首页> 外文期刊>Indian drugs >DEVELOPMENT AND VALIDATION OF SPECTROPHOTOMETRIC METHOD FOR SIMULTANEOUS ESTIMATION OF FAMOTIDINE, DICLOFENAC AND PARACETAMOL IN THEIR COMBINED DOSAGE FORM
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DEVELOPMENT AND VALIDATION OF SPECTROPHOTOMETRIC METHOD FOR SIMULTANEOUS ESTIMATION OF FAMOTIDINE, DICLOFENAC AND PARACETAMOL IN THEIR COMBINED DOSAGE FORM

机译:分光光度法同时估算法莫替丁,双氯芬酸和帕拉他莫的分光光度法的建立和验证

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摘要

Famotidine (FAM), Diclofenac (DCF) and Paracetamol (PCM) are used in combination for musculoskeletal disorders. A simple, sensitive, rapid, precise, reproducible and accurate spectrophotometric method for simultaneous determination of FAM, DCF and PCM was developed. The method was based on UV spectrophotometric determination of three drugs using simultaneous equation method. The stock solutions were prepared in methanol AR. Absorbance measurement was carried out at 288.4 nm, 281.2nm and 248.2 nm for FAM, DCF and PCM respectively. Beer Lambert law was obeyed in the concentration range of 1-30ug/ml_ for FAM, 2-40ug/ml_ for DCF and 1-20ug/ml_ for PCM. The results of the analysis were tested and validated for various validation parameters statistically and by recovery studies according to the International Conference on Harmonization Q2B guidelines. The utility of the developed method has been demonstrated by analysis of commercially available tablet dosage form.
机译:法莫替丁(FAM),双氯芬酸(DCF)和扑热息痛(PCM)组合使用可解决肌肉骨骼疾病。开发了一种同时测定FAM,DCF和PCM的简单,灵敏,快速,精确,可重现和准确的分光光度法。该方法基于紫外分光光度法,采用联立方程法测定三种药物。储备溶液在甲醇AR中制备。 FAM,DCF和PCM分别在288.4 nm,281.2 nm和248.2 nm处进行吸光度测量。对于FAM,在1-30ug / mL的浓度范围内,在DCF为2-40ug / mL的浓度下,对于PCM为1-20ug / mL的浓度范围,遵守比尔朗伯定律。根据国际协调Q2B指南,通过统计和恢复研究对分析结果进行了测试,并针对各种验证参数进行了验证。通过对市售片剂剂型的分析证明了该开发方法的实用性。

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