Key result
Dialdehyde heparin cross-linked porcine acellular dermal matrix improved thermal stability, biocompatibility, and anticoagulant properties compared to glutaraldehyde cross-linked matrix.
Why the study?
Porcine acellular dermal matrix used in heart valve materials easily forms life-threatening thrombi due to collagen-induced coagulation, and current glutaraldehyde cross-linked valves have poor anticoagulant performance, calcification, and cytotoxicity.
Does dialdehyde heparin crosslinking improve the anticoagulant properties of porcine acellular dermal matrix compared to glutaraldehyde crosslinking?
Does dialdehyde heparin crosslinking improve the anticoagulant properties of porcine acellular dermal matrix compared to glutaraldehyde crosslinking?
Dialdehyde heparin crosslinking improves the anticoagulant properties and biocompatibility of porcine acellular dermal matrix, showing potential for use in artificial heart valves.
The anticoagulant properties of valve materials are essential to maintain blood patency after artificial valve implantation. Porcine acellular dermal matrix (pADM) has low immunogenicity, good biocompatibility, and can reduce calcification by eliminating heterogeneous cells. However, its main component is collagen, which has strong coagulation function and poor anticoagulant activity. When used in heart valve materials, it can easily coagulate and form a life-threatening thrombus. Therefore, it is necessary to improve its anticoagulant performance. The glutaraldehyde (GA) cross-linked valves widely used clinically are easy to calcify with poor anticoagulant performance and cytotoxicity. In this study, dialdehyde heparin containing cross-linking active aldehyde groups was prepared by sodium periodate oxidation, then it was used for crosslinking with pADM to chemically modify its anticoagulant performance. Compared with GA cross-linked pADM (GA-pA), dialdehyde heparin cross-linked pADM (OL-pA) has better thermal stability and biocompatibility, especially its anticoagulant and antiplatelet adhesion were significantly improved, which can reduce the incidence of coagulation, thrombocytopenia and bleeding. In summary, dialdehyde heparin is expected to be applied to modify the anticoagulant properties of pADM and has great potential for the preparation and clinical application of anticoagulant materials such as heart valves and artificial blood vessels.
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Feng et al. (2022) studied Thrombosis in heart valve materials. Dialdehyde heparin cross-linked porcine acellular dermal matrix (OL-pA) vs. Glutaraldehyde cross-linked pADM (GA-pA) was evaluated on Thermal stability, biocompatibility, anticoagulant properties, and antiplatelet adhesion. Dialdehyde heparin cross-linked porcine acellular dermal matrix improved thermal stability, biocompatibility, and anticoagulant properties compared to glutaraldehyde cross-linked matrix.
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