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Cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility

NO is the earliest discovered gas signal molecule which is produced by normal healthy endothelial cells, and it has many functions, such as maintaining cardiovascular homeostasis, regulating vasodilation, inhibiting intimal hyperplasia and preventing atherosclerosis in the blood system. Insufficient...

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Autores principales: Zhou, Lei, Li, Xin, Wang, Kebing, Shen, Fangyu, Zhang, Lu, Li, Peichuang, Shang, Tengda, Wang, Jin, Huang, Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147359/
https://www.ncbi.nlm.nih.gov/pubmed/32296534
http://dx.doi.org/10.1093/rb/rbz043
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author Zhou, Lei
Li, Xin
Wang, Kebing
Shen, Fangyu
Zhang, Lu
Li, Peichuang
Shang, Tengda
Wang, Jin
Huang, Nan
author_facet Zhou, Lei
Li, Xin
Wang, Kebing
Shen, Fangyu
Zhang, Lu
Li, Peichuang
Shang, Tengda
Wang, Jin
Huang, Nan
author_sort Zhou, Lei
collection PubMed
description NO is the earliest discovered gas signal molecule which is produced by normal healthy endothelial cells, and it has many functions, such as maintaining cardiovascular homeostasis, regulating vasodilation, inhibiting intimal hyperplasia and preventing atherosclerosis in the blood system. Insufficient NO release is often observed in the pathological environment, for instance atherosclerosis. It was discovered that NO could be released from the human endogenous NO donor by many compounds, and these methods can be used for the treatment of certain diseases in the blood system. In this work, a series of copper-loaded polydopamine (PDA) coatings were produced through self-polymerization time for 24, 48 and 72 h. The chemical composition and structure, coating thickness and hydrophilicity of the different copper-loaded PDA coatings surfaces were characterized by phenol hydroxyl quantitative, X-ray photoelectron spectroscopy, ellipsometry atomic force microscopy and water contact angles. The results indicate that the thickness and the surface phenolic hydroxyl density of the PDA coatings increased with the polymerization time.This copper-loaded coating has glutathione peroxidase-like activity, and it has the capability of catalyzing NO releasing from GSNO. The surface of the coating showed desirable hemocompatibility, the adhesion and activation of platelets were inhibited on the copper-loaded coatings. At the same time, the formation of the thrombosis was also suppressed. These copper-loaded PDA coatings could provide a promising platform for the development of blood contact materials.
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spelling pubmed-71473592020-04-15 Cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility Zhou, Lei Li, Xin Wang, Kebing Shen, Fangyu Zhang, Lu Li, Peichuang Shang, Tengda Wang, Jin Huang, Nan Regen Biomater Research Articles NO is the earliest discovered gas signal molecule which is produced by normal healthy endothelial cells, and it has many functions, such as maintaining cardiovascular homeostasis, regulating vasodilation, inhibiting intimal hyperplasia and preventing atherosclerosis in the blood system. Insufficient NO release is often observed in the pathological environment, for instance atherosclerosis. It was discovered that NO could be released from the human endogenous NO donor by many compounds, and these methods can be used for the treatment of certain diseases in the blood system. In this work, a series of copper-loaded polydopamine (PDA) coatings were produced through self-polymerization time for 24, 48 and 72 h. The chemical composition and structure, coating thickness and hydrophilicity of the different copper-loaded PDA coatings surfaces were characterized by phenol hydroxyl quantitative, X-ray photoelectron spectroscopy, ellipsometry atomic force microscopy and water contact angles. The results indicate that the thickness and the surface phenolic hydroxyl density of the PDA coatings increased with the polymerization time.This copper-loaded coating has glutathione peroxidase-like activity, and it has the capability of catalyzing NO releasing from GSNO. The surface of the coating showed desirable hemocompatibility, the adhesion and activation of platelets were inhibited on the copper-loaded coatings. At the same time, the formation of the thrombosis was also suppressed. These copper-loaded PDA coatings could provide a promising platform for the development of blood contact materials. Oxford University Press 2020-03 2020-01-17 /pmc/articles/PMC7147359/ /pubmed/32296534 http://dx.doi.org/10.1093/rb/rbz043 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhou, Lei
Li, Xin
Wang, Kebing
Shen, Fangyu
Zhang, Lu
Li, Peichuang
Shang, Tengda
Wang, Jin
Huang, Nan
Cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility
title Cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility
title_full Cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility
title_fullStr Cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility
title_full_unstemmed Cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility
title_short Cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility
title_sort cu(∥)-loaded polydopamine coatings with in situ nitric oxide generation function for improved hemocompatibility
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147359/
https://www.ncbi.nlm.nih.gov/pubmed/32296534
http://dx.doi.org/10.1093/rb/rbz043
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