Evidence map›Paper›PMID 21536929›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2011

A beta-camera integrated with a microfluidic chip for radioassays based on real-time imaging of glycolysis in small cell populations.

Nam T Vu, Zeta T F Yu, Begonya Comin-Anduix, Jonas N Søndergaard, Robert W Silverman, Canny Y N Chang, Antoni Ribas, Hsian-Rong Tseng, Arion F Chatziioannou

Open access · bronzeAbstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.3field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Development of a Lensless Radiomicroscope for Cellular-Resolution Radionuclide Imaging.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2023
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  5. Performance evaluation ofMedical physics · 2017
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  13. High-resolution radioluminescence microscopy of 18F-FDG uptake by reconstructing the β-ionization track.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2013
    Article
  14. Fast metabolic response to drug intervention through analysis on a miniaturized, highly integrated molecular imaging system.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2013
    Article
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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

9 authors at 2 institutions in 1 country.

Nam T VuCrump Institute for Molecular Imaging, University of California, Los Angeles, California 90095-1770, USA.
Zeta T F Yu
Begonya Comin-Anduix
Jonas N Søndergaard
Robert W Silverman
Canny Y N Chang
Antoni Ribas
Hsian-Rong Tseng
Arion F Chatziioannou
University of California, Los Angeles · USInstitute for Molecular Medicine · US

Funding

QUANTITATIVE IMAGE ANALYSIS SPECIALIZED RESOURCE COREU54CA119347 · NCI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI WITTE, OWEN N. · 2005 to 2009
$17.8M
Research Training in Biomedical PhysicsT32EB002101 · NIBIB · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Michael F McNitt-Gray · 2003 to 2026
$5.3M
NCI NIH HHS U54 CA119347NIBIB NIH HHS 5T32EB002101NIBIB NIH HHS T32 EB002101
6 · The paper itself

Abstract

unlabelledAn integrated β-camera and microfluidic chip was developed that is capable of quantitative imaging of glycolysis radioassays using (18)F-FDG in small cell populations down to a single cell. This paper demonstrates that the integrated system enables digital control and quantitative measurements of glycolysis in B-Raf(V600E)-mutated melanoma cell lines in response to specific B-Raf inhibition.

methodsThe β-camera uses a position-sensitive avalanche photodiode to detect charged particle-emitting probes within a microfluidic chip. The integrated β-camera and microfluidic chip system was calibrated, and the linearity was measured using 4 different melanoma cell lines (M257, M202, M233, and M229). Microfluidic radioassays were performed with cell populations ranging from hundreds of cells down to a single cell. The M229 cell line has a homozygous B-Raf(V600E) mutation and is highly sensitive to a B-Raf inhibitor, PLX4032. A microfluidic radioassay was performed over the course of 3 days to assess the cytotoxicity of PLX4032 on cellular (18)F-FDG uptake.

resultsThe β-camera is capable of imaging radioactive uptake of (18)F-FDG in microfluidic chips. (18)F-FDG uptake for a single cell was measured using a radioactivity concentration of 37 MBq/mL during the radiotracer incubation period. For in vitro cytotoxicity monitoring, the β-camera showed that exposure to 1 μM PLX4032 for 3 days decreased the (18)F-FDG uptake per cell in highly sensitive M229 cells, compared with vehicle controls.

conclusionThe integrated β-camera and microfluidic chip can provide digital control of live cell cultures and allow in vitro quantitative radioassays for multiple samples simultaneously.

Indexed as

Beta ParticlesGlycolysisMicrofluidic Analytical TechniquesSystems IntegrationBiological TransportCalibrationCell Line, TumorFluorodeoxyglucose F18GlucoseHumansIndolesMolecular ImagingRadiometrySingle-Cell AnalysisSulfonamidesTime FactorsFluorodeoxyglucose F18GlucoseIndolesSulfonamidesVemurafenib

Identifiers

PMID21536929
PMCPMC3270819
OpenAlexW2102777056

What OpenQuestion holds

Textmetadata
LicenceTDM
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.