IMPROVED THERAPY OF EXPERIMENTAL LEISHMANIASIS BY USE OF A LIPOSOME-ENCAPSULATED ANTIMONIAL DRUG

被引:93
作者
ALVING, CR
STECK, EA
HANSON, WL
LOIZEAUX, PS
CHAPMAN, WL
WAITS, VB
机构
[1] WALTER REED ARMY INST RES,DIV MED CHEM,WASHINGTON,DC 20012
[2] UNIV GEORGIA,COLL VET MED,DEPT PARASITOL,ATHENS,GA 30602
关键词
D O I
10.1016/0024-3205(78)90270-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The anti-leishmanial antimonial drug meglumine antimoniate (Glucantime ®) was incorporated into liposomes, and was tested for effects against experimental leishmanial infection in hamsters. When the hamsters had been infected for a short period before treatment (3 days), treatment doses of 416 mg/kg of free meglumine antimoniate, or 4 mg/kg of liposome-encapsulated drug, each gave 99.8% suppression of parasites. After 10 or 17 days of infection prior to treatment liposome-encapsulated compound was more than 300 times as effective as the antimonial drug alone. Use of liposomes containing appropriate drugs is proposed as a markedly superior means to treat certain chronic intracellular parasitic infections. © 1978.
引用
收藏
页码:1021 / 1026
页数:6
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