Accelerating protein release from microparticles for regenerative medicine applications

被引:55
|
作者
White, Lisa J. [1 ]
Kirby, Giles T. S. [1 ]
Cox, Helen C. [1 ]
Qodratnama, Roozbeh [1 ]
Qutachi, Omar [1 ]
Rose, Felicity R. A. J. [1 ]
Shakesheff, Kevin M. [1 ]
机构
[1] Univ Nottingham, Sch Pharm, Nottingham NG7 2RD, England
基金
英国生物技术与生命科学研究理事会;
关键词
Poly; (D; L-lactic -co-glycolic acid) (PLGA); Microparticles; Microspheres; Controlled release; Double emulsion solvent evaporation; Growth factor delivery; BONE MORPHOGENETIC PROTEIN; IN-VITRO; SPATIOTEMPORAL DELIVERY; PLGA MICROSPHERES; CO-ENCAPSULATION; GROWTH-FACTORS; STABILITY; LYSOZYME; DEGRADATION; POLYMERS;
D O I
10.1016/j.msec.2013.02.020
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
There is a need to control the spatio-temporal release kinetics of growth factors in order to mitigate current usage of high doses. A novel delivery system, capable of providing both structural support and controlled release kinetics, has been developed from PLGA microparticles. The inclusion of a hydrophilic PLGA-PEG-PLGA triblock copolymer altered release kinetics such that they were decoupled from polymer degradation. A quasi zero order release profile over four weeks was produced using 10% w/w PLGA-PEG-PLGA with 50:50 PLGA whereas complete and sustained release was achieved over ten days using 30% w/w PLGA-PEG-PLGA with 85:15 PLGA and over four days using 30% w/w PLGA-PEG-PLGA with 50:50 PLGA. These three formulations are promising candidates for delivery of growth factors such as BMP-2, PDGF and VEGF. Release profiles were also modified by mixing microparticles of two different formulations providing another route, not previously reported, for controlling release kinetics. This system provides customisable, localised and controlled delivery with adjustable release profiles, which will improve the efficacy and safety of recombinant growth factor delivery. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:2578 / 2583
页数:6
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