Evidence map›Paper›PMID 26388460›Full record

ArticleJournal of biomedical optics2015

Optical properties of mouse brain tissue after optical clearing with FocusClear™.

Austin J Moy, Bernard V Capulong, Rolf B Saager, Matthew P Wiersma, Patrick C Lo, Anthony J Durkin, Bernard Choi

Open access · bronzeAbstract read
In one paragraph

Article in Journal of biomedical optics, 2015. 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
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Austin J MoyUniversity of California, Irvine, Beckman Laser Institute and Medical Clinic, Department of Surgery, 1002 Health Sciences Road East, Irvine, California 92617, United StatesbUniversity of California, Irvine, Department of Biomedical Engineering, 3120 Natur.
Bernard V CapulongUniversity of California, Irvine, Beckman Laser Institute and Medical Clinic, Department of Surgery, 1002 Health Sciences Road East, Irvine, California 92617, United States.
Rolf B SaagerUniversity of California, Irvine, Beckman Laser Institute and Medical Clinic, Department of Surgery, 1002 Health Sciences Road East, Irvine, California 92617, United States.
Matthew P WiersmaUniversity of California, Irvine, Beckman Laser Institute and Medical Clinic, Department of Surgery, 1002 Health Sciences Road East, Irvine, California 92617, United StatesbUniversity of California, Irvine, Department of Biomedical Engineering, 3120 Natur.
Patrick C LoUniversity of California, Irvine, Beckman Laser Institute and Medical Clinic, Department of Surgery, 1002 Health Sciences Road East, Irvine, California 92617, United StatesbUniversity of California, Irvine, Department of Biomedical Engineering, 3120 Natur.
Anthony J DurkinUniversity of California, Irvine, Beckman Laser Institute and Medical Clinic, Department of Surgery, 1002 Health Sciences Road East, Irvine, California 92617, United States.
Bernard ChoiUniversity of California, Irvine, Beckman Laser Institute and Medical Clinic, Department of Surgery, 1002 Health Sciences Road East, Irvine, California 92617, United StatesbUniversity of California, Irvine, Department of Biomedical Engineering, 3120 Natur.
University of California, Irvine · USBeckman Laser Institute and Medical Clinic · US

Funding

Virtual Photonocs TechnologiesP41EB015890 · NIBIB · UNIVERSITY OF CALIFORNIA-IRVINE · PI DURKIN, ANTHONY · 2012 to 2017
$7.0M
Novel Optical Treatment Approach for Vascular BirthmarksR01HD065536 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI CHOI, BERNARD, KELLY, KRISTEN M · 2010 to 2014
$1.4M
NIBIB NIH HHS EB015890NIBIB NIH HHS P41 EB015890NICHD NIH HHS R01 HD065536
6 · The paper itself

Abstract

Fluorescence microscopy is commonly used to investigate disease progression in biological tissues. Biological tissues, however, are strongly scattering in the visible wavelengths, limiting the application of fluorescence microscopy to superficial (<200µm) regions. Optical clearing, which involves incubation of the tissue in a chemical bath, reduces the optical scattering in tissue, resulting in increased tissue transparency and optical imaging depth. The goal of this study was to determine the time- and wavelength-resolved dynamics of the optical scattering properties of rodent brain after optical clearing with FocusClear™. Light transmittance and reflectance of 1-mm mouse brain sections were measured using an integrating sphere before and after optical clearing and the inverse adding doubling algorithm used to determine tissue optical scattering. The degree of optical clearing was quantified by calculating the optical clearing potential (OCP), and the effects of differing OCP were demonstrated using the optical histology method, which combines tissue optical clearing with optical imaging to visualize the microvasculature. We observed increased tissue transparency with longer optical clearing time and an analogous increase in OCP. Furthermore, OCP did not vary substantially between 400 and 1000 nm for increasing optical clearing durations, suggesting that optical histology can improve ex vivo visualization of several fluorescent probes.

Indexed as

Models, BiologicalAnimalsBrainComputer SimulationImage Interpretation, Computer-AssistedLightMiceMice, Inbred C3HMicroscopy, FluorescenceOrgan Culture TechniquesOrgan Preservation SolutionsScattering, RadiationSolutionsOrgan Preservation SolutionsSolutions

Identifiers

PMID26388460
PMCPMC4963466
OpenAlexW2113057341

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.