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机构地区:[1]吉林市第五医院,吉林吉林132001 [2]吉林市食品药品检验所,吉林吉林132001
出 处:《中国中医药杂志》2008年第12期1-4,共4页
摘 要:目的:建立利节散的含量测定方法。方法:采用高效液相色谱法。色谱柱:Agilent Extend—C18(4.6mm×250mm,5μm),流动相:乙腈-0.3%磷酸溶液(19:81,V/V),流速:1.0ml·min^-1,检测波长:203nm,柱温:40℃。结果:三七皂苷R1在0.03~0.90μg范围内线性关系良好(r=0.9999);平均加样回收率为100.00%,RSD=1.3%(n=5);人参皂苷Rg1在0.10~3.00μg范围内线性关系良好(r=1.0000);平均加样回收率为99.50%,RSD=0.6%(n=5)。结论:该方法简便易行,结果准确可靠,可适用于利节散的质量控制。Objective: To set up a method for quality control of Lijiesan. Method:HPLC method was developed to quantitative determination. COLUMN C18-Agilent Extend(4.6mm× 250mm, 5 μ m).The mobilic phase was acetonifrile-0.3%phosphoric acid solution (19:81V/V) as mobilic phase. The column temperature was 40℃, the wavelength for detection was 203nm, flow rate was 1.0ml · min^-1. Results:The notoginsenoside R,average of recovery rate was 100.00%, and RSD was 1.3%(n=5); The ginsenoside Rg, average of recovery rate was 99.50%, and RSD was 0.6%(n=5). C The method is simple, accurate and suitable for its assaying.
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