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Bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering
Three-dimensional (3D) bioprinting technologies have shown great potential in the fabrication of 3D models for different human tissues. Stem cells are an attractive cell source in tissue engineering as they can be directed by material and environmental cues to differentiate into multiple cell types...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Whioce Publishing Pte. Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310267/ https://www.ncbi.nlm.nih.gov/pubmed/32596547 http://dx.doi.org/10.18063/ijb.v5i2.2.204 |
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author | Kolan, Krishna C. R. Semon, Julie A. Bromet, Bradley Day, Delbert E. Leu, Ming C. |
author_facet | Kolan, Krishna C. R. Semon, Julie A. Bromet, Bradley Day, Delbert E. Leu, Ming C. |
author_sort | Kolan, Krishna C. R. |
collection | PubMed |
description | Three-dimensional (3D) bioprinting technologies have shown great potential in the fabrication of 3D models for different human tissues. Stem cells are an attractive cell source in tissue engineering as they can be directed by material and environmental cues to differentiate into multiple cell types for tissue repair and regeneration. In this study, we investigate the viability of human adipose-derived mesenchymal stem cells (ASCs) in alginate-gelatin (Alg-Gel) hydrogel bioprinted with or without bioactive glass. Highly angiogenic borate bioactive glass (13-93B3) in 50 wt% is added to polycaprolactone (PCL) to fabricate scaffolds using a solvent-based extrusion 3D bioprinting technique. The fabricated scaffolds with 12 × 12 × 1 mm(3) in overall dimensions are physically characterized, and the glass dissolution from PCL/glass composite over a period of 28 days is studied. Alg-Gel composite hydrogel is used as a bioink to suspend ASCs, and scaffolds are then bioprinted in different configurations: Bioink only, PCL+bioink, and PCL/glass+bioink, to investigate ASC viability. The results indicate the feasibility of the solvent-based bioprinting process to fabricate 3D cellularized scaffolds with more than 80% viability on day 0. The decrease in viability after 7 days due to glass concentration and static culture conditions is discussed. The feasibility of modifying Alg-Gel with 13-93B3 glass for bioprinting is also investigated, and the results are discussed. |
format | Online Article Text |
id | pubmed-7310267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Whioce Publishing Pte. Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73102672020-06-25 Bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering Kolan, Krishna C. R. Semon, Julie A. Bromet, Bradley Day, Delbert E. Leu, Ming C. Int J Bioprint Research Article Three-dimensional (3D) bioprinting technologies have shown great potential in the fabrication of 3D models for different human tissues. Stem cells are an attractive cell source in tissue engineering as they can be directed by material and environmental cues to differentiate into multiple cell types for tissue repair and regeneration. In this study, we investigate the viability of human adipose-derived mesenchymal stem cells (ASCs) in alginate-gelatin (Alg-Gel) hydrogel bioprinted with or without bioactive glass. Highly angiogenic borate bioactive glass (13-93B3) in 50 wt% is added to polycaprolactone (PCL) to fabricate scaffolds using a solvent-based extrusion 3D bioprinting technique. The fabricated scaffolds with 12 × 12 × 1 mm(3) in overall dimensions are physically characterized, and the glass dissolution from PCL/glass composite over a period of 28 days is studied. Alg-Gel composite hydrogel is used as a bioink to suspend ASCs, and scaffolds are then bioprinted in different configurations: Bioink only, PCL+bioink, and PCL/glass+bioink, to investigate ASC viability. The results indicate the feasibility of the solvent-based bioprinting process to fabricate 3D cellularized scaffolds with more than 80% viability on day 0. The decrease in viability after 7 days due to glass concentration and static culture conditions is discussed. The feasibility of modifying Alg-Gel with 13-93B3 glass for bioprinting is also investigated, and the results are discussed. Whioce Publishing Pte. Ltd. 2019-07-12 /pmc/articles/PMC7310267/ /pubmed/32596547 http://dx.doi.org/10.18063/ijb.v5i2.2.204 Text en Copyright: © 2019, Whioce Publishing Pte. Ltd. http://creativecommons.org/licenses/cc-by-nc/4.0/ This is an open-access article distributed under the terms of the Attribution-NonCommercial 4.0 International 4.0 (CC BY-NC 4.0), which permits all non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited. |
spellingShingle | Research Article Kolan, Krishna C. R. Semon, Julie A. Bromet, Bradley Day, Delbert E. Leu, Ming C. Bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering |
title | Bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering |
title_full | Bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering |
title_fullStr | Bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering |
title_full_unstemmed | Bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering |
title_short | Bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering |
title_sort | bioprinting with human stem cell-laden alginate-gelatin bioink and bioactive glass for tissue engineering |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310267/ https://www.ncbi.nlm.nih.gov/pubmed/32596547 http://dx.doi.org/10.18063/ijb.v5i2.2.204 |
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