An ultrasensitive enzyme-free electrochemical immunosensor based on redox cycling amplification using methylene blue. Issue 18 (23rd August 2017)

• Record Type: Journal Article
• Authors: Dutta, Gorachand; Lillehoj, Peter B.
• Is Part Of: Analyst. Volume 142:Issue 18(2017)
• Page Start: 3492
• Page End: 3499
• Publication Date: 2017-08-23
• Subjects: Chemistry, Analytic -- Periodicals; 543
• DOI: 10.1039/c7an00789b
• Languages: English
• ISSNs: 0003-2654

Abstract

Abstract : An enzyme-free immunosensor based on methylene blue redox cycling was developed for ultrasensitive analytical measurements in plasma and whole blood samples. 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 )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 ( Pf HRP2) 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.