Tissue implantable microbiosensor

• US 9,468,402 B2
• Filed: 12/01/2011
• Issued: 10/18/2016
• Est. Priority Date: 12/01/2010
• Status: Active Grant

• Current Assignee: Pinnacle Technology, Inc.
• Original Assignee: Pinnacle Technology, Inc.
• Inventors: Petillo, Peter A., Wilson, George S., Wu, Judy Z., Richter, Mark L., Johnson, David A., Aillon, Daniel V.
• Primary Examiner(s): JANG, CHRISTIAN YONGKYUN
• Application Number:
  US13/991,113
• Publication Number:
  US 20130324820A1
• Time in Patent Office: 1,783 Days
• US Class Current: 1/1
• CPC Class Codes: A61B 2562/12 Manufacturing methods specially adapted for producing sensors for in-vivo measurements
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/14865 invasive, e.g. introduced into the body by a catheter or needle or using implanted sensors
• CPC Class Codes: C25D 7/00 Electroplating characterised by the article coated

Abstract

A biosensor system comprises a capillary substrate, conductive electrode, and a plurality of nanoparticles having an enzyme deposited thereon formed in a cavity at one end of the capillary substrate. The substrate may have an optional reinforcing layer (which may be conductive or non-conductive) and optional insulating layer thereon. A cannula having an optional conductive layer, insulating layer, and reference electrode may also form part of the system.

Claims

1. A tissue implantable biosensor system comprising:

a capillary substrate;

a conductive electrode within said capillary substrate, said capillary substrate having a cavity at one end;

a plurality of nanoparticles having an enzyme immobilized thereon deposited in said cavity; and

a reference electrode.

2. The tissue implantable biosensor system of claim 1, wherein said capillary substrate has an exterior surface coated with a reinforcing material coating.

3. The tissue implantable biosensor system of claim 2, wherein said reinforcing material coating selected from the group consisting of a para-aramid polymer coating, carbon nanotube coating, and grapheme coating.

4. The tissue implantable biosensor system of claim 3, wherein said reinforcing material forms an electric shield around said capillary substrate which reduces electrical noise and dielectric absorption effects in said system.

5. The tissue implantable biosensor system of claim 2, wherein said reinforcing material coating has a thickness from about 2 nm to about 100 nm.

6. The tissue implantable biosensor system of claim 2, wherein said reinforcing material coating has an overlying insulating layer.

7. The tissue implantable biosensor system of claim 1, wherein said conductive electrode comprises a metal or metal alloy wire which is sealed in the capillary substrate and etched to a depth to form said cavity.

8. The tissue implantable biosensor system of claim 7, wherein a resin seals said wire in said capillary substrate.

9. The tissue implantable biosensor system of claim 1, wherein said capillary substrate is housed in a cannula.

10. The tissue implantable biosensor system of claim 9, wherein said reference electrode is integrated in said cannula.

11. The tissue implantable biosensor system of claim 10, wherein said cannula is tapered.

12. The tissue implantable biosensor system of claim 10, wherein a conducting layer is formed on said cannula, said conducting layer forming an electric shield around said biosensor which reduces electrical noise and dielectric absorption effects in said system.

13. The tissue implantable biosensor system of claim 12, wherein an insulating layer overlies said conducting layer.

14. The tissue implantable biosensor system of claim 1, wherein said nanoparticles comprise a nanoparticle core and a coating on said nanoparticle core, said coating comprising an activated group for covalent attachment of said enzyme to said nanoparticle core.

15. The tissue implantable biosensor system of claim 14, wherein said nanoparticle core comprises a metal, a metal alloy, or a combination thereof.

16. The tissue implantable biosensor system of claim 14, wherein said nanoparticle core is magnetic.

17. The tissue implantable biosensor system of claim 16, wherein said nanoparticle core is selected from the group consisting of iron, nickel, cobalt, yttrium, neodymium, samarium, and combinations thereof.

18. The tissue implantable biosensor system of claim 14, wherein said nanoparticle core is non-magnetic.

19. The tissue implantable biosensor system of claim 18, wherein said nanoparticle core is selected from group consisting of gold, silver, platinum, manganese, palladium, copper, zinc, ruthenium, rhodium, cadmium, stainless steel, iridium, and combinations thereof.

20. The tissue implantable biosensor system of claim 14, wherein said coating is non-conducting.

21. The tissue implantable biosensor system of claim 14, wherein said coating comprises a carbohydrate polymer.

22. The tissue implantable biosensor system of claim 14, wherein said coating comprises a linear carbohydrate polymer.

23. The tissue implantable biosensor system of claim 14, wherein said coating comprises a polymer selected from the group consisting of glycosaminoglycans (including hyaluronan, chondroitin, chondroitin sulfate, heparin, heparan sulfate, dermatan, dermatan sulfate, keratan, keratan sulfate), mucopolysaccharides, celluloses, pectins, glucomannans, galactomannans, agars, alginic acids, chitins, inulins, glucans amylases, amylopectins, xanthan gums, dextrans, glycogens, arabinoxylans, and combinations thereof.

24. The tissue implantable biosensor system of claim 14, wherein said nanoparticle core is completely coated with said coating.

25. The tissue implantable biosensor system of claim 14, wherein said coating is from about 5 nm to about 10 nm thick.

26. The tissue implantable biosensor system of claim 14, wherein said enzyme is attached to said coating via a group selected from the group consisting of primary amines, carboxylates, thiols, aldehyde moieties, and non-covalently attachments using bioaffinities.

27. The tissue implantable biosensor system of claim 14, wherein said enzyme is an oxidase enzyme selected from the group consisting of malate oxidase, hexose oxidase, aryl-alcohol oxidase, L-gulonolactone oxidase, pyranose oxidase, L-sorbose oxidase, pyridoxine 4-oxidase (S)-2-hydroxy-acid oxidase, ecdysone oxidase, secondary-alcohol oxidase, 4-hydroxymandelate oxidase, long-chain-alcohol oxidase, thiamine oxidase, hydroxyphytanate oxidase, N-acylhexosamine oxidase, polyvinyl-alcohol oxidase, D-arabinono-1,4-lactone oxidase, vanillyl-alcohol oxidase, D-mannitol oxidase, alditol oxidase, choline dehydrogenase, gluconate 2-dehydrogenase, glucooligosaccharide oxidase, alcohol dehydrogenase, cellobiose dehydrogenase, aldehyde oxidase, glyoxylate oxidase, indole-3-acetaldehyde oxidase, aryl-aldehyde oxidase, retinal oxidase, abscisic-aldehyde oxidase, aldehyde ferredoxin oxidoreductase, indolepyruvate ferredoxin oxidoreductase, aldehyde dehydrogenase, dihydroorotate oxidase, dihydrouracil oxidase, tetrahydroberberine oxidase, tryptophan alpha,beta-oxidase, L-galactonolactone oxidase, acyl-CoA dehydrogenase, isoquinoline 1-oxidoreductase, quinaldate 4-oxidoreductase, D-aspartate oxidase, L-amino-acid oxidase, monoamine oxidase, pyridoxal 5′

-phosphate synthase, D-glutamate oxidase, ethanolamine oxidase, putrescine oxidase, cyclohexylamine oxidase, protein-lysine 6-oxidase, D-glutamate(D-aspartate) oxidase, L-lysine 6-oxidase, primary-amine oxidase, 7-chloro-L-tryptophan oxidase, N-methyl-L-amino-acid oxidase, non-specific polyamine oxidase, N8-acetylspermidine oxidase (propane-1,3-diamine-forming), N6-methyl-lysine oxidase, polyamine oxidase (propane-1,3-diamine-forming), N1-acetylpolyamine oxidase, spermine oxidase, L-pipecolate oxidase, dimethylglycine oxidase, polyamine oxidase, E-dihydrobenzophenanthridine oxidase, NAD(P)H oxidase, urate oxidase, aci-nitropropanoate oxidase, sulfite oxidase, methanethiol oxidase, prenylcysteine oxidase, L-ascorbate oxidase, 3-hydroxyanthranilate oxidase, rifamycin-B oxidase, superoxide dismutase, reticuline oxidase, lactate oxidase, D-amino acid oxidase, (S)-6-hydroxynicotine oxidase, (R)-6-hydroxynicotine oxidase, alcohol oxidase, pyruvate oxidase, glucose oxidase, glutamate oxidase, acyl coenzyme A oxidase, choline oxidase, glutathione sulfhydryl oxidase, glycerolphosphate oxidase, sarcosine oxidase, xanthine oxidase, oxalate oxidase, cholesterol oxidase, gamma-glutamyl-putrescine oxidase, GABA oxidase, histamine oxidase, diamine oxidase, nucleoside oxidase, L-lysine oxidase, L-aspartate oxidase, glycine oxidase, and galactose oxidase.

28. The tissue implantable biosensor system of claim 14, wherein said enzyme is an oxidase enzyme selected from the group consisting of lactate oxidase, D-amino acid oxidase, (S)-6-hydroxynicotine oxidase, (R)-6-hydroxynicotine oxidase, alcohol oxidase, pyruvate oxidase, glucose oxidase, glutamate oxidase, acyl coenzyme A oxidase, choline oxidase, glutathione sulfhydryl oxidase, glycerolphosphate oxidase, sarcosine oxidase, xanthine oxidase, oxalate oxidase, cholesterol oxidase, gamma-glutamyl-putrescence oxidase, GABA oxidase, histamine oxidase, diamine oxidase, nucleoside oxidase, L-lysine oxidase, L-aspartate oxidase, glycine oxidase, and galactose oxidase.

29. The tissue implantable biosensor system of claim 1, wherein said nanoparticles are from about 30 am to about 200 nm in diameter.

30. The tissue implantable biosensor system of claim 1, wherein the number of capillary substrates is from about one to about eight.