Evidence map›Paper›PMID 38223174›Full record

ArticleBiomedical optics express2024

Fast Fourier ptychographic quantitative phase microscopy for in vitro label-free imaging.

Ruofei Wu, Zicong Luo, Mingdi Liu, Haiqi Zhang, Junrui Zhen, Lisong Yan, Jiaxiong Luo, Yanxiong Wu

Open access · goldAbstract read
In one paragraph

Article in Biomedical optics express, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
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

1 citing paper in PubMed, 14 citations in OpenAlex.

  1. Article
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 at 2 institutions in 1 country.

Ruofei WuSchool of Physics and Optoelectronic Engineering, Foshan University, Foshan 528000, China.ORCID https://orcid.org/0009-0005-6331-4458
Zicong LuoSchool of Physics and Optoelectronic Engineering, Foshan University, Foshan 528000, China.ORCID https://orcid.org/0009-0000-6452-8056
Mingdi LiuSchool of Physics and Optoelectronic Engineering, Foshan University, Foshan 528000, China.
Haiqi ZhangSchool of Physics and Optoelectronic Engineering, Foshan University, Foshan 528000, China.
Junrui ZhenSchool of Physics and Optoelectronic Engineering, Foshan University, Foshan 528000, China.
Lisong YanSchool of Optical and Electronic Information, Huazhong University of Science and Technology, Wuhan 430074, China.
Jiaxiong LuoSchool of Physics and Optoelectronic Engineering, Foshan University, Foshan 528000, China.
Yanxiong WuSchool of Physics and Optoelectronic Engineering, Foshan University, Foshan 528000, China.
Foshan University · CNHuazhong University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantitative phase microscopy (QPM) is indispensable in biomedical research due to its advantages in unlabeled transparent sample thickness quantification and obtaining refractive index information. Fourier ptychographic microscopy (FPM) is among the most promising QPM methods, incorporating multi-angle illumination and iterative phase recovery for high-resolution quantitative phase imaging (QPI) of large cell populations over a wide field of-view (FOV) in a single pass. However, FPM is limited by data redundancy and sequential acquisition strategies, resulting in low imaging efficiency, which in turn limits its real-time application in in vitro label-free imaging. Here, we report a fast QPM based on Fourier ptychography (FQP-FPM), which uses an optimized annular downsampling and parallel acquisition strategy to minimize the amount of data required in the front end and reduce the iteration time of the back-end algorithm (3.3% and 4.4% of conventional FPM, respectively). Theoretical and data redundancy analyses show that FQP-FPM can realize high-throughput quantitative phase reconstruction at thrice the resolution of the coherent diffraction limit by acquiring only ten raw images, providing a precondition for in vitro label-free real-time imaging. The FQP-FPM application was validated for various in vitro label-free live-cell imaging. Cell morphology and subcellular phenomena in different periods were observed with a synthetic aperture of 0.75 NA at a 10× FOV, demonstrating its advantages and application potential for fast high-throughput QPI.

Identifiers

PMID38223174
PMCPMC10783909
OpenAlexW4388939336

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.