a comparative cytotoxic evaluation of disulfiram encapsulated plga nanoparticles on mcf-7 cells

background: disulfiram is oral aldehyde dehydrogenase (aldh) inhibitor that has been used in the treatment of alcoholism. recent studies show that this drug has anticancer properties; however, its rapid degradation has limited its clinical application. encapsulation of disulfiram polymeric nanoparticles (nps) may improve its anticancer activities and protect rapid degradation of the drug. materials and methods: a poly (lactide-co-glycolide) (plga) was developed for encapsulation of disulfiram and its delivery into breast cancer cells. disulfiram encapsulated plga nps were prepared by nanoprecipitation method and were characterized by scanning electron microscopy (sem). the loading and encapsulation efficiency of nps were determined using uv-visible spectroscopy. cell cytotoxicity of free and encapsulated form of disulfiram is also determined using mtt assay. results: disulfiram encapsulated plga nps had uniform size with 165 nm. drug loading and entrapment efficiency were 5.35 ±0.03% and 58.85±1.01%. the results of mtt assay showed that disulfiram encapsulated plga nps were more potent in induction of apoptosis compare to free disulfiram. conclusion: based on the results obtained in the present study it can be concluded that encapsulation of disulfiram with plga can protect its degradation in improve its cytotoxicity on breast cancer cells.