4.6 Article

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

Journal

ANALYST
Volume 142, Issue 18, Pages 3492-3499

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7an00789b

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Funding

  1. National Institutes of Health [R01 AI113257]

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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)(6)(3+) 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.

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