An elastomer with in situ generated pure zwitterionic surfaces for fibrosis-resistant implants
- PMID: 38972625
- DOI: 10.1016/j.actbio.2024.06.047
An elastomer with in situ generated pure zwitterionic surfaces for fibrosis-resistant implants
Abstract
Polymeric elastomers are widely utilized in implantable biomedical devices. Nevertheless, the implantation of these elastomers can provoke a robust foreign body response (FBR), leading to the rejection of foreign implants and consequently reducing their effectiveness in vivo. Building effective anti-FBR coatings on those implants remains challenging. Herein, we introduce a coating-free elastomer with superior immunocompatibility. A super-hydrophilic anti-fouling zwitterionic layer can be generated in situ on the surface of the elastomer through a simple chemical trigger. This elastomer can repel the adsorption of proteins, as well as the adhesion of cells, platelets, and diverse microbes. The elastomer elicited negligible inflammatory responses after subcutaneous implantation in rodents for 2 weeks. No apparent fibrotic capsule formation was observed surrounding the elastomer after 6 months in rodents. Continuous subcutaneous insulin infusion (CSII) catheters constructed from the elastomer demonstrated prolonged longevity and performance compared to commercial catheters, indicating its great potential for enhancing and extending the performance of various implantable biomedical devices by effectively attenuating local immune responses. STATEMENT OF SIGNIFICANCE: The foreign body response remains a significant challenge for implants. Complicated coating procedures are usually needed to construct anti-fibrotic coatings on implantable elastomers. Herein, a coating-free elastomer with superior immunocompatibility was achieved using a zwitterionic monomer derivative. A pure zwitterionic layer can be generated on the elastomer surface through a simple chemical trigger. This elastomer significantly reduces protein adsorption, cell and bacterial adhesion, and platelet activation, leading to minimal fibrotic capsule formation even after six months of subcutaneous implantation in rodents. CSII catheters constructed from the PQCBE-H elastomer demonstrated prolonged longevity and performance compared to commercial catheters, highlighting the significant potential of PQCBE-H elastomers for enhancing and extending the performance of various implantable biomedical devices.
Keywords: Elastomer; Foreign body response; Implant; Inflammation; Zwitterionic surface.
Copyright © 2024 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Similar articles
-
Immunocompatible elastomer with increased resistance to the foreign body response.Nat Commun. 2024 Aug 30;15(1):7526. doi: 10.1038/s41467-024-52023-z. Nat Commun. 2024. PMID: 39214984 Free PMC article.
-
Reducing the foreign body response on human cochlear implants and their materials in vivo with photografted zwitterionic hydrogel coatings.Acta Biomater. 2023 Aug;166:212-223. doi: 10.1016/j.actbio.2023.05.011. Epub 2023 May 13. Acta Biomater. 2023. PMID: 37187301 Free PMC article.
-
A Sprayable Polyelectrolyte Coating to Mitigate the Foreign Body Response of Implants.Langmuir. 2025 Apr 8;41(13):9131-9140. doi: 10.1021/acs.langmuir.5c00868. Epub 2025 Mar 27. Langmuir. 2025. PMID: 40145243
-
Beyond Encapsulation: Exploring Macrophage-Fibroblast Cross Talk in Implant-Induced Fibrosis.Tissue Eng Part B Rev. 2024 Dec;30(6):596-606. doi: 10.1089/ten.TEB.2023.0300. Epub 2024 Mar 27. Tissue Eng Part B Rev. 2024. PMID: 38420650 Review.
-
Macrophage responses to implants: prospects for personalized medicine.J Leukoc Biol. 2015 Dec;98(6):953-62. doi: 10.1189/jlb.5VMR0415-166R. Epub 2015 Jul 13. J Leukoc Biol. 2015. PMID: 26168797 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials