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电化学可再生表面增强拉曼光谱传感器:用于检测参与过氧化物生成的代谢物的新平台。

Electrochemically renewable SERS sensor: A new platform for the detection of metabolites involved in peroxide production.

作者信息

Jiang Lei, Wang Lu, Zhan De-Sheng, Jiang Wen-Rong, Fodjo Essy Kouadio, Hafez Mahmoud Elsayed, Zhang Yan-Mei, Zhao Hu, Qian Ruo-Can, Li Da-Wei

机构信息

Key Laboratory for Advanced Materials, Shanghai Key Laboratory of Functional Materials Chemistry, Joint International Laboratory for Precision Chemistry, Frontiers Science Center for Materiobiology & Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, PR China.

Department of Laboratory Medicine, Huadong Hospital Affiliated to Fudan University, Shanghai, 200040, PR China.

出版信息

Biosens Bioelectron. 2021 Mar 1;175:112918. doi: 10.1016/j.bios.2020.112918. Epub 2020 Dec 29.

Abstract

The accurate detection of hydrogen peroxide (HO)-involved metabolites plays a significant role in the early diagnosis of metabolism-associated diseases, whereas most of current metabolite-sensing systems are often hindered by low sensitivity, interference of coexisting species, or tedious preparation. Herein, an electrochemistry-regenerated surface-enhanced Raman scattering (SERS) sensor was developed to serve as a universal platform for detecting HO-involved metabolites. The SERS sensor was constructed by modifying newly synthesized 2-mercaptohydroquinone (2-MHQ) molecules on the surface of gold nanoparticles (AuNPs) that were electrochemically predeposited on an ITO electrode. Metabolites were detected through the changes in the SERS spectrum as a result of the reaction of 2-MHQ with HO induced by the metabolites. Combining the superiority of SERS fingerprint identification and the specificity of the related enzymatic reactions producing HO, the designed SERS sensor was highly selective in detecting glucose and uric acid as models of HO-involved metabolite with limits of detection (LODs) of 0.159 μM and 0.0857 μM, respectively. Moreover, the sensor maintained a high SERS activity even after more than 10 electrochemical regenerations within 2 min, demonstrating its effectiveness for the rapid detection of various metabolites with electrochemistry-driven regulation. Importantly, the presented SERS sensor showed considerable practicability for the detection of metabolites in real serum samples. Accordingly, the SERS sensor is a new detection platform for HO-involved metabolites detection in biological fluids, which may aid the early diagnosis of metabolism-related diseases.

摘要

准确检测过氧化氢(HO)相关代谢物在代谢相关疾病的早期诊断中起着重要作用,然而目前大多数代谢物传感系统常常受到灵敏度低、共存物质干扰或制备繁琐的阻碍。在此,开发了一种电化学再生表面增强拉曼散射(SERS)传感器,作为检测HO相关代谢物的通用平台。该SERS传感器是通过在预先电化学沉积在ITO电极表面的金纳米颗粒(AuNPs)上修饰新合成的2-巯基对苯二酚(2-MHQ)分子构建而成。通过2-MHQ与代谢物诱导产生的HO反应导致的SERS光谱变化来检测代谢物。结合SERS指纹识别的优势和产生HO的相关酶促反应的特异性,所设计的SERS传感器在检测作为HO相关代谢物模型的葡萄糖和尿酸时具有高度选择性,检测限(LOD)分别为0.159 μM和0.0857 μM。此外,该传感器即使在2分钟内进行了10多次电化学再生后仍保持高SERS活性,证明了其通过电化学驱动调节快速检测各种代谢物的有效性。重要的是,所展示的SERS传感器在实际血清样品中检测代谢物时显示出相当的实用性。因此,该SERS传感器是一种用于生物流体中HO相关代谢物检测的新型检测平台,可能有助于代谢相关疾病的早期诊断。

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