Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Environmental Chemistry Environmental Chemistry Society
Environmental problems - Chemical approaches
RESEARCH ARTICLE

Determination of Selective Quinones and Quinoid Radicals in Airborne Particulate Matter and Vehicular Exhaust Particles

Athanasios Valavanidis A B , Konstantinos Fiotakis A , Thomais Vlahogianni A , Vasilios Papadimitriou A and Vayia Pantikaki A
+ Author Affiliations
- Author Affiliations

A Department of Chemistry, University of Athens, University Campus Zografou, 15784 Athens, Greece.

B Corresponding author. Email: valavanidis@chem.uoa.gr

Environmental Chemistry 3(2) 118-123 https://doi.org/10.1071/EN05089
Submitted: 16 November 2005  Accepted: 17 February 2006   Published: 5 May 2006

Environmental Context. Fine and coarse airborne particulate matter (PM) has been linked to increases in respiratory diseases and lung cancer. PM contains a variety of compounds, such as metals, polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs, and quinones adsorbed in a carbonaceous polymeric matrix. Although quinones are found in small amounts in PM, they are capable of redox cycling and in the presence of oxygen catalyse the generation of reactive oxygen species (ROS) in biological systems. ROS are responsible for the induction of oxidative stress, especially oxidative damage to cellular proteins and DNA. This paper investigated quantitatively selected quinones and hydroquinones by high performance liquid chromatography in various airborne PM samples. Also, we investigated the presence of persistent semiquinone radicals in solid samples and quinoid radicals in aqueous extracts of alkaline solution by electron paramagnetic resonance spectroscopy.

Abstract. In recent years, there has been an increasing interest in the study of the health effects of respirable particulate matter (PM) because of its deposition in the human lungs and adverse health effects. Analysis of PM content focused on substances of toxicological importance, such as polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs, aliphatic hydrocarbons, alkyl-substituted benzenes and naphthalenes, transition metals and various quinones. Recent studies shifted their attention to quinones and their toxicological role in PM. Quinones can be transformed into their semiquinones, which undergo redox cycling and reduce oxygen to produce reactive oxygen species (ROS) in biological systems, resulting in the induction of oxidative stress, especially oxidative damage to cellular components and DNA. In the present study, the presence of five quinones, 1,2-benzenediol (catechol) and 1,4-benzenediol (hydroquinone) in various PM samples was identified and measured quantitatively by high performance liquid chromatography. Mean concentrations of individual target quinones ranged from 15–140 ng mg–1 in diesel and gasoline exhaust particles to 1.5–60 ng mg–1 (or 150–1100 pg m–3) in airborne PM (total suspended particulates, PM aerodynamic diameter 10 μm, PM aerodynamic diameter 2.1 μm) samples. Precision (repeatability and reproducibility) varied from 5 to 15%. Also, examples of electron paramagnetic resonance spectra for the single broad unstructured signal are presented, corresponding to the persistent stable semiquinone radicals of solid samples of PM, and the formation of quinoid radicals in aqueous extracts of PM samples in air-saturated carbonate-buffered solution, pH 9.5–10.

Keywords. : analysis — free radicals — particulate matter — quinoid radicals — quinones


Acknowledgements

The authors wish to acknowledge the financial support of the Research Grants Committee of the University of Athens. We would like to thank the scientists of Atmospheric Pollution and Noise Control Division of Athens and Dr E. Bakeas of the Laboratory of Analytical Chemistry for their support during our sampling of airborne PM. Also, we would like to thank our anonymous reviewers for their interesting and stimulating comments and suggestions concerning the quinoid radicals of PM and the chromatographic details.


References


[1]   R. P. Peng, F. Dominici, R. Pastor-Barriuso, S. L. Zeger, J. M. Samet, Am. J. Epidemol. 2005, 161,  585.
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         open url image1