Evidence map›Paper›PMID 40143999›Full record

ArticleJPhys photonics2025

High-resolution multi-modal imaging of sub-cellular structures with low numerical aperture objective.

Somaiyeh Khoubafarin, Peuli Nath, Saloni Malla, Durgesh Desai, William D Gorgas, Amit K Tiwari, Aniruddha Ray

Abstract read
In one paragraph

Article in JPhys photonics, 2025. 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

7 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
Peuli NathDepartment of Physics and Astronomy, University of Toledo, Toledo, OH 43606, United States of America.ORCID https://orcid.org/0000-0003-1285-0240
Saloni MallaDepartment of Pharmacology and Experimental Therapeutics, University of Toledo, Toledo, OH 43606, United States of America.
Durgesh DesaiDepartment of Physics and Astronomy, University of Toledo, Toledo, OH 43606, United States of America.
William D GorgasDepartment of Electrical and Computer Science, University of Toledo, Toledo, OH 43606, United States of America.ORCID https://orcid.org/0009-0007-9849-2603
Amit K TiwariDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas of Medical Sciences, Little Rock, AR, 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

High-throughput high-resolution microscopy for phenotypic drug discovery applicationsR15EB034552 · NIBIB · UNIVERSITY OF TOLEDO · PI RAY, ANIRUDDHA · 2023 to 2024
$650k
NIBIB NIH HHS R15 EB034552
6 · The paper itself

Abstract

Imaging of subcellular structures, which underpins many of the advances in biological and medical sciences, requires microscopes with high numerical aperture (N.A.) objectives which are costly, complex, requires oil immersion and have very limited field-of-view, typically covering a handful of cells. Here, we leverage a low N.A. objective to simultaneously capture scattering, phase, and fluorescence images of subcellular structures in breast cancer cells (BT-20) and observe nanoparticle uptake, with sub-diffraction-limited resolution (<400 nm with a 0.25 N.A. objective) utilizing a 2-dimensional (2-D) microlens substrate. High resolution labeled and label-free images of subcellular components is made possible by implementing a specific configuration, wherein the sample is placed in close proximity to the microlens substrate, which results in efficient collection of the rapidly decaying evanescent waves that contains the high frequency information, thereby improving resolution and the light capture efficiency. The microlens-assisted imaging provides an easy-to-implement and cost-effective means of drastically improving the resolution of any microscope with low N.A. objective lenses, paving the way for the development of affordable, portable multi-modal imaging systems with high-resolution imaging capabilities. This technology has broad implications for various fields and could democratize access to high-quality microscopy, particularly for application in resource-limited settings.

Indexed as

field of viewmicrolens substrateresolution

Identifiers

PMID40143999
PMCPMC11933920

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.