Tissue engineered esophagus
A tissue engineering and esophagus technology, applied in medical science, prosthesis, etc., can solve the problems of unsatisfactory biocompatibility and cell affinity, and achieve good cell compatibility and good degradation rate.
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Embodiment 1
[0018] Isolation and culture of epidermal keratinocytes
[0019] The patient's epidermis was trimmed into strips with a width of 1-2 stomachs, rinsed twice in PBS without calcium and magnesium, and immersed in 0.5% neutral protease overnight with the epidermis facing upward. After the epidermis was torn off from the dermis, it was cut into pieces and digested with 0.05% trypsin-0.53mM EDTA at 37°C for 20 minutes, and 10ml of trypsin inhibitor was used to terminate the digestion. Filter through a 150-mesh stainless steel filter, centrifuge (1200 rpm, 10 minutes) and count to make a single-cell suspension, press 10 5 / m 2 Density seeding culture, serum-free epidermal cell medium, plus bovine pituitary extract and recombinant epidermal growth factor, at 37°C, 5% CO 2 Cultured in an incubator with saturated humidity, the culture medium was changed every 3 days. When the cells reached 60%-70% confluence, they were digested with 0.05% trypsin at 37°C for 10 minutes, and subcultur...
Embodiment 2
[0021] Dermal Fibroblast Isolation and Culture Isolation and Digestion
[0022] The leather fragments in Example 1 were digested with 2% collagenase at 37°C for 2 hours, filtered through a 150-mesh stainless steel filter, centrifuged at 1200 rpm for 5 minutes, the supernatant was discarded, and calcium and magnesium-free PBS was added to wash 3 times. Add 10ml of culture medium containing 10% fetal bovine serum, mix well, and count by trypan blue staining.
[0023] After counting the primary culture, make a single cell suspension, press 10 5 / cm 2 Density inoculation culture, DMEM culture solution containing 10% fetal bovine serum, cultivated in an incubator at 37°C and 10% relative humidity, and the culture solution was changed every 3 days. When the cells are confluent to 60%-75% density, wash with 1% calcium and magnesium-free PBS, digest with 0.25% trypsin at 37°C for 5 minutes, add DMEM medium containing 10% fetal bovine serum, mix well, count, press Subculture at a r...
Embodiment 3
[0025] Constructing tissue engineered esophagus
[0026] Vascular endothelial cells and dermal fibroblasts cultured in vitro were collected, seeded on tissue-engineered skin scaffold materials, and vascular endothelial cells, fibroblasts-acellular dermal complexes were constructed. Seeding density is 10 5 -10 8 . The culture medium was changed every 3 days, and the culture time was 7-10 days.
[0027] Form a double-layer structure: collect epidermal cells and inoculate them on the surface of vascular endothelial cells, fibroblasts-degradable scaffold material composites. After one week, an air-liquid interface formed on the surface of the complex, promoting further differentiation of vascular endothelial cells.
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