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作 者:陈方剑[1] 宋洪杰[1] 高鸿彬[1] 王志君[1] 傅芃[1] 陆松伟[1] 袁文琳[1]
机构地区:[1]第二军医大学长海医院药学部,上海200433
出 处:《药学服务与研究》2012年第6期427-430,共4页Pharmaceutical Care and Research
基 金:上海市卫生局中药新药及院内制剂研发项目(No.2011ZJ028)
摘 要:目的:建立用HPLC法同时测定感冒安颗粒中没食子酸、绿原酸及咖啡酸的含量。方法:采用Kromasil C18色谱柱(150mm×4.6mm,5μm);流动相:乙腈(A)-0.4%磷酸溶液(B),梯度洗脱:0~7.50min A相2%,7.50~7.51min A相2%→12%,7.51~25.00min A相12%;流速:0.8ml/min;柱温:室温;检测波长:272nm(没食子酸)、327nm(绿原酸和咖啡酸)。结果:没食子酸在0.27~8.64μg/ml范围内线性关系良好(r=0.999 9),平均回收率为100.14%,RSD为1.66%(n=9);绿原酸在1.00~32.00μg/ml范围内线性关系良好(r=0.999 7),平均回收率为98.10%,RSD为2.38%(n=9);咖啡酸在0.30~9.60μg/ml范围内线性关系良好(r=0.999 8),平均回收率为100.48%,RSD为2.28%(n=9)。结论:该方法准确、灵敏,专属性强,重现性好,对感冒安颗粒质量控制标准的提高具有参考意义。Objective: To establish a HPLC method for simultaneous determination of gallic acid,chlorogenic acid and caffeic acid contents in Ganmao'an granules.Methods: The separation column of Kromasil C18(150 mm×4.6 mm,5 μm) was used,acetonitrile(A)-0.4% phosphoric acid(B) was applied as the mobile phase with gradient elution: 0-7.50 min 2% A,7.50-7.51 min 2%→12% A,7.51-25.00 min 12% A.The flow rate was 0.8 ml/min.The column temperature was room temperature.The detection wavelengths were 272 nm for gallic acid,327 nm for chlorogenic acid and caffeic acid.Results: The linear ranges of gallic acid,chlorogenic acid and caffeic acid were 0.27-8.64 μg/ml(r=0.999 9),1.00-32.00 μg/ml(r=0.999 7) and 0.30-9.60 μg/ml(r=0.999 8),respectively.The average recoveries of gallic acid,chlorogenic acid and caffeic acid were 100.14%,RSD 1.66%(n=9),98.10%,RSD 2.38%(n=9) and 100.48%,RSD 2.28%(n=9),respectively.Conclusion: The method is accurate,sensitive,selective and reproducible,and could provide the reference for the improvement of quality control standard of Ganmao'an granules.
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