Evidence map›Paper›PMID 41867837›Full record

ArticlebioRxiv : the preprint server for biology2026

Scanless temporal focusing enables high-speed three-dimensional quantitative phase microscopy.

Yuechuan Lin, Xiang Zhang, Rebecca E Zubajlo, Zahid Yaqoob, Brian W Anthony, Peter T C So

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

6 authors.

Yuechuan LinLaser Biomedical Research Center, G. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.ORCID 0000-0002-1336-0668
Xiang ZhangDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Rebecca E ZubajloDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Zahid YaqoobLaser Biomedical Research Center, G. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Brian W AnthonyDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Peter T C SoLaser Biomedical Research Center, G. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.

Funding

Wide-Field Short-Wave Infrared (SWIR) multiphoton (MP) tissue imagingP41EB015871 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2012 to 2021
$11.3M
High Throughput End-to-End Design of Quantitative Phase Microscopy based on Customizable Nano-OpticsR01GM160726 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2025 to 2025
$2.0M
Characterizing mechanisms of sickle cell crisis via dynamic optical assayR01HL121386 · NHLBI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2014 to 2016
$1.7M
Acoustically-driven optical-interferometric microscope for cell characterizationR21GM140613 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI ANTHONY, BRIAN W, SO, PETER T. · 2021 to 2022
$424k
NHLBI NIH HHS R01 HL121386NIBIB NIH HHS P41 EB015871NIGMS NIH HHS R01 GM160726NIGMS NIH HHS R21 GM140613
6 · The paper itself

Abstract

Quantitative phase microscopy (QPM) enables label-free imaging of structure and dynamics in biological and physical systems, yet achieving high-speed three-dimensional (3D) QPM with strong optical sectioning remains a central challenge. Here, we introduce a single-shot reflection-mode temporal focusing QPM (TF-QPM) that provides sub-micron optical sectioning without needs of any mechanical scanning or multiplexed acquisitions. By extending temporal focusing beyond its conventional use in multiphoton fluorescence microscopy, TF-QPM enables diffraction-limited label-free phase-sensitive volumetric imaging with 402 nm lateral and 920 nm axial resolution, markedly reduced speckle noise, and depth-resolved imaging at 3,709 Hz frame rate -an order of magnitude faster than most existing techniques and currently only limited by the camera speed. The resulting spatiotemporal phase sensitivity enables precise 3D tracking of particle motion and quantitative characterization of fast dynamics in complex and anisotropic media. For tissue imaging applications, TF-QPM achieves histology-level resolution in intact samples and supports pixel-level virtual staining, providing a rapid, label-free alternative to conventional sectioning-based workflows. Together, these results establish TF-QPM as a scanless, high-speed platform for rapid, label-free volumetric imaging across both basic research and translational applications.

Identifiers

PMID41867837
PMCPMC13001468

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.