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机构地区:[1]吉林金柏氏食品科技有限公司,吉林白山135200 [2]吉林大学白求恩制药厂,长春130021 [3]吉林大学白求恩第一临床学院,长春130021
出 处:《特产研究》2013年第1期57-59,共3页Special Wild Economic Animal and Plant Research
基 金:吉林省科技发展计划医药产业发展专项资金(YYZX201123-4)
摘 要:建立参松养心胶囊中人参皂苷Rb1含量测定的HPLC方法。色谱柱Alltima C18(250mm×4.6mm,5μm),流动相乙腈-0.02%磷酸水溶液(32∶68),流速1.0mL/min;检测波长203nm。人参皂苷Rb1进样量在0.4~4.0μg与峰面积呈良好线性关系(r=0.999 1);平均加样回收率100.3%,RSD 1.72%。本方法结果准确,精密度及重现性较好,可以用于参松养心胶囊中人参皂苷Rb1的含量测定。To develop an HPLC method for determination of active ginsenoside Rbl in Sheasongyangxin Capsules. Chromatographic separation was performed on an Alltima Cls (250mm × 4.6mm, 5μm) column; mobile phase was acetonitrile - 0.02% phosphorie acid, flow rate was 1.0mL/min;detector wavelength was 203nm. Good linear relationships of gimenoside Rb1 was provided over investigated concentration between 0.4- 4.0/μg( r = 0.999 1 ). The average recoveries of ginsenoside Rb1 was 100.3 %. Repeatability experiments showed that relative standard deviation(RSD) values of ginsenoside Rb1 was 1.72 %. The developed method was acurate, sensitive and repeatable, and can be used for the deten'nination of ginsenoside Rb1 in Shensongyangxin Capsules.
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