Evidence map›Paper›PMID 28562033›Full record

ArticleAnalytical chemistry2017

Toward a Droplet-Based Single-Cell Radiometric Assay.

Maria Elena Gallina, Tae Jin Kim, Mark Shelor, Jaime Vasquez, Amy Mongersun, Minkyu Kim, Sindy K Y Tang, Paul Abbyad, Guillem Pratx

Abstract read
In one paragraph

Article in Analytical chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Flow radiocytometry using droplet optofluidics.Biosensors & bioelectronics · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Radio-Fluorogenic Gel Dosimetry with Coumarin.Bioengineering (Basel, Switzerland) · 2018
    Article
  10. 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

9 authors.

Maria Elena GallinaDivision of Medical Physics, Department of Radiation Oncology, Stanford University , 300 Pasteur Drive, Palo Alto, California 94305, United States.ORCID 0000-0002-3949-5536
Tae Jin KimDivision of Medical Physics, Department of Radiation Oncology, Stanford University , 300 Pasteur Drive, Palo Alto, California 94305, United States.
Mark ShelorUniversity of California-Merced , Department of Bioengineering, 5200 North Lake Road, Merced, California 95343, United States.
Jaime VasquezUniversity of California-San Francisco , School of Pharmacy, 600 16th Street, San Francisco, California, 94158, United States.
Amy MongersunDepartment of Chemistry and Biochemistry, Santa Clara University , Daly Science 123500 El Camino Real, Santa Clara, California 95053, United States.
Minkyu KimDepartment of Mechanical Engineering, Stanford University , 418 Panama Mall, Stanford, California 94305, United States.
Sindy K Y TangDepartment of Mechanical Engineering, Stanford University , 418 Panama Mall, Stanford, California 94305, United States.
Paul AbbyadDepartment of Chemistry and Biochemistry, Santa Clara University , Daly Science 123500 El Camino Real, Santa Clara, California 95053, United States.
Guillem PratxDivision of Medical Physics, Department of Radiation Oncology, Stanford University , 300 Pasteur Drive, Palo Alto, California 94305, United States.

Funding

Stanford Molecular Imaging Scholars (SMIS) ProgramT32CA118681 · NCI · STANFORD UNIVERSITY · PI CRAIG S LEVIN · 2016 to 2026
$4.3M
Quantitative Imaging of Cancer Drug Resistance via Radioluminescence MicroarraysR01CA186275 · NCI · STANFORD UNIVERSITY · PI PRATX, GUILLEM · 2014 to 2018
$1.7M
High-throughput radionuclide counting and sorting of single cellsR21CA193001 · NCI · STANFORD UNIVERSITY · PI PRATX, GUILLEM · 2015 to 2017
$698k
NCI NIH HHS R01 CA186275NCI NIH HHS R21 CA193001NCI NIH HHS T32 CA118681
6 · The paper itself

Abstract

Radiotracers are widely used to track molecular processes, both in vitro and in vivo, with high sensitivity and specificity. However, most radionuclide detection methods have spatial resolution inadequate for single-cell analysis. A few existing methods can extract single-cell information from radioactive decays, but the stochastic nature of the process precludes high-throughput measurement (and sorting) of single cells. In this work, we introduce a new concept for translating radioactive decays occurring stochastically within radiolabeled single-cells into an integrated, long-lasting fluorescence signal. Single cells are encapsulated in radiofluorogenic droplets containing molecular probes sensitive to byproducts of ionizing radiation (primarily reactive oxygen species, or ROS). Different probes were examined in bulk solutions, and dihydrorhodamine 123 (DHRh 123) was selected as the lead candidate due to its sensitivity and reproducibility. Fluorescence intensity of DHRh 123 in bulk increased at a rate of 54% per Gy of X-ray radiation and 15% per MBq/ml of 2-deoxy-2-[

Indexed as

RadiometrySingle-Cell AnalysisFluorescenceHumansMolecular StructureMonte Carlo MethodOptical ImagingParticle SizeReactive Oxygen SpeciesTumor Cells, CulturedReactive Oxygen Species

Identifiers

PMID28562033
PMCPMC5480233

What OpenQuestion holds

Textmetadata
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.