Encapsulation of protein nanoparticles into uniform-sized microspheres formed in a spinning oil film

被引:35
|
作者
Leach, WT
Simpson, DT
Val, TN
Yu, ZS
Lim, KT
Park, EJ
Williams, RO
Johnston, KP [1 ]
机构
[1] Univ Texas, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas, Coll Pharm, Div Pharmaceut, Austin, TX 78712 USA
[3] Pukyong Natl Univ, Div Image & Informat Engn, Pusan 608739, South Korea
关键词
microsphere size control; monodisperse emulsions; spray freezing into liquid process; bovine serum albumin; solid-in-oil-in-oil processing; PLGA; initial burst;
D O I
10.1208/pt060475
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A new spinning oil film (SOF) solid-in-oil-in-oil emulsion process was developed to produce uniform-sized protein-loaded biodegradable microspheres. A thin SOF on a cylindrical rotor was used to shear droplets from a nozzle tip to control droplet size. The resulting microspheres with low polydispersity (6%) produced a low burst (6%-11%) release even at high loadings (13%-18% encapsulated solids, 8%-12% protein). The SOF process had a high yield and did not require the presence of water, which can cause protein denaturation, or surfactants, which may be unwanted in the final product. Amorphous protein and crystalline excipient solids were encapsulated into 3 different polymers, giving a homogenous drug distribution throughout the microspheres, and an essentially complete protein encapsulation efficiency (average = 99%). In contrast, large burst release was observed for polydisperse microspheres produced by a conventional emulsification technique, particularly for microspheres smaller than 25 mu m in diameter, which gave 93% burst at 15% loading. The uniform encapsulation of high loadings of proteins into microspheres with low polydispersity in an anhydrous process is of practical interest in the development of controlled-release protein therapeutics.
引用
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页数:13
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