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Fluidic integrated 3D bioprinting system to sustain cell viability towards larynx fabrication
Herein, we report the first study to create a three‐dimensional (3D) bioprinted artificial larynx for whole‐laryngeal replacement. Our 3D bio‐printed larynx was generated using extrusion‐based 3D bioprinter with rabbit's chondrocyte‐laden gelatin methacryloyl (GelMA)/glycidyl‐methacrylated hyal...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013754/ https://www.ncbi.nlm.nih.gov/pubmed/36925698 http://dx.doi.org/10.1002/btm2.10423 |
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author | Park, Hae Sang Lee, Ji Seung Kim, Chang‐Beom Lee, Kwang‐Ho Hong, In‐Sun Jung, Harry Lee, Hanna Lee, Young Jin Ajiteru, Olatunji Sultan, Md Tipu Lee, Ok Joo Kim, Soon Hee Park, Chan Hum |
author_facet | Park, Hae Sang Lee, Ji Seung Kim, Chang‐Beom Lee, Kwang‐Ho Hong, In‐Sun Jung, Harry Lee, Hanna Lee, Young Jin Ajiteru, Olatunji Sultan, Md Tipu Lee, Ok Joo Kim, Soon Hee Park, Chan Hum |
author_sort | Park, Hae Sang |
collection | PubMed |
description | Herein, we report the first study to create a three‐dimensional (3D) bioprinted artificial larynx for whole‐laryngeal replacement. Our 3D bio‐printed larynx was generated using extrusion‐based 3D bioprinter with rabbit's chondrocyte‐laden gelatin methacryloyl (GelMA)/glycidyl‐methacrylated hyaluronic acid (GMHA) hybrid bioink. We used a polycaprolactone (PCL) outer framework incorporated with pores to achieve the structural strength of printed constructs, as well as to provide a suitable microenvironment to support printed cells. Notably, we established a novel fluidics supply (FS) system that simultaneously supplies basal medium together with a 3D bioprinting process, thereby improving cell survival during the printing process. Our results showed that the FS system enhanced post‐printing cell viability, which enabled the generation of a large‐scale cell‐laden artificial laryngeal framework. Additionally, the incorporation of the PCL outer framework with pores and inner hydrogel provides structural stability and sufficient nutrient/oxygen transport. An animal study confirmed that the transplanted 3D bio‐larynx successfully maintained the airway. With further development, our new strategy holds great potential for fabricating human‐scale larynxes with in vivo‐like biological functions for laryngectomy patients. |
format | Online Article Text |
id | pubmed-10013754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100137542023-03-15 Fluidic integrated 3D bioprinting system to sustain cell viability towards larynx fabrication Park, Hae Sang Lee, Ji Seung Kim, Chang‐Beom Lee, Kwang‐Ho Hong, In‐Sun Jung, Harry Lee, Hanna Lee, Young Jin Ajiteru, Olatunji Sultan, Md Tipu Lee, Ok Joo Kim, Soon Hee Park, Chan Hum Bioeng Transl Med Research Articles Herein, we report the first study to create a three‐dimensional (3D) bioprinted artificial larynx for whole‐laryngeal replacement. Our 3D bio‐printed larynx was generated using extrusion‐based 3D bioprinter with rabbit's chondrocyte‐laden gelatin methacryloyl (GelMA)/glycidyl‐methacrylated hyaluronic acid (GMHA) hybrid bioink. We used a polycaprolactone (PCL) outer framework incorporated with pores to achieve the structural strength of printed constructs, as well as to provide a suitable microenvironment to support printed cells. Notably, we established a novel fluidics supply (FS) system that simultaneously supplies basal medium together with a 3D bioprinting process, thereby improving cell survival during the printing process. Our results showed that the FS system enhanced post‐printing cell viability, which enabled the generation of a large‐scale cell‐laden artificial laryngeal framework. Additionally, the incorporation of the PCL outer framework with pores and inner hydrogel provides structural stability and sufficient nutrient/oxygen transport. An animal study confirmed that the transplanted 3D bio‐larynx successfully maintained the airway. With further development, our new strategy holds great potential for fabricating human‐scale larynxes with in vivo‐like biological functions for laryngectomy patients. John Wiley & Sons, Inc. 2022-10-20 /pmc/articles/PMC10013754/ /pubmed/36925698 http://dx.doi.org/10.1002/btm2.10423 Text en © 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Park, Hae Sang Lee, Ji Seung Kim, Chang‐Beom Lee, Kwang‐Ho Hong, In‐Sun Jung, Harry Lee, Hanna Lee, Young Jin Ajiteru, Olatunji Sultan, Md Tipu Lee, Ok Joo Kim, Soon Hee Park, Chan Hum Fluidic integrated 3D bioprinting system to sustain cell viability towards larynx fabrication |
title | Fluidic integrated 3D bioprinting system to sustain cell viability towards larynx fabrication |
title_full | Fluidic integrated 3D bioprinting system to sustain cell viability towards larynx fabrication |
title_fullStr | Fluidic integrated 3D bioprinting system to sustain cell viability towards larynx fabrication |
title_full_unstemmed | Fluidic integrated 3D bioprinting system to sustain cell viability towards larynx fabrication |
title_short | Fluidic integrated 3D bioprinting system to sustain cell viability towards larynx fabrication |
title_sort | fluidic integrated 3d bioprinting system to sustain cell viability towards larynx fabrication |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013754/ https://www.ncbi.nlm.nih.gov/pubmed/36925698 http://dx.doi.org/10.1002/btm2.10423 |
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