Carvacrol solid lipid nanoparticle dispersion with antibacterial activity and its preparation method and application
A technology of solid lipid nanometer and antibacterial activity, which is applied in the field of fungicides, can solve the problems of low absorption rate and bioavailability, darker carvacrol color, and low solubility, so as to increase solubility, inhibit growth, The effect of simple preparation process
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[0022] The second aspect of the present invention provides a kind of preparation method of above-mentioned carvacrol solid lipid nanoparticle dispersion liquid with bacteriostatic activity, and this preparation method comprises:
[0023] (1) Melting and mixing carvacrol, glyceryl monostearate and 1,2-propylene glycol ester to obtain an oil phase;
[0024] (2) Mix Tween-80 and part of water evenly to obtain an aqueous phase;
[0025] (3) The oil phase and the water phase are mixed uniformly, and then ethanol is added to obtain a microemulsion;
[0026] (4) Mix the microemulsion with the remaining water evenly to obtain a carvacrol solid lipid nanoparticle dispersion.
[0027] According to the present invention, preferably, in step (1), the melting temperature is 40-80°C.
[0028] According to the present invention, preferably, in step (2), the mixing temperature is 40-80°C.
[0029] According to the present invention, preferably, step (3) is at 40-80°C, rapidly mixing the oi...
Embodiment 1
[0037] The present embodiment provides a carvacrol solid lipid nanoparticle dispersion with antibacterial activity, the specific preparation method is: weigh 4g 1,2-propanediol ester, 4g glyceryl monostearate and 0.4g carvacrol Mix and heat to 70°C until completely melted to obtain a liquid oil phase; additionally weigh 12g of Tween-80 and 200g of distilled water, stir and heat to 70°C to obtain an aqueous phase. Mix the two phases of oil and water rapidly within 0.5min at 70°C, heat the temperature to 80°C and stir for 10 minutes to form a coarse milk, add 40g of absolute ethanol dropwise to the coarse milk to form a clear, transparent and stable microemulsion, The microemulsion was quickly dispersed into 400mL of 2-4°C cold water within 0.5min, and kept stirring for 30 minutes to obtain a carvacrol solid lipid nanoparticle dispersion;
[0038] The carvacrol solid lipid nanoparticle dispersion in Example 1 was placed for 3 months without aggregation and precipitation of nanop...
Embodiment 2
[0040] The present embodiment provides a carvacrol solid lipid nanoparticle with antibacterial activity, the specific preparation method is: take 4g 1,2-propanediol ester, 4g glyceryl monostearate and 0.8g carvacrol and mix and heat to 70°C until completely melted to obtain a liquid oil phase; additionally weigh 12g of Tween-80 and 200g of distilled water, stir and heat to 70°C to obtain an aqueous phase. Mix the two phases of oil and water rapidly within 0.5min at 70°C, heat the temperature to 80°C and stir for 10 minutes to form a coarse milk, add 40g of absolute ethanol dropwise to the coarse milk to form a clear, transparent and stable microemulsion, The microemulsion was quickly dispersed into 400mL of 2-4°C cold water within 0.5min, and kept stirring for 30 minutes to obtain a carvacrol solid lipid nanoparticle dispersion;
[0041] The carvacrol solid lipid nanoparticle dispersion of Example 2 was placed for 3 months without aggregation and precipitation of nanoparticles...
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