Stem cell bioactive composition and preparation method and application thereof
A stem cell biology and composition technology, applied in biochemical equipment and methods, cell culture active agents, non-embryonic pluripotent stem cells, etc. The effect of promoting growth and maintaining undifferentiated state, avoiding safety hazards, and high yield
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Embodiment 1
[0021] Embodiment 1, separation and purification of adipose stromal cells
[0022] After informed consent of the patients, adipose tissue was obtained by liposuction. The age of the patient is between 37-54 years old, and the body mass index (kg / m 2 ) between 28-35, in good health except obesity, without diabetes or other complications. After liposuction, put the adipose tissue in normal saline and send it to the laboratory within 2 hours after the operation, wash with 2 times the volume of Krebs-Ringer Bicarbonate buffer 3-4 times to remove blood stains, and then use 1 times the volume of type Ⅰ collagenase (1g / L of KRB, 1% BSA) was digested at 37°C for 60min with intermittent stirring. After digestion, centrifuge at 300 g for 5 min to remove floating adipocytes. Inoculate the obtained stromal cells into cell culture flasks at 37°C, 5% CO 2 The cells were cultured in an incubator at an initial density of 3.5×10 3 piece / cm 2 , the cells grow to about 80% after 4-5 days o...
Embodiment 2
[0023] Embodiment 2, separation and purification of placental mesenchymal stem cells
[0024] Take the placental tissue of full-term normal delivery or caesarean section, strip off the maternal side decidua, cut small pieces of fetal decidua side placental tissue, wash with PBS, and remove blood. Cut the placental tissue into pieces, add 0.1% type IV collagenase, digest at 37°C for 30 minutes, pass through a 100-mesh sieve, collect the cell suspension, add the prepared medium (containing DMEM, 10% FBS, 5ng / mL bFGF, 100U / mL penicillin, 100μg / mL streptomycin, 25mmol / L glutamine), adjust the culture cell density to 1×10 5 cells / mL, placed at 37°C, 5% CO 2 cultured in an incubator, and the medium was changed every 3-4 days. Only a small amount of adherent cells were obtained in the cells obtained after the fetal decidua side placental tissue was digested. After 2 weeks, flat monolayer cells gradually formed. The cells were passaged and frozen according to conventional methods. S...
Embodiment 3
[0025] Example 3, Establishment of a co-culture system of adipose stromal cells and mesenchymal stem cells
[0026] A non-contact co-culture of adipose stromal cells and mesenchymal stem cells was carried out using a Transwell hanging culture chamber with a PET membrane combined with a 6-well plate. Cells in the logarithmic growth phase were taken, digested with 0.05% / 0.25% trypsin to make a single cell suspension, counted, adjusted the cell density and inoculated, and the medium was MSC serum-free medium. In the experimental group, adipose stromal cells were inoculated in the lower chamber of the Transwell culture chamber, and then the upper chamber of the Transwell suspension culture chamber was placed in the hole, and MSCs were inoculated in the Transwell suspension culture chamber, so that the culture medium in the upper and lower chambers could communicate with each other, thereby A co-culture system of adipose stromal cells and mesenchymal stem cells was established; in ...
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