Coated magnolia fargesii volatile oil nano liposome nasal drops
A technology of nano-liposomes and nasal drops, which can be used in liposome delivery, plant raw materials, respiratory diseases, etc. It can solve the problems of no patent report of magnolia volatile oil liposomes, etc., so as to improve the effective utilization rate and drug absorption Rapid, easily absorbed effect
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Embodiment 1
[0039] Preparation of Nanoliposome Nasal Drops Coated with Magnolia Magnolia Volatile Oil (1)
[0040] 200mg soybean lecithin, 750mg magnolia volatile oil, 100mg cholesterol, 0.2mg sodium cholate, 1mg collagen, dissolved in 20ml of 2:1 methanol / chloroform mixed solvent. Constant temperature at 38°C, evaporate under reduced pressure to form a lipid film, add 20ml of phosphate buffer to shake and dissolve, adjust the pH value to 5.5, add 10mg of stearic acid amine, 0.05mg of polysorbate 80, and obtain a multilocular liposome dispersion. Ultrasonic treatment at an ultrasonic temperature of 10°C and an ultrasonic frequency of 200 Hz in an ice-water bath for 20 minutes, filtering through a 0.15 μm microporous membrane to form a uniform monolayer liposome suspension, adding 8.5 mg of phosphatidylglycerol to the filtrate to prepare Nasal administration formulations. The average particle size of liposomes encapsulating the drug carrier in the suspension was determined to be 73nm, and...
Embodiment 2
[0042] Preparation of Nanoliposome Nasal Drops Coated with Magnolia Magnolia Volatile Oil (2)
[0043] 200mg egg yolk lecithin, 330mg magnolia volatile oil, 66mg cholesterol, 0.01mg sodium deoxycholate, 10mg vitamin A acetate, dissolved in a mixed solvent of 30ml methanol. Constant temperature at 28°C, evaporate under reduced pressure to form a lipid film, add 20ml of phosphate buffer to shake and dissolve, adjust the pH value to 7.0, add 100mg of diacetyl phosphate, 0.1mg of methylparaben, and obtain a multilocular liposome dispersion . Ultrasonic treatment at an ultrasonic temperature of 1°C and an ultrasonic frequency of 600 Hz in an ice-water bath for 10 minutes, filtered through a 0.15 μm microporous membrane to form a uniform monolayer liposome suspension, and adding 4 mg of phosphatidic acid to the filtrate to prepare nasal administration pharmaceutical preparations. The average particle size of the liposomes encapsulating the drug carrier in the suspension was determ...
Embodiment 3
[0045] Preparation of Nanoliposome Nasal Drops Coated with Magnolia Magnolia Volatile Oil (3)
[0046]Dissolve 200mg soybean lecithin, 1600mg magnolia volatile oil, 200mg cholesterol, 5mg Triton-100, 5mg vitamin E in 40ml chloroform mixed solvent, evaporate under reduced pressure at 65°C to form a lipid film, add 20ml phosphate buffer to shake and dissolve, and adjust the pH value 7.5, add 20 mg of stearic acid amine, 50 mg of diacetyl phosphate, and 0.1 mg of phenylparaben methyl ester to obtain a multilocular liposome dispersion, and conduct ultrasonic treatment in an ice-water bath for 1 minute at an ultrasonic temperature of 5 ° C and an ultrasonic frequency of 1000 Hz. After filtering through a 0.15 μm microporous membrane to form a uniform monolayer liposome suspension, 2 mg stearylamine was added to the filtrate to prepare a nasal administration preparation. The average particle size of liposomes encapsulating the drug carrier in the suspension was determined to be 66nm...
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