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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.

SUBMITTER: Dutta G 

PROVIDER: S-EPMC5600201 | biostudies-literature | 2017 Sep

REPOSITORIES: biostudies-literature

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

Dutta Gorachand G   Lillehoj Peter B PB  

The Analyst 20170901 18


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(NH<sub>3</sub>)<sub>6</sub><sup>3+</sup> and a highly exergonic reaction with tris(2-carboxyethyl)phosphine (TCEP). This approach offers improved detection  ...[more]

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