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机构地区:[1]南京中医药大学附属常州市中医医院,江苏常州213003 [2]江苏健民制药有限公司,江苏常州213018
出 处:《中医学报》2013年第12期1851-1853,共3页Acta Chinese Medicine
基 金:国家自然基金项目(编号:50827530)
摘 要:目的:建立保元排毒丸中丹参酮ⅡA的含量测定的方法,并对制剂中丹参酮ⅡA含量的稳定性进行研究。方法:采用高效液相色谱法对保元排毒丸中丹参酮ⅡA的含量进行测定,将制剂分别置温度为(60±2)℃条件下、湿度为(75±5)%条件下3个月,对制剂中丹参酮ⅡA进行稳定性研究。结果:高效液相色谱法测定保元排毒丸中丹参酮ⅡA含量的方法较好,丹参酮ⅡA在0.03~0.30μg范围内线性关系良好(n=5,r=0.9999);保元排毒丸制剂在(60±20)℃温度条件下、湿度为(75±5)%条件下稳定性良好。结论:高效液相色谱法测定保元排毒丸中丹参酮ⅡA的含量,方法简便、准确,适用于组方丹参中丹参酮ⅡA成分的含量测定;同时稳定性实验表明保元排毒丸制剂中丹参酮ⅡA成分稳定性良好。Objective :To establish the content determination method and stability study of tanshinone Ⅱ A in Baoyuan paidu pill. Meth- ods : detected the content of tanshinone Ⅱ A in Baoyuan Paidu Pill by high performance liquid chromatography ( HPLC ), and put the pill under the condition of temperature ( 60 ± 2 ) ℃, humidity ( 75± 5 ) % for 3 months, and stability study of tanshinone ⅡA in the pill. Re- sults :The content of tanshinone Ⅱ A in Baoyuan Paidu Pill detection by HPLC was better, and Tanshinone Ⅱ A had a good linear rela- tionship in the range of 0.03 -0.30 μg( n = 5, r = 0.999 9 ). Baoyuan Paidu Pill had good stability under the condition of temperature ( 60 ± 20) ℃, humidity of ( 75 ± 5 ) %. Conclusion : The method of HPLC determination of tanshinone Ⅱ A in Baoyuan Paidu Pill content is simple and accurate,which can be used for the content determination of tanshinone Ⅱ A in salvia miltiorrhiza of the composition. At the same time, stability test shows that tanshinone Ⅱ A composition in Baoyuan Paidu Pill has good stability.
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