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基于肽核酸的分子鉴定用于通过内转录间隔区 2 区域的熔解曲线分析鉴定四种药用牡丹品种。

Peptide Nucleic Acid Based Molecular Authentication for Identification of Four Medicinal Paeonia Species Using Melting Array Analysis of the Internal Transcribed Spacer 2 Region.

机构信息

K-herb Research Center, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon 305-811, Korea.

出版信息

Molecules. 2017 Nov 7;22(11):1922. doi: 10.3390/molecules22111922.

DOI:10.3390/molecules22111922
PMID:29112146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6150393/
Abstract

Accurate taxonomic identification of plant materials in herbal medicines is important for product quality control. The genus (Saxifragales) is the source of the herbal preparations Paeoniae Radix (Paeoniae Radix Alba and Paeoniae Radix Rubra) and Moutan Radicis Cotex. However, confusion has arisen regarding their contents due to linguistic and taxonomic ambiguities, similar morphologies and different definitions of Paeoniae Radix in the Korean and Chinese national pharmacopoeias, leading to the distribution of adulterated products. To develop a method for identifying the four species used in these medicines, three fluorescently-labeled peptide nucleic acid (PNA) probes were designed against ITS2 sequences containing single nucleotide polymorphisms (SNPs) and used in a real-time PCR melting curve assay. Each of the four species was accurately identified using this analysis. The accuracy and analytical stability of the PNA melting curve assay was confirmed using commercially available samples of the four species. This assay is a reliable genetic tool to distinguish between different -derived herbal medicines and identify the botanical origins of Paeoniae Radix and Moutan Radicis Cortex. This technique may also contribute to quality control and standardization of herbal medicines by providing a reliable authentication tool and preventing the distribution of inauthentic adulterants.

摘要

准确鉴定草药中的植物材料对于产品质量控制非常重要。属(虎耳草目)是草药制剂白芍(白芍和赤芍)和牡丹皮的来源。然而,由于语言和分类上的歧义、相似的形态和韩国及中国国家药典中对白芍的不同定义,导致其成分混淆,出现了掺假产品。为了开发一种鉴定这些药物中使用的四种物种的方法,设计了三种针对 ITS2 序列的荧光标记肽核酸(PNA)探针,该序列包含单核苷酸多态性(SNP),并用于实时 PCR 熔解曲线分析。使用该分析方法可以准确鉴定出这四种物种。使用市售的四种物种的商业样本验证了 PNA 熔解曲线分析的准确性和分析稳定性。该方法是一种可靠的遗传工具,可用于区分不同来源的草药,并鉴定白芍和牡丹皮的植物来源。该技术还可以通过提供可靠的鉴定工具和防止掺假品的传播,为草药的质量控制和标准化做出贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/020933a8dd22/molecules-22-01922-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/1c03249dfd25/molecules-22-01922-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/a16720f61ed7/molecules-22-01922-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/1e2b5dc35c26/molecules-22-01922-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/f1dce82d5949/molecules-22-01922-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/020933a8dd22/molecules-22-01922-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/1c03249dfd25/molecules-22-01922-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/a16720f61ed7/molecules-22-01922-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/1e2b5dc35c26/molecules-22-01922-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/f1dce82d5949/molecules-22-01922-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a3/6150393/020933a8dd22/molecules-22-01922-g005.jpg

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