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作 者:吴宏伟[1] 郭伟斌[1] 苏智阳[1] 邱元素[1]
出 处:《中国药品标准》2003年第6期52-54,共3页Drug Standards of China
摘 要:目的:建立新的HPLC流动相分析方法,使米诺环素与甲基米诺环素达到有效的分离,测定准确的米诺环素含量。方法:流动相为醋酸铵缓冲溶液(pH6.55):乙腈:甲醇=830:185:5,检测波长为280nm,流速为1.0ml/min,进样量为20μl。结果:米诺环素与甲基米诺环素的分离度大于2.3,线性范围在0.2mg/ml~2mg/ml,r=0.9999;回收率为99.22%,95%可信限范围为99.22±0.52%(n=9),RSD=1.14%。Objective: To establish a new analytical method of HPLC to determinate accurately the potency of Minocycline by Changing mobile phase. It can make Minocycline and Methylol Minocycline to achieve an effective separation. Method: Mobile phase is ammonium acetate buffer solution(pH6. 55) : acetonitrile : methanol = 830:185 :5. wavelength was 280nm,flow rate was 1.0ml/min,volume injected was 20μl. Result: Separablity of Minocycline exceed 2. 3,the linear range was 0. 2-2mg/ ml,r = 0. 9999,the recovery was 99. 22%,the 95% creditability range was 99. 22±0. 52% (n = 9) ,RSD= 1. 14%.
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