Preparation method of hydrogen-microbubble-containing aqueous solution, and product and application of method
An aqueous solution and hydrogen technology, applied in the field of biomedicine, can solve the problems of unstable concentration, difficult to control, short storage time, etc., and achieve the effects of improving solubility, reducing dosage and controllable concentration.
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Embodiment 1
[0064] Preparation of Hydrogen Microbubble Aqueous Solution
[0065] In S1, a certain amount of 1,2-arachidylglycerylphosphatidylcholine (20:0, PC) and 1,2-distearoylglycerylphosphatidylcholine modified by polyethylene glycol 2000 were added in a 90:10 molar ratio. Ethanolamine (DSPE-PEG) was mixed in chloroform with a vortex mixer. The chloroform was removed with a dry nitrogen flow to form a uniform film of the dissolved material on the wall of the test tube, and dried in a vacuum oven at 45°C for more than 2 hours.
[0066] S2 According to the total mass of the above-mentioned phospholipids, add a certain volume of buffer solution with a pH of 7.4 (containing 10% (volume ratio) glycerol, 10% (volume ratio) propylene glycol and 80% (volume ratio) 0.1M Tris Tris trihydroxyaminomethane) , the phospholipid mixture film was hydrated so that the final concentration of phospholipids was 3 mg / ml. Heat to above 70°C to make it fall off the wall of the test tube. Keep the water ...
Embodiment 2
[0086] Preparation of Hydrogen Microbubble Aqueous Solution
[0087] In S1, a certain amount of 1,2-docosyl fatty acylglyceryl phosphatidylcholine (22:0PC), polyethylene glycol 2000 modified 1,2-distearoyl Glycerylphosphatidylethanolamine (DSPE-PEG) was mixed in chloroform with a vortex mixer. The chloroform was removed with a dry nitrogen flow to form a uniform film of the dissolved material on the wall of the test tube, and dried in a vacuum oven at 45°C for more than 2 hours.
[0088] S2 According to the total mass of the above-mentioned phospholipids, add a certain volume of buffer solution with a pH of 7.4 (containing 10% (volume ratio) glycerol, 10% (volume ratio) propylene glycol and 80% (volume ratio) 0.1M Tris Tris trihydroxyaminomethane) , the phospholipid mixture film was hydrated so that the final concentration of phospholipids was 3 mg / ml. Heat to above 70°C to make it fall off the wall of the test tube. Keep the water temperature above 80°C with a water-bath...
Embodiment 3
[0094] Preparation of Hydrogen Microbubble Aqueous Solution
[0095] S1 A certain amount of 1,2-arachidylglycerylphosphatidylcholine (20:0, PC) and polyethylene glycol 2000 stearate (PEG40S) were mixed in chloroform with a vortex at a molar ratio of 85:15. Spin mixer to mix. The chloroform was removed with a dry nitrogen flow to form a uniform film of the dissolved material on the wall of the test tube, and dried in a vacuum oven at 45°C for more than 2 hours.
[0096] S2 According to the total mass of the above-mentioned phospholipids, add a certain volume of buffer solution with a pH of 7.4 (containing 10% (volume ratio) glycerol, 10% (volume ratio) propylene glycol and 80% (volume ratio) 0.1M Tris Tris trihydroxyaminomethane) , the phospholipid mixture film was hydrated so that the final concentration of phospholipids was 3 mg / ml. Heat to above 70°C to make it fall off the wall of the test tube. Keep the water temperature above 70°C with a water-bath ultrasonic oscilla...
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