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3D-bioprinted all-inclusive bioanalytical platforms for cell studies

Innovative drug screening platforms should improve the discovery of novel and personalized cancer treatment. Common models such as animals and 2D cell cultures lack the proper recapitulation of organ structure and environment. Thus, a new generation of platforms must consist of cell models that accu...

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Autores principales: Mazrouei, Roya, Velasco, Vanessa, Esfandyarpour, Rahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474064/
https://www.ncbi.nlm.nih.gov/pubmed/32887912
http://dx.doi.org/10.1038/s41598-020-71452-6
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author Mazrouei, Roya
Velasco, Vanessa
Esfandyarpour, Rahim
author_facet Mazrouei, Roya
Velasco, Vanessa
Esfandyarpour, Rahim
author_sort Mazrouei, Roya
collection PubMed
description Innovative drug screening platforms should improve the discovery of novel and personalized cancer treatment. Common models such as animals and 2D cell cultures lack the proper recapitulation of organ structure and environment. Thus, a new generation of platforms must consist of cell models that accurately mimic the cells’ microenvironment, along with flexibly prototyped cell handling structures that represent the human environment. Here, we adapted the 3D-bioprinting technology to develop multiple all-inclusive high throughputs and customized organ-on-a-chip-like platforms along with printed 3D-cell structures. Such platforms are potentially capable of performing 3D cell model analysis and cell-therapeutic response studies. We illustrated spherical and rectangular geometries of bio-printed 3D human colon cancer cell constructs. We also demonstrated the utility of directly 3D-bioprinting and rapidly prototyping of PDMS-based microfluidic cell handling arrays in different geometries. Besides, we successfully monitored the post-viability of the 3D-cell constructs for seven days. Furthermore, to mimic the human environment more closely, we integrated a 3D-bioprinted perfused drug screening microfluidics platform. Platform’s channels subject cell constructs to physiological fluid flow, while its concave well array hold and perfused 3D-cell constructs. The bio-applicability of PDMS-based arrays was also demonstrated by performing cancer cell-therapeutic response studies.
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spelling pubmed-74740642020-09-08 3D-bioprinted all-inclusive bioanalytical platforms for cell studies Mazrouei, Roya Velasco, Vanessa Esfandyarpour, Rahim Sci Rep Article Innovative drug screening platforms should improve the discovery of novel and personalized cancer treatment. Common models such as animals and 2D cell cultures lack the proper recapitulation of organ structure and environment. Thus, a new generation of platforms must consist of cell models that accurately mimic the cells’ microenvironment, along with flexibly prototyped cell handling structures that represent the human environment. Here, we adapted the 3D-bioprinting technology to develop multiple all-inclusive high throughputs and customized organ-on-a-chip-like platforms along with printed 3D-cell structures. Such platforms are potentially capable of performing 3D cell model analysis and cell-therapeutic response studies. We illustrated spherical and rectangular geometries of bio-printed 3D human colon cancer cell constructs. We also demonstrated the utility of directly 3D-bioprinting and rapidly prototyping of PDMS-based microfluidic cell handling arrays in different geometries. Besides, we successfully monitored the post-viability of the 3D-cell constructs for seven days. Furthermore, to mimic the human environment more closely, we integrated a 3D-bioprinted perfused drug screening microfluidics platform. Platform’s channels subject cell constructs to physiological fluid flow, while its concave well array hold and perfused 3D-cell constructs. The bio-applicability of PDMS-based arrays was also demonstrated by performing cancer cell-therapeutic response studies. Nature Publishing Group UK 2020-09-04 /pmc/articles/PMC7474064/ /pubmed/32887912 http://dx.doi.org/10.1038/s41598-020-71452-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mazrouei, Roya
Velasco, Vanessa
Esfandyarpour, Rahim
3D-bioprinted all-inclusive bioanalytical platforms for cell studies
title 3D-bioprinted all-inclusive bioanalytical platforms for cell studies
title_full 3D-bioprinted all-inclusive bioanalytical platforms for cell studies
title_fullStr 3D-bioprinted all-inclusive bioanalytical platforms for cell studies
title_full_unstemmed 3D-bioprinted all-inclusive bioanalytical platforms for cell studies
title_short 3D-bioprinted all-inclusive bioanalytical platforms for cell studies
title_sort 3d-bioprinted all-inclusive bioanalytical platforms for cell studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474064/
https://www.ncbi.nlm.nih.gov/pubmed/32887912
http://dx.doi.org/10.1038/s41598-020-71452-6
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