黏膜黏附
壳聚糖
聚合物
儿茶酚
药物输送
部分
表面改性
材料科学
生物粘附
化学改性
组合化学
胶粘剂
高分子化学
化学
纳米技术
有机化学
复合材料
图层(电子)
物理化学
作者
Kyuri Kim,Keumyeon Kim,Ji Hyun Ryu,Haeshin Lee
出处
期刊:Biomaterials
[Elsevier BV]
日期:2015-02-24
卷期号:52: 161-170
被引量:277
标识
DOI:10.1016/j.biomaterials.2015.02.010
摘要
Numerous mucoadhesive polymers have been exploited for prolonging the residence time of formulated drugs or pharmaceuticals at specific delivery sites. However, it has been difficult to achieve satisfactory mucoadhesive properties. The two major modification strategies such as thiolation or lectin functionalization have been extensively studied, but disulfide bond reversibility in the case of thiolation and the toxicity of lectins have been problems. Thus, approaches for further improvement of mucoadhesive properties need to be developed. With an overwhelming library of mucoadhesive polymers, one practical way to improve mucoadhesion is chemical modification of existing mucoadhesive polymers. In other words, the method is based on utilizing the cooperative effect that might be achieved by chemical tethering of a small adhesive moiety to an available mucoadhesive polymer. Here, we conjugated catechols derived from mussel adhesive proteins to chitosan, which is a widely known mucoadhesive polymer. We demonstrated that the gastrointestinal (GI) tract retention of chitosan-catechol was improved compared to unmodified chitosan, which is due to the formation of irreversible catechol mediated-crosslinking with mucin. The results indicate that catechol modification of mucoadhesive polymers may possibly lead to a new generation of mucoadhesive polymers for mucosal drug delivery.
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