Riess J G
Unité de Chimie Moléculaire, Université de Nice Sophia-Antipolis, Faculté des Sciences, France.
J Drug Target. 1994;2(5):455-68. doi: 10.3109/10611869408996822.
Stable fluorinated vesicles--i.e. vesicles with a hydrophobic and lipophobic fluorinated film within their bilayer membranes--have been obtained from a variety of neutral, zwitterionic or anionic fluorinated amphiphiles, including single chain phosphocholine derivatives, double-chain phospholipids, glycolipids and glycophospholipids, as well as from combinations of standard phospholipids with amphiphilic mixed fluorocarbon/hydrocarbon compounds. The strong hydrophobic interactions developed by perfluoroalkyl chains result in increased membrane stability, as strikingly illustrated by the fact that even short single-chain fluorinated amphiphiles can form stable, heat-sterilizable vesicles without the need for any additive. They also result in increased versatility in the aggregation behavior of fluorinated surfactants, as shown by the formation, depending on molecular structure and experimental conditions, of a range of supramolecular assemblies other than vesicles, including disks, helical tubules and fibers, for example from fluorinated glycolipids. The more impermeable, adjustable fluorinated core within the liposomal membrane confers to liposomes added drug and probe encapsulation stability as compared to their hydrogenated analogs, whether in buffer or in serum. Fluorinated vesicles made from perfluoroalkylated phospholipids were also found to have 3 to 6 times longer circulation half-lives in mice than similarly sized conventional DSPC/cholesterol liposomes. Finally, the incorporation of mixed fluorocarbon/hydrocarbon alkanes or alkenes into standard liposomes may provide an alternative, straightforward and cost efficient approach to fluorinated vesicles.
稳定的氟化囊泡——即双分子层膜内具有疏水和疏脂氟化膜的囊泡——已由多种中性、两性离子或阴离子氟化两亲物制备得到,包括单链磷酸胆碱衍生物、双链磷脂、糖脂和糖磷脂,以及标准磷脂与两亲性氟碳/烃类化合物的组合。全氟烷基链产生的强疏水相互作用导致膜稳定性增加,这一点从以下事实可以明显看出:即使是短链单链氟化两亲物也能形成稳定的、可热灭菌的囊泡,而无需任何添加剂。它们还导致氟化表面活性剂聚集行为的多功能性增加,例如由氟化糖脂形成的一系列除囊泡外的超分子聚集体,包括盘状、螺旋管状和纤维状,这取决于分子结构和实验条件。与氢化类似物相比,脂质体膜内更具不透性、可调节的氟化核心赋予脂质体添加药物和探针包封稳定性,无论是在缓冲液中还是在血清中。还发现由全氟烷基化磷脂制成的氟化囊泡在小鼠体内的循环半衰期比同样大小的传统DSPC/胆固醇脂质体长3至6倍。最后,将氟碳/烃类烷烃或烯烃掺入标准脂质体中可能为氟化囊泡提供一种替代的、直接且经济高效的方法。