Pulmonary toxicity of molybdenum disulphide after inhalation in mice

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Pulmonary toxicity of molybdenum disulphide after inhalation in mice. / Sørli, Jorid B; Jensen, Alexander C Ø; Mortensen, Alicja; Szarek, Józef; Gutierrez, Claudia A T; Givelet, Lucas; Loeschner, Katrin; Loizides, Charis; Hafez, Iosif; Biskos, George; Vogel, Ulla; Hadrup, Niels.

In: Toxicology, Vol. 485, 153428, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Sørli, JB, Jensen, ACØ, Mortensen, A, Szarek, J, Gutierrez, CAT, Givelet, L, Loeschner, K, Loizides, C, Hafez, I, Biskos, G, Vogel, U & Hadrup, N 2023, 'Pulmonary toxicity of molybdenum disulphide after inhalation in mice', Toxicology, vol. 485, 153428. https://doi.org/10.1016/j.tox.2023.153428

APA

Sørli, J. B., Jensen, A. C. Ø., Mortensen, A., Szarek, J., Gutierrez, C. A. T., Givelet, L., Loeschner, K., Loizides, C., Hafez, I., Biskos, G., Vogel, U., & Hadrup, N. (2023). Pulmonary toxicity of molybdenum disulphide after inhalation in mice. Toxicology, 485, [153428]. https://doi.org/10.1016/j.tox.2023.153428

Vancouver

Sørli JB, Jensen ACØ, Mortensen A, Szarek J, Gutierrez CAT, Givelet L et al. Pulmonary toxicity of molybdenum disulphide after inhalation in mice. Toxicology. 2023;485. 153428. https://doi.org/10.1016/j.tox.2023.153428

Author

Sørli, Jorid B ; Jensen, Alexander C Ø ; Mortensen, Alicja ; Szarek, Józef ; Gutierrez, Claudia A T ; Givelet, Lucas ; Loeschner, Katrin ; Loizides, Charis ; Hafez, Iosif ; Biskos, George ; Vogel, Ulla ; Hadrup, Niels. / Pulmonary toxicity of molybdenum disulphide after inhalation in mice. In: Toxicology. 2023 ; Vol. 485.

Bibtex

@article{7b36ef3333db40f9a18a79dd88a5d376,
title = "Pulmonary toxicity of molybdenum disulphide after inhalation in mice",
abstract = "Molybdenum disulphide (MoS2) is a constituent of many products. To protect humans, it is important to know at what air concentrations it becomes toxic. For this, we tested MoS2 particles by nose-only inhalation in mice. Exposures were set to 13, 50 and 150 mg MoS2/m3 (=8, 30 and 90 mg Mo/m3), corresponding to Low, Mid and High exposure. The duration was 30 min/day, 5 days/week for 3 weeks. Molybdenum lung-deposition levels were estimated based on aerosol particle size distribution measurements, and empirically determined with inductively coupled plasma-mass spectrometry (ICP-MS). Toxicological endpoints were body weight gain, respiratory function, pulmonary inflammation, histopathology, and genotoxicity (comet assay). Acellular reactive oxygen species (ROS) production was also determined. The aerosolised MoS2 powder had a mean aerodynamic diameter of 800 nm, and a specific surface area of 8.96 m2/g. Alveolar deposition of MoS2 in lung was estimated at 7, 27 and 79 µg/mouse and measured as 35, 101 and 171 µg/mouse for Low, Mid and High exposure, respectively. Body weight gain was lower than in controls at Mid and High exposure. The tidal volume was decreased with Low and Mid exposure on day 15. Increased genotoxicity was seen in bronchoalveolar lavage (BAL) fluid cells at Mid and High exposures. ROS production was substantially lower than for carbon black nanoparticles used as bench-mark, when normalised by mass. Yet if ROS of MoS2 was normalised by surface area, it was similar to that of carbon black, suggesting that a ROS contribution to the observed genotoxicity cannot be ruled out. In conclusion, effects on body weight gain and genotoxicity indicated that Low exposure (13 mg MoS2/m3, corresponding to 0.8 mg/m3 for an 8-hour working day) was a No Observed Adverse Effect Concentration (NOAEC,) while effects on respiratory function suggested this level as a Lowest Observed Adverse Effect Concentration (LOAEC).",
keywords = "Humans, Mice, Animals, Molybdenum/toxicity, Reactive Oxygen Species, Soot, Respiratory Aerosols and Droplets, Lung/pathology, Bronchoalveolar Lavage Fluid/chemistry, Weight Gain, Inhalation Exposure/adverse effects, Particle Size",
author = "S{\o}rli, {Jorid B} and Jensen, {Alexander C {\O}} and Alicja Mortensen and J{\'o}zef Szarek and Gutierrez, {Claudia A T} and Lucas Givelet and Katrin Loeschner and Charis Loizides and Iosif Hafez and George Biskos and Ulla Vogel and Niels Hadrup",
note = "Copyright {\textcopyright} 2023 The Authors. Published by Elsevier B.V. All rights reserved.",
year = "2023",
doi = "10.1016/j.tox.2023.153428",
language = "English",
volume = "485",
journal = "Toxicology",
issn = "0300-483X",
publisher = "Elsevier Ireland Ltd",

}

RIS

TY - JOUR

T1 - Pulmonary toxicity of molybdenum disulphide after inhalation in mice

AU - Sørli, Jorid B

AU - Jensen, Alexander C Ø

AU - Mortensen, Alicja

AU - Szarek, Józef

AU - Gutierrez, Claudia A T

AU - Givelet, Lucas

AU - Loeschner, Katrin

AU - Loizides, Charis

AU - Hafez, Iosif

AU - Biskos, George

AU - Vogel, Ulla

AU - Hadrup, Niels

N1 - Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.

PY - 2023

Y1 - 2023

N2 - Molybdenum disulphide (MoS2) is a constituent of many products. To protect humans, it is important to know at what air concentrations it becomes toxic. For this, we tested MoS2 particles by nose-only inhalation in mice. Exposures were set to 13, 50 and 150 mg MoS2/m3 (=8, 30 and 90 mg Mo/m3), corresponding to Low, Mid and High exposure. The duration was 30 min/day, 5 days/week for 3 weeks. Molybdenum lung-deposition levels were estimated based on aerosol particle size distribution measurements, and empirically determined with inductively coupled plasma-mass spectrometry (ICP-MS). Toxicological endpoints were body weight gain, respiratory function, pulmonary inflammation, histopathology, and genotoxicity (comet assay). Acellular reactive oxygen species (ROS) production was also determined. The aerosolised MoS2 powder had a mean aerodynamic diameter of 800 nm, and a specific surface area of 8.96 m2/g. Alveolar deposition of MoS2 in lung was estimated at 7, 27 and 79 µg/mouse and measured as 35, 101 and 171 µg/mouse for Low, Mid and High exposure, respectively. Body weight gain was lower than in controls at Mid and High exposure. The tidal volume was decreased with Low and Mid exposure on day 15. Increased genotoxicity was seen in bronchoalveolar lavage (BAL) fluid cells at Mid and High exposures. ROS production was substantially lower than for carbon black nanoparticles used as bench-mark, when normalised by mass. Yet if ROS of MoS2 was normalised by surface area, it was similar to that of carbon black, suggesting that a ROS contribution to the observed genotoxicity cannot be ruled out. In conclusion, effects on body weight gain and genotoxicity indicated that Low exposure (13 mg MoS2/m3, corresponding to 0.8 mg/m3 for an 8-hour working day) was a No Observed Adverse Effect Concentration (NOAEC,) while effects on respiratory function suggested this level as a Lowest Observed Adverse Effect Concentration (LOAEC).

AB - Molybdenum disulphide (MoS2) is a constituent of many products. To protect humans, it is important to know at what air concentrations it becomes toxic. For this, we tested MoS2 particles by nose-only inhalation in mice. Exposures were set to 13, 50 and 150 mg MoS2/m3 (=8, 30 and 90 mg Mo/m3), corresponding to Low, Mid and High exposure. The duration was 30 min/day, 5 days/week for 3 weeks. Molybdenum lung-deposition levels were estimated based on aerosol particle size distribution measurements, and empirically determined with inductively coupled plasma-mass spectrometry (ICP-MS). Toxicological endpoints were body weight gain, respiratory function, pulmonary inflammation, histopathology, and genotoxicity (comet assay). Acellular reactive oxygen species (ROS) production was also determined. The aerosolised MoS2 powder had a mean aerodynamic diameter of 800 nm, and a specific surface area of 8.96 m2/g. Alveolar deposition of MoS2 in lung was estimated at 7, 27 and 79 µg/mouse and measured as 35, 101 and 171 µg/mouse for Low, Mid and High exposure, respectively. Body weight gain was lower than in controls at Mid and High exposure. The tidal volume was decreased with Low and Mid exposure on day 15. Increased genotoxicity was seen in bronchoalveolar lavage (BAL) fluid cells at Mid and High exposures. ROS production was substantially lower than for carbon black nanoparticles used as bench-mark, when normalised by mass. Yet if ROS of MoS2 was normalised by surface area, it was similar to that of carbon black, suggesting that a ROS contribution to the observed genotoxicity cannot be ruled out. In conclusion, effects on body weight gain and genotoxicity indicated that Low exposure (13 mg MoS2/m3, corresponding to 0.8 mg/m3 for an 8-hour working day) was a No Observed Adverse Effect Concentration (NOAEC,) while effects on respiratory function suggested this level as a Lowest Observed Adverse Effect Concentration (LOAEC).

KW - Humans

KW - Mice

KW - Animals

KW - Molybdenum/toxicity

KW - Reactive Oxygen Species

KW - Soot

KW - Respiratory Aerosols and Droplets

KW - Lung/pathology

KW - Bronchoalveolar Lavage Fluid/chemistry

KW - Weight Gain

KW - Inhalation Exposure/adverse effects

KW - Particle Size

U2 - 10.1016/j.tox.2023.153428

DO - 10.1016/j.tox.2023.153428

M3 - Journal article

C2 - 36641057

VL - 485

JO - Toxicology

JF - Toxicology

SN - 0300-483X

M1 - 153428

ER -

ID: 356430554