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Functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing

In-situ three-dimensional (3D) bioprinting has been emerging as a promising technology designed to rapidly seal cutaneous defects according to their contour. Improvements in the formulations of multi-component bioink are needed to support cytocompatible encapsulation and biological functions. Platel...

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Autores principales: Zhao, Ming, Wang, Jing, Zhang, Jinxin, Huang, Jingman, Luo, Liang, Yang, Yunshu, Shen, Kuo, Jiao, Tian, Jia, Yanhui, Lian, Weilong, Li, Jin, Wang, Yunchuan, Lian, Qin, Hu, Dahai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254123/
https://www.ncbi.nlm.nih.gov/pubmed/35799896
http://dx.doi.org/10.1016/j.mtbio.2022.100334
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author Zhao, Ming
Wang, Jing
Zhang, Jinxin
Huang, Jingman
Luo, Liang
Yang, Yunshu
Shen, Kuo
Jiao, Tian
Jia, Yanhui
Lian, Weilong
Li, Jin
Wang, Yunchuan
Lian, Qin
Hu, Dahai
author_facet Zhao, Ming
Wang, Jing
Zhang, Jinxin
Huang, Jingman
Luo, Liang
Yang, Yunshu
Shen, Kuo
Jiao, Tian
Jia, Yanhui
Lian, Weilong
Li, Jin
Wang, Yunchuan
Lian, Qin
Hu, Dahai
author_sort Zhao, Ming
collection PubMed
description In-situ three-dimensional (3D) bioprinting has been emerging as a promising technology designed to rapidly seal cutaneous defects according to their contour. Improvements in the formulations of multi-component bioink are needed to support cytocompatible encapsulation and biological functions. Platelet-rich plasma (PRP), as a source of patient-specific autologous growth factors, exhibits capabilities in tissue repair and rejuvenation. This study aimed to prepare PRP-integrated alginate-gelatin (AG) composite hydrogel bioinks and evaluate the biological effects in vitro and in vivo. 3D bioprinted constructs embedded with dermal fibroblasts and epidermal stem cells were fabricated using extrusion strategy. The integration of PRP not only improved the cellular behavior of seeded cells, but regulate the tube formation of vascular endothelial cells and macrophage polarization in a paracrine manner, which obtained an optimal effect at an incorporation concentration of 5%. For in-situ bioprinting, PRP integration accelerated the high-quality wound closure, modulated the inflammation and initiated the angiogenesis compared with the AG bioink. In conclusion, we revealed the regenerative potential of PRP, readily available at the bedside, as an initial signaling provider in multi-component bioink development. Combined with in-situ printing technology, it is expected to accelerate the clinical translation of rapid individualized wound repair.
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spelling pubmed-92541232022-07-06 Functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing Zhao, Ming Wang, Jing Zhang, Jinxin Huang, Jingman Luo, Liang Yang, Yunshu Shen, Kuo Jiao, Tian Jia, Yanhui Lian, Weilong Li, Jin Wang, Yunchuan Lian, Qin Hu, Dahai Mater Today Bio Full Length Article In-situ three-dimensional (3D) bioprinting has been emerging as a promising technology designed to rapidly seal cutaneous defects according to their contour. Improvements in the formulations of multi-component bioink are needed to support cytocompatible encapsulation and biological functions. Platelet-rich plasma (PRP), as a source of patient-specific autologous growth factors, exhibits capabilities in tissue repair and rejuvenation. This study aimed to prepare PRP-integrated alginate-gelatin (AG) composite hydrogel bioinks and evaluate the biological effects in vitro and in vivo. 3D bioprinted constructs embedded with dermal fibroblasts and epidermal stem cells were fabricated using extrusion strategy. The integration of PRP not only improved the cellular behavior of seeded cells, but regulate the tube formation of vascular endothelial cells and macrophage polarization in a paracrine manner, which obtained an optimal effect at an incorporation concentration of 5%. For in-situ bioprinting, PRP integration accelerated the high-quality wound closure, modulated the inflammation and initiated the angiogenesis compared with the AG bioink. In conclusion, we revealed the regenerative potential of PRP, readily available at the bedside, as an initial signaling provider in multi-component bioink development. Combined with in-situ printing technology, it is expected to accelerate the clinical translation of rapid individualized wound repair. Elsevier 2022-06-24 /pmc/articles/PMC9254123/ /pubmed/35799896 http://dx.doi.org/10.1016/j.mtbio.2022.100334 Text en © 2022 The Authors https://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 Full Length Article
Zhao, Ming
Wang, Jing
Zhang, Jinxin
Huang, Jingman
Luo, Liang
Yang, Yunshu
Shen, Kuo
Jiao, Tian
Jia, Yanhui
Lian, Weilong
Li, Jin
Wang, Yunchuan
Lian, Qin
Hu, Dahai
Functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing
title Functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing
title_full Functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing
title_fullStr Functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing
title_full_unstemmed Functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing
title_short Functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing
title_sort functionalizing multi-component bioink with platelet-rich plasma for customized in-situ bilayer bioprinting for wound healing
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254123/
https://www.ncbi.nlm.nih.gov/pubmed/35799896
http://dx.doi.org/10.1016/j.mtbio.2022.100334
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