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Spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels

We demonstrate spatial control over cell attachment on biodegradable surfaces by flowing cell adhesive poly (D-lysine) (PDL) in a trifluoroethanol (TFE)–water mixture through microfluidic channels placed on a biodegradable poly (lactic acid)–poly (ethylene glycol) (PLA–PEG) substrate. The partial so...

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Detalles Bibliográficos
Autores principales: Baman, Nicki K, Schneider, Galen B, Terry, Treniece L, Zaharias, Rebecca, Salem, Aliasger K
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426782/
https://www.ncbi.nlm.nih.gov/pubmed/17722538
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author Baman, Nicki K
Schneider, Galen B
Terry, Treniece L
Zaharias, Rebecca
Salem, Aliasger K
author_facet Baman, Nicki K
Schneider, Galen B
Terry, Treniece L
Zaharias, Rebecca
Salem, Aliasger K
author_sort Baman, Nicki K
collection PubMed
description We demonstrate spatial control over cell attachment on biodegradable surfaces by flowing cell adhesive poly (D-lysine) (PDL) in a trifluoroethanol (TFE)–water mixture through microfluidic channels placed on a biodegradable poly (lactic acid)–poly (ethylene glycol) (PLA–PEG) substrate. The partial solvent mixture swells the PLA–PEG within the confines of the microfluidic channels allowing PDL to diffuse on to the surface gel layer. When excess water is flowed through the channels substituting the TFE–water mixture, the swollen PLA surface collapses, entrapping PDL polymer. Results using preosteoblast human palatal mesenchymal cells (HEPM) indicate that this new procedure can be used for facile attachment of cells in localized regions. The PEG component of the PLA–PEG copolymer prevents cells from binding to the nonpatterned regions.
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spelling pubmed-24267822008-06-20 Spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels Baman, Nicki K Schneider, Galen B Terry, Treniece L Zaharias, Rebecca Salem, Aliasger K Int J Nanomedicine New Technologies We demonstrate spatial control over cell attachment on biodegradable surfaces by flowing cell adhesive poly (D-lysine) (PDL) in a trifluoroethanol (TFE)–water mixture through microfluidic channels placed on a biodegradable poly (lactic acid)–poly (ethylene glycol) (PLA–PEG) substrate. The partial solvent mixture swells the PLA–PEG within the confines of the microfluidic channels allowing PDL to diffuse on to the surface gel layer. When excess water is flowed through the channels substituting the TFE–water mixture, the swollen PLA surface collapses, entrapping PDL polymer. Results using preosteoblast human palatal mesenchymal cells (HEPM) indicate that this new procedure can be used for facile attachment of cells in localized regions. The PEG component of the PLA–PEG copolymer prevents cells from binding to the nonpatterned regions. Dove Medical Press 2006-06 /pmc/articles/PMC2426782/ /pubmed/17722538 Text en © 2006 Dove Medical Press Limited. All rights reserved
spellingShingle New Technologies
Baman, Nicki K
Schneider, Galen B
Terry, Treniece L
Zaharias, Rebecca
Salem, Aliasger K
Spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels
title Spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels
title_full Spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels
title_fullStr Spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels
title_full_unstemmed Spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels
title_short Spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels
title_sort spatial control over cell attachment by partial solvent entrapment of poly lysine in microfluidic channels
topic New Technologies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426782/
https://www.ncbi.nlm.nih.gov/pubmed/17722538
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