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Spectrofluorimetric determination of gemifloxacin mesylate and linezolid in pharmaceutical formulations: Application of quinone-based fluorophores and enhanced native fluorescence

机译:药物制剂中甲磺酸吉非沙星和利奈唑胺的荧光光谱法测定:基于醌的荧光团和增强的天然荧光的应用

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摘要

Quinone-based fluorophores and enhanced native fluorescence techniques were applied for a fast quantitative analysis of gemifloxacin mesylate (GEM) and linezolid (LIN) in pharmaceutical formulations. For this purpose, three sensitive, accurate and precise spectrofluorimetric methods were developed. GEM, as an n-electron donor, reacts with 7,7,8,8-tetracyanoquinodimethane (method A) and 2,5-dichloro-3,6-dihydroxy-p-benzoquinone (method B) as π-electron acceptors, forming charge transfer complexes that exhibit high fluorescence intensity at 441 and 390 nm upon excitation at 260 and 339 nm, respectively. Method C depends on measurement of enhanced native fluorescence of LIN in phosphate buffer (pH 5) at 380 nm upon excitation at 260 nm. Experimental factors affecting the fluorescence intensity were optimized. Linearity was obtained over concentration ranges 50–500, 10–60 and 20–400 ng mL−1 for methods A, B and C, respectively. The developed methods were validated and successfully applied for determination of the cited drugs in tablets.
机译:基于醌的荧光团和增强的天然荧光技术可用于药物制剂中甲磺酸吉非沙星(GEM)和利奈唑胺(LIN)的快速定量分析。为此,开发了三种灵敏,准确和精确的荧光光谱法。 GEM作为n电子给体,与7,7,8,8-四氰基喹二甲烷(方法A)和2,5-二氯-3,6-二羟基-对苯醌(方法B)反应,作为π电子受体,形成电荷转移复合物,分别在260和339 nm激发后在441和390 nm处显示高荧光强度。方法C取决于在260 nm激发后在380 nm磷酸盐缓冲液(pH 5)中LIN增强的天然荧光的测量。优化了影响荧光强度的实验因素。方法A,B和C分别在50–500、10–60和20–400 ng mL-1的浓度范围内获得线性。验证了所开发的方法,并成功地应用于片剂中所引用药物的测定。

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