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作 者:晏海军 陈一波 张福利[2] 林丽娅 王禄 YAN Haijun;CHEN Yibo;ZHANG Fuli;LIN Liya;WANG Lu(College of Chemistry and Chemical Engineering,Shanghai University of Engineering Science,Shanghai 201620,China;State Pharmaceutical Administration of Shanghai Institute of Pharmaceutical Industry,Shanghai 201203,China;China National Pharmaceutical Industry Corporation Ltd.,Langfang Company,Langfang 065000,China)
机构地区:[1]上海工程技术大学化学化工学院,上海201620 [2]上海医药工业研究院有限公司,上海201203 [3]国药集团工业有限公司廊坊分公司,河北廊坊065000
出 处:《中国现代应用药学》2022年第5期633-637,共5页Chinese Journal of Modern Applied Pharmacy
摘 要:目的建立HPLC检测盐酸氯胺酮原料药中有关物质的方法。方法采用Waters Xbridge C18色谱柱,以0.005 mol·L^(-1)己烷磺酸钠水溶液-乙腈-磷酸(90︰10︰0.1)为流动相A,乙腈为流动相B,梯度洗脱,流速1.0 mL·min^(-1),检测波长215 nm,柱温30℃。结果主成分与各杂质间最小分离度>1.5;主成分以及其6个杂质在各自的浓度范围内呈良好的线性关系(r>0.999);平均回收率为97.6%~103.0%,RSD为0.8%~2.8%。结论本方法准确、灵敏、可靠,适用于盐酸氯胺酮有关物质的测定。OBJECTIVE To establish an HPLC method for determination of the related substances in ketamine hydrochloride.METHODS Waters Xbridge C18 column was used;the mobile phase A consisted of 0.005 mol·L^(-1) sodium hexanesulfonate aqueous solution-acetonitrile-phosphoric acid(90︰10︰0.1),the mobile phase B was acetonitrile,with gradient elution at the flow rate of 1.0 mL·min^(-1);the detection wavelength was 215 nm;the column temperature was 30℃.RESULTS The minimum separation between the main component and each impurity was>1.5;ketamine and its six impurities showed a good linear relationship in the self-concentration range(r>0.999);and the average recoveries were 97.6%-103.0% with RSDs of 0.8%-2.8%.CONCLUSION The method is accurate,sensitive and reliable,which is suitable for the determination of related substances in ketamine hydrochloride.
分 类 号:R917.101[医药卫生—药物分析学]
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