Chemical and Biological Characterization of Particulate Matter (PM 2.5) and Volatile Organic Compounds Collected at Different Sites in the Los Angeles Basin
Authors:
- Arthur K. ChoACArthur K. Cho
- Yasuhiro ShinkaiYSYasuhiro Shinkai
- Debra A. SchmitzDSDebra A. Schmitz
- Emma Di StefanoESEmma Di Stefano
- Arantza Eiguren-FernandezAEArantza Eiguren-Fernandez
- Aline Lefol Nani GuarieiroAGAline Lefol Nani Guarieiro
- Erika M. SalinasESErika M. Salinas
- John R. FroinesJFJohn R. Froines
- William P. MelegaWMWilliam P. Melega
Open Access
- 7 May 2020
- journal article
- research article
- Published by MDPI AG in Applied Sciences
- Vol. 10 (9) , 3245
Abstract
Background: Most studies on air pollution (AP) exposure have focused on adverse health effects of particulate matter (PM). Less well-studied are the actions of volatile organic compounds (VOCs) not retained in PM collections. These studies quantified chemical and biological properties of both PM2.5 and VOCs. Methods: Samples were collected near the Port of Los Angeles (Long Beach, LB), railroads (Commerce, CM), and a pollution-trapping topography-site (San Bernardino, SB). Quantitative assays were conducted: (1) chemical—prooxidant and electrophile content, (2) biological—tumor necrosis factor-α (TNF-α) and heme oxygenase-1 (HO-1) expression (3), VOC modulation of PM effects and (4), activation of the antioxidant response element (ARE) using murine RAW 264.7 macrophages. Results: SB site samples were the most potent in the chemical and biological assays, followed by a CM railroad site. Only PM2.5 exhibited significant proinflammatory responses. VOCs were more potent than PM2.5 in generating anti-inflammatory responses; further, VOC pretreatment reduced PM-associated TNF-α expression. VOCs significantly increased ARE activation compared to their corresponding PM2.5 which remained at background levels. Conclusion: Ambient VOCs are major contributors to adaptive responses that can modulate PM effects, in vitro, and, as such, need to be included in comprehensive assessments of AP.Keywords
Funding Information
- Fogarty International Center (NIH Research Grant # D43TW000623)
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