Evidence map›Paper›PMID 28703922›Full record

ArticleMedical physics2017

Sensitivity evaluation and selective plane imaging geometry for x-ray-induced luminescence imaging.

Bryan P Quigley, Corey D Smith, Shih-Hsun Cheng, Jeffrey S Souris, Charles A Pelizzari, Chin-Tu Chen, Leu-Wei Lo, Chester S Reft, Rodney D Wiersma, Patrick J La Riviere

Abstract read
In one paragraph

Article in Medical physics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. X-ray luminescence imaging for small animals.Proceedings of SPIE--the International Society for Optical Engineering · 2020
    Article
  4. Review
  5. 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

10 authors.

Bryan P QuigleyDepartment of Radiology, The University of Chicago, Chicago, IL, 60637, USA.
Corey D SmithDepartment of Radiology, The University of Chicago, Chicago, IL, 60637, USA.
Shih-Hsun ChengDepartment of Radiology, The University of Chicago, Chicago, IL, 60637, USA.
Jeffrey S SourisDepartment of Radiology, The University of Chicago, Chicago, IL, 60637, USA.
Charles A PelizzariDepartment of Radiation and Cellular Oncology, The University of Chicago, Chicago, IL, 60637, USA.
Chin-Tu ChenDepartment of Radiology, The University of Chicago, Chicago, IL, 60637, USA.
Leu-Wei LoDepartment of Radiology, The University of Chicago, Chicago, IL, 60637, USA.
Chester S ReftDepartment of Radiation and Cellular Oncology, The University of Chicago, Chicago, IL, 60637, USA.
Rodney D WiersmaDepartment of Radiation and Cellular Oncology, The University of Chicago, Chicago, IL, 60637, USA.
Patrick J La RiviereDepartment of Radiology, The University of Chicago, Chicago, IL, 60637, USA.

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI CHIEN-MIN KAO · 1985 to 2026
$122.1M
University of Chicago Initiative for Maximizing Student Development (IMSD) - Renewal 01R25GM109439 · NIGMS · UNIVERSITY OF CHICAGO · PI SCHWARTZ, NANCY B · 2014 to 2023
$5.7M
Radiation response within the tumor microenvironmentR01CA164492 · NCI · UNIVERSITY OF CHICAGO · PI KRON, STEPHEN J. · 2011 to 2015
$4.8M
RESEARCH TRAINING IN MEDICAL PHYSICST32EB002103 · NIBIB · UNIVERSITY OF CHICAGO · PI ARMATO, SAMUEL G. · 2003 to 2019
$4.7M
Development of a benchtop x-ray fluorescence tomography system using a novel geomR01EB017293 · NIBIB · UNIVERSITY OF CHICAGO · PI LA RIVIERE, PATRICK JEAN, MENG, LING-JIAN · 2014 to 2017
$1.8M
Nanotheranostics for Early Colorectal Cancer Detection and TreatmentR01CA171785 · NCI · UNIVERSITY OF CHICAGO · PI SOURIS, JEFFREY S. · 2013 to 2017
$1.6M
High-Performance Computer Cluster for Image AnalysisS10RR021039 · NCRR · UNIVERSITY OF CHICAGO · PI NISHIKAWA, ROBERT M · 2007 to 2007
$230k
NCI NIH HHS P30 CA014599NCI NIH HHS R01 CA164492NCI NIH HHS R01 CA171785NCRR NIH HHS S10 RR021039NIBIB NIH HHS R01 EB017293NIBIB NIH HHS T32 EB002103NIGMS NIH HHS R25 GM109439
6 · The paper itself

Abstract

purposeX-ray-induced luminescence (XIL) is a hybrid x-ray/optical imaging modality that employs nanophosphors that luminescence in response to x-ray irradiation. X-ray-activated phosphorescent nanoparticles have potential applications in radiation therapy as theranostics, nanodosimeters, or radiosensitizers. Extracting clinically relevant information from the luminescent signal requires the development of a robust imaging model that can determine nanophosphor distributions at depth in an optically scattering environment from surface radiance measurements. The applications of XIL in radiotherapy will be limited by the dose-dependent sensitivity at depth in tissue. We propose a novel geometry called selective plane XIL (SPXIL), and apply it to experimental measurements in optical gel phantoms and sensitivity simulations.

methodsAn imaging model is presented based on the selective plane geometry which can determine the detected diffuse optical signal for a given x-ray dose and nanophosphor distribution at depth in a semi-infinite, optically homogenous material. The surface radiance in the model is calculated using an analytical solution to the extrapolated boundary condition. Y

resultsNanophosphor characterizations showed a peak emission at 611 nm, a linear luminescent response to tube current and nanoparticle concentration, and a quadratic luminescent response to tube voltage. The luminescent efficiency calculation accomplished with calibrated bioluminescence mouse phantoms determines 1.06 photons were emitted per keV of x-ray radiation absorbed per g/mL of nanophosphor concentration. Sensitivity simulations determined that XIL could detect a concentration of 1 mg/mL of nanophosphors with a dose of 1 cGy at a depth ranging from 2 to 4 cm, depending on the optical parameters of the homogeneous diffuse optical environment. The deconvolution applied to the SPXIL measurements could resolve two sources 1 cm apart up to a depth of 1.75 cm in the diffuse phantom.

conclusionsWe present a novel imaging geometry for XIL in a homogenous, diffuse optical environment. Basic characterization of Y

Indexed as

LuminescenceCalibrationNanoparticlesOptical ImagingPhantoms, ImagingSignal-To-Noise RatioX-Raysdeconvolutionluminescencenanoparticlesoptical imagingx-rays

Identifiers

PMID28703922
PMCPMC5646227

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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.