CN1239714C - Preparing method for biological chip - Google Patents
Preparing method for biological chip Download PDFInfo
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- CN1239714C CN1239714C CN 02127335 CN02127335A CN1239714C CN 1239714 C CN1239714 C CN 1239714C CN 02127335 CN02127335 CN 02127335 CN 02127335 A CN02127335 A CN 02127335A CN 1239714 C CN1239714 C CN 1239714C
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Abstract
The present invention provides a method for preparing a biological wafer. The present invention comprises the following steps: hydrophobic substances are sprayed on base material in a microinjection way, and a hydrophobic area is formed on the surface of the base material; the base material is partitioned into a plurality of small compartments by the hydrophobic area; a probe is respectively fixed on the small compartments in the microinjection way.
Description
Invention field
The present invention relates to a kind of preparation method of biochip; Particularly, relate to the preparation method who adopts the biochip that the microinjection mode makes.
Background of invention
Biochip is the breakthrough invention of twentieth century ultimogeniture thing science and technology the next item up, can match in excellence or beauty auto production line that Henry Ford then organized to the great revolution of automotive industry for the development of biotech industry, or similar semi-conductor is for the revolutionary character development of computer industry.In broad terms, biochip is meant on glass (glass), silicon chip (slica), plastics (plastic) or nitrocotton materials such as (nitrocellulose), utilize industrial technologies such as microelectronics, micromechanics, photoelectricity, automatization to make the product that is applied to biochemical analysis, its effective object can be gene, protein or cell tissue etc.The principal feature of biochip technology be analyze confidence level and tolerance range height, analysis speed is fast, employed sample and reagent are few, can handle a large amount of samples simultaneously, and obtain the experimental data of globality and parallelization.
On the whole, biochip research still belongs to the initial stage developmental stage in the world, but existing many great achievements.The kind of biochip has microarray (microarray), DNA wafer (DNAchip), protein/antibody wafer (protein/antibody chip), organizes wafer (tissue chip) and laboratory wafer (lab-on-a-chip) etc. at present, and is wherein comparatively ripe with microarray (microarray) and DNA wafer (DNA chip) development.And the purposes of biochip is very extensive, comprise application, the screening of medicine and the detecting of chemical and biological weapons etc. on gene sequencing, toxicological analysis, disease gene performance, the calibrating of single Yeast Nucleic Acid polymorphism, the medical jurisprudence, this shows that biochip must be the large flat bread that Mirae Corp. circle competitively strives food.But, how to grasp competitive edge and then depend on and prepare highdensity biochip how at lower cost.
Biochip can be divided into three kinds according to the mode difference of probe (probe) preparation, first kind of light guiding in-situ synthesis (light-directed synthesis) that the photo-engraving process (photolithography) that is Affymetrix company develops combines with chemical synthesis.Second kind is Stanford University's employed contact point sample method (pin), is to utilize in advance synthetic good DNA, RNA or protein with robotic arm fast, be fixed on the matrix to high-density.The third is microinjection (micro-injection method), utilizes microinjection (micro-injection) mode to remove to prepare complementary nucleotide as Rosetta Inpharmatics company.The interpretation mode of last data is that sample and wafer that desire detects are carried out hybridization (hybridization), again with the mark (label) on the subject matter in the sample (target), for example modes such as fluorescent, radiating material or ferment colour generation are carried out cat scanner and data analysis afterwards.
Making the common method of biochip at present may be: (a) utilize microarray point system machine that the synthetic probe solution is planted on the wafer by precise positioning mechanism cloth, or (b) utilize the technology of optical etching to carry out Nucleotide light direct in-situ synthesis method (light-directed in-situ synthesis).Wherein, carry the physical construction of probe solution can be divided into the syringe needle (pin) of contact and contactless micro-syringe (micro-injector) in the some system machine.The syringe needle of contact (pin) cost is low, but drop is bigger, array density lower (about 150～200 μ m of every bit), and destructible wafer surface; And contactless micro-syringe (micro-injector) can not destroyed wafer surface, and drop is less, array density higher (about 50～150 μ m of every bit).
For example, carry out the mode of light direct in-situ DNA synthesis method at glass surface with the technology that is derived from optical etching, can be at area 1.6cm
2The preparation kind on glass high-density micro-array of 400,000 kinds of nucleic acid probes nearly.Though be leading present technology, be subject to the too fast and light shield cost costliness of speed that the photochemical reaction rate is successively decreased according to the increase of nucleic acid probe length, so fail to popularize.Therefore, method commonly used at present is point-needle type (pin) and microinjection (micro-injection method), and wherein microinjection is divided into piezoelectric type microinjection and hot bubble type microinjection again.For example Protogene company utilizes piezoelectric type microinjection technology (piezo micro-injection, U.S.Pat.No.5985551; 6,177,558 B1) carry out DNA original position synthetic (DNA in-situ synthesis) in wafer surface, cost is lower, but density only is about 10～10
4Spots/cm
2
Though above-mentioned mentioned be that photo-engraving process, the some skill of handling needles or piezoelectric method all have its shortcoming, therefore with regard to the preparation of biochip, how preparing quality better, resolution, enough to reach low-cost biochip will be the main factor of winning victory.Prepare biochip in the microinjection mode and note the pollution to each other of probe drop.In order to overcome pollution problem, United States Patent (USP) the 5th, 552, disclosed for No. 270 with polyacrylamide colloid (polyacrylamide) and made many boothes, its colloidal thickness is 30 μ m, can prevent the mutual pollution of probe solution, and can increase probe solution fixed amount, so but shortcoming to be processing procedure trouble, cost high and because of moisture easily evaporation need be stored in the nonvolatile oil, therefore, need before using to clean with chloroform (chloroform) or ethanol (ethanol) again, generally speaking use and inconvenient.In addition, also can utilize the mode of conductor etching on silicon chip (silicon), to be etched into many sulculuses chamber and prevent pollution between probe solution, but this legal system journey trouble and spend high.The shortcoming of above-mentioned prior art promptly is the problem that institute of the present invention desire solves.
Summary of the invention
The purpose of this invention is to provide a kind of preparation method of simple and cheap biochip, it comprises the following steps: in the microinjection mode one lyophobic dust to be sprayed on the base material; Form a hydrophobicity district in this substrate surface, and be separated out a plurality of boothes by this hydrophobicity is trivial; And with the microinjection mode with a probe stationary on this booth.The inventive method not only can prevent between the probe drop interference phenomenon each other, also can increase the resolution of probe density and wafer.Therefore, the inventive method can be prepared high-density, drop is little, parsing power is good and cost is low biochip.
Description of drawings
Figure 1A to Figure 1B is sprayed on synoptic diagram base material on micro-syringe with lyophobic dust for showing the present invention.Figure 1A demonstration utilizes micro-syringe vertical direction to spray lyophobic dust to substrate surface; Figure 1B demonstration utilizes micro-syringe horizontal direction to spray lyophobic dust to substrate surface.
Fig. 2 A to Fig. 2 B shows that the present invention utilizes micro-syringe to spray lyophobic dust to substrate surface, forms the possible shape of booth at substrate surface.Fig. 2 A shows the quadrate booth; Fig. 2 B shows circular booth.
Fig. 3 shows the distribution of lyophobic dust on the substrate surface of the present invention and the sectional view that the probe drop covers situation.
After Fig. 4 A to Fig. 4 D showed the booth that the present invention separates out with lyophobic dust, the fixed nucleic acid probe was to the synoptic diagram of base material.Fig. 4 A demonstration splashes into different booth (wetting ability district) with the Nucleotide solution that micro-syringe will have protecting group; Fig. 4 B demonstration is removed protecting group with acidic solution; Fig. 4 C demonstration splashes into different booth (wetting ability district) with micro-syringe with the Nucleotide solution that the 2nd floor has protecting group; And Fig. 4 D shows the biochip that preparation is finished.
Fig. 5 is the structural map of the hot bubble type micro-syringe that adopts of most preferred embodiment of the present invention.
Fig. 6 A-Fig. 6 D is the operation chart of the micro-syringe of Fig. 5, Fig. 6 A is the cross-sectional view of micro-syringe, Fig. 6 B is for forming the situation of first bubble, Fig. 6 C is for then forming second bubble, make two bubble incorporation and extrude the situation of drop, Fig. 6 D is that two bubble collapses make unnecessary liquid flow back to the situation of liquid tank.
Embodiment
The invention provides a kind of preparation method of biochip, at first one lyophobic dust is sprayed on the base material, form a hydrophobicity district, and separate out a plurality of boothes by this lyophobic dust in this substrate surface in the microinjection mode.Then, again with the microinjection mode with a probe stationary in each booth.
Usually the material that can be used as biochip substrate can be hydrophobic substrates or hydrophilic base.Hydrophobic substrates includes but not limited to following material--glass, silicon chip, plastic cement, nylon membrane, resin, quartz, pottery and metal material.Hydrophilic base then mostly is polymkeric substance, comprise as polystyrene (polystyrene), polyester (polyester), polycarbonate (polycarbonate), polyvinyl chloride (polyvinylchloride), polyethylene (polyethylene), polypropylene (polypropylene), polysulfones (polysulfone), polyurethane(s) (polyurethane) or poly-basic methyl acrylate materials such as (PMMA), but be not limited thereto the place person of enumerating.
If adopt hydrophobic substrates, then when having sprayed lyophobic dust after, the booth surface that the hydrophobicity district of lyophobic dust formation is separated out, must be processed into possess hydrophilic property functional group earlier could combine with probe.The hydrophilic functional group of indication can be amido (NH herein
2), carboxyl (COOH), thiol (SH), epoxy group(ing) (epoxide), aldehyde radical (aldehyde) or streptavidin (Streptavidin) etc.
If the employing hydrophilic base then needs earlier surface treatment to be become hydrophobicity, could spray lyophobic dust then, to form the hydrophobicity district.Afterwards, need again booth to be processed into wetting ability, could combine with probe.The substrate surface modifying method can be with reference to following paper: Souther, Chem.abst.113; 152979r (1990) and Anal.Biochem.157; 283 (1986), do not repeat them here.
Microinjection mode of the present invention is to adopt a micro-syringe (micro-injector), with vertical, level or any direction, unidirectionally or two-way sprays back and forth, as shown in Figure 1A and Figure 1B.The micro-syringe that is adopted comprises hot bubble type micro-syringe and piezoelectric type micro-syringe.The hot bubble type micro-syringe that is adopted comprises: a groove chamber, in order to place liquid; One microinjection hole is positioned on the groove chamber, and the liquid in the groove chamber is flowed out; And a primary heater and a secondary heater, be arranged in the both sides in this microinjection hole respectively.When the filled with fluid of groove chamber, primary heater can produce first bubble, and then, secondary heater can produce second bubble, utilizes two bubbles that liquid is cut off ejection, and primary heater and secondary heater are driven by a common signal.In addition, the generation of first bubble is as a valve, and the liquid that limits in this groove chamber flows out, and hereinafter will describe in detail.
The lyophobic dust that the present invention sprays in the microinjection mode includes, but not limited to tetrafluoroethylene (Teflon), polyimide (polyimide), siliceous and fluorine-containing water-sprinkling agent and fluorine-containing and silicon-containing compound etc.After being sprayed to lyophobic dust on the base material, lyophobic dust can form hydrophobic region at substrate surface, separates out a plurality of boothes by hydrophobic region, and booth can be for square, circular or any geometricdrawing, shown in Fig. 2 A and Fig. 2 B.The booth magnitude range can be 20～200 μ m, and the thickness range of lyophobic dust can be 1～30 μ m, and width range can be 5～100 μ m.
As shown in Figure 3, the form of desiring to be fixed in probe on the substrate surface and being with drop is sprayed out by micro-syringe, covers in the booth (wetting ability district).Probe solution is housed in the micro-syringe, this probe solution can be thymus nucleic acid (DNA), Yeast Nucleic Acid (RNA), Nucleotide (Nucleotides), oligonucleotide (Oligonucleotides), protein (Protein), antibody (Antibodies) or peptide (Peptides) etc., but is not limited to the above person of enumerating.Above-mentioned probe stationary is to reach via the mode of a functional groups in the method for booth, and the functional groups mode comprises absorption (adsorption) method, covalent attachment method (covalent binding), coating method (encapsulation), crosslinking (cross-linking) and entrapping method (entrapment) etc., but is not limited to aforesaid method.If common probe solution DNA; when RNA or Nucleotide; must be earlier make that through some chemically modifieds the functional groups on itself and the substrate surface is tightr; for example be modified into phosphonate (phosphonate); phosphonic acids hydrogen salt (hydrogen phosphonate); phosphoramide (phosphonamidite); phosphoramidite (phosphoramidite); phosphite (phosphite) or methyl phosphoramide (methylphosphonamidite) compounds; if preparation oligonucleotide microarray (oligonucleotide microarray), in 5 of Nucleotide ' or 3 ' end must connect protecting group and combine with the Nucleotide that prevents same layer.
Produce the little micro-array biochip of drop, wherein the size in the surface tension of Nucleotide solution itself, viscosity and microinjection hole is the major decision factor, and usually general drop size is about 25～250 μ m.
If prepare the Nucleotide microarray, then must more consider the viscosity of choice of Solvent in the Nucleotide solution and solvent with the hot bubble type micro-syringe.In general, therefore the drop little then more easily volatilization of healing, must contain a kind of high boiling solvent in the common employed solvent at least, and for example boiling point prevents the volatilization of nucleic acid solution greater than 140 ℃ solvent.Selected solvent is comparatively suitable with polar aprotic solvent, commonly used just like two nitriles (dinitriles), mononitriles (mononitriles), glyme class (glymes), diethylene glycol diformazan ethers (diglymes), triglyme class (triglymes), trimethyl phosphate (trimethylphosphates), dimethyl formamide (dimethylformamides, DMF) and N-Methyl pyrrolidone (N-methyl pyrrolidinone, NMP) etc.
When preparation oligonucleotide microarray (oligonucleotide microarray) wafer; utilize micro-syringe that each shielded Nucleotide (protected nucleotides) is fixed on the base material in order just like the mode of piling up wood, the protecting group that connects on Nucleotide is to be used for preventing the Nucleotide of each layer to overlap each other together.After the Nucleotide solution of the first layer fixedly gets on; utilize acidic solution that the protecting group on the Nucleotide is removed; and then the fixing Nucleotide of going up the second layer, can prepare desired biochip apace by that analogy, this kind method is more flexible in the design of nucleotide probe.If when preparation DNA, RNA or protein chip, then directly will synthesize good thymus nucleic acid (DNA), Yeast Nucleic Acid (RNA) or protein and directly be sprayed in the booth of base material.Then peptide is connected one by one during preparation peptide (peptides) wafer as the Nucleotide micro-array.
Sample and the above-mentioned biochip for preparing that desire is detected carries out hybridization (hybridization) at last, carry out differential responses by the mark (label) on the subject matter in the sample (target) more afterwards, for example modes such as fluorescent, radiating material, ferment colour generation are carried out cat scanner and data analysis.
Embodiment
Below will specify the present invention with embodiment, right category of the present invention is not limited to the scope shown in the embodiment.
1: the first kind of preparation method who carries out batch oligonucleotide microarray (oligonucleotide microarray) with the hot bubble type micro-syringe of embodiment.
1. the glass surface with micro-syringe forms booth
With glass is base material, and lyophobic dust to contain lyophobic dust, directly, regularly sprays as the hot bubble type micro-syringe of teflon (Teflon) at glass surface in elder generation, to form the square booth that lyophobic dust separates, shown in Fig. 2 A.The width range of its intermediate chamber is about 50 μ m, and the thickness that lyophobic dust sprays is 2 μ m, and width is 5 μ m.
2. carrying out wetting ability in booth handles
In the square booth that hydrophobicity separates out, to contain the micro-syringe of octyl group trichlorosilane (octyltrichlorosilane), carrying out silanization (silanization) handles, make the booth zone become the wetting ability district, its surface has thiol and (SH) is able to combine with nucleotide probe detailed method such as United States Patent (USP) the 6th, 159, No. 695, can form a nonvolatil thioether bond or the reversible cystine linkage of a chemistry selection thiol key to surface, wetting ability district.
3. oligonucleotide is incorporated on the microarray sheet
The dimethoxy tribenzyl Nucleotide phosphamic acid solution (DMTr-nucleotide phosphoramidite) that will contain tetrazolium (tetrazole) activator is sprayed on micro-syringe in the wetting ability district of hexasilane processing, and the first layer Nucleotide can (SH) combine with the thiol in the wetting ability district.Utilize acidic solution then, protecting group is removed, spray second layer Nucleotide again as Tricholroacetic Acid (trichloroacetic acid) or hydrochloric acid (HCl) solution.Connect each Nucleotide successively with said procedure, can obtain oligonucleotide microarray (oligonucleotide microarray) at last, detailed steps can be with reference to United States Patent (USP) the 6th, 184, and 347B No. 1, the 5th, 985, No. 551 does not repeat them here.
4. carry out hybridization (hybridization) with the oligonucleotide microarray that obtains
Target nucleotide sequence (target) that desire is detected and above-mentioned oligonucleotide microarray carry out hybridization at last, then by the mark (Label) on the target Nucleotide (target), what the sequence that can learn target Nucleotide (target) is, way can be with reference to United States Patent (USP) the 5th in detail, 985, No. 551.
The preparation method of 2: the second kinds of batch oligonucleotide microarrays of embodiment.
The compartment shape of oligonucleotide microarray (oligonucleotide microarray) can also be circle, shown in Fig. 2 B.Can directly spray lyophobic dust and form circular compartment with micro-syringe.Or doing a corresponding circular slab earlier covers on the base material, sprays lyophobic dust with micro-syringe then, takes away circular slab subsequently, can obtain circular compartment at last.Wherein the circular slab material is good with hydroaropic substance, for example nylon membrane etc.Preparation process afterwards is identical with embodiment 1.
Embodiment 3: the preparation method who carries out protein chip (Protein chip) with the piezoelectric type micro-syringe.
1. form the hydrophobicity compartment with micro-syringe at glass surface
With glass is base material, earlier at glass surface to contain lyophobic dust, as polyimide (polyimide), the piezoelectric type micro-syringe spray lyophobic dust directly, regularly, in order to form square hydrophobicity compartment, shown in Fig. 2 A, the width range of its intermediate chamber is about 50 μ m, and the thickness that lyophobic dust sprays is 2 μ m, and width is 5 μ m.
2. make protein bound on the microarray sheet
With octyl group trichlorosilane (octyltrichlorosilane), make square booth finishing that lyophobic dust is separated out become to have thiol and (SH), make that protein probe can be in conjunction with thereon.The combining method of protein probe and base material can 047B1 number, not repeat them here with reference to United States Patent (USP) the 6th, 225.
3. detect the proteic test of target with protein chip
After above-mentioned protein chip prepared, in the booth on protein example (sample) the adding wafer, (Cy3 Cy5) can learn to contain which kind of protein in the sample by the fluorescent subject matter on the sample.
Though the present invention is described with preferred embodiment; right its is not in order to limit the present invention; those of ordinary skill in the art is familiar with this skill person; do not breaking away under the spirit and scope of the present invention; can do various changes and modification, so protection scope of the present invention is as the criterion with the scope of claims.
For above-mentioned and other purposes of the present invention, feature and advantage can be become apparent, hereinafter, be described in detail below by preferred embodiment and in conjunction with appended diagram:
The explanation of symbol
The symbol of Fig. 1-4D:
10～micro-syringe;
12～lyophobic dust;
14～micro-syringe moving direction;
16～base material;
18～hydrophobicity district;
20～booth;
21～wetting ability district;
22～nucleic acid drop;
24～have a Nucleotide drop of protecting group;
26～protecting group;
28～acidic solution;
The symbol of Fig. 5-6D:
1～jet orifice;
2～primary heater;
3～secondary heater;
4～electrode;
5～groove chamber;
6～microchannel;
7～liquid;
8～wafer;
A～first bubble;
B～second bubble;
P～bubble direction of expansion;
F～drop emission direction.
Claims (29)
1. the preparation method of a biochip comprises the following steps:
(a) provide a base material;
(b) in the microinjection mode one lyophobic dust is sprayed on this base material, forms a hydrophobicity district, and be separated out a plurality of boothes by this hydrophobicity is trivial in this substrate surface; And
(c) in the microinjection mode with a probe stationary in this booth.
2. the preparation method of biochip as claimed in claim 1, wherein this lyophobic dust comprises tetrafluoroethylene (Teflon), polyimide (polyimide), siliceous and fluorine-containing water-sprinkling agent and fluorine-containing or silicon-containing compound.
3. the preparation method of biochip as claimed in claim 1, wherein this microinjection mode is to adopt a micro-syringe, with vertical, level, unidirectional or two-way sprinkling.
4. the preparation method of biochip as claimed in claim 1, wherein this microinjection mode is to adopt a micro-syringe, with any direction, unidirectional or two-way sprinkling.
5. as the preparation method of claim 3 or 4 described biochips, wherein this micro-syringe comprises hot bubble type micro-syringe or piezoelectric type micro-syringe.
6. the preparation method of biochip as claimed in claim 1, wherein this base material is a hydrophobic substrates, it is made up of following arbitrary material: glass, silicon wafer, quartz, mica, stupalith or metal material.
7. the preparation method of biochip as claimed in claim 6 in step (b) afterwards, also comprises step (d), handles carrying out a wetting ability in each booth, makes the surface of each booth have a hydrophilic functional group.
8. the preparation method of biochip as claimed in claim 7, wherein this hydrophilic functional group comprises amido (NH
2), (COOH), thiol (SH) or streptavidin (Streptavidin) for carboxyl.
9. the preparation method of biochip as claimed in claim 1, wherein this base material is a hydrophilic base, and it is made up of following arbitrary material: polystyrene, polyester, PC, polyvinyl chloride, polyethylene, polypropylene, polysulfones, polyurethane(s) or polymethylene MALEIC ANHYDRIDE.
10. the preparation method of biochip as claimed in claim 9 also comprises the following step:
(e) afterwards, carry out a hydrophobicity on this hydrophilic substrates surface and handle, make this substrate surface treatment become hydrophobic in step (a); And
(f) afterwards, in each booth, carry out a wetting ability and handle, make each booth surface have a hydrophilic functional group in step (b).
11. the preparation method of biochip as claimed in claim 10, wherein this hydrophilic functional group comprises amido (NH
2), (COOH), thiol (SH) or streptavidin (Streptavidin) for carboxyl.
12. the preparation method of biochip as claimed in claim 1, wherein the shape of this booth comprises square, circular or other geometricdrawing.
13. the preparation method of biochip as claimed in claim 1, wherein this probe comprises thymus nucleic acid (DNA), Yeast Nucleic Acid (RNA), Nucleotide (Nucleotides), oligonucleotide (Oligonucleotides), protein (Protein), antibody (Antibodies) or peptide (Peptides).
14. the preparation method of biochip as claimed in claim 1, wherein this probe stationary is via a functional groups mode in this booth.
15. the preparation method of biochip as claimed in claim 14, wherein this functional groups mode comprises absorption (absorption) method, covalent attachment method (covalent binding), coating method (encapsulation), crosslinking (cross-linking) or entrapping method (entrapment).
16. the preparation method of biochip as claimed in claim 1, wherein this microinjection mode is to use a hot bubble type micro-syringe, and this hot bubble type micro-syringe comprises:
One groove chamber is in order to place liquid;
One microinjection hole is positioned on the groove chamber, and the liquid in the groove chamber is flowed out; And
One primary heater and a secondary heater are arranged in the both sides in this microinjection hole respectively; When the filled with fluid of this groove chamber, this primary heater can produce one first bubble, and this secondary heater can produce one second bubble, utilizes two bubbles that liquid is cut off ejection.
17. the preparation method of biochip as claimed in claim 16, wherein this primary heater and this secondary heater are driven by a common signal.
18. the preparation method of biochip as claimed in claim 16, wherein the generation of first bubble is as a valve, and the liquid that limits in this groove chamber flows out.
19. a biochip, it comprises:
(i) base material;
(ii) the booth that separated out of a hydrophobicity district and a plurality of hydrophobicitys district is positioned on the base material, and wherein this hydrophobicity district sprays a lyophobic dust by the microinjection mode to be formed; And
(iii) a probe is to be fixed on this booth in the microinjection mode.
20. biochip as claimed in claim 19, wherein this base material is a hydrophobic substrates, and it is made up of following arbitrary material: glass, silicon wafer, quartz, mica, stupalith or metal material.
21. biochip as claimed in claim 20, the hydrophobic substrates surface in each booth wherein, after handling through a wetting ability, this substrate surface has a hydrophilic functional group.
22. biochip as claimed in claim 21, wherein this hydrophilic functional group comprises amido (NH
2), (COOH), thiol (SH) or streptavidin (Streptavidin) for carboxyl.
23. biochip as claimed in claim 22, wherein this base material is a hydrophilic base, can be made up of following arbitrary material: polystyrene, polyester, PC, polyvinyl chloride, polyethylene, polypropylene, polysulfones, polyurethane(s) or polymethylene MALEIC ANHYDRIDE.
24. biochip as claimed in claim 21 wherein forms before these a plurality of boothes, also carries out a hydrophobicity pre-treatment on this hydrophilic substrates, makes this substrate surface treatment become hydrophobic.
25. biochip as claimed in claim 24 wherein after this booth forms, also carries out a wetting ability and handles, and makes this booth surface have a hydrophilic functional group.
26. biochip as claimed in claim 25, wherein this hydrophilic functional group comprises amido (NH
2), (COOH), thiol (SH) or streptavidin (Streptavidin) for carboxyl.
27. biochip as claimed in claim 19, wherein this lyophobic dust comprises tetrafluoroethylene (Teflon), polyimide (polyimide), siliceous and fluorine-containing water-sprinkling agent or fluorine-containing and silicon-containing compound.
28. biochip as claimed in claim 19, wherein this probe comprises thymus nucleic acid (DNA), Yeast Nucleic Acid (RNA), Nucleotide (Nucleotides), oligonucleotide (Oligonucleotides), protein (Protein), antibody (Antibodies) or peptide (Peptides).
29. biochip as claimed in claim 19, wherein this probe is a kind of being fixed on this booth in the following manner: absorption (absorption) method, covalent attachment method (covalent binding), coating method (encapsulation), crosslinking (cross-linking) or entrapping method (entrapment).
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| CN 02127335 CN1239714C (en) | 2002-08-02 | 2002-08-02 | Preparing method for biological chip |
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| CN 02127335 CN1239714C (en) | 2002-08-02 | 2002-08-02 | Preparing method for biological chip |
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| CN1239714C true CN1239714C (en) | 2006-02-01 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102692515A (en) * | 2011-03-23 | 2012-09-26 | 成功大学 | Biomedical chip used for blood coagulation tests, its manufacturing method and application |
| TWI636244B (en) * | 2017-03-24 | 2018-09-21 | 國立清華大學 | Manufacturing device and manufacturing method for test strips |
-
2002
- 2002-08-02 CN CN 02127335 patent/CN1239714C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102692515A (en) * | 2011-03-23 | 2012-09-26 | 成功大学 | Biomedical chip used for blood coagulation tests, its manufacturing method and application |
| CN102692515B (en) * | 2011-03-23 | 2014-09-17 | 成功大学 | Biomedical chip used for blood coagulation tests, its manufacturing method and application |
| TWI636244B (en) * | 2017-03-24 | 2018-09-21 | 國立清華大學 | Manufacturing device and manufacturing method for test strips |
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| CN1472340A (en) | 2004-02-04 |
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