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胶束增敏荧光光度法测定药物制剂中利巴韦林的含量。

Determination of the anti-viral drug Ribavirin in dosage forms via micelle-enhanced spectrofluorimetric method.

机构信息

Department of Chemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.

出版信息

Luminescence. 2013 Mar-Apr;28(2):190-4. doi: 10.1002/bio.2361. Epub 2012 Apr 3.

Abstract

A simple and sensitive spectrofluorimetric method was developed for the determination of Ribavirin in pharmaceutical formulations. The proposed method was based on the fluorescence spectral behaviour of Ribavirin in a sodium dodecyl sulfate (SDS) micellar system. In an aqueous acetate buffer solution of pH 4.0, the fluorescence intensity of Ribavirin was significantly enhanced by about 217% in the presence of SDS. Fluorescence intensity was measured at 396 nm after excitation at 270 nm for Ribavirin. The fluorescence-concentration plot was rectilinear over the range of 0.01-3.0 µg/mL for Ribavirin with a lower detection limit of 5.02 x 10(-3) µg/mL. The method was successfully applied to the analysis of the drug in its commercial capsules. Results were in good agreement with those obtained with the official method. The application of the proposed method was extended to stability studies of Ribavirin after exposure to different forced degradation conditions such as acidic, alkaline, photo and oxidative conditions according to ICH guidelines.

摘要

建立了一种简单灵敏的荧光分光光度法用于测定药物制剂中的利巴韦林。该方法基于利巴韦林在十二烷基硫酸钠(SDS)胶束体系中的荧光光谱行为。在 pH 值为 4.0 的醋酸盐缓冲水溶液中,利巴韦林在 SDS 的存在下荧光强度显著增强约 217%。利巴韦林在 270nm 激发后于 396nm 处测量荧光强度。利巴韦林的荧光浓度曲线在 0.01-3.0μg/mL 范围内呈线性,检测限为 5.02×10^(-3)μg/mL。该方法成功地应用于其商业胶囊中药物的分析。结果与官方方法获得的结果吻合良好。根据 ICH 指南,该方法的应用扩展到利巴韦林在不同强制降解条件下(如酸、碱、光和氧化条件)的稳定性研究。

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