INSTITUTE OF PHYSICS PUBLISHING JOURNAL OF MICROMECHANICS AND MICROENGINEERING
J. Micromech. Microeng. 16 (2006) 113–121 doi:10.1088/0960-1317/16/1/016
A novel fabrication method of flexible and
monolithic 3D microfluidic structures
using lamination of SU-8 films
Patrick Abgrall
1
, Christine Lattes
2
, V´ eronique Con´ ed´ era
1
,
Xavier Dollat
1
, St´ ephane Colin
2
and Anne Marie Gu´ e
1
1
LAAS-CNRS, 7 avenue du Colonel Roche, 31077 Toulouse Cedex 4, France
2
LGMT-INSAT,135 avenue de Rangueil, 31077 Toulouse Cedex 4, France
E-mail: pabgrall@laas.fr
Received 15 May 2005, in final form 20 October 2005
Published 13 December 2005
Online at stacks.iop.org/JMM/16/113
Abstract
The fabrication of three-dimensional (3D) microfluidic networks entirely
made of SU-8 with integrated electrodes is reported. The described
technology allows the fabrication of uncrosslinked SU-8 dry film on a
polyester (PET) sheet and its subsequent lamination to form closed
microstructures. Unlike other reported methods, transferred layers are
patterned following the bonding step allowing a more accurate and simple
alignment between levels than techniques using already patterned layers.
Dry release of the complete polymer microstructure was demonstrated.
Flexible microfluidic chips were obtained. This technique uses simple tools
and no wafer bonder is used but lamination techniques which are more
collective processes. Limitations in the method for layers thicker than
50 µm have been observed and are discussed. Hydraulic flow experiments
have been performed to study the deformation of the cover layer which
could influence adjacent flow in a three-dimensional configuration.
Important deformations have been observed for layers 10 µm thick and an
average pressure greater than 100 kPa. No deformations have been noted for
layers with thicknesses greater than 35 µm and for average pressures up to
200 kPa. No failures occurred within the range of the experimental set-up,
i.e. up to 300 kPa.
1. Introduction
Since the early works of Terry et al in the 1970s and
particularly the introduction of the concept of micro total
analysis systems (µTAS) by Manz in the 1990s [1, 2],
there is a growing interest in coupling microfluidic structures
(e.g. microchannels, microchambers) with conventional
microsystems to form what is nowadays called a lab-on-a-chip
(LOC).
An important characteristic of these microfluidic chips
compared to conventional microsystems is the large
size necessary for many analytical functions such as
chromatography and capillary electrophoresis where the
integration of several centimetres long microchannels is
required. Though monolithic approaches have driven the
works in the 1990s with silicon and glass micromachining,
it is obvious that these processes are not well adapted to
microfluidic applications for many purposes. The high voltage
often required in LOC excludes silicon. Glass processing
is difficult and not cost effective. Polymer microfabrication
techniques including casting, hot embossing, liquid injection,
thermoforming, lamination and low-temperature bonding
represent more suitable ways to fabricate such large
microfluidic parts at low cost [3, 4]. So hybrid microsystems
mixing polymer microfluidic devices and silicon electronic
components are now investigated especially for high value
added LOC.
Another major concern is the control of surface properties
since surface effects become increasingly dominant as size
is diminished. Therefore, it is often necessary to fabricate
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