Factors affecting protein release behavior from surfactant-protein complexes under physiological conditions

被引:17
|
作者
Yoshiura, Hiromu
Hashida, Masakazu
Kamiya, Noriho
Goto, Masahiro
机构
[1] Kyushu Univ, Dept Appl Chem, Grad Sch Engn, Fukuoka 8190395, Japan
[2] Kyushu Univ, Ctr Future Chem, Fukuoka 8190395, Japan
关键词
drug delivery; emulsions; peptide drug; protein drug; protein release; protein stability; surfactant-protein complex;
D O I
10.1016/j.ijpharm.2007.01.041
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein release behavior from its complex with edible surfactants was investigated under physiological conditions using hen egg lysozyme and Aspergillus niger glucose oxidase as model proteins. It revealed that protein release rates could be controlled by hydrophobicity of surfactants and the molar ratio of proteins to surfactants in the preparation of the complexes. Evaluation of functional integrity of a protein on the basis of specific activity of an enzyme released from the complex suggested that lower hydrophobicity of surfactants led to higher retention of catalytic activity. In addition, it was found that protein release rates from the complexes were correlated with the aqueous droplet size of water-in-oil emulsions in the preparation of the complexes. The results suggest the potential of surfactant-protein complexes in pharmaceutical formulations for mucosal delivery of therapeutic proteins. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:174 / 179
页数:6
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