Application of ginsenoside composition in preparation of medicine for preventing and treating alopecia by acting on hair follicle tissue
A technology of ginsenosides and compositions, applied in the field of medicine, to achieve the effect of simple ingredients
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Embodiment 1
[0027] Embodiment 1: the effect of preventing and treating alopecia of ginsenoside composition of the present invention
[0028] In order that the ginsenoside composition of the present invention has the effect of preventing hair loss and growing hair, 80 hair loss subjects were selected, aged 18-60, with an average age of 30.5 years, half male and half male. The above-mentioned hair loss subjects were divided into 4 groups, 20 subjects in each group.
[0029] Each group is given the following conventional hair care essence respectively: (1) blank conventional hair care essence matrix: (2) the composition containing ginsenoside Rg1 and ginsenoside Re and the hair care essence of the conventional hair care essence matrix, wherein by weight percentage Ginsenoside Rg1 accounts for 5% of the total weight of the hair care essence, and ginsenoside Re accounts for 4% of the total weight of the hair care essence; Ginsenoside CK accounts for 1% of the total weight of hair care essence...
Embodiment 2
[0034] Example 2: Effects of the ginsenoside composition of the present invention on the growth of mouse hair follicles and the proliferation of hair follicle bulb cells in vitro
[0035] In Vitro Experiment of Mouse Vibrissa Hair Follicles
[0036] 1. Mouse vibrissae hair follicle organ culture
[0037] C57BL / 6J mice aged 4-6 weeks were sacrificed by cervical dislocation, their beards on both sides were cut off, and their vibrissae were disinfected with 75% alcohol three times. Then put them in Williams culture medium, under a dissecting microscope, use micro scissors and tweezers to separate the anagen hair follicles, and cut off the upper 1 / 3 part of the hair follicles. Hair follicle culture was carried out in a 96-well plate, one hair follicle was placed in each well, and 0.2 mL of Williams culture medium serum-free medium was added to each well, which contained transferrin 10 mg / L, penicillin 100 U / mL, streptomycin 100μg / mL and other components, placed in 37 ℃, 5% CO ...
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