Pelepasan Ibuprofen dari Mikrokapsul Tersalut Paduan Lilin Lebah dan Poli(asam laktat) Secara In Vitro

Abstract

Ibuprofen as an anti-inflammatory drug has a short elimination rate which can causes gastric irritation. Microencapsulation technique can be used to overcome these problems and provide a better therapeutic efficacy through controlled drug release mechanism. In this research, microencapsulation of ibuprofen carried out by blending process and emulsion-solvent evaporation method. Ibuprofen was coated by blend beeswax and poly(lactic acid) (PLA) with various compositions (9:1, 8:2, 7:3, and 6:4) and concentration of gelatin (1%, 1.5%, and 2%) as an emulsifier. Efficiency of encapsulation performed in simulated intestinal medium pH 7.2. The highest value of ibuprofen encapsulation efficiencies was equal to 84.21% had been produced by microcapsules with ratio bees wax:PLA 6:4 and concentration of gelatin 2%. Release test of ibuprofen was performed by beeswax:PLA blend with ratio 8:2 and 6:4 produces the highest average percentage release about 15.31% and 19.25% at minute 225 in the same medium. The release pattern of ibuprofen had followed zero order kinetics model explaining that concentration of ibuprofen released relative constant for each release time. Observation of surface morphology of microcapsules using a scanning electron microscop (SEM) showed subtle bulges irregularly shaped scattered on its surface.