HPLC法测定跌打巴布剂中三七皂苷R1和人参皂苷Rg1含量  被引量:2

HPLC Determination of Notoginsenoside R1 and Ginsenoside Rg1 in Dieda Cataplasm

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作  者:陈文珠[1] 袁小红[1] 

机构地区:[1]广东省中医院,广东广州510120

出  处:《中国医药指南》2013年第9期62-63,共2页Guide of China Medicine

摘  要:目的建立跌打巴布剂中三七皂苷R1和人参皂苷Rg1的含量测定方法。方法采用HPLC法,以Agilent TC-C18ODS柱为色谱柱,以乙腈-水(24:76)为流动相,检测波长203nm,流速1mL/min。结果三七皂苷R1线性范围为0.583~29.15μg(r=0.9999,n=5),回收率为99.9%~100.3%。人参皂苷Rg1线性范围为0.336~16.8μg(r=0.9999,n=5),回收率为99.8%~100.2%。结论本方法准确、可靠、灵敏度高,可用于跌打巴布剂的定量检测。Objective Determine notoginsenoside R1 and ginsenoside Rg1 in Dieda cataplasm by HPLC.Methods Agilent TC-C18 ODS column was used with the mobile phase containing acetonitrile-water(24:76).The wavelength of detector was set at 203nm.The flow rate was 1mL/min.Results The calibration curves were linear in the range of 0.583~29.15μg for notoginsenoside R1(r=0.9999,n=5) and 0.336~16.8μg for ginsenoside Rg1(r=0.9999,n=5).The recovery of notoginsenoside R1 was 99.9%~100.3%,and that of ginsenoside Rg1 was 99.8%~100.2%.Conclusion The method is accurate,reliable and simple,and is suitable for the determination of Dieda cataplasm.

关 键 词:跌打巴布剂 高效液相色谱法 三七皂苷R1 人参皂苷RG1 

分 类 号:R282.710.3[医药卫生—中药学]

 

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