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Polydopamine/poly(sulfobetaine methacrylate) Co-deposition coatings triggered by CuSO(4)/H(2)O(2) on implants for improved surface hemocompatibility and antibacterial activity

Implanted biomaterials such as medical catheters are prone to be adhered by proteins, platelets and bacteria due to their surface hydrophobicity characteristics, and then induce related infections and thrombosis. Hence, the development of a versatile strategy to endow surfaces with antibacterial and...

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Autores principales: Zhu, Zhongqiang, Gao, Qiang, Long, Ziyue, Huo, Qiuyi, Ge, Yifan, Vianney, Ntakirutimana, Daliko, Nishimwe Anodine, Meng, Yongchun, Qu, Jia, Chen, Hao, Wang, Bailiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7887402/
https://www.ncbi.nlm.nih.gov/pubmed/33665495
http://dx.doi.org/10.1016/j.bioactmat.2021.01.025
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author Zhu, Zhongqiang
Gao, Qiang
Long, Ziyue
Huo, Qiuyi
Ge, Yifan
Vianney, Ntakirutimana
Daliko, Nishimwe Anodine
Meng, Yongchun
Qu, Jia
Chen, Hao
Wang, Bailiang
author_facet Zhu, Zhongqiang
Gao, Qiang
Long, Ziyue
Huo, Qiuyi
Ge, Yifan
Vianney, Ntakirutimana
Daliko, Nishimwe Anodine
Meng, Yongchun
Qu, Jia
Chen, Hao
Wang, Bailiang
author_sort Zhu, Zhongqiang
collection PubMed
description Implanted biomaterials such as medical catheters are prone to be adhered by proteins, platelets and bacteria due to their surface hydrophobicity characteristics, and then induce related infections and thrombosis. Hence, the development of a versatile strategy to endow surfaces with antibacterial and antifouling functions is particularly significant for blood-contacting materials. In this work, CuSO(4)/H(2)O(2) was used to trigger polydopamine (PDA) and poly-(sulfobetaine methacrylate) (PSBMA) co-deposition process to endow polyurethane (PU) antibacterial and antifouling surface (PU/PDA(Cu)/PSBMA). The zwitterions contained in the PU/PDA(Cu)/PSBMA coating can significantly improve surface wettability to reduce protein adsorption, thereby improving its blood compatibility. In addition, the copper ions released from the metal-phenolic networks (MPNs) imparted them more than 90% antibacterial activity against E. coli and S. aureus. Notably, PU/PDA(Cu)/PSBMA also exhibits excellent performance in vivo mouse catheter-related infections models. Thus, the PU/PDA(Cu)/PSBMA has great application potential for developing multifunctional surface coatings for blood-contacting materials so as to improve antibacterial and anticoagulant properties.
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spelling pubmed-78874022021-03-03 Polydopamine/poly(sulfobetaine methacrylate) Co-deposition coatings triggered by CuSO(4)/H(2)O(2) on implants for improved surface hemocompatibility and antibacterial activity Zhu, Zhongqiang Gao, Qiang Long, Ziyue Huo, Qiuyi Ge, Yifan Vianney, Ntakirutimana Daliko, Nishimwe Anodine Meng, Yongchun Qu, Jia Chen, Hao Wang, Bailiang Bioact Mater Article Implanted biomaterials such as medical catheters are prone to be adhered by proteins, platelets and bacteria due to their surface hydrophobicity characteristics, and then induce related infections and thrombosis. Hence, the development of a versatile strategy to endow surfaces with antibacterial and antifouling functions is particularly significant for blood-contacting materials. In this work, CuSO(4)/H(2)O(2) was used to trigger polydopamine (PDA) and poly-(sulfobetaine methacrylate) (PSBMA) co-deposition process to endow polyurethane (PU) antibacterial and antifouling surface (PU/PDA(Cu)/PSBMA). The zwitterions contained in the PU/PDA(Cu)/PSBMA coating can significantly improve surface wettability to reduce protein adsorption, thereby improving its blood compatibility. In addition, the copper ions released from the metal-phenolic networks (MPNs) imparted them more than 90% antibacterial activity against E. coli and S. aureus. Notably, PU/PDA(Cu)/PSBMA also exhibits excellent performance in vivo mouse catheter-related infections models. Thus, the PU/PDA(Cu)/PSBMA has great application potential for developing multifunctional surface coatings for blood-contacting materials so as to improve antibacterial and anticoagulant properties. KeAi Publishing 2021-02-05 /pmc/articles/PMC7887402/ /pubmed/33665495 http://dx.doi.org/10.1016/j.bioactmat.2021.01.025 Text en © 2021 [The Author/The Authors] http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Zhu, Zhongqiang
Gao, Qiang
Long, Ziyue
Huo, Qiuyi
Ge, Yifan
Vianney, Ntakirutimana
Daliko, Nishimwe Anodine
Meng, Yongchun
Qu, Jia
Chen, Hao
Wang, Bailiang
Polydopamine/poly(sulfobetaine methacrylate) Co-deposition coatings triggered by CuSO(4)/H(2)O(2) on implants for improved surface hemocompatibility and antibacterial activity
title Polydopamine/poly(sulfobetaine methacrylate) Co-deposition coatings triggered by CuSO(4)/H(2)O(2) on implants for improved surface hemocompatibility and antibacterial activity
title_full Polydopamine/poly(sulfobetaine methacrylate) Co-deposition coatings triggered by CuSO(4)/H(2)O(2) on implants for improved surface hemocompatibility and antibacterial activity
title_fullStr Polydopamine/poly(sulfobetaine methacrylate) Co-deposition coatings triggered by CuSO(4)/H(2)O(2) on implants for improved surface hemocompatibility and antibacterial activity
title_full_unstemmed Polydopamine/poly(sulfobetaine methacrylate) Co-deposition coatings triggered by CuSO(4)/H(2)O(2) on implants for improved surface hemocompatibility and antibacterial activity
title_short Polydopamine/poly(sulfobetaine methacrylate) Co-deposition coatings triggered by CuSO(4)/H(2)O(2) on implants for improved surface hemocompatibility and antibacterial activity
title_sort polydopamine/poly(sulfobetaine methacrylate) co-deposition coatings triggered by cuso(4)/h(2)o(2) on implants for improved surface hemocompatibility and antibacterial activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7887402/
https://www.ncbi.nlm.nih.gov/pubmed/33665495
http://dx.doi.org/10.1016/j.bioactmat.2021.01.025
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