Biosensing systems for measurement of lactose

Patent metadata

Field	Value
Publication number	US-10024797-B2
Application number	US-201113988723-A
Country	US
Kind code	B2
Filing date	Nov 22, 2011
Priority date	Nov 22, 2010
Publication date	Jul 17, 2018
Grant date	Jul 17, 2018

Abstract

Herein disclosed are biosensing systems that measure lactose concentration in a solution.

First claim

What is claimed:

1. A biosensing system that measures lactose concentration in a solution, said biosensing system comprising:
an optode comprising an optical fiber having a first tip and a second tip,
a luminescent transducer layer covering said first tip,
a biocomponent layer covering said luminescent transducer layer,
said biocomponent layer comprising at least one biocomponent that catalyzes a reaction with lactose in said solution, wherein
said at least one biocomponent is immobilized within said biocomponent layer using a hydrogel or polymer matrix,
a porous membrane covering said biocomponent layer, wherein said porous membrane provides a mass transfer resistance between said biocomponent layer and said solution,
a photon-detection device coupled to said second tip, wherein the photon-detection device is configured to detect photons emitted from the luminescent transducer layer through the optical fiber, and
a signal processing system coupled to said photon-detection device.

2. The biosensing system of claim 1 whereby said lactose concentration in said solution, the depth of said biocomponent layer, the depth of said porous membrane, the diffusion coefficient of lactose in said porous membrane, and the K M and V max of said catalytic reaction between said biocomponent and lactose are selected such that Da is greater than the value of 1−β and the quotient between Da 2 and 4β is from about 10 to at least 1000,
wherein V max is the maximum reaction rate of said biocomponent with lactose under saturating lactose concentrations, and
wherein K M is the lactose concentration at which the reaction rate of said biocomponent and lactose is half of V max , and
wherein β is the lactose concentration in said solution divided by said K M of said biocomponent for lactose, and
wherein Da is a dimensionless Damköhler number, and
wherein Da is (h e V max h p )/(D p K M ), and
wherein h e is the thickness of said biocomponent layer, and
wherein h p is the thickness of said porous membrane, and
wherein D p is the diffusion coefficient of lactose in said porous membrane.

3. The biosensing system of claim 1 wherein said luminescent transducer layer contains a luminescent agent that is selected from the group consisting of
a fluorescent agent,
a phosphorescent agent,
a bioluminescent agent, or
a chemiluminescent agent.

4. The biosensing system of claim 1 wherein said luminescent transducer layer contains a luminescent agent that is selected from the group consisting of:
trisodium 8-hydroxy-1,3,6-trisulphonate, fluoro (8-anilino-l-naphthalene sulphonate), tris(bipyridine)ruthenium(II) complex, Tris(4,7-diphenyl-1,10-phenanthroline)Ru(II) (RuDPP), ruthenium complexes, and acridinium- and quinidinium-based reagents, fluorescein, fluoresceinamine, or a fluorescein containing compound.

5. The biosensing system of claim 1 wherein said biocomponent layer comprises a biocomponent selected from the group consisting of at least one enzyme from Enzyme Commission numbers 1.1.3, 1.2.3, 1.3.3, 1.4.3, 1.5.3, 1.6.3, 1.7.3, 1.8.3, 1.9.3, 1.10.3, 1.16.3, 1.17.3, 1.21.3, and 3.2.1.23.

6. The biosensing system of claim 1 wherein said polymer matrix comprises one or more of polyacrylamide, polystyrene, polymethacrylate, polyvinylalcohol and polyurethane, and wherein said biocomponent is entrapped within said polymer matrix.

7. The biosensing system of claim 6 wherein said biocomponent is bound to said matrix layer through adding crosslinking agents to said biocomponent entrapped within said matrix layer, and
wherein said crosslinking agents are selected from the group consisting of glutaraldehyde, hexamethylene diisocyanate and 1,5-dinitro-2,4-difluorobenzene, polyethyleneimine, hexamethylenediamine and formaldehyde.

8. The biosensing system of claim 1 wherein said luminescent transducer layer is bound in a layer of molecules bound to the first tip of said optical fiber, said layer of molecules is selected from the group consisting of cellulose, cellulose derivatives, silica, glass, dextran, starch, agarose, porous silica, chitin and chitosan.

9. The biosensing system of claim 1 , said porous membrane is polycarbonate having a pore size of from about 0.005 μm to about 0.025 μm.

10. The biosensing system of claim 9 , said porous membrane comprises a coating of polyurethane.

11. The biosensing system of claim 1 wherein said biocomponent comprises beta-galactosidase and glucose oxidase and wherein luminescence of said luminescent transducer layer is at least partially quenched with oxygen.

12. The biosensing system of claim 11 wherein said biocomponent further comprises catalase.

13. The biosensing system of claim 1 wherein said biocomponent comprises beta-galactosidase and galactose oxidase and wherein luminescence of said luminescent transducer layer is at least partially quenched with oxygen.

14. The biosensing system of claim 13 wherein said biocomponent further comprises catalase.

15. The biosensing system of claim 1 wherein said biocomponent is carbohydrate oxidase and wherein luminescence of said luminescent transducer layer is at least partially quenched with oxygen.

16. The biosensing system of claim 1 wherein said biocomponent further comprises catalase.

17. The biosensing system of claim 1 wherein said biocomponent is cellobiose dehydrogenase and wherein luminescence of said luminescent transducer layer interacts with protons.

18. The biosensing system of claim 1 wherein said biocomponent comprises beta-galactosidase and hexose oxidase and wherein luminescence of said luminescent transducer layer is at least partially quenched with oxygen.

19. The biosensing system of claim 18 wherein said biocomponent further comprises catalase.

20. The biosensing system of claim 1 , wherein said hydrogel comprises one or more of algal polysaccharides, agarose, alginate, gelatin, collagen, pectin, poly(carbamoyl)sulfonate, locust bean gum, and gellan, and wherein said biocomponent is entrapped within said hydrogel.

21. The biosensing system of claim 1 , wherein said biocomponent layer further comprises one or more of a gel-hardening agent and a stabilizing agent.

22. The biosensing system of claim 21 , wherein said one or more of a gel-hardening agent and a stabilizing agent comprises one or more of glutaraldehyde, polyethyleneimine, hexamethylenediamine and formaldehyde.

23. The biosensing system of claim 1 , wherein said porous membrane enables said biosensing system to measure lactose in said solution at concentrations up to and including 20 mM.

24. The biosensing system of claim 1 , wherein said porous membrane enables said biosensing system to measure lactose in said solution at concentrations up to and including 100 mM.

25. The biosensing system of claim 1 , wherein said luminescent transducer layer comprises one or more fluorophores capable of interacting with protons.

Assignees

• Reardon Kenneth F
• Dandy David S
• Holcomb Ryan E
• Univ Colorado State Res Found

Inventors

• Reardon Kenneth F
• Dandy David S
• Holcomb Ryan E

Classifications

• G01N21/6486 Primary

  Measuring fluorescence of biological material, e.g. DNA, RNA, cells (G01N21/6428 takes precedence) · CPC title

• G01N2021/772

  Tip coated light guide · CPC title

• G01N2021/7786

  Fluorescence · CPC title

• G01N21/6428

  Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" (in vivo A61B5/00; immunoassay G01N33/53) · CPC title

• G01N2021/775

  Indicator and selective membrane · CPC title