方法稳定性表明了恩曲他滨的方法开发和紫外光谱和反相高效液相色谱法的验证

Ashwini V. Shelke, Pooja Surwae, Atul R. Bendale, Laxmikany Borse, A. Jadhav
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引用次数: 1

摘要

恩曲他滨(通常称为FTC,系统名称2 & 3′-二脱氧-5-氟-3-硫胞苷)是一种核苷类逆转录酶抑制剂(NRTI),用于预防和治疗成人和儿童的HIV感染。在240nm波长上对药物进行紫外分析。建立了一种简便、灵敏、准确的反相高效液相色谱法测定恩曲他滨原料药的含量。本方法灵敏度高,线性范围为10 ~ 50µg/ml (r2 = 0.9991)。根据ICH指南的各种参数来验证和测试该方法。检出限为0.1534µgml,定量限为0.4649µgml。结果表明,该方法准确、专属性好、重现性好,操作简便、成本低、耗时短,适用于恩曲他滨原料药的测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Method stability indicating method development and validation for emtricitabina by UV spectroscopic and RP-HPLC methods
Emtricitabine (commonly called FTC, systematic name 2 & 3’-dideoxy-5-fluoro-3-thiacytidine) is a nucleoside reverse-transcriptase inhibitor (NRTI) for the prevention and treatment of HIV infection in adults and children. The UV analysis of the drug was carried out on the 240nm wavelength. A simple, sensitive and accurate RP-HPLC method has been developed& validated for the determination of Emtricitabine in bulk formulation. Present method shows high sensitivity with linearity 10 to 50µg/ml (r2 = 0.9991). Various parameters according to ICH guidelines are followed for validating and testing of this method. Detection limit and quantitation limit were found to be 0.1534 µg ml and 0.4649 µgml respectively. The results demonstrated that the procedure is accurate, specific and reproducible and also being simple, cheap and less time consuming and appropriate for the determination of Emtricitabine in bulk formulation.
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