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A poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment

Wound repair remains a huge clinical challenge, which can cause bleeding, infection, and patient death. In our current research, a bioactive, injectable, multifunctional composite hydrogel doped with nanospheres was prepared with antibacterial and angiogenesis-promoting functions for the treatment o...

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Autores principales: Luo, Jiajia, Sun, Fenglei, Rao, Pinhua, Zhu, Tonghe, Liu, Yonghang, Du, Juan, Chen, Sihao, Jin, Xiangyun, Jin, Jiale, Chai, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9877222/
https://www.ncbi.nlm.nih.gov/pubmed/36714634
http://dx.doi.org/10.3389/fbioe.2022.1091122
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author Luo, Jiajia
Sun, Fenglei
Rao, Pinhua
Zhu, Tonghe
Liu, Yonghang
Du, Juan
Chen, Sihao
Jin, Xiangyun
Jin, Jiale
Chai, Yi
author_facet Luo, Jiajia
Sun, Fenglei
Rao, Pinhua
Zhu, Tonghe
Liu, Yonghang
Du, Juan
Chen, Sihao
Jin, Xiangyun
Jin, Jiale
Chai, Yi
author_sort Luo, Jiajia
collection PubMed
description Wound repair remains a huge clinical challenge, which can cause bleeding, infection, and patient death. In our current research, a bioactive, injectable, multifunctional composite hydrogel doped with nanospheres was prepared with antibacterial and angiogenesis-promoting functions for the treatment of wounds. Amino groups in ε-polylysine (ε-EPL) undergo dynamic Schiff base reaction cross-linking with oxidized hyaluronic acid (OHA), and F127 exhibits unique temperature sensitivity to form an injectable thermosensitive hydrogel (FHE10), which can form a hydrogel to cover the wound at body temperature. Nanospheres (PNs) prepared using poly (glyceryl-sebacate-acrylate) (PGSA) were loaded into hydrogels (FHE10) for promoting wound repair. The prepared FHE10 exhibited rapid gelation, good injectable abilities, and showed resistance to the flourish of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). In vitro investigations showed that FHE10 had good hemocompatibility and cytocompatibility. FHE10@PNs exhibited good proliferation, migration, and tube formation of human umbilical vein endothelial cells (HUVECs) and human foreskin fibroblasts (HFF-1). Furthermore, FHE10@PNs significantly promoted reepithelialization and collagen deposition as well as micro-vascularization compared with the use of FHE10 or PNs alone, thereby accelerating the repair of wounds. In general, this study demonstrated that the multifunctional injectable composite hydrogel showed great potential in wound treatment.
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spelling pubmed-98772222023-01-27 A poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment Luo, Jiajia Sun, Fenglei Rao, Pinhua Zhu, Tonghe Liu, Yonghang Du, Juan Chen, Sihao Jin, Xiangyun Jin, Jiale Chai, Yi Front Bioeng Biotechnol Bioengineering and Biotechnology Wound repair remains a huge clinical challenge, which can cause bleeding, infection, and patient death. In our current research, a bioactive, injectable, multifunctional composite hydrogel doped with nanospheres was prepared with antibacterial and angiogenesis-promoting functions for the treatment of wounds. Amino groups in ε-polylysine (ε-EPL) undergo dynamic Schiff base reaction cross-linking with oxidized hyaluronic acid (OHA), and F127 exhibits unique temperature sensitivity to form an injectable thermosensitive hydrogel (FHE10), which can form a hydrogel to cover the wound at body temperature. Nanospheres (PNs) prepared using poly (glyceryl-sebacate-acrylate) (PGSA) were loaded into hydrogels (FHE10) for promoting wound repair. The prepared FHE10 exhibited rapid gelation, good injectable abilities, and showed resistance to the flourish of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). In vitro investigations showed that FHE10 had good hemocompatibility and cytocompatibility. FHE10@PNs exhibited good proliferation, migration, and tube formation of human umbilical vein endothelial cells (HUVECs) and human foreskin fibroblasts (HFF-1). Furthermore, FHE10@PNs significantly promoted reepithelialization and collagen deposition as well as micro-vascularization compared with the use of FHE10 or PNs alone, thereby accelerating the repair of wounds. In general, this study demonstrated that the multifunctional injectable composite hydrogel showed great potential in wound treatment. Frontiers Media S.A. 2023-01-12 /pmc/articles/PMC9877222/ /pubmed/36714634 http://dx.doi.org/10.3389/fbioe.2022.1091122 Text en Copyright © 2023 Luo, Sun, Rao, Zhu, Liu, Du, Chen, Jin, Jin and Chai. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Luo, Jiajia
Sun, Fenglei
Rao, Pinhua
Zhu, Tonghe
Liu, Yonghang
Du, Juan
Chen, Sihao
Jin, Xiangyun
Jin, Jiale
Chai, Yi
A poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment
title A poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment
title_full A poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment
title_fullStr A poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment
title_full_unstemmed A poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment
title_short A poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment
title_sort poly (glycerol-sebacate-acrylate) nanosphere enhanced injectable hydrogel for wound treatment
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9877222/
https://www.ncbi.nlm.nih.gov/pubmed/36714634
http://dx.doi.org/10.3389/fbioe.2022.1091122
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