Method for preparing artificial skin containing hair follicle
A technology of artificial skin and hair follicles, applied in the fields of biomedicine and artificial skin preparation, can solve the problems of no epidermis, easy infection, small culture area, etc., and achieve the effects of promoting normal healing, easy large-scale production, and convenient operation
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Embodiment 1
[0017] (1) Use microsurgical scissors and microsurgical photography to separate a number of mouse vibrissae hair follicles (>100) under a dissecting microscope, add 0.5% dissociating enzyme, digest for 16-18 hours at 4°C, and transfer the hair follicles into D-Hanks solution, centrifuged to remove the isolated enzyme. Squeeze out the hair shaft from the hair follicle, digest the hair follicle epithelial cells with 0.125% trypsin plus 0.02% EDTA, stop the digestion with 5% D-Hanks solution of newborn bovine serum, blow the cells, sieve, count, and centrifuge.
[0018] (2) Digest rat vibrissa follicles with 0.3% collagenase D at 37°C for 4 to 6 hours after removal of the hair shaft, and stop when the dermal sheath surrounding the hair follicles has been digested into single cells and the dermal papilla inside has not yet begun to digest Digest, wash with D-Hanks solution, centrifuge to remove collagenase D three times, centrifuge at low speed (300rpm) for 5 minutes, collect supe...
Embodiment 2
[0021] The preparation method refers to Example 1, and the subcultured dermal papilla cells (4 / ml. A small amount of hair follicle-like structures were observed after 8 weeks of culture.
Embodiment 3
[0023] The preparation method refers to Example 1, and the subcultured dermal papilla cells (5 / ml. A small amount of hair follicle-like structures were observed after 8 weeks of culture.
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