Evidence map›Paper›PMID 24689603›Full record

ArticleThe Review of scientific instruments2014

Design and evaluation of a device for fast multispectral time-resolved fluorescence spectroscopy and imaging.

Diego R Yankelevich, Dinglong Ma, Jing Liu, Yang Sun, Yinghua Sun, Julien Bec, Daniel S Elson, Laura Marcu

Abstract read
In one paragraph

Article in The Review of scientific instruments, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

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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

8 authors.

Diego R YankelevichDepartment of Electrical and Computer Engineering, University of California, 3101 Kemper Hall, Davis, California 95616, USA.
Dinglong MaDepartment of Biomedical Engineering, University of California, 451 Health Sciences Drive, Davis, California 95616, USA.
Jing LiuDepartment of Biomedical Engineering, University of California, 451 Health Sciences Drive, Davis, California 95616, USA.
Yang SunDepartment of Biomedical Engineering, University of California, 451 Health Sciences Drive, Davis, California 95616, USA.
Yinghua SunDepartment of Biomedical Engineering, University of California, 451 Health Sciences Drive, Davis, California 95616, USA.
Julien BecDepartment of Biomedical Engineering, University of California, 451 Health Sciences Drive, Davis, California 95616, USA.
Daniel S ElsonHamlyn Centre for Robotic Surgery, Department of Surgery and Cancer, Imperial College London, Exhibition Road, London SW7 2AZ, United Kingdom.
Laura MarcuDepartment of Biomedical Engineering, University of California, 451 Health Sciences Drive, Davis, California 95616, USA.

Funding

Time-Resolved Spectroscopy of Unstable Arterial PlaquesR01HL067377 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MARCU, LAURA · 2001 to 2015
$5.2M
NHLBI NIH HHS R01 HL067377NHLBI NIH HHS R01-HL67377
6 · The paper itself

Abstract

The application of time-resolved fluorescence spectroscopy (TRFS) to in vivo tissue diagnosis requires a method for fast acquisition of fluorescence decay profiles in multiple spectral bands. This study focusses on development of a clinically compatible fiber-optic based multispectral TRFS (ms-TRFS) system together with validation of its accuracy and precision for fluorescence lifetime measurements. It also presents the expansion of this technique into an imaging spectroscopy method. A tandem array of dichroic beamsplitters and filters was used to record TRFS decay profiles at four distinct spectral bands where biological tissue typically presents fluorescence emission maxima, namely, 390, 452, 542, and 629 nm. Each emission channel was temporally separated by using transmission delays through 200 μm diameter multimode optical fibers of 1, 10, 19, and 28 m lengths. A Laguerre-expansion deconvolution algorithm was used to compensate for modal dispersion inherent to large diameter optical fibers and the finite bandwidth of detectors and digitizers. The system was found to be highly efficient and fast requiring a few nano-Joule of laser pulse energy and <1 ms per point measurement, respectively, for the detection of tissue autofluorescent components. Organic and biological chromophores with lifetimes that spanned a 0.8-7 ns range were used for system validation, and the measured lifetimes from the organic fluorophores deviated by less than 10% from values reported in the literature. Multi-spectral lifetime images of organic dye solutions contained in glass capillary tubes were recorded by raster scanning the single fiber probe in a 2D plane to validate the system as an imaging tool. The lifetime measurement variability was measured indicating that the system provides reproducible results with a standard deviation smaller than 50 ps. The ms-TRFS is a compact apparatus that makes possible the fast, accurate, and precise multispectral time-resolved fluorescence lifetime measurements of low quantum efficiency sub-nanosecond fluorophores.

Indexed as

LasersOptical FibersFluorescent DyesImage Processing, Computer-AssistedSpectrometry, FluorescenceFluorescent Dyes

Identifiers

PMID24689603
PMCPMC3971822

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.