Hernia bioremediation mesh and preparation method thereof
A biological and mesh technology, applied in medical science, prosthesis, etc., can solve the problems of tissue regeneration mismatch, cytotoxicity, slow degradation rate, etc., to reduce the incidence of inflammation and infection, accelerate functional reconstruction, good The effect of mechanical properties
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Embodiment 1
[0055] Preparation of biorepair mesh for submucosal hernia of pig small intestine, please refer to Figure 5 :
[0056] (1) Pretreatment
[0057] Take freshly slaughtered pig small intestine tissue and clean it, soak it in 0.5% acetic acid solution for 30 minutes, the ratio of pig small intestine to acetic acid solution is 1:5, use physical curettage to remove the mucosal layer, muscle layer, serous layer of the pig small intestine jejunum , Lymph nodes, separate the submucosa, cut into thin strips evenly longitudinally, and rinse with purified water 3 times to obtain the biorepair material, namely the submucosa of the small intestine, which is referred to as SIS material below.
[0058] (2) Virus inactivation
[0059] Using a mixed aqueous solution containing 1.0% peroxyacetic acid and 15% ethanol, the ratio of the SIS material to the mixed aqueous solution is 1:10, and the virus is inactivated by soaking at room temperature for 100 minutes under ultrasonic conditions. Then use pur...
Embodiment 2
[0070] Preparation of pig small intestinal submucosal hernia repairing mesh
[0071] (1) Pretreatment
[0072] Clean the small intestine tissue of the freshly slaughtered animal and soak it in 0.01% acetic acid solution for 120 minutes. The ratio of the small intestine to the acetic acid solution is 1:10. Use physical scraping to remove the mucosal, muscle, and serous layers of the small intestine and jejunum. , Lymph nodes, separate the submucosa, cut into fragments, and rinse 3 times with purified water.
[0073] (2) Virus inactivation
[0074] Using a mixed aqueous solution containing 0.5% peroxyacetic acid and 25% ethanol, the ratio of the SIS material to the mixed aqueous solution is 1:15, and the virus is inactivated by soaking at room temperature for 120 minutes under ultrasonic conditions. Then use purified water ultrasonic cleaning 3 times.
[0075] (3) Degreasing
[0076] Use ethanol with a concentration of 90%, the ratio of SIS material to ethanol is 1:15, and soak at room t...
Embodiment 3
[0085] For the safety of the samples, the samples prepared in Example 1-2 were tested for immunogenic substances.
[0086] (1) Cell residue detection method: fixed with 10% neutral formalin, embedded in paraffin, cut into 0.4 micron slices, dewaxed with xylene, dehydrated with serial alcohol, stained with hematoxylin and eosin, microscope Observe the cell residue and matrix fiber structure.
[0087] (2) DNA content detection method: in accordance with YY / T 0606.25-2014 "Determination of DNA Residues of Biological Materials of Animal Origin: Fluorescence Staining Method".
[0088] (3) Detection method of α-Gal antigen content: After the sample is fixed with paraformaldehyde, the slice is embedded in conventional paraffin, and the slice thickness is 3 microns. The specific affinity between biotin-labeled BSI-B4 and α-Gal antigen was used for immunohistochemical reaction. Staining result judgment: dark brown particles are strongly positive (+++), brown particles are positive (++), yel...
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