Co-lyophilization of bovine serum albumin (BSA) with poly(ethylene glycol) improves efficiency of BSA encapsulation and stability in polyester microspheres by a solid-in-oil-in-oil technique
被引:18
作者:
Al-Azzam, W
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机构:Univ Puerto Rico, Dept Chem, San Juan, PR 00931 USA
Al-Azzam, W
Pastrana, EA
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h-index: 0
机构:Univ Puerto Rico, Dept Chem, San Juan, PR 00931 USA
Pastrana, EA
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机构:
Griebenow, K
机构:
[1] Univ Puerto Rico, Dept Chem, San Juan, PR 00931 USA
[2] Univ Puerto Rico, Dept Biol, San Juan, PR 00931 USA
drug delivery;
protein aggregation;
protein stability;
sustained release;
D O I:
10.1023/A:1019881505734
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The effect of the co-lyophilization of bovine serum albumin (BSA) with poly(ethylene glycol) (PEG) on the BSA encapsulation efficiency and formation of soluble BSA aggregates upon solid-in-oil-in-oil (s/o/o) encapsulation in poly(lactic-co-glycolic) acid (PLGA) microspheres was investigated. Suspension of the lyophilized BSA-PEG formulations in methylene chloride produced small protein powder particles of less than 1 mum diam. and this afforded high encapsulation efficiencies of typically greater than or equal to90% ameliorating one of the problems in s/o/o encapsulation. Formation of soluble BSA aggregates upon s/o/o encapsulation followed by 24 h in vitro release was between 5% and 22%, much lower than values of 59% reported for BSA without stabilizing excipients. Therefore, PEG also afforded BSA stabilization during s/o/o encapsulation. Sustained release occurred over ca. 2 months and was complete.