Application of a CuS/Au heterostructure with peroxidase-like activity in immunosensors. (5th July 2022)

• Record Type: Journal Article
• Authors: Li, Pengli; Wang, Min; Jiang, Mingzhe; Lai, Wenjing; Li, Jiajia; Liu, Kailin; Li, Hongling; Hong, Chenglin
• Is Part Of: New journal of chemistry. Volume 46:Number 29(2022)
• Page Start: 13963
• Page End: 13970
• Publication Date: 2022-07-05
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/d2nj02738k
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : This work synthesized CuS–Au heterojunction by galvanic substitution method. The synthesis method is green and simple. CuS NPs exhibit remarkable oxidase-like activity. The immunosensor prepared under the optimized conditions has excellent analytical performance. Abstract : The early detection of tumour markers is essential for the timely treatment of cancer, and thus realising the sensitive detection of carcinoembryonic antigen (CEA) is significant. Herein, we employed an electrochemical immunosensor as a simple analytical method. The loading of precious metals significantly amplifies the signal of electrochemical immunosensors. In this study, the successful loading of Au NPs was achieved via the galvanic displacement method. Moreover, CuS nanoflowers possessed intrinsic peroxidase-like activity, which could catalyse the oxidation of o -phenylenediamine (OPD) to generate a light-orange product in the presence of hydrogen peroxide (H2 O2 ). The flower-shaped CuS not only provided active sites for the catalytic reaction, but also possessed a large specific surface area, which could provide abundant sites for the placement of Au nanoparticles. Thus, it was suitable for the labelling of Ab2 for the sensitive detection of CEA. The instant current response ( i – t ) method detected CEA quantitatively, and the immunosensor prepared under the optimized conditions exhibited an excellent analytical performance. The detection range of the sensor prepared in this study was 0.1–80 ng mL −1 and its detection limit was 5.5 pg mL −1 (S/N = 3).