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出 处:《中成药》2006年第6期812-815,共4页Chinese Traditional Patent Medicine
摘 要:目的:建立心可宁胶囊(蟾酥等)中华蟾酥毒基和脂蟾毒配基的含量测定方法。方法:采用HPLC法进行含量测定。色谱柱:十八烷基硅烷键合硅胶为填充剂,流动相:甲醇-水(50∶40),流速:0.8 mL/m in,检测波长:296 nm;柱温:室温。结果:线性范围:华蟾酥毒基3.5μg^0.28μg,脂蟾毒配基3.75μg^0.30μg。平均回收率:华蟾酥毒基为99.86%,RSD为1.8%(n=5),脂蟾毒配基为99.84%,RSD为1.2%(n=5)。结论:该方法简便、灵敏、准确、专属强,能够控制产品质量。AIM: To establish the method of determining cinobufagin and resibufogenin in Xinkening Capsules (Venenum Bufonis, etc. ). METHODS: HPLC was applied to determining cinobufagin and resibufogenin. The determination was carried out using an ODS column with a solvent system: methanol-water (50: 40). The flow rate was 1.0 mL/min, detection wavelength was at 296 nm. RESULTS : The linear ranges of cinobufagin and resibufogenin were 3.5 μg-0.28 μg and 3.75 μg-0.30 μg, respectively. The average recoveries of cinobufagin and resibu- fogenin were 99.86% ( RSD = 1.8%, n = 5 ), and 99.84% ( RSD = 1.2%, n = 5 ), respectively. CONCLUSION : This method is simple, accurate with strong specificity and can be used to control the quality of Xinkening Capsules.
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