Evidence map›Paper›PMID 41515924›Full record

ArticleInternational journal of molecular sciences2025

Protective Effect of PEG-EDTA and Its Zinc(II) Complex on Human Cells.

Tashneet Dhaliwal, Cole Babcock, Brynmar Degenhardt, Isaac Osorio Passos, Tigran Stepanyan, Makan Golizeh

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Tashneet DhaliwalMetals in Environment and Health (MEH) Research Cluster, Concordia University of Edmonton, Edmonton, AB T5B 4E4, Canada.
Cole BabcockMetals in Environment and Health (MEH) Research Cluster, Concordia University of Edmonton, Edmonton, AB T5B 4E4, Canada.ORCID 0009-0001-1774-7886
Brynmar DegenhardtMetals in Environment and Health (MEH) Research Cluster, Concordia University of Edmonton, Edmonton, AB T5B 4E4, Canada.
Isaac Osorio PassosSchool of Engineering, Faculty of Nanotechnology Engineering, Universidad Pontificia Bolivariana, Medellín 050031, Colombia.
Tigran StepanyanMetals in Environment and Health (MEH) Research Cluster, Concordia University of Edmonton, Edmonton, AB T5B 4E4, Canada.
Makan GolizehMetals in Environment and Health (MEH) Research Cluster, Concordia University of Edmonton, Edmonton, AB T5B 4E4, Canada.ORCID 0000-0001-7746-5533

Funding

Babcocks Synthetics Ltd. N/AConcordia University of Edmonton CSG-PROJ-2311-12Natural Sciences and Engineering Research Council of Canada RGPIN-2022-03625
6 · The paper itself

Abstract

The most widely used chelating agent, ethylenediaminetetraacetic acid (EDTA), can cause mild to serious side effects when used for clinical applications. Introducing a polyethylene glycol (PEG) moiety into the molecular structure of EDTA has been shown to lower its toxicity; however, it is unclear whether this could affect EDTA chelation efficiency due to the steric hindrance and the loss of a coordination site caused by the PEGylation reaction. This research aimed to determine if PEGylation could reduce EDTA toxicity without affecting its chelation efficiency. To this end, effective formation constants were determined for EDTA and PEG-EDTA rare earth metal ion complexes using spectrophotometric and titrimetric methods. The stability of PEG-EDTA complexes with the target metal ions was assessed under different conditions using Fourier-transform infrared spectroscopy. The cytotoxicity and metal detoxification capacity of EDTA, PEG-EDTA, and their zinc(II) complexes were determined in two selected human cell types exposed to toxic heavy metal ions. This study suggests that PEG-EDTA has lower toxicity than EDTA, especially when complexed with a nontoxic metal ion, such as zinc(II), while only slightly losing chelation efficiency, potentially making PEG-EDTA a more favourable metal detoxification reagent for clinical applications.

Indexed as

Chelating AgentsCoordination ComplexesEdetic AcidPolyethylene GlycolsZincCell SurvivalHumansSpectroscopy, Fourier Transform InfraredChelating AgentsCoordination ComplexesEdetic AcidPolyethylene GlycolsZincchelationcytotoxicityEDTAhuman umbilical vein endothelial cells (HUVECs)metal displacementPEG-EDTAPEGylationspectroscopytitrationtriple-negative breast cancer (TNBC)

Identifiers

PMID41515924
PMCPMC12785647

What OpenQuestion holds

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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.