Evidence map›Paper›PMID 40352520›Full record

ArticleACS omega2025

Synthesis, Characterization, and Toxicity Assessment of Superparamagnetic Iron Oxide Nanoparticles Coated with Antitumor Molecules.

Camila Chagas, Emerson B da Silva, Beatriz da C A Alves, Glaucia L da Veiga, Edimar C Pereira, Paula Haddad, Maria Lúcia Schumacher, Tatiane Nassar Britos, Lídia M Lima, Eliezer J L Barreiro and 2 more

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Camila ChagasClinical Analysis Laboratory of the Centro Universitário FMABC, Av. Príncipe de Gales, 821, Bairro Vila Príncipe de Gales, Santo André, São Paulo 09060-650, Brazil.
Emerson B da SilvaClinical Analysis Laboratory of the Centro Universitário FMABC, Av. Príncipe de Gales, 821, Bairro Vila Príncipe de Gales, Santo André, São Paulo 09060-650, Brazil.
Beatriz da C A AlvesClinical Analysis Laboratory of the Centro Universitário FMABC, Av. Príncipe de Gales, 821, Bairro Vila Príncipe de Gales, Santo André, São Paulo 09060-650, Brazil.ORCID https://orcid.org/0000-0001-9930-7747
Glaucia L da VeigaClinical Analysis Laboratory of the Centro Universitário FMABC, Av. Príncipe de Gales, 821, Bairro Vila Príncipe de Gales, Santo André, São Paulo 09060-650, Brazil.
Edimar C PereiraChemistry Department, Federal University of São Paulo-Campus Diadema, Rua São Nicolau, 210, Centro, Diadema, São Paulo 09913-030, Brazil.
Paula HaddadChemistry Department, Federal University of São Paulo-Campus Diadema, Rua São Nicolau, 210, Centro, Diadema, São Paulo 09913-030, Brazil.ORCID https://orcid.org/0000-0001-5362-1861
Maria Lúcia SchumacherChemistry Department, Federal University of São Paulo-Campus Diadema, Rua São Nicolau, 210, Centro, Diadema, São Paulo 09913-030, Brazil.
Tatiane Nassar BritosChemistry Department, Federal University of São Paulo-Campus Diadema, Rua São Nicolau, 210, Centro, Diadema, São Paulo 09913-030, Brazil.
Lídia M LimaLASSBio, Institute of Biomedical Sciences, Federal University of Rio de Janeiro (UFRJ), Sala 35-Prédio Do Centro de Ciências da Saúde, Av. Carlos Chagas, 373-Bloco K, 2° Andar, Cidade Universitária, Ilha do Fundão, Rio de Janeiro, Rio de Janeiro 21941-902, Brazil.ORCID https://orcid.org/0000-0002-8625-6351
Eliezer J L BarreiroLASSBio, Institute of Biomedical Sciences, Federal University of Rio de Janeiro (UFRJ), Sala 35-Prédio Do Centro de Ciências da Saúde, Av. Carlos Chagas, 373-Bloco K, 2° Andar, Cidade Universitária, Ilha do Fundão, Rio de Janeiro, Rio de Janeiro 21941-902, Brazil.
Fabio F FerreiraCenter for Natural and Human Sciences (CCNH), Federal University of ABC (UFABC), Santo André, São Paulo 09280-560, Brazil.ORCID https://orcid.org/0000-0003-1516-1221
Fernando L A FonsecaClinical Analysis Laboratory of the Centro Universitário FMABC, Av. Príncipe de Gales, 821, Bairro Vila Príncipe de Gales, Santo André, São Paulo 09060-650, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New definitions describe cancer as a condition where cells, transformed by natural selection, undergo uncontrolled proliferation. Currently, several available drugs for treating cancer present side effects and are nonselective, thus complicating patient treatment. To overcome such issues, alternative therapies using inorganic nanoparticles and parent compounds are becoming more attractive. Here, we demonstrate the use of biocompatible superparamagnetic iron oxide nanoparticles (SPIONs) coated with the LASSBio-1735 parent compound in BALB/c mice inoculated with the Ehrlich tumor. We first characterize the formed nanoparticles and confirm and quantify the anchoring of LASSBio-1735 on the surface of the SPIONs. Tests conducted after 7, 14, and 30 days show that no significant alterations were found in erythrocyte count analysis, hemoglobin and hematocrit determination, platelet and leukocyte counts, neutrophil/lymphocyte ratio, serum iron dosage, alanine aminotransferase, aspartate aminotransferase, serum creatinine, and urea determination, as well as analysis of the animals' and tumor weights. This confirms that this new alternative can be considered in clinical trials to treat solid tumors.

Identifiers

PMID40352520
PMCPMC12060056

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.