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De novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation

Biomaterial-enabled de novo formation of non-fibrotic tissue in situ would provide an important tool to physicians. One example application, glottic insufficiency, is a debilitating laryngeal disorder wherein vocal folds do not fully close, resulting in difficulty speaking and swallowing. Preferred...

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Autores principales: Pruett, Lauren J., Kenny, Hannah L., Swift, William M., Catallo, Katarina J., Apsel, Zoe R., Salopek, Lisa S., Scumpia, Philip O., Cottler, Patrick S., Griffin, Donald R., Daniero, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950481/
https://www.ncbi.nlm.nih.gov/pubmed/36823180
http://dx.doi.org/10.1038/s41536-023-00281-8
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author Pruett, Lauren J.
Kenny, Hannah L.
Swift, William M.
Catallo, Katarina J.
Apsel, Zoe R.
Salopek, Lisa S.
Scumpia, Philip O.
Cottler, Patrick S.
Griffin, Donald R.
Daniero, James J.
author_facet Pruett, Lauren J.
Kenny, Hannah L.
Swift, William M.
Catallo, Katarina J.
Apsel, Zoe R.
Salopek, Lisa S.
Scumpia, Philip O.
Cottler, Patrick S.
Griffin, Donald R.
Daniero, James J.
author_sort Pruett, Lauren J.
collection PubMed
description Biomaterial-enabled de novo formation of non-fibrotic tissue in situ would provide an important tool to physicians. One example application, glottic insufficiency, is a debilitating laryngeal disorder wherein vocal folds do not fully close, resulting in difficulty speaking and swallowing. Preferred management of glottic insufficiency includes bulking of vocal folds via injectable fillers, however, the current options have associated drawbacks including inflammation, accelerated resorption, and foreign body response. We developed a novel iteration of microporous annealed particle (MAP) scaffold designed to provide persistent augmentation. Following a 14-month study of vocal fold augmentation using a rabbit vocal paralysis model, most MAP scaffolds were replaced with tissue de novo that matched the mixture of fibrotic and non-fibrotic collagens of the contralateral vocal tissue. Further, persistent tissue augmentation in MAP-treated rabbits was observed via MRI and via superior vocal function at 14 months relative to the clinical standard.
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spelling pubmed-99504812023-02-25 De novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation Pruett, Lauren J. Kenny, Hannah L. Swift, William M. Catallo, Katarina J. Apsel, Zoe R. Salopek, Lisa S. Scumpia, Philip O. Cottler, Patrick S. Griffin, Donald R. Daniero, James J. NPJ Regen Med Article Biomaterial-enabled de novo formation of non-fibrotic tissue in situ would provide an important tool to physicians. One example application, glottic insufficiency, is a debilitating laryngeal disorder wherein vocal folds do not fully close, resulting in difficulty speaking and swallowing. Preferred management of glottic insufficiency includes bulking of vocal folds via injectable fillers, however, the current options have associated drawbacks including inflammation, accelerated resorption, and foreign body response. We developed a novel iteration of microporous annealed particle (MAP) scaffold designed to provide persistent augmentation. Following a 14-month study of vocal fold augmentation using a rabbit vocal paralysis model, most MAP scaffolds were replaced with tissue de novo that matched the mixture of fibrotic and non-fibrotic collagens of the contralateral vocal tissue. Further, persistent tissue augmentation in MAP-treated rabbits was observed via MRI and via superior vocal function at 14 months relative to the clinical standard. Nature Publishing Group UK 2023-02-23 /pmc/articles/PMC9950481/ /pubmed/36823180 http://dx.doi.org/10.1038/s41536-023-00281-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pruett, Lauren J.
Kenny, Hannah L.
Swift, William M.
Catallo, Katarina J.
Apsel, Zoe R.
Salopek, Lisa S.
Scumpia, Philip O.
Cottler, Patrick S.
Griffin, Donald R.
Daniero, James J.
De novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation
title De novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation
title_full De novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation
title_fullStr De novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation
title_full_unstemmed De novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation
title_short De novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation
title_sort de novo tissue formation using custom microporous annealed particle hydrogel provides long-term vocal fold augmentation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950481/
https://www.ncbi.nlm.nih.gov/pubmed/36823180
http://dx.doi.org/10.1038/s41536-023-00281-8
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