Kirby C J, Gregoriadis G
Division of Clinical Sciences, Clinical Research Centre, Harrow, Middlesex, England.
J Microencapsul. 1984 Jan-Mar;1(1):33-45. doi: 10.3109/02652048409031535.
Different types of liposomes composed of a variety of lipids have been compared for their ability to incorporate Factor VIII, with a view to attempting oral therapy of haemophilia. Reverse evaporation liposomes (REV) composed of unsaturated phospholipids, allowed adequate levels of entrapment for administration to haemophilic dogs, but failed to promote entry of Factor VIII into the vasculature, possibly due to liposome breakdown and denaturation of Factor VIII within the gastrointestinal tract. A novel technique was therefore developed which made possible high-yield entrapment of Factor VIII in much more stable liposomes based on the saturated phospholipid, distearoyl phosphatidylcholine. This new technique has a number of other important features which make it an attractive method for the incorporation of a wide range of materials into liposomes.
为了尝试对血友病进行口服治疗,已对由多种脂质组成的不同类型脂质体结合凝血因子VIII的能力进行了比较。由不饱和磷脂组成的逆相蒸发脂质体(REV),能使足够水平的凝血因子VIII被包封用于给血友病犬给药,但未能促进凝血因子VIII进入脉管系统,这可能是由于脂质体在胃肠道内分解以及凝血因子VIII变性所致。因此开发了一种新技术,该技术能使凝血因子VIII以高产率包封在基于饱和磷脂二硬脂酰磷脂酰胆碱的更稳定的脂质体中。这项新技术还有许多其他重要特性,使其成为将多种物质包封到脂质体中的一种有吸引力的方法。