Hair restoring liquid containing dermal papilla cell derived exosome and collagen and preparation method thereof
A dermal papilla cell and collagen technology, which is applied in the field of hair growth liquid containing dermal papilla cell-derived exosomes and collagen and its preparation field, can solve the problem of inability to treat both the symptoms and root causes, difficulty in lifting finasteride, poor effect, etc. It can improve the structural stability and long-term efficacy, promote proliferation activity and migration activity, and improve the effect of oily scalp and hair loss.
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preparation example 1
[0071] Isolation and culture of human scalp dermal papilla cells:
[0072] (1) The discarded human scalp hair follicles after hair transplantation (with the patient's signature and consent), were immediately placed in a sterile centrifuge tube filled with Bingsheng Ringer's solution, and quickly transferred to the laboratory. Human scalp tissue needs to separate the hair follicles under a microscope, cut the hair bulbs with micro scissors and move them to a new PBS petri dish.
[0073] (2) Collect all excised dermal papillae and wash them three times with fresh PBS. Use a syringe to carefully aspirate the PBS washing solution under the microscope, taking care not to aspirate the dermal papilla. Digest the dermal papilla with 0.2% type I collagenase, and digest it in a cell culture incubator at 37°C for 1.5 hours. Under the microscope, it can be seen that some black dermal papilla cells are separated from the white dermal sheath. At this time, pipette Pipette with a gun and c...
preparation example 2
[0077] Extraction of exosomes from low-generation human dermal papilla cells:
[0078] When the 3rd or 5th generation human scalp dermal papilla cells are within 25cm 2When the growth in the culture bottle reaches 90% confluence, replace the culture medium with 5 mL low-sugar DMEM medium containing no fetal bovine serum and culture for 3 days, then transfer it to a special centrifuge tube of 50 mL high-speed centrifuge, centrifuge at 2000 g at 4 °C for 20 min. Remove the supernatant and transfer it to a polyethylene glycol tube suitable for ultracentrifugation rotors. Mark one side of each ultracentrifuge tube with a waterproof marker, place the tube on the rotor with the marked side up, and centrifuge at 10,000 g, 4 °C for 30 min, then transfer the supernatant to the same size polyethylene glycol as above centrifuge at 4°C for 1 h at 100,000 g, remove the supernatant thoroughly, and resuspend the pellet in each tube in 1 mL of PBS using a micropipette.
[0079] The exosomes...
Embodiment 1
[0081] This embodiment provides a hair tonic, which includes an exosome composition and auxiliary materials. The exosome composition is dermal papilla cell-derived exosomes and collagen coated therein at a mass ratio of 7:1; the auxiliary material and hair papilla The mass ratio of cell-derived exosomes is 20:1; the excipients are 2 parts of stabilizer (1 part of sodium hyaluronate, 1 part of hydroxyethyl starch), 3 parts of humectant (propylene glycol), and 2 parts of scalp absorption promoter ( 1 part of dimethyl sulfoxide, 1 part of menthol), 1 part of antioxidant (citric acid) and 100 parts of water.
[0082] The preparation method of this hair tonic is as follows:
[0083] (1) Mix the third-generation dermal papilla cell-derived exosomes prepared in Preparation Example 2 with the electrotransfection buffer to prepare the first solution;
[0084] (2) mixing the first solution obtained in step (1) with collagen, and performing electroporation transduction to obtain a secon...
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