Novel two electrode-based correction approach for elimination of biofouling from label-free affinity biosensors for detection

Patent metadata

Field	Value
Publication number	US-2025224394-A1
Application number	US-202218699807-A
Country	US
Kind code	A1
Filing date	Oct 11, 2022
Priority date	Oct 11, 2021
Publication date	Jul 10, 2025
Grant date	—

Abstract

The invention relates to a novel two-electrode approach that obviates non-specific adsorption (NSA) commonly termed, “biofouling” on biosensors. The unique two-electrode approach is based on baseline and sensing electrodes that are exposed to conditions with and without the detecting analyte. Proper corrections for normalization of the baseline and the intercept are made to eliminate the prevalence of biofouling and accurately detect the presence of the biomarkers without any interference. A corrective method nullifies the influence of any interfering factors present in animal and human blood, serum, biological body fluids or in any natural or synthetic solution that could bind to the label free biosensor (i.e., non-specific adsorption) and influence its sensitivity, accuracy, rapid detectability, specificity, precision, and reproducibility.

First claim

We claim:

1 . A biosensor system to detect biomarkers of interest in a patient and reduce or preclude non-biomarker interference, comprising:
a baseline biosensor, comprising:
an electrically conductive material interface having a surface,
an immobilization agent applied or deposited onto the surface of the conductive material interface; and
biotin conjugated with the immobilization agent;
a sensing biosensor, comprising:
a conductive material interface having a surface, and
a biological sensor agent applied to the surface of the conductive material interface, the biological sensor agent comprising:
an immobilization agent; and
at least one aptamer or antibody selected to interact with the immobilization agent and selected to bind with the biomarkers of interest;
a signaling agent comprising an electrochemical impedance signal generated by binding of the aptamer or antibody with the biomarkers of interest; and a bodily fluid sample derived from the patient and in contact with the biotin of the baseline biosensor and at least one aptamer or antibody of the sensing biosensor, wherein the baseline biosensor detects interference in the bodily fluid sample, and the sensing biosensor detects a presence of the cardiac biomarker of interest in the bodily fluid sample; and a correction applied to the baseline biosensor and the sensing biosensor to reduce or preclude non-biomarker interference from the bodily fluid sample.

2 . The system of claim 1 , wherein the bodily fluid sample is selected from blood, serum, plasma, and urine samples of animals or humans.

3 . The system of claim 1 , wherein the biomarkers are selected from C-reactive protein, Creatinine Kinase, Creatinine Phosphokinase, TroponinT, Myoglobin, IL-6, IL-18, Brain Natriuretic Peptide, and D-Dimer, immunosuppression drugs, Tacrolimus; Sirolimus, Tau protein, glial fibrillary acidic protein and breakdown products (GFAP-BDP) and ubiquitin C-terminal hydrolase L1 (UCH-L1).

4 . The system of claim 1 , wherein the immobilization agent is a binding agent.

5 . The system of claim 4 , wherein the binding agent is selected from the group consisting of avidin, streptavidin, neutravidin and mixtures thereof.

6 . The system of claim 1 , wherein the conductive material interface comprises a multi-array of vertically aligned platinum wires.

7 . The system of claim 1 , wherein the aptamer or antibody is effective to impedimetrically detect simultaneously a plurality of biomarkers in the bodily fluid sample.

8 . The system of claim 6 , wherein the multi-arrays of vertically aligned platinum wires are arranged in a circular configuration.

9 . A biosensing method of detecting biomarkers of interest in a bodily fluid sample of a patient and to reduce or preclude non-biomarker interference, comprising:
obtaining the bodily fluid sample from the patient; forming a detection device, comprising:
a baseline biosensor, comprising:
a conductive material interface having a surface,
an immobilization agent applied or deposited onto the surface of the conductive material interface; and
biotin conjugated with the immobilization agent;

a sensing biosensor, comprising:
a conductive material interface having a surface, and
a biological sensor agent applied to the surface of the conductive material interface, the biological sensor agent comprising:
an immobilization agent; and
at least one aptamer or antibody selected to interact with the immobilization agent and selected to bind with the biomarkers of interest;

contacting the biotin of the baseline biosensor and the aptamer or antibody of the sensing biosensor with the bodily fluid sample; generating an electrochemical impedance signal for each of the baseline biosensor and the sensing biosensor; and applying a correction to the sensing biosensor based on the baseline biosensor to reduce or preclude non-biomarker interference from the bodily sample.

10 . The method of claim 9 , wherein the electrochemical impedance signal is transduced to a read-out value.

11 . The method of claim 10 , wherein the electrochemical impedance signal is connected to a portable device such as a hand-held device that is effective to display the read-out value.

12 . The method of claim 9 , wherein the detection device is in the form of a test strip and the method, comprises:
contacting the bodily fluid sample with the test strip; assessing a visual change to the test strip; correlating the visual change with a chart or key; and based on said correlating, determining if the visual change is indicative of the presence of a change in electrochemical impedance and the presence of the cardiac biomarkers in the bodily fluid sample.

13 . The method of claim 12 , wherein the visual change is a color change.

14 . The method of claim 9 , wherein the electrochemical impedance signal is generated as a result of the biomarker of interest interacting with the aptamer or antibody.

15 . The method of claim 9 , wherein prior to applying the immobilization agent, the surface of the conductive interface material is treated with a thiol-based compound.

16 . The method of claim 15 , wherein the thiol-based compound is an aminothiol selected from cysteamine and/or glutaraldehyde.

Assignees

• Univ Pittsburgh Commonwealth Sys Higher Education

Inventors

• Kumta Prashant N
• Roy Abhijit
• Patil Mitali S
• Datta Moni Kanchan
• Kunjukunju Sangeetha

Classifications

• G01N33/68

  involving proteins, peptides or amino acids {(involving lipoproteins G01N33/92)} · CPC title

• G01N2333/54

  Interleukins [IL] · CPC title

• G01N2333/4737

  C-reactive protein · CPC title

• G01N33/70

  involving creatine or creatinine · CPC title

• G01N2333/58

  Atrial natriuretic factor complex; Atriopeptin; Atrial natriuretic peptide [ANP]; Brain natriuretic peptide [BNP, proBNP]; Cardionatrin; Cardiodilatin · CPC title