Cargando…
Alginate based antimicrobial hydrogels formed by integrating Diels–Alder “click chemistry” and the thiol–ene reaction
In recent years medical devices manufacturers have been looking for antimicrobial coatings which are biocompatible and non-toxic for a wide range of medical devices. The demand for these antimicrobial coatings has increased significantly, owing to the increased incidence of hospital-associated infec...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078979/ https://www.ncbi.nlm.nih.gov/pubmed/35541529 http://dx.doi.org/10.1039/c8ra00668g |
_version_ | 1784702459788132352 |
---|---|
author | Wang, Gang Zhu, Jiehua Chen, Xiaofeng Dong, Hua Li, Qingtao Zeng, Lei Cao, Xiaodong |
author_facet | Wang, Gang Zhu, Jiehua Chen, Xiaofeng Dong, Hua Li, Qingtao Zeng, Lei Cao, Xiaodong |
author_sort | Wang, Gang |
collection | PubMed |
description | In recent years medical devices manufacturers have been looking for antimicrobial coatings which are biocompatible and non-toxic for a wide range of medical devices. The demand for these antimicrobial coatings has increased significantly, owing to the increased incidence of hospital-associated infections (HAIs). Hydrogels have been widely used in biomedical applications due to their hydrophilicity, biodegradability, non-toxicity and biocompatibility. In this work, sodium alginate (SA) based antibacterial hydrogels SA/PEG–HHC10 were designed and prepared by combining Diels–Alder (DA) click chemistry and the thiol–ene reaction. The hydrogels were first prepared using DA click chemistry with good mechanical strength, then the cysteine-terminated antimicrobial peptide HHC10–CYS (HHC10) was grafted into the hydrogel by the thiol–ene reaction between the oxy-norbornene group and the thiol group. The results showed that the antimicrobial hydrogels had a strong antibacterial property and good biocompatibility. Therefore, the antimicrobial hydrogels have significant potential application as coatings for implantable medical devices. |
format | Online Article Text |
id | pubmed-9078979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90789792022-05-09 Alginate based antimicrobial hydrogels formed by integrating Diels–Alder “click chemistry” and the thiol–ene reaction Wang, Gang Zhu, Jiehua Chen, Xiaofeng Dong, Hua Li, Qingtao Zeng, Lei Cao, Xiaodong RSC Adv Chemistry In recent years medical devices manufacturers have been looking for antimicrobial coatings which are biocompatible and non-toxic for a wide range of medical devices. The demand for these antimicrobial coatings has increased significantly, owing to the increased incidence of hospital-associated infections (HAIs). Hydrogels have been widely used in biomedical applications due to their hydrophilicity, biodegradability, non-toxicity and biocompatibility. In this work, sodium alginate (SA) based antibacterial hydrogels SA/PEG–HHC10 were designed and prepared by combining Diels–Alder (DA) click chemistry and the thiol–ene reaction. The hydrogels were first prepared using DA click chemistry with good mechanical strength, then the cysteine-terminated antimicrobial peptide HHC10–CYS (HHC10) was grafted into the hydrogel by the thiol–ene reaction between the oxy-norbornene group and the thiol group. The results showed that the antimicrobial hydrogels had a strong antibacterial property and good biocompatibility. Therefore, the antimicrobial hydrogels have significant potential application as coatings for implantable medical devices. The Royal Society of Chemistry 2018-03-21 /pmc/articles/PMC9078979/ /pubmed/35541529 http://dx.doi.org/10.1039/c8ra00668g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Wang, Gang Zhu, Jiehua Chen, Xiaofeng Dong, Hua Li, Qingtao Zeng, Lei Cao, Xiaodong Alginate based antimicrobial hydrogels formed by integrating Diels–Alder “click chemistry” and the thiol–ene reaction |
title | Alginate based antimicrobial hydrogels formed by integrating Diels–Alder “click chemistry” and the thiol–ene reaction |
title_full | Alginate based antimicrobial hydrogels formed by integrating Diels–Alder “click chemistry” and the thiol–ene reaction |
title_fullStr | Alginate based antimicrobial hydrogels formed by integrating Diels–Alder “click chemistry” and the thiol–ene reaction |
title_full_unstemmed | Alginate based antimicrobial hydrogels formed by integrating Diels–Alder “click chemistry” and the thiol–ene reaction |
title_short | Alginate based antimicrobial hydrogels formed by integrating Diels–Alder “click chemistry” and the thiol–ene reaction |
title_sort | alginate based antimicrobial hydrogels formed by integrating diels–alder “click chemistry” and the thiol–ene reaction |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078979/ https://www.ncbi.nlm.nih.gov/pubmed/35541529 http://dx.doi.org/10.1039/c8ra00668g |
work_keys_str_mv | AT wanggang alginatebasedantimicrobialhydrogelsformedbyintegratingdielsalderclickchemistryandthethiolenereaction AT zhujiehua alginatebasedantimicrobialhydrogelsformedbyintegratingdielsalderclickchemistryandthethiolenereaction AT chenxiaofeng alginatebasedantimicrobialhydrogelsformedbyintegratingdielsalderclickchemistryandthethiolenereaction AT donghua alginatebasedantimicrobialhydrogelsformedbyintegratingdielsalderclickchemistryandthethiolenereaction AT liqingtao alginatebasedantimicrobialhydrogelsformedbyintegratingdielsalderclickchemistryandthethiolenereaction AT zenglei alginatebasedantimicrobialhydrogelsformedbyintegratingdielsalderclickchemistryandthethiolenereaction AT caoxiaodong alginatebasedantimicrobialhydrogelsformedbyintegratingdielsalderclickchemistryandthethiolenereaction |