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Titanium Dioxide Nanoparticles (TiO2) Quenching Based Aptasensing Platform: Application to Ochratoxin A Detection

机译:基于二氧化钛纳米粒子(TiO2)淬火的传感平台:在O曲霉毒素A检测中的应用

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摘要

We demonstrate for the first time, the development of titanium dioxide nanoparticles (TiO2) quenching based aptasensing platform for detection of target molecules. TiO2 quench the fluorescence of FAM-labeled aptamer (fluorescein labeled aptamer) upon the non-covalent adsorption of fluorescent labeled aptamer on TiO2 surface. When OTA interacts with the aptamer, it induced aptamer G-quadruplex complex formation, weakens the interaction between FAM-labeled aptamer and TiO2, resulting in fluorescence recovery. As a proof of concept, an assay was employed for detection of Ochratoxin A (OTA). At optimized experimental condition, the obtained limit of detection (LOD) was 1.5 nM with a good linearity in the range 1.5 nM to 1.0 µM for OTA. The obtained results showed the high selectivity of assay towards OTA without interference to structurally similar analogue Ochratoxin B (OTB). The developed aptamer assay was evaluated for detection of OTA in beer sample and recoveries were recorded in the range from 94.30%–99.20%. Analytical figures of the merits of the developed aptasensing platform confirmed its applicability to real samples analysis. However, this is a generic aptasensing platform and can be extended for detection of other toxins or target analyte.
机译:我们首次展示了基于二氧化钛纳米粒子(TiO2)猝灭的适体检测平台,用于检测目标分子。当荧光标记的适体非共价吸附在TiO2表面上时,TiO2淬灭FAM标记的适体(荧光素标记的适体)的荧光。当OTA与适体相互作用时,它会诱导适体G-四链体复合物的形成,削弱FAM标记的适体与TiO2之间的相互作用,从而导致荧光恢复。作为概念的证明,采用了一种测定方法来检测A曲霉毒素A(OTA)。在优化的实验条件下,对于OTA,获得的检出限(LOD)为1.5 nM,线性范围为1.5 nM至1.0 µM。获得的结果表明对OTA的测定具有很高的选择性,而不会干扰结构相似的类似O曲毒素B(OTB)。对开发的适体测定法进行了评估,以检测啤酒样品中的OTA,记录的回收率在94.30%–99.20%之间。所开发的适体平台的优点的分析数据证实了其在真实样品分析中的适用性。但是,这是一个通用的适体平台,可以扩展用于检测其他毒素或目标分析物。

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