ArticleScientific reports2025
Femtosecond laser microfabrication of a fully-integrated optofluidic device for 3D imaging flow cytometry.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Ultrafast Laser-Enabled 3D Glass Microchannel Reactors.Sensors (Basel, Switzerland) · 2025Review
Corrections and comments
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Authors and funding
7 authors.
Funding
Abstract
In recent years imaging flow cytometry (IFC) is gaining increasing attention as it combines the characteristics of conventional flow cytometry with optical microscopy techniques, allowing for high-throughput, multi-parameter screening of single cell populations. In the field of biology, the always increasing demand for high content morphological and spatial information led to the development of systems for volumetric imaging. However, current 3D IFC systems are often limited by the incompatibility with available microfluidic devices or by instrumental complexity that might lead to optical misalignment or mechanical instabilities in day-by-day operation. To this end, here we demonstrate the importance of advancing the laser fabrication technique by reporting on a fully integrated optofluidic platform composed of a borosilicate glass chip encompassing reconfigurable integrated photonic circuits for patterned light generation, bonded to a fused silica glass chip incorporating cylindrical hollow lenses, for light-sheet illumination, perfectly aligned to a microchannel where the sample under investigation flows. The system is capable of high-resolution imaging flow cytometry by implementing structured light sheet microscopy in a heterogeneously integrated platform with unprecedented stability. All the components are realized by femtosecond laser irradiation followed by chemical etching. The extreme level of integration permitted by the advanced optimization of the laser fabrication technique allowed the reduction of the assembled components and the absence of moving parts, thus ensuring durable alignment as well as mechanical and thermal stability both in short and long-term operation of the device, for the automated fluorescence signal acquisition during the sample flow.
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Registered trials
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