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In vivo tracking of toxic diesel particulate matter in mice using radiolabeling and nuclear imaging
  • Park, Jung Eun ;
  • Lee, Jun Young ;
  • Chae, Jungho ;
  • Min, Chang Ho ;
  • Shin, Hee Soon ;
  • Lee, So Young ;
  • Lee, Jae Young ;
  • Park, Jeong Hoon ;
  • Jeon, Jongho
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Publication Year
2023-02-01
Publisher
Elsevier Ltd
Citation
Chemosphere, Vol.313
Keyword
BiodistributionDiesel particulate matterPositron emission tomography imagingRadiolabelingToxicological study
Mesh Keyword
Adverse health effectsBiodistributionsDiesel particulate mattersIn-vivoIntratrachealNuclear imagingPositron emission tomography imagingRadiolabellingTomography imagingToxicological studyAnimalsInhalation ExposureLungMiceMolecular ImagingParticulate MatterVehicle Emissions
All Science Classification Codes (ASJC)
Environmental EngineeringEnvironmental ChemistryChemistry (all)PollutionPublic Health, Environmental and Occupational HealthHealth, Toxicology and Mutagenesis
Abstract
Exposure to diesel particulate matter (DPM) is associated with several adverse health effects, including severe respiratory diseases. Quantitative analysis of DPM in vivo can provide important information on the behavior of harmful chemicals, as well as their toxicological impacts in living subjects. This study presents whole-body images and tissue distributions of DPM in animal models, using molecular imaging and radiolabeling techniques. The self-assembly of the 89Zr-labeled pyrene analog with a suspension of DPM efficiently produced 89Zr-incorporated DPM (89Zr-DPM). Positron emission tomography images were obtained for mice exposed to 89Zr-DPM via three administration routes: intratracheal, oral, and intravenous injection. DPM was largely distributed in the lungs and only slowly cleared after 7 days in mice exposed via the intratracheal route. In addition, a portion of 89Zr-DPM was translocated to other organs, such as the heart, spleen, and liver. Uptake values in these organs were also noticeable following exposure via the intravenous route. In contrast, most of the orally administered DPM was excreted quickly within a day. These results suggest that continuous inhalation exposure to DPM causes serious lung damage and may cause toxic effects in the extrapulmonary organs.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/33098
DOI
https://doi.org/10.1016/j.chemosphere.2022.137395
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Type
Article
Funding
This work was supported by the National Research Foundation of Korea (Grant number: 2022R1A2C1003577 ), a research grant from the Korea Food Research Institute (Grant number: E0210200-01 ) and Nuclear R&D Program of Ministry of Science and ICT (Grant number: 1711174197 ).
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Lee, Jae Young 이재영
Department of Environmental and Safety Engineering
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