Process for the manufacture of wholly microfabricated biosensors

• US 5,837,446 A
• Filed: 06/07/1995
• Issued: 11/17/1998
• Est. Priority Date: 11/14/1988
• Status: Expired due to Fees

• Current Assignee: i STAT Corporation (Abbott Laboratories)
• Original Assignee: i STAT Corporation (Abbott Laboratories)
• Inventors: Lauks, Imants R., Van Der Werf, Paul, Mier, deceased, Randall M., Steiner, Susan, Itak, Jeanne, Davis, Graham, Wieck, Henry J., Smit, Nicolaas, Cozzette, Stephen N., Piznik, Sylvia
• Primary Examiner(s): Chin, Christopher L.
• Application Number:
  US08/482,517
• Time in Patent Office: 1,259 Days
• Field of Search: 204/400, 204/403, 204/411, 204/412, 204/414-419, 204/430-432, 422/57, 422/82.08, 435/6, 435/14, 435/25, 435/177, 435/817, 435/287.1, 435/287.2, 436/518, 436/528, 436/531, 436/532, 436/149-151, 436/806
• US Class Current: 435/6.11
• CPC Class Codes: B01L 2200/12 Specific details about manufacturing devices
• CPC Class Codes: B01L 2300/0636 Integrated biosensor, microarrays
• CPC Class Codes: B01L 2300/0645 Electrodes
• CPC Class Codes: B01L 2300/0877 Flow chambers
• CPC Class Codes: B01L 3/0268 using pulse dispensing or spraying, eg. inkjet type, piezo actuated ejection of droplets from capillaries
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: B01L 3/5088 confining liquids at a location by surface tension, e.g. virtual wells on plates, wires B01L3/50857 takes precedence
• CPC Class Codes: C12Q 1/001 Enzyme electrodes
• CPC Class Codes: G01N 2035/00059 vacuum chucks
• CPC Class Codes: G01N 2035/00237 Handling microquantities of analyte, e.g. microvalves, capillary networks
• CPC Class Codes: G01N 2035/00455 Controlling humidity in analyser
• CPC Class Codes: G01N 2035/00534 Mixing by a special element, e.g. stirrer
• CPC Class Codes: G01N 2035/1034 Transferring microquantities of liquid
• CPC Class Codes: G01N 2035/1076 plurality or independently movable heads
• CPC Class Codes: G01N 33/5438 Electrodes
• CPC Class Codes: G01N 35/0099 comprising robots or similar manipulators robots per se B25J
• CPC Class Codes: G01N 35/109 with two horizontal degrees of freedom
• CPC Class Codes: G01V 9/00 Prospecting or detecting by methods not provided for in groups G01V1/00 - G01V8/00
• CPC Class Codes: G10K 11/006 Transducer mounting in underwater equipment, e.g. sonobuoys
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode
• CPC Class Codes: Y10S 436/806 : Electrical property or magnetic property

Abstract

An efficient method for the microfabrication of electronic devices which have been adapted for the analyses of biologically significant analyte species is described. The techniques of the present invention allow for close control over he dimensional features of the various components and layers established on a suitable substrate. Such control extends to those parts of the devices which incorporate the biological components which enable these devices to function as biological sensors. The materials and methods disclosed herein thus provide an effective means for the mass production of uniform wholly microfabricated biosensors. Various embodiments of the devices themselves are described herein which are especially suited for real time analyses of biological samples in a clinical setting. In particular, the present invention describes assays which can be performed using certain ligand/ligand receptor-based biosensor embodiments. The present invention also discloses a novel method for the electrochemical detection of particular analyte species of biological and physiological significance using an substrate/label signal generating pair which produces a change in the concentration of electroactive species selected from the group consisting of dioxygen and hydrogen peroxide.

Claims

1. A method of detecting the presence and quantity of at least one analyte species in a liquid sample which comprises:

(a) contacting a microfabricated biosensor with a liquid sample, said biosensor comprising;

(i) a base sensor, (ii) a permselective layer, superimposed over at least a portion of said base sensor, having a thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a biolayer superimposed over at least a portion of said permselective layer and said base sensor, which biolayer comprises a sufficient amount of a bioactive molecule capable of selectively interacting with a particular analyte species, and a support matrix in which said bioactive molecule is incorporated, which matrix is selected from the group consisting of a photoformable proteinaceous mixture, a film-forming latex, and combinations thereof and through which matrix said analyte species may freely permeate and interact with said bioactive molecule; and

b) obtaining a measured signal output from said biosensor, from which signal output the presence and quantity of an analyte species may be deduced.

2. The method of claim 1 which further comprises contacting said biosensor with a suitable calibrant solution to obtain a reference signal output to which said measured signal output may be compared.

3. The method of claim 1 or 2 in which said liquid sample is a biological fluid.

4. The method of claim 1 or 2 in which said analyte species is selected from the group consisting of sodium ion, potassium ion, protons, chloride ion, ionized calcium, dissolved carbon dioxide, total carbon dioxide, dissolved oxygen, hydrogen peroxide, ethanol, glucose, cholesterol, uric acid, ascorbic acid, bilirubin, creatinine, creatine, triglyceride, lactate dehydrogenase, creatine kinase, alkaline phosphatase, alanine transaminase, aspartate transaminase, amylase, and lipase.

5. A method of detecting a plurality of analyte species in a single liquid sample which comprises (a) contacting said liquid sample with a calibrated wholly microfabricated biosensor comprising an array of overlaid structures each sensitive to a particular analyte species which structures are comprised of (i) a base sensor, (ii) a permselective layer, superimposed over at least a portion of said base sensor, having a thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a biolayer superimposed over at least a portion of said permselective layer, which biolayer comprises a sufficient amount of a bioactive molecule capable of selectively interacting with a particular analyte species, and a support matrix in which said bioactive molecule is incorporated, which matrix is selected from the group consisting of a photoformable proteinaceous mixture, a film-forming latex, and combinations thereof and through which matrix said analyte species may freely permeate and interact with said bioactive molecule;

(b) obtaining a plurality of signal outputs from said biosensor; and

(c) processing said signal outputs to deduce the presence and quantity of each analyte species.

6. A method for assaying a sample for a particular ligand species which comprises:

(a) providing reagents capable of interacting with a sample suspected of containing a particular ligand species to produce a change in the concentration of an electroactive detactable species, which change in the concentration of said detectable species is proportional to the amount of said particular ligand species in said sample;

(b) contacting said sample and said reagents with a microfabricated biosensor comprising (i) a base sensor sensitive to the concentration of said detectable species;

(ii) a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less; and

(iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of an immobilized ligand receptor capable of binding said particular ligand species or any complex comprising said particular ligand species;

(c) measuring a signal output from said biosensor from which signal output the concentration of said detectable species may be deduced;

(d) assessing a change in the concentration of said detectable species compared to a base line concentration of said detectable species; and

(e) relating said change to the amount of said particular ligand species in said sample.

10. The method of claim 6, 7, 8 or 9 in which said microfabricated biosensor further comprises a photoresist layer, comprising a photoformable proteinaceous mixture, interposed between said permselective layer and said receptor layer.

11. The method of claim 6, 7, 8 or 9 in which said microfabricated biosensor further comprises an electrolyte layer interposed between said base sensor and said permselective layer.

12. The method of claim 6, 7, 8 or 9 in which said immobilized ligand receptor is selected from the group consisting of ionophores, cofactors, enzymes, antibodies, antigens, lectins, neurochemical receptors, active fragments or subunits of the preceding molecules and mixtures thereof.

13. The method of claim 6, 7, 8 or 9 in which said permselective layer is photodefined.

14. The method of claim 6, 7, 8 or 9 in which said particular ligand species is selected from the group consisting of ionophores, cofactors, enzymes, antibodies, antigens, lectins, neurochemical receptors, fragments or subunits of the preceding molecules and mixtures thereof.

29. The method of claim 6, 7, 8 or 9 in which said immobilized ligand receptor is a glycoprotein.

30. The method of claim 6, 7, 8 or 9 in which said particular ligand species is a glycoprotein.

31. The method of claim 6, 7, 8 or 9 in which said immobilized ligand receptor is an oligonucleotide or polynucleotide or a single strand thereof.

32. The method of claim 6, 7, 8 or 9 in which said particular ligand species is an oligonucleotide or polynucleotide or a single strand thereof.

33. The method of claim 6, 7, 8 or 9 in which said immobilized ligand receptor is a polypeptide or protein.

34. The method of claim 6, 7, 8 or 9 in which said particular ligand species is a polypeptide or protein.

35. The method of claim 6, 7, 8 or 9 in which said particular ligand species is a virus or fungus.

7. A method for assaying a sample for a particular ligand species, which method comprises:

(a) providing a reagent capable of interacting with a sample suspected of containing a particular ligand species, which reagent comprises a labeled ligand or a labeled ligand receptor capable of forming a complex with said particular ligand species,

said label being capable of acting on an added substrate to produce a change in the concentration of an electroactive detectable species and which change is proportional to the amount of said particular ligand species in said sample;

(b) contacting said sample and said reagent with a microfabricated biosensor comprising (i) a base sensor sensitive to the concentration of said detectable species, (ii) a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of an immobilized ligand receptor capable of binding said labeled, particular ligand species or any complex comprising said labeled, particular ligand species,

for a period of time sufficient to allow said immobilized ligand receptor to bind with said labeled ligand, particular ligand species, or any complex comprising said labeled ligand, particular ligand species;

(c) removing any material which remains unbound to said immobilized ligand receptor followed by the addition of said substrate;

(d) measuring the change in the concentration of said detectable species; and

(e) relating said change to the amount of said particular ligand species in said sample.

16. The method of claim 7, 8 or 9 in which the operation of step (c) is accomplished by adding a substrate with the concomitant removal of any materials which remain unbound to said immobilized ligand receptor.

8. A method for assaying a sample for a particular ligand species which comprises:

(a) providing a reagent capable of interacting with a sample suspected of containing a particular ligand species, which reagent comprises a labeled ligand receptor capable of forming a complex with said particular ligand species,

said label being capable of acting on an added substrate to produce a change in the concentration of an electroactive detactable and which change is proportional to the amount of said particular ligand species in said sample;

(b) contacting a sample and said reagent with a microfabricated biosensor comprising;

(i) a base sensor sensitive to the concentration of said detectable species, (ii) a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of an immobilized ligand receptor capable of binding said particular ligand species or any complex thereof,

for a period of time sufficient to allow said immobilized ligand receptor to bind with said particular ligand species or any complex thereof;

(c) removing any material which remains unbound to said immobilized ligand receptor followed by the addition of said substrate;

(d) measuring the change in the concentration of said detectable species; and

(e) relating said change to the amount of said particular ligand species in said sample.

15. The method of claim 8 which further comprises removing any material which remains unbound to said immobilized ligand receptor between steps (b) and (c).

9. A method for assaying a sample for a particular ligand species which comprises:

(a) providing a reagent capable of interacting with a sample suspected of containing a particular ligand species, which reagent comprises a labeled ligand capable of competing with said particular ligand species for available immobilized ligand receptors,

said label being capable of acting on an added substrate to produce a change in the concentration of an electroactive detactable, which change is proportional to the amount of said particular ligand species in said sample;

(b) contacting said sample and said reagent with a microfabricated biosensor comprising (i) a base sensor sensitive to the concentration of said detectable species, (ii) a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of said immobilized ligand receptor capable of binding said labeled ligand or particular ligand species,

for a period of time sufficient to allow said immobilized ligand receptor to bind with said labeled ligand or particular ligand species;

(c) removing any material which remains unbound to said immobilized ligand receptor followed by the addition of said substrate;

(d) measuring the change in the concentration of said detectable species; and

(e) relating said change to the amount of said particular ligand species in said sample.

17. A method for assaying a sample for a particular antigenic species which comprises:

(a) providing a reagent capable of interacting with a sample suspected of containing a particular antigenic species, which reagent comprises a labeled antibody capable of forming a complex with said particular antigenic species,

said label being capable of acting on an added substrate to produce a change in the concentration of an electroactive detactable and which change is proportional to the amount of said particular antigenic species in said sample;

(b) contacting a sample and said reagent with a microfabricated biosensor comprising (i) a base sensor sensitive to the concentration of said detectable species, (ii) a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of an immobilized ligand receptor comprising an antibody capable of binding said particular antigenic species or any complex thereof,

(c) removing any material which remains unbound to said immobilized ligand receptor followed by the addition of said substrate;

(d) measuring the change in the concentration of said detectable species; and

(e) relating said change to the amount of said particular antigenic species in said sample.

21. The method of claim 17, 18, 19 or 20 in which the operation of step (c) is accomplished by adding a substrate with the concomitant removal of any materials which remain unbound to said immobilized ligand receptor.

22. The method of claim 6, 7, 8, 9, 17, 18, 19 or 20 in which said label is an enzyme.

23. The method of claim 6, 7, 8, 9, 17, 18, 19 or 20 in which said detectable species is dioxygen or hydrogen peroxide.

24. The method of claim 6, 7, 8, 9, 17, 18, 19 or 20 in which said substrate is an indoxyl phosphate, analog, or derivative thereof.

28. The method of claim 6, 7, 8, 9, 17, 18, 19, 20 or 25 in which said base sensor is an electrochemical sensor.

18. A method for assaying a sample for a particular antigenic species, which method comprises:

(a) providing a reagent capable of interacting with a sample suspected of containing a particular antigenic species, which reagent comprises a labeled antigenic species,

said label being capable of acting on an added substrate to produce a change in the concentration of an electroactive detectable species and which change is proportional to the amount of said particular antigenic species in said sample;

(b) contacting said sample and said reagent with a microfabricated biosensor comprising (i) a base sensor sensitive to the concentration of said detectable species;

(ii)a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of an immobilized ligand receptor comprising an antibody capable of binding said labeled antigenic species, particular antigenic species or any complex comprising said labeled antigenic species or particular antigenic species,

for a period of time sufficient to allow said immobilized ligand receptor to bind with said labeled antigenic species, particular antigenic species or any complex comprising said labeled antigenic species or particular antigenic species;

(c) removing any material which remains unbound to said immobilized ligand receptor to bind with said labeled antigenic species, particular antigenic species or any complex comprising said labeled antigenic species or particular antigenic species;

(d) measuring the change in the concentration of said detectable species; and

(e) relating said change to the amount of said particular antigenic species in said sample.

19. A method for assaying a sample for a particular antibody which comprises:

(a) providing a reagent capable of interacting with a sample suspected of containing a particular antibody, which reagent comprises a labeled antigenic species or a labeled anti-antibody capable of forming a complex with said particular antibody,

said label being capable of acting on an added substrate to produce a change in the concentration of an electroactive detectable species and which change is proportional to the amount of said particular antibody in said sample;

(a) contacting a sample and said reagent with a microfabricated biosensor comprising (i) a base sensor sensitive to the concentration of said detectable species;

(ii) a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of an immobilized ligand receptor comprising an antigenic species or anti-antibody capable of binding said particular antibody or any complex thereof,

for a period of time sufficient to allow said immobilized ligand receptor to bind with said particular antibody or any complex thereof;

(c) removing any material which remains unbound to said immobilized ligand receptor followed by the addition of said substrate;

(d) measuring the change in the concentration of said detectable species; and

(e) relating said change to the amount of said particular antibody in said sample.

20. A method for assaying a sample for a particular antibody, which method comprises:

(a) providing a reagent capable of interacting with a sample suspected of containing a particular antibody, which reagent comprises a labeled antibody,

said label being capable of acting on an added substrate to produce a change in the concentration of an electroactive detectable species and which change is proportional to the amount of said particular antibody in said sample;

(b) contacting said sample and said reagent with a microfabricated biosensor comprising (i) a base sensor sensitive to the concentration of said detectable species, (ii) a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of an immobilized ligand receptor comprising an antigenic species or anti-antibody capable of binding said particular antibody or labeled antibody,

for a period of time sufficient to allow said immobilized ligand receptor to bind with said particular antibody or labeled antibody;

(c) removing any material which remains unbound to said immobilized ligand receptor followed by the addition of said substrate;

(d) measuring the change in the concentration of said detectable species; and

(e) relating said change to the amount of said particular antibody in said sample.

25. A method for assaying a sample for a particular oligonucleotide sequence, which method comprises:

(a) providing a reagent capable of interacting with a sample suspected of containing a particular oligonucleotide sequence, which reagent comprises a labeled probe having a base sequence which is complementary to at least a portion of said oligonucleotide sequence and capable of forming a hybrid complex therewith,

said label being capable of acting on an added substrate to produce a change in the concentration of an electroactive detectable species and which change is proportional to the amount of said oligonucleotide sequence in said sample;

(b) contacting said sample and said reagent with a microfabricated biosensor comprising (i) a base sensor sensitive to the concentration of said detectable species, (ii) a permselective layer, superimposed over at least a portion of said base sensor, having a composition and thickness sufficient to exclude substantially molecules with a molecular weight of about 120 or more while allowing the free permeation of molecules with a molecular weight of about 50 or less, and (iii) a receptor layer, superimposed over said base sensor and at least a portion of said permselective layer, comprising a sufficient amount of an immobilized ligand receptor capable of binding said oligonucleotide sequence or complex hybrid thereof,

for a period of time sufficient to allow said immobilized ligand receptor to bind with said oligonucleotide sequence or complex hybrid thereof;

(c) removing any material which remains unbound to said immobilized ligand receptor followed by the addition of said substrate;

(d) measuring the change in the concentration of said detectable species; and

(e) relating said change to the amount of said oligonucleotide sequence in said sample.

26. The method of claim 25 in which said immobilized ligand receptor is a preselected probe having a base sequence which is complementary to at least a portion of said oligonucleotide sequence and which binds said oligonucleotide sequence or hybrid complex thereof at a site other than that engaged by said labeled probe.

27. The method of claim 25 in which said immobilized ligand receptor is an antibody which recognizes said hybrid complex.