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J.Health Sci., 51(5), 597-606, 2005
Determination of Benzo[a]pyrene, Benz[a]anthracene and Dibenz[a,h]anthracene in Creosotes and Creosote-Treated Woods
Yoshiaki Ikarashi,* Masa-aki Kaniwa, and Toshie Tsuchiya
Division of Medical Devices, National Institute of Health Sciences, 1-18-1, Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan
The amount of benzo[a]pyrene (BaP), benz[a]anthracene (BaA), and dibenz[a,h]anthracene (DBA) has been restricted to a concentration of 10 mu g/g each in creosotes, and 3 mu g/g each in creosote-treated woods, respectively, because of the possibility of the risk of skin cancer in consumers, and creosotes can otherwise contain high concentrations of each chemical. We already reported the content of 16 polycyclic aromatic hydrocarbons (PAHs) and phenols in creosotes and creosote-treated wood as determined by gas chromatography-mass spectrometry (GC-MS) and absorptiometry [Chemosphere, 60, 1279-1287 (2005)]. However, the limit of determination of each PAH per sample was > 40 mu g/g according to that method, the sensitivity of which was insufficient for determining the allowable levels of these 3 compounds. Moreover, a substantial amount of time was needed for GC-MS analysis. In the present study, we improved upon our previous analytical method in order to increase the sensitivity of the test and to reduce the duration of GC-MS analysis. Creosote was extracted from treated wood samples by dichloromethane-soak incubation, and was placed on a Sep-Pak silica cartridge and eluted with dichloromethane. The eluates were evaporated and dissolved in dichloromethane. The sample solution spiked with the internal standard solution was injected into the GC-MS system. The limit of determination of each chemical in the test solution was approximately 0.2 mu g/ml, which corresponded to 1-2 mu g/g in each sample. The duration of GC-MS analysis was approximately 17 min. A collaborative study was also carried out in order to evaluate the reproducibility of the method for determining low levels of BaP and related compounds in creosotes. The present method was applied for the analysis of certain commercially available creosotes and creosote-treated wood samples in Japan. It was confirmed that some creosotes and railway sleepers contained these compounds in high concentrations, thus exceeding the allowed control value.
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