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Rapid Authentication of Ginkgo biloba Herbal Products Using the Recombinase Polymerase Amplification Assay

机译:使用重组酶聚合酶扩增法快速鉴定银杏叶草药产品

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摘要

Species adulteration in herbal products (HPs) exposes consumers to health risks. Chemical and morphological methods have their own deficiencies when dealing with the detection of species containing the same active compounds in HPs. In this study, we developed a rapid identification method using the recombinase polymerase amplification (RPA) assay to detect two species, Ginkgo biloba and Sophora japonica (as adulteration), in Ginkgo biloba HPs. Among 36 Ginkgo biloba HP samples, 34 were found to have Ginkgo biloba sequences, and 9 were found to have Sophora japonica sequences. During the authentication process, the RPA-LFS assay showed a higher specificity, sensitivity and efficiency than PCR-based methods. We initially applied the RPA-LSF technique to detect plant species in HPs, demonstrating that this assay can be developed into an efficient tool for the rapid on-site authentication of plant species in Ginkgo biloba HPs.
机译:草药产品(HP)中的物种掺假使消费者面临健康风险。在检测HP中含有相同活性化合物的物种时,化学和形态学方法有其自身的缺陷。在这项研究中,我们开发了一种利用重组酶聚合酶扩增(RPA)分析的快速鉴定方法,以检测银杏叶HP中的两种银杏和日本槐(掺假)。在36个银杏HP样品中,发现34个具有银杏序列,9个具有槐花序列。在认证过程中,RPA-LFS分析显示出比基于PCR的方法更高的特异性,灵敏度和效率。我们最初将RPA-LSF技术用于检测HP中的植物种类,证明该测定法可以发展成为一种快速现场验证银杏HP中植物种类的有效工具。

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