The pentapeptide thymopentin was englobed in solid lipid nanoparticles
prepared from warm microemulsions following two different methods: fr
om O/W microemulsion by forming the more lipophilic ion-pair with hexa
decylphosphate, and from W/O/W microemulsion by dissolving the pentape
ptide in the aqueous internal phase. The incorporation of the hydrophi
lic drug was 5.2% and 1.7% respectively; in both cases, the in vitro r
elease of thymopentin from the solid lipid nanoparticles followed a ps
eudo-zero-order kinetics.