Application of endometrium stem cell in preparation of medicine for curing liver fibrosis
A technology of endometrial stem cells and liver fibrosis, applied in animal cells, drug combinations, vertebrate cells, etc., can solve the problems of donor shortage and high cost, and achieve the effect of improving liver function and reducing the degree of liver fibrosis
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Embodiment 1
[0015] Example 1: Preparation of chronic liver injury mouse model
[0016] Utilize 10% (volume concentration) carbon tetrachloride (CCl 4 , the solvent is olive oil) to induce chemical liver injury to eight-week-old ICR mice (about 25 grams in body weight), intraperitoneal injection, the dose is 1ml CCl 4 / kg body weight, 2 times a week, continuous injection for 4 weeks, to establish the liver fibrosis model, and the injected mice were fed normally in a sterile environment.
Embodiment 2
[0017] Embodiment 2: the preparation of serum preparation
[0018] Serum preparation: Blood was collected from the orbital blood method of liver fibrosis model mice as described in Example 1, or venous blood was collected from patients with liver fibrosis, kept in a water bath at 37°C for 30 minutes, centrifuged at 3500rpm for 10 minutes, and the supernatant was taken at -20 ℃ frozen for later use.
[0019] Serum preparation preparation: DMEM culture fluid + penicillin + 100U / ml streptomycin + volume concentration 1% amphotericin B + volume concentration 1% glutamine + volume concentration 20% fetal bovine serum, add volume final concentration of 1 to 5% The above-mentioned serums are ready-to-use and ready-to-use.
Embodiment 3
[0020] Example 3: Endometrial Stem Cell Preparation
[0021] (1) Isolation and culture of endometrial stem cells
[0022] Collect menstrual blood samples from donors for routine microbial and infectious disease pathogen safety testing, use 1.0779 / ml Ficoll for density gradient centrifugation, separate mononuclear cells, wash the isolated mononuclear cells 3 times with normal saline, and use DMEM culture medium (add 100U / ml penicillin+100U / ml streptomycin+volume concentration 1% amphotericin B+volume concentration 1% glutamine+volume concentration 20% fetal bovine serum) adjust cell density to (3~5)×10 6 cells / ml, seeded on the bottom area of 75cm 2 culture flask at 37°C, 5% CO 2 Cultivate in an incubator; after 48 hours, wash off non-adherent cells, continue to culture until about 80% confluence, digest with 0.25% trypsin-EDTA, and pass passage.
[0023] (2) Preparation of endometrial stem cell preparation
[0024] Take the endometrial stem cells that have grown to about...
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