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Controlled drug release through carboxymethyl-chitosan/poly(vinyl alcohol) blend films

机译:通过羧甲基壳聚糖/聚乙烯醇共混膜控制药物释放

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Carboxymethyl-chitosan (CMCS)/poly(vinyl alcohol) (PVA) blend film was studied for an application as a coating material in the site-specific drug delivery system. Films were prepared by blending varying amounts of 4 wt% CMCS with 4 wt% PVA, casting and drying at 50 degrees C for 24 h. The cross-sectional SEM micrograph of the film revealed that an increase in the amount of CMCS in the blend resulted in the film surface less smooth in the dry state and the network less uniform and more porous in the hydrated state, which became appreciable at 50%. The inclusion of CMCS in the blend also made the swelling of the films pH dependent, and lead to an increase in the degree of swelling with pH increase. When the permeation of three model drugs, salicylic acid, theophyline, and ornidazole, was studied using a static diffusion vessel, it followed a zero-order kinetics and increased with an increase in the CMCS content in the blend, a decrease in the molecular weight of drug, an increase in the pH of medium, and a decrease in the film thickness.
机译:研究了羧甲基壳聚糖(CMCS)/聚乙烯醇(PVA)混合膜在特定部位给药系统中作为涂料的应用。通过将不同量的4 wt%CMCS与4 wt%PVA混合,流延并在50摄氏度下干燥24小时来制备薄膜。薄膜的截面SEM显微照片显示,共混物中CMCS的增加导致薄膜在干燥状态下较不光滑,在水合状态下网络较不均匀且多孔,在50℃时变得可观%。在共混物中包含CMCS也使膜的溶胀与pH有关,并导致溶胀度随pH增加而增加。当使用静态扩散容器研究三种模型药物水杨酸,茶碱和奥硝唑的渗透时,其遵循零级动力学,并且随着共混物中CMCS含量的增加而增加,分子量降低药物的作用,介质pH的增加和膜厚度的减小。

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