Pulsatile Protein Release from Monodisperse Liquid-Core Microcapsules of Controllable Shell Thickness

被引:15
|
作者
Xia, Yujie [1 ]
Pack, Daniel W. [2 ,3 ]
机构
[1] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[2] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
[3] Univ Kentucky, Dept Pharmaceut Sci, Lexington, KY 40536 USA
关键词
bovine serum albumin; controlled release; monodisperse microcapsules; poly( lactide-co-glycolide); pulsatile release; DOUBLE-WALLED MICROSPHERES; DRUG-DELIVERY; PLG MICROSPHERES; POLYMER MATRICES; GENE-THERAPY; DEGRADATION; DOXORUBICIN;
D O I
10.1007/s11095-014-1412-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pulsatile delivery of proteins, in which release occurs over a short time after a period of little or no release, is desirable for many applications. This paper investigates the effect of biodegradable polymer shell thickness on pulsatile protein release from biodegradable polymer microcapsules. Using precision particle fabrication (PPF) technology, monodisperse microcapsules were fabricated encapsulating bovine serum albumin (BSA) in a liquid core surrounded by a drug-free poly(lactide-co-glycolide) (PLG) shell of uniform, controlled thickness from 14 to 19 mu m. When using high molecular weight PLG (Mw 88 kDa), microparticles exhibited the desired core-shell structure with high BSA loading and encapsulation efficiency (55-65%). These particles exhibited very slow release of BSA for several weeks followed by rapid release of 80-90% of the encapsulated BSA within 7 days. Importantly, with increasing shell thickness the starting time of the pulsatile release could be controlled from 25 to 35 days. Biodegradable polymer microcapsules with precisely controlled shell thickness provide pulsatile release with enhanced control of release profiles.
引用
收藏
页码:3201 / 3210
页数:10
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