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作 者:曹园[1,2] 姚毅 范慧佳 王强[3] 段金廒[2]
机构地区:[1]南京中医药大学附属医院,南京210036 [2]南京中医药大学,南京210023 [3]中国药科大学,南京210009
出 处:《中国药事》2015年第6期581-587,共7页Chinese Pharmaceutical Affairs
基 金:国家自然科学基金项目(编号81102772);国家科技重大专项资助项目"中药质量标准研究和信息化体系建设平台"中药材质量标准研究(编号2009X09308-04);江苏省博士后基金(编号1302083B)
摘 要:目的:完善卷柏的质量标准。方法:依据《中国药典》2010年版附录相关方法,对卷柏药材进行显微鉴别,对灰分、酸不溶性灰分进行检查。采用HPLC检测selaginellin和穗花杉双黄酮的含量,选用Waters Cosmosil C18柱(250 mm×4.6 mm id,5μm);检测波长:300、337 nm;流速:1 m L·min-1;柱温:30℃;流动相:乙腈-0.1%甲酸水梯度洗脱。结果:确定了卷柏药材的显微特征;酸不溶性灰分限度≤11.0%,总灰分限度≤15.0%;建立同时测定卷柏药材中穗花杉双黄酮和selaginellin的HPLC含量检测方法。结论:卷柏药材的显微鉴别,以及同时测定穗花杉双黄酮和selaginellin的HPLC含量测定等方法简便、准确、重现性好,可有效控制卷柏药材的质量。Objective: To improve quality standards of Herba Selaginellae. Methods: According to the methods recorded in the appendix of Chinese Pharmacopeia(2010 edition), the microscopic identification ofHerba Selaginellae was conducted, and the tests of ash and acid-insoluble ash were carried out. The contents of bioactive constituents in selaginellin and amentoflavone were determined by HPLC on a Waters Cosmosil C18 column(250 mm× 4.6 mm id, 5 μm) and eluted with acetonitrile-0.1% formic acid as the mobile phase at a flow rate of 1 m L·min-1.The column temperature was 30 ℃ and the detection wavelength was 300 nm and 337 nm.Results: Microscopic characteristics were identified. The limit for acid insoluble ash was ≤ 11.0%, and the total ash limit was ≤ 15.0%. The HPLC method for simultaneous determination of amentoflavone andSelaginellin was established. Conclution: The developed method is accurate, sensitive and reproducible, which is effective for the quality control of Herba Selaginellae.
关 键 词:卷柏 穗花杉双黄酮 selaginellin HPLC含量测定 显微鉴别
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