紫外分光光度法测定微乳中吉非罗齐含量分析方法的验证

IF 1.9 Q3 COMPUTER SCIENCE, ARTIFICIAL INTELLIGENCE
M. Herrera P., José Cantos C., Kevin Muñoz S., Jovan Durán A., Julio Vinueza G., Fernanda Kolenyak dos Santos
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引用次数: 0

摘要

本研究旨在验证紫外分光光度法定量微乳液中掺入的吉非罗齐的分析方法。通过构建用于鉴定微乳液的三元相图进行的实验开发。采用偏光显微镜技术对微乳液进行了表征。根据美国药典(USP)39 NF34和国际协调会议(ICH)(2005)描述的参数对分析方法进行了验证,该参数评估了线性、稳健性、日内和日间准确度、特异性准确度、检测和定量限。所开发的方法证明了线性,确定系数(R2)为0.9898,此外,每个测试的精度、准确度和稳健性都低于5%的变异系数。所获得的结果是有利的,因为它们符合USP 39-NF34(2016)和ICH(2005)规定的参数,表明该方法对预期目的是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
VALIDATION OF ANALYTICAL METHOD BY UV SPECTROPHOTOMETRIC QUANTIFICATION OF GEMFIBROZIL INCORPORATED IN THE MICROEMULSIONS
The present study aims to validate an analytical method by UV spectrophotometric for the quantification of gemfibrozil incorporated into microemulsions. Experimental development by constructing a ternary phase diagram for the identification of microemulsions. The characterization of the microemulsions was carried out by the polarized light microscopy technique. The analytical method was validated according to the parameters described by the United State Pharmacopeia (USP) 39 NF34 and International Conference on Harmonization (ICH) (2005), which evaluated linearity, robustness, intra and inter day accuracy, specificity accuracy, limits of detection and quantification. The developed method demonstrated linearity with a coefficient of determination (R2) of 0.9898, in addition to precision, accuracy and robustness for each of the tests with values that presented a coefficient of variation of less than 5 %. The results obtained were favorable, since they comply with the parameters stipulated by USP 39-NF34 (2016) and ICH (2005), indicating that the method is effective for the intended purpose.
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来源期刊
Intelligenza Artificiale
Intelligenza Artificiale COMPUTER SCIENCE, ARTIFICIAL INTELLIGENCE-
CiteScore
3.50
自引率
6.70%
发文量
13
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