Hepatotoxicity is the most serious adverse effect of rifampicin (RIF). We aimed to investigate the potential hepatoprotective effect of mannose-functionalized poly(lactic-co-glycolic acid)(PLGA)/RIF nanoparticles (NPs) in rats as a possible promising approach to minimize RIF-induced hepatotoxicity. Mannose-functionalized PLGA/RIF NPs were fabricated and characterized , then the hepatoprotective effect of optimized NPs was studied on rat and cell culture models.
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