Journal Article

Agglomeration of titanium dioxide nanoparticles increases toxicological responses in vitro and in vivo

van den Brule, Sybille, Sebaihi, Noham, Van Landuyt, Kirsten L., Godderis, Lode, Petry, Jasmine, Lison, Dominique, Cokic, Stevan M., Hoet, Peter H., Murugadoss, Sivakumar, Brassinne, Frederic, Mast, Jan

2020

Overview

Background The terms agglomerates and aggregates are frequently used in the regulatory definition(s) of nanomaterials (NMs) and hence attract attention in view of their potential influence on health effects. However, the influence of nanoparticle (NP) agglomeration and aggregation on toxicity is poorly understood although it is strongly believed that smaller the size of the NPs greater the toxicity. A toxicologically relevant definition of NMs is therefore not yet available, which affects not only the risk assessment process but also hinders the regulation of nano-products. In this study, we assessed the influence of NP agglomeration on their toxicity/biological responses in vitro and in vivo. Results We tested two TiO 2 NPs with different primary sizes (17 and 117 nm) and prepared ad-hoc suspensions composed of small or large agglomerates with similar dispersion medium composition. For in vitro testing, human bronchial epithelial (HBE), colon epithelial (Caco2) and monocytic (THP-1) cell lines were exposed to these suspensions for 24 h and endpoints such as cytotoxicity, total glutathione, epithelial barrier integrity, inflammatory mediators and DNA damage were measured. Large agglomerates of 17 nm TiO 2 induced stronger responses than small agglomerates for glutathione depletion, IL-8 and IL-1β increase, and DNA damage in THP-1, while no effect of agglomeration was observed with 117 nm TiO 2 . In vivo, C57BL/6JRj mice were exposed via oropharyngeal aspiration or oral gavage to TiO 2 suspensions and, after 3 days, biological parameters including cytotoxicity, inflammatory cell recruitment, DNA damage and biopersistence were measured. Mainly, we observed that large agglomerates of 117 nm TiO 2 induced higher pulmonary responses in aspirated mice and blood DNA damage in gavaged mice compared to small agglomerates. Conclusion Agglomeration of TiO 2 NPs influences their toxicity/biological responses and, large agglomerates do not appear less active than small agglomerates. This study provides a deeper insight on the toxicological relevance of NP agglomerates and contributes to the establishment of a toxicologically relevant definition for NMs.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Administration, Oral / Agglomerates / Animals / Biological responses / Biomedical and Life Sciences / Biomedicine / Bronchoalveolar Lavage Fluid - chemistry / Caco-2 Cells / Cell Survival - drug effects / Chemical properties / Cytotoxicity / Deoxyribonucleic acid / Development and progression / DNA / DNA Damage / Dosimetry / Environmental Health / Epithelial Cells - drug effects / Female / Health aspects / Humans / Hypotheses / Influence / Inhalation Exposure - adverse effects / Mice, Inbred C57BL / Nanomaterials / Nanoparticles / Nanoparticles - chemistry / Nanoparticles - toxicity / Nanotechnology / Particle Size / Pharmacology/Toxicology / Pneumology/Respiratory System / Public Health / Risk assessment / Surface Properties / Surgical implants / Testing / THP-1 Cells / Titanium - chemistry / Titanium - toxicity / Titanium dioxide / Toxicity