Synthesis of lipid-based amphiphilic block copolymer and its evaluation as nano drug carrier

被引:18
|
作者
Arshad, Muhammad [1 ]
Pradhan, Rehan A. [1 ]
Ullah, Aman [1 ]
机构
[1] Univ Alberta, Dept Agr Food & Nutr Sci, Edmonton, AB T6G 2P5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Fatty acids; Block copolymer; Self-assembly; Drug delivery; RADICAL POLYMERIZATION; FATTY-ACID; DELIVERY; MICELLES; NANOPARTICLES; PEG; FLUORESCENCE; DOXORUBICIN; BEHAVIOR; SOLVENT;
D O I
10.1016/j.msec.2017.03.109
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In current study, we report the synthesis and characterization of renewable fatty acid-based block copolymer. The block copolymer was synthesized via RAFT polymerization under microwave irradiations. Firstly, the homopolymer of N,N-dimethylacrylamide (DMA) was prepared and used as a macro-CTA to copolymerize with modified stearic acid monomer (SAM). The characterization of copolymer p-DMA-b-SAM was done by H-1 NMR, ATR-FTIR and GPC. The block copolymer was allowed to self-assemble and the entrapment of carbamazepine (CBZ) into hydrophobic core of polymeric micelles was investigated in aqueous media. A high drug entrapment efficiency (69%) was observed for block copolymer micelles. The spherical appearance of micelles in the size range of 20-70 nm was determined with transmission electron microscopy (TEM). An effort was also made to investigate the in vitro release profile of CBZ from micelles. A sustained drug release rate was observed, showing complete release of drug within 70 h. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:217 / 223
页数:7
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