| Literature DB >> 29784509 |
Asim Halder1, Divanshu Shukla2, Suvadra Das1, Partha Roy3, Arup Mukherjee4, Bhaskar Saha5.
Abstract
Visceral Leishmaniasis (VL), caused by the protozoan parasite Leishmania donovani, is a potentially fatal disease. The only orally bioavailable drug miltefosine is toxic and the effective liposomal Amphotericin B (AmBisome) is limited by its prohibitive cost and requirement for parenteral administration. Therefore, finding a new potential drug candidate and an alternative delivery system is imperative. We report that Betulinic acid (BA), a pentacyclic triterpenoid from Betula alba bark, was loaded onto uniformly spherical PLGA nanoparticles (BANPs; diameter 187.5 ± 5.60 nm) coated with Lactoferrin (Lf-BANPs). The amastigotes count in macrophages was more effectively reduced by Lf-BANP than BA and BANP. Lf-BANPs reduced the pro-parasitic, anti-inflammatory cytokine IL-10, but increased nitric oxide (NO), production in L. donovani-infected macrophages indicating that Lf-BANP possesses a significant anti-leishmanial activity.Entities:
Keywords: Betulinic acid; Cytokine; Lactoferrin; Leishmania; Macrophage; PLGA nanoparticles
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Year: 2018 PMID: 29784509 DOI: 10.1016/j.cyto.2018.05.010
Source DB: PubMed Journal: Cytokine ISSN: 1043-4666 Impact factor: 3.861