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基于 HPRR 的双原子催化剂电化学生物传感器用于检测与癌症相关的细胞外囊泡。

A HPRR-based diatomic catalyst electrochemical biosensor for detecting cancer-related extracellular vesicles.

机构信息

State Key Laboratory of Digital Medical Engineering, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering & Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing 211102, P. R. China.

Central Laboratory, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210011, P. R. China.

出版信息

Anal Methods. 2024 Nov 7;16(43):7381-7389. doi: 10.1039/d4ay01573h.

Abstract

Cancer-associated extracellular vesicles (EVs) are crucial biomarkers for cancer diagnosis as they contain abundant tumor cell information. To efficiently and accurately detect cancer-associated EVs, an electrochemical hydrogen peroxide reduction reaction (HPRR)-based biosensor was developed, utilizing enzyme-linked immunosorbent and diatomic catalyst strategies for catalytic HPRR current amplification for specific identification and highly sensitive detection. The anti-CXCR4 antibody was immobilized on a Au-plated electrode to selectively capture EVs from the sample. Subsequently, Fe/Cu diatomic catalysts, modified with an anti-CD63 antibody, were bound to the CD63 on the EVs. Quantitative detection of EVs was achieved by measuring the electrical signals from the HPRR catalyzed by the labeled Fe/Cu diatomic catalysts. Under optimized conditions, the electrochemical signals exhibited a linear relationship with EV concentration in the range of 500 to 1 × 10 particles mL, with a detection limit of 117 particles mL, maintaining accuracy even in FBS. With its affordability, high sensitivity, and ease of use, this sensor holds significant potential for medication guidance and postoperative evaluation.

摘要

癌症相关细胞外囊泡 (EVs) 是癌症诊断的重要生物标志物,因为它们包含丰富的肿瘤细胞信息。为了高效、准确地检测癌症相关 EVs,开发了一种基于电化学过氧化氢还原反应 (HPRR) 的生物传感器,利用酶联免疫吸附和双原子催化剂策略进行催化 HPRR 电流放大,用于特异性识别和高灵敏度检测。将抗 CXCR4 抗体固定在 Au 修饰的电极上,以选择性地从样品中捕获 EVs。随后,用抗 CD63 抗体修饰的 Fe/Cu 双原子催化剂与 EV 上的 CD63 结合。通过测量标记的 Fe/Cu 双原子催化剂催化的 HPRR 的电信号来实现 EVs 的定量检测。在优化条件下,电化学信号在 500 至 1×10 个颗粒 mL 的范围内与 EV 浓度呈线性关系,检测限为 117 个颗粒 mL,即使在 FBS 中也保持准确性。该传感器具有价格低廉、灵敏度高、使用方便等优点,在药物指导和术后评估方面具有重要的应用潜力。

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