Co-conveying nano composition of phenylethyl resorcinol and preparation method and application of co-conveying nano composition
A technology of phenylethyl resorcinol and nano composition, which is applied in skin care preparations, medical preparations containing active ingredients, pharmaceutical formulas, etc., and can solve the problem of insignificant whitening effect and phenylethylresorcinol It is easy to cause allergies, high retention, etc., to achieve the effect of increasing skin penetration and retention, no drug leakage, and reducing irritation
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[0091] The present invention also provides a preparation method for co-transporting nanocomposites of phenylethylresorcinol described in the above technical solution, comprising the following steps:
[0092] A. Dissolving phenylethyl resorcinol, other water-insoluble whitening active ingredients, emulsifiers, and co-emulsifiers with complex lipids to obtain an oil phase;
[0093] B. Dissolving other water-soluble whitening active ingredients and polyols in water to obtain an aqueous phase;
[0094] C. Mix and emulsify the oil phase obtained in step A with the water phase obtained in step B, and micronize to obtain a micron-scale dispersion;
[0095] D, the micron-scale dispersion obtained in step C is subjected to nano-processing to obtain a nano-scale dispersion, which is a co-transport nanocomposite of phenylethyl resorcinol;
[0096] There is no sequence between the steps A and B.
[0097] According to the water solubility of other whitening active ingredients, the presen...
Embodiment 1
[0115] 4.0% polyoxyethylene sorbitan fatty acid ester, 1.0% polyoxyethylene castor oil, 25.0% 1,3-propylene glycol, 3.0% hydrogenated polydecene, 0.1% phenylethyl resorcinol, 5.0% papaya Protease and 0.4% phloretin were stirred and dissolved in a water bath at 40°C to obtain an oil phase, which was set aside;
[0116] Stir and dissolve 0.1% heparin sodium, 0.1% vitamin C ethyl ether, 0.05% allantoin, 0.05% carnosine, 5.0% glycerin and 59.29% water in a water bath at 40°C to obtain an aqueous phase for later use;
[0117] After the oil phase and the water phase are obtained, add the oil phase to the water phase at a rate of 1 drop / second under the condition of a water bath at 40°C, and control the stirring rate at 15 rpm during the dropping process. Shear emulsification for 1min to make a micron-sized dispersion;
[0118] The micron-scale dispersion was subjected to high-pressure homogenization treatment under the condition of a pressure of 1200 bar, and the circulation was pe...
Embodiment 2
[0121] 15.0% polyoxyethylene castor oil, 2.0% polyoxyethylene hydrogenated castor oil, 7.0% 1,2-hexanediol, 3.0% isopropyl myristate, 1.0% phenylethyl resorcinol, 0.5% licorice Subacid, 1.0% curcumin, and 2.0% salicylic acid were stirred and dissolved in a water bath at 45°C to obtain an oil phase, which was set aside;
[0122] Stir and dissolve 6.0% nicotinamide, 6.0% vitamin C ethyl ether, 10.0% glycerin and 46.5% water in a water bath at 45°C to obtain an aqueous phase for later use;
[0123] After the oil phase and the water phase are obtained, add the oil phase to the water phase at a rate of 2 drops / second under the condition of a water bath at 45°C, and control the stirring rate at 10 rpm during the dropping process. Shear emulsification for 3 minutes to make a micron-scale dispersion;
[0124] The micron-scale dispersion was subjected to high-pressure homogenization treatment under the condition of a pressure of 1000 bar, and the circulation was repeated twice to obta...
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