In Vitro Aerosol Exposure to Nanomaterials: From Laboratory to Environmental Field Toxicity Testing

Exposure to nanomaterials (NMs) is inevitable, requiring robust toxicological assessment to understand potential environmental and human health effects. NMs are favored in many applications because of their small size; however, this allows them to easily aerosolize and, subsequently, expose humans v...

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Veröffentlicht in:Chemical research in toxicology 2020-05, Vol.33 (5), p.1179-1194
Hauptverfasser: Tilly, Trevor B, Nelson, M. Tyler, Chakravarthy, Karthik B, Shira, Emily A, Debrose, Madeline C, Grabinski, Christin M, Salisbury, Richard L, Mattie, David R, Hussain, Saber M
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container_issue 5
container_start_page 1179
container_title Chemical research in toxicology
container_volume 33
creator Tilly, Trevor B
Nelson, M. Tyler
Chakravarthy, Karthik B
Shira, Emily A
Debrose, Madeline C
Grabinski, Christin M
Salisbury, Richard L
Mattie, David R
Hussain, Saber M
description Exposure to nanomaterials (NMs) is inevitable, requiring robust toxicological assessment to understand potential environmental and human health effects. NMs are favored in many applications because of their small size; however, this allows them to easily aerosolize and, subsequently, expose humans via inhalation. Toxicological assessment of NMs by conventional methods in submerged cell culture is not a relevant way to assess inhalation toxicity of NMs because of particle interference with bioassays and changes in particokinetics when dispersed in medium. Therefore, an in vitro aerosol exposure chamber (AEC) was custom designed and used for direct deposition of NMs from aerosols in the environment to the air–liquid interface of lung cells. Human epithelial lung cell line, A549, was used to assess the toxicity of copper, nickel, and zinc oxide nanopowders aerosolized by acoustic agitation in laboratory study. Post optimization, the AEC was used in the field to expose the A549 cells to NM aerosols generated from firing a hand gun and rifle. Toxicity was assessed using nondestructive assays for cell viability and inflammatory response, comparing the biologic effect to the delivered mass dose measured by inductively coupled plasma-mass spectrometry. The nanopowder exposure to submerged and ALI cells resulted in dose-dependent toxicity. In the field, weapon exhaust from the M4 reduced cell viability greater than the M9, while the M9 stimulated inflammatory cytokine release of IL-8. This study highlights the use of a portable chamber with the capability to assess toxicity of NM aerosols exposed to air–liquid interface in vitro lung cell culture.
doi_str_mv 10.1021/acs.chemrestox.9b00237
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