Defective UIO66 metal-organic framework nanoparticles assisted by cascade isothermal amplification technology for the detection of aflatoxin B1.

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Talanta Pub Date : 2025-04-01 Epub Date: 2024-12-19 DOI:10.1016/j.talanta.2024.127411
Yanyan Shao, Qian Tao, Luyao Shao, Jing Bi, Qian Wang, Zhigang Wang, Xuan Sun
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引用次数: 0

Abstract

Aflatoxin B1 (AFB1) exhibits significant toxicity and pose a serious threat to food safety, environmental hygiene, and public health even in trace amounts. Hence, the development of a rapid, accurate, and sensitive detection technology has become a pivotal aspect of ensuring control standards. In this study, we introduce the UIO66 and two defective dichloroacetic acid@UIO66 (DCA@UIO66, DU) metal-organic framework nanoparticles, named DU1 and DU2, characterized by different defect levels. It is noteworthy that DU1 exhibits superior DNA sensing capability compared to UIO66 and DU2. With a fluorescence quenching efficiency of 92.66 % and a recovery efficiency of 1256.75 %, DU1 demonstrates the substantial potential in the detection field. Furthermore, we employ cascade isothermal amplification to assist DU1-mediated fluorescence sensors in detecting AFB1. AFB1 is efficiently identified through an aptamer competition process facilitated by magnetic nanoparticles, which initiates the exponential amplification triggered rolling circle amplification reaction, and converts trace amounts of toxin signal into a large number of long single-stranded DNA molecules. Upon recognition of the amplification product by the fluorescent probe on DU1, a more stable double-stranded DNA is formed and leaves the surface of DU1, leading to a significant change in fluorescence intensity. This method exhibits acceptable sensitivity, with a detection limit of 0.09 pg mL-1 and a wide detection range spanning from 0.2 pg mL-1 to 20 pg mL-1. Additionally, this assay exhibits satisfactory specificity and high accuracy in practical sample applications. Our proposed method offers a solid theoretical framework and technical backing, thereby facilitating the establishment of a new generation of mycotoxin detection standards.

级联等温扩增技术辅助缺陷UIO66金属有机框架纳米颗粒检测黄曲霉毒素B1。
黄曲霉毒素B1 (AFB1)具有显著的毒性,即使微量也会对食品安全、环境卫生和公众健康造成严重威胁。因此,发展一种快速、准确、灵敏的检测技术已成为保证控制标准的关键方面。在本研究中,我们引入了UIO66和两种缺陷的二氯乙酸acid@UIO66 (DCA@UIO66, DU)金属有机框架纳米粒子,命名为DU1和DU2,它们具有不同的缺陷水平。值得注意的是,与UIO66和DU2相比,DU1具有更强的DNA传感能力。DU1的荧光猝灭效率为92.66%,回收率为1256.75%,在检测领域具有很大的潜力。此外,我们采用级联等温扩增来辅助du1介导的荧光传感器检测AFB1。AFB1是通过磁性纳米粒子介导的适体竞争过程高效鉴定的,该过程启动指数扩增触发滚圈扩增反应,将微量毒素信号转化为大量长单链DNA分子。DU1上的荧光探针识别扩增产物后,形成更稳定的双链DNA并离开DU1表面,导致荧光强度发生显著变化。该方法具有可接受的灵敏度,检测限为0.09 pg mL-1,检测范围从0.2 pg mL-1到20 pg mL-1。此外,该分析在实际样品应用中表现出令人满意的特异性和高精度。该方法为新一代霉菌毒素检测标准的建立提供了坚实的理论框架和技术支持。
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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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