Abstract:
The potential of chitosan microparticles as a carrier of doxorubicin for the treatment of visceral leishmaniasis was evaluated by macrophage mediated drug targeting approach. Cationic charge of doxorubicin was masked by complexing it with dextran sulfate (a poly anion) in order to facilitate its incorporation into cationic chitosan microparticles. Prior to in vitro and in vivo studies, characterization studies were carried out systematically: particle size distribution (~ 1.049 µm), surface morphology (fluorescence microscopy- spherical structured microparticles), FTIR (to characterize effective cross-linking) and differential scanning calorimetry. In vitro studies were carried out in J774.1 in order to check the effective endocytotic uptake of microparticles by macrophages. In vivo studies were conducted in syrian golden hamsters as per well established protocols and the results drawn from in vivo studies displayed substantial reduction in leishmanial parasite load for doxorubicin encapsulated chitosan microparticles: ~78.2±10.4%, when compared to the control (free doxorubicin): 33.3±2.4%.
