Toxicity and magnetometry evaluation of the uptake of core-shell maghemite-silica nanoparticles by neuroblastoma cells

Author:

López-Martín Raúl1ORCID,Aranda-Sobrino Nieves2,De Enciso-Campos Nerea2,Sánchez Elena H.1,Castañeda-Peñalvo Gregorio3,Lee Su Seong4,Binns Chris1,Ballesteros-Yáñez Inmaculada25,De Toro Jose A.1ORCID,Castillo-Sarmiento Carlos A.56ORCID

Affiliation:

1. Departamento de Física Aplicada, Instituto Regional de Investigación Científica Aplicada (IRICA), Universidad de Castilla-La Mancha , Ciudad Real 13071, Spain

2. Department of Inorganic and Organic Chemistry and Biochemistry, School of Medicine, University of Castilla-La Mancha , Ciudad Real 13071, Spain

3. Departamento de Química Analítica y Tecnología de los Alimentos, Facultad de Ciencias y Tecnología Química, Universidad de Castilla-La Mancha , Ciudad Real 13071, Spain

4. NanoBio Lab, Institute of Materials Research and Engineering, 31 Biopolis Way, #09-01, The Nanos , Singapore 138669, Singapore

5. BIomedicine Institute, Universidad de Castilla-La Mancha , Albacete 02008, Spain

6. Department of Nursing, Physiotherapy and Occupational Therapy, School of Physiotherapy and Nursing, University of Castilla-La Mancha , Toledo 45071, Spain

Abstract

Nanoparticle uptake by cells is a key parameter in their performance in biomedical applications. However, the use of quantitative, non-destructive techniques to obtain the amount of nanoparticles internalized by cells is still uncommon. We have studied the cellular uptake and the toxicity of core-shell maghemite-silica magnetic nanoparticles (MNPs), with a core diameter of 9 nm and a shell thickness of 3 nm. The internalization of the nanoparticles by mouse neuroblastoma 2a cells was evaluated by sensitive and non-destructive Superconducting Quantum Interference Device (SQUID) magnetometry and corroborated by graphite furnace atomic absorption spectroscopy. We were thus able to study the toxicity of the nanoparticles for well-quantified MNP uptake in terms of nanoparticle density within the cell. No significant variation in cell viability or growth rate was detected for any tested exposure. Yet, an increase in both the amount of mitochondrial superoxide and in the lysosomal activity was detected for the highest concentration (100 μg ml −1 ) and incubation time (24 h), suggesting the onset of a disruption in ROS homeostasis, which may lead to an impairment in antioxidant responses. Our results validate SQUID magnetometry as a sensitive technique to quantify MNP uptake and demonstrate the non-toxic nature of these core-shell MNPs under our culture conditions.

Funder

Ministerio de Ciencia e Innovación

European Social Fund Plus

Junta de Comunidades de Castilla-La Mancha

Universidad de Castilla-La Mancha

Publisher

The Royal Society

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