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光谱荧光法研究测定舒马曲坦琥珀酸盐:应用于片剂和加标人血浆。

Spectrofluorimetric investigation for determination of sumatriptan succinate: application to tablets and spiked human plasma.

机构信息

Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Delta University for Science and Technology, Gamasa, Egypt.

出版信息

Luminescence. 2021 May;36(3):755-760. doi: 10.1002/bio.4000. Epub 2021 Jan 14.

Abstract

A simple and highly sensitive spectrofluorimetric method for the estimation of sumatriptan succinate has been investigated. The suggested method depends on the determination of the intrinsic fluorescence properties of the drug in aqueous systems at λ 350 nm following λ at 225 nm. The linearity range was 10-100 ng/ml, with a detection limit and quantitation limit of 1.2 and 3.6 ng/ml, respectively. The suggested method was sufficiently successful for determination of sumatriptan its pharmaceutical tablets as well as in spiked human plasma. Moreover, the validation parameters were determined following International Council for Harmonisation guidelines. Statistical analysis of the obtained results from the proposed and reference methods showed no significance difference between the two methods regarding accuracy and precision.

摘要

已研究出一种简单且灵敏的马来酸舒马曲坦测定法。该方法取决于在 225nm 激发波长下测定药物在水相体系中的本征荧光性质,在 350nm 处检测。该方法的线性范围为 10-100ng/ml,检测限和定量限分别为 1.2ng/ml 和 3.6ng/ml。该方法成功地应用于马来酸舒马曲坦片剂及其在人血浆中的加标测定。此外,验证参数是按照国际协调理事会的指导方针确定的。对从所提议的和参考方法获得的结果进行的统计学分析表明,两种方法在准确性和精密度方面没有显著差异。

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