Evidence map›Paper›PMID 32499958›Full record

ArticleBiomedical optics express2020

Single-cavity dual-wavelength all-fiber femtosecond laser for multimodal multiphoton microscopy.

Farhad Akhoundi, N Peyghambarian

Abstract read
In one paragraph

Article in Biomedical optics express, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

2 authors.

Farhad AkhoundiCollege of Optical Sciences, University of Arizona, Tucson, AZ 85721, USA.
N PeyghambarianCollege of Optical Sciences, University of Arizona, Tucson, AZ 85721, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A single-cavity dual-wavelength all-fiber femtosecond laser is designed to generate 1030 nm wavelength for high resolution multiphoton imaging and 1700 nm wavelength for long penetration depth imaging. Considering two-photon and three-photon microscopy (2PM and 3PM), the proposed laser provides the single-photon wavelength equivalent to 343 nm, 515 nm, 566 nm and 850 nm, that can be employed to excite a wide variety of intrinsic fluorophores, dyes, and fluorescent proteins. Generating two excitation wavelengths from a single laser reduces the footprint and cost significantly compared to having two separate lasers. Furthermore, an all-reflective microscope is designed to eliminate the chromatic aberration while employing two excitation wavelengths. The compact all-fiber alignment-free laser design makes the overall size of the microscope appropriate for clinical applications.

Identifiers

PMID32499958
PMCPMC7249830

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.