Application of stromal vascular fraction cells and mesenchymal progenitor cells to prevention or treatment of osteoarthritis
An osteoarthritis, vascular layer technology, applied in the application field of interstitial vascular layer cells and mesenchymal progenitor cells in the prevention or treatment of osteoarthritis, can solve the lack of methods for prevention or treatment of knee osteoarthritis, Donor site destruction, inability to treat cartilage defects, etc.
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Embodiment 1
[0154] SVF and haMPCs for Knee Osteoarthritis (KOA)
example 1
[0156]The patient is a 45-year-old woman with bilateral knee joint pain for more than 3 years, morning stiffness, limited mobility, difficulty in going up and down stairs, and pain when walking on level ground. X-ray examination showed obvious osteophytes, joint space narrowing, and sclerotic changes . The WOMAC score is 92 points. Diagnosis: moderate knee osteoarthritis.
[0157] About 30ml of fat was extracted from the lower abdomen of KOA patients, and the vascular matrix part was separated from 10ml of freshly obtained adipose tissue, and the SVF was obtained after collagenase digestion, filtration, and centrifugation to remove mature adipocytes, and the surface antigen of the SVF was identified. For identification results, see figure 2 .
[0158] Dose each side as 5*10 6 Each cell / 2ml of SVF was injected into the bilateral joint cavity of the patient. The remaining adipose tissue was isolated and purified, and the P2-P5 generations were cultured to obtain haMPCs. T...
Embodiment 2
[0165] Identification of embodiment 2SVF and haMPCs
[0166] 1. Flow detection
[0167] Cells were collected into centrifuge tubes by enzymatic digestion, and the cell suspension was adjusted to a density of 1×10 5 / mL, 800r / min (120g), centrifuge for 5min, discard the supernatant, wash the resuspended cells with cold D-Hanks at 4°C, centrifuge the cell suspension again at 800r / min for 5min, and then discard the supernatant. Then the cells were resuspended to 1 mL with D-Hanks, 5-10 μL of antibody was added, protected from light, and placed on ice for 30 min. Rinse with D-Hanks, centrifuge, discard the supernatant, repeat the washing process 2-3 times to ensure that unbound antibodies are removed, and finally, add about 200 to 300 μL of D-Hanks to make a suspension, and use a flow cytometer to detect ( figure 2 ).
[0168] The flow cytometric detection results of SVF are shown in Table 1.
[0169] Table 1
[0170]
[0171] The expression of cell surface antigen marke...
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