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Study on Quality Standard of Tibetan Medicine Corydalis dasyptera Maxim.
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作者 Yi SHI Yunfeng HAN +5 位作者 Xi TANG Jie GAO Lin PAN Yi ZHANG Xianrong LAI Duojie LONGZHU 《Medicinal Plant》 CAS 2021年第5期28-32,共5页
[Objectives]To establish the quality standard of Tibetan medicine Corydalis dasyptera Maxim.[Methods]According to the research method of drug quality standard in the appendix of 2020 edition of Chinese Pharmacopoeia,8... [Objectives]To establish the quality standard of Tibetan medicine Corydalis dasyptera Maxim.[Methods]According to the research method of drug quality standard in the appendix of 2020 edition of Chinese Pharmacopoeia,8 batches of C.dasyptera Maxim.from different habitats were studied by character identification,microscopic identification and TLC identification.The content of water,total ash,acid-insoluble ash and alcohol-soluble extract was determined,and the content of protopine in medicinal materials was determined by high performance liquid chromatography(HPLC).[Results]The properties and microscopic characteristics of C.dasyptera Maxim.were determined.The TLC characteristic spots of the medicinal materials were clear,the degree of separation was good,and the specificity was strong.Both the test sample and the control sample showed the same yellow-green spots in the corresponding position.It was tentatively determined that the water content of C.dasyptera Maxim.should not exceed 14.0%,the total ash content should not exceed 14.0%,the acid-insoluble ash content should not exceed 3.0%,and the alcohol-soluble extract content should not be less than 18.0%.There was a good linear relationship between the concentration of protopine and the peak area in the range of 16.64-166.40μg·10-3(r=0.9996).The average recovery rate was 98.47%and the RSD was 1.21%(n=6).The content of protopine in 8 batches of C.dasyptera Maxim.was 0.023%-0.093%.[Conclusions]The established quality research method is simple,stable and reliable,and can be used for the quality control of C.dasyptera Maxim. 展开更多
关键词 Corydalis dasyptera Maxim. Microscopic identification TLC identification Content determination
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藏药迭裂黄堇的质量标准研究
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作者 石懿 韩云凤 +5 位作者 唐茜 高洁 潘琳 张艺 赖先荣 龙主多杰 《中药与临床》 2021年第2期6-10,共5页
目的:建立藏药迭裂黄堇的质量标准。方法:按照2020版《中国药典》附录中药品质量标准研究方法,对不同产地的8批次迭裂黄堇药材进行性状鉴别、显微鉴别、薄层色谱鉴别,对药材水分、总灰分、酸不溶性灰分以及醇溶性浸出物含量进行检测,利... 目的:建立藏药迭裂黄堇的质量标准。方法:按照2020版《中国药典》附录中药品质量标准研究方法,对不同产地的8批次迭裂黄堇药材进行性状鉴别、显微鉴别、薄层色谱鉴别,对药材水分、总灰分、酸不溶性灰分以及醇溶性浸出物含量进行检测,利用高效液相色谱法对药材中的原阿片碱成分进行含量测定。结果:确定了迭裂黄堇的药材性状及显微特征。药材的薄层色谱特征斑点清晰,分离度良好,专属性强。供试品与对照品在相应位置上均显示相同的黄绿色斑点。暂定迭裂黄堇药材的水分不得过14.0%,总灰分不得过14.0%,酸不溶性灰分不得过3.0%,醇溶性浸出物含量不得少于18.0%。原阿片碱质量浓度在16.64~166.40μg·10^(-3)内与峰面积线性关系良好(r=0.9996)。平均加样回收率为98.47%,RSD为1.21%(n=6)。8批迭裂黄堇药材中原阿片碱的含量为0.023%~0.093%。结论:建立的质量研究方法操作简便、稳定性好、结果可靠,可用于迭裂黄堇的质量控制。 展开更多
关键词 迭裂黄堇 显微鉴别 薄层鉴别 含量测定
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