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Preparation method of biogenic vein containing venous valve

A bio-derived, venous valve technology, applied in the field of biomedical engineering, can solve problems such as higher requirements for anti-immune rejection, inability to mass-produce autologous blood vessel transplantation, and limited promotion

Active Publication Date: 2021-04-20
曾祥军
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the experimental object of the method in the above-mentioned literature is autologous blood vessel transplantation, which does not involve immune rejection. Transplanting a vein containing a venous valve from a cow to a dog’s vein is a xenograft, and there will be greater rejection between different species, which will seriously cause veins and veins. The anastomotic stoma is narrow or even occluded, and the requirements for anti-immune rejection are higher, which cannot be met by the methods in the literature
The treatment method in the literature is to add rapamycin to the bioprotein glue and then inject it in the space around the grafted vein. Inhibiting the hyperplasia of the venous intimal, the concentration of rapamycin in the venous intimal cannot be guaranteed. In the literature, rapamycin is used after the anastomosis is completed. Different operators and different patients vary in the dosage and There are individual differences in the specific location, which is not conducive to ensuring the stability of the effect. Autologous blood vessel transplantation cannot be mass-produced on a large scale, which limits the promotion. The acquisition of autologous blood vessels will cause secondary trauma to patients that cannot be ignored.

Method used

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  • Preparation method of biogenic vein containing venous valve
  • Preparation method of biogenic vein containing venous valve
  • Preparation method of biogenic vein containing venous valve

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] a. Take fresh bovine jugular vein pipes with a diameter of 0.5-1.5 cm and with valves slaughtered daily in slaughterhouses, turn them over and find the valve part, cut out a section with a length of 3-5 cm that contains a complete valve, turn it back and trim it Adipose tissue and excess connective tissue around the veins were removed, and blood clots were removed by antegrade lavage with normal saline, then immersed in 0.1% (W / V) brogeramine solution for disinfection for 30 minutes, and then rinsed with PBS solution for later use.

[0029] b. The material obtained in step a was treated with PBS solution containing 0.5% (W / V) Triton X-100 for 48 hours, the cells were lysed, and washed with PBS solution. Then immerse in PBS solution containing 0.025% (W / V) trypsin and 0.02% (W / V) EDTA (0.025g trypsin, 0.02g EDTA dissolved in 100mL PBS solution) for 30min, digest the cells, and use PBS solution rinse. Finally, immerse in PBS solution containing 30u / ml DNase I and 0.3mg / m...

Embodiment 2

[0036]Except that the formulation of the treatment solution is different in step d, all the other are the same as in Example 1. In this example, each 1 L of rapamycin solution was obtained by dissolving 125 mg of rapamycin in 100 ml of absolute ethanol and adding PBS solution to constant volume, and each 1 L of rapamycin solution was mixed with 500 mg of PLGA in proportion to obtain a treatment solution.

Embodiment 3

[0038] Except that the formulation of the treatment solution is different in step d, all the other are the same as in Example 1. In this example, each 1 L of rapamycin solution was obtained by dissolving 300 mg of rapamycin in 150 ml of absolute ethanol and adding PBS solution to constant volume, and each 1 L of rapamycin solution was mixed with 1000 mg of PLGA in proportion to obtain a treatment solution.

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Abstract

The invention discloses a preparation method of a biogenic vein containing a venous valve, which is characterized in that the steps are: a. cutting the jugular vein of a cow with a diameter of 0.5 to 1.5 cm and a length of 3 to 5 cm containing a complete venous valve, and cleaning and sterilize; b. Cell lysis treatment, cell digestion and nucleic acid digestion treatment are performed on the material obtained in step a; c. The material treated in step b is sequentially subjected to covalent bonded heparin treatment → ion-bound heparin treatment → covalent bond Heparin treatment; d. Immerse the material treated in step c into the mixture of rapamycin solution and PLGA and pull it at a constant speed for 1 to 10 minutes, and then treat the vein intima with the same steps; after natural drying, put it in 20 ℃ oven drying for 12 hours. The present invention coats the venous intima and adventitia with rapamycin, so that the treated bovine jugular vein containing venous valves can significantly inhibit the hyperplasia of the venous intima and anastomosis after being implanted in the dog vein.

Description

technical field [0001] The invention relates to biomedical engineering, in particular to a method for preparing a biogenic vein containing a venous valve. Background technique [0002] Varicose veins of lower extremities is a common clinical disease, which is prone to occur in people over 45 years old. Patients rarely have obvious clinical symptoms in the early stage, but in the later stage, the superficial veins of the lower limbs may be exposed, accompanied by symptoms such as acidity, sinking, swelling, pain, and fatigue. In severe cases, superficial thrombophlebitis, stasis dermatitis, Stasis ulcer, varicose vein bleeding. The cause of varicose veins of the lower extremities is venous valve insufficiency, which leads to venous blood filling and high pressure in the lower extremities, resulting in varicose veins. Varicose veins cause local blood circulation disorders and affect the appearance of the limbs. Saphenous vein stripping, these methods are only symptomatic tre...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61L27/34A61L27/36A61L27/50A61L27/54A61L33/10
CPCA61L27/34A61L27/3625A61L27/3687A61L27/507A61L27/54A61L33/0011A61L33/08A61L2300/216A61L2300/232A61L2300/416A61L2300/42A61L2420/06C08L67/04
Inventor 曾祥军
Owner 曾祥军