Active external essence solution with functions of diminishing inflammation, facilitating skin reparation and regeneration and whitening skin and preparation method of essence solution
A skin repair and essence technology, applied in the direction of medical preparations containing active ingredients, skin care preparations, anti-inflammatory agents, etc., can solve skin redness, suppuration or pain, pathogenic bacteria are prone to drug resistance, and skin irritation Major problems, achieve the effect of restoring skin health, promoting the formation of new epidermis, and strict compatibility
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Embodiment 1
[0038] The preparation of embodiment 1 plant extract
[0039] (1) Wash, dry and pulverize the nine plant raw materials of Akebia vine, Angelica dahurica, Sophora japonica, Trichosanthes pollen, Nocturnal vine, Polygonum cuspidatum, Selaginella chinensis, Aloe vera and Mint, and pass through a 20-mesh sieve to obtain The powder is extracted according to steps (2)-(4) respectively;
[0040] (2) Carry out reflux extraction with 90% ethanol by volume at 80°C, the mass volume ratio of crude drug to ethanol g / mL is 1:20, reflux extraction for 4 hours, a total of 4 times, and then combine the extracts;
[0041] (3) The remaining residue is leached 3 times with hot water, 4 hours each time, the extract is combined with the extract of step (2) and then cooled to 20°C to 30°C, filtered through a 100-mesh filter cloth to obtain the filtrate;
[0042] (4) in the filtrate that step (3) obtains, add the 1,3-butanediol miscibility of the same volume as ethanol, concentrate under reduced pre...
Embodiment 2
[0045] Embodiment 2 has anti-inflammation, promotes the active external application essence of skin repair regeneration and whitening effect
[0046] 1. Formula
[0047] Calculated by weight percentage, glycerin stearate 3.5%, polydimethylsiloxane 2.0%, isononyl isononanoate 1.5%, jojoba oil 1.5%, Moroccan argan oil 1.5%, tamanu oil 4.0% , Isopropyl Myristate 1.5%, Octyl Stearate 2.5%, Linoleic Acid 1.5%, Caprylic / Capric Triglyceride 2.0%, Xanthan Gum 0.1%, Propylene Glycol 2.0%, Butylene Glycol 1.5%, Seaweed Sugar 0.5%, L-pyrrolidone sodium carboxylate 1.0%, hydrogenated castor oil 1.5%, Va palmitate 0.5%, Ve acetate 0.1%, hyaluronic acid 0.3%, the plant extract prepared in Example 1 5.0%, tobacco Amide 2.0%, preservative (phenoxyethanol) 0.1%, water make up 100%.
[0048] The hyaluronic acid consists of large molecular weight hyaluronic acid with a molecular weight of 1 800 000 to 2 200 000 Da, medium molecular weight hyaluronic acid with a molecular weight of 1 000 000 to...
experiment example 1
[0059] Anti-inflammatory activity evaluation of plant extract part in Experimental Example 1 product of the present invention
[0060] Hyaluronidase and trypsin are important enzymes in the occurrence and development of inflammation. Reducing or inhibiting the activity of these two enzymes is an effective way to prevent inflammation. This example studies the effect of the product of the present invention on hyaluronidase To illustrate the anti-inflammatory effect of the plant extract part in the product of the present invention.
[0061] Experimental group I: plant extract I, prepared according to the method of Example 1
[0062] Experimental group II: plant extract II, prepared according to the method of Example 1, the difference is that it does not contain Akebia extract
[0063] Experimental group II: Akebia extract, prepared according to the method in Example 1
[0064] The above plant extracts were dissolved by adding 10 times the weight of distilled water, and prepared...
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