Evidence map›Paper›PMID 18596334›Full record

ReviewAnnals of the New York Academy of Sciences2008

Fluorescence interferometry: principles and applications in biology.

Alberto Bilenca, Jing Cao, Max Colice, Aydogan Ozcan, Brett Bouma, Laurel Raftery, Guillermo Tearney

Abstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2008. 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
–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

1 citing paper in PubMed.

  1. Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure.Proceedings of the National Academy of Sciences of the United States of America · 2009
    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.

Alberto BilencaHarvard Medical School and Wellman Center for Photomedicine, Massachusetts General Hospital, 50 Blossom St., BAR 720, Boston, Massachusetts 02114, USA. abilenca@partners.org
Jing Cao
Max Colice
Aydogan Ozcan
Brett Bouma
Laurel Raftery
Guillermo Tearney

Funding

TGF-BETA FAMILY REGULATION OF EPITHELIAL MORPHOGENESISR01GM060501 · NIGMS · UNIVERSITY OF NEVADA LAS VEGAS · PI RAFTERY, LAUREL A · 2000 to 2012
$4.5M
In-site Measurement of Plaque Biomechanical PropertiesR01HL070039 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BOUMA, BRETT E · 2002 to 2005
$1.4M
NHLBI NIH HHS R01 HL070039NIGMS NIH HHS R01 GM060501
6 · The paper itself

Abstract

The use of fluorescence radiation is of fundamental importance for tackling measurement problems in the life sciences, with recent demonstrations of probing biological systems at the nanoscale. Usually, fluorescent light-based tools and techniques use the intensity of light waves, which is easily measured by detectors. However, the phase of a fluorescence wave contains subtle, but no less important, information about the wave; yet, it has been largely unexplored. Here, we introduce the concept of fluorescence interferometry to allow the measurement of phase information of fluorescent light waves. In principle, fluorescence interferometry can be considered a unique form of optical low-coherence interferometry that uses fluorophores as a light source of low temporal coherence. Fluorescence interferometry opens up new avenues for developing new fluorescent light-based imaging, sensing, ranging, and profiling methods that to some extent resemble interferometric techniques based on white light sources. We propose two experimental realizations of fluorescence interferometry that detect the interference pattern cast by the fluorescence fields. This article discusses their measurement capabilities and limitations and compares them with those offered by optical low-coherence interferometric schemes. We also describe applications of fluorescence interferometry to imaging, ranging, and profiling tasks and present experimental evidences of wide-field cross-sectional imaging with high resolution and large range of depth, as well as quantitative profiling with nanometer-level precision. Finally, we point out future research directions in fluorescence interferometry, such as fluorescence tomography of whole organisms and the extension to molecular interferometry by means of quantum dots and bioluminescence.

Indexed as

FluorescenceAnimalsBiologyEquipment DesignFluorescent DyesFourier AnalysisHumansInterferometryLightLuminescenceMicroscopy, FluorescenceMicroscopy, Phase-ContrastNanotechnologyQuantum DotsTomographyFluorescent Dyes

Identifiers

PMID18596334
PMCPMC10902801

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.