Jörg Kutter

Jörg Kutter


Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 April 2010 in Microfluidics and Nanofluidics
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Journal Article
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PNPedro S. Nunes
Pedro S. Nunes
POPelle Ohlsson
Pelle Ohlsson
OOOlga Ordeig
Olga Ordeig
JKJörg Kutter
Jörg Kutter

23 January 2003 in Lab on a Chip
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Journal Article
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AWAnders Wolff
Anders Wolff
IPI. R. Perch-Nielsen
I. R. Perch-Nielsen
ULU. D. Larsen
U. D. Larsen
PFP. Friis
P. Friis
GGG. Goranovic
G. Goranovic
PTP. Telleman
P. Telleman
The integration of complete analyses systems “on chip” is one of the great potentials of microfabricated devices. In this study we present a new pressure-driven microfabricated fluorescent-activated cell sorter chip with advanced functional integration. Using this sorter, fluorescent latex beads are sorted from chicken red blood cells, achieving substantial enrichments at a sample throughput of 12000 cells s−1. As a part of the sorter chip, we have developed a monolithically integrated single step coaxial flow compound for hydrodynamic focusing of samples in flow cytometry and cell sorting. The structure is simple, and can easily be microfabricated and integrated with other microfluidic components. We have designed an integrated chamber on the chip for holding and culturing of the sorted cells. By integrating this chamber, the risk of losing cells during cell handling processes is eliminated. Furthermore, we have also developed integrated optics for cell detection. Our new design contributes to the ongoing efforts for building a fully integrated micro cell sorting and analysing system.

8 August 2009 in Journal of Applied Crystallography
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Journal Article
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SNS. S. Nielsen
S. S. Nielsen
KTK. Noergaard Toft
K. Noergaard Toft
DSD. Snakenborg
D. Snakenborg
MJM. G. Jeppesen
M. G. Jeppesen
JJJ. K. Jacobsen
J. K. Jacobsen
LAL. Arleth
L. Arleth

1 February 2016 in Biosensors and Bioelectronics
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Journal Article
Closed access
JLJosiane P. Lafleur
Josiane P. Lafleur
AJAlexander Jönsson
Alexander Jönsson
SSSilja Senkbeil
Silja Senkbeil
JKJörg Kutter
Jörg Kutter

22 December 2005 in Lab on a Chip
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Journal Article
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SBS. Balslev
S. Balslev
AJA. M. Jorgensen
A. M. Jorgensen
BBB. Bilenberg
B. Bilenberg
KMK. B. Mogensen
K. B. Mogensen
DSD. Snakenborg
D. Snakenborg
AKAnders Kristensen
Anders Kristensen
Taking the next step from individual functional components to higher integrated devices, we present a feasibility study of a lab-on-a-chip system with five different components monolithically integrated on one substrate. These five components represent three main domains of microchip technology: optics, fluidics and electronics. In particular, this device includes an on-chip optically pumped liquid dye laser, waveguides and fluidic channels with passive diffusive mixers, all defined in one layer of SU-8 polymer, as well as embedded photodiodes in the silicon substrate. The dye laser emits light at 576 nm, which is directly coupled into five waveguides that bring the light to five different locations along a fluidic channel for absorbance measurements. The transmitted portion of the light is collected at the other side of this cuvette, again by waveguides, and finally detected by the photodiodes. Electrical read-out is accomplished by integrated metal connectors. To our knowledge, this is the first time that integration of all these components has been demonstrated.

20 April 2004 in Lab on a Chip
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Journal Article
Closed access
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ZWZ. Wang
Z. Wang
JEJ. El-Ali
J. El-Ali
MEM. Engelund
M. Engelund
TGT. Gotsæd
T. Gotsæd
IPI. R. Perch-Nielsen
I. R. Perch-Nielsen
AWAnders Wolff
Anders Wolff
Flow cytometry is widely used for analyzing microparticles, such as cells and bacteria. In this paper, we report an innovative microsystem, in which several different optical elements (waveguides, lens and fiber-to-waveguide couplers) are integrated with microfluidic channels to form a complete microchip flow cytometer. All the optical elements, the microfluidic system, and the fiber-to-waveguide couplers were defined in one layer of polymer (SU-8, negative photoresist) by standard photolithography. With only a single mask procedure required, all the fabrication and packaging processes can be finished in one day. Polystyrene beads were measured in the microchip flow cytometer, and three signals (forward scattering, large angle scattering and extinction) were measured simultaneously for each bead. To our knowledge this is the first time forward scattered light and incident light extinction were measured in a microsystem using integrated optics. The microsystem can be applied for analyzing different kinds of particles and cells, and can easily be integrated with other microfluidic components.