Poly-2-methyl-2-oxazoline–modified bioprosthetic heart valve leaflets have enhanced biocompatibility and resist structural degeneration

Author:

Zakharchenko Andrey1,Xue Yingfei2ORCID,Keeney Samuel1,Rock Christopher A.1ORCID,Alferiev Ivan S.1,Stachelek Stanley J.1,Takano Hajime3,Thomas Tina1,Nagaswami Chandrasekaran4,Krieger Abba M.5,Chorny Michael1,Ferrari Giovanni2ORCID,Levy Robert J.1

Affiliation:

1. Pediatric Heart Valve Center, Division of Cardiology, Department of Pediatrics, The Children’s Hospital of Philadelphia, Philadelphia, PA 19104

2. Department of Surgery and Biomedical Engineering, Columbia University, New York, NY, 10032

3. Division of Neurology, Department of Pediatrics, The Children’s Hospital of Philadelphia, Philadelphia, PA 19104

4. Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104

5. Department of Statistics, The Wharton School, University of Pennsylvania, Philadelphia, PA, 19104

Abstract

Significance Heart valve disease affects millions, and since there is no effective medical therapy, surgical repair when possible—or more commonly, replacement—are the only treatments available. Bioprosthetic heart valves (BHV), the most frequently used valve replacements, are composed of heterograft tissue, typically fixed in glutaraldehyde, and prepared for human use either as surgically implantable devices or for transcatheter delivery. Protein-glycation limits the durability of BHV, contributing to device failure, often requiring reoperation after only a decade or less of functionality. This problem is addressed by modifying BHV leaflets with poly-2-methyl-2-oxazoline, effectively mitigating glycation and serum protein infiltration and enhancing biocompatibility.

Funder

HHS | National Institutes of Health

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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