Method for preparing adipose-derived stem cell sap for cosmetic maintenance
A technology of fat stem cells and cells, which is applied in the field of medical cosmetology, can solve the problems of not being able to effectively promote the metabolism of epidermal cells, having no biologically active substances, and many harmful substances remaining, so as to promote skin wound healing, prolong storage time, and prevent discoloration. spot effect
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[0025] The embodiment of the present invention provides a preparation method of adipose stem cell fluid for beauty maintenance, comprising the following steps:
[0026] Step 1: Obtain adipose stem cells, obtain adipose tissue, wash with D-Hanks buffer to remove residual blood and tissue fragments, cut the adipose tissue into small fat pieces, add the adipose tissue to the digestive juice, and put it in a constant temperature shaking box at 37°C Digest in medium for 20-60 minutes, then let it stand until it is stratified, absorb the upper fat cell liquid, transfer it into the DMEM medium containing fetal bovine serum, seal and centrifuge, the speed of centrifugation is 800rpm-1800rpm, and the centrifugation time is 5min- After centrifugation for 15 minutes, remove the supernatant, add an appropriate amount of DMEM medium containing fetal bovine serum again, pipette the cells to make adipose-derived stem cell suspension, inoculate into culture flasks, and store at 37°C in 5% CO ...
Embodiment 1
[0034] Prepare adipose-derived stem cell fluid by the following steps:
[0035] Step 1: Obtain adipose stem cells. First, obtain adipose tissue. The adipose tissue can be obtained from the human body through liposuction. The adipose tissue is washed with D-Hanks buffer to remove residual blood and tissue fragments, and the adipose tissue is cut into For small fat pieces, add the fat tissue into the digestion solution, put it in a 37°C constant temperature shaking box for digestion for 20 minutes, then let it stand until it is layered, absorb the upper fat cell liquid, transfer it into the DMEM medium containing fetal bovine serum, seal and centrifuge Separation, the speed of centrifugation is 800rpm, and the centrifugation time is 15min. After centrifugation, the supernatant is removed, and an appropriate amount of DMEM medium containing fetal bovine serum is added again. At 37°C, 5% CO 2 Culture at a constant temperature, and replace the medium regularly until the adipose st...
Embodiment 2
[0040] Prepare adipose-derived stem cell fluid by the following steps:
[0041] Step 1, to obtain adipose stem cells, first obtain adipose tissue, wash the adipose tissue with D-Hanks buffer to remove residual blood and tissue fragments, cut the adipose tissue into small fat pieces, add the adipose tissue to the digestive juice, and put it in 37℃ Digest in a constant temperature shaking box for 30 minutes, then let it stand until it is layered, absorb the upper fat cell liquid, transfer it into the DMEM medium containing fetal bovine serum, seal and centrifuge, the speed of centrifugation is 800rpm, and the centrifugation time is 15min. Remove the supernatant after separation, add an appropriate amount of DMEM medium containing fetal bovine serum again, pipette the cells to make adipose stem cell suspension, inoculate into culture flasks, and store at 37°C, 5% CO 2 Culture at a constant temperature, and replace the medium regularly until the adipose stem cells cover the bottom...
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