Literature DB >> 17886044

Comparative toxicity of size-fractionated airborne particulate matter obtained from different cities in the United States.

M Ian Gilmour1, John McGee, Rachelle M Duvall, Lisa Dailey, Mary Daniels, Elizabeth Boykin, Seung-Hyun Cho, Donald Doerfler, Terry Gordon, Robert B Devlin.   

Abstract

Hundreds of epidemiological studies have shown that exposure to ambient particulate matter (PM) is associated with dose-dependent increases in morbidity and mortality. While early reports focused on PM less than 10 microm (PM10), numerous studies have since shown that the effects can occur with PM stratified into ultrafine (UF), fine (FI), and coarse (CO) size modes despite the fact that these materials differ significantly in both evolution and chemistry. Furthermore the chemical makeup of these different size fractions can vary tremendously depending on location, meteorology, and source profile. For this reason, high-volume three-stage particle impactors with the capacity to collect UF, FI, and CO particles were deployed to four different locations in the United States (Seattle, WA; Salt Lake City, UT; Sterling Forest and South Bronx, NY), and weekly samples were collected for 1 mo in each place. The particles were extracted, assayed for a standardized battery of chemical components, and instilled into mouse lungs (female BALB/c) at doses of 25 and 100 microg. Eighteen hours later animals were euthanized and parameters of injury and inflammation were monitored in the bronchoalveolar lavage fluid and plasma. Of the four locations, the South Bronx coarse fraction was the most potent sample in both pulmonary and systemic biomarkers, with a strong increase in lung inflammatory cells as well as elevated levels of creatine kinase in the plasma. These effects did not correlate with lipopolysaccharide (LPS) or total zinc or sulfate content, but were associated with total iron. Receptor source modeling on the PM2.5 samples showed that the South Bronx sample was heavily influenced by emissions from coal fired power plants (31%) and mobile sources (22%). Further studies will assess how source profiles correlate with the observed effects for all locations and size fractions.

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Year:  2007        PMID: 17886044     DOI: 10.1080/08958370701490379

Source DB:  PubMed          Journal:  Inhal Toxicol        ISSN: 0895-8378            Impact factor:   2.724


  27 in total

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4.  Differential pulmonary effects of wintertime California and China particulate matter in healthy young mice.

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5.  The effect of particle size, location and season on the toxicity of urban and rural particulate matter.

Authors:  Jaime Mirowsky; Christina Hickey; Lori Horton; Martin Blaustein; Karen Galdanes; Richard E Peltier; Steven Chillrud; Lung Chi Chen; James Ross; Arthur Nadas; Morton Lippmann; Terry Gordon
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6.  Hospital admissions and chemical composition of fine particle air pollution.

Authors:  Michelle L Bell; Keita Ebisu; Roger D Peng; Jonathan M Samet; Francesca Dominici
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7.  Mouse lung inflammation after instillation of particulate matter collected from a working dairy barn.

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Journal:  Toxicol Appl Pharmacol       Date:  2009-03-09       Impact factor: 4.219

8.  Variation in the composition and in vitro proinflammatory effect of urban particulate matter from different sites.

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Journal:  J Biochem Mol Toxicol       Date:  2013-01       Impact factor: 3.642

9.  Pulmonary inflammatory effects of source-oriented particulate matter from California's San Joaquin Valley.

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10.  Comparative toxicity of size-fractionated airborne particulate matter collected at different distances from an urban highway.

Authors:  Seung-Hyun Cho; Haiyan Tong; John K McGee; Richard W Baldauf; Q Todd Krantz; M Ian Gilmour
Journal:  Environ Health Perspect       Date:  2009-06-29       Impact factor: 9.031

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