Development of drug-loaded polymer microcapsules for treatment of epilepsy

被引:14
|
作者
Chen, Yu [1 ]
Gu, Qi [1 ,2 ]
Yue, Zhilian [1 ]
Crook, Jeremy M. [1 ,3 ,4 ]
Moulton, Simon E. [5 ]
Cook, Mark J. [1 ,6 ,7 ]
Wallace, Gordon G. [1 ]
机构
[1] Univ Wollongong, AIIM Facil, Intelligent Polymer Res Inst, ARC Ctr Excellence Electromat Sci, Innovat Campus,Northfields Ave, Wollongong, NSW 2522, Australia
[2] Chinese Acad Sci, Inst Zool, State Key Lab Stem Cell & Reprod Biol, 1 Beichen West Rd, Beijing 100101, Peoples R China
[3] Univ Melbourne, St Vincents Hosp, Dept Surg, 35 Victoria Parade, Fitzroy, Vic 3065, Australia
[4] Univ Wollongong, Illawarra Hlth & Med Res Inst, Wollongong, NSW 2522, Australia
[5] Swinburne Univ Technol, ARC Ctr Excellence Electromat Sci, Fac Sci Engn & Technol, Hawthorn, Vic 3122, Australia
[6] St Vincents Hosp, Clin Neurosci, 5th Floor,Daly Wing,35 Victoria Parade, Fitzroy, Vic 3065, Australia
[7] Univ Melbourne, St Vincents Hosp, Dept Med, 35 Victoria Parade, Fitzroy, Vic 3065, Australia
基金
澳大利亚研究理事会;
关键词
BLOOD-BRAIN-BARRIER; ACID) COMPOSITE NANOFIBERS; TEMPORAL-LOBE EPILEPSY; ANTIBACTERIAL ACTIVITY; CONTROLLED-RELEASE; ELECTROSPUN NANOFIBERS; SOLVENT EVAPORATION; DELIVERY-SYSTEMS; MICROSPHERES; THERAPY;
D O I
10.1039/c7bm00623c
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
Despite significant progress in developing new drugs for seizure control, epilepsy still affects 1% of the global population and is drug-resistant in more than 30% of cases. To improve the therapeutic efficacy of epilepsy medication, a promising approach is to deliver anti-epilepsy drugs directly to affected brain areas using local drug delivery systems. The drug delivery systems must meet a number of criteria, including high drug loading efficiency, biodegradability, neuro-cytocompatibility and predictable drug release profiles. Here we report the development of fibre-and sphere-based microcapsules that exhibit controllable uniform morphologies and drug release profiles as predicted by mathematical modelling. Importantly, both forms of fabricated microcapsules are compatible with human brain derived neural stem cells and differentiated neurons and neuroglia, indicating clinical compliance for neural implantation and therapeutic drug delivery.
引用
收藏
页码:2159 / 2168
页数:10
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