Fujikawa Shelly M, Chen Irene A, Szostak Jack W
Howard Hughes Medical Institute, and Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Langmuir. 2005 Dec 20;21(26):12124-9. doi: 10.1021/la052590q.
We describe a simple approach to the controlled removal of molecules from the membrane of large unilamellar vesicles made of fatty acids. Such vesicles shrink dramatically upon mixing with micelles composed of a mixture of fatty acid and a phospholipid (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC)), as fatty acid molecules leave the vesicle membrane and accumulate within the mixed micelles. Vesicle shrinkage was confirmed by dynamic light scattering, fluorescence recovery after photobleaching of labeled vesicles, and fluorescence resonance energy transfer between lipid dyes incorporated into the vesicle membrane. Most of the encapsulated impermeable solute is retained during shrinkage, becoming concentrated by a factor of at least 50-fold in the final small vesicles. This unprecedented combination of vesicle shrinkage with retention of contents allows for the preparation of small vesicles containing high solute concentrations, and may find applications in liposomal drug delivery.
我们描述了一种从由脂肪酸制成的大单层囊泡膜中可控去除分子的简单方法。当这些囊泡与由脂肪酸和磷脂(1-棕榈酰-2-油酰-sn-甘油-3-磷酸胆碱(POPC))混合物组成的胶束混合时,会显著收缩,因为脂肪酸分子离开囊泡膜并积聚在混合胶束内。通过动态光散射、标记囊泡光漂白后的荧光恢复以及掺入囊泡膜的脂质染料之间的荧光共振能量转移证实了囊泡收缩。在收缩过程中,大多数包裹的不可渗透溶质被保留下来,在最终的小囊泡中浓缩至少50倍。这种前所未有的囊泡收缩与内容物保留的组合使得制备含有高溶质浓度的小囊泡成为可能,并可能在脂质体药物递送中找到应用。