Method for preparing nanoliposomes of medium chain fatty acids (MCFAs) by dynamic high-pressure microfluidization (DHPM)-freezing and thawing method
A high-pressure micro-jet, medium-chain fatty acid technology, applied in the field of food nutrition, can solve the problems of large toxic reagents, unsuitable for industrial production, etc., and achieve the effect of stable liposome properties and good storage stability
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Embodiment 1
[0018] Weigh 0.45g of medium-chain fatty acids (MCFAs), 2.06g of lecithin, 0.34g of cholesterol, 0.62g of Tween-80 and 0.04g of vitamin E, dissolve them completely in 42ml of absolute ethanol, and remove them by vacuum rotation in a water bath at 40°C. Anhydrous ethanol, forming a uniform film. Take 30ml of phosphate buffered saline solution (PBS) with a concentration of 0.05M and a pH of 7.4, add 0.9g of maltose, add the obtained maltose solution to the film for hydration and wash the film, and the uniform suspension formed is the thick liposome. The crude liposomes were added to DHPM, and subjected to microfluidization treatment 4 times under the condition of 140MPa to obtain medium-chain fatty acid (MCFAs) liposomes. Put medium-chain fatty acid (MCFAs) liposomes in -80°C for 0.5 hours, take them out, thaw them in a water bath at 40°C for 15 minutes, and freeze them again in -80°C. Repeat this process 3 times to obtain medium-chain fatty acids (MCFAs) Nanoliposomes. The pr...
Embodiment 2
[0020] Weigh 0.90g of medium-chain fatty acids (MCFAs), 4.12g of lecithin, 0.68g of cholesterol, 1.23g of Tween-80 and 0.08g of vitamin E, dissolve them completely in 83ml of absolute ethanol, and remove them by vacuum rotation in a water bath at 40°C. Anhydrous ethanol, forming a uniform film. Take 60ml of phosphate buffered saline solution (PBS) with a concentration of 0.05M and a pH of 7.4, add 1.8g of maltose, add the resulting maltose solution to the film for hydration and wash the film, and form a uniform suspension that is thick liposomes. The crude liposomes were added to DHPM, and subjected to microfluidization treatment 4 times under the condition of 140MPa to obtain medium-chain fatty acid (MCFAs) liposomes. Put medium-chain fatty acid (MCFAs) liposomes in -80°C for 0.5 hours, take them out, thaw them in a water bath at 40°C for 15 minutes, and freeze them again in -80°C. Repeat this process 3 times to obtain medium-chain fatty acids (MCFAs) Nanoliposomes. The pre...
Embodiment 3
[0022] Weigh 0.45g of medium-chain fatty acids (MCFAs), 2.06g of lecithin, 0.34g of cholesterol, 0.84g of Tween-80 and 0.08g of vitamin E, dissolve them completely in 42ml of absolute ethanol, and remove them by vacuum rotation in a water bath at 40°C. Anhydrous ethanol, forming a uniform film. Take 30ml of phosphate buffered saline solution (PBS) with a concentration of 0.05M and a pH of 7.4, add 0.9g of maltose, add the obtained maltose solution to the film for hydration and wash the film, and the uniform suspension formed is the thick liposome. The crude liposomes were added to DHPM, and subjected to microfluidization treatment 4 times under the condition of 140MPa to obtain medium-chain fatty acid (MCFAs) liposomes. Put medium-chain fatty acid (MCFAs) liposomes in -80°C for 1.0h, take them out, thaw them in a water bath at 40°C for 15 minutes, put them in -80°C for freezing again, and repeat this process 3 times to obtain medium-chain fatty acids (MCFAs) Nanoliposomes. T...
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