Smartphone-Based Photoelectrochemical Immunoassay with Co 9 S 8 @ZnIn 2 S 4 for Point-of-Care Diagnosis of Breast Cancer Biomarker

光电流 异质结 材料科学 检出限 免疫分析 线性范围 注意事项 光电子学 纳米技术 分析化学(期刊) 化学 色谱法 医学 病理 免疫学 抗体
作者
Ruijin Zeng,Yuxuan Li,Yanli Li,Qing Wan,Zhisheng Huang,Zhenli Qiu,Dianping Tang
出处
期刊:Research [American Association for the Advancement of Science]
卷期号:2022 被引量:51
标识
DOI:10.34133/2022/9831521
摘要

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 Co 9 S 8 @ZnIn 2 S 4 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 Co 9 S 8 @ZnIn 2 S 4 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 Co 9 S 8 @ZnIn 2 S 4 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).
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