IP Library Granted Patent US 12,213,784
Granted Patent B2
US 12,213,784 · App. 16/468,146 · Granted Feb 4, 2025

Durable enzyme-based biosensor and process for drop deposition immobilization

Inventors: Yunqing Du (Quincy, MA); Ming L. Wang (Ipswich, MA)
Assignee: Northeastern University
A61B5/1486A61B5/14532G01N27/3271A61B2562/0285
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Quick Facts
Patent No.
US 12,213,784
App. No.
16/468,146
Granted
Feb 4, 2025
Kind
B2
Abstract

A sensor having improved shelf life is provided for determining concentration of a biomarker in a liquid sample. The sensor functions by electrochemical detection and requires use of a biomolecule, e.g., an enzyme that catalyzes an electron transfer reaction specific for the biomarker. The sensor requires use of a quaternary ammonium compound as a bio-linker. It further requires crosslinking of the biomolecule for improved stability.

Claims (55)

1. A sensor for determining a concentration of a biomarker in a liquid sample, the sensor comprising:

an insulating or semiconducting substrate;

at least one working electrode, a counter electrode, and a reference electrode, and

a sample placement area on a surface of the substrate for containing the liquid sample during a determination of the biomarker concentration in the liquid sample;

wherein each of the working electrode(s), counter electrode, and reference electrode comprises a conductive metal layer deposited on the substrate in the sample placement area;

wherein the working electrode is coated in the sample placement area with a plurality of sensor elements;

wherein the sensor elements are functionalized with a functionalization coating comprising a quaternary ammonium compound, a plurality of metal nanoparticles, a crosslinked enzyme that catalyzes an electron transfer reaction specific for the biomarker;

wherein the working electrode, counter electrode, and reference electrode are connected to an amperometry circuit;

wherein the sensor measures electron transfer into the working electrode;

wherein an output voltage of the amperometry circuit correlates with concentration of the biomarker in the liquid sample deposited in the sample placement area; and

wherein the sensor has been fabricated by a method comprising drop deposition of the functionalization coating from a single suspension comprising the quaternary ammonium compound, the metal nanoparticles, and the enzyme.

2. The sensor of claim 1 , wherein the sensor elements comprise a material selected from the group consisting of single-walled carbon nanotubes (SWNT), double-walled carbon nanotubes, multi-walled carbon nanotubes, graphite, graphene, carbon nanofibers, carbon nanowires, carbon nanorods, and combinations thereof.

3. The sensor of claim 1 , wherein the functionalization coating does not contain a polycationic polymer.

4. The sensor of claim 1 , wherein the quaternary ammonium compound comprises alkyl chains having a chain length from about C 2 to about C 16 .

5. The sensor of claim 1 , wherein the quaternary ammonium compound is a chloride or bromide salt.

6. The sensor of claim 1 , wherein the quaternary ammonium compound is selected from the group consisting of tetraethylammonium bromide, tetrapropylammonium bromide, tetrabutylammonium bromide, hexadecyltrimethylammonium bromide, benzalkonium chloride, alkyldimethylbenzylammonium chloride having alkyl chain lengths from C 12 to C 16 , and dialkyldimethylammonium chloride having alkyl chain lengths from C 8 to C 10 .

7. The sensor of claim 1 , wherein the enzyme is crosslinked using a homobifunctional or heterobifunctional crosslinking reagent.

8. The sensor of claim 1 , wherein the enzyme is crosslinked by a reagent selected from the group consisting of glutaraldehyde, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, N-hydroxysuccinimide, N-hydroxysulfosuccinimide, dicyclohexylcarbodiimide, dimethyl adipimidate, dimethyl suberimidate, and combinations thereof.

9. The sensor of claim 1 , further comprising a protective membrane covering the functionalized sensor elements.

10. The sensor of claim 1 having a shelf life of at least nine months.

11. The sensor of claim 1 , wherein the enzyme is glucose oxidase and the biomarker is glucose.

12. The sensor of claim 11 that is capable of detecting glucose at concentrations down to 5 μM.

13. The sensor of claim 11 that is configured for determination of glucose concentration in saliva.

14. A biomarker analysis system comprising:

the sensor of claim 1 ;

a signal conditioning and/or analysis device that processes an electrical signal from the sensor.

15. A biomarker sensor array comprising a plurality of sensors according to claim 1 sharing a common substrate.

16. A kit comprising the sensor of claim 1 in a vacuum storage container.

17. A method of determining a concentration of a biomarker in a liquid sample, the method comprising the steps of:

(a) providing a sensor comprising:

an insulating or semiconducting substrate;

at least one working electrode, a counter electrode, and a reference electrode, and

a sample placement area on a surface of the substrate for containing the liquid sample during a determination of the biomarker concentration in the liquid sample;

wherein each of the working electrode(s), counter electrode, and reference electrode comprises a conductive metal layer deposited on the substrate in the sample placement area;

wherein the working electrode is coated in the sample placement area with a plurality of sensor elements;

wherein the sensor elements are functionalized with a functionalization coating comprising a quaternary ammonium compound, a plurality of metal nanoparticles, a crosslinked enzyme that catalyzes an electron transfer reaction specific for the biomarker;

wherein the working electrode, counter electrode, and reference electrode are connected to an amperometry circuit;

wherein the sensor measures electron transfer into the working electrode; and

wherein an output voltage of the amperometry circuit correlates with concentration of the biomarker in the liquid sample deposited in the sample placement area;

wherein the sensor has been fabricated by a method comprising drop deposition of the functionalization coating from a single suspension comprising the quaternary ammonium compound, the metal nanoparticles, and the enzyme;

(b) introducing a liquid sample into the sample placement area of the sensor; and

(c) determining the concentration in the liquid sample from an electrical output of the sensor.

18. The method of claim 17 further comprising the steps of:

(d) removing the liquid sample introduced in step (b);

(e) introducing a new liquid sample into the sample placement area of the sensor; and

(f) determining a new biomarker concentration in the new liquid sample from an electrical output of the sensor.

19. The method of claim 17 , wherein the liquid sample is saliva.

20. A method of fabricating a biomarker sensor, comprising the steps of:

(a) microfabricating one or more working electrodes, a reference electrode, and a counter electrode on the surface of an insulating substrate, wherein each of said electrodes contacts a sample placement area on the substrate;

(b) depositing a plurality of sensor elements onto the working electrode;

(c) depositing a functionalization coating onto the sensor elements, the functionalization coating comprising one or more functionalization layers; wherein each functionalization layer comprises a quaternary ammonium compound, a plurality of metal nanoparticles, an enzyme that catalyzes an electron transfer reaction specific for the biomarker, wherein the one or more functionalization layers are deposited through drop deposition of a single suspension comprising the quaternary ammonium compound, the metal nanoparticles, and the enzyme; and

(d) crosslinking the enzyme by applying a crosslinking reagent to the functionalization coating.

21. The method of claim 20 , wherein the crosslinking reagent is applied to the top of the functionalization coating, or wherein the crosslinking reagent is applying by its inclusion in one or more of the one or more functionalization layers.

22. The method of claim 20 , wherein the single suspension further comprises a homobifunctional or heterobifunctional crosslinking reagent.

23. The method of claim 20 , wherein the sensor elements are deposited onto the working electrode by a self-assembly process comprising depositing a liquid suspension of sensor elements onto the electrode.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2024
From: DU, YUNQING; WANG, MING L.
To: NORTHEASTERN UNIVERSITY
Reel/Frame 069624/0470 →
Continuity (2)
Provisional Application 62432513 · Dec 9, 2016
Related Publication 20200405200A1 · Dec 31, 2020
References Cited (31)
US 5116729A · Ismail et al. · 1992 [cited by applicant]
US 20070042496A1 · Okamoto · 2007 [cited by examiner]
US 20100009456A1 · Prins et al. · 2010 [cited by applicant]
US 20110236951A1 · Grate · 2011 [cited by examiner]
US 20110263011A1 · Qiu et al. · 2011 [cited by applicant]
US 20120216936A1 · Forrow et al. · 2012 [cited by applicant]
US 20120228149A1 · Boal · 2012 [cited by examiner]
US 20120325679A1 · Forrow · 2012 [cited by examiner]
US 20130324820A1 · Petillo · 2013 [cited by examiner]
US 20140197042A1 · Zhang · 2014 [cited by examiner]
CN 1815236A · 2006 [cited by applicant]
CN 101393159A · 2009 [cited by applicant]
CN 103175884A · 2013 [cited by applicant]
CN 10502972A · 2015 [cited by applicant]
CN 105708416A · 2016 [cited by applicant]
EP 1688742A1 · 2006 [cited by applicant]
WO 2003035891A2 · 2003 [cited by applicant]
Du et al., “Sensing of Salivary Glucose Using Nano-Structured Biosensors”. Biosensors 2016, 6(1): p. 10; Journal of Diabetes Science and Technology, pp. 1344-1352. [cited by applicant]
Gibson, T. D., “Biosensors: The Stability Problem”, Analusis, 1999, 27(7): p. 630-638. [cited by applicant]
Double-Do Protein Cross-Linkers, Handbook & Selection Guide, Archived, Dec. 7, 2017; Retrieved from www.GBiosciences.com. [cited by applicant]
Castagnola et al., “Potential applications of human saliva as diagnostic fluid”, Acta Otorhinolaryngologica Italica, 2011; 31:347-357. [cited by applicant]
Zhang et al., “On-chip highly sensitive saliva glucose sensing using multilayer films composed of single-walled carbon hanotubes, gold nanoparticles, and glucose oxidase”, Sensing and Bio-Sensing Research, vol. 4, Jun. … [cited by applicant]
Malon et al., “Saliva-Based Biosensors: Noninvasive Monitoring Tool for Clinical Diagnostics”, BioMed Research International, vol. 2014, Article ID 962903, 20 pages, 2014. [cited by applicant]
Lichter et al., “Design of Antibacterial Surfaces and Interfaces: Polyelectrolyte Multilayers as a Multifunctional Platform”, Macromolecules, 2009, 42(22), pp. 8573-8586. [cited by applicant]
Petkova et al., “Gold and silver nanoparticles for biomolecule immobilization and enzymatic catalysis”, Nanoscale Research Letters, 2012, 7, Article No. 287, 10 pages. [cited by applicant]
Moore et al., “Improving the Environment for Immobilized Dehydrogenase Enzymes by Modifying Nation with Tetraalkylammonium Bromides”, Biomacromolecules 2004, 5(4), pp. 1241-1247. [cited by applicant]
Meredith et al., “Hydrophobic Salt-modified Nafion for Enzyme Immobilization and Stabilization”, Jove-Journal of Visualized Experiments, 2012 (65), 5 pages. [cited by applicant]
Zhou et al., “Immunoassays for cortisol using antibody-doped sol-gel silica”, Journal of Materials Chemistry, 2004, 12 (14): p. 2311-2316. [cited by applicant]
Zucca and Sanjust, “Inorganic Materials as Supports for Covalent Enzyme Immobilization: Methods and Mechanisms”, Methods and Mechanisms. Molecules, 2014, 19(9): p. 14139-14194. [cited by applicant]
Wong, “Salivary diagnostics powered by nanotechnologies, proteomics and genomics”, J Am Dent Assoc, 2006, 137 (3): p. 313-21. [cited by applicant]
Wang et al., “A novel glucose biosensor based on the immobilization of glucose oxidase onto gold nanoparticles-modified Pb nanowires”, Biosensors and Bioelectronics 25 (2009) 142-146. [cited by applicant]