Article ID Journal Published Year Pages File Type
7869096 Materials Science and Engineering: C 2016 6 Pages PDF
Abstract
The analyses of detailed structure characterized by TEM and DLS confirmed the nano-size of the particle 10-20 nm and FTIR confirmed for antileishmanial drug encapsulation in to PLGA-PEG. The dose of miltefosine is decreased by fifty percent as the IC50 value is decreased from 0.2 to 0.1 μg. Further inhibitions of amastigotes in the splenic tissue with these nanoparticles are significantly more than the conventional miltefosine and PLGA-PEG encapsulated Amphoterecin B (23.21 ± 23/89.09 ± 52.7/92.12 ± 55.1).63
Related Topics
Physical Sciences and Engineering Materials Science Biomaterials
Authors
, , , , , , , ,