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A Rapid Label-Free Fluorescent Aptasensor PicoGreen-Based Strategy for Aflatoxin B1 Detection in Traditional Chinese Medicines

机译:一种快速的无标签荧光Aptasensor Picogreen基于中药中的黄曲霉毒素B1检测的策略

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摘要

Aflatoxin B1 (AFB1) is a very hazardous carcinogen, readily contaminating foodstuffs and traditional Chinese medicines (TCMs) that has inspired increasing health concerns due to dietary exposure. Colloidal nanocrystals have been proposed as optical labels for aptasensor assembly, but these typically require tedious multistep conjugation and suffer from unsatisfactory robustness when used for complex matrices. In the present study, we report a rapid and sensitive method for screening for trace AFB1 levels in TCMs using a label-free fluorescent aptasensor PicoGreen dye-based strategy. Using PicoGreen to selectively measure complementary double-stranded DNA, fluorescence enhancement due to dsDNA is ‘turned off’ in the presence of AFB1 due binding of aptamer target over complementary sequence. Self-assembly of a label-free fluorescent aptasensor based on AFB1 aptamer and PicoGreen dye was performed. Due to competition between the complementary sequence and AFB1 target, this rapid method was capable of highly sensitive and selective screening for AFB1 in five types of TCMs. This proposed approach had a limit of detection as low as 0.1 μg·L−1 and good linearity with a range of 0.1–10 μg·L−1 (0.1–10 ppb). Among the 20 samples tested, 6 batches were found to be contaminated with AFB1 using this method, which was confirmed using sophisticated liquid chromatography-electrospray ionization-tandem mass spectrometry/mass spectrometry analysis. The results of this study indicate the developed method has the potential to be a simple, quick, and sensitive tool for detecting AFB1 in TCMs.
机译:黄曲霉毒素B1(AFB1)是一种非常危险的致癌物,容易污染食品和中药(TCMS),其由于饮食暴露而激发了越来越多的健康问题。已经提出了胶体纳米晶体作为适当传感器组件的光学标记,但是当用于复合矩阵时,这些通常需要繁琐的多学期缀合并遭受不令人满意的鲁棒性。在本研究中,我们通过基于标记的荧光Aptasensor Picogreen染料的策略报告了一种快速和敏感的方法,用于筛选TCMS中TCMS中的痕量AFB1水平。使用Picogreen选择性地测量互补的双链DNA,在AFB1在Aptamer靶标过后的AFB1的存在下,荧光增强在互补序列上的Aptamer靶标的存在。进行基于AFB1 Aptamer和Picogreen染料的无标签荧光Aptasensor的自组装。由于互补序列和AFB1目标之间的竞争,这种快速方法能够对五种TCMS中的AFB1具有高度敏感和选择性筛选。该所提出的方法具有低至0.1μg·1-1的检测限,良好的线性度,范围为0.1-10μg·l-1(0.1-10ppb)。在测试的20个样品中,使用该方法发现6批次被AFB1污染,使用复杂的液相色谱 - 电喷雾电离 - 串联质谱/质谱分析来确认。本研究的结果表明,开发方法具有用于检测TCMS中的AFB1的简单,快速,敏感的工具。

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