Method for promoting hair growth
A technology for hair growth and hair follicles, applied in the field of beauty and health care, can solve problems such as affecting hair growth, slow growth, and falling off, and achieve the effects of less toxic and side effects, easy absorption, and simple operation.
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Embodiment 1
[0022] The specific process of Bpv (phen) promoting mouse telogen hair follicles to enter the growth phase is as follows:
[0023] 1. Anesthetize 7-9 week old mice with sodium pentobarbital;
[0024] 2. Use depilatory cream to remove the hair on the back of the mouse;
[0025] 3. Dissolve 0.2mg of bpv (phen) inhibitor and 10mg of PLGA / TPGS nanomaterials in 5ml of acetone, stir and centrifuge, resuspend with 50ul PBS, PLGA / TPGS / PBS as a control, and then subcutaneously injected into the back of the mouse;
[0026] 4. After 15 days and 21 days, observe the hair growth situation of two groups of mice, the inventors found that the bpv (phen) inhibitor treated part hair grows very fast, while other parts hardly have;
[0027] Experimental results: 15 days after the mice were depilated, no hair entered the anagen phase at all, while the areas treated with the inhibitor had already grown hair. Twenty-one days after depilation, the skin of the mice had just begun to darken, while t...
Embodiment 2
[0029] Analyze the phosphorylation of mouse epidermal cells and hair follicle cells treated with bpv (phen) inhibitors:
[0030] 1. Get the skin tissues of bpv (phen) inhibitor treatment group and control group respectively;
[0031] 2. After 4% PFA fixation and sucrose dehydration, perform tissue sectioning;
[0032] 3. Immunofluorescence staining showed that the epidermal cells and hair follicle cells of the mice treated with the inhibitor almost all expressed AKT-P 3 days after depilation, while the epidermal cells and hair follicle cells of the control group almost did not express;
[0033] 4. Experimental results: 3 days after hair removal in mice, the hair follicles were in the telogen stage, and the expression of AKT-P in the hair follicles and their epidermis was very low, almost no expression, while the expression of KAT-P in the hair follicles and epidermis of the inhibitor treated parts was very high , indicating that these cells are activated.
Embodiment 3
[0035] Analysis of bpv (phen) inhibitor treated mouse hair follicle growth cycle and hair follicle stem cell proliferation:
[0036] 1. Get the skin tissues of bpv (phen) inhibitor treatment group and control group respectively;
[0037] 2. After 4% PFA fixation and sucrose dehydration, perform tissue sectioning;
[0038] 3. Immunofluorescence staining showed that the hair follicles in the bpv (phen) inhibitor-treated area entered the anagen phase after 5 days, while the hair follicles in other areas were in the resting phase;
[0039] 4. Experimental results: Immunofluorescence staining of the cell proliferation marker Ki67 showed that hair follicle stem cells proliferated in large numbers after 5 days in the hair follicles treated with bpv (phen) inhibitors, while other control hair follicle stem cells rarely proliferated.
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