Preparation method and application of pancreas substrate hydrogel for repairing pancreatic tissue
A technology of hydrogel and pancreas, applied in the field of preparation of pancreatic matrix hydrogel, can solve the problems of large side effects and poor operability of drugs, and achieve the effects of mild implementation conditions, low immunogenicity, and promotion of endogenous repair.
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[0053] A method for preparing pancreatic matrix hydrogel for repairing pancreatic tissue, comprising the steps of:
[0054] B. Preparation of porcine pancreatic matrix hydrogel:
[0055] The decellularized pancreas tissue is freeze-dried and made into powder, then mixed with hydrochloric acid-pepsin solution in proportion, and the pH value is adjusted to a physiological state to obtain the porcine pancreas matrix hydrogel.
[0056] Further, the preparation method of the pancreatic matrix hydrogel for repairing pancreatic tissue also includes the steps of:
[0057] A. Decellularization of the pancreas:
[0058] (1) cutting the pancreatic tissue into thin slices, and rinsing with physiological saline to obtain thin slices of pancreatic tissue;
[0059] (2) immersing the thin slice of pancreatic tissue in a physiological saline solution containing sodium lauryl sulfate and stirring to obtain pancreatic tissue;
[0060] (3) The pancreatic tissue is soaked in Triton X-100 soluti...
Embodiment 1
[0063] The preparation of embodiment 1 porcine pancreas matrix hydrogel
[0064] Specific steps are as follows:
[0065] (1) Decellularization of porcine pancreas: first cut porcine pancreas tissue into thin slices about 2 mm thick and rinse with normal saline, then immerse it in 0.5% sodium lauryl sulfate / normal saline, stir at room temperature for 24 hours ;Finally transfer it to 1% Triton X-100 solution, stir at room temperature until the tissue is transparent, it takes about 1 hour, and rinse with normal saline 3-5 times, 15 minutes each time, to remove residual detergent.
[0066] (2) Preparation of porcine pancreatic matrix hydrogel: Grind the decellularized pancreatic tissue freeze-dried into powder with a pulverizer, then add it into hydrochloric acid-pepsin solution at a ratio of 10 mg / mL, stir slowly at room temperature until dissolved, Adjust to the physiological state (pH=7.4) by adding 0.1M sodium hydroxide and 10x PBS, so that the final concentration of the hydr...
Embodiment 2
[0068] Example 2 Use of porcine pancreatic matrix hydrogel in the preparation of drugs that promote endogenous repair of the pancreas
[0069] A. Preparation and identification of porcine pancreatic matrix hydrogel
[0070] (1) Preparation of porcine pancreatic matrix hydrogel: take fresh porcine pancreas, cut off the surface adipose tissue and adventitia, cut the porcine pancreas tissue into thin slices about 2 mm thick and rinse with normal saline several times to remove blood cells, and then Immerse in 0.5% sodium lauryl sulfate / normal saline, stir at room temperature for 24 hours; finally transfer it to 1% Triton X-100 solution, stir at room temperature until the tissue is transparent, about 1 hour, and rinse with normal saline for 3- 5 times, 15 minutes each time, to remove residual detergent. Decellularized pancreases were stored at -80°C.
[0071] (2) Identification of decellularized porcine pancreas: the decellularized porcine pancreas tissue was directly embedded wi...
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