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Biological testing of chitosan‐collagen‐based porous scaffolds loaded with PLGA/Triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus

OBJECTIVES: Endoscopic submucosal dissection (ESD), a preferential approach for early oesophageal neoplasms, inevitably results in oesophageal strictures in patients. Clinical use of glucocorticoids through submucosal injection is beneficial for inhibiting oesophageal stricture following injury; how...

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Autores principales: Ni, Wenkai, Lin, Shengli, Bian, Saiyan, Xiao, Mingbing, Wang, Yongjun, Yang, Yumin, Lu, Cuihua, Zheng, Wenjie, Zhou, Pinghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941226/
https://www.ncbi.nlm.nih.gov/pubmed/33543561
http://dx.doi.org/10.1111/cpr.13004
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author Ni, Wenkai
Lin, Shengli
Bian, Saiyan
Xiao, Mingbing
Wang, Yongjun
Yang, Yumin
Lu, Cuihua
Zheng, Wenjie
Zhou, Pinghong
author_facet Ni, Wenkai
Lin, Shengli
Bian, Saiyan
Xiao, Mingbing
Wang, Yongjun
Yang, Yumin
Lu, Cuihua
Zheng, Wenjie
Zhou, Pinghong
author_sort Ni, Wenkai
collection PubMed
description OBJECTIVES: Endoscopic submucosal dissection (ESD), a preferential approach for early oesophageal neoplasms, inevitably results in oesophageal strictures in patients. Clinical use of glucocorticoids through submucosal injection is beneficial for inhibiting oesophageal stricture following injury; however, it also has limitations, such as dose loss and perforation. Hence, alternatives to glucocorticoid therapy should be developed. METHODS: A novel porous composite scaffold, ChCo‐TAMS, composed of chitosan, collagen‐I and triamcinolone acetonide (TA) loaded into poly (lactic‐co‐glycolic) acid (PLGA) microspheres (TAMS), was successfully constructed and subjected to biological testing to ameliorate oesophageal ESD‐related stenosis. RESULTS: The synthesized biomaterials displayed unique properties in inhibiting the activation of macrophages, chemokine‐mediated cell recruitment and fibrogenesis of fibroblasts. Further application of the scaffolds in the rat dermal defect and porcine oesophageal ESD model showed that these novel scaffolds played a robust role in inhibiting wound contracture and oesophageal ESD strictures. CONCLUSIONS: The developed composite scaffolds provide a promising clinical medical device for the prevention of post‐operative oesophageal stricture.
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spelling pubmed-79412262021-03-16 Biological testing of chitosan‐collagen‐based porous scaffolds loaded with PLGA/Triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus Ni, Wenkai Lin, Shengli Bian, Saiyan Xiao, Mingbing Wang, Yongjun Yang, Yumin Lu, Cuihua Zheng, Wenjie Zhou, Pinghong Cell Prolif Original Articles OBJECTIVES: Endoscopic submucosal dissection (ESD), a preferential approach for early oesophageal neoplasms, inevitably results in oesophageal strictures in patients. Clinical use of glucocorticoids through submucosal injection is beneficial for inhibiting oesophageal stricture following injury; however, it also has limitations, such as dose loss and perforation. Hence, alternatives to glucocorticoid therapy should be developed. METHODS: A novel porous composite scaffold, ChCo‐TAMS, composed of chitosan, collagen‐I and triamcinolone acetonide (TA) loaded into poly (lactic‐co‐glycolic) acid (PLGA) microspheres (TAMS), was successfully constructed and subjected to biological testing to ameliorate oesophageal ESD‐related stenosis. RESULTS: The synthesized biomaterials displayed unique properties in inhibiting the activation of macrophages, chemokine‐mediated cell recruitment and fibrogenesis of fibroblasts. Further application of the scaffolds in the rat dermal defect and porcine oesophageal ESD model showed that these novel scaffolds played a robust role in inhibiting wound contracture and oesophageal ESD strictures. CONCLUSIONS: The developed composite scaffolds provide a promising clinical medical device for the prevention of post‐operative oesophageal stricture. John Wiley and Sons Inc. 2021-02-04 /pmc/articles/PMC7941226/ /pubmed/33543561 http://dx.doi.org/10.1111/cpr.13004 Text en © 2021 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. 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 Original Articles
Ni, Wenkai
Lin, Shengli
Bian, Saiyan
Xiao, Mingbing
Wang, Yongjun
Yang, Yumin
Lu, Cuihua
Zheng, Wenjie
Zhou, Pinghong
Biological testing of chitosan‐collagen‐based porous scaffolds loaded with PLGA/Triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus
title Biological testing of chitosan‐collagen‐based porous scaffolds loaded with PLGA/Triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus
title_full Biological testing of chitosan‐collagen‐based porous scaffolds loaded with PLGA/Triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus
title_fullStr Biological testing of chitosan‐collagen‐based porous scaffolds loaded with PLGA/Triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus
title_full_unstemmed Biological testing of chitosan‐collagen‐based porous scaffolds loaded with PLGA/Triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus
title_short Biological testing of chitosan‐collagen‐based porous scaffolds loaded with PLGA/Triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus
title_sort biological testing of chitosan‐collagen‐based porous scaffolds loaded with plga/triamcinolone microspheres for ameliorating endoscopic dissection‐related stenosis in oesophagus
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941226/
https://www.ncbi.nlm.nih.gov/pubmed/33543561
http://dx.doi.org/10.1111/cpr.13004
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