Title of article :
Preparation, Statistical Optimization and Characterization of Propolis-Loaded Solid Lipid Nanoparticles Using Box-Behnken Design
Author/Authors :
Taherzadeh ، Sahar Department of Pharmaceutics - Faculty of Pharmacy - Hamadan University of Medical Sciences , Naeimifar ، Atefeh Department of Pharmaceutics - Faculty of Pharmacy - Tehran University of Medical Sciences , Mehrabani Yeganeh ، Ehsan Department of Pharmaceutics - Faculty of Pharmacy - Hamadan University of Medical Sciences , Esmaili ، Zahra Department of Pharmaceutics - Faculty of Pharmacy - Tehran University of Medical Sciences , Mahjoub ، Reza Department of Pharmaceutics - Faculty of Pharmacy - Hamadan University of Medical Sciences , Akbari Javar ، Hamid Department of Pharmaceutics - Faculty of Pharmacy - Tehran University of Medical Sciences
Abstract :
Purpose: Propolis is a resinous material obtained by honeybees with many biological and pharmacological properties which can be used for treatment of various diseases. Current study aims to formulate and characterize propolis-loaded solid lipid nanoparticles (SLNs) carrier system. Methods: The prepared SLNs, composed of glyceryl monostearate (GMS), Soy lecithin, Tween 80 and polyethylene glycol 400 (PEG 400), were fabricated employing solvent emulsificationevaporation technique. In addition, the impact of several variables including concentration ratios of GMS/Soy lecithin and PEG 400/Tween 80 along with emulsification time were evaluated on the size, polydispersity index (PDI) and zeta potential of particles. SLN formulations were optimized using Box-Behnken design. The particles were freeze dried and morphologically studied by scanning electron microscopy (SEM). The in-vitro release profile of propolis entrapped in the optimized nanoparticles was investigated. Results: The mean particle size, PDI, zeta potential, entrapment efficiency (EE) and loading efficiency (LE) of optimized propolis-loaded SLNs were found to be 122.6±22.36 nm, 0.28±0.06, -26.18±3.3 mV, 73.57±0.86% and 3.29±0.27%, respectively. SEM images exhibited nanoparticles to be non-aggregated and in spherical shape. The in-vitro release study showed prolonged release of propolis from nanoparticles. Conclusion: The results implied that the proposed way of SLN preparation could be considered as a proper method for production of propolis loaded colloidal carrier system.
Keywords :
Propolis , Solid lipid nanoparticles (SLN) , Drug delivery , Solvent emulsification , evaporation method , Box , Behnken design
Journal title :
Advanced Pharmaceutical Bulletin
Journal title :
Advanced Pharmaceutical Bulletin