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Preeti Irny*, Ratan S. Tone, Namdeo R. Jadhav Department if pharmaceutics,Bharati vidyapeeth college of pharmacy, Near Chitranagari, Kolhapur 416013, India. Email: preetie_88@yahoo.co.in Abstract The present investigation was aimed at developing and exploring the use of mannosylated gelatin nanoparticles for the selective delivery of an anti-HIV drug, Zidovudine. Zidovudine (AZT) is an antiretroviral agent used in treatment of AIDS having low biological half life (0.5-3hrs) with numerous dose dependant side effects and thus it is good candidate for the formulation of sustained release dosage forms.The mannosylated gelatin nanoparticles (MN-G-NPs) were prepared using a two-step desolvation technique and coupled with mannose using the amino group of gelatin present on the surface of nanoparticles. The mannosylation was confirmed using infrared spectroscopy. MN-G-NPs were characterized for shape, particle size, zeta potential, and percentage drug entrapment. The size of nanoparticles was found to be in range of 200-800 nm. In-Vitro drug release studies showed release up to 79.98% to 88.04% up to 18 hrs .Coupling of the nanoparticles with mannose significantly enhances the lung, liver, and lymph nodes uptake of drug, could possibility be advantageous in reducing viral load with efficacy. increased therapeutic