Peanut oligopeptide-coated nano liposome as well as preparation method and application thereof
A nano-liposome and short peptide technology, which is applied in the directions of liposome delivery, peptide/protein components, medical preparations of inactive ingredients, etc., can solve problems such as low encapsulation rate, and achieve low cost and simple preparation process. , the effect of strong operability
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Embodiment 1
[0077] Example 1 The effect of different pressure treatments of high-pressure microjet on liposome particle size and encapsulation efficiency
[0078] Step 1: Weigh 421 mg of lecithin, 36.7 mg of peanut short peptide, 44.2 mg of cholesterol, 95.7 mg of sodium deoxycholate, add 100 mL of 95% ethanol, and sonicate in a water bath until it is completely dissolved;
[0079] The second step: depressurize the solution in a water bath at 45°C, and remove the ethanol by rotary evaporation, with a vacuum of -0.09MPa, until a uniform lipid film is formed on the wall of the eggplant bottle. Add 100 mL of 0.01 mol / L PBS (pH 7.4) buffer to the rotary evaporating flask, spin and hydrate for 60 minutes to obtain a crude liposome suspension;
[0080] The third step: pass the crude liposome suspension through a high-pressure micro-jet homogenizer, and the treatment pressure is 60, 90, 120, 150, and 180 MPa, respectively, and cycle treatment once to determine the liposome particle size and encapsulati...
Embodiment 2
[0084] Example 2 The effect of different cycles of high-pressure micro-jet 120MPa treatment on liposome particle size and encapsulation efficiency
[0085] Step 1: Weigh 421 mg of lecithin, 36.7 mg of peanut short peptide, 44.2 mg of cholesterol, 95.7 mg of sodium deoxycholate, add 100 mL of 95% ethanol, and sonicate in a water bath until it is completely dissolved;
[0086] The second step: depressurize the solution in a water bath at 45°C, and remove the ethanol by rotary evaporation, with a vacuum of -0.09MPa, until a uniform lipid film is formed on the wall of the eggplant bottle. Add 100 mL of 0.01 mol / L PBS (pH 7.4) buffer to the rotary evaporating flask, spin and hydrate for 60 minutes to obtain a crude liposome suspension;
[0087] The third step: pass the crude liposome suspension through a high-pressure micro-jet homogenizer at a treatment pressure of 120 MPa, and cycle treatment for 1-5 times to determine the liposome particle size and encapsulation efficiency of different...
Embodiment 3
[0090] Example 3 The effect of Ostwald maturation of nanoliposomes on the encapsulation efficiency
[0091] Step 1: Weigh 421 mg of lecithin, 36.7 mg of peanut short peptide, 44.2 mg of cholesterol, 95.7 mg of sodium deoxycholate, add 100 mL of 95% ethanol, and sonicate in a water bath until it is completely dissolved;
[0092] The second step: depressurize the solution in a water bath at 45°C, and remove the ethanol by rotary evaporation, with a vacuum of -0.09MPa, until a uniform lipid film is formed on the wall of the eggplant bottle. Add 100 mL of 0.01 mol / L PBS (pH 7.4) buffer to the rotary evaporating flask, spin and hydrate for 60 minutes to obtain a crude liposome suspension;
[0093] The third step: pass the crude liposome suspension through a high-pressure micro-jet homogenizer at a treatment pressure of 120 MPa, and perform 4 cycles of treatment to obtain nano liposomes;
[0094] The fourth step: stir the nanoliposomes at 20, 50, and 100 rpm under room temperature condition...
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