Camellia oil lipidosome, preparation method thereof and application of camellia oil lipidosome to preparing acute liver injury treating drugs
A technology of oil liposome and camellia oil, applied in the directions of liposome delivery, drug combination, pharmaceutical formulation, etc., can solve problems such as unfavorable mass preparation, cumbersomeness, etc., achieves alleviation of necrosis and cell shrinkage, good repeatability, and easy preparation the effect obtained
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[0019] The invention provides a kind of preparation method of camellia oil liposome, comprising the following steps:
[0020] Suspending 1 mL of camellia oil, 0.05-1.5 g of lecithin and 0.01-0.2 g of phosphatidylserine in 5-50 mL of deionized water, ultrasonication, oscillation and standing still to obtain camellia oil liposomes.
[0021] In the present invention, the suspension system is preferably 1mL camellia oil, 0.1-1.0g lecithin and 0.02-0.15g phosphatidylserine suspended in 10-40mL deionized water, more preferably 1mL camellia oil, 0.2g lecithin and 0.02g Phosphatidylserine was suspended in 10 mL of deionized water.
[0022] In the present invention, the power of the ultrasound is preferably 30-200W, more preferably 50-150W, more preferably 100W. The temperature of the ultrasound is preferably lower than 50°C, more preferably 10-40°C. The time of the ultrasound is preferably 10-20 min. In the present invention, there is no special limitation on the instrument used fo...
Embodiment 1
[0029] 1mL camellia oil (SCY), 0.2g lecithin, 0.02g phosphatidylserine, suspended in 10mL deionized water. The sonicator was used for 5 minutes, the ultrasonic power was 200W, the temperature of the mixture was 40°C during the sonication, and the mixture was vortexed for 5 minutes. Stand still for 5 minutes to obtain camellia oil liposomes. The morphology of liposomes was observed by light microscopy.
[0030] result figure 1 shown. In aqueous solution, the prepared camellia oil liposome (Lip-SCY) was in uniform white emulsion state ( figure 1 -A). Microscopic observation shows that liposomes are spherical or nearly spherical, with a diameter of 1-10 μm ( figure 1 -B).
Embodiment 2
[0032] 1mL camellia oil, 1.0g lecithin, 0.1g phosphatidylserine, suspended in 30mL deionized water. Ultrasonic breaker was used for 10 minutes, the power of ultrasound was 150W, the temperature of the mixture was 40°C during the ultrasound process, and the mixture was vortexed for 5 minutes. Stand still for 8 minutes to obtain camellia oil liposomes. The morphology of liposomes was observed by light microscopy.
[0033] In aqueous solution, the prepared camellia oil liposome (Lip-SCY) was in the state of uniform white emulsion. Microscopic observation showed that the liposome was spherical or nearly spherical, with a diameter of 1-10 μm.
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