摘要
Poly-γ-glutamic acid (γ-PGA) prepared by fermentation of microbe was used as drug carrier for vanadium sulfate to obtain vanadyl-poly-γ-glutamic acid (VO-γ-PGA) complex. The FI-IR spectrum of the complex demonstrated that the expected VO-γ-PGA complex is formed by the coordination of VO2+ through the side chain carboxylic groups of the γ-PGA. Studies of the complex in treating type I diabetes were carried out on alloxan induced diabetes rats. The results of treating the rats in 2 weeks and then stopping administration for 10 days showed that VO-γ-PGA can effectively lower blood glucose levels of diabetic rats during administration. But after ceasing treatment there were no differences between groups in blood glucose level and water intake. The results of oral glucose tolerance and some serum parameters also demonstrated that VO-γ-PGA was more effective than vanadium sulfate in treating diabetic rats.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 3041-3047 |
| 页数 | 7 |
| 期刊 | Journal of Pharmaceutical Sciences |
| 卷 | 99 |
| 期 | 7 |
| DOI | |
| 出版状态 | 已出版 - 7月 2010 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 3 良好健康与福祉
指纹
探究 'Effects of insulin-mimetic vanadyl-poly(γ-glutamic acid) complex on diabetic rat model' 的科研主题。它们共同构成独一无二的指纹。引用此
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