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机构地区:[1]天津大学药物科学与技术学院,天津300072 [2]天津药物研究院,天津300193 [3]江南大学生物工程学院,江苏无锡214122
出 处:《中国实验方剂学杂志》2013年第4期75-78,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(81001627);天津市科技支撑计划项目(11ZCKFSY01200)
摘 要:目的:建立川西獐牙莱药材的质量标准。方法:采用薄层色谱法对川西獐牙菜药材进行定性鉴别,采用高效液相色谱法测定主要活性成分獐牙莱苦苷、芒果苷、当药醇苷和齐墩果酸的含量。色谱柱为Diamonsil C18(4.6 mm×250 mm,5μm),检测獐芽菜苦苷、芒果苷和当药醇苷的流动相甲醇-0.02%磷酸水(45∶55),检测波长254 nm,检测齐墩果酸的流动相乙腈-甲醇-0.2%冰醋酸水(65∶15∶20),检测波长210 nm,流速1.0 mL.min-1,柱温30℃。结果:川西獐牙菜药材的薄层色谱鉴别特征明显,专属性强;獐牙菜苦苷、芒果苷、当药醇苷和齐墩果酸的HPLC含量测定线性范围分别为0.075~0.75μg(r=0.999 9),0.05~0.5μg(r=0.999 7),0.032~0.32μg(r=0.999 3),0.116~11.6μg(r=0.999 4),平均回收率分别为98.91%(RSD 0.77%),99.61%(RSD 1.38%),100.35%(RSD 0.69%),99.26%(RSD 0.40%),并根据10批药材中相应成分的含量初步制定了其含量限度。结论:川西獐牙菜定性定量测定方法简单准确,能够为川西獐牙菜药材的质量控制提供有效依据。Objective: To establish a method of quality control of Swertia mussotii. Method: TLC method was applied in the qualitative identification of S. mussotii. The content of swertiamarin, mangiferin, swertianolin and oleanolic acid were determined by HPLC equipped with Diamonsil Cls (4.6 mm x 250 mm, 5 μm) column. The mobile phase of swertiamarin, mangiferin and swertianolin consisted of methanol-0.02% phosphoric acid, and detected at the wavelength of 254 nm. The mobile phase of 01eanolic acid consisted of methanol-0.2% glacial acetic acid, and detected at the wavelength of 210 nm. The analysis was done at a flow rate of 1.0 mL min-l. The column temperature was kept at 30 ℃. Result: The linearity of swertiamarin, mangiferin, swertianolin and oleanolic acid was in the range of 0. 075-0.75 μg ( r = o. 999 9 ) , 0.05-0.5 μg ( r = 0.999 7 ) , O. 032-0. 98.91% swertiano accurate 32 μg (r = 0. 999 3) and 0. 116-11.6 μg (r = 0. 999 4) , respectively. The average recoveries were (RSD 0.77% ) for swertiamain, 99.61% (RSD 1.38% ) for mangiferin, 100.35% (RSD 0.69% ) for 1in and 99.26% ( RSD 0.40% ) for oleanolic acid respectively. Conclusion: This method is simple, with good reproducibility. It is suitable for quality control of S. mussotii
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