生脉超微粉中3种人参皂苷含量测定方法学研究  被引量:2

Content Determination of Three Ginsenosides in Shengmai Ultra-micro Powder

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作  者:邱新建 李守信 刘武占 苏瑞强 张则平 赵志全 

机构地区:[1]鲁南制药集团股份有限公司/中药制药共性技术国家重点实验室/中药制药新技术山东省企业重点实验室,临沂276006

出  处:《世界科学技术-中医药现代化》2013年第8期1801-1804,共4页Modernization of Traditional Chinese Medicine and Materia Medica-World Science and Technology

基  金:科学技术部国家重点基础研究发展计划(973计划)项目(2010CB735604):新药研制过程化学机理--中药制药过程控制技术模式和方式研究;负责人:萧伟

摘  要:目的:建立生脉超微粉中3种人参皂苷的含量测定方法。方法:采用kromasil C18(250 mm×4.6 mm,5μm)色谱柱,以乙腈(A)-水(B)为流动相,梯度洗脱0-35 min,19%A;35-55 min,19%-29% A;55-70 min,29%A;70-100 min,29%-40%A,流速1 mL·min-1,检测波长203 nm,柱温30℃,进样量10μL。结果:人参皂苷Rg1、人参皂苷Re、人参皂苷Rb1线性范围分别为0.083-0.834μg、0.086-0.863μg、0.091-0.911μg;平均加样回收率(n=6)分别为100.7%、100.5%、100.5%。结论:本方法快速、灵敏,重现性好,适合于生脉超微粉中人参皂苷Rg1、人参皂苷Re、人参皂苷Rb1的含量测定。This study was aimed to establish an HPLC method to determine three ginsenosides in Shengmai ultra-micro powder. The kromasil C18 (250 mm í 4.6 mm, 5 μm) was used as analytical column. The mobile phase was composed of acetonitrile (A) and water (B) with gradient elution (0-35 min, 19% A; 35-55 min, 19%-29% A; 55-70 min, 29% A; 70-100 min, 29%-40% A) at a flow rate of 1 mL·min-1. The detection wavelength was 203 nm and the column temperature was 30℃. The injection volume was 10 μL. The results showed that the linear ranges of ginsenoside Rg1, ginsenoside Re, ginsenoside Rb1 were 0.083-0.834 μg, 0.086-0.863 μg, 0.091-0.911 μg, respec-tively. The average recovery rates (n = 6) were 100.7%, 100.5%, 100.5%, respectively. It was concluded that this method was quick, sensitive, repeatable and suitable to determine contents of ginsenoside Rg1, ginsenoside Re and ginsenoside Rb1 in Shengmai ultra-micro powder.

关 键 词:生脉超微粉 人参皂苷Rg1 人参皂苷RB1 含量测定 GINSENOSIDE RG1 ginsen oside RB1 

分 类 号:R917[医药卫生—药物分析学]

 

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