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1.
Sensors (Basel) ; 22(15)2022 Aug 02.
Article in English | MEDLINE | ID: mdl-35957340

ABSTRACT

Label-free field-effect transistor-based immunosensors are promising candidates for proteomics and peptidomics-based diagnostics and therapeutics due to their high multiplexing capability, fast response time, and ability to increase the sensor sensitivity due to the short length of peptides. In this work, planar junctionless field-effect transistor sensors (FETs) were fabricated and characterized for pH sensing. The device with SiO2 gate oxide has shown voltage sensitivity of 41.8 ± 1.4, 39.9 ± 1.4, 39.0 ± 1.1, and 37.6 ± 1.0 mV/pH for constant drain currents of 5, 10, 20, and 50 nA, respectively, with a drain to source voltage of 0.05 V. The drift analysis shows a stability over time of -18 nA/h (pH 7.75), -3.5 nA/h (pH 6.84), -0.5 nA/h (pH 4.91), 0.5 nA/h (pH 3.43), corresponding to a pH drift of -0.45, -0.09, -0.01, and 0.01 per h. Theoretical modeling and simulation resulted in a mean value of the surface states of 3.8 × 1015/cm2 with a standard deviation of 3.6 × 1015/cm2. We have experimentally verified the number of surface sites due to APTES, peptide, and protein immobilization, which is in line with the theoretical calculations for FETs to be used for detecting peptide-protein interactions for future applications.


Subject(s)
Biosensing Techniques , Transistors, Electronic , Biosensing Techniques/methods , Electricity , Immunoassay , Silicon Dioxide
2.
Lab Chip ; 16(8): 1514-22, 2016 Apr 21.
Article in English | MEDLINE | ID: mdl-27025866

ABSTRACT

The use of high quality semen for artificial insemination in the livestock industry is essential for successful outcome. Insemination using semen with a high number of sperm cells containing morphological defects has a negative impact on fertilization outcome. Therefore, semen with a high number of these abnormal cells is discarded in order to maintain high fertilization potential, resulting in the loss of a large number of morphologically normal sperm cells (up to 70-80% of original sample). A commonly occurring morphological sperm anomaly is the cytoplasmic droplet on the sperm flagella. Currently, no techniques are available to extract morphologically normal sperm cells from rejected samples. Therefore, we aim to develop a microfluidic setup which is able to detect and sort morphologically normal sperm cells label-free and non-invasively. In a proof-of-concept experiment, differential impedance measurements were used to detect the presence of cytoplasmic droplets on sperm flagella, which was quantified by calculating the area under the curve (AUC) of the corresponding impedance peaks. A receiver operating characteristic curve of this electrical analysis method showed the good predictive power of this analysis method (AUC value of 0.85). Furthermore, we developed a label-free cell sorting system using LabVIEW, which is capable of sorting sperm cells based on impedance. In a proof-of-concept experiment, sperm cells and 3 µm beads were sorted label-free and non-invasively using impedance detection and dielectrophoresis sorting. These experiments present our first attempt to perform sperm refinement using microfluidic technology.


Subject(s)
Cell Separation/instrumentation , Lab-On-A-Chip Devices , Spermatozoa/cytology , Animals , Cytoplasm/metabolism , Electric Impedance , Electrophoresis , Male , Swine
3.
Lab Chip ; 15(5): 1294-301, 2015 Mar 07.
Article in English | MEDLINE | ID: mdl-25578490

ABSTRACT

Selection of healthy spermatozoa is of crucial importance for the success rates of assisted reproduction technologies (ART) such as in vitro fertilization and intra-cytoplasmic sperm injection. Although sperm selection for ART procedures is predominantly based on sperm motility, successful fertilization is not predicted by good motility alone. For example, sperm characteristics such as the acrosome state and DNA integrity have shown significant impact on ART outcome. Although fertilization can be achieved with a single spermatozoon of high quality, current quality assessments are population-based and do not allow investigation of multiple sperm characteristics on a single spermatozoon simultaneously. In order to study sperm cells on the single cell level, we designed and characterized a PDMS microfluidic platform that allows single sperm entrapment. After spatially confining individual sperm cells within microfluidic cell traps, the cell viability, chromosomal content and acrosome state were studied. This platform is suitable for the analysis of individual sperm cells, which could be exploited for (non-invasive) sperm analysis and selection by impedance or Raman spectroscopy.


Subject(s)
Microfluidic Analytical Techniques/methods , Spermatozoa/cytology , Cell Survival , Equipment Design , Humans , Hydrodynamics , In Situ Hybridization, Fluorescence , Male , Microfluidic Analytical Techniques/instrumentation , Spectrum Analysis, Raman
4.
Lab Chip ; 14(15): 2635-41, 2014 Aug 07.
Article in English | MEDLINE | ID: mdl-24615285

ABSTRACT

In this article, we describe the development of a high throughput platform to spatially manipulate viable sperm for motility measurements and recovery of the best single sperm for fertilization purposes. Micro-contact printing was used to pattern islands of adhesive proteins (fibronectin) separated by sperm repellent species (Pluronic acid F-127) on commercially available polystyrene substrates. Following washing, arrays of viable single sperm were captured onto the islands demonstrating for the first time that sperm can be trapped by micro-contact printing with patterning efficiency of 90% while retaining 100% viability. These were then subjected to motility analysis whilst remaining spatially confined to the islands. Single sperm motility was assessed (n = 37) by software analysis measuring the number of rotations per second (degrees s⁻¹). The assignment of array coordinates allows the more active single sperm to be easily identified and recovered by a simple micromanipulator pipette aspiration step with automated possibility for assisted reproductive technologies or further quality correlation analysis. Taken together, we show for the first time a technique to simultaneously screen thousands of viable single sperm for motility assessment while retaining the ability for single species recovery for enhanced fertilization purposes.


Subject(s)
Cell Separation/veterinary , Fibronectins/chemistry , Immobilized Proteins/chemistry , Lab-On-A-Chip Devices/veterinary , Semen Analysis/veterinary , Single-Cell Analysis/veterinary , Spermatozoa/cytology , Animals , Cell Adhesion , Cell Separation/instrumentation , Cell Survival , Equipment Design/veterinary , Fertilization in Vitro/veterinary , Fibronectins/metabolism , Immobilized Proteins/metabolism , Male , Materials Testing/veterinary , Netherlands , Poloxamer/chemistry , Polystyrenes/chemistry , Printing, Three-Dimensional , Semen Analysis/instrumentation , Single-Cell Analysis/instrumentation , Software , Sperm Motility , Spermatozoa/metabolism , Surface Properties , Sus scrofa
5.
Anal Chem ; 79(15): 5567-73, 2007 Aug 01.
Article in English | MEDLINE | ID: mdl-17585833

ABSTRACT

This paper describes the design, modeling, and experimental characterization of an electrochemical sensor array for on-line monitoring of fermentor conditions in both miniaturized cell assays and in industrial scale fermentations. The viable biomass concentration is determined from impedance spectroscopy. As a miniaturized electrode configuration with high cell constant is applied, the spectral conductivity variation is monitored instead of the permittivity variation. The dissolved oxygen concentration is monitored amperometrically using an ultramicroelectrode array, which is shown to have negligible flow dependence. pH is monitored using an ion-sensitive field effect transistor (ISFET), and a platinum thermistor is included for temperature measurements. All sensors were shown to be sufficiently accurate within the range relevant to yeast fermentations. The sensor array is shown to be very stable and durable and withstands steam-sterilization.


Subject(s)
Biosensing Techniques/methods , Fermentation , Saccharomyces cerevisiae/metabolism , Biomass , Biosensing Techniques/instrumentation , Electrochemistry , Equipment Design , Hydrogen-Ion Concentration , Industrial Microbiology , Microelectrodes , Platinum/chemistry , Saccharomyces cerevisiae/cytology , Sensitivity and Specificity , Temperature , Thermometers , Transistors, Electronic
6.
Phys Rev Lett ; 95(25): 256107, 2005 Dec 16.
Article in English | MEDLINE | ID: mdl-16384480

ABSTRACT

Measurements are shown indicating that the drying rate of nanochannels can be enhanced by up to 3 orders of magnitude relative to drying by vapor diffusion, and that the drying rate is independent of the relative humidity of the environment up to a relative humidity of more than 90%. Micromachined Pyrex glass nanochannels of 72 nm height and with sharp corners (corner angles 7 degrees) were used. Available theory shows that the sharp corners function as a low-resistance pathway for liquid water, siphoning (wicking) the water to a location close to the channel exit before it evaporates. The described phenomena are of importance for the understanding of drying processes in industry and agriculture. The introduction of sharp corners or grooves can furthermore be beneficial for the functioning of microheat pipes and capillary-pumped loops.

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