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剂型中硫利达嗪和氟哌噻吨的荧光分光光度法测定;在含量均匀度测试中的应用。

Spectrofluorimetric determination of thioridazine and flupentixol in dosage forms; application to content uniformity test.

作者信息

Attia Tamer Z, Omar Mahmoud A

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Minia University, Minia, Egypt.

出版信息

Luminescence. 2016 Aug;31(5):1091-7. doi: 10.1002/bio.3076. Epub 2015 Dec 16.

Abstract

A reliable, sensitive, cheap and non-extractive spectrofluorimetric method has been developed and validated for determination of thioridazine and flupentixol based on ternary complex formation with eosin and lead(II) in the presence of methylcellulose as surfactant at pH 3.2. Under the optimum conditions, the quantitative quenching effect of investigated drugs on the native fluorescence of eosin has been investigated. The quenching of the eosin fluorescence was measured at 517 nm after excitation at 462 nm. The different experimental parameters affecting the development and stability of the reaction products were carefully studied and optimized, and the results were satisfactory. The calibration plots were constructed over the range of 0.5-3.0 µg mL(-1) . The developed method was successfully applied for determination of investigated drugs in commercial tablets without interference from common excipients. It was further applied for content uniformity testing of flupentixol in its tablets. Statistical comparisons of the results with those of the reference methods revealed excellent agreement and indicated no significant difference in accuracy and precision. Copyright © 2015 John Wiley & Sons, Ltd.

摘要

基于在pH 3.2条件下,在甲基纤维素作为表面活性剂存在时,与曙红和铅(II)形成三元配合物,已开发并验证了一种可靠、灵敏、廉价且无需萃取的荧光分光光度法,用于测定硫利达嗪和氟哌噻吨。在最佳条件下,研究了所研究药物对曙红天然荧光的定量猝灭作用。在462 nm激发后,于517 nm处测量曙红荧光的猝灭。仔细研究并优化了影响反应产物形成和稳定性的不同实验参数,结果令人满意。校准曲线在0.5 - 3.0 µg mL⁻¹范围内构建。所开发的方法成功应用于测定市售片剂中的所研究药物,不受常见辅料干扰。它还进一步应用于氟哌噻吨片剂的含量均匀度测试。结果与参考方法的统计比较显示出极好的一致性,表明在准确度和精密度方面无显著差异。版权所有© 2015约翰威立父子有限公司。

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