反应 #568462
ord-78251c4bc637447c935d2066ecc3b015
溶剂
反应条件
后处理
- 1其他Liposomes were formed by the reversed-phase evaporation method
- 2其他This mixture was sonicated for 5 minutes under a low flow of nitrogen
- 3其他The organic phase was removed under vacuum on a rotary evaporator at 40° until all frothing
- 4workup.ADDITIONAn additional 1.3 ml aliquot of the dye solution was added
- 5其他except that the usual sonication step
- 6其他Finally, to remove any unencapsulated dye
- 7过滤filtered on a 1×14 cm Sephadex G-50 column
- 8其他dialyzed overnight against TBS at 4° C
- 9其他stored at 4° C.
- 10其他of 9 months
实验过程
Liposomes were formed by the reversed-phase evaporation method, as described in Szoka, et al., Biochim. Biophys. Acta, 601 (1980) 559, and O'Connell, et al., Anal. Chem., 31 (1985) 142, the disclosures of which are hereby incorporated by reference, from a mixture of DPPC, cholesterol, DPPG, and Alachlor-DPPE conjugate in a molar ration of 5:5:0.5:0.01. Forty-three μmol of this mixture were dissolved in 4.2 ml of a solvent mixture containing chloroform-isopropyl ether-methanol (6:6:1,v/v). This solution was warmed to 45° C. and 0.7 ml of the dye solution was added with swirling. This mixture was sonicated for 5 minutes under a low flow of nitrogen. The organic phase was removed under vacuum on a rotary evaporator at 40° until all frothing had stopped. An additional 1.3 ml aliquot of the dye solution was added, and the liposomes were then sequentially extruded twice through each of two polycarbonate filters of decreasing pore sizes of 1.0 μm and 0.4 μm. The diameters of the liposome preparations were measured by laser scattering in a LA-900 particle size distribution analyzer (Horiba, Irvine, Calif.), using the manufacturers method, except that the usual sonication step was omitted to avoid lysis (rupture) of the liposomes. Finally, to remove any unencapsulated dye, the liposomes were gel filtered on a 1×14 cm Sephadex G-50 column and dialyzed overnight against TBS at 4° C. When stored at 4° C., there was no significant leakage of dye over a period of 9 months as described below.