壳聚糖
聚电解质
阳离子聚合
海藻酸钙
肿胀 的
药物输送
微球
海藻酸钠
剂型
化学工程
分散性
材料科学
化学
钙
核化学
色谱法
钠
高分子化学
纳米技术
有机化学
聚合物
复合材料
工程类
作者
S.-B. Park,Hyeonsoo Kang,Seokjin Haam,H.-Y. Park,W.-S. Kim
标识
DOI:10.1080/02652040410001729269
摘要
Chitosan beads (CBs) incorporating Ca-alginate microspheres (CAMs), containing a drug, were prepared as an oral sustained delivery system. Stable and monodisperse Ca-alginate microspheres loaded with drug were obtained by a membrane emulsification method. The Ca-alginate microspheres were encapsulated in chitosan beads by the ionotropic gelation method with a polyelectrolyte complex reaction between two oppositely charged polyions. The surface and internal characteristics of the beads were improved by ionic cross-linking in tripolyphosphate (TPP) solution adjusted to pH 5.0. The release experiments were performed using lidocaine.HCl (cationic drug) and sodium salicylate (anionic drug) as model drugs. Initial release of drugs depended on the degree of swelling. Ca-alginate microspheres encapsulated in chitosan beads were superior to both drug-loaded CBs and CAMs beads for sustained release because they had a three-layer composition; a calcium alginate core bounded by an inter-phasic chitosan-alginate membrane, which itself was surrounded by a layer of chitosan-TPP.
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