Yamaguchi H, Iwata K
Antimicrob Agents Chemother. 1979 May;15(5):706-11. doi: 10.1128/AAC.15.5.706.
The specific affinity for membrane lipids and the membrane selectivity of three imidazole derivatives, clotrimazole, miconazole, and econazole, were studied using various types of liposomes with respect to the lecithin fatty acyl group composition and the liposome content and composition of sterol as membrane models. The sensitivity of liposomes to these drugs was primarily dependent upon the lecithin fatty acyl group composition. With sterol-free liposome systems, each imidazole induced maximum release of trapped glucose as a marker from the unsaturated dioleoyl lecithin liposomes, minimum release from the saturated dipalmitoyl lecithin liposomes, and intermediate release from egg lecithin liposomes. The sensitivity of the dipalmitoyl lecithin liposomes to any imidazole drug was not influenced by the incorporation of cholesterol or ergosterol. On the other hand, clotrimazole-induced permeability changes of liposomes prepared from unsaturated dioleoyl lecithin or egg lecithin were greatly enhanced by the incorporation of ergosterol, whereas they were suppressed by cholesterol incorporation. The sensitivity of liposomes prepared from these unsaturated lecithins to miconazole and econazole was also augmented by ergosterol incorporation, although it was scarcely altered by cholesterol incorporation. Negatively charged liposomes were more sensitive to the three imidazole drugs than positively charged liposomes.
以卵磷脂脂肪酰基组成以及作为膜模型的脂质体中甾醇的含量和组成各异的各类脂质体为对象,研究了克霉唑、咪康唑和益康唑这三种咪唑衍生物对膜脂质的特异性亲和力和膜选择性。脂质体对这些药物的敏感性主要取决于卵磷脂脂肪酰基组成。在无甾醇脂质体系统中,每种咪唑均能使包封的葡萄糖作为标记物从不饱和二油酰卵磷脂脂质体中最大程度释放,从饱和二棕榈酰卵磷脂脂质体中最小程度释放,而从蛋黄卵磷脂脂质体中释放程度居中。二棕榈酰卵磷脂脂质体对任何咪唑药物的敏感性不受胆固醇或麦角固醇掺入的影响。另一方面,由不饱和二油酰卵磷脂或蛋黄卵磷脂制备的脂质体,其因克霉唑诱导的通透性变化在掺入麦角固醇时会大大增强,而在掺入胆固醇时则受到抑制。尽管掺入胆固醇几乎不会改变,但掺入麦角固醇也会增强由这些不饱和卵磷脂制备的脂质体对咪康唑和益康唑的敏感性。带负电荷的脂质体对这三种咪唑药物的敏感性高于带正电荷的脂质体。