Usefulness of microspheres composed of gelatin with various cross-linking density

被引:40
|
作者
Iwanaga, K
Yabuta, T
Kakemi, M
Morimoto, K
Tabata, Y
Ikada, Y
机构
[1] Osaka Univ Pharmaceut Sci, Dept Pharmaceut, Takatsuki, Osaka 5691094, Japan
[2] Hokkaido Coll Pharamacy, Dept Pharmaceut, Otaru, Hokkaido 0470264, Japan
[3] Kyoto Univ, Inst Frontier Med Sci, Dept Biomat, Sakyo Ku, Kyoto 6068507, Japan
关键词
gelatin; microsphere; cross-linking density; insulin; glutaraldehyde;
D O I
10.1080/02652040310001600523
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The release rate of insulin, as a model peptide, from gelatin microspheres (GM) prepared with gelatin having various cross-linking densities in vitro was examined. The release of insulin from GM showed the burst effect, followed by a slow release phase regardless of the cross-linking density of gelatin. The total amount of insulin released in 2 weeks decreased with increasing cross-linking density of gelatin. The release rate of insulin within 6 h was well correlated with the cross-linking density of gelatin. The remaining amounts of both insulin and GM after injection of insulin incorporated in GM to mice femoral muscle tissue were also examined in vivo . Both insulin and GM rapidly disappeared from the injection site within 1 day, and thereafter slowly disappeared over 14 days. The time courses of the remaining amounts were fairly similar to each other. Furthermore, the remaining amount of insulin 1 day after administration was well correlated with the cross-linking density of gelatin. These data suggest that insulin was released from GM with the degradation of GM in mice muscular tissue and that the release rate of insulin can be controlled by modifying the cross-linking density of gelatin. In conclusion, the control of the release rate of insulin from GM can be achieved under both in vitro and in vivo conditions by gelatin through the alteration of cross-linking conditions.
引用
收藏
页码:767 / 776
页数:10
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