Itraconazole in cyclodextrin solution

被引:91
作者
Stevens, DA
机构
[1] Santa Clara Valley Med Ctr, Dept Med, Div Infect Dis, San Jose, CA 95128 USA
[2] Calif Inst Med Res, San Jose, CA 95128 USA
[3] Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA
来源
PHARMACOTHERAPY | 1999年 / 19卷 / 05期
关键词
D O I
10.1592/phco.19.8.603.31529
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Itraconazole, a water-insoluble oral triazole antifungal, has been formulated in cyclodextrin as a solution. Cyclodextrin is a ring of glucose molecules that can accept a lipophilic guest molecule within the ring. This enables solubilization and delivery to the lipid interface of the gut lumen, resulting in absorption of the guest molecule without absorption of the ring. This new system enhances the absorption of itraconazole. Improved blood and tissue levels of itraconazole and topical effect in mucosal disease should result in greater efficacy for a variety of indications, particularly patients with gastroenteropathy in whom absorption of earlier preparations was sometimes problematic.
引用
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页码:603 / 611
页数:9
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