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首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >DEVELOPMENT AND VALIDATION OF UV SPECTROSCOPIC METHODS FOR SIMULTANEOUS ESTIMATION OF PARACETAMOL AND ZALTOPROFEN IN BULK AND TABLET FORMULATION
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DEVELOPMENT AND VALIDATION OF UV SPECTROSCOPIC METHODS FOR SIMULTANEOUS ESTIMATION OF PARACETAMOL AND ZALTOPROFEN IN BULK AND TABLET FORMULATION

机译:紫外分光光度法同时估算散装和片剂配方中帕拉西他莫和唑来普芬的方法的建立和验证

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Two methods for simultaneous estimation of Pracetamol and Zaltoprofen in combined tablet dosage form have been developed. The first UV spectrophotometric method was a determination using the simultaneous equation method at 245 nm and 227 nm. The second UV spectrophotometric method is the Q – analysis (absorption ratio) method, which involves the formation of absorbance equation at 237.5 nm (isobestic point) and at 227 nm the maximum absorption of Zaltoprofen. The linearity ranges for Paracetamol and Zaltoprofen were 2 – 18 μg/ml and 2 – 18 μg/ml respectively. The accuracy of the methods was assessed by recovery studies was found to be 100.02 ± 0.467 and 99.87 ± 0.532 for simultaneous equation method and 99.82 ± 0.483 and 99.84 ± 0.512 for Q analysis (absorption ratio) method for Paracetamol and Zaltoprofen respectively. These methods are simple, accurate and rapid; those require no preliminary separation and can therefore be used for routine analysis of both drugs in quality control laboratories
机译:已经开发出了两种方法来同时估算联合片剂剂型中的扑热息痛和扎洛特芬。第一种紫外分光光度法是使用联立方程法在245 nm和227 nm处测定。第二种紫外分光光度法是Q-分析(吸收率)方法,它涉及形成237.5 nm(等吸收点)和227 nm时Zaltoprofen的最大吸收率的吸收率方程。扑热息痛和扎托洛芬的线性范围分别为2 – 18μg/ ml和2 – 18μg/ ml。通过回收率研究对方法的准确性进行评估,联立方程法分别为100.02±0.467和99.87±0.532,对乙酰氨基酚和Zaltoprofen的Q分析(吸收比)方法分别为99.82±0.483和99.84±0.512。这些方法简单,准确,快速;这些不需要初步分离,因此可以在质量控制实验室中用于两种药物的常规分析

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