TY - JOUR
T1 - Integrated microfluidic probe station
AU - Perrault, C. M.
AU - Qasaimeh, M. A.
AU - Brastaviceanu, T.
AU - Anderson, K.
AU - Kabakibo, Y.
AU - Juncker, D.
N1 - Funding Information:
The authors wish to acknowledge support from Canadian Foundation for Innovation (CF), Canada Institute for Health Research (CIHR) Regenerative and Nanomedicine grants, Natural Science and Engineering Research Council of Canada (NSERC), the McGill Nanotools Microfab Laboratory (funded by CFI, NSERC, and VRQ), and thank Matthieu Nannini and Nikolas Pekas for their help and advice, and Adiel Mallik for proof reading. M.A.Q. acknowledges the Alexander Graham Bell Canada Graduate NSERC Scholarship and D.J. acknowledges the Canada Research Chair.
PY - 2010/11
Y1 - 2010/11
N2 - The microfluidic probe (MFP) consists of a flat, blunt tip with two apertures for the injection and reaspiration of a microjet into a solution-thus hydrodynamically confining the microjet-and is operated atop an inverted microscope that enables live imaging. By scanning across a surface, the microjet can be used for surface processing with the capability of both depositing and removing material; as it operates under immersed conditions, sensitive biological materials and living cells can be processed. During scanning, the MFP is kept immobile and centered over the objective of the inverted microscope, a few micrometers above a substrate that is displaced by moving the microscope stage and that is flushed continuously with the microjet. For consistent and reproducible surface processing, the gap between the MFP and the substrate, the MFP's alignment, the scanning speed, the injection and aspiration flow rates, and the image capture need all to be controlled and synchronized. Here, we present an automated MFP station that integrates all of these functionalities and automates the key operational parameters. A custom software program is used to control an independent motorized Z stage for adjusting the gap, a motorized microscope stage for scanning the substrate, up to 16 syringe pumps for injecting and aspirating fluids, and an inverted fluorescence microscope equipped with a charge-coupled device camera. The parallelism between the MFP and the substrate is adjusted using manual goniometer at the beginning of the experiment. The alignment of the injection and aspiration apertures along the scanning axis is performed using a newly designed MFP screw holder. We illustrate the integrated MFP station by the programmed, automated patterning of fluorescently labeled biotin on a streptavidin-coated surface.
AB - The microfluidic probe (MFP) consists of a flat, blunt tip with two apertures for the injection and reaspiration of a microjet into a solution-thus hydrodynamically confining the microjet-and is operated atop an inverted microscope that enables live imaging. By scanning across a surface, the microjet can be used for surface processing with the capability of both depositing and removing material; as it operates under immersed conditions, sensitive biological materials and living cells can be processed. During scanning, the MFP is kept immobile and centered over the objective of the inverted microscope, a few micrometers above a substrate that is displaced by moving the microscope stage and that is flushed continuously with the microjet. For consistent and reproducible surface processing, the gap between the MFP and the substrate, the MFP's alignment, the scanning speed, the injection and aspiration flow rates, and the image capture need all to be controlled and synchronized. Here, we present an automated MFP station that integrates all of these functionalities and automates the key operational parameters. A custom software program is used to control an independent motorized Z stage for adjusting the gap, a motorized microscope stage for scanning the substrate, up to 16 syringe pumps for injecting and aspirating fluids, and an inverted fluorescence microscope equipped with a charge-coupled device camera. The parallelism between the MFP and the substrate is adjusted using manual goniometer at the beginning of the experiment. The alignment of the injection and aspiration apertures along the scanning axis is performed using a newly designed MFP screw holder. We illustrate the integrated MFP station by the programmed, automated patterning of fluorescently labeled biotin on a streptavidin-coated surface.
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U2 - 10.1063/1.3497302
DO - 10.1063/1.3497302
M3 - Article
C2 - 21133501
AN - SCOPUS:78650256484
SN - 0034-6748
VL - 81
JO - Review of Scientific Instruments
JF - Review of Scientific Instruments
IS - 11
M1 - 115107
ER -