Evidence map›Paper›PMID 25706293›Full record

ArticlePloS one2015

Ultraviolet germicidal irradiation and its effects on elemental distributions in mouse embryonic fibroblast cells in x-ray fluorescence microanalysis.

Qiaoling Jin, Stefan Vogt, Barry Lai, Si Chen, Lydia Finney, Sophie-Charlotte Gleber, Jesse Ward, Junjing Deng, Rachel Mak, Nena Moonier and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. 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

11 authors at 2 institutions in 1 country.

Qiaoling JinDepartment of Physics & Astronomy, Northwestern University, Evanston, Illinois, USA.
Stefan VogtX-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois, USA.
Barry LaiX-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois, USA.
Si ChenX-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois, USA.
Lydia FinneyX-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois, USA.
Sophie-Charlotte GleberX-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois, USA.
Jesse WardX-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois, USA.
Junjing DengDepartment of Physics & Astronomy, Northwestern University, Evanston, Illinois, USA.
Rachel MakDepartment of Physics & Astronomy, Northwestern University, Evanston, Illinois, USA.
Nena MoonierAPS Engineering Support Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois, USA.
Chris JacobsenDepartment of Physics & Astronomy, Northwestern University, Evanston, Illinois, USA; X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois, USA; Chemistry of Life Processes Institute, Northwestern University, Evanston, Illinois, USA.
Argonne National Laboratory · USNorthwestern University · US

Funding

Cryo ptychography combined with x-ray fluorescence analysis of metals in cellsR01GM104530 · NIGMS · NORTHWESTERN UNIVERSITY · PI JACOBSEN, CHRIS JOHNSON · 2013 to 2020
$2.2M
NIGMS NIH HHS R01 GM104530
6 · The paper itself

Abstract

Rapidly-frozen hydrated (cryopreserved) specimens combined with cryo-scanning x-ray fluorescence microscopy provide an ideal approach for investigating elemental distributions in biological cells and tissues. However, because cryopreservation does not deactivate potentially infectious agents associated with Risk Group 2 biological materials, one must be concerned with contamination of expensive and complicated cryogenic x-ray microscopes when working with such materials. We employed ultraviolet germicidal irradiation to decontaminate previously cryopreserved cells under liquid nitrogen, and then investigated its effects on elemental distributions under both frozen hydrated and freeze dried states with x-ray fluorescence microscopy. We show that the contents and distributions of most biologically important elements remain nearly unchanged when compared with non-ultraviolet-irradiated counterparts, even after multiple cycles of ultraviolet germicidal irradiation and cryogenic x-ray imaging. This provides a potential pathway for rendering Risk Group 2 biological materials safe for handling in multiuser cryogenic x-ray microscopes without affecting the fidelity of the results.

Indexed as

CryopreservationAnimalsElectron Probe MicroanalysisEmbryonic Stem CellsFibroblastsMiceMicroscopy, FluorescenceUltraviolet Rays

Identifiers

PMID25706293
PMCPMC4338249
OpenAlexW2004005117

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.