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Development of Biocompatible HA Hydrogels Embedded with a New Synthetic Peptide Promoting Cellular Migration for Advanced Wound Care Management

In the past few years, there have been many efforts underway to develop effective wound healing treatments for traumatic injuries. In particular, wound‐healing peptides (WHPs) and peptide‐grafted dressings hold great promise for novel therapeutic strategies for wound management. This study reports a...

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Autores principales: Wang, Sun Young, Kim, Hyosuk, Kwak, Gijung, Yoon, Hong Yeol, Jo, Sung Duk, Lee, Ji Eun, Cho, Daeho, Kwon, Ick Chan, Kim, Sun Hwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247053/
https://www.ncbi.nlm.nih.gov/pubmed/30479928
http://dx.doi.org/10.1002/advs.201800852
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author Wang, Sun Young
Kim, Hyosuk
Kwak, Gijung
Yoon, Hong Yeol
Jo, Sung Duk
Lee, Ji Eun
Cho, Daeho
Kwon, Ick Chan
Kim, Sun Hwa
author_facet Wang, Sun Young
Kim, Hyosuk
Kwak, Gijung
Yoon, Hong Yeol
Jo, Sung Duk
Lee, Ji Eun
Cho, Daeho
Kwon, Ick Chan
Kim, Sun Hwa
author_sort Wang, Sun Young
collection PubMed
description In the past few years, there have been many efforts underway to develop effective wound healing treatments for traumatic injuries. In particular, wound‐healing peptides (WHPs) and peptide‐grafted dressings hold great promise for novel therapeutic strategies for wound management. This study reports a topical formulation of a new synthetic WHP (REGRT, REG) embedded in a hyaluronic acid (HA)‐based hydrogel dressing for the enhancement of acute excisional wound repair. The copper‐free click chemistry is utilized to form biocompatible HA hydrogels by cross‐linking dibenzocyclooctyl‐functionalized HA with 4‐arm poly(ethylene glycol) (PEG) azide. The HA hydrogels are grafted with the REG peptide, a functional derivative of erythroid differentiation regulator1, displaying potent cell motility‐stimulating ability, thus sustainably releasing physiologically active peptides for a prolonged period. Combined with the traditional wound healing benefits of HA, the HA hydrogel embedded REG (REG‐HAgel) accelerates re‐epithelialization in skin wound healing, particularly by promoting migration of fibroblasts, keratinocytes, and endothelial cells. REG‐HAgels improve not only rate, but quality of wound healing with higher collagen deposition and more microvascular formation while being nontoxic. The peptide‐grafted HA hydrogel system can be considered as a promising new wound dressing formulation strategy for the treatment of different types of wounds with combinations of various natural and synthetic WHPs.
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spelling pubmed-62470532018-11-26 Development of Biocompatible HA Hydrogels Embedded with a New Synthetic Peptide Promoting Cellular Migration for Advanced Wound Care Management Wang, Sun Young Kim, Hyosuk Kwak, Gijung Yoon, Hong Yeol Jo, Sung Duk Lee, Ji Eun Cho, Daeho Kwon, Ick Chan Kim, Sun Hwa Adv Sci (Weinh) Full Papers In the past few years, there have been many efforts underway to develop effective wound healing treatments for traumatic injuries. In particular, wound‐healing peptides (WHPs) and peptide‐grafted dressings hold great promise for novel therapeutic strategies for wound management. This study reports a topical formulation of a new synthetic WHP (REGRT, REG) embedded in a hyaluronic acid (HA)‐based hydrogel dressing for the enhancement of acute excisional wound repair. The copper‐free click chemistry is utilized to form biocompatible HA hydrogels by cross‐linking dibenzocyclooctyl‐functionalized HA with 4‐arm poly(ethylene glycol) (PEG) azide. The HA hydrogels are grafted with the REG peptide, a functional derivative of erythroid differentiation regulator1, displaying potent cell motility‐stimulating ability, thus sustainably releasing physiologically active peptides for a prolonged period. Combined with the traditional wound healing benefits of HA, the HA hydrogel embedded REG (REG‐HAgel) accelerates re‐epithelialization in skin wound healing, particularly by promoting migration of fibroblasts, keratinocytes, and endothelial cells. REG‐HAgels improve not only rate, but quality of wound healing with higher collagen deposition and more microvascular formation while being nontoxic. The peptide‐grafted HA hydrogel system can be considered as a promising new wound dressing formulation strategy for the treatment of different types of wounds with combinations of various natural and synthetic WHPs. John Wiley and Sons Inc. 2018-09-21 /pmc/articles/PMC6247053/ /pubmed/30479928 http://dx.doi.org/10.1002/advs.201800852 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Wang, Sun Young
Kim, Hyosuk
Kwak, Gijung
Yoon, Hong Yeol
Jo, Sung Duk
Lee, Ji Eun
Cho, Daeho
Kwon, Ick Chan
Kim, Sun Hwa
Development of Biocompatible HA Hydrogels Embedded with a New Synthetic Peptide Promoting Cellular Migration for Advanced Wound Care Management
title Development of Biocompatible HA Hydrogels Embedded with a New Synthetic Peptide Promoting Cellular Migration for Advanced Wound Care Management
title_full Development of Biocompatible HA Hydrogels Embedded with a New Synthetic Peptide Promoting Cellular Migration for Advanced Wound Care Management
title_fullStr Development of Biocompatible HA Hydrogels Embedded with a New Synthetic Peptide Promoting Cellular Migration for Advanced Wound Care Management
title_full_unstemmed Development of Biocompatible HA Hydrogels Embedded with a New Synthetic Peptide Promoting Cellular Migration for Advanced Wound Care Management
title_short Development of Biocompatible HA Hydrogels Embedded with a New Synthetic Peptide Promoting Cellular Migration for Advanced Wound Care Management
title_sort development of biocompatible ha hydrogels embedded with a new synthetic peptide promoting cellular migration for advanced wound care management
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247053/
https://www.ncbi.nlm.nih.gov/pubmed/30479928
http://dx.doi.org/10.1002/advs.201800852
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