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APTES-modified mesoporous silicas as the carriers for poorly water-soluble drug. Modeling of diflunisal adsorption and release

机译:APTES改性的介孔二氧化硅作为水溶性差的药物的载体。二氟烷吸附和释放的模型

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摘要

Four mesoporous siliceous materials such as SBA-16, SBA-15, PHTS and MCF functionalized with (3-aminopropyl)triethoxysilane were successfully prepared and applied as the carriers for poorly water-soluble drug diflunisal. Several techniques including nitrogen sorption analysis, XRD, TEM, FUR and thermogravimetric analysis were employed to characterize mesoporous matrices. Adsorption isotherms were analyzed using Langmuir, Freundlich, Temkin and Dubinin-Radushkevich models. In order to find the best-fit isotherm for each model, both linear and nonlinear regressions were carried out. The equilibrium data were best fitted by the Langmuir isotherm model revealing maximum adsorption capacity of 217.4 mg/g for aminopropyl group-modified SBA-15. The negative values of Gibbs free energy change indicated that the adsorption of diflunisal is a spontaneous process. Weibull release model was employed to describe the dissolution profile of diflunisal. At pH 4.5 all prepared mesoporous matrices exhibited the improvement of drug dissolution kinetics as compared to the dissolution rate of pure diflunisal. (C) 2016 Elsevier B.V. All rights reserved.
机译:成功制备了四种用(3-氨基丙基)三乙氧基硅烷官能化的介孔硅质材料,例如SBA-16,SBA-15,PHTS和MCF,并将其用作水溶性差的药物二氟菊酯的载体。包括氮吸附分析,XRD,TEM,FUR和热重分析在内的几种技术被用来表征介孔基体。使用Langmuir,Freundlich,Temkin和Dubinin-Radushkevich模型分析吸附等温线。为了找到每个模型的最佳拟合等温线,进行了线性和非线性回归。平衡数据最好由Langmuir等温模型拟合,该模型显示氨丙基修饰的SBA-15的最大吸附容量为217.4 mg / g。吉布斯自由能变化的负值表明二氟乙醛的吸附是自发过程。用Weibull释放模型描述双氟尼醛的溶出曲线。在pH 4.5下,与纯二氟尼醛的溶解速率相比,所有制备的中孔基质均表现出药物溶解动力学的改善。 (C)2016 Elsevier B.V.保留所有权利。

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