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基于智能手机的CoS@ZnInS光电化学免疫分析法用于乳腺癌生物标志物的即时诊断

Smartphone-Based Photoelectrochemical Immunoassay with CoS@ZnInS for Point-of-Care Diagnosis of Breast Cancer Biomarker.

作者信息

Zeng Ruijin, Li Yuxuan, Li Yanli, Wan Qing, Huang Zhisheng, Qiu Zhenli, Tang Dianping

机构信息

Key Laboratory of Analytical Science for Food Safety and Biology (MOE & Fujian Province), State Key Laboratory of Photocatalysis on Energy and Environment, Department of Chemistry, Fuzhou University, Fuzhou 350108, China.

School of Electronics and Information Engineering, Hubei University of Science and Technology, Xianning 437100, China.

出版信息

Research (Wash D C). 2022 Aug 18;2022:9831521. doi: 10.34133/2022/9831521. eCollection 2022.

Abstract

Photoelectrochemical immunoassays incorporating specific antigen-antibody recognition reactions with the photon-electron conversion capabilities of photocatalysts have been developed for biomarker detection, but most involve bulky and expensive equipment and are unsuitable for point-of-care testing. Herein, a portable smartphone-based photoelectrochemical immunoassay was innovatively designed for the on-site detection of breast cancer biomarkers (human epidermal growth factor receptor 2; HER2). The system consists of a split-type immunoassay mode, disposable screen-printed electrode covered with hierarchical CoS@ZnInS heterostructures, an integrated circuit board, and a Bluetooth smartphone equipped with a specially designed app. Using alkaline phosphatase (ALP) catalytic strategy to in situ generate ascorbic acid (AA) for electron-donating toward CoS@ZnInS heterostructures, an immunoreaction was successfully constructed for the HER2 detection in the real sample due to the positive correlation of the photocurrent signal to electron donor concentration. Differential charge density indicates that the formation of CoS@ZnInS heterojunction can facilitate the flow of charges in the interface and enhance the photocurrent of the composite. More importantly, the measured photocurrent signal can be wirelessly transmitted to the software and displayed on the smartphone screen to obtain the corresponding HER2 concentration value. The photocurrent values linearly with the logarithm of HER2 concentrations range spanned from 0.01 ng/mL to 10 ng/mL with a detection limit of 3.5 pg/mL. Impressively, the clinical serum specimen results obtained by the proposed method and the wireless sensing device are in good agreement with the enzyme-linked immunosorbent assay (ELISA).

摘要

结合特定抗原-抗体识别反应与光催化剂的光-电子转换能力的光电化学免疫分析方法已被开发用于生物标志物检测,但大多数方法需要庞大且昂贵的设备,不适合即时检测。在此,创新性地设计了一种基于便携式智能手机的光电化学免疫分析方法,用于现场检测乳腺癌生物标志物(人表皮生长因子受体2;HER2)。该系统由分离式免疫分析模式、覆盖有分级CoS@ZnInS异质结构的一次性丝网印刷电极、集成电路板以及配备专门设计应用程序的蓝牙智能手机组成。利用碱性磷酸酶(ALP)催化策略原位生成抗坏血酸(AA)作为向CoS@ZnInS异质结构供电子的物质,由于光电流信号与电子供体浓度呈正相关,成功构建了用于实际样品中HER2检测的免疫反应。差分电荷密度表明CoS@ZnInS异质结的形成可促进界面处电荷的流动并增强复合材料的光电流。更重要的是,测得的光电流信号可无线传输至软件并显示在智能手机屏幕上,以获得相应的HER2浓度值。光电流值与HER2浓度的对数在0.01 ng/mL至10 ng/mL范围内呈线性关系,检测限为3.5 pg/mL。令人印象深刻的是,所提出的方法和无线传感设备获得的临床血清标本结果与酶联免疫吸附测定(ELISA)结果高度一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c09/9422330/97e9c78e3f21/RESEARCH2022-9831521.sch.001.jpg

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