Evidence map›Paper›PMID 41476510›Full record

ArticleACS omega2025

Benzalkonium Chloride-Coated Iron Oxide Nanoparticles: Cytotoxic Potential on Murine Leydig Cells (TM3).

Pedro Igor Macário Viana, Thalita Marcolan Valverde, Daniele Alves Fagundes, Carla Cristina Martins Silva, Graziela de Paula Ferreira Dantas, Larissa Kennedy Moreira Freitas, Danilo Roberto Carvalho Ferreira, Bruna de Paula Dias, Pedro Lana Gastelois, Clascídia Aparecida Furtado and 3 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. 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

13 authors.

Pedro Igor Macário VianaLaboratório de Biologia Celular, Departamento de Morfologia, Instituto de Ciências Biológicas (ICB-UFMG), Universidade Federal de Minas Gerais, Belo Horizonte, MG 31270-901, Brazil.ORCID https://orcid.org/0000-0002-0195-9534
Thalita Marcolan ValverdeLaboratório de Biologia Celular, Departamento de Morfologia, Instituto de Ciências Biológicas (ICB-UFMG), Universidade Federal de Minas Gerais, Belo Horizonte, MG 31270-901, Brazil.
Daniele Alves FagundesLaboratório de Física Aplicada, Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN), Belo Horizonte, MG 31270-901, Brazil.
Carla Cristina Martins SilvaLaboratório de Biologia Celular, Departamento de Morfologia, Instituto de Ciências Biológicas (ICB-UFMG), Universidade Federal de Minas Gerais, Belo Horizonte, MG 31270-901, Brazil.ORCID https://orcid.org/0009-0006-8613-0835
Graziela de Paula Ferreira DantasLaboratório de Biologia Celular, Departamento de Morfologia, Instituto de Ciências Biológicas (ICB-UFMG), Universidade Federal de Minas Gerais, Belo Horizonte, MG 31270-901, Brazil.
Larissa Kennedy Moreira FreitasLaboratório de Biologia Celular, Departamento de Morfologia, Instituto de Ciências Biológicas (ICB-UFMG), Universidade Federal de Minas Gerais, Belo Horizonte, MG 31270-901, Brazil.
Danilo Roberto Carvalho FerreiraLaboratório de Química de Nanoestruturas de Carbono, Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN), Belo Horizonte, MG 31270-901, Brazil.
Bruna de Paula DiasLaboratório de Química de Nanoestruturas de Carbono, Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN), Belo Horizonte, MG 31270-901, Brazil.
Pedro Lana GasteloisCentro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN), Belo Horizonte, MG 31270-901, Brazil.ORCID https://orcid.org/0000-0001-7849-5013
Clascídia Aparecida FurtadoLaboratório de Química de Nanoestruturas de Carbono, Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN), Belo Horizonte, MG 31270-901, Brazil.ORCID https://orcid.org/0000-0001-7812-4319
José Domingos ArdissonLaboratório de Física Aplicada, Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN), Belo Horizonte, MG 31270-901, Brazil.
Ângela Leão AndradeDepartamento de Química, Instituto de Ciências Exatas e Biológicas (ICEB/UFOP), Universidade Federal de Ouro Preto, Ouro Preto, MG 35400-000, Brazil.ORCID https://orcid.org/0000-0002-0888-5072
Guilherme Mattos Jardim CostaLaboratório de Biologia Celular, Departamento de Morfologia, Instituto de Ciências Biológicas (ICB-UFMG), Universidade Federal de Minas Gerais, Belo Horizonte, MG 31270-901, Brazil.ORCID https://orcid.org/0000-0002-2907-7760

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study presents a novel nanocomplex, Mag-Bc, combining magnetite (Mag) and benzalkonium chloride (Bc). The objective was to evaluate the cytotoxic potential of Mag-Bc across three cell lines (TM3, VERO, and AML-12) and to assess its antiandrogenic effects specifically on TM3 cells. Physicochemical characterization confirmed the formation of partially oxidized magnetite and successful Bc coating, which conferred a positive charge to the nanoparticles. Viability assays on TM3 cells demonstrated no reduction below 70% at any dose or exposure time. Cellular internalization studies revealed efficient uptake of both coated and uncoated nanoparticles, indicating that the Bc coating did not impair cellular internalization. The nanocomplex exhibited intermediate superoxide anion production, maintaining levels comparable to control groups and demonstrating superior biocompatibility compared to magnetite and benzalkonium chloride alone. Testosterone levels remained unchanged following exposure to the Bc-coated nanoparticles. Collectively, these findings demonstrate that the Mag-Bc nanocomplex exhibits enhanced biocompatibility, characterized by a maintained cell viability, preserved cellular internalization capacity, reduced oxidative stress, and unchanged endocrine function. In contrast, cell growth kinetics of TM3 cells exposed to Bc-coated nanoparticles demonstrated reduced proliferation between days 3 and 8 compared with controls, suggesting potential time-dependent effects. The growth inhibition of Leydig cells induced by the nanocomplex may have implications for applications requiring suppression of testicular cell proliferation or for the development of nanoparticle-based therapeutic strategies targeting cell growth arrest.

Identifiers

PMID41476510
PMCPMC12750389

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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.