TY - JOUR
T1 - Rapid and specific detection of nanoparticles and viruses one at a time using microfluidic laminar flow and confocal fluorescence microscopy
AU - Drori, Paz
AU - Mouhadeb, Odelia
AU - Moya Muñoz, Gabriel G.
AU - Razvag, Yair
AU - Alcalay, Ron
AU - Klocke, Philipp
AU - Cordes, Thorben
AU - Zahavy, Eran
AU - Lerner, Eitan
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/10/18
Y1 - 2024/10/18
N2 - Mainstream virus detection relies on the specific amplification of nucleic acids via polymerase chain reaction, a process that is slow and requires extensive laboratory expertise and equipment. Other modalities, such as antigen-based tests, allow much faster virus detection but have reduced sensitivity. In this study, we introduce an approach for rapid and specific detection of single nanoparticles using a confocal-based flow virometer. The combination of laminar flow in a microfluidic channel and correlated fluorescence signals emerging from both free dyes and fluorescently labeled primary antibodies provide insights into nanoparticle volumes and specificities. We evaluate and validate the assay using fluorescent beads and viruses, including SARS-CoV-2 with fluorescently labeled primary antibodies. Additionally, we demonstrate how hydrodynamic focusing enhances the assay sensitivity for detecting viruses at relevant loads. Based on our results, we envision the future use of this technology for clinically relevant bio-nanoparticles, supported by the implementation of the assay in a portable and user-friendly setup.
AB - Mainstream virus detection relies on the specific amplification of nucleic acids via polymerase chain reaction, a process that is slow and requires extensive laboratory expertise and equipment. Other modalities, such as antigen-based tests, allow much faster virus detection but have reduced sensitivity. In this study, we introduce an approach for rapid and specific detection of single nanoparticles using a confocal-based flow virometer. The combination of laminar flow in a microfluidic channel and correlated fluorescence signals emerging from both free dyes and fluorescently labeled primary antibodies provide insights into nanoparticle volumes and specificities. We evaluate and validate the assay using fluorescent beads and viruses, including SARS-CoV-2 with fluorescently labeled primary antibodies. Additionally, we demonstrate how hydrodynamic focusing enhances the assay sensitivity for detecting viruses at relevant loads. Based on our results, we envision the future use of this technology for clinically relevant bio-nanoparticles, supported by the implementation of the assay in a portable and user-friendly setup.
KW - Biological sciences
KW - Biotechnology
KW - Fluidics
KW - Optical imaging
UR - http://www.scopus.com/inward/record.url?scp=85207352843&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2024.110982
DO - 10.1016/j.isci.2024.110982
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C2 - 39391727
AN - SCOPUS:85207352843
SN - 2589-0042
VL - 27
JO - iScience
JF - iScience
IS - 10
M1 - 110982
ER -