Evidence map›Paper›PMID 29359102›Full record

ArticleBiomedical optics express2018

13-fold resolution gain through turbid layer via translated unknown speckle illumination.

Kaikai Guo, Zibang Zhang, Shaowei Jiang, Jun Liao, Jingang Zhong, Yonina C Eldar, Guoan Zheng

Abstract read
In one paragraph

Article in Biomedical optics express, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Ptychography at all wavelengths.Nature reviews. Methods primers · 2025
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Organic Hyperbolic Material Assisted Illumination Nanoscopy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. 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

7 authors.

Kaikai Guo *Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.
Zibang Zhang *Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.
Shaowei Jiang *Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.
Jun LiaoBiomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.
Jingang ZhongDepartment of Optoelectronic Engineering, Jinan University, Guangzhou 510632, China.
Yonina C EldarElectrical Engineering, Israel Institute of Technology, Haifa 32000, Israel.
Guoan ZhengBiomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.

Funding

Fluorescence ptychographic microscopy for 4D live-cell imaging with high-spatiotemporal resolution and reduced phototoxicityR03EB022144 · NIBIB · UNIVERSITY OF CONNECTICUT STORRS · PI ZHENG, GUOAN · 2016 to 2017
$148k
NIBIB NIH HHS R03 EB022144
6 · The paper itself

Abstract

Fluorescence imaging through a turbid layer holds great promise for various biophotonics applications. Conventional wavefront shaping techniques aim to create and scan a focus spot through the turbid layer. Finding the correct input wavefront without direct access to the target plane remains a critical challenge. In this paper, we explore a new strategy for imaging through turbid layer with a large field of view. In our setup, a fluorescence sample is sandwiched between two turbid layers. Instead of generating one focus spot via wavefront shaping, we use an unshaped beam to illuminate the turbid layer and generate an unknown speckle pattern at the target plane over a wide field of view. By tilting the input wavefront, we raster scan the unknown speckle pattern via the memory effect and capture the corresponding low-resolution fluorescence images through the turbid layer. Different from the wavefront-shaping-based single-spot scanning, the proposed approach employs many spots (i.e., speckles) in parallel for extending the field of view. Based on all captured images, we jointly recover the fluorescence object, the unknown optical transfer function of the turbid layer, the translated step size, and the unknown speckle pattern. Without direct access to the object plane or knowledge of the turbid layer, we demonstrate a 13-fold resolution gain through the turbid layer using the reported strategy. We also demonstrate the use of this technique to improve the resolution of a low numerical aperture objective lens allowing to obtain both large field of view and high resolution at the same time. The reported method provides insight for developing new fluorescence imaging platforms and may find applications in deep-tissue imaging.

Indexed as

(110.0113) Imaging through turbid media(170.0110) Imaging systems(180.0180) Microscopy

Identifiers

PMID29359102
PMCPMC5772581

What OpenQuestion holds

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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 OpenQuestion graph.