Cosmetic or plastic composition comprising multipotent stem cells derived from human adipose tissue, fibroblast, and adipose or adiopocyte
A fibroblast and adipose tissue technology, applied in bone/connective tissue cells, animal cells, tissue culture, etc., can solve problems such as stem cell plastic surgery and plastic surgery with less effort
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Embodiment 1
[0033] Example 1: Isolation of multiplastic adult stem cells from adipose tissue and preparation of compositions for plastic surgery
preparation Embodiment 1
[0035] Uniformly resuspend the adipocyte-containing suspension obtained by liposuction in saline with an appropriate amount of saline, and place a sufficient amount of the resuspended suspension in a cell culture flask or a shaker flask Incubate by standing or shaking. A minimum of 6-12 hours is required for static cultures. Next, the cell layer (MSCs from adipose, fibroblasts) attached to the surface of the culture flask was collected by treating with trypsin ( figure 1 ). At this time, the cells suspended in a small amount of saline are directly collected for use, or the cell layer collected from the saline is centrifuged at 1000 rpm for 10 minutes to use only the pelleted pellet in the case where the volume of the cell layer should be reduced . The separated cell layer contains adult stem cells and fibroblasts. The composition for cosmetic or plastic surgery containing adult stem cells, fibroblasts, fat and adipocytes according to the present invention is prepared by mi...
preparation Embodiment 2
[0037] Pluriplastic stem cells were isolated and purified from human adipose tissue. That is, the isolated human adipose tissue was washed 3 times with PBS and then finely dissected. The dissected tissue was digested at a ratio of 1:3 (adipose tissue:DMEM) in DMEM-LG (low glucose) medium supplemented with type 1 collagenase (1 mg / ml) at 37° C. for 1 hour. After washing the digested tissue with PBS, it was centrifuged at 1000 rpm for 5 minutes. The supernatant was aspirated, and the remaining pellets on the bottom were washed with a mixture of 10% FBS and DMEM-LG (low sugar) at a ratio of 1:1, followed by centrifugation at 1000 rpm for 5 minutes. The resulting pellet was filtered through a 100 μm mesh to remove debris and washed with PBS. The obtained cells were cultured in DMEM medium (10% FBS, 2 mM NAC, 0.2 mM ascorbic acid). After one night, unattached cells were washed with PBS and incubated in K-NAC medium (keratinocyte-SFM medium + 2 mM NAC + 0.2 mM ascorbic acid + 0.0...
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