A soft tissue construction method and application of synovial mesenchymal stem cells
A technology of mesenchymal stem cells and construction methods, applied in the field of soft tissue construction of synovial mesenchymal stem cells, to achieve strong chondrogenic potential, easy to obtain materials, and good application prospects
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Embodiment 1
[0035] The preparation method of embodiment 1 soft tissue (1)
[0036] The soft tissue was prepared as follows:
[0037](1) Isolation and culture of synovial mesenchymal stem cells: The fresh human synovial specimens were surface-sterilized twice with 75% ethanol, washed twice with PBS, placed in a petri dish, and the tissues were cut with sterilized surgical scissors. For small fragments, put them in a 50ml centrifuge tube, add an appropriate amount of PBS, centrifuge, discard the supernatant, add an appropriate amount of type II collagenase, shake on a shaker (200rpm, 37°C) for 2 hours, centrifuge to discard the collagenase, and finally in the tissue Add an appropriate amount of low-sugar DMEM culture solution containing 10% FBS to the fragments, then transfer to a petri dish and place at 37°C, 5% CO 2 Culture in an incubator with saturated humidity, transfer the tissue block to a new culture dish two days later, continue culturing for two days and then discard the tissue b...
Embodiment 2
[0042] Embodiment 2 The preparation method of soft tissue (two)
[0043] The soft tissue was prepared as follows:
[0044] (1) Isolation and culture of synovial mesenchymal stem cells: sterilize the surface of fresh human synovial specimens with 70% ethanol once, wash them once with PBS, put them in a petri dish, and cut the tissue with sterilized surgical scissors. For small fragments, put in a 50ml centrifuge tube, add appropriate amount of PBS, centrifuge, discard the supernatant, add appropriate amount of type II collagenase, shake on a shaker (200rpm, 37°C) for 1 hour, centrifuge to discard the collagenase, and finally in the tissue Add an appropriate amount of low-sugar DMEM medium containing 5% FBS to the fragments, then transfer to a petri dish, and place at 32°C, 3% CO 2 Culture in an incubator with saturated humidity, transfer the tissue block to a new culture dish two days later, continue to culture for two days and then discard the tissue block until the mesenchym...
Embodiment 3
[0049] Embodiment 3 The preparation method of soft tissue (three)
[0050] The soft tissue was prepared as follows:
[0051] (1) Isolation and culture of synovial mesenchymal stem cells: The fresh human synovial specimens were surface-sterilized with 80% ethanol for 3 times, washed with PBS for 3 times, placed in a petri dish, and the tissues were cut with sterilized surgical scissors. For small fragments, put in a 50ml centrifuge tube, add appropriate amount of PBS, centrifuge, discard the supernatant, add appropriate amount of type II collagenase, shake on a shaker (200rpm, 37°C) for 3 hours, centrifuge to discard the collagenase, and finally in the tissue Add an appropriate amount of low-sugar DMEM culture solution containing 15% FBS to the fragments, then transfer to a petri dish and place at 42°C, 7% CO 2 Culture in an incubator with saturated humidity, transfer the tissue block to a new culture dish two days later, continue to culture for two days and then discard the t...
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