Wouter Olthuis

Dr. Wouter Olthuis

orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

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

Representative Publications

View All Publications
15 January 2020 in The Analyst
Verified
Journal Article
Open access
PDF file
JLJasper J. A. Lozeman
Jasper J. A. Lozeman
PFPascal Führer
Pascal Führer
WOWouter Olthuis
Wouter Olthuis
MOMathieu Odijk
Mathieu Odijk
Reviewing the future of electrochemistry combined with infrared, Raman, and nuclear magnetic resonance spectroscopy as well as mass spectrometry.

6 October 2005 in Chemphyschem
Verified
Journal Article
Closed access
PDF file
EFErik J. Faber
Erik J. Faber
LSLouis De Smet
Louis De Smet
WOWouter Olthuis
Wouter Olthuis
HZHan Zuilhof
Han Zuilhof
ESErnst J. R. Sudhölter
Ernst J. R. Sudhölter
ABAlbert van Den Berg
Albert van Den Berg

28 May 2018 in Frontiers in Neuroscience
Verified
Journal Article
Open access
PDF file
EREmil H. Rijnbeek
Emil H. Rijnbeek
NENick Eleveld
Nick Eleveld
WOWouter Olthuis
Wouter Olthuis
In this paper various types of electrodes for stimulation and recording activity of peripheral nerves for the control of neuroprosthetic limbs are reviewed. First, an overview of interface devices for (feedback-) controlled movement of a prosthetic device is given, after which the focus is on peripheral nervous system (PNS) electrodes. Important electrode properties, i.e., longevity and spatial resolution, are defined based upon the usability for neuroprostheses. The cuff electrode, longitudinal intrafascicular electrodes (LIFE), transverse intrafascicular multichannel electrode (TIME), Utah slanted electrode array (USEA), and the regenerative electrode are discussed and assessed on their longevity and spatial resolution. The cuff electrode seems to be a promising electrode for the control of neuroprostheses in the near future, because it shows the best longevity and good spatial resolution and it has been used on human subjects in multiple studies. The other electrodes may be promising in the future, but further research on their longevity and spatial resolution is needed. A more quantitatively uniform study protocol used for all electrodes would allow for a proper comparison of recording and stimulation performance. For example, the discussed electrodes could be compared in a large in vivo study, using one uniform comparison protocol.

1 November 2016 in Talanta
Verified
Journal Article
Closed access
LVL. van de Velde
L. van de Velde
EDE. D'ANgremont
E. D'ANgremont
WOWouter Olthuis
Wouter Olthuis

1 January 2017 in Biomicrofluidics
Verified
Journal Article
Open access
MRMehdi Rafeie
Mehdi Rafeie
MWMarcel Welleweerd
Marcel Welleweerd
AHAmin Hassanzadeh-Barforoushi
Amin Hassanzadeh-Barforoushi
MAMohsen Asadnia
Mohsen Asadnia
WOWouter Olthuis
Wouter Olthuis
Majid Ebrahimi WarkianiMajid Ebrahimi Warkiani
Majid Ebrahimi Warkiani
Mixing fluid samples or reactants is a paramount function in the fields of micro total analysis system (μTAS) and microchemical processing. However, rapid and efficient fluid mixing is difficult to achieve inside microchannels because of the difficulty of diffusive mass transfer in the laminar regime of the typical microfluidic flows. It has been well recorded that the mixing efficiency can be boosted by migrating from two-dimensional (2D) to three-dimensional (3D) geometries. Although several 3D chaotic mixers have been designed, most of them offer a high mixing efficiency only in a very limited range of Reynolds numbers (Re). In this work, we developed a 3D fine-threaded lemniscate-shaped micromixer whose maximum numerical and empirical efficiency is around 97% and 93%, respectively, and maintains its high performance (i.e., >90%) over a wide range of 1 < Re < 1000 which meets the requirements of both the μTAS and microchemical process applications. The 3D micromixer was designed based on two distinct mixing strategies, namely, the inducing of chaotic advection by the presence of Dean flow and diffusive mixing through thread-like grooves around the curved body of the mixers. First, a set of numerical simulations was performed to study the physics of the flow and to determine the essential geometrical parameters of the mixers. Second, a simple and cost-effective method was exploited to fabricate the convoluted structure of the micromixers through the removal of a 3D-printed wax structure from a block of cured polydimethylsiloxane. Finally, the fabricated mixers with different threads were tested using a fluorescent microscope demonstrating a good agreement with the results of the numerical simulation. We envisage that the strategy used in this work would expand the scope of the micromixer technology by broadening the range of efficient working flow rate and providing an easy way to the fabrication of 3D convoluted microstructures.

29 December 2020 in ACS Sensors
Verified
Journal Article
Open access
ETEsther Tanumihardja
Esther Tanumihardja
RSRolf H. Slaats
Rolf H. Slaats
AMAndries D. van der Meer
Andries D. van der Meer
RPRobert Passier
Robert Passier
WOWouter Olthuis
Wouter Olthuis
ABAlbert van Den Berg
Albert van Den Berg
In vitro studies which focus on cellular metabolism can benefit from time-resolved readouts from the living cells. pH and O2 concentration are fundamental parameters upon which cellular metabolism is often inferred. This work demonstrates a novel use of a ruthenium oxide (RuOx) electrode for in vitro studies. The RuOx electrode was characterized to measure both pH and O2 using two different modes. When operated potentiometrically, continuous pH reading can be obtained, and O2 concentration can be measured chronoamperometrically. In this work, we demonstrate the use of the RuOx electrodes in inferring two different types of metabolism of human pluripotent stem cell-derived cardiomyocytes. We also show and discuss the interpretation of the measurements into meaningful extracellular acidification rates and oxygen consumption rates of the cells. Overall, we present the RuOx electrode as a versatile and powerful tool in in vitro cell metabolism studies, especially in comparative settings.