Sehgal S, Rogers J A
Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, Canada.
J Microencapsul. 1995 Jan-Feb;12(1):37-47. doi: 10.3109/02652049509051125.
Liposomes of dimyristoylphosphatidylcholine (DMPC) or dipalmitoylphosphatidylcholine (DPPC), cholesterol (CHOL) and dicetylphosphate (DCP) containing Ara-C were prepared at pH 4.5 and subsequently coated with a derivatized polysaccharide, O-palmitoylpullulan (OPP). Encapsulation efficiencies (EEF) of DMPC:CHOL:DCP (3:1:2 mol ratio) and DPPC:CHOL:DCP (3:1:0.5 mol ratio) liposomes were respectively 28 and 40% before and 15 and 27% after coating with polymer. Stabilities of liposomes in sodium cholate (SC) concentrations up to 16 mM at pH 5.6 or in SC solutions at pH 7.4 were increased by coating with OPP. At pH 2.0 and 37 degrees C, Ara-C was released at a slow rate, kuo (uncoated) or kco (coated), for 24 h after an initial rapid release phase that lasted for about 6 h and the ratio kuo/kco, was 1.9 and 5.7 for the DMPC:CHOL:DCP and the DPPC:CHOL:DCP compositions respectively. At pH 7.4 and 37 degrees C in the presence of 10 mM SC, the ratio kuo/kco was 5.1 and 1.4 respectively. It is concluded that coating liposomes with OPP increases the potential of using liposomes as a drug delivery system in harsh environments such as encountered after oral administration, although the magnitude of the effect is dependent on the liposome composition.
在pH 4.5条件下制备了含有阿糖胞苷的二肉豆蔻酰磷脂酰胆碱(DMPC)或二棕榈酰磷脂酰胆碱(DPPC)、胆固醇(CHOL)和磷酸二鲸蜡酯(DCP)的脂质体,随后用衍生化多糖O-棕榈酰普鲁兰(OPP)进行包衣。DMPC:CHOL:DCP(摩尔比3:1:2)和DPPC:CHOL:DCP(摩尔比3:1:0.5)脂质体在包衣前的包封率(EEF)分别为28%和40%,包衣后的包封率分别为15%和27%。用OPP包衣可提高脂质体在pH 5.6时高达16 mM的胆酸钠(SC)浓度中或pH 7.4的SC溶液中的稳定性。在pH 2.0和37℃下,阿糖胞苷在最初持续约6小时的快速释放阶段后,以缓慢速率释放,未包衣的释放速率为kuo,包衣的释放速率为kco,持续24小时,DMPC:CHOL:DCP和DPPC:CHOL:DCP组合物的kuo/kco比值分别为1.9和5.7。在pH 7.4和37℃且存在10 mM SC的条件下,kuo/kco比值分别为5.1和1.4。结论是,用OPP包衣脂质体增加了在口服给药后等恶劣环境中使用脂质体作为药物递送系统地可能性,尽管效果的程度取决于脂质体的组成。