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1.
Lab Chip ; 12(7): 1289-95, 2012 Apr 07.
Article in English | MEDLINE | ID: mdl-22334354

ABSTRACT

We present a novel centrifugal microfluidic platform for the highly efficient manipulation and analysis of particles for applications in bead-based assays. The platform uses an array of geometrical V-cup barriers to trap particles using stopped-flow sedimentation under highly reproducible hydrodynamic conditions. The impact parameters governing the occupancy distribution and capture efficiency of the arrayed traps are investigated. The unique, nearly 100% capture efficiency paired with the capability to establish sharply peaked, single occupancy distributions enables a novel, digital readout mode for color-multiplexed, particle-based assays with low-complexity instrumentation. The presented technology marks an essential step towards a versatile platform for the integration of bead- and cell-based biological assays.


Subject(s)
Microfluidic Analytical Techniques/instrumentation , Antibodies/immunology , Centrifugation , Dimethylpolysiloxanes/chemistry , Humans , Immunoassay , Immunoglobulin G/chemistry , Immunoglobulin G/immunology , Particle Size , Polystyrenes/chemistry
2.
Lab Chip ; 9(17): 2591-5, 2009 Sep 07.
Article in English | MEDLINE | ID: mdl-19680583

ABSTRACT

Embryonic stem (ES) cells are pluripotent cells, which can differentiate into any cell type. This cell type has often been implicated as an eminent source of renewable cells for tissue regeneration and cellular replacement therapies. Studies on manipulation of the various differentiation pathways have been at the forefront of research. There are many ways in which ES cells can be differentiated. One of the most common techniques is to initiate the development of embryoid bodies (EBs) by in vitro aggregation of ES cells. Thereafter, EBs can be induced to undergo differentiation into various cell lineages. In this article, we present a microfluidic platform using biocompatible materials, which is suitable for culturing EBs. The platform is based on a Y-channel device with two inlets for two different culturing media. An EB is located across both streams. Using the laminar characteristics at low Reynolds number and high Peclet numbers, we have induced cell differentiation on half of the EB while maintaining the other half in un-induced stages. The results prove the potential of using microfluidic technology for manipulation of EBs and ES cells in tissue engineering.


Subject(s)
Cell Differentiation , Embryonic Stem Cells/cytology , Microfluidics/instrumentation , Animals , Blotting, Western , Fluorescent Antibody Technique , Mice
3.
Anal Chem ; 80(7): 2326-41, 2008 Apr 01.
Article in English | MEDLINE | ID: mdl-18321133

ABSTRACT

Recent developments in micro- and nanotechnologies made possible the fabrication of devices integrating a deterministic network of nanochannels, i.e., with at least one dimension in a range from 1 to 100 nm. The proximity of this dimension and the Debye length, the size of biomolecules such as DNA or proteins, or even the slip length, added to the excellent control on the geometry gives unique features to nanofluidic devices. This new class of devices not only finds applications wherever less well-defined porous media, such as electrophoresis gels, have been traditionally used but also give a new insight into the sieving mechanisms of biomolecules and the fluid flow at the nanoscale. Beyond this, the control on the geometry allows smarter design resulting, among others, in new separation principles by taking advantage of the anisotropy. This perspective gives an overview on the fabrication technologies of nanofluidic devices and their applications. In the first part, the current state of the art of nanofluidic fabrication is presented. The second part first discusses the key transport phenomena in nanochannels. Current applications of nanofluidic devices are next discussed. Finally, future challenges and possible applications are highlighted.

4.
Electrophoresis ; 28(24): 4539-51, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18072221

ABSTRACT

Since its introduction in the nineties, the negative resist SU-8 has been increasingly used in micro- and nanotechnologies. SU-8 has made the fabrication of high-aspect ratio structures accessible to labs with no high-end facilities such as X-ray lithography systems or deep reactive ion etching systems. These low-cost techniques have been applied not only in the fabrication of metallic parts or molds, but also in numerous other micromachining processes. Its ease of use has made SU-8 to be used in many applications, even when high-aspect ratios are not required. Beyond these pattern transfer applications, SU-8 has been used directly as a structural material for microelectromechanical systems and microfluidics due to its properties such as its excellent chemical resistance or the low Young modulus. In contrast to conventional resists, which are used temporally, SU-8 has been used as a permanent building material to fabricate microcomponents such as cantilevers, membranes, and microchannels. SU-8-based techniques have led to new low-temperature processes suitable for the fabrication of a wide range of objects, from the single component to the complete lab-on-chip. First, this article aims to review the different techniques and provides guidelines to the use of SU-8 as a structural material. Second, practical examples from our respective labs are presented.


Subject(s)
Electrochemistry/instrumentation , Miniaturization , Nanotechnology , Microscopy, Electron, Scanning , Surface Properties
5.
Lab Chip ; 7(4): 520-2, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17389971

ABSTRACT

Planar nanochannels are of particular significance in nanofluidics: keeping the width on the micrometre scale prevents the use of nanolithography while the depth stays in the nanometric range, i.e. below 100 nm. Fabrication of wide and shallow nanochannels in a plastic is known to be challenging due to the collapse of the structure during the sealing step. In this Technical Note, we demonstrate the simple and low-cost fabrication without nanolithography of monolithic and planar nanochannels by hot-embossing and bonding below the glass transition temperature.


Subject(s)
Microfluidic Analytical Techniques/instrumentation , Microfluidics , Electrochemistry/methods , Equipment Design , Glass , Hot Temperature , Ions , Micromanipulation , Microscopy, Atomic Force , Nanostructures , Nanotechnology/methods , Polymethyl Methacrylate/chemistry , Silicon/chemistry , Surface Properties , Temperature
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