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首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >QUANTITATIVE ANALYSIS OF PARACETAMOL AND DICLOFENAC IN COMBINED DOSAGE FORM BY FIRST DERIVATIVE AND SIMULTANEOUS EQUATION METHOD IN APPLICATION TO THE DETERMINATION OF DISSOLUTION STUDY
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QUANTITATIVE ANALYSIS OF PARACETAMOL AND DICLOFENAC IN COMBINED DOSAGE FORM BY FIRST DERIVATIVE AND SIMULTANEOUS EQUATION METHOD IN APPLICATION TO THE DETERMINATION OF DISSOLUTION STUDY

机译:一次导数-同时方程法定量分析扑热息痛和双氯芬酸混合剂型在溶出度测定中的应用

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摘要

Two simple, economical, precise, and accurate methods are described for the simultaneous determination of Paracetamol and Diclofenac in combined tablet dosage form. The first method is first- order derivative zero crossing method. The first order derivative absorption at 275.6 nm (zero cross point of Diclofenac) was used for Paracetamol and 242.69 nm (zero cross point of Paracetamol) for Diclofenac. The second one is simultaneous equation method in application to dissolution study. Simultaneous equation method was successfully applied to carry out dissolution study of commercial tablet formulation by using USP type II dissolution test apparatus. The solvent used is pH 6.8 phosphate buffer. Linearity range was 2-10μg/ml and 5-25 μg/ml for Paracetamol and Diclofenac respectively. The methods were validated with respect to linearity, precision and accuracy.
机译:描述了两种简单,经济,准确和准确的方法,用于同时测定组合片剂剂型中的扑热息痛和双氯芬酸。第一种方法是一阶导数过零方法。扑热息痛使用275.6 nm(双氯芬酸的零交叉点)的一阶导数吸收,双氯芬酸使用242.69 nm(对乙酰氨基酚的零交叉点)的一阶导数吸收。第二种是联立方程法在溶出度研究中的应用。通过使用USP II型溶出度测试仪,成功地将联立方程法应用于商业片剂的溶出度研究。使用的溶剂是pH 6.8磷酸盐缓冲液。扑热息痛和双氯芬酸的线性范围分别为2-10μg/ ml和5-25μg/ ml。这些方法在线性,精度和准确性方面得到了验证。

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