Zhao Xiao-Mei, Tian Shuang-Shuang, Liu Shan-Shan, Qu Qian, Zhao Jing-Yuan, Yan Li-Hua, Wang Zhi-Min
National Engineering Laboratory for Quality Control Technology of Chinese Herbal Medicines, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences Beijing 100700, China Shanxi University of Chinese Medicine Jinzhong 030619, China.
National Engineering Laboratory for Quality Control Technology of Chinese Herbal Medicines, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences Beijing 100700, China.
Zhongguo Zhong Yao Za Zhi. 2020 Apr;45(7):1566-1577. doi: 10.19540/j.cnki.cjcmm.20200202.202.
The present research was launched to improve the quality standards of Alismatis Rhizoma and supply scientific evidence and recommendations for the quality control of Alismatis Rhizoma in Chinese Pharmacopoeia(Ch. P) 2020 edition. The contents of water, total ash, heavy metals and deleterious element, pesticide residues and alcohol-soluble extract were analyzed according to the methods listed in the volume Ⅳ of Ch. P 2015 edition. Alisol B 23-acetate, alisol C 23-acetate and reference herbs were used to identify Alismatis Rhizoma by TLC method, which was developed by using a mixture of dichloromethane-methanol(15∶1) as developing solvent on silica gel GF_(254 )precoated plates. In HPLC method, alisol B 23-acetate and alisol C 23-acetate were separated with acetonitrile-water as the mobile phase and detected at 208 nm and 246 nm, respectively. Thirty-seven batches of crude drugs, thirty batches of prepared slices and nineteen batches of salt prepared slices of Alismatis Rhizoma were determined according to the methods established. The quality standards established based on the research results were specific and repeatable, and suitable for the quality evaluation of Alismatis Rhizoma. We recommended that the botanical sources, TLC examination, alcohol-soluble extract of salt prepared slices and content determination should be revised in the Ch. P 2020 edition.
开展本研究旨在提高泽泻的质量标准,为《中国药典》2020年版泽泻的质量控制提供科学依据和建议。按照2015年版《中国药典》四部中所列方法,对水分、总灰分、重金属及有害元素、农药残留量和醇溶性浸出物的含量进行分析。以泽泻醇B 23-乙酸酯、泽泻醇C 23-乙酸酯及对照药材为对照,采用硅胶GF254预制板,以二氯甲烷-甲醇(15∶1)为展开剂,用薄层色谱法对泽泻进行鉴别。高效液相色谱法中,以乙腈-水为流动相,分别在208 nm和246 nm波长处测定泽泻醇B 23-乙酸酯和泽泻醇C 23-乙酸酯的含量。按照所建立的方法,对37批泽泻药材、30批泽泻饮片和19批泽泻盐炙饮片进行了测定。基于研究结果所建立的质量标准具有专属性和重复性,适用于泽泻的质量评价。建议《中国药典》2020年版修订泽泻的植物来源、薄层色谱检查、盐炙饮片醇溶性浸出物及含量测定等项内容。