壳聚糖
聚电解质
肿胀 的
化学
聚合物
药物输送
复合数
傅里叶变换红外光谱
共聚物
材料科学
溶解
毒品携带者
自愈水凝胶
化学工程
高分子化学
核化学
有机化学
复合材料
工程类
作者
Yu Chen,Xiaoting Yan,Jian Zhao,Huaiyu Feng,Puwang Li,Zongrui Tong,Ziming Yang,Sidong Li,Jueying Yang,Shaohua Jin
标识
DOI:10.1016/j.carbpol.2018.02.065
摘要
In the current study, a novel semi-dissolution/acidification/sol-gel transition (SD-A-SGT) method was explored for the preparation of polyelectrolyte complexing (PEC) composite hydrogels with natural polymers only. A chitosan (CS) powder was uniformly dispersed in a solution of poly(glutamic acid) (PGA) and alginate (SA) to form a semi-dissolved slurry mixture that was then exposed to an gaseous acidic atmosphere. CS was gradually dissolved and interacted with PGA and SA to form a CS/PGA/SA PEC composite hydrogel with a homogeneous structure. The SD-A-SGT procedure was able to overcome the shortcomings of direct mixing method via the PEC interaction. The effects of the hydrogel composition on its structure and properties were investigated by FTIR, XRD, rheology study, XPS, SEM, and swelling kinetics. The drug delivery performance of the CS/PGA/SA hydrogel was explored using piroxicam (PXC) as a model drug. PXC was in situ embedded in the hydrogel by the SD-A-SGT method. The hydrogel exhibited pH responsive drug release behaviors that were affected by the hydrogel composition. In all, the SD-A-SGT method for preparing PEC composite hydrogels has a great application potential in constructing the CS based hydrogels as medical materials.
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