生甘遂与制甘遂中的二萜类成分甘遂大戟萜酯D的含量研究  

Determination of Kansuiphorin D in Kansui Radix and its Processed Products

作　　者：程显隆[1] 肖新月[1] 邹秦文 刘薇[1] 石岩[1] 魏锋[1] 马双成[1] 林瑞超[1] 

机构地区：[1]中国食品药品检定研究院,北京100050 [2]北京联馨药业有限公司,北京102628

出　　处：《中国现代中药》2011年第7期25-28,共4页Modern Chinese Medicine

基　　金：国家科技支撑计划--常见与重要药品安全标准研究(2006BAI14B01);国家科技重大专项--中药质量标准研究和信息化体系建设平台(2009ZX093008-004)

摘　　要：目的:建立甘遂中甘遂大戟萜酯D的含量测定方法,并比较生甘遂和醋甘遂中甘遂大戟萜酯D的含量差异。方法:样品以甲醇为提取溶剂,超声处理后,以HPLC法分析。采用菲罗门lunarC18色谱柱(250mm×4.6mm,5μm)色谱柱分离,柱温40℃,以乙腈-水(70:30)为流动相,流速1.0mL·min-1;检测波长235nm。结果:甘遂大戟萜酯D线性范围分别为0.216～8.64μg(r=0.9999),平均加样回收率为103.5%(n=9);44批次甘遂中,甘遂大戟萜酯D的含量为0.008%～0.036%。结论:该方法准确、可靠,具有良好的重复性和稳定性,可用于甘遂大戟萜酯D的定量分析。Objective： To develop an HPLC method for determination of Kansuiphorin D in Kansui Radix and to compare the differences of the contents of euphol and tirueallol in Kansui Radix and its processed product （processed with vinegar） by HPLC. Methods： The sample was extracted by methanol. HPLC analysis was performed on an lunar C18 column, column temperature was 40 ℃. The mobile phase was the system of acetonitrile-water（70：30）. The flow rate was 1.0 mL. min^-1 and UV detection was set at 235 nm. Results： Determined the contents of Kansuiphorin D of 44 samples by HPLC. Conclusion： The methad was simple, rapid and accurate with good productivity, which can be used to determine of Kansuiphorin D in Kansui Radix and its processed product.

关 键 词：甘遂 醋甘遂 甘遂大戟萜酯D 高效液相色谱法 

分 类 号：R284.1[医药卫生—中药学]