首页> 外文期刊>Luminescence: The journal of biological and chemical luminescence >Spectrofluorimetric determination of oseltamivir phosphate through derivatization with o-phthalaldehyde. Application to pharmaceutical preparations with a preliminary study on spiked plasma samples
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Spectrofluorimetric determination of oseltamivir phosphate through derivatization with o-phthalaldehyde. Application to pharmaceutical preparations with a preliminary study on spiked plasma samples

机译:邻苯二甲醛衍生化荧光荧光法测定磷酸奥司他韦。对加标血浆样品的初步研究在药物制剂中的应用

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摘要

A simple and sensitive spectrofluorimetric method has been developed and validated for the determination of oseltamivir phosphate (OST) in pharmaceutical preparations. The method is based on the reaction between oseltamivir phosphate and o-phthalaldehyde in presence of 2-mercapto-ethanol in borate buffer, pH 10.8, to give a highly fluorescent product measured at 450 nm after excitation at 336 nm. The different experimental parameters affecting the development and stability of the reaction product were studied and optimized. The fluorescence intensity-concentration plot is rectilinear over the range 0.05-1.0 μg/mL, with a lower detection limit of 5 ng/mL and limit of quantitation of 16 ng/mL. The developed method was successfully applied to the analysis of the drug in its commercial capsules and suspension, mean recoveries of OST were 99.97 ± 1.67% and 100.17 ± 1.18%, respectively (n = 3). Statistical comparison of the results obtained by the proposed and comparison method revealed no significant difference in the performance of the two methods regarding accuracy and precision. The proposed method was further extended to in vitro determination of the studied drug in spiked human plasma as a preliminary investigation; the mean recovery (n = 3) was 98.68 ± 5.8%. A reaction pathway was postulated.
机译:已经开发了一种简单而灵敏的荧光光谱法,并已用于药物制剂中磷酸奥司他韦(OST)的测定。该方法基于磷酸奥司他韦和邻苯二甲醛在2-巯基乙醇在pH 10.8的硼酸盐缓冲液中的反应,得到在336 nm激发后在450 nm处测得的高荧光产物。研究和优化了影响反应产物发展和稳定性的不同实验参数。荧光强度-浓度图在0.05-1.0μg/ mL范围内呈直线,检测下限为5 ng / mL,定量下限为16 ng / mL。所开发的方法已成功地应用于药物在其商业胶囊和悬浮液中的分析,OST的平均回收率分别为99.97±1.67%和100.17±1.18%(n = 3)。通过提议的和比较方法获得的结果的统计比较表明,就准确性和准确性而言,两种方法的性能没有显着差异。拟议的方法进一步扩展到了体外测定加标人血浆中所研究药物的方法,作为初步研究。平均回收率(n = 3)为98.68±5.8%。假定反应途径。

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