Issue 18, 2017

An ultrasensitive enzyme-free electrochemical immunosensor based on redox cycling amplification using methylene blue

Abstract

We report a new enzyme-free electrochemical sensor for ultrasensitive measurements of protein biomarkers in plasma and whole blood samples based on a unique electrochemical–chemical–chemical (ECC) redox cycling signal amplification scheme. This scheme uses methylene blue (MB) as a redox indicator which undergoes an endergonic reaction with Ru(NH3)63+ and a highly exergonic reaction with tris(2-carboxyethyl)phosphine (TCEP). This approach offers improved detection sensitivity and sensor stability compared with enzyme-based ECC redox cycling techniques, while involving a simpler sensor modification process and detection protocol. This redox cycling scheme was combined with a robust immunosandwich assay for quantitative measurements of protein biomarkers. For proof of principle, Plasmodium falciparum histidine-rich protein 2 (PfHRP2) was measured in human plasma and whole blood samples, which could be detected down to 10 fg mL−1 and 18 fg mL−1, respectively. Furthermore, this immunosensor exhibits high selectivity, excellent reproducibility and good stability for up to 2 weeks, making it a promising platform for point-of-care testing, especially for detecting extremely low biomarker concentrations in raw biofluids.

Graphical abstract: An ultrasensitive enzyme-free electrochemical immunosensor based on redox cycling amplification using methylene blue

Supplementary files

Article information

Article type
Paper
Submitted
12 May 2017
Accepted
04 Aug 2017
First published
09 Aug 2017

Analyst, 2017,142, 3492-3499

An ultrasensitive enzyme-free electrochemical immunosensor based on redox cycling amplification using methylene blue

G. Dutta and P. B. Lillehoj, Analyst, 2017, 142, 3492 DOI: 10.1039/C7AN00789B

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