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Perfusable Vessel-on-a-Chip for Antiangiogenic Drug Screening with Coaxial Bioprinting
Vessel-on-a-chips, which can be used to study microscale fluid dynamics, tissue-level biological molecules delivery and intercellular communication under favorable three-dimensional (3D) extracellular matrix microenvironment, are increasingly gaining traction. However, not many of them can allow for...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Whioce Publishing Pte. Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668575/ https://www.ncbi.nlm.nih.gov/pubmed/36404784 http://dx.doi.org/10.18063/ijb.v8i4.619 |
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author | Gu, Zeming Xie, Mingjun Lv, Shang Liu, Nian He, Jing Li, Yuanrong Zhu, Yuanbo Fu, Jianzhong Lin, Hui Xie, Chaoqi He, Yong |
author_facet | Gu, Zeming Xie, Mingjun Lv, Shang Liu, Nian He, Jing Li, Yuanrong Zhu, Yuanbo Fu, Jianzhong Lin, Hui Xie, Chaoqi He, Yong |
author_sort | Gu, Zeming |
collection | PubMed |
description | Vessel-on-a-chips, which can be used to study microscale fluid dynamics, tissue-level biological molecules delivery and intercellular communication under favorable three-dimensional (3D) extracellular matrix microenvironment, are increasingly gaining traction. However, not many of them can allow for long-term perfusion and easy observation of angiogenesis process. Since angiogenesis is necessary for the expansion of tumor, antiangiogenic drugs play a significant role in cancer treatment. In this study, we established an innovative and reliable antiangiogenic drug screening chip that was highly modularly integrated for long-term perfusion (up to 10 days depending on the hydrogel formula) and real-time monitoring. To maintain an unobstructed flow of cell-laden tubes for subsequent perfusion culture on the premise of excellent bioactivities, a polycaprolactone stent inspired by coronary artery stents was introduced to hold up the tubular lumen from the inside, while the perfusion chip was also elaborately designed to allow for convenient observation. After 3 days of perfusion screening, distinct differences in human umbilical vein endothelial cell sprouting were observed for a gradient of concentrations of bevacizumab, which pointed to the effectiveness and reliability of the drug screening perfusion system. Overall, a perfusion system for antiangiogenic drug screening was developed, which can not only conduct drug evaluation, but also be potentially useful in other vessel-mimicking scenarios in the area of tissue engineering, drug screening, pharmacokinetics, and regenerative medicine. |
format | Online Article Text |
id | pubmed-9668575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Whioce Publishing Pte. Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96685752022-11-17 Perfusable Vessel-on-a-Chip for Antiangiogenic Drug Screening with Coaxial Bioprinting Gu, Zeming Xie, Mingjun Lv, Shang Liu, Nian He, Jing Li, Yuanrong Zhu, Yuanbo Fu, Jianzhong Lin, Hui Xie, Chaoqi He, Yong Int J Bioprint Research Article Vessel-on-a-chips, which can be used to study microscale fluid dynamics, tissue-level biological molecules delivery and intercellular communication under favorable three-dimensional (3D) extracellular matrix microenvironment, are increasingly gaining traction. However, not many of them can allow for long-term perfusion and easy observation of angiogenesis process. Since angiogenesis is necessary for the expansion of tumor, antiangiogenic drugs play a significant role in cancer treatment. In this study, we established an innovative and reliable antiangiogenic drug screening chip that was highly modularly integrated for long-term perfusion (up to 10 days depending on the hydrogel formula) and real-time monitoring. To maintain an unobstructed flow of cell-laden tubes for subsequent perfusion culture on the premise of excellent bioactivities, a polycaprolactone stent inspired by coronary artery stents was introduced to hold up the tubular lumen from the inside, while the perfusion chip was also elaborately designed to allow for convenient observation. After 3 days of perfusion screening, distinct differences in human umbilical vein endothelial cell sprouting were observed for a gradient of concentrations of bevacizumab, which pointed to the effectiveness and reliability of the drug screening perfusion system. Overall, a perfusion system for antiangiogenic drug screening was developed, which can not only conduct drug evaluation, but also be potentially useful in other vessel-mimicking scenarios in the area of tissue engineering, drug screening, pharmacokinetics, and regenerative medicine. Whioce Publishing Pte. Ltd. 2022-09-22 /pmc/articles/PMC9668575/ /pubmed/36404784 http://dx.doi.org/10.18063/ijb.v8i4.619 Text en Copyright: © 2022 Gu et al. https://creativecommons.org/licenses/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 Gu, Zeming Xie, Mingjun Lv, Shang Liu, Nian He, Jing Li, Yuanrong Zhu, Yuanbo Fu, Jianzhong Lin, Hui Xie, Chaoqi He, Yong Perfusable Vessel-on-a-Chip for Antiangiogenic Drug Screening with Coaxial Bioprinting |
title | Perfusable Vessel-on-a-Chip for Antiangiogenic Drug Screening with Coaxial Bioprinting |
title_full | Perfusable Vessel-on-a-Chip for Antiangiogenic Drug Screening with Coaxial Bioprinting |
title_fullStr | Perfusable Vessel-on-a-Chip for Antiangiogenic Drug Screening with Coaxial Bioprinting |
title_full_unstemmed | Perfusable Vessel-on-a-Chip for Antiangiogenic Drug Screening with Coaxial Bioprinting |
title_short | Perfusable Vessel-on-a-Chip for Antiangiogenic Drug Screening with Coaxial Bioprinting |
title_sort | perfusable vessel-on-a-chip for antiangiogenic drug screening with coaxial bioprinting |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668575/ https://www.ncbi.nlm.nih.gov/pubmed/36404784 http://dx.doi.org/10.18063/ijb.v8i4.619 |
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