M. Fresta et al., INTRACELLULAR ACCUMULATION OF OFLOXACIN-LOADED LIPOSOMES IN HUMAN SYNOVIAL FIBROBLASTS, Antimicrobial agents and chemotherapy, 39(6), 1995, pp. 1372-1375
In order to incorporate ofloxacin within liposomes, the reverse-phase
evaporation technique was carried out, The liposome lipid matrix consi
sted of osphatidylcholine-cholesterol-dihexadecylphosphate (4:3:4 mola
r ratio). The liposome formulation presented a mean size of 185 +/- 31
nm and had an encapsulation capacity of 5.3 mu l/mu mol. The liposome
formulation was able to deliver ofloxacin into McCoy cells in a great
er amount (2.6-fold) than the free drug, improving antibiotic accumula
tion.