Synthesis, characterization and in vivo drug delivery study of a biodegradable nano-structured molecularly imprinted polymer based on cross-linker of fructose

被引:41
作者
Asadi, Ebadullah [1 ]
Abdouss, Majid [1 ]
Leblanc, Roger M. [2 ]
Ezzati, Noushin [3 ]
Wilson, James N. [2 ]
Kordestani, Davood [1 ]
机构
[1] Amirkabir Univ Technol, Dept Chem, POB 15875-4413, Tehran, Iran
[2] Univ Miami, Dept Chem, Coral Gables, FL 33124 USA
[3] Islamic Azad Univ, Saveh Branch, Young Researchers & Elite Club, Saveh, Iran
关键词
Targeting drug delivery; Biodegradable; Controlled drug release; SELECTIVE RECOGNITION; VITRO DEGRADATION; EXTRACTION; OLANZAPINE; ACID; NANOPARTICLES; CHLORAMPHENICOL; ADSORPTION; NETWORKS; CARRIERS;
D O I
10.1016/j.polymer.2016.05.031
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, a new biodegradable cross-linker agent based on fructose was reported for fabrication of brain targeted molecularly imprinted polymer (MIP). The applied strategy for targeting drug delivery was based on two mechanisms. Firstly, the magnetic structure of prepared MIP which facilitates the aggregation of carrier near target tissue under magnetic field. Second, the tendency of brain cell to use the produced fructose during degradation of MIP as fuel. In synthesis procedure magnetic fluorescent multi core shell structure MIP was prepared via co-precipitation polymerization in the presence of olanzapine as template and fructose with double acts, as monomer and cross-linker. Various kinds of in vitro and in vivo experiments were carried out to indicate the considered properties of carrier. The obtained data confirmed the designed carrier olanzapine satisfactorily meet the requirement in brain drug delivery application. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:226 / 237
页数:12
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