伏马菌素 B1 的近红外驱动双光电阴极光电化学传感:光子上转换生物光电阴极与增强型光捕获光阳极的集成。

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL Talanta Pub Date : 2025-01-01 Epub Date: 2024-10-14 DOI:10.1016/j.talanta.2024.127047
Jiang Guo, Xuqiao Liu, Jianqiao Liu, Kai Yan, Jingdong Zhang
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引用次数: 0

摘要

伏马菌毒素 B1(FB1)是伏马菌毒素家族中最常见、毒性最强的霉菌毒素,即使在痕量水平也会对人类,尤其是儿童和婴儿造成威胁。因此,设计一种简便灵敏的检测策略至关重要。本文揭示了一种用于在近红外照射下检测 FB1 的全新双光电电极光电化学(PEC)传感平台。该平台集成了光子上转换生物光阴极基底(UCNPs/Au/CuInS2,UCNPs:NaYF4:Yb3+、Er3+、Nd3+),并使用 SnO2/SnS2@Bi/Bi2S3 异质结光电阳极来大大提高光捕获能力。此外,还使用了涂有多巴胺的氧化锌(ZnO@PDA)作为信号抑制剂。光电流的恢复是由于 FB1 与其适配体(FB1-Apt)之间的强结合亲和力促进了 FB1-Apt/ZnO@PDA 与光电极的解离。对 PEC 传感性能和电子传递过程进行了深入研究。所开发的 "信号恢复型 "PEC灵敏传感器的动态线性范围从1.0 × 10-3到1.0 × 102 ng/mL,检测下限为0.13 pg/mL。以 FB1 酶联免疫吸附测定(ELISA)试剂盒为参照物,该传感器在玉米糊等未添加添加剂的真实样品中表现出卓越的实际检测性能,这表明它具有对其他霉菌毒素进行常规分析的潜力。因此,这项研究为有效检测霉菌毒素和其他有害物质建立了一个可行的双光电电极 PEC 框架。
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Near-infrared-driven dual-photoelectrode photoelectrochemical sensing for fumonisin B1: Integrating a photon up-conversion bio-photocathode with an enhanced light-capturing photoanode.

Fumonisin B1 (FB1), the most prevalent and highly toxic mycotoxin within the fumonisins family, poses threats to humans, especially in children and infants, even at trace levels. Therefore, it is essential to design an easy and sensitive detection strategy. Herein, a brand-new dual-photoelectrode photoelectrochemical (PEC) sensing platform for FB1 detection under near-infrared irradiation was unveiled. This platform integrated a photon up-conversion bio-photocathode substrate (UCNPs/Au/CuInS2, UCNPs: NaYF4: Yb3+, Er3+, Nd3+) and used a SnO2/SnS2@Bi/Bi2S3 heterojunction photoanode to greatly enhance light capture. Additionally, ZnO coated with polydopamine (ZnO@PDA) was utilized as a signal inhibitor. The restoration of photocurrent occurred due to the strong binding affinity between FB1 and its aptamer (FB1-Apt), facilitating the dissociation of FB1-Apt/ZnO@PDA from the photoelectrode. The PEC sensing performance and the electron transfer process were thoroughly examined. The developed "signal-restoration" PEC aptasensor exhibited a wider dynamic linear range from 1.0 × 10-3 to 1.0 × 102 ng/mL, with a lower limit of detection (0.13 pg/mL). It has demonstrated excellent practical detection performance in unspiked real samples, such as corn paste, with the FB1 enzyme-linked immunosorbent assay (ELISA) Kit serving as a reference, indicating its potential for routine analysis of other mycotoxins. Thus, this research establishes a feasible dual-photoelectrode PEC framework for the effective detection of mycotoxins and other hazardous substances.

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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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