Formulation and optimization of Retapamulin loaded PLGA nanoparticles for burn wounds

Abstract

In the present study, PLGA nanoparticles (PLGA-NP) of retapamulin (RP) were prepared and optimized by studying the effect of various formulation and process variables for effective delivery at burn wound site. Drug loaded PLGA-NP were successfully prepared and characterized by TEM, XRD and DSC study. Formulation and process variables like surfactant concentration, drug concentration, polymer concentration etc. showed significant effect on the particle size, entrapment efficiency and drug loading. PLGA-NP exhibited prolonged drug release following Higuchi release kinetics (R2= 0.9907). In vitro study demonstrated systemic escape of drug from PLGA-NP which might eliminate side effects associated with topical exposure through conventional treatment. Further retention of activity of entrapped drug was confirmed by in vitro antimicrobial assay. Optimized PLGA nanoparticle of Retapamulin was incorporated into PVA-Chitosan hydrogel slurry and casted into film to prepare multiphase hydrogel.Thus, present optimized system can be effectively used for delivery of drug at burn wound site in especially compromised wounds.