Trigone-leaf dioscorea opposita saponin liposome, method for preparing the same and use of the same
A technology of dioscin and trigonum saponin, which is applied in the field of medicine, can solve the problems that there is no preparation of dioscin trigonum saponin, and achieve the effect of treating cardiovascular diseases, uniform particle size and shape, and good stability
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Embodiment 1
[0015] Example 1 Preparation of Diosgenin Liposomes by High Pressure Homogenization
[0016] Get lecithin (Chengdu Kelong Chemical Reagent Co., Ltd.) 2.5g, cholesterol (Chengdu Kelong Chemical Reagent Co., Ltd.) 0.5g, add 15ml dioscin phosphate buffer (containing dioscin 0.5g) and heat up to 80°C; add this high-temperature liquid phase into the double myristyl phosphatidylglycerol solution at the same temperature, mix quickly for 1min (8500rpm), and then mix with 500bar high pressure for 3 times; finally cool down and solidify. The encapsulation efficiency was 65%.
Embodiment 2
[0017] Example 2 Preparation of dioscin liposomes by thin film method
[0018] Dissolve 1.25 g of lecithin (Chengdu Kelong Chemical Reagent Co., Ltd.) and 0.3 g of cholesterol (Chengdu Kelong Chemical Reagent Co., Ltd.) in 60 ml of ether, and use a 250 ml eggplant-shaped bottle to evaporate under reduced pressure on a rotary evaporator to remove ether. The lipid forms a thin film on the wall of the Erlenmeyer flask, and then 15 ml of dioscin phosphate buffer (containing 0.3 g of dioscin) is added to rotate and hydrate to obtain dioscin liposomes. The encapsulation efficiency is 70%.
Embodiment 3
[0019] Example 3 Preparation of Dioscin Liposomes by Reverse Evaporation
[0020] Dissolve 2.5g of lecithin and 1g of cholesterol in a 250ml Erlenmeyer flask with 120ml of ether, then add 20ml of 8% mannitol aqueous solution of diosgenin (containing 0.4g of diosgenin), and ultrasonically make it into a homogeneous single-phase system , and then evaporated under reduced pressure to remove ether to a gel state, and then continued to evaporate under reduced pressure for 10 minutes to obtain diosgenin liposomes. The encapsulation efficiency is 50%.
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