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翻转体:包含基于反式-2-吗啉环己醇的脂质的 pH 敏感脂质体,该脂质能够进行构象翻转,并在酸性介质中触发即时货物释放。

Fliposomes: pH-Sensitive Liposomes Containing a trans-2-morpholinocyclohexanol-Based Lipid That Performs a Conformational Flip and Triggers an Instant Cargo Release in Acidic Medium.

机构信息

Department of Pharmaceutics and Medicinal Chemistry, University of the Pacific, 751 Brookside Road, Stockton, CA 95211, USA.

出版信息

Pharmaceutics. 2011 Jul 11;3(3):379-405. doi: 10.3390/pharmaceutics3030379.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac36/3857072/9c727139eba2/pharmaceutics-03-00379f1.jpg

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