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Instrumented cardiac microphysiological devices via multi-material 3D printing

Biomedical research has relied on animal studies and conventional cell cultures for decades. Recently, microphysiological systems (MPS), also known as organs-on-chips, that recapitulate the structure and function of native tissues in vitro, have emerged as a promising alternative(1). However, curren...

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Autores principales: Lind, Johan U., Busbee, Travis A., Valentine, Alexander D., Pasqualini, Francesco S., Yuan, Hongyan, Yadid, Moran, Park, Sung-Jin, Kotikian, Arda, Nesmith, Alexander P., Campbell, Patrick H., Vlassak, Joost J., Lewis, Jennifer A., Parker, Kevin K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321777/
https://www.ncbi.nlm.nih.gov/pubmed/27775708
http://dx.doi.org/10.1038/nmat4782
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author Lind, Johan U.
Busbee, Travis A.
Valentine, Alexander D.
Pasqualini, Francesco S.
Yuan, Hongyan
Yadid, Moran
Park, Sung-Jin
Kotikian, Arda
Nesmith, Alexander P.
Campbell, Patrick H.
Vlassak, Joost J.
Lewis, Jennifer A.
Parker, Kevin K.
author_facet Lind, Johan U.
Busbee, Travis A.
Valentine, Alexander D.
Pasqualini, Francesco S.
Yuan, Hongyan
Yadid, Moran
Park, Sung-Jin
Kotikian, Arda
Nesmith, Alexander P.
Campbell, Patrick H.
Vlassak, Joost J.
Lewis, Jennifer A.
Parker, Kevin K.
author_sort Lind, Johan U.
collection PubMed
description Biomedical research has relied on animal studies and conventional cell cultures for decades. Recently, microphysiological systems (MPS), also known as organs-on-chips, that recapitulate the structure and function of native tissues in vitro, have emerged as a promising alternative(1). However, current MPS typically lack integrated sensors and their fabrication requires multi-step lithographic processes(2). Here, we introduce a facile route for fabricating a new class of instrumented cardiac microphysiological devices via multi-material 3D printing. Specifically, we designed six functional inks, based on piezo-resistive, high conductance, and biocompatible soft materials that enable integration of soft strain gauge sensors within micro-architectures that guide the self-assembly of physio-mimetic laminar cardiac tissues. We validated that these embedded sensors provide non-invasive, electronic readout of tissue contractile stresses, inside cell incubator environments. We further applied these devices to study drug responses, as well as the contractile development of human stem cell derived laminar cardiac tissues over four weeks.
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spelling pubmed-53217772017-04-24 Instrumented cardiac microphysiological devices via multi-material 3D printing Lind, Johan U. Busbee, Travis A. Valentine, Alexander D. Pasqualini, Francesco S. Yuan, Hongyan Yadid, Moran Park, Sung-Jin Kotikian, Arda Nesmith, Alexander P. Campbell, Patrick H. Vlassak, Joost J. Lewis, Jennifer A. Parker, Kevin K. Nat Mater Article Biomedical research has relied on animal studies and conventional cell cultures for decades. Recently, microphysiological systems (MPS), also known as organs-on-chips, that recapitulate the structure and function of native tissues in vitro, have emerged as a promising alternative(1). However, current MPS typically lack integrated sensors and their fabrication requires multi-step lithographic processes(2). Here, we introduce a facile route for fabricating a new class of instrumented cardiac microphysiological devices via multi-material 3D printing. Specifically, we designed six functional inks, based on piezo-resistive, high conductance, and biocompatible soft materials that enable integration of soft strain gauge sensors within micro-architectures that guide the self-assembly of physio-mimetic laminar cardiac tissues. We validated that these embedded sensors provide non-invasive, electronic readout of tissue contractile stresses, inside cell incubator environments. We further applied these devices to study drug responses, as well as the contractile development of human stem cell derived laminar cardiac tissues over four weeks. 2016-10-24 2017-03 /pmc/articles/PMC5321777/ /pubmed/27775708 http://dx.doi.org/10.1038/nmat4782 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Lind, Johan U.
Busbee, Travis A.
Valentine, Alexander D.
Pasqualini, Francesco S.
Yuan, Hongyan
Yadid, Moran
Park, Sung-Jin
Kotikian, Arda
Nesmith, Alexander P.
Campbell, Patrick H.
Vlassak, Joost J.
Lewis, Jennifer A.
Parker, Kevin K.
Instrumented cardiac microphysiological devices via multi-material 3D printing
title Instrumented cardiac microphysiological devices via multi-material 3D printing
title_full Instrumented cardiac microphysiological devices via multi-material 3D printing
title_fullStr Instrumented cardiac microphysiological devices via multi-material 3D printing
title_full_unstemmed Instrumented cardiac microphysiological devices via multi-material 3D printing
title_short Instrumented cardiac microphysiological devices via multi-material 3D printing
title_sort instrumented cardiac microphysiological devices via multi-material 3d printing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321777/
https://www.ncbi.nlm.nih.gov/pubmed/27775708
http://dx.doi.org/10.1038/nmat4782
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