Encapsulation of clotrimazole into solid lipid nanoparticles by microwave-assisted microemulsion technique

Recently, we reported a novel microwave-assisted one-pot microemulsion procedure for the production of solid lipid nanoparticles (SLN5). In the current study, the suitability of the microwave-assisted procedure in encapsulation of clotrimazole was investigated. Clotrimazole, a synthetic, imidazole-type anti-fungal drug, was used as lipophilic model drug. The particle sizes of microwave-produced stearic acid-based clotrimazole-loaded SLN5 were within the nanometer size range with zeta potential values high enough to predict good physical stability. High encapsulation efficiency and loading capacity demonstrated the high encapsulation capability of microwave-produced SLN5. Physicochemical characterization of SLN5 and bulk stearic acid, performed by differential scanning calorimetry (DSC) and X-ray diffraction (XRD), indicated decreased crystallinity of stearic acid, a factor that influences incorporation and release of drug. The release studies demonstrated a slow and sustained but incomplete release of drugs (<50% after 12 h and <70% after 24 h). The release of clotrimazole was found to be governed by both diffusion and swelling, i.e. anomalous or non-Fickian diffusion. The release data, however, fitted more appropriately to the Weibull model. The clotrimazole-loaded SLN5 were found to be non-toxic, investigated by cell viability assays using human epithelial A549 and mouse epithelial 3T3-L1 cell lines. The cytotoxic concentration (CC50) value was greater than 100 mu g/mL. Internalization of SLN5 into A549 cells by endocytosis was demonstrated by confocal imaging. The antifungal efficacy of drug-loaded SLN5 was evaluated on Candida albicans. These encouraging results suggest that microwave-produced SLN5 can be considered as efficient carriers for clotrimazole and will further assist their development for administration via different routes. Crown Copyright (C) 2016 Published by Elsevier Ltd. All rights reserved.