Key result
Non-glutaraldehyde porcine pericardium improves anticoagulation and cuts calcification vs glutaraldehyde in preclinical models.
Why the study?
Transcatheter bioprosthetic heart valves carry an early risk of thrombosis, but antithrombotic drugs increase bleeding risk, highlighting the need to improve the intrinsic anticoagulant properties of valve materials.
Does non-glutaraldehyde cross-linked porcine pericardium grafted with heparin improve anticoagulant and anti-calcification properties compared to glutaraldehyde cross-linked porcine pericardium in bioprosthetic heart valve models?
Does non-glutaraldehyde cross-linked porcine pericardium grafted with heparin improve anticoagulant and anti-calcification properties compared to glutaraldehyde cross-linked porcine pericardium in bioprosthetic heart valve models?
A novel non-glutaraldehyde cross-linked porcine pericardium material grafted with heparin demonstrates improved anticoagulant, anti-calcification, and endothelial proliferation properties for potential use in bioprosthetic heart valves.
Hypothesis-generating for improved bioprosthetic valves; human trials required before any practice consideration.
In the last decade, the number of transcatheter heart valve replacement for severe heart valve disease has increased exponentially. Although the bioprosthetic artificial heart valve (BHV) has similar fluid dynamics performance to the original heart valve compared with mechanical heart valve so that there is no need to take long-term anticoagulant drugs to prevent thromboembolism, transcatheter BHV replacement are still at risk for thrombosis during the first few months according to the clinical data. However, the use of antithrombotic drugs can also increase the risk of bleeding. Therefore, it is particularly important to improve the anticoagulant properties for the BHV itself. In this work, a kind of non-glutaraldehyde cross-linked BHV material with excellent antithrombotic ability has been prepared from carboxylated oxazolidine treated porcine pericardium (consisting of collagen, elastin and glycoprotein) with the further graft of the anticoagulant heparin sodium via hydrophilic modified chitosan. Along with the similar mechanical properties and collagen stability comparable to the glutaraldehyde cross-linked porcine pericardium (PP), these functional non-glutaraldehyde cross-linked PPs exhibit better biocompatibility, promoted endothelial proliferation and superior anti-calcification ability. More importantly, excellent anticoagulant activity can be observed in the hematological experiments in vivo and in vitro. In summary, these excellent performances make these functional non-glutaraldehyde cross-linked PPs great potentialities in the BHV applications.
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Chen et al. (2022) studied Severe heart valve disease. Functional non-glutaraldehyde treated porcine pericardium (OX-SH-PP) vs. Glutaraldehyde cross-linked porcine pericardium (G-PP) and decellularized porcine pericardium (D-PP) was evaluated on Anticoagulant activity, anti-calcification, and biocompatibility. The functional non-glutaraldehyde cross-linked porcine pericardium (OX-SH-PP) exhibited superior anticoagulant activity, reduced calcification, and promoted endothelial proliferation compared to glutaraldehyde cross-linked pericardium in vitro and in animal models.
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