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Large area micropatterning of cells on polydimethylsiloxane surfaces
BACKGROUND: Precise spatial control and patterning of cells is an important area of research with numerous applications in tissue engineering, as well as advancing an understanding of fundamental cellular processes. Poly (dimethyl siloxane) (PDMS) has long been used as a flexible, biocompatible subs...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223844/ https://www.ncbi.nlm.nih.gov/pubmed/25383093 http://dx.doi.org/10.1186/1754-1611-8-24 |
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author | Moustafa, Mahmoud E Gadepalli, Venkat S Elmak, Ahmed A Lee, Woomin Rao, Raj R Yadavalli, Vamsi K |
author_facet | Moustafa, Mahmoud E Gadepalli, Venkat S Elmak, Ahmed A Lee, Woomin Rao, Raj R Yadavalli, Vamsi K |
author_sort | Moustafa, Mahmoud E |
collection | PubMed |
description | BACKGROUND: Precise spatial control and patterning of cells is an important area of research with numerous applications in tissue engineering, as well as advancing an understanding of fundamental cellular processes. Poly (dimethyl siloxane) (PDMS) has long been used as a flexible, biocompatible substrate for cell culture with tunable mechanical characteristics. However, fabrication of suitable physico-chemical barriers for cells on PDMS substrates over large areas is still a challenge. RESULTS: Here, we present an improved technique which integrates photolithography and cell culture on PDMS substrates wherein the barriers to cell adhesion are formed using the photo-activated graft polymerization of polyethylene glycol diacrylate (PEG-DA). PDMS substrates with varying stiffness were prepared by varying the base to crosslinker ratio from 5:1 to 20:1. All substrates show controlled cell attachment confined to fibronectin coated PDMS microchannels with a resistance to non-specific adhesion provided by the covalently immobilized, hydrophilic PEG-DA. CONCLUSIONS: Using photolithography, it is possible to form patterns of high resolution stable at 37°C over 2 weeks, and microstructural complexity over large areas of a few cm(2). As a robust and scalable patterning method, this technique showing homogenous and stable cell adhesion and growth over macroscales can bring microfabrication a step closer to mass production for biomedical applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1754-1611-8-24) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4223844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42238442014-11-08 Large area micropatterning of cells on polydimethylsiloxane surfaces Moustafa, Mahmoud E Gadepalli, Venkat S Elmak, Ahmed A Lee, Woomin Rao, Raj R Yadavalli, Vamsi K J Biol Eng Methodology BACKGROUND: Precise spatial control and patterning of cells is an important area of research with numerous applications in tissue engineering, as well as advancing an understanding of fundamental cellular processes. Poly (dimethyl siloxane) (PDMS) has long been used as a flexible, biocompatible substrate for cell culture with tunable mechanical characteristics. However, fabrication of suitable physico-chemical barriers for cells on PDMS substrates over large areas is still a challenge. RESULTS: Here, we present an improved technique which integrates photolithography and cell culture on PDMS substrates wherein the barriers to cell adhesion are formed using the photo-activated graft polymerization of polyethylene glycol diacrylate (PEG-DA). PDMS substrates with varying stiffness were prepared by varying the base to crosslinker ratio from 5:1 to 20:1. All substrates show controlled cell attachment confined to fibronectin coated PDMS microchannels with a resistance to non-specific adhesion provided by the covalently immobilized, hydrophilic PEG-DA. CONCLUSIONS: Using photolithography, it is possible to form patterns of high resolution stable at 37°C over 2 weeks, and microstructural complexity over large areas of a few cm(2). As a robust and scalable patterning method, this technique showing homogenous and stable cell adhesion and growth over macroscales can bring microfabrication a step closer to mass production for biomedical applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1754-1611-8-24) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-24 /pmc/articles/PMC4223844/ /pubmed/25383093 http://dx.doi.org/10.1186/1754-1611-8-24 Text en © Moustafa et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Moustafa, Mahmoud E Gadepalli, Venkat S Elmak, Ahmed A Lee, Woomin Rao, Raj R Yadavalli, Vamsi K Large area micropatterning of cells on polydimethylsiloxane surfaces |
title | Large area micropatterning of cells on polydimethylsiloxane surfaces |
title_full | Large area micropatterning of cells on polydimethylsiloxane surfaces |
title_fullStr | Large area micropatterning of cells on polydimethylsiloxane surfaces |
title_full_unstemmed | Large area micropatterning of cells on polydimethylsiloxane surfaces |
title_short | Large area micropatterning of cells on polydimethylsiloxane surfaces |
title_sort | large area micropatterning of cells on polydimethylsiloxane surfaces |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223844/ https://www.ncbi.nlm.nih.gov/pubmed/25383093 http://dx.doi.org/10.1186/1754-1611-8-24 |
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