Diffraction-based diagnostic devices

• US 7,485,453 B2
• Filed: 05/03/2002
• Issued: 02/03/2009
• Est. Priority Date: 05/03/2002
• Status: Active Grant

• Current Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Original Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Inventors: Kaylor, Rosann, Cohen, David
• Primary Examiner(s): Le; Long V
• Assistant Examiner(s): Yu; Melanie J.
• Application Number:
  US10/139,018
• Publication Number:
  US 20030207257A1
• Time in Patent Office: 2,468 Days
• Field of Search: 435/283.1, 435/287.1, 435/287.2, 435/288.3, 435/4, 435/7.1, 422/50, 422/61, 422/68.1, 422/82.11, 356/300, 356/302, 356/305, 436/518, 436/524, 436/525
• US Class Current: 435/287.1
• CPC Class Codes: B82Y 15/00 Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
• CPC Class Codes: B82Y 30/00 Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: C12Q 1/003 Functionalisation
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings

Abstract

A biosensor includes a substrate with areas of active receptive material disposed thereon. The receptive material is specific for an analyte of interest. A pattern of the active areas is defined on the substrate by an oxidizing photo-masking process.

Claims

1. A method for producing biosensors, comprising:

forming a blocking layer of thiol-containing molecules on a metalized substrate member, the thiol-containing molecules forming thiol-metal bonds with the metal surface of the substrate member;

exposing the substrate member to an oxidizing enhancing stimulus through a mask having a pattern of exposed areas and protected areas, said exposure being of sufficient time to oxidize the thiol-metal bonds in the exposed areas of the blocking layer under the mask;

exposing the substrate member to a first source of thiolated biomolecules without an intervening washing step, for a time sufficient to remove the oxidized thiol-metal bonds in the exposed areas and form a layer of the first thiolated biomolecules directly on the metalized substrate member at the oxidized areas of the blocking layer by displacing the oxidized thiol-containing molecules in the exposed areas with the first thiolated biomolecule, the first thiolated biomolecules being specific for an analyte of interest having a particular size, the first thiolated biomolecules defining active areas of receptive material in a pattern corresponding to the oxidized areas defined by the exposing to oxidize step, wherein when the biosensor is exposed to a medium containing the analyte of interest, the analyte binds to the receptive material in the active areas such that the particular size of the analyte of interest, with or without a diffraction enhancing element, facilitates subsequent diffraction of light in a diffraction pattern corresponding to the active areas.

2. The method as in claim 1, wherein the first thiolated biomolecules are selected from at least one of antigens, antibodies, nucleotides, chelators, enzymes, bacteria, yeasts, fungi, viruses, bacterial pili, bacterial flagellar materials, nucleic acids, polysaccharides, lipids, proteins, carbohydrates, metals, hormones, and respective receptors for said materials.

3. The method as in claim 1, wherein the oxidizing enhancing stimulus is a UV light source.

4. The method as in claim 1, wherein the metalized substrate is gold-coated.

5. The method as in claim 1, comprising selecting the substrate member from the group of materials consisting of plastics, metal coated plastics and glass, functionalized plastics and glass, silicon wafers, and foils.

6. The method as in claim 1, wherein the substrate member comprises a polymer film coated with a metal.

7. The method as in claim 6, wherein the polymer film comprises polyethylene-terephthalate.

8. The method as in claim 6, comprising selecting the metal from the group consisting of gold, silver, chromium, nickel, platinum, aluminum, iron, copper, gold oxide, chromium oxide and zirconium.

9. The method as in claim 1, comprising viewing a diffraction pattern of active areas with a naked eye.

10. The method as in claim 1, wherein the analyte of interest is selected from at least one of a bacteria, yeast, fungus, virus, rheumatoid factor, IgG, IgM, IgA, IgD and IgE antibodies, carcinoembryonic antigen, streptococcus Group A antigen, viral antigens, antigens associated with autoimmune disease, allergens, tumor antigens, streptococcus group B antigen, IIV I or HIV II antigen, antibodies viruses, antigens specific to RSV, an antibody, antigen, enzyme, hormone, polysaccharide, protein, lipid, carbohydrate, drug, nucleic acid, Neisseria meningitides groups A, B, C, Y and W sub 135, Streptococcus pneumoniae, E. coli K1, Haemophllus influenza type A/B, an antigen derived from microorganisms, PSA and CRP antigens, a hapten, a drug of abuse, a therapeutic drug, an environmental agents, or antigens specific to Hepatitis.

11. The method as in claim 1, wherein the first thiolated biomolecules are non-specific for a particular analyte of interest, and further comprising exposing the substrate member a second time to the oxidizing stimulus without the mask for a sufficient time to oxidize the thiol-metal bonds in the remaining areas of the blocking layer, and subsequently exposing the substrate member to a second source of thiolated biomolecules that are specific for the analyte of interest for a time sufficient for a layer of the second thiolated biomolecules to form at the second oxidized areas, the areas containing the second thiolated biomolecules defining active areas of receptive material, and the areas containing the first thiolated biomolecules defining shielded areas of the substrate, and wherein when the biosensor is exposed to a medium containing the analyte of interest, the analyte binds to the receptive material in the active areas and facilitate subsequent diffraction of transmitted light in a diffraction pattern corresponding to the active areas.

12. The method as in claim 11, wherein the second thiolated biomolecules are selected from at least one of antigens, antibodies, nucleotides, chelators, enzymes, bacteria, yeasts, fungi, viruses, bacterial pili, bacterial flagellar materials, nucleic acids, polysaccharides, lipids, proteins, carbohydrates, metals, hormones, and respective receptors for said materials.

13. The method as in claim 11, wherein the analyte of interest is selected from at least one of a bacteria, yeast, fungus, virus, rheumatoid factor, IgG, IgM, IgA, IgD and IgE antibodies, carcinoembryonic antigen, streptococcus Group A antigen, viral antigens, antigens associated with autoimmune disease, allergens, tumor antigens, streptococcus group B antigen, IIV I or HIV II antigen, antibodies viruses, antigens specific to RSV, an antibody, antigen, enzyme, hormone, polysaccharide, protein, lipid, carbohydrate, drug, nucleic acid, Neisseria meningitides groups A, B, C, Y and W sub 135, Streptococcus pneumoniae, E. coil K1, Haemophllus influenza type A/B, an antigen derived from microorganisms, PSA and CRP antigens, a hapten, a drug of abuse, a therapeutic drug, an environmental agents, or antigens specific to Hepatitis.

14. The method as in claim 11, wherein the oxidizing enhancing stimulus is a UV light source.

15. The method as in claim 11, wherein the metalized substrate is gold-coated.

16. The method as in claim 11, comprising selecting the substrate member from the group of materials consisting of plastics, metal coated plastics and glass, functionalized plastics and glass, silicon wafers, and foils.

17. The method as in claim 11, wherein the substrate member comprises a polymer film coated with a metal.

18. The method as in claim 17, wherein the polymer film comprises polyethylene-terephthalate.

19. The method as in claim 1, wherein the thiol-containing molecules consist essentially of thioglucose.