高效液相色谱法测定原料中氟康唑及其有机杂质的方法验证

IF 0.8 4区 医学 Q4 TROPICAL MEDICINE
Biomedica Pub Date : 2023-08-31 DOI:10.7705/biomedica.6850
James Alexander Castillo, Natalia Afanasjeva
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引用次数: 0

摘要

介绍每个国家的真实实验室条件,包括气候,都会影响该方法分析药理学物质的效率。因此,有必要根据相应的指导方针验证流程,并对其进行优化,以确保成功并对结果充满信心。客观的目的是在热带气候条件下,使用二极管阵列检测器,使用高效液相色谱法,验证原料中氟康唑及其有机杂质的定量方法,并符合所有监管要求。材料和方法。我们对该方法进行了预验证测试,包括系统充分性、过滤器研究、量化极限、无系统误差、强制降解研究和溶液稳定性。此外,我们还验证了该系统的特异性、线性、准确性、精密度和稳健性。后果将降解产物与分析物峰分离可以实现该方法的光谱纯度。在室温和冷藏条件下的评估时间(24小时)内,溶液的稳定性没有受到影响。线性导致评估的相关系数大于或等于0.999,杂质的相关系数小于或等于0.997。我们获得的氟康唑回收率在98%到102%之间,杂质检测的准确度在80%到120%之间。评估的重复性和再现性因子不超过2.0%的相对标准差,杂质的相对标准偏差不超过5.0%,表明该方法具有足够的稳健性。此外,短的分析执行时间允许快速确定原材料质量。结论我们证明,通过高效液相色谱法验证的氟康唑定量方法具有足够的选择性、精确性、准确性、线性和稳健性,能够在包括哥伦比亚热带气候在内的真实条件下产生准确的分析结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Method validation for the quantification of fluconazole and its organic impurities in raw material using high-performance liquid chromatography

Method validation for the quantification of fluconazole and its organic impurities in raw material using high-performance liquid chromatography

Method validation for the quantification of fluconazole and its organic impurities in raw material using high-performance liquid chromatography

Method validation for the quantification of fluconazole and its organic impurities in raw material using high-performance liquid chromatography

Introduction. The real laboratory conditions of each country, including climate, can affect the method’s efficiency in analyzing a pharmacological substance. Thus, it is necessary to validate the process according to the corresponding guidelines and optimize it to ensure success and confidence in the results. Objective. The objective was to validate a methodology for fluconazole and its organic impurities quantification in raw material using high-performance liquid chromatography, with a diode array detector, under tropical climate conditions, and complying with all regulatory requirements. Materials and methods. We performed pre-validation tests of the method consisting of system adequacy, filters study, quantification limit, absence of systematic error, forced degradation studies, and solutions stability. In addition, we validated the specificity, linearity, accuracy, precision, and robustness of the system. Results. Separation of the degradation products from the analyte peaks allowed the achievement of the method’s spectral purity. The solution’s stability was not affected during the evaluated time (24 hours) at room temperature and under refrigeration. Linearity resulted in correlation coefficients greater than or equal to 0.999 for the evaluation and greater than or equal to 0.997 for impurities. We obtained a fluconazole recovery varying from 98 to 102% with an accuracy between 80 to 120% for impurities detection. The repeatability and reproducibility factor did not exceed a relative standard deviation of 2.0% for the evaluation and of 5.0% for the impurities, demonstrating the adequate robustness of the method. In addition, a short analysis execution time allowed the quick determination of the raw material quality. Conclusion. We demonstrated that the fluconazole quantification method validated by high-performance liquid chromatography is sufficiently selective, precise, exact, linear, and robust to generate accurate analytical results under real conditions, including the tropical climate of Colombia.

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来源期刊
Biomedica
Biomedica 医学-热带医学
CiteScore
1.60
自引率
0.00%
发文量
76
审稿时长
>12 weeks
期刊介绍: Biomédica is the quarterly journal of the Instituto Nacional de Salud of Colombia [Colombia’s National Health Institute]. Its purpose is to publish the results of original research that contributes meaningfully to knowledge in health and biomedical sciences.
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