A kind of dressing for promoting wound healing and preparation method thereof
A wound healing and mixed solution technology, applied in the field of biomedical engineering, can solve problems such as poor wound healing effect, poor barrier effect, and exogenous infection
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[0021] alpha 2 Method for preparing M crude tissue:
[0022] Fresh pig plasma was added to a 0.1% (w / v) soy trypsin inhibitor under -5 ° C, and EDTA (ethylenediamine tetracetate) solution was added to a final concentration to 10 mmol / L, after 5% - The 18% polyethylene glycol 6000 was graded, stirred with stirring for 60 min, 40 mm / min at 4 ° C for 30 min, 5 times mass 50 mmol / L Tris-HCl (pH 7.4) solution dissolved precipitation, 50 mmol / L Tris-HCl (pH7 .4) The buffer is fully dialyzed, that is, α 2 M rough.
Embodiment 1
[0024] 1, take α 2 M crude extract was concentrated and subjected to Sephacryl S-300 gel chromatography column, the eluate was a 100 mmol / l Tris-HCl (pH 8.0) buffer containing 0.5 mol / l NaCl, and the flow out of the absorption peak was detected. The first peak outflow is collected and the ultrafiltration membrane ultrafiltration of 400 kDa is used. 2 Gully globulin solution, its protein concentration is measured to 90 μg / L using a BCA protein quantitative kit;
[0025] 2, 0.42 g of blue copper wins, 0.12 g of copper sulfate, 2.2 g of bright peptide, 5 g of a total molecular weight of 5.0 × 10 5 , The deacetylacetin is 82.5% of the carboxymethyl chitosan and 15g average molecular weight of 1.0 × 10 6 The polyoxyethylene is dissolved in 1 L of water, stirred and uniformly prepared, then the α obtained by 1.25 ml of step 1 2 Gully globulin solution to obtain spinning fluid;
[0026] 3, use the spinning liquid for electrospinning, the syringe specification is 10ml, the needle sp...
Embodiment 2
[0028] 1, take α 2 M crude extract was concentrated and subjected to Sephacryl S-300 gel chromatography column, the eluate was a 100 mmol / l Tris-HCl (pH 8.0) buffer containing 0.5 mol / l NaCl, and the flow out of the absorption peak was detected. The first peak outflow was collected and the ultrafiltration membrane ultrafiltration was concentrated by ultrafiltration membrane ultrafiltration of 300 kDa. 2 Gully globulin solution, its protein concentration was measured by a BCA protein quantitative kit was 80 μg / L;
[0029] 2, 0.17 g of blue copper wins, 0.08 g of copper sulfate, 1.1 g of bright peptide, 5 g of a bonded molecular weight of 5.0 × 10 5 , The deacetylatin is 80% of the carboxymethyl chitosan and 5g average molecular weight of 1.0 × 10 6 The polyoxyethylene is dissolved in 1 L of water, stirred and uniformly prepared, then the alpha obtained by 1 ml of step 1 was added. 2 Gully globulin solution to obtain spinning fluid;
[0030] 3, use the spinning liquid for elec...
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