Development of PLGA-PEG encapsulated miltefosine based drug delivery system against visceral leishmaniasis
详细信息    查看全文
文摘

Synthesis of PLGA-PEG encapsulated miltefosine nanoparticles has been done.

An IC50 value of PPEM (0.1 ug/ml), miltefosine (0.2 μg/ml) and AmpB (1 μg/ml) were observed two fold better efficacies.

Inhibition of amastigotes of PPEM (23.21 ± 23) was significantly more than miltefosine (89.22 ± 52.7) and AmpB (94.12 ± 55.1).

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700