Sullivan S M, Huang L
Biochim Biophys Acta. 1985 Jan 10;812(1):116-26. doi: 10.1016/0005-2736(85)90528-0.
Immunoliposomes able to bind specifically to target cells and to release their encapsulated contents upon brief heating were prepared. Monoclonal anti-H2Kk was covalently derivatized with palmitic acid by the method of Huang, A. et al. (Huang, A., Tsao, Y.S., Kennel, S.J. and Huang, L. (1982) Biochim. Biophys. Acta 716, 140-150). The palmitoyl antibody was injected at a controlled rate into a suspension of fused unilamellar dipalmitoylphosphatidylcholine liposomes maintained at a constant temperature. The final protein-to-lipid ratio of the resultant liposomes with incorporated antibody (immunoliposomes) was dependent upon the rate of antibody injection and the lipid concentration. Injection of palmitoyl antibody into a liposome suspension containing 50 mM carboxyfluorescein at 41 degrees C resulted in simultaneous antibody incorporation and entrapment of dye. Immunoliposomes were able to release the entrapped carboxyfluorescein upon heating. The release of dye at temperatures between the pre- and main-transition temperatures of DPPC was abolished by the addition of calf serum (5%). Furthermore, the presence of serum resulted in an increase in the temperature of the maximal release rate and also in the rate of release at that temperature. Retention of antigen-binding capacity was demonstrated by the ability of the immunoliposomes to bind specifically to the target cells. Rapid release of entrapped carboxyfluorescein from immunoliposomes bound to target cells at 4 degrees C was achieved upon brief exposure (less than 3 min) at 41 degrees C. These heat-sensitive immunoliposomes may be useful in enhancing drug delivery to target cells.
制备了能够特异性结合靶细胞并在短暂加热时释放其包封内容物的免疫脂质体。采用Huang等人(Huang, A., Tsao, Y.S., Kennel, S.J.和Huang, L. (1982) Biochim. Biophys. Acta 716, 140 - 150)的方法将单克隆抗H2Kk与棕榈酸共价衍生化。将棕榈酰化抗体以可控速率注入保持在恒定温度的融合单层二棕榈酰磷脂酰胆碱脂质体悬浮液中。所得掺入抗体的脂质体(免疫脂质体)的最终蛋白质与脂质比率取决于抗体注入速率和脂质浓度。在41℃将棕榈酰化抗体注入含有50 mM羧基荧光素的脂质体悬浮液中,导致抗体同时掺入并捕获染料。免疫脂质体在加热时能够释放捕获的羧基荧光素。在DPPC的预转变温度和主转变温度之间的温度下,加入小牛血清(5%)可消除染料的释放。此外,血清的存在导致最大释放速率温度升高,以及该温度下的释放速率增加。免疫脂质体与靶细胞特异性结合的能力证明了其抗原结合能力的保留。在4℃下与靶细胞结合的免疫脂质体在41℃短暂暴露(少于3分钟)后,可实现捕获的羧基荧光素的快速释放。这些热敏免疫脂质体可能有助于增强药物向靶细胞的递送。