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Updated: Mar 30, 2026

Mitigation of Blood Borne Cell Attachment to Metal Implants through CD47-Derived Peptide Immobilization
Published on: December 3, 2020
Immobilization of bioactive plasmin reduces the thrombogenicity of metal surfaces
Steven G Wise1, Praveesuda L Michael2, Anna Waterhouse3
1The Heart Research Institute, Sydney, NSW 2042, Australia; Sydney Medical School, University of Sydney, NSW 2006, Australia; School of Molecular Bioscience, University of Sydney, NSW 2006, Australia.
Abstract:
Components of many vascular prostheses including endovascular stents, heart valves and ventricular assist devices are made using metal alloys. In these blood contacting applications, metallic devices promote blood clotting, which is managed clinically by profound platelet suppression and/or anticoagulation. Here it is proposed that the localized immobilization of bioactive plasmin, a critical mediator of blood clot stability, may attenuate metallic prosthesis-induced thrombus formation. Previously described approaches to covalently immobilize biomolecules on implantable materials have relied on complex chemical linker chemistry, increasing the possibility of toxic side effects and reducing bioactivity. We utilize a plasma deposited thin film platform to covalently immobilize biologically active plasmin on stainless steel substrates, including stents. A range of in vitro whole blood assays demonstrate striking reductions in thrombus formation. This approach has profound potential to improve the efficacy of a wide range of metallic vascular implants.
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