Papahadjopoulos D, Allen T M, Gabizon A, Mayhew E, Matthay K, Huang S K, Lee K D, Woodle M C, Lasic D D, Redemann C
Department of Pharmacology, University of California, San Francisco 94143.
Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11460-4. doi: 10.1073/pnas.88.24.11460.
The results obtained in this study establish that liposome formulations incorporating a synthetic polyethylene glycol-derivatized phospholipid have a pronounced effect on liposome tissue distribution and can produce a large increase in the pharmacological efficacy of encapsulated antitumor drugs. This effect is substantially greater than that observed previously with conventional liposomes and is associated with a more than 5-fold prolongation of liposome circulation time in blood, a marked decrease in uptake by tissues such as liver and spleen, and a corresponding increased accumulation in implanted tumors. These and other properties described here have expanded considerably the prospects of liposomes as an effective carrier system for a variety of pharmacologically active macromolecules.
本研究获得的结果表明,掺入合成聚乙二醇衍生化磷脂的脂质体制剂对脂质体的组织分布有显著影响,并且可使包封的抗肿瘤药物的药理疗效大幅提高。这种效果大大超过了先前用传统脂质体所观察到的效果,并且与脂质体在血液中的循环时间延长5倍以上、肝脏和脾脏等组织的摄取显著减少以及植入肿瘤中的蓄积相应增加有关。这里描述的这些以及其他特性大大拓展了脂质体作为多种药理活性大分子的有效载体系统的前景。