- 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
- 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载。
- 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
- 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
- 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们。
- 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
- 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
甘肃黄芪与红芪总黄酮含量对比测定方法探索研究
甘肃黄芪与红芪总黄酮含量对比测定方法探索研究
摘要:目的 探索建立甘肃黄芪和红芪药材中总黄酮含量对比的测定方法。方法 以毛蕊异黄酮苷等为对照品,采用紫外分光光度法和比色法(显色剂:NaNO2-Al(NO3)3-NaOH、AlCl3、Mg(Ac)2、NaOH、磷钼酸、盐酸-镁粉),考察样品和对照品吸收曲线。结果 采用比色法,黄芪、红芪样品和对照品的最大吸收波长不一致,峰形有差别或差别较大。采用紫外法测定,毛蕊异黄酮苷在Ⅱ带260 nm处呈现特征肩峰吸收,黄芪和红芪亦在Ⅱ带呈现特征肩峰吸收,吸收波长分别为263、265 nm,吸收波长与对照品基本一致。结论 常用的显色反应不适合甘肃黄芪和红芪中总黄酮含量的对比测定;异黄酮类化合物吸收Ⅱ带作为特征吸收带,适于黄芪和红芪样品中总黄酮含量的对比研究。
关键词:黄芪;红芪;总黄酮;紫外-可见分光光度法;比色法;含量测定
DOI:10.3969/j.issn.1005-5304.2016.09.024
中图分类号:R284.1 文献标识码:A 文章编号:1005-5304(2016)09-0099-07
Study on Determination Method of Total Flavonoids in Gansu Astragali Radix and Hedysarum Polybotrys YE Ying1, BAO Qiang2, WANG Rui-hai1, BAI Dong1, XUE Xin1, ZHANG Li-shi1, LIU Li-mei1 (1. Institute of Basic Theory Research of TCM, China Academy of Chinese Medical Sciences, Beijing 100700, China; 2. Department of Pharmacy, Gansu Province Hospital of TCM, Lanzhou 730050, China)
Abstract: Objective To study the determination method of total flavonoids in Gansu Astragali Radix and Hedysarum Polybotrys. Methods Calycosin glycosides etc. was selected as reference substances, comparison on the difference of absorption curves was done by ultraviolet spectroscopy and colorimetric method (NaNO2-Al(NO3)3- NaOH, AlCl3, Mg(Ac)2, NaOH, phosphomolybdic acid, HCl-Mg power). Results With colorimetric method, the maximum absorption wavelength of referrence and the test was inconsistent. The absorption peak shape was also different. With UV method, Calycosin glycosides in band Ⅱ (260 nm) showed a shoulder absorption. Astragali Radix and Hedysarum Polybotrys also showed characteristic shoulder absorptions in band Ⅱ with absorption wavelength at 263 nm and 265 nm. So the sample absorption wavelength is basically the same as that of the control sample. Conclusion Colorimetries usually used for determination of total flavonoids are not suitable for the comparison determination of Gansu Astragali Radix and Hedysarum Polybotrys. It is suitable for determining the contents of total flavonoids in samples
文档评论(0)