Diffraction-based diagnostic devices

• US 7,169,550 B2
• Filed: 09/26/2002
• Issued: 01/30/2007
• Est. Priority Date: 09/26/2002
• Status: Expired due to Fees

• Current Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Original Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Inventors: Kaylor, Rosann, Cohen, David, Sayre, Curtis
• Primary Examiner(s): Chin; Christopher L.
• Application Number:
  US10/256,278
• Publication Number:
  US 20040063146A1
• Time in Patent Office: 1,587 Days
• Field of Search: None
• US Class Current: 435/4
• CPC Class Codes: G01N 21/4788 Diffraction for sizing particles G01N15/0205
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G03H 1/182 Post-exposure processing, e.g. latensification
• CPC Class Codes: Y10S 436/805 Optical property
• CPC Class Codes: Y10S 436/815 Test for named compound or class of compounds
• CPC Class Codes: Y10S 436/82 Hepatitis associated antigens and antibodies
• CPC Class Codes: Y10S 436/901 Drugs of abuse, e.g. narcotics, amphetamine

Abstract

A biosensor includes a substrate with a receptive material layer of radiation-absorbing member (RAM)-tagged biomolecules disposed thereon. The receptive material is specific for an analyte of interest. A pattern of active and deactivated areas of the receptive material are defined in the receptive material layer by a masking process wherein areas are exposed through a mask with a light source to induce deactivation.

Claims

1. A method of making a biosensor, comprising the steps of:

forming a receptive material layer of biomolecules and a radiation-absorbing member generally uniformly over a surface of a substrate member in a light protected environment, the biomolecules being specific for an analyte of interest;

placing a mask over the substrate member, the mask having a configuration so as to cover at least one underlying area of the substrate member while exposing at least one adjacent area;

exposing the substrate member and mask combination with a radiation source sufficient to excite said radiation-absorbing member and, deactivate the biomolecules in the areas exposed by the mask;

removing the mask from the substrate member; and

wherein a resulting pattern of active and inactive areas of the receptive material are defined, the inactive areas corresponding to the areas exposed by the mask and the active areas corresponding to the areas underlying the mask such that 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 subsequently facilitates diffraction of transmitted, reflected, or phase-shifted light in a diffraction pattern corresponding to the active areas.

2. The method as in claim 1, wherein the radiation absorbing member is a fluorophore.

3. The method as in claim 2, wherein said step of exposing with the radiation source includes illuminating the substrate member at a wavelength and amplitude sufficient for inducing fluorescence without photo-bleaching the fluorophore.

4. The method as in claim 1, wherein the radiation-absorbing member is a photoinitiator.

5. The method as in claim 4, wherein the step of exposing with the radiation source includes illuminating with a light at a wavelength and amplitude sufficient to generate free radicals sufficient to deactivate the biomolecules in the areas exposed by the mask.

6. The method as in claim 4, wherein the step of exposing with radiation source includes illuminating with a light at a wavelength and amplitude sufficient to generate thermally excited molecules sufficient to deactivate the biomolecules in the areas exposed by the mask.

7. 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, glass, and foils.

8. The method as in claim 7, wherein the substrate member is a metal coated plastic, and comprising selecting the metal from the group consisting of gold, silver, chromium, nickel, platinum, aluminum, iron, copper, titanium, gold oxide, chromium oxide, silver oxide, and zirconium.

9. The method as in claim 8, comprising depositing the gold coating onto the polymer film at a thickness between about 1 nanometer and 1000 nanometers.

10. The method as in claim 1, wherein the receptive material is a protein or proteins.

11. The method as in claim 10, wherein the receptive material is an antibody.

12. The method as in claim 1, comprising selecting the receptive material 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, aptamers, peptides, and respective receptors for said materials.

13. 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, HIV 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, Haemophilus 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 1, further comprising defining a plurality of openings through the mask in a desired pattern, the openings defining the pattern of inactive areas.