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Construction and Application of in vitro Alveolar Models Based on 3D Printing Technology

Increasing lung diseases, mutating coronaviruses, and the development of new compounds urgently require biomimetic in vitro lung models for lung pathology, toxicology, and pharmacology. The current construction strategies for lung models mainly include animal models, 2D cell culture, lung-on-a-chip,...

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Autores principales: Liu, Tiankun, Zhou, Chang, Shao, Yongchun, Xiong, Zhuo, Weng, Ding, Pang, Yuan, Sun, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Ltd on behalf of Chinese Mechanical Engineering Society (CMES). 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213023/
http://dx.doi.org/10.1016/j.cjmeam.2022.100025
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author Liu, Tiankun
Zhou, Chang
Shao, Yongchun
Xiong, Zhuo
Weng, Ding
Pang, Yuan
Sun, Wei
author_facet Liu, Tiankun
Zhou, Chang
Shao, Yongchun
Xiong, Zhuo
Weng, Ding
Pang, Yuan
Sun, Wei
author_sort Liu, Tiankun
collection PubMed
description Increasing lung diseases, mutating coronaviruses, and the development of new compounds urgently require biomimetic in vitro lung models for lung pathology, toxicology, and pharmacology. The current construction strategies for lung models mainly include animal models, 2D cell culture, lung-on-a-chip, and lung organoids. However, current models face difficulties in reproducing in vivo-like alveolar size and vesicle-like structures, and are unable to contain multiple cell types. In this study, a strategy for constructing alveolar models based on degradable hydrogel microspheres is proposed. Hydrogel microspheres, 200–250 µm in diameter, were prepared using a self-developed printing technique driven by alternating viscous and inertial forces. Microcapsules were further constructed using a coacervation-based layer-by-layer technique and core liquefaction. Three types of cells were inoculated and co-cultured on hydrogel capsules based on optimized microcapsule surface treatment strategies. Finally, an in vitro three-dimensional endothelial alveolar model with a multicellular composition and vesicle-like structure with a diameter of approximately 230 µm was successfully constructed. Cells in the constructed alveolar model maintained a high survival rate. The LD(50) values of glutaraldehyde based on the constructed models were in good agreement with the reference values, validating the potential of the model for future toxicant and drug detection.
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spelling pubmed-92130232022-06-22 Construction and Application of in vitro Alveolar Models Based on 3D Printing Technology Liu, Tiankun Zhou, Chang Shao, Yongchun Xiong, Zhuo Weng, Ding Pang, Yuan Sun, Wei Chinese Journal of Mechanical Engineering: Additive Manufacturing Frontiers Article Increasing lung diseases, mutating coronaviruses, and the development of new compounds urgently require biomimetic in vitro lung models for lung pathology, toxicology, and pharmacology. The current construction strategies for lung models mainly include animal models, 2D cell culture, lung-on-a-chip, and lung organoids. However, current models face difficulties in reproducing in vivo-like alveolar size and vesicle-like structures, and are unable to contain multiple cell types. In this study, a strategy for constructing alveolar models based on degradable hydrogel microspheres is proposed. Hydrogel microspheres, 200–250 µm in diameter, were prepared using a self-developed printing technique driven by alternating viscous and inertial forces. Microcapsules were further constructed using a coacervation-based layer-by-layer technique and core liquefaction. Three types of cells were inoculated and co-cultured on hydrogel capsules based on optimized microcapsule surface treatment strategies. Finally, an in vitro three-dimensional endothelial alveolar model with a multicellular composition and vesicle-like structure with a diameter of approximately 230 µm was successfully constructed. Cells in the constructed alveolar model maintained a high survival rate. The LD(50) values of glutaraldehyde based on the constructed models were in good agreement with the reference values, validating the potential of the model for future toxicant and drug detection. The Authors. Published by Elsevier Ltd on behalf of Chinese Mechanical Engineering Society (CMES). 2022-06 2022-06-16 /pmc/articles/PMC9213023/ http://dx.doi.org/10.1016/j.cjmeam.2022.100025 Text en © 2022 The Authors. Published by Elsevier Ltd on behalf of Chinese Mechanical Engineering Society (CMES). Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Liu, Tiankun
Zhou, Chang
Shao, Yongchun
Xiong, Zhuo
Weng, Ding
Pang, Yuan
Sun, Wei
Construction and Application of in vitro Alveolar Models Based on 3D Printing Technology
title Construction and Application of in vitro Alveolar Models Based on 3D Printing Technology
title_full Construction and Application of in vitro Alveolar Models Based on 3D Printing Technology
title_fullStr Construction and Application of in vitro Alveolar Models Based on 3D Printing Technology
title_full_unstemmed Construction and Application of in vitro Alveolar Models Based on 3D Printing Technology
title_short Construction and Application of in vitro Alveolar Models Based on 3D Printing Technology
title_sort construction and application of in vitro alveolar models based on 3d printing technology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213023/
http://dx.doi.org/10.1016/j.cjmeam.2022.100025
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