Dressing for treating diabetic foot and preparation method thereof
A glycosaminoglycan and stem cell technology, applied in the field of stem cells, can solve the problems of difficult to obtain curative effect, unable to fully heal diabetic foot wound healing, etc., and achieve the effect of promoting rapid healing, reducing immune rejection, and easy to obtain.
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[0024] The present invention has no special limitation on the source of umbilical cord mesenchymal stem cells, and those familiar to those skilled in the art can be used, such as commercially available umbilical cord mesenchymal stem cells; conventional umbilical cord mesenchymal stem cells well known to those skilled in the art can also be used The preparation method is prepared. In the present invention, the preparation method of umbilical cord mesenchymal stem cells is preferably the following specific steps:
[0025] Take the freshly collected human umbilical cord, wash the blood stains on the surface with PBS buffer, cut the umbilical cord into 1-2cm long pieces with surgical scissors, remove the arteriovenous and adventitia respectively, and cut to (20-50)mm with ophthalmic scissors 3 size organization block.
[0026] Flatten an appropriate amount of tissue pieces into a Petri dish with tweezers, add to DMEM / F12 culture medium containing 10% FBS, and transfer to 5% CO ...
Embodiment 1
[0043] Step 1 Isolation of human umbilical cord mesenchymal stem cells
[0044] Take the freshly collected human umbilical cord, wash the blood stains on the surface with PBS buffer, cut the umbilical cord into 1-2cm long pieces with surgical scissors, remove the arteriovenous and adventitia respectively, and cut to (20-50)mm with ophthalmic scissors 3 size organization block.
[0045] Flatten an appropriate amount of tissue pieces into a Petri dish with tweezers, add to DMEM / F12 culture medium containing 10% FBS, and transfer to 5% CO 2 , 37°C, and a saturated humidity of 95% in an incubator, the first 5-7 days are static culture, and the first rehydration is performed when the color of the culture solution changes to light yellow; when at least 5 places crawl out of each dish are observed After forming a sheet of cells, use a pipette to suck off the culture medium and tissue pieces in the dish, and then perform liquid replacement treatment to continue culturing, and then ob...
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