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Digitally Driven Aerosol Jet Printing to Enable Customisable Neuronal Guidance

Digitally driven manufacturing technologies such as aerosol jet printing (AJP) can make a significant contribution to enabling new capabilities in the field of tissue engineering disease modeling and drug screening. AJP is an emerging non-contact and mask-less printing process which has distinct adv...

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Autores principales: Capel, Andrew J., Smith, Matthew A. A., Taccola, Silvia, Pardo-Figuerez, Maria, Rimington, Rowan P., Lewis, Mark P., Christie, Steven D. R., Kay, Robert W., Harris, Russell A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435718/
https://www.ncbi.nlm.nih.gov/pubmed/34527674
http://dx.doi.org/10.3389/fcell.2021.722294
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author Capel, Andrew J.
Smith, Matthew A. A.
Taccola, Silvia
Pardo-Figuerez, Maria
Rimington, Rowan P.
Lewis, Mark P.
Christie, Steven D. R.
Kay, Robert W.
Harris, Russell A.
author_facet Capel, Andrew J.
Smith, Matthew A. A.
Taccola, Silvia
Pardo-Figuerez, Maria
Rimington, Rowan P.
Lewis, Mark P.
Christie, Steven D. R.
Kay, Robert W.
Harris, Russell A.
author_sort Capel, Andrew J.
collection PubMed
description Digitally driven manufacturing technologies such as aerosol jet printing (AJP) can make a significant contribution to enabling new capabilities in the field of tissue engineering disease modeling and drug screening. AJP is an emerging non-contact and mask-less printing process which has distinct advantages over other patterning technologies as it offers versatile, high-resolution, direct-write deposition of a variety of materials on planar and non-planar surfaces. This research demonstrates the ability of AJP to print digitally controlled patterns that influence neuronal guidance. These consist of patterned poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) tracks on both glass and poly(potassium 3-sulfopropyl methacrylate) (PKSPMA) coated glass surfaces, promoting selective adhesion of SH-SY5Y neuroblastoma cells. The cell attractive patterns had a maximum height ≥0.2 μm, width and half height ≥15 μm, Ra = 3.5 nm, and RMS = 4.1. The developed biocompatible PEDOT:PSS ink was shown to promote adhesion, growth and differentiation of SH-SY5Y neuronal cells. SH-SY5Y cells cultured directly onto these features exhibited increased nuclei and neuronal alignment on both substrates. In addition, the cell adhesion to the substrate was selective when cultured onto the PKSPMA surfaces resulting in a highly organized neural pattern. This demonstrated the ability to rapidly and flexibly realize intricate and accurate cell patterns by a computer controlled process.
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spelling pubmed-84357182021-09-14 Digitally Driven Aerosol Jet Printing to Enable Customisable Neuronal Guidance Capel, Andrew J. Smith, Matthew A. A. Taccola, Silvia Pardo-Figuerez, Maria Rimington, Rowan P. Lewis, Mark P. Christie, Steven D. R. Kay, Robert W. Harris, Russell A. Front Cell Dev Biol Cell and Developmental Biology Digitally driven manufacturing technologies such as aerosol jet printing (AJP) can make a significant contribution to enabling new capabilities in the field of tissue engineering disease modeling and drug screening. AJP is an emerging non-contact and mask-less printing process which has distinct advantages over other patterning technologies as it offers versatile, high-resolution, direct-write deposition of a variety of materials on planar and non-planar surfaces. This research demonstrates the ability of AJP to print digitally controlled patterns that influence neuronal guidance. These consist of patterned poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) tracks on both glass and poly(potassium 3-sulfopropyl methacrylate) (PKSPMA) coated glass surfaces, promoting selective adhesion of SH-SY5Y neuroblastoma cells. The cell attractive patterns had a maximum height ≥0.2 μm, width and half height ≥15 μm, Ra = 3.5 nm, and RMS = 4.1. The developed biocompatible PEDOT:PSS ink was shown to promote adhesion, growth and differentiation of SH-SY5Y neuronal cells. SH-SY5Y cells cultured directly onto these features exhibited increased nuclei and neuronal alignment on both substrates. In addition, the cell adhesion to the substrate was selective when cultured onto the PKSPMA surfaces resulting in a highly organized neural pattern. This demonstrated the ability to rapidly and flexibly realize intricate and accurate cell patterns by a computer controlled process. Frontiers Media S.A. 2021-08-30 /pmc/articles/PMC8435718/ /pubmed/34527674 http://dx.doi.org/10.3389/fcell.2021.722294 Text en Copyright © 2021 Capel, Smith, Taccola, Pardo-Figuerez, Rimington, Lewis, Christie, Kay and Harris. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Capel, Andrew J.
Smith, Matthew A. A.
Taccola, Silvia
Pardo-Figuerez, Maria
Rimington, Rowan P.
Lewis, Mark P.
Christie, Steven D. R.
Kay, Robert W.
Harris, Russell A.
Digitally Driven Aerosol Jet Printing to Enable Customisable Neuronal Guidance
title Digitally Driven Aerosol Jet Printing to Enable Customisable Neuronal Guidance
title_full Digitally Driven Aerosol Jet Printing to Enable Customisable Neuronal Guidance
title_fullStr Digitally Driven Aerosol Jet Printing to Enable Customisable Neuronal Guidance
title_full_unstemmed Digitally Driven Aerosol Jet Printing to Enable Customisable Neuronal Guidance
title_short Digitally Driven Aerosol Jet Printing to Enable Customisable Neuronal Guidance
title_sort digitally driven aerosol jet printing to enable customisable neuronal guidance
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435718/
https://www.ncbi.nlm.nih.gov/pubmed/34527674
http://dx.doi.org/10.3389/fcell.2021.722294
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