Drug Loading and Release Behavior Depending on the Induced Porosity of Chitosan/Cellulose Multilayer Nanofilms

被引:47
作者
Park, Sohyeon [1 ]
Choi, Daheui [1 ]
Jeong, Hyejoong [1 ]
Heo, Jiwoong [1 ]
Hong, Jinkee [1 ]
机构
[1] Chung Ang Univ, Sch Chem Engn & Mat Sci, 84 Heukseok Ro, Seoul 06974, South Korea
关键词
polysaccharide; layer-by-layer; cross-linking; structural change; drug loading and release behavior; MESOPOROUS SILICA NANOPARTICLES; CROSS-LINKING; POLYELECTROLYTE MULTILAYERS; SURFACE MODIFICATION; PROTEIN RELEASE; THIN-FILM; DELIVERY; CHITOSAN; STABILITY; COLLAGEN;
D O I
10.1021/acs.molpharmaceut.7b00371
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The ability to control drug loading and release is the most important feature in the development of medical devices. In this research, we prepared a functional nanocoating technology to incorporate a drug-release layer onto a desired substrate. The multilayer films were prepared using chitosan (CHI) and carboxymethyl cellulose (CMC) polysaccharides by the layer-by-layer (LbL) method. By using chemical cross linking to change the inner structure of the assembled multilayer, we could control the extent of drug loading and release. The cross-linked multilayer film had a porous structure and enhanced water wettability. Interestingly, more of the small-molecule drug was loaded into and released from the non-cross-linked multilayer film, whereas more of the macromolecular drug was loaded into and released from the cross-linked multilayer film. These results indicate that drug loading and release can be easily controlled according to the molecular weight of the desired drug by changing the structure of the film.
引用
收藏
页码:3322 / 3330
页数:9
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