ArticleBiomedical optics express2025
Multi-culture label-free quantitative cell migration sensing with single-cell precision.
Article in Biomedical optics express, 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.
- Recent breakthroughs in digital holography, 2D/3D imaging, and holographic optical elements: introduction.Biomedical optics express · 2025Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A fair comparison of multiple live cell cultures requires examining them under identical environmental conditions, which can only be done accurately if all cells are prepared simultaneously and studied at the same time and place. This contribution introduces a multiplexed lensless digital holographic microscopy system (MLS), enabling synchronous, label-free, quantitative observation of multiple live cell cultures with single-cell precision. The innovation of this setup lies in its ability to robustly compare the behaviour, i.e., migratory pathways, of cells cultured or contained in different ways (with varied stimuli applied), making it a valuable tool for dynamic biomedical diagnostics on a cellular level. The system's design allows for potential expansion to accommodate as many samples as needed, thus broadening its application scope in future quantitative diagnostics on global multi-culture cellular behaviours via their localized single-cell spatiotemporal optical signatures. We believe that our method has the potential to empower reliable live cell multi-culture comparisons through simultaneous quantitative imaging, enhancing label-free investigations into cell cultures and the effects of biochemical or physical stimuli over large areas, and unlocking novel mechanistic understandings through high-throughput time-lapse observations.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.