반응 #2375747
ord-820fea7ff16c46c8bf9ee516170c8895
반응 조건
후처리
- 1기타The lipids were dried to a film under vacuum
- 2온도with heating for 1-2 mins
- 3기타in a 60° C.
- 4workup.ADDITIONThis solution was added to the solvent mixture
- 5기타The solvent was removed under vacuum
- 6기타in a 60° C.
- 7기타Once the solvent was removed
- 8기타was resuspended in 0.5 ml 60° C. sodium acetate buffer
- 9세척The preparation was washed by addition of 0.5 ml of 60° C. sodium acetate buffer
- 10기타The supernatant was decanted
- 11기타resuspended with 1 ml of 60° C. sodium acetate buffer
- 12workup.WAITg for 10 minutes
- 13workup.ADDITIONThe resuspended DSPC-cholesterol lipomes containing calcitonin
- 14기타retention of the liposomal preparation to that of free calcitonin
- 15기타was at least about 70% present one day
- 16workup.WAITpersisted for about 3 to 7 days
실험 절차
8.27 mg DSPC (1:1 initial L:D ratio) and 1.73 mg cholesterol (7:3 mole % ratio DSPC: cholesterol), both in chloroform, were transferred to a 50 ml round bottom flask. The lipids were dried to a film under vacuum using rotoevaporation. The lipids were then solubilized in 0.500 ml methanol with heating for 1-2 mins. in a 60° C. water bath. Ten milligrams of calcitonin (Mitsubishi Chemical Co., Japan MCI-536) was solubilized in 0.100 ml sodium acetate buffer. This solution was added to the solvent mixture. The solvent was removed under vacuum, using rotoevaporation in a 60° C. water bath. Once the solvent was removed, the lipid/drug film was resuspended in 0.5 ml 60° C. sodium acetate buffer. The preparation was washed by addition of 0.5 ml of 60° C. sodium acetate buffer followed by centrifugation at 12,100×g for 10 minutes. The supernatant was decanted and the liposomal pellet resuspended with 1 ml of 60° C. sodium acetate buffer. The suspension was again centrifuged at 12,100×g for 10 minutes and resuspended. The resuspended DSPC-cholesterol lipomes containing calcitonin were administered s.c. to mice to compare retention of the liposomal preparation to that of free calcitonin. Free calcitonin was undetectable after one hour in mice. The calcitonin of liposomes of the instant invention was at least about 70% present one day after administration and persisted for about 3 to 7 days disclosing a substantial increase in retention time over free calcitonin.