Supported membranes meet flat fluidics: monitoring dynamic cell adhesion on pump-free microfluidics chips functionalized with supported membranes displaying mannose domains

In this paper we demonstrate the combination of supported membranes and so-called flat microfluidics, which enables one to manipulate liquids on flat chip surfaces via “inverse piezoelectric effect”. Here, an alternating external electric field applied to the inter-digital transducers excites a sur...

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Main Authors: Oelke, Jochen (Author) , Kaindl, Thomas (Author) , Pasc, Andreea (Author) , Guttenberg, Zeno (Author) , Wixforth, Achim (Author) , Tanaka, Motomu (Author)
Format: Article (Journal)
Language:English
Published: 22 February 2013
In: Materials
Year: 2013, Volume: 6, Issue: 2, Pages: 669-681
ISSN:1996-1944
DOI:10.3390/ma6020669
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/ma6020669
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/1996-1944/6/2/669
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Author Notes:Jochen Oelke, Thomas Kaindl, Andreea Pasc, Zeno Guttenberg, Achim Wixforth and Motomu Tanaka
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Summary:In this paper we demonstrate the combination of supported membranes and so-called flat microfluidics, which enables one to manipulate liquids on flat chip surfaces via “inverse piezoelectric effect”. Here, an alternating external electric field applied to the inter-digital transducers excites a surface acoustic wave on a piezoelectric substrate. Employing lithographic patterning of self-assembled monolayers of alkoxysilanes, we successfully confine a free-standing, hemi-cylindrical channel with the volume of merely 7 µL . The experimentally determined maximum flow velocity scales linearly with the acoustic power, suggesting that our current setup can drive liquids at the speed of up to 7 cm/s (corresponding to a shear rate of 280 s−1) without applying high pressures using a fluidic pump. After the establishment of the functionalization of fluidic chip surfaces with supported membranes, we deposited asymmetric supported membranes displaying well-defined mannose domains and monitored the dynamic adhesion of E. Coli HB101 expressing mannose-binding receptors. Despite of the further technical optimization required for the quantitative analysis, the obtained results demonstrate that the combination of supported membranes and flat fluidics opens a large potential to investigate dynamic adhesion of cells on biofunctional membrane surfaces with the minimum amount of samples, without any fluidic pump.
Item Description:Gesehen am 06.12.2021
Physical Description:Online Resource
ISSN:1996-1944
DOI:10.3390/ma6020669