A Real‐Time Antifouling Multivalent Aptamer Platform for Wash‐Free Electrochemical Detection of Low‐Abundance Biomarkers in Human Plasma

P Payel Sen S Survanshu Saxena (School of Biomedical Engineering McMaster University Hamilton Canada) Z Zijie Zhang N Navreen Sandhu (Department of Engineering Physics McMaster University Hamilton Canada) P Pranati Das (Department of Engineering Physics McMaster University Hamilton Canada) J Jimmy Gu (Department of Biochemistry and Biomedical Sciences McMaster University Hamilton Canada) T Todd Hoare (School of Biomedical Engineering McMaster University Hamilton Canada) Y Yingfu Li (Department of Biochemistry and Biomedical Sciences, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4K1, Canada) L Leyla Soleymani (Department of Engineering Physics McMaster University Hamilton Canada)

Abstract

ABSTRACT Sensitive and specific detection of low‐abundance proteins in complex biofluids is essential for early disease diagnosis and real‐time health monitoring. Electrochemical aptamer‐based biosensors offer rapid, point‐of‐care potential, but their clinical translation has been limited by biofouling, matrix variability, and signal instability in samples such as human plasma. Here, we introduce the Real‐Time Magnetic Multivalent Aptamer (RT‐MagMAp) assay, a one‐pot, wash‐free electrochemical platform that detects the low‐abundance biomarker VEGF 165 directly in diluted human plasma. The RT‐MagMAp system integrates three enabling chemical designs: (i) a hierarchical multivalent aptamer architecture combining bead‐immobilized monomeric aptamers with electrode‐bound trimeric aptamers to form highly stable electroactive sandwich assemblies; (ii) antifouling zwitterionic polymer coatings that house trimeric aptamers while suppressing nonspecific adsorption; and (iii) a dynamic internal calibration mechanism using nonfunctional mutant aptamers to correct for plasma‐dependent variability. Together, these elements enable femtomolar VEGF 165 detection (32–354 fM, depending on calibration method) and quantitative performance across 124 blinded plasma samples, achieving a Pearson correlation coefficient of 1.00 and a concordance correlation coefficient of 0.996 relative to a commercial ELISA. Together, these results establish RT‐MagMAp as a robust, clinically relevant electrochemical platform capable of quantitative, wash‐free protein detection directly in complex biological fluids.

Article Details

Volume / Issue Vol. 65, Issue 16
Published April 13, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

P

Payel Sen

S

Survanshu Saxena

School of Biomedical Engineering McMaster University Hamilton Canada

Z

Zijie Zhang

N

Navreen Sandhu

Department of Engineering Physics McMaster University Hamilton Canada

P

Pranati Das

Department of Engineering Physics McMaster University Hamilton Canada

J

Jimmy Gu

Department of Biochemistry and Biomedical Sciences McMaster University Hamilton Canada

T

Todd Hoare

School of Biomedical Engineering McMaster University Hamilton Canada

Y

Yingfu Li

Department of Biochemistry and Biomedical Sciences, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4K1, Canada

L

Leyla Soleymani

Department of Engineering Physics McMaster University Hamilton Canada