Evidence map›Paper›PMID 23668322›Full record

ArticleACS nano2013

Cellular interaction and toxicity depend on physicochemical properties and surface modification of redox-active nanomaterials.

Janet M Dowding, Soumen Das, Amit Kumar, Talib Dosani, Rameech McCormack, Ankur Gupta, Thi X T Sayle, Dean C Sayle, Laurence von Kalm, Sudipta Seal and 1 more

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
8.6field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 204 citations in OpenAlex.

  1. Article
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  7. Ceria nanoparticles: biomedical applications and toxicity.Journal of Zhejiang University. Science. B · 2024
    Review
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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

11 authors at 2 institutions in 2 countries.

Janet M DowdingBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, Florida 32816, USA.
Soumen Das
Amit Kumar
Talib Dosani
Rameech McCormack
Ankur Gupta
Thi X T Sayle
Dean C Sayle
Laurence von Kalm
Sudipta Seal
William T Self
University of Central Florida · USUniversity of Kent · GB

Funding

Catalytic properties of NanoceriaR01AG031529 · NIA · UNIVERSITY OF CENTRAL FLORIDA · PI SEAL, SUDIPTA, SELF, WILLIAM T · 2008 to 2011
$1.0M
NIA NIH HHS R01 AG031529NIA NIH HHS R01AG031529-01
6 · The paper itself

Abstract

The study of the chemical and biological properties of CeO2 nanoparticles (CNPs) has expanded recently due to its therapeutic potential, and the methods used to synthesize these materials are diverse. Moreover, conflicting reports exist regarding the toxicity of CNPs. To help resolve these discrepancies, we must first determine whether CNPs made by different methods are similar or different in their physicochemical and catalytic properties. In this paper, we have synthesized several forms of CNPs using identical precursors through a wet chemical process but using different oxidizer/reducer; H2O2 (CNP1), NH4OH (CNP2), or hexamethylenetetramine (HMT-CNP1). Physicochemical properties of these CNPs were extensively studied and found to be different depending on the preparation methods. Unlike CNP1 and CNP2, HMT-CNP1 was readily taken into endothelial cells and the aggregation can be visualized using light microscopy. Exposure to HMT-CNP1 also reduced cell viability at a 10-fold lower concentration than CNP1 or CNP2. Surprisingly, exposure to HMT-CNP1 led to substantial decreases in ATP levels. Mechanistic studies revealed that HMT-CNP1 exhibited substantial ATPase (phosphatase) activity. Though CNP2 also exhibits ATPase activity, CNP1 lacked ATPase activity. The difference in catalytic (ATPase) activity of different CNPs preparation may be due to differences in their morphology and oxygen extraction energy. These results suggest that the combination of increased uptake and ATPase activity of HMT-CNP1 may underlie the biomechanism of the toxicity of this preparation of CNPs and may suggest that ATPase activity should be considered when synthesizing CNPs for use in biomedical applications.

Indexed as

Chemical PhenomenaAdenosine TriphosphatasesAdenosine TriphosphateAmmonium HydroxideCatalysisCeriumChemical PrecipitationHumansHuman Umbilical Vein Endothelial CellsHydrogen PeroxideHydroxidesIntracellular SpaceMethenamineNanoparticlesOxidation-ReductionParticle SizeAdenosine TriphosphatasesAdenosine TriphosphateAmmonium Hydroxideceric oxideCeriumHydrogen PeroxideHydroxidesMethenaminePhosphoric Monoester HydrolasesWater

Identifiers

PMID23668322
PMCPMC3700371
OpenAlexW2029231128

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.