Department of Pharmaceutics and Medicinal Chemistry, University of the Pacific, 751 Brookside Road, Stockton, CA 95211, USA.
Pharmaceutics. 2011 Jul 11;3(3):379-405. doi: 10.3390/pharmaceutics3030379.
Incorporation of a pH-sensitive conformational switch into a lipid structure enables a drastic conformational flip upon protonation that disrupts the liposome membrane and causes rapid release of cargo specifically in areas of increased acidity. pH-sensitive liposomes containing the amphiphile (1) with trans-2-morpholinocyclohexanol conformational switch, a phospholipid, and a PEG-lipid conjugate were constructed and characterized. The optimized composition-1/POPC/PEG-ceramide (50/45/5)-could be stored at 4 °C and pH 7.4 for up to 1.5 years, and was stable in blood serum in vitro after 48 h at 37 °C. Liposomes loaded with ANTS/DPX or methotrexate demonstrated an unusually quick content release (in a few seconds) at pH below 5.5, which was independent of inter-liposome contact. The pH-titration curve for the liposome leakage paralleled the curve for the acid-induced conformational flip of 1 studied by 1H-NMR. Freeze-fracture electron microscopy images showed budding and division of the bilayer at pH 5.5. A plausible mechanism of pH-sensitivity involves an acid-triggered conformational flip of 1, shortening of lipid tails, and membrane perturbations, which cause the content leakage. The methotrexate-loaded liposomes demonstrated much higher cytotoxicity in HeLa cells than the free drug indicating that they can serve as viable drug delivery systems.
将 pH 敏感构象开关整合到脂质结构中,可以在质子化时实现剧烈的构象翻转,破坏脂质体膜,并导致货物在酸度增加的区域迅速释放。构建并表征了含有反式-2-吗啉环己醇构象开关的两亲物(1)、磷脂和 PEG-脂质缀合物的 pH 敏感脂质体。优化的组成-1/POPC/PEG-神经酰胺(50/45/5)可以在 4°C 和 pH 7.4 下储存长达 1.5 年,并且在 37°C 下体外血清中 48 小时后稳定。负载 ANTS/DPX 或甲氨蝶呤的脂质体在 pH 低于 5.5 时表现出异常快速的内容物释放(几秒钟内),这与脂质体之间的接触无关。脂质体泄漏的 pH 滴定曲线与通过 1H-NMR 研究的 1 酸性诱导构象翻转的曲线平行。冷冻断裂电子显微镜图像显示在 pH 5.5 时双层的出芽和分裂。一种合理的 pH 敏感性机制涉及 1 的酸触发构象翻转,脂质尾部缩短和膜扰动,导致内容物泄漏。与游离药物相比,负载甲氨蝶呤的脂质体在 HeLa 细胞中表现出更高的细胞毒性,表明它们可以作为可行的药物递送系统。