Functional cosmetic composition comprising growth factors and amino acids
A cosmetic composition and growth factor technology, applied in cosmetics, cosmetic preparations, medical preparations containing active ingredients, etc., to achieve the effect of improving skin wrinkles, excellent skin wrinkles, and improving skin elasticity
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Embodiment 1
[0042] In Example 1, after adding human growth factors (EGF, FGF, VEGF) to the cell culture solution, the proliferation promoting effect on skin fibroblasts was observed.
[0043] (1) Isolate fibroblasts from human tissues
[0044] The human abdomen skin tissue was taken into a sterilized 10cmbeaker, and washed with phosphorylation buffer solution (D-PBS) of the same skin (1:1). Put 20ml of D-PBS into Cleanbench, grab the tissue with forceps with one hand, and cut the skin tissue into a size less than 2mm with a scalpel. Recover the cut tissue and solution and put 20ml into multiple 50ml conicaltubes for centrifugation. The same amount of 0.15% collagenasetype-1 solution (Invitrogen) was added and reacted at 37°C for 1-2 hours. After washing with D-PBS, centrifugation was performed at 400×g for 5 minutes. Remove the supernatant. After adding 10-40ml of D-PBS to the pellet remaining at the bottom to dissolve the precipitated and agglomerated cells, it is passed through a 70-100m...
Embodiment 2
[0053] In Example 2, the synthesis performance of collagen (collagen) of human fibroblasts was observed in the DMEM medium supplemented with human growth factors and collagen precursors.
[0054] (1) Isolate fibroblasts from human tissues
[0055] The human abdomen skin tissue was taken into a sterilized 10cmbeaker, and washed with phosphorylation buffer solution (D-PBS) of the same skin (1:1). Put 20ml of D-PBS into Cleanbench, grab the tissue with forceps with one hand, and cut the skin tissue into a size less than 2mm with a scalpel. Recover the cut tissue and solution and put 20ml into multiple 50ml conicaltubes for centrifugation. The same amount of 0.15% collagenasetype-1 solution (Invitrogen) was added and reacted at 37°C for 1-2 hours. After washing with D-PBS, centrifugation was performed at 400×g for 5 minutes. Remove the supernatant. After adding 10-40ml of D-PBS to the pellet remaining at the bottom to dissolve the precipitated and agglomerated cells, it is passed t...
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