首页> 外文期刊>American Journal of PharmTech Research >Development and Validation of Solvent Extraction Spectrophotometric Method for Simultaneous Estimation of Doxofylline and Terbutaline sulphate In their Combined Dosage Form
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Development and Validation of Solvent Extraction Spectrophotometric Method for Simultaneous Estimation of Doxofylline and Terbutaline sulphate In their Combined Dosage Form

机译:溶剂萃取分光光度法同时估算多索茶碱和硫酸特布他林混合剂型的建立和验证

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  ABSTRACT Simple, specific, accurate, precise and reproducible method have been developed and validated for the simultaneous estimation of both drugs in their combined dosage form. UV spectrophotometric method was a determination using the solvent extraction method at 277 nm and 279 nm over the concentration range 10-50 and 20-60 μg/ml for Doxofylline in chloroform and terbutaline sulphate in water respectively. The % recoveries of the both the drugs were found to be 100.34% – 100.72 % and 98.25– 99.19 % respectively. Method was statistically validated for accuracy, precision, specificity, LOQ, robustness and ruggedness according to ICH guidelines and can be used for analysis of combined dosage form. Key words: Doxofylline, Terbutaline sulphate, Solvent Extraction Spectrophotometric method.
机译:摘要已经开发并验证了简单,特异性,准确,精确和可重现的方法,可同时估算两种药物在其组合剂型中的使用。紫外分光光度法是使用溶剂萃取法在浓度分别为10-50和20-60μg/ ml的氯仿中的多沙茶碱和水中的硫酸特布他林在277 nm和279 nm处测定的。两种药物的回收率分别为100.34%– 100.72%和98.25 – 99.19%。根据ICH指南,对该方法的准确性,精密度,特异性,LOQ,稳健性和耐用性进行了统计验证,可用于组合剂型的分析。关键词:多索茶碱硫酸特布他林溶剂萃取分光光度法

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