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Effect of detergent type on the performance of liver decellularized extracellular matrix-based bio-inks
Decellularized extracellular matrix-based bio-inks (dECM bio-inks) for bioprinting technology have recently gained attention owing to their excellent ability to confer tissue-specific functions and 3D-printing capability. Although decellularization has led to a major advancement in bio-ink developme...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919203/ https://www.ncbi.nlm.nih.gov/pubmed/33717429 http://dx.doi.org/10.1177/2041731421997091 |
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author | Jeong, Wonwoo Kim, Min Kyeong Kang, Hyun-Wook |
author_facet | Jeong, Wonwoo Kim, Min Kyeong Kang, Hyun-Wook |
author_sort | Jeong, Wonwoo |
collection | PubMed |
description | Decellularized extracellular matrix-based bio-inks (dECM bio-inks) for bioprinting technology have recently gained attention owing to their excellent ability to confer tissue-specific functions and 3D-printing capability. Although decellularization has led to a major advancement in bio-ink development, the effects of detergent type, the most important factor in decellularization, are still unclear. In this study, the effects of various detergent types on bio-ink performance were investigated. Porcine liver-derived dECM bio-inks prepared using widely used detergents, including sodium dodecyl sulfate (SDS), sodium deoxycholate (SDC), Triton X-100 (TX), and TX with ammonium hydroxide (TXA), were characterized in detail. SDS and SDC severely damaged glycosaminoglycan and elastin proteins, TX showed the lowest rate of decellularization, and TXA-based dECM bio-ink possessed the highest ECM content among all bio-inks. Differences in biochemical composition directly affected bio-ink performance, with TXA-dECM bio-ink showing the best performance with respect to gelation kinetics, intermolecular bonding, mechanical properties, and 2D/3D printability. More importantly, cytocompatibility tests using primary mouse hepatocytes also showed that the TXA-dECM bio-ink improved albumin secretion and cytochrome P450 activity by approximately 2.12- and 1.67-fold, respectively, compared with the observed values for other bio-inks. Our results indicate that the detergent type has a great influence on dECM damage and that the higher the dECM content, the better the performance of the bio-ink for 3D bioprinting. |
format | Online Article Text |
id | pubmed-7919203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-79192032021-03-11 Effect of detergent type on the performance of liver decellularized extracellular matrix-based bio-inks Jeong, Wonwoo Kim, Min Kyeong Kang, Hyun-Wook J Tissue Eng Original Article Decellularized extracellular matrix-based bio-inks (dECM bio-inks) for bioprinting technology have recently gained attention owing to their excellent ability to confer tissue-specific functions and 3D-printing capability. Although decellularization has led to a major advancement in bio-ink development, the effects of detergent type, the most important factor in decellularization, are still unclear. In this study, the effects of various detergent types on bio-ink performance were investigated. Porcine liver-derived dECM bio-inks prepared using widely used detergents, including sodium dodecyl sulfate (SDS), sodium deoxycholate (SDC), Triton X-100 (TX), and TX with ammonium hydroxide (TXA), were characterized in detail. SDS and SDC severely damaged glycosaminoglycan and elastin proteins, TX showed the lowest rate of decellularization, and TXA-based dECM bio-ink possessed the highest ECM content among all bio-inks. Differences in biochemical composition directly affected bio-ink performance, with TXA-dECM bio-ink showing the best performance with respect to gelation kinetics, intermolecular bonding, mechanical properties, and 2D/3D printability. More importantly, cytocompatibility tests using primary mouse hepatocytes also showed that the TXA-dECM bio-ink improved albumin secretion and cytochrome P450 activity by approximately 2.12- and 1.67-fold, respectively, compared with the observed values for other bio-inks. Our results indicate that the detergent type has a great influence on dECM damage and that the higher the dECM content, the better the performance of the bio-ink for 3D bioprinting. SAGE Publications 2021-02-24 /pmc/articles/PMC7919203/ /pubmed/33717429 http://dx.doi.org/10.1177/2041731421997091 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Jeong, Wonwoo Kim, Min Kyeong Kang, Hyun-Wook Effect of detergent type on the performance of liver decellularized extracellular matrix-based bio-inks |
title | Effect of detergent type on the performance of liver decellularized
extracellular matrix-based bio-inks |
title_full | Effect of detergent type on the performance of liver decellularized
extracellular matrix-based bio-inks |
title_fullStr | Effect of detergent type on the performance of liver decellularized
extracellular matrix-based bio-inks |
title_full_unstemmed | Effect of detergent type on the performance of liver decellularized
extracellular matrix-based bio-inks |
title_short | Effect of detergent type on the performance of liver decellularized
extracellular matrix-based bio-inks |
title_sort | effect of detergent type on the performance of liver decellularized
extracellular matrix-based bio-inks |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919203/ https://www.ncbi.nlm.nih.gov/pubmed/33717429 http://dx.doi.org/10.1177/2041731421997091 |
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