Collagen/chitosan film containing biotinylated glycol chitosan nanoparticles for localized drug delivery

被引:29
作者
Chen, Ming-Mao [1 ]
Huang, Yu-Qing [1 ]
Cao, Huan [1 ]
Liu, Yan [2 ]
Guo, Hao [1 ]
Chen, Lillian S. [1 ]
Wang, Jian-Hua [1 ]
Zhang, Qi-Qing [1 ,3 ,4 ]
机构
[1] Fuzhou Univ, Inst Biomed & Pharmaceut Technol, Fuzhou 350002, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[3] Chinese Acad Med Sci, Inst Biomed Engn, Key Lab Biomed Mat Tianjin, Tianjin 300192, Peoples R China
[4] Peking Union Med Coll, Tianjin 300192, Peoples R China
基金
中国国家自然科学基金;
关键词
Collagen; Drug film; Silver carp skin; Glycol chitosan; Self-assembled nanoparticles; SELF-ASSEMBLED NANOPARTICLES; AGGREGATED NANOPARTICLES; CONTROLLED-RELEASE; SKIN; MICROSPHERES; COLLAGENS; CONJUGATE; MEMBRANES; ALBUMIN; ACID;
D O I
10.1016/j.colsurfb.2015.02.024
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
The objective of this study was to design a drug delivery system consisting of biotinylated cholesterol-modified glycol chitosan (Bio-CHGC) nanoparticles and fish collagen/chitosan (Col/Ch) film for localized chemotherapy. Bio- CHGC was synthesized, and then its self-assembled nanoparticles were prepared by probe sonication. Doxorubicin (DOX)-loaded Bio-CHGC (DBC) nanoparticles prepared by dialysis had spherical shape, and their sizes were in the range of 330-397 nm. Col/Ch/DBC nanoparticle films were fabricated by freeze-drying. SEM showed that the DBC nanoparticles were uniformly distributed into the films, and the films retained their structural integrity. A higher degradation and swelling rate of the drug films led to a higher diffusion rate of the nanoparticles from the films, resulting in an increase in the drug release from nanoparticles. The release of DOX from the films or Bio-CHGC nanoparticles was sensitive to the pH value of the release medium. In addition, the DOX release ratio of the drug,films was lower than that of the nanoparticles alone, suggesting that the drug films had a double-sustained effect on the drug release. MTT assay implied that the DBC nanoparticle film showed a higher inhibitory ratio than the film containing nanoparticles without biotin, indicating that biotin moieties in the nanoparticles played an important role in exerting a cytotoxic effect. These data demonstrate that Col/Ch/DBC nanoparticle film has the potential to be used as a localized delivery system for hydrophobic antitumor drugs. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:339 / 346
页数:8
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