Formulation of amphotericin B as nanosuspension for oral administration

被引:138
作者
Kayser, O
Olbrich, C
Yardley, V
Kiderlen, AF
Croft, SL
机构
[1] Free Univ Berlin, Inst Pharm Pharmazeut Technol Biopharm & Biotechn, D-12169 Berlin, Germany
[2] Robert Koch Inst, D-13353 Berlin, Germany
[3] London Sch Hyg & Trop Med, London WC1 7HT, England
关键词
amphotericin; Leishmania; nanosuspension; oral;
D O I
10.1016/S0378-5173(02)00686-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Amphotherin B was formulated in a nanosuspension as a new oral drug delivery system for the treatment of experimental visceral leishmaniasis. Amphotericin B (AmB) nanosuspensions were produced by high pressure homogenisation obtaining particles with a PCs diameter of 528 nm. Environmental stability was determined in artificial gastrointestinal fluids at different pH and electrolyte concentrations. In vivo efficacy was determined in a mouse model of visceral leishmaniasis. Following oral administration (5 mg kg(-1)), micronised amphotericin B did not show any curative effect. However, administrations of amphotericin B nanosuspension, reduced liver parasite load by 28.6% compared to untreated controls. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:73 / 75
页数:3
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