ArticleJournal of biomedical optics2025
Quantitative evaluation of the site-dependent cell viability in three-dimensional hepatocyte spheroids based on dynamic optical coherence tomography.
Article in Journal of biomedical optics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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
4 citing papers in PubMed.
- Transcriptomic responses to repeated exposure of human C3A liver spheroids to polystyrene nanoplastics.Archives of toxicology · 2026Article
- Physics-informed deep learning enables reliable and scalable organoid quantification for drug screening via OCT.NPJ digital medicine · 2026Article
- Longitudinal investigation of prostate tumor spheroid proliferation with dynamic line-field optical coherence tomography.Biomedical optics express · 2026Article
- A modular and reconfigurable microfluidic device for culturing spheroids under continuous perfusion.APL bioengineering · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Significance: Hepatocyte spheroids (HCSs) are three-dimensional (3D) Aim: We aim to achieve long-term, non-invasive monitoring and quantification of HCS cell viability based on dynamic optical coherence tomography (D-OCT) and enhance visualization of HCS internal activity with D-OCT pseudo-color images. Approach: We employed D-OCT based on power spectrum analysis with an appropriate optical coherence tomography time-series image acquisition rate to obtain the motion frequency distribution of cells within HCS, thus distinguishing and segmenting the viable and necrotic cell layers based on the average frequency of cellular activity, and quantify the tissue activity using the pixel ratio of the segmented viable region to the total spheroid region. Meanwhile, we used the hue saturation value color mapping method to enable enhanced visualization and high-precision segmentation of viable and necrotic cell layers in HCS. Results: The feasibility of the D-OCT method was verified experimentally with three sets of HCS samples (HCS-2000, HCS-5000, and HCS-10000) by comparison with a confocal laser scanning microscope. The cells in C3A-HCS were found to be active mainly in the range of 8 to 13 Hz by D-OCT detection. 3D D-OCT pseudo-color images of HCS with a maximum diameter of Conclusions: The employed D-OCT method can be used to quantitatively evaluate the site-dependent cell viability in HCS and possesses the potential for long-term, non-invasive monitoring and quantification of HCS viability.
Indexed as
Identifiers
What OpenQuestion holds
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.