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奥格列汀胶束增强同步荧光光谱法的析因设计优化:应用于含量均匀度测试和体外药物释放

Factorial design optimization of micelle enhanced synchronous spectrofluorimetric assay of Omarigliptin: Applied to content uniformity testing and in vitro drug release.

作者信息

Ayoub Bassam M, Mowaka Shereen, Arafa Mona G

机构信息

Pharmaceutical Chemistry Department, Faculty of Pharmacy, The British University in Egypt (BUE), El-Sherouk city, Cairo, Egypt.

The Center for Drug Research and Development (CDRD), Faculty of Pharmacy, The British University in Egypt (BUE), El-Sherouk city, Cairo, Egypt.

出版信息

Luminescence. 2018 Jun;33(4):797-805. doi: 10.1002/bio.3479. Epub 2018 Apr 1.

Abstract

A micelle enhanced spectrofluorimetric method was developed for determination of Omarigliptin (OMG) based on its native fluorescence behavior. The interaction of OMG with surfactants and macromolecules was studied. In aqueous solution, the relative fluorescence intensity (RFI) of OMG was enhanced by 24% in the presence of Tween 80 at pH 3.5. The optimal conditions for the micelle enhanced fluorescence were attained by Minitab® program using Plackett-Burman factorial design. Pareto chart, contour plots and surface plots were used to exclude the insignificant variables and optimize the significant factors. The spectrofluorimeter was operated under synchronous mode using ∆λ = 30 nm and recording the RFI of the intense narrow band at 267 nm for OMG in 0.5% w/v Tween 80 + 0.2 M acetate buffer (pH 3.5) system using water as diluent. Using synchronous scan mode offered many advantages including considerable reduction of spectral overlap and enhanced linearity of the calibrators. Validation parameters were satisfied over the concentration range 0.1-2 μg/ml. The developed method was the first analytical procedure for OMG assay in Marizev® tablets. Moreover, content uniformity testing and in vitro drug release of tablets were performed.

摘要

基于奥格列汀(OMG)的固有荧光行为,开发了一种胶束增强荧光光谱法用于测定奥格列汀。研究了OMG与表面活性剂和大分子的相互作用。在水溶液中,在pH 3.5的吐温80存在下,OMG的相对荧光强度(RFI)提高了24%。使用Minitab®程序通过Plackett-Burman析因设计获得胶束增强荧光的最佳条件。使用帕累托图、等高线图和表面图来排除不显著的变量并优化显著因素。荧光光谱仪在同步模式下运行,使用∆λ = 30 nm,并以水为稀释剂,在0.5% w/v吐温80 + 0.2 M醋酸盐缓冲液(pH 3.5)体系中记录OMG在267 nm处强烈窄带的RFI。使用同步扫描模式具有许多优点,包括显著减少光谱重叠和增强校准物的线性。在0.1 - 2 μg/ml的浓度范围内,验证参数均符合要求。所开发的方法是用于测定Marizev®片剂中OMG的首个分析程序。此外,还进行了片剂的含量均匀度测试和体外药物释放研究。

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