Evidence map›Paper›PMID 26968385›Full record

ArticleJournal of biomedical optics2016

Characterization and standardization of tissue-simulating protoporphyrin IX optical phantoms.

Mikael Marois, Jaime Bravo, Scott C Davis, Stephen Chad Kanick

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomedical optics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 27 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

4 authors at 3 institutions in 2 countries.

Mikael MaroisPolytechnique Montreal, 2500 Chemin de Polytechnique, Montreal, Quebec H3T 1J4, CanadabDartmouth College, 14 Engineering Drive, Hanover, New Hampshire 03755, United States.
Jaime BravoPolytechnique Montreal, 2500 Chemin de Polytechnique, Montreal, Quebec H3T 1J4, Canada.
Scott C DavisDartmouth College, 14 Engineering Drive, Hanover, New Hampshire 03755, United StatescNorris Cotton Cancer Center, Dartmouth Hitchcock Medical Center, 1 Medical Center Drive, Lebanon, New Hampshire 03766, United States.
Stephen Chad KanickDartmouth College, 14 Engineering Drive, Hanover, New Hampshire 03755, United StatescNorris Cotton Cancer Center, Dartmouth Hitchcock Medical Center, 1 Medical Center Drive, Lebanon, New Hampshire 03766, United States.
Dartmouth College · USDartmouth–Hitchcock Medical Center · USPolytechnique Montréal · CA

Funding

Coregistered Fluorescence-Enhanced Resection of Malignant GliomaR01NS052274 · NINDS · DARTMOUTH-HITCHCOCK CLINIC · PI ROBERTS, DAVID W · 2007 to 2018
$4.6M
Quantitative optical dosimetry of magnetic nanoparticle cancer treatmentsK25CA164248 · NCI · DARTMOUTH COLLEGE · PI KANICK, STEPHEN CHAD · 2013 to 2015
$498k
NCI NIH HHS K25 CA164248NCI NIH HHS K25CA164248-01NINDS NIH HHS R01 NS052274NINDS NIH HHS R01NS052274-06
6 · The paper itself

Abstract

Optical devices for measuring protoporphryin IX (PpIX) fluorescence in tissue are routinely validated by measurements in optical phantoms. Yet there exists limited data to form a consensus on the recipe for phantoms that both mimic the optical properties found in tissue and yield a reliable and stable relationship between PpIX concentration and the fluorescence remission intensity. This study characterizes the influence of multiple phantom components on PpIX fluorescence emission intensity, using Intralipid as the scattering source, bovine whole blood as the background absorber, and Tween as a surfactant to prevent PpIX aggregation. Optical measurements showed a linear proportionality (r > 0.99) between fluorescence intensity and PpIX concentration (0.1 to 10 μg/mL) over a range of Intralipid (1 to 2%) and whole blood (0.5 to 3%) for phantoms containing low surfactant (≤ 0.1%), with fluorescence intensities and scattering and absorption properties stable for 5 h after mixing. The role of surfactant in PpIX phantoms was found to be complex, as aggregation was evident in aqueous nonturbid phantoms with no surfactant (0% Tween), and avoided in phantoms containing Intralipid as the scattering source with no additional or low amounts of added surfactant (≤ 0.1% Tween). Conversely, phantoms containing higher surfactant content (>0.1% Tween) and whole blood showed interactions that distorted the fluorescence emissions.

Indexed as

Models, BiologicalPhantoms, ImagingOptical ImagingProtoporphyrinsSpectrometry, FluorescenceSurface-Active Agentsprotoporphyrin IXProtoporphyrinsSurface-Active Agents

Identifiers

PMID26968385
PMCPMC5994807
OpenAlexW2295636863

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.