An electrochemical aptasensor-based CoxP-decorated porous carbon microspheres and AuNRs labelled methylene blue as signal labels for the sensitive detection of PCB77. Issue 37 (4th September 2020)

• Record Type: Journal Article
• Authors: Tian, Panpan; Zhang, Baozhong; Lv, Lina; Xie, Lingling; Chen, Hanyu; He, Baoshan
• Is Part Of: Analytical methods. Volume 12:Issue 37(2020)
• Page Start: 4579
• Page End: 4587
• Publication Date: 2020-09-04
• Subjects: Chemistry, Analytic -- Periodicals; Analytical biochemistry -- Periodicals; Chemical laboratories -- Standards -- Periodicals; 543.1905
• DOI: 10.1039/d0ay01462a
• Languages: English
• ISSNs: 1759-9660

Abstract

Abstract : Diagram of the electrochemical aptasensor construction and the mechanism for detection of PCB77. Abstract : In this work, a simple, specific and ultra-sensitive electrochemical aptasensor was successfully developed based on a novel signal reduction strategy for the detection of polychlorinated biphenyls (PCB77). This aptasensor was prepared by the electrodeposition of gold nanoparticles (AuNPs) on an Au electrode (AuE) modified with cobalt phosphide (Co x P, a mixture of CoP and Co2 P) decorated porous carbon microspheres. In this study, the thiolated single-complementary DNA (cDNA) was immobilized on the surface of the modified electrode via the Au–S bond. Subsequently, the gold nanorod@methylene blue connection aptamer (AuNRs@MB-Apt) signal labels were immobilized onto the modified electrode through the principle of complementary base pairing. Further, the aptamer preferentially binds to PCB77, decreasing the amount of AuNR@MB-Apt. The DPV current response was related to the PCB77 concentration. Under the optimized experimental conditions, a low detection limit of 5.9 × 10 −2 ng L −1 and a wide linear range of 1 × 10 −11 mg mL −1 to 1 × 10 −4 mg mL −1 (S/N = 3) for PCB77 were achieved. Moreover, the proposed aptasensor offered high selectivity, stability and reproducibility, indicating the broad potential application in environmental monitoring.