Studies of combined NO-eluting/CD47-modified polyurethane surfaces for synergistic enhancement of biocompatibility

• Published in: Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2020-08, Vol.192, p.111060-111060, Article 111060
• Main Authors: Zhang, Qi, Stachelek, Stanley J., Inamdar, Vaishali V., Alferiev, Ivan, Nagaswami, Chandrasekaran, Weisel, John W., Hwang, Jeong Hyun, Meyerhoff, Mark E.
• Format: Article
• Language: English
• Subjects: Biocompatibility; Inflammation; Intravascular Devices; Nitric Oxide; Platelets
• ISSN: 0927-7765; 1873-4367; 1873-4367
• DOI: 10.1016/j.colsurfb.2020.111060

[Display omitted] •Peptide CD47 can be covalently immobilized to a range of polyurethane configurations.•The anti-inflammatory properties of pepCD47 were not inhibited by NO exposure.•Released NO and pepCD47 demonstrated a cumulative anti-inflammatory effect. The blood compatibility of various intravascular (IV) devices (e.g., catheters, sensors, etc.) is compromised by activation of platelets that can cause thrombus formation and device failure. Such devices also carry a high risk of microbial infection. Recently, nitric oxide (NO) releasing polymers/devices have been proposed to reduce these clinical problems. CD47, a ubiquitously expressed transmembrane protein with proven anti-inflammation/anti-platelet properties when immobilized on polymeric surfaces, is a good candidate to complement NO release in both effectiveness and longevity. In this work, we successfully appended CD47 peptides (pepCD47) to the surface of biomedical grade polyurethane (PU) copolymers. SIRPα binding and THP-1 cell attachment experiments strongly suggested that the pepCD47 retains its biological properties when bound to PU films. In spite of the potentially high reactivity of NO toward various amino acid residues in CD47, the efficacy of surface-immobilized pepCD47 to prevent inflammatory cell attachment was not inhibited after being subjected to a high flux of NO for three days, demonstrating excellent compatibility of the two species. We further constructed a CD47 surface immobilized silicone tubing filled with NO releasing S-nitrosoglutathione/ascorbic acid (GSNO/AA) solution for synergistic biocompatibility evaluation. Via an ex vivo Chandler loop model, we demonstrate for the first time that NO release and CD47 modification could function synergistically at the blood/material interface and produce greatly enhanced anti-inflammatory/anti-platelet effects. This concept should be readily implementable to create a new generation of thromboresistant/antimicrobial implantable devices.