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首页> 外文期刊>Molecules >Rapid Authentication of the Herbal Medicine Plant Species Aralia continentalis Kitag. and Angelica biserrata C.Q. Yuan and R.H. Shan Using ITS2 Sequences and Multiplex-SCAR Markers
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Rapid Authentication of the Herbal Medicine Plant Species Aralia continentalis Kitag. and Angelica biserrata C.Q. Yuan and R.H. Shan Using ITS2 Sequences and Multiplex-SCAR Markers

机译:草药植物种Aralia continentalis Kitag的快速认证。和当归比塞拉塔C.Q. Yuan和R.H. Shan使用ITS2序列和Multiplex-SCAR标记

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Accurate identification of the plant species that are present in herbal medicines is important for quality control. Although the dried roots of Aralia continentalis (Araliae Continentalis Radix) and Angelica biserrata (Angelicae Pubescentis Radix) are used in the same traditional medicine, namely Dok-Hwal in Korean and Du-Huo in Chinese, the medicines are described differently in the national pharmacopeia. Further confusion arises from the distribution of dried Levisticum officinale and Heracleum moellendorffii roots as the same medicine. Medicinal ingredients from all four plants are morphologically similar, and discrimination is difficult using conventional methods. Molecular identification methods offer rapidity and accuracy. The internal transcribed spacer 2 (ITS2) region of the nuclear ribosomal RNA gene (rDNA) was sequenced in all four plant species, and the sequences were used to design species-specific primers. Primers for each species were then combined to allow sample analysis in a single PCR reaction. Commercial herbal medicine samples were obtained from Korea and China and analyzed using the multiplex assay. The assay successfully identified authentic medicines and also identified inauthentic or adulterated samples. The multiplex assay will be a useful tool for identification of authentic Araliae Continentalis Radix and/or Angelicae Pubescentis Radix preparations in Korea and China. View Full-Text
机译:准确鉴定草药中存在的植物种类对于质量控制很重要。尽管在相同的传统药物中使用了非洲五味子(Araliae Continentalis Radix)和当归比塞洛奇(Angelicae Pubescentis Radix)的干燥根,即朝鲜语中的Dok-Hwal和中文中的Du-Houo,但在国家药典中对药物的描述有所不同。与相同药物相比,干枯叶紫草和莫拉氏干根的分布引起了进一步的混乱。来自所有四种植物的药用成分在形态上相似,并且使用常规方法很难区分。分子鉴定方法可提供快速性和准确性。在所有四个植物物种中对核糖体RNA基因(rDNA)的内部转录间隔区2(ITS2)区域进行了测序,并将这些序列用于设计物种特异性引物。然后将每种物种的引物合并在一起,以便在单个PCR反应中进行样品分析。商业草药样品从韩国和中国获得,并使用多重分析进行分析。该测定法成功鉴定出了真正的药物,还鉴定出了未经鉴定或掺假的样品。多重分析将是鉴定韩国和中国正宗的欧亚大陆(Araliae Continentalis Radix)和/或当归(Angelicae Pubescentis Radix)制剂的有用工具。查看全文

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