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Thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model

Tissue adhesion is a common complication after surgery. In this work, a dexamethasone loaded polymeric micelles in thermosensitive hydrogel composite (Dex hydrogel) was prepared, which combined the anti-adhesion barrier with controlled release of anti-adhesion drug. Dexamethasone (Dex) was encapsula...

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Autores principales: Wu, Qinjie, Wang, Ning, He, Tao, Shang, Jinfeng, Li, Ling, Song, Linjiang, Yang, Xi, Li, Xia, Luo, Na, Zhang, Wenli, Gong, Changyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555101/
https://www.ncbi.nlm.nih.gov/pubmed/26324090
http://dx.doi.org/10.1038/srep13553
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author Wu, Qinjie
Wang, Ning
He, Tao
Shang, Jinfeng
Li, Ling
Song, Linjiang
Yang, Xi
Li, Xia
Luo, Na
Zhang, Wenli
Gong, Changyang
author_facet Wu, Qinjie
Wang, Ning
He, Tao
Shang, Jinfeng
Li, Ling
Song, Linjiang
Yang, Xi
Li, Xia
Luo, Na
Zhang, Wenli
Gong, Changyang
author_sort Wu, Qinjie
collection PubMed
description Tissue adhesion is a common complication after surgery. In this work, a dexamethasone loaded polymeric micelles in thermosensitive hydrogel composite (Dex hydrogel) was prepared, which combined the anti-adhesion barrier with controlled release of anti-adhesion drug. Dexamethasone (Dex) was encapsulated in polymeric micelles (Dex micelles), and then the Dex micelles were loaded into biodegradable and thermosensitive hydrogel. The obtained Dex hydrogel showed a temperature-dependent sol-gel-sol phase transition behavior. The Dex hydrogel could form a non-flowing gel in situ upon subcutaneous injection and gradually degrade in about 20 days. In addition, Dex hydrogel was assigned for anti-adhesion studies in a more rigorous recurrent adhesion animal model. Compared with normal saline (NS) and Dex micelles group, tissue adhesions in hydrogel and Dex hydrogel group were significantly alleviated. In Dex hydrogel group, the media adhesion score is 0, which was dramatically lower than that in blank hydrogel group (2.50, P < 0.001). In histopathological examination and scanning electron microscopy (SEM) analysis, an integral neo-mesothelial cell layer with microvilli on their surface was observed, which revealed that the injured parietal and visceral peritoneum were fully recovered without the concerns of adhesion formation. Our results suggested that Dex hydrogel may serve as a potential anti-adhesion candidate.
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spelling pubmed-45551012015-09-11 Thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model Wu, Qinjie Wang, Ning He, Tao Shang, Jinfeng Li, Ling Song, Linjiang Yang, Xi Li, Xia Luo, Na Zhang, Wenli Gong, Changyang Sci Rep Article Tissue adhesion is a common complication after surgery. In this work, a dexamethasone loaded polymeric micelles in thermosensitive hydrogel composite (Dex hydrogel) was prepared, which combined the anti-adhesion barrier with controlled release of anti-adhesion drug. Dexamethasone (Dex) was encapsulated in polymeric micelles (Dex micelles), and then the Dex micelles were loaded into biodegradable and thermosensitive hydrogel. The obtained Dex hydrogel showed a temperature-dependent sol-gel-sol phase transition behavior. The Dex hydrogel could form a non-flowing gel in situ upon subcutaneous injection and gradually degrade in about 20 days. In addition, Dex hydrogel was assigned for anti-adhesion studies in a more rigorous recurrent adhesion animal model. Compared with normal saline (NS) and Dex micelles group, tissue adhesions in hydrogel and Dex hydrogel group were significantly alleviated. In Dex hydrogel group, the media adhesion score is 0, which was dramatically lower than that in blank hydrogel group (2.50, P < 0.001). In histopathological examination and scanning electron microscopy (SEM) analysis, an integral neo-mesothelial cell layer with microvilli on their surface was observed, which revealed that the injured parietal and visceral peritoneum were fully recovered without the concerns of adhesion formation. Our results suggested that Dex hydrogel may serve as a potential anti-adhesion candidate. Nature Publishing Group 2015-09-01 /pmc/articles/PMC4555101/ /pubmed/26324090 http://dx.doi.org/10.1038/srep13553 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wu, Qinjie
Wang, Ning
He, Tao
Shang, Jinfeng
Li, Ling
Song, Linjiang
Yang, Xi
Li, Xia
Luo, Na
Zhang, Wenli
Gong, Changyang
Thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model
title Thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model
title_full Thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model
title_fullStr Thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model
title_full_unstemmed Thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model
title_short Thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model
title_sort thermosensitive hydrogel containing dexamethasone micelles for preventing postsurgical adhesion in a repeated-injury model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555101/
https://www.ncbi.nlm.nih.gov/pubmed/26324090
http://dx.doi.org/10.1038/srep13553
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