Soybean-source anti-oxidative peptide nano-liposome and preparation method thereof
A soybean antioxidant peptide and nanoliposome technology, which is applied in the directions of liposome delivery, peptide/protein components, antitoxins, etc., can solve the problems of increased viscosity, microbial growth, complicated operation, etc., and achieves low cost of raw materials, The effect of method innovation and simple process route
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Embodiment 1
[0021] A method for preparing soybean-derived antioxidant peptide nanoliposomes, comprising the steps of:
[0022] Using soybean antioxidant peptides of 3-10 kDa as raw materials, accurately weigh 15 mg of soybean antioxidant peptides, and dissolve them in PBS buffer solution with a pH value of 6 and a concentration of 0.05M at room temperature to obtain an aqueous phase system. Then weigh phospholipids and cholesterol with a mass ratio of 2:1, put them in a round bottom flask, dissolve them in ether at room temperature, and plug cotton on the bottle mouth to obtain a lipid phase system, and place them in -10 ℃ environment for standby. In a fume hood, place a medical needle on a 2mL syringe, quickly draw the aqueous phase and inject it into the lipid phase, and the lipid phase:water phase volume ratio is 5:1. The mixed phase was treated with an ultrasonic cell crushing instrument with a power of 700W and ultrasonication at -10°C for 6min to form a stable W / O emulsion. Transf...
Embodiment 2
[0028]Using 3-10kDa soybean antioxidant peptides as raw materials, accurately weigh 20mg of soybean antioxidant peptides, and dissolve them in PBS buffer solution with a pH value of 6.8 and a concentration of 0.1M at room temperature to obtain an aqueous phase system. Then weigh phospholipids and cholesterol with a mass ratio of 3:1, put them in a round-bottomed flask, dissolve them in ether at room temperature, and plug cotton on the bottle mouth to obtain a lipid phase system, and place them in -8 ℃ environment for standby. In a fume hood, place a medical needle on a 2mL syringe, quickly draw up the aqueous phase and inject it into the lipid phase, and the lipid phase:water phase volume ratio is 1:1. The mixed phase was treated with an ultrasonic cell crushing instrument with a power of 550W and ultrasonication at -8°C for 7 minutes to form a stable W / O emulsion. Transfer the mixed phase to a 100mL spin-dried bottle, and rotate it at 40°C for 12 minutes under low pressure t...
Embodiment 3
[0031] Using 3-10kDa soybean antioxidant peptides as raw materials, accurately weigh 25mg soybean antioxidant peptides, dissolve them in a PBS buffer solution with a pH value of 7.4 and a concentration of 0.5M at room temperature to obtain an aqueous phase system. Then weigh phospholipid and cholesterol with a mass ratio of 5:1, put them in a round-bottomed flask, dissolve them in ether at room temperature, and plug cotton on the bottle mouth to obtain a lipid phase system, and place them in -4 ℃ environment for standby. In a fume hood, place a medical needle on a 2mL syringe, quickly draw up the volume of the aqueous phase and inject it into the volume of the lipid phase, and the volume ratio of lipid phase:water phase is 2:1. The mixed phase was treated with an ultrasonic cell crushing instrument with a power of 500W and ultrasonication at -6°C for 9 minutes to form a stable W / O emulsion. Transfer the mixed phase to a 100mL spin-dried bottle, and evaporate under low pressur...
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