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

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.

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Publication Details

Journal
ACS Omega
Published
2025-12-10
DOI
https://doi.org/10.1021/acsomega.5c09618
Primary Topic
Environmental Chemistry and Analysis
Type
article
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article

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

Graziela de Paula Ferreira Dantas, Guilherme Mattos Jardim Costa, José D. Ardisson, Pedro Lana Gastelois et al.
ACS Omega
Environmental Chemistry and Analysis
article

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

Graziela de Paula Ferreira Dantas, Guilherme Mattos Jardim Costa, José D. Ardisson, Pedro Lana Gastelois, Daniele Alves Fagundes, Thalita Marcolan Valverde, Pedro Igor Macário Viana, Ângela Leão Andrade, Clascídia Aparecida Furtado, Danilo Roberto Carvalho Ferreira, Bruna de Paula Dias, Luiz Felipe Mota Freitas, Carla Jeany Teixeira Silva
article en

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.

ACS OmegaVol. 10(50)
Universidade Federal de Ouro Preto (BR), Universidade Federal de Minas Gerais (BR), Centro de Desenvolvimento da Tecnologia Nuclear (BR), Instituto de Investigaciones en Ciencias de la Salud (AR), Instituto de Biología Molecular y Celular de Rosario (AR), Nano Carbon (Poland) (PL)
Openalex Percentile: Top 65%
Environmental Chemistry and Analysis
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