Bovine serum albumin (BSA) was used to prepare microspheres and microc
apsules containing progesterone. The microparticles were obtained by m
eans of a multiple emulsion method and by thermal or chemical crosslin
king. The drug loading was higher for microspheres than microcapsules
and varied for the different crosslinking methods: higher with thermal
than chemical crosslinking and, among the chemical crosslinkers, load
ing was higher for formaldehyde than 2,3-butanedione and glutaraldehyd
e, respectively. Drug release was well differentiated for the differen
t systems: the microspheres released 60% of their content according to
an anomalous diffusion mechanism in the shorter periods, whereas micr
ocapsules released 60% of their content according to different kinetic
trends and for longer periods of time. The duration of each kinetic p
eriod and the relative drug fraction released, depends on the crosslin
king method (thermal or chemical) and the nature of the crosslinking a
gent. Among the systems examined, the glutaraldehyde crosslinked micro
spheres show the higher release rate while the thermally crosslinked m
icrocapsules had the lowest release rate which is characterized by the
longest lasting zero order period.