Brain-targeted delivery of protein using chitosan- and RVG peptide-conjugated, pluronic-based nano-carrier

被引:161
|
作者
Kim, Ja-Young [1 ,2 ]
Choi, Won Il [1 ,2 ]
Kim, Young Ha [3 ]
Tae, Giyoong [1 ,2 ]
机构
[1] Gwangju Inst Sci & Technol, Sch Mat Sci & Engn, Kwangju 500712, South Korea
[2] Gwangju Inst Sci & Technol, Dept Nanobio Mat & Elect, Kwangju 500712, South Korea
[3] Chung Ang Univ, Dept Chem, Seoul 156755, South Korea
基金
新加坡国家研究基金会;
关键词
Pluronic; Chitosan; BBB; Rabies virus glycoprotein (RVG); beta-galactosidase; IN-VITRO; NANOPARTICLES; BARRIER; THERAPEUTICS; TRANSDUCTION; SYSTEM;
D O I
10.1016/j.biomaterials.2012.09.047
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Brain-targeted delivery of drug or imaging agent is hard to achieve efficiently due to the infiltrative nature of the blood-brain barrier (BBB). Moreover, delivery of therapeutic proteins to brain tissue is further limited by the size and physic-chemical properties of proteins. In this work, we developed a chitosan-conjugated Pluronic-based nano-carrier with a specific target peptide for the brain (rabies virus glycoprotein; RVG29) and applied for the protein delivery to the brain. The in-vivo brain accumulation of the nano-carrier in mice followed i.v injection was optically monitored with Cy5.5-conjugation to the nano-carrier, and the result showed that the Pluronic-based nano-carrier conjugated with both chitosan and the peptide was very efficient for the accumulation in brain tissue and was remarkably better than the nano-carrier conjugated with the peptide only. beta-galactosidase, a model protein, was also delivered and accumulated efficiently in the brain by loading in the nano-carrier, analyzed by the bio-distribution of beta-galactosidase. The delivered protein in the brain also maintained its bioactivity. Therefore, RVG29- and chitosan-conjugated Pluronic-based nano-carrier could be potentially useful for the diagnosis and therapy of brain diseases. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1170 / 1178
页数:9
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