Evidence map›Paper›PMID 42367260›Full record

ArticleJPhys photonics2026

Compact on-chip fluorescence microscope for dynamic imaging of cellular processes and biomimetic systems.

Somaiyeh Khoubafarin, Aakash Subramanian, William Daniel Gorgas, Cyrus Koogan, Indira Sigdel, Md Alamgir Kabir, Yuan Tang, Aniruddha Ray

Abstract read
In one paragraph

Article in JPhys photonics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Somaiyeh KhoubafarinDepartment of Physics and Astronomy, University of Toledo, Toledo, OH 43606, United States of America.ORCID https://orcid.org/0000-0001-7947-568X
Aakash SubramanianDepartment of Electrical Engineering and Computer Science, University of Toledo, Toledo, OH 43606, United States of America.
William Daniel GorgasDepartment of Physics and Astronomy, University of Toledo, Toledo, OH 43606, United States of America.ORCID https://orcid.org/0009-0007-9849-2603
Cyrus KooganDepartment of Chemistry and Biochemistry, University of Toledo, Toledo, OH 43606, United States of America.ORCID https://orcid.org/0009-0003-5440-5636
Indira SigdelDepartment of Bioengineering, College of Engineering, University of Toledo, Toledo, OH 43606, United States of America.
Md Alamgir KabirDepartment of Physics and Astronomy, University of Toledo, Toledo, OH 43606, United States of America.
Yuan TangDepartment of Bioengineering, College of Engineering, University of Toledo, Toledo, OH 43606, United States of America.
Aniruddha RayDepartment of Physics and Astronomy, University of Toledo, Toledo, OH 43606, United States of America.ORCID https://orcid.org/0000-0003-2561-2217

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Real-time and High-throughput fluorescence imaging is essential for probing dynamic cellular behavior in biomimetic and tissue-on-chip systems. While fluorescence microscopy provides high sensitivity and subcellular resolution, the intrinsic heterogeneity of these engineered tissues requires imaging multiple regions to obtain representative biological information. Meeting this need typically demands mechanical scanning systems, which add both hardware and software complexity and substantially increase cost. Here, we developed a compact and low-cost on-chip fluorescence microscopy platform that integrates a two-dimensional microlens substrate directly onto a complementary metal-oxide-semiconductor sensor to achieve high resolution and signal-to-noise ratio (SNR). Excitation light is delivered laterally through a prism to induce total internal reflection, effectively rejecting background illumination and allowing only fluorescence emission to reach the detector. The system's optical geometry was optimized using analytical modeling and numerical simulations to maximize photon collection and SNR. Using this optimized system, we first demonstrated its capability at the cellular level by capturing drug-induced oxidative stress and rapid intracellular signaling dynamics in BT-20 breast cancer cells. Once we were successfully able to monitor these dynamic processes, we next applied the system to biomimetic models. In a microfluidic tumor-endothelial co-culture, we visualized the passage of small molecules, nanoparticles, and ions across the endothelial barrier under controlled flow conditions. Integration with microfluidic co-culture systems further demonstrated its ability to study complex interactions within tumor microenvironments. By combining simplicity, sensitivity, and compatibility with biomimetic platforms, this on-chip fluorescence microscope enables wide-field monitoring of cellular dynamics across large populations, allowing observation of cell-to-cell variability and supporting applications in drug screening, cellular signaling studies, and tissue-on-chip research.

Indexed as

biomimetic systemsCMOS sensoron-chip fluorescence microscope

Identifiers

PMID42367260
PMCPMC13295382

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.