Chan H C, Magin R L
Department of Electrical and Computer Engineering, University of Illinois, Urbana 61801.
J Pharm Sci. 1989 Apr;78(4):311-3. doi: 10.1002/jps.2600780410.
Liposome blood clearance and temperature-dependent drug release were studied using an electron spin resonance technique on whole blood samples. Temperature-sensitive liposomes composed of dipalmitoylphosphatidylcholine and dipalmitoylphosphatidylglycerol (4:1 by weight) were formed by reversed-phase evaporation. The liposomes were stable in the blood for greater than 2 h after iv injection. Liposome blood clearance exhibited a fast and slow component which may be due to the presence of both large and small liposomes in the preparation. The onset temperature for liposome release of the water-soluble nitroxide spin label was reduced from 40 degrees C in Hepes buffered saline to 38 degrees C in the rat blood, and the total release in the blood was approximately 25% greater than that measured in saline. These results show the influence of blood constituents on temperature-dependent drug release from liposomes.
使用电子自旋共振技术对全血样本进行研究,以考察脂质体的血液清除率和温度依赖性药物释放。通过反相蒸发法制备了由二棕榈酰磷脂酰胆碱和二棕榈酰磷脂酰甘油(重量比为4:1)组成的温度敏感脂质体。静脉注射后,脂质体在血液中稳定存在超过2小时。脂质体的血液清除率呈现出快速和缓慢两个组分,这可能是由于制剂中同时存在大、小脂质体。水溶性氮氧化物自旋标记物从脂质体释放的起始温度在Hepes缓冲盐溶液中为40℃,在大鼠血液中降至38℃,并且在血液中的总释放量比在盐溶液中测得的约高25%。这些结果表明血液成分对脂质体温度依赖性药物释放的影响。