Foong W C, Green K L
School of Pharmacy, Portsmouth Polytechnic, UK.
J Pharm Pharmacol. 1988 Mar;40(3):171-5. doi: 10.1111/j.2042-7158.1988.tb05212.x.
The association of free or liposome-entrapped [3H]methotrexate [( 3H]MTX) with thioglycollate-elicited macrophages was investigated in-vitro. [14C]Cholesteryl oleate was incorporated into the liposomes as a lipid marker. [3H]MTX association with the macrophages was 5 to 9-fold higher with liposome-entrapped [3H]MTX than with the free drug. Macrophage-liposome association was biphasic, temperature-dependent and saturable at high liposomal lipid concentration. A high liposome cholesterol (CH) content or the presence of 2,4-dinitrophenol or colchicine also reduced macrophage-liposome association.
在体外研究了游离或脂质体包裹的[3H]甲氨蝶呤([3H]MTX)与巯基乙酸诱导的巨噬细胞的结合情况。将[14C]胆固醇油酸酯作为脂质标记物掺入脂质体中。脂质体包裹的[3H]MTX与巨噬细胞的结合比游离药物高5至9倍。巨噬细胞与脂质体的结合是双相的,依赖温度,并且在高脂质体脂质浓度下可饱和。高脂质体胆固醇(CH)含量或2,4-二硝基苯酚或秋水仙碱的存在也会降低巨噬细胞与脂质体的结合。