Abstract
This work describes the stability and in vitro release of letrozole (drug)-loaded poly(lactic-
co
-glycolic acid) (PLGA) microparticles. To control the release capacity of the drug, the microparticles were fabricated with different ratios of biopolymer using solvent evaporation techniques. Further, the drug encapsulation efficiency, physicochemical properties, and morphologies were measured. In vitro release data of the drug were fitted to three theoretical models to evaluate the release kinetics. The highest correlation coefficient was found in Higuchi and Korsmeyer–Peppas that ensured the controlled release of the encapsulated drug from the microparticles. Scanning electron microscopy and Fourier-transform infrared spectroscopy analysis with gradual degradation time up to 80 days revealed the stability of PLGA, and stabilized the drug bioavailability.