Fresta M, Spadaro A, Cerniglia G, Ropero I M, Puglisi G, Furneri P M
Institute of Pharmaceutical and Toxicological Chemistry, Catania, Italy.
Antimicrob Agents Chemother. 1995 Jun;39(6):1372-5. doi: 10.1128/AAC.39.6.1372.
In order to incorporate ofloxacin within liposomes, the reverse-phase evaporation technique was carried out. The liposome lipid matrix consisted of dipalmitoylphosphatidylcholine-cholesterol-dihexadecylphosphate (4: 3:4 molar ratio). The liposome formulation presented a mean size of 185 +/- 31 nm and had an encapsulation capacity of 5.3 microliters/mumol. The liposome formulation was able to deliver ofloxacin into McCoy cells in a greater amount (2.6-fold) than the free drug, improving antibiotic accumulation.
为了将氧氟沙星包封于脂质体中,采用了逆相蒸发技术。脂质体脂质基质由二棕榈酰磷脂酰胆碱 - 胆固醇 - 二己基磷酸酯(摩尔比4:3:4)组成。该脂质体制剂的平均粒径为185±31nm,包封容量为5.3微升/微摩尔。与游离药物相比,该脂质体制剂能够将更多量的氧氟沙星递送至McCoy细胞中(2.6倍),提高了抗生素的蓄积。