V.Viswanath1*, B. Narasimha Rao1, K. Gnana prakash1, D. Sai Padmini2, B. Gowthami1
Solid lipid nanoparticles (SLN) were novel colloidal drug carrier systems offering controlled release profiles for many pharmaceutically active agents. The objective of present research work was to develop Tolnaftate-solid lipid nanoparticles using solid lipid as drug carrier. As the drug was inactive orally, it was delivered by topical route. Hot homogenization along with ultrasonication were used for such purpose. Then they were converted to gel. The drug compatibility was checked by using FTIR studies. Seven different formulations were prepared by variable concentrations of lipids and its effect on drug loading was studied. Produced Tolnaftate- SLN gels were evaluated for the parameters like Homogenity, Spreadability, Viscosity, pH, Drug content, Entrapment Efficiency, invitro drug release & invitro drug permeation studies. Antifungal activity of the optimized formulation (F7) was also studied. Tolnaftate -SLNs have good potential in treating topical fungal infections.
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