Poneurosis stent and preparation method and application thereof
A membrane scaffold and solution technology, applied in medical science, tissue regeneration, surgery, etc., can solve problems affecting the physical and mental health of patients
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[0051]In the first aspect, the present invention provides a method for preparing an aponeurotic scaffold, comprising the following steps: breaking the aponeurotic cells, then breaking the nucleus, removing deoxyribonucleic acid by DNase, and finally preparing the aponeurotic scaffold by slicing.
[0052] The aponeurosis of the present invention is derived from animal aponeurosis tissue, such as porcine aponeurosis tissue, sheep aponeurosis tissue and bovine mucosal tissue. The preparation method of the aponeurosis support of the present invention uses animal aponeurosis tissue as a raw material, first the aponeurotic cells are broken, and the cell membrane is removed; then the nucleus is broken, the nuclear membrane and most of the nucleic acid are removed; and the residual deoxyribonucleic acid is removed by DNase, Avoid exogenous deoxyribonucleic acid or protein contact with the wound to cause immune rejection; finally slice the aponeurosis to obtain aponeurotic scaffold with...
Embodiment 1
[0092] A preparation method of aponeurosis support, comprising the following steps:
[0093] Select fresh pig limbs, and remove the pig's aponeurosis tissue under aseptic conditions, such as figure 1 As shown in the picture on the left (native), cut it into a size of about 2cm*1cm, put it in a 15mL sterile centrifuge tube, rinse with heparin PBS buffer for 30 minutes, and shake it in a laboratory shaker with the speed set at 80 rpm, and the temperature was set at 4 °C. The oscillating liquids are as follows: 2% TritonX-100 solution for 24 hours, sterile PBS solution for 30 minutes, and 0.25% SDS solution for 24 hours. After shaking, rinse with sterile PBS solution for 30 minutes, digest with 1 mg / mL DNase at 37°C for 1 hour, and rinse with sterile PBS solution for 30 minutes. Place in a cryostat, set the slice thickness to 200 microns, and cut the tissue into 200 microns thick slices. Rinse with sterile PBS solution for 10 minutes to prepare the aponeurotic scaffold, such a...
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