Quercetin crosslinking method for preparing artificial bioprosthesis heart valve materials

A heart valve, quercetin technology, applied in the field of biomedical engineering, can solve problems such as fragility, affecting the working period of biological valves, and becoming brittle

Inactive Publication Date: 2008-07-23
SHANGHAI INST OF CERAMIC CHEM & TECH CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, glutaraldehyde itself has cytotoxicity, inhibits the completion of endothelialization of the valve host, affects the growth of normal human tissue, and results in a short working life of the valve; at the same time, the cytotoxicity and excessive cross-linking of glutaraldehyde itself also promotes valve calcification, Weaken the mechanical strength of the biological valve, making it brittle and

Method used

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  • Quercetin crosslinking method for preparing artificial bioprosthesis heart valve materials
  • Quercetin crosslinking method for preparing artificial bioprosthesis heart valve materials
  • Quercetin crosslinking method for preparing artificial bioprosthesis heart valve materials

Examples

Experimental program
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Effect test

Embodiment 1

[0056] Use the balanced salt buffer D-Hanks solution at 1-6°C as the storage and transportation solution, take the fresh porcine aortic heart valve from the slaughterhouse, cut the valve leaflets at 4°C within 4 hours, and use D-Hanks Fluid clean. Afterwards, the decellularized porcine heart aortic valve was prepared according to the aforementioned method, washed and washed, and the decellularized valve material with the structure and shape shown in Figure 1 was obtained. Then add 2ml of quercetin to each valve to soak in ethanol-containing D-Hanks special solution, shake and cross-link at 120rpm at 37°C for 48 hours. Add 2ml of D-Hanks solution to each valve to soak the valve, shake and wash at 120rpm at 37°C for 48 hours, and repeat the washing 3 times. The obtained biological valve material was evaluated for the above performance. 2 in Figure 2 is a decellularized valve cross-linked with 6.25 mg / ml glutaraldehyde, which is as loose as the non-cross-linked decellularized v...

Embodiment 2

[0058] Prepare the decellularized porcine heart aortic valve according to the method described in the summary of the invention and clean it, add 2.5mg / ml quercetin-containing D-Hanks special solution with ethanol at a ratio of 2ml per valve. Example 1 Method Cross-linking, the resulting cross-linked biological valve material can also maintain the original shape of the valve, soft and moist without shrinking. Figure 3 shows that the maximum tensile strength of the decellularized valve cross-linked by 2.5 mg / ml quercetin is 13.9 MPa. Figure 5 shows that only 28.5% of the decellularized valve cross-linked with 2.5 mg / ml quercetin was degraded after 24 hours of enzymatic hydrolysis. It shows that this concentration of quercetin also has a cross-linking effect on the decellularized valve, and has good mechanical properties and stability against enzymolysis.

Embodiment 3

[0060] Get fresh porcine aortic heart valve from slaughterhouse by the method of embodiment 1 and clean up. After washing with D-Hanks solution three times, valve cells were removed by shaking with decellularization solution at 60 rpm at 4°C for 96 hours. Use D-Hanks solution to shake the decellularized heart valve material at 21°C (room temperature) at 120rpm to wash valve cell residues, debris, free protein, nucleic acid and other macromolecules for 96 hours. Add 0.1mg / ml, 0.2mg / ml, 0.5mg / ml, 2mg / ml and 5mg / ml quercetin in ethanol-containing D-Hanks special solution at a rate of 20ml per valve, at 20°C, at 240rpm shaking speed, cross-linked for 96 hours. Add 20ml of D-Hanks solution to each valve to soak the valve, and wash at 120rpm for 10 minutes at room temperature. The bioprosthetic valve material of the present invention that makes like this is done aforementioned performance evaluation, and its maximum tensile strength is respectively 10.4MPa, 12.5MPa, 14.4MPa, 14.9M...

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Abstract

The invention discloses a cross-linking preparing method for heart valve prosthesis material, comprising a cross-linker, cross-linking steps and preserving treatment after cross-linking. The method is characterized in that the collected cardiac valve of a pig is timely and appropriately treated and cleaned, and then the cells are completely removed and cleaned, then the obtained cells are cross-linked by quercetin, thus improving the mechanical strength, further eliminating the antigenicity and enhancing the stability. The acellular bioprothesis cardiac valve of the pig adopts heart valve prosthesis prepared by the method has the advantages of non-toxic valve, high tensile strength, resistance to enzymic degradation and minimum release of the cross-linker and self-protein of valves. The cross-linking properties of the acellular bioprothesis cardiac valve made of cardiac valve material of the pig are beneficial to transplanting, proliferation, covering and long-term anti-calcification of interstitial cells of valves of the body of man and vascular endothelial cells after being transplanted into the human body.

Description

technical field [0001] The invention relates to a crosslinking preparation method of an artificial biological heart valve material, which belongs to the field of biomedical engineering. Background technique [0002] Worldwide, heart valve disease is associated with high morbidity and mortality. In the United States, 60,000 artificial heart valve replacement operations are performed every year, and about 20,000 people die directly from the disease [Julie R, BorisAN, Vacanti JP. Tissue engineering: a 21st century solution to surgical reconstruction. Ann thorac surg, 2001, 72 : 577-591.]. Clinically, artificial heart valves are mainly treated with mechanical valves and heterogeneous biological valves. Human allograft biological valves stored at low temperature are also used clinically, but they are rarely used due to insufficient sources. The coagulation effect of heterogeneous biological valves is weak, and patients do not need to take anticoagulant drugs after surgery. Co...

Claims

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Application Information

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IPC IPC(8): A61L27/38A61F2/24
Inventor 常江翟万银
Owner SHANGHAI INST OF CERAMIC CHEM & TECH CHINESE ACAD OF SCI
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