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Validated liquid chromatographic method for simultaneous estimation of albendazole and ivermectin in tablet dosage form

机译:经验证的液相色谱法同时测定片剂剂型中的阿苯达唑和伊维菌素

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A reverse phased liquid chromatography(LC)method was developed and validated for simultaneous estimation of albendazole and ivermectin in tablet dosage fonn.The isocratic LC analysis was performed on NUCLEODUR Cl 8 RP column(250 X 4.6 mm,5 mu)using mobile phase composed of acetonitrile,methanol and water in ratio of 60:30:10(v/v/v)at a flow rate of 1.8 mL/min.Quantitation was performed using UV detector at 245 nm and the run time was 20 min.The retention times were found to be 3.56 min for albendazole and 10.08 min for ivermectin.The analytical method was validated according to ICH guidelines.The linearity was observed in the range of 400-800 and 6-12 mu g/mL with correlation coefficient,r=0.9975 and 0.9969 for albendazole and ivermectin respectively.The relative standard deviation values for repeatability and intermediate precision studies were less than 2%,and the accuracy(% recovery)was greater than 98% for both the drugs.The method was successfully applied for market sample analysis and mean percentage assay values were 98.68±0.28 and 98.6710.50 for albendazole and ivermectin respectively.The present method is precise and accurate and can be used for the routine estimation of albendazole and ivermectin in tablet dosage forms.
机译:建立了反相液相色谱(LC)方法并验证了片剂剂量形式中阿苯达唑和伊维菌素的同时估算方法。使用流动相组成的NUCLEODUR Cl 8 RP色谱柱(250 X 4.6 mm,5 mu)进行等度LC分析以1.8 mL / min的流速以60:30:10(v / v / v)的比例混合乙腈,甲醇和水。使用UV检测器在245 nm处进行定量,运行时间为20分钟。阿苯达唑的分析时间为3.56分钟,伊维菌素的分析时间为10.08分钟。分析方法根据ICH指南进行了验证,线性在400-800和6-12μg / mL范围内具有相关系数,r =阿苯达唑和伊维菌素分别为0.9975和0.9969。两种药物的重复性和中等精密度研究的相对标准偏差小于2%,两种药物的准确度(回收率%)均大于98%。该方法已成功应用于市场。样本分析阿苯达唑和伊维菌素的平均测定值分别为98.68±0.28和98.6710.50。本方法准确,准确,可用于片剂剂型中阿苯达唑和伊维菌素的常规估计。

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