be recognized by a particular target. The term
"probe" refers to a molecule having a probe function, such as an
individual polynucleotide molecule, or a group of molecules having
the same probe function, such as polynucleotides of the same
sequence surface fixed at dispersed positions, and often includes
molecules called ligands. The probe and the target are often used
in a replaceable manner, and the probe can bind, as part of a
ligand-anti-ligand antibody (may be called a receptor) pair, to the
target, or can become a form binding to it. The probe and the
target herein can include bases which can be found in nature, or
matters similar thereto.
[0086] An example of the probe supported on the carrier is one
which has a site of binding to the carrier via a linker in part of
an oligonucleotide comprising a base sequence hybridizable to a
target nucleic acid, and which has a structure connected to the
surface of the carrier at the site of binding to the carrier. The
probe is, preferably, a single-strand nucleic acid having a
complementary base sequence to all or a part of the target nucleic
acid, the probe can be hybridized specifically with the target
substance. The location, in the molecule of the oligonucleotide, of
the site of binding to the carrier in this configuration is not
limited as long as the desired hybridization reaction is not
impaired.
[0087] The probe employed in the probe carrier, to which the method
of the present invention is applied, is properly selected according
to the purpose of its use. For preferred practice of the method of
the present invention, the two-dimensional probe carrier to be
produced has the probe which is preferably at least one of DNA's,
RNA's, cDNA's (complementary DNA's), PNA's, oligonucleotides,
polynucleotides, other nucleic acids, oligopeptides, polypeptides,
proteins, enzymes, substrates for enzymes, antibodies, epitopes for
antibodies, antigens, hormones, hormone receptors, ligands, ligand
receptors, oligosaccharides, and polysaccharides.
[0088] The probe carrier produced by the method of the present
invention preferably includes a probe having a structure capable of
binding to the surface of a carrier. Fixing of the probe onto the
carrier is desirably performed by binding the probe to the surface
of the carrier.
[0089] The structure capable of binding to the carrier surface,
which the probe has, is preferably one which has been formed by
treatment for introducing previously to a molecular of a probe
material at least one of organic functional groups, such as an
amino group, a mercapto group, a carboxyl group, a hydroxyl group,
an acid halide (a haloformyl group: --COX), a halide (--X), an
aziridine group, a maleimide group, a succinimide group, an
isothiocyanate group, a sulfonyl chloride (--SO.sub.2Cl) group, an
aldehyde group (formyl group: --CHO), hydrazine, and iodinated
acetamide. In this case, it is necessary previously to induce onto
the surface of the substrate a structure (an organic functional
group) which reacts with each of various types of the above
mentioned organic functional groups to form covalent bonding. For
example, when the probe material has an amino group, succinimide
ester, isothiocyanate, sulfonylchloride and aldehyde can be induced
onto the surface of the substrate. When the probe material has
mercapto group (thiol group), maleimide can be induced onto the
surface of the substrate. When glass material is used as the
subtrate, a required functional group can be induced onto the
surface of the substrate by using a silane coupling agent having
the required fuctional group, and additionally a crosslinker having
the required fuctional group.
[0090] When probe solution imparted on the carrier is dried
drastically, the probe can not be fixed sufficiently onto the
carrier. In order to prevent this problem, it is preferable to
control not only the environmental humidity of the liquid ejection
part but also that of a path for transporting the carrier. And, it
is preferable to determine the time up to that the probe has fixed
sufficiently onto the carrier, to set up the time to exposure the
probe carrier to the environmental humidity according to the
determined time, and, after the set time passed, to take out the
probe carrier from the environmental humidity.
[0091] (Other)
[0092] The present invention achieves distinct effect when applied
to a recording head or a recording apparatus which has means for
generating thermal energy such as electrothermal transducers or
laser light, and which causes changes in ink by the thermal energy
so as to eject ink. This is because such a system can achieve a
high density of probe imparting and high resolution of probe
carrier.
[0093] A typical structure and operational principle thereof is
disclosed in U.S. Pat. Nos. 4,723,129 and 4,740,796, and it is
preferable to use this basic principle to implement such a system.
Although this system can be applied either to on-demand type or
continuous type ink jet recording systems, it is particularly
suitable for the on-demand type apparatus. This is because the
on-demand type apparatus has electrothermal transducers, each
disposed on a sheet or liquid passage that retains liquid (ink),
and operates as follows: first, one or more drive signals are
applied to the electrothermal transducers to cause thermal energy
corresponding to recording information; second, the thermal energy
induces sudden temperature rise that exceeds the nucleate boiling
so as to cause the film boiling on heating portions of the
recording head; and third, bubbles are grown in the liquid (ink)
corresponding to the drive signals. By using the growth and
collapse of the bubbles, the ink is expelled from at least one of
the ink ejection orifices of the head to form one or more ink
drops. The drive signal in the form of a pulse is preferable
because the growth and collapse of the bubbles can be achieved
instantaneously and suitably by this form of drive signal. As a
drive signal in the form of a pulse, those described in U.S. Pat.
Nos. 4,463,359 and 4,345,262 are preferable. In addition, it is
preferable that the rate of temperature rise of the heating
portions described in U.S. Pat. No. 4,313,124 be adopted to achieve
better recording.
[0094] U.S. Pat. Nos. 4,558,333 and 4,459,600 disclose the
following structure of a recording head, which is incorporated to
the present invention: this structure includes heating portions
disposed on bent portions in addition to a combination of the
ejection orifices, liquid passages and the electrothermal
transducers disclosed in the above patents. Moreover, the present
invention can be applied to structures disclosed in Japanese Patent
Application Laid-open Nos. 59-123670 (1984) and 59-138461 (1984) in
order to achieve similar effects. The former discloses a structure
in which a slit common to all the electrothermal transducers is
used as ejection orifices of the electrothermal transducers, and
the latter discloses a structure in which openings for absorbing
pressure waves caused by thermal energy are formed corresponding to
the ejection orifices. Thus, irrespective of the type of the
recording head, the present invention can achieve probe imparting
positively and effectively.
[0095] The present invention can be also applied to a so-called
full-line type liquid ejecting head whose length equals the maximum
length across a probe carrier. Such a recording head may consists
of a plurality of recording heads combined together, or one
integrally arranged recording head.
[0096] In addition, the present invention can be applied to various
serial type liquid ejecting heads: a liquid ejecting head fixed to
the main assembly of a liquid ejecting apparatus; a conveniently
replaceable chip type liquid ejecting head which, when loaded on
the main assembly of a liquid ejecting apparatus, is electrically
connected to the main assembly, and is supplied with probe solution
therefrom; and a cartridge type liquid ejecting head integrally
including a probe solution reservoir.
[0097] It is further preferable to add a recovery system, or a
preliminary auxiliary system for a liquid ejecting head as a
constituent of the liquid ejecting apparatus because they serve to
make the effect of the present invention more reliable. Examples of
the recovery system are a capping means and a cleaning means for
the liquid ejecting head, and a pressure or suction means for the
liquid ejecting head. Examples of the preliminary auxiliary system
are a preliminary heating means utilizing electrothermal
transducers or a combination of other heater elements and the
electrothermal transducers, and a means for carrying out
preliminary ejection of probe solution independently of the
ejection for probe imparting. These systems are effective for
reliable liquid ejecting.
[0098] The most effective method for the above-described solution
is to carry out film boiling stated above.
[0099] As described above, the present invention is characterized
in that ambient humidity for the plurality of nozzles of the liquid
ejection device for ejecting droplets of solutions containing
probes to the surface of the carrier is controlled to 50% or more,
preferably 60% or more, part of the solution supply passages
leading to the plurality of nozzles are composed of gas permeable
membranes capable of gas-liquid separation under reduced pressure,
and these portions are gathered and altogether placed under reduced
pressure, whereby air bubbles are removed from the solutions
supplied to the plurality of nozzles, and the amount of a dissolved
gas, a cause of air bubble formation, is decreased.
[0100] Accordingly, the present invention makes it possible to
produce a high quality probe carrier in a high yield.
[0101] The present invention has been described in detail with
respect to the preferred embodiments, but it is to be understood
that changes and modifications may be made without departing from
the invention in its broader aspects, and it is our intention in
the appended claims to cover all such changes and modifications as
fall within the true spirit of the invention.
* * * * *