壮药了刁竹含量测定方法的建立  

DETERMINATION OF THE CONTENT OF CYNANCHUM PANICULATUM(BGE.)KITAG.OF ZHUANG MEDICINE

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作  者:黄琴[1] 蒋伟哲[2] 黄瑞松 陆峥琳 叶积秀 

机构地区:[1]中国人民解放军第303医院 [2]广西医科大学药学院,南宁530021 [3]广西民族医药研究院,南宁530021 [4]广西中医药大学药学院,南宁530021

出  处:《广西医科大学学报》2016年第1期153-156,共4页Journal of Guangxi Medical University

基  金:广西科学研究与技术开发计划项目重大专项计划资助项目(No.桂科重1355001-4);广西医疗卫生重点科研课题资助项目(No.重2012015)

摘  要:目的:建立了刁竹丹皮酚含量测定方法,为控制该药材质量提供技术支撑。方法:对HPLC的色谱柱、流动相、检测波长等色谱条件进行摸索,采用正交设计的方法对供试品溶液的制备条件进行筛选。结果:建立的含量测定方法色谱条件:色谱柱为ZORBAX SB-C18柱(4.6 mm×150 mm,5μm,柱温25℃),流动相为甲醇∶水(55∶45),流速1.0 mL/min,检测波长274nm;供试品溶液制备条件:药材破碎度为过三号筛的粉末,提取溶剂为甲醇,溶剂加入量25mL,回流时间30min。结论:该测定方法简便、准确、重现性好,适用于了刁竹药材的质量控制。Objective: To investigate method for content determination of paeonol of Cynanchum paniculatum (Bge.) Kitag. , and to provide technical support for quality control of the medicinal material. Methods:Comparing different chromatographic column, flow velocity, detection wavelength to confirm the chromatographic conditions. Orthogonal design was applied to study the samples' preparation conditions. Results:The chromategraphic column was Agilent ZORBAX SB-C18 (4.6 mm× 150 mm, 5 μm) ; themobile phase was methanol : water (55 : 45) with the flow of 1.0 mL/min, and the detection wavelength was 274 nm. The preparation condition of sample solution was as follow:the pulverization degree of medicinal materials was over No. 3 sieve powder, methanol amount was of 25 mL, and the reflux time was 30 rains. Conclusion: The established method is accurate, reliable and reproducible, which might be suitable for quality control of the medicinal materials.

关 键 词:了刁竹 丹皮酚 含量测定方法 

分 类 号:R-33[医药卫生]

 

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