Preparation method of deer blood peptide liposome
A liposome and deer blood peptide technology, applied in the field of deer blood, can solve the problems of restricting the consumption of deer blood, achieve good application prospects, improve bioavailability, and expand the application range
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Embodiment 1
[0018] Using fresh deer blood as raw material, deer blood peptides are prepared according to the following process:
[0019] Take 1 liter of fresh deer blood, centrifuge at 4°C and 3000 rpm for 1 hour, take the supernatant and denature it at 100°C for 1 hour, add 1 liter of pH 2 Tris-HCl buffer solution to the deer blood plasma protein after denaturation, Add pepsin, the amount of enzyme added is enzyme: protein (plasma protein) mass ratio = 1:100, hydrolyze at 20°C for 0.5 hours, freeze-dry after the reaction, and obtain powdered deer blood active peptide.
[0020] Take 50mg of dry phospholipid and cholesterol mixture, the mass ratio of phospholipid to cholesterol is 1:0.1, dissolve the mixture in 50ml of chloroform and mix well, then vacuum rotary evaporation at 80℃ to form a lipid film. Hydrate the lipid film with 500ml of deionized water, add glass beads with a diameter of 0.5-3mm, stir at 90°C for 60 minutes, and then stir at room temperature for 60 minutes to form liposo...
Embodiment 2
[0022] Take 1 liter of fresh deer blood, centrifuge at 4°C and 15,000 rpm for 0.1 hour, take the supernatant and add 480 grams of urea, denature it for 1 hour, add 25 liters of pH 8 phosphate buffer, add neutral protease, enzyme The amount added is enzyme: protein = 1:500, hydrolyzed at 80°C for 24 hours, and freeze-dried after the reaction to obtain powdered deer blood active peptide.
[0023] Take 50mg of dry phospholipid and cholesterol mixture, the mass ratio of phospholipid and cholesterol is 1:0.01, dissolve the mixture in 1000ml of chloroform and mix well, then evaporate in vacuum at 40℃ to form a layer of lipid film. Add 500ml of deionized water to hydrate the lipid film, add glass beads with a diameter of 0.5-3mm, stir at 90°C for 60 minutes, and then stir at room temperature for 60 minutes to form liposomes. The above-prepared buckblood peptide was dissolved in pH 7.4 phosphate buffer to prepare a buckblood peptide solution with a concentration of 5 mg / ml; 50 ml of b...
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