Preparation method of hair follicle stem cell active factor freeze-dried powder for treating alopecia
A technology for hair follicle stem cells and active factors, which is applied in the field of preparation of lyophilized powder of hair follicle stem cell active factors for the treatment of hair loss, can solve the problems of short storage time, reduced activity, unfavorable transportation, etc. The effect of various activities and easy access to materials
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[0037] see figure 1 Shown, the preparation method of the hair follicle stem cell active factor freeze-dried powder provided by the invention comprises the following steps:
[0038] S1. Acquisition of hair follicle stem cells: Under sterile conditions, cut the hair root to obtain hair follicle tissue, then wash the hair follicle tissue in DPBS containing double antibody, then cut it into pieces, and inoculate it in the primary medium for primary Subculture, then digest and purify to obtain hair follicle stem cells;
[0039] S2. Acquisition of active factors of hair follicle stem cells: the hair follicle stem cells are subcultured, and then enriched, centrifuged, and concentrated by ultrafiltration to obtain a concentrate of active factors of hair follicle stem cells;
[0040] S3. Mixing and freeze-drying: after mixing the hair follicle stem cell active factor concentrated solution and the auxiliary solution in a mixer, a mixed solution is obtained; after the mixed solution is ...
Embodiment 1-1
[0047] Acquisition of hair follicle stem cells: Under sterile conditions, cut the hair root to obtain hair follicle tissue, then wash the hair follicle tissue in DPBS containing penicillin and streptomycin, and then cut it into pieces (0.8mm 3 ), and inoculated in primary medium for primary culture, then digested and purified to obtain hair follicle stem cells;
[0048] Among them, the primary culture medium is HG-DMEM culture medium containing 10% fetal bovine serum by volume fraction, and the medium is changed every 3 days in the primary culture; the specific operation of digestion is to obtain hair follicles when the cell density is 70-75%. Tissue cells, then add neutral protease, hair follicle tissue cells, and PBS buffer into a centrifuge tube to seal, and place on a shaker at 37°C at 100r / min to digest for 1.5h, centrifuge at 2000rpm, discard the supernatant, and then use sterile PBS buffer Rinse twice with liquid to wash away neutral protease, then add 0.01% trypsin-EDT...
Embodiment 1-2
[0050] Acquisition of hair follicle stem cells: Under sterile conditions, cut the hair root to obtain hair follicle tissue, then wash the hair follicle tissue in DPBS containing penicillin and streptomycin, and then cut it into pieces (0.8mm 3 ), and inoculated in primary medium for primary culture, then digested and purified to obtain hair follicle stem cells;
[0051] Among them, the primary culture medium is HG-DMEM culture medium containing 10% fetal bovine serum by volume fraction, and the medium is changed every 3 days in the primary culture; the specific operation of digestion is to obtain hair follicles when the cell density is 75-85%. Tissue cells, then add neutral protease, hair follicle tissue cells and PBS buffer into a centrifuge tube to seal, and place on a shaker at 37°C at 100r / min for digestion for 2h, centrifuge at 2000rpm, discard the supernatant, and then use sterile PBS buffer Rinse twice to remove neutral protease, then add 0.125% trypsin-EDTA solution, s...
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