Smart-agriculture technologies comprise a set of management systems designed to sustainably increase the efficiency and productivity of farming. In this paper, we present a lab-on-a-chip device that can be employed...
In this study, we
present a microdevice for the capture and quantification
of
Sclerotinia sclerotiorum
spores,
pathogenic agents of one of the most harmful infectious diseases of
crops,
Sclerotinia
stem rot. The early prognosis
of an outbreak is critical to avoid severe economic losses and can
be achieved by the detection of a small number of airborne spores.
However, the current lack of simple and effective methods to quantify
fungal airborne pathogens has hindered the development of an accurate
early warning system. We developed a device that remedies these limitations
based on a microfluidic design that contains a nanothick aluminum
electrode structure integrated with a picoliter well array for dielectrophoresis-driven
capture of spores and on-chip quantitative detection employing impedimetric
sensing. Based on experimental results, we demonstrated a highly efficient
spore trapping rate of more than 90% with an effective impedimetric
sensing method that allowed the spore quantification of each column
in the array and achieved a sensitivity of 2%/spore at 5 kHz and 1.6%/spore
at 20 kHz, enabling single spore detection. We envision that our device
will contribute to the development of a low-cost microfluidic platform
that could be integrated into an infectious plant disease forecasting
tool for crop protection.
Current approaches in targeted patient treatments often require the rapid isolation of specific rare target cells. Stream-based dielectrophoresis (DEP) based cell sorters have the limitation that the maximum number of sortable cell types is equivalent to the number of output channels, which makes upscaling to a higher number of different cell types technically challenging. Here, we present a microfluidic platform for selective single-cell sorting that bypasses this limitation. The platform consists of 10 000 nanoliter wells which are placed on top of interdigitated electrodes (IDEs) that facilitate dielectrophoresis-driven capture of cells. By use of a multisectorial design formed by 10 individually addressable IDE structures, our platform can capture a large number of different cell types. The sectorial approach allows for fast and straightforward modification to sort complex samples as different cell types are captured in different sectors and therefore removes the need for individual output channels per cell type. Experimental results obtained with a mixed sample of benign (MCF-10A) and malignant (MDA-MB-231) breast cells showed a target to nontarget sorting accuracy of over 95%. We envision that the high accuracy of our platform, in addition to its versatility and simplicity, will aid clinical environments where reliable sorting of varying complex samples is essential.
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