Fate and partitioning of selected pharmaceuticals in aquatic environment
Hiroshi Yamamoto1, Akihide Hayashi, Yuki Nakamura
1Department of Mathematical and Natural Sciences, Faculty of Integrated Arts and Sciences, The University of Tokushima, 1-1 Minamijosanjima-cho, Tokushima, 770-8502, Japan. hiroshi@ias.tokushima-u.ac.jp
Abstract:
Two nonsteroidal anti-inflammatory drugs (NSAIDs), ibuprofen and acetaminophen, a beta-blocker atenolol, and an antidepressant fluoxetine were selected, and their sorption coefficients (Koc values) on the basis of dissolved organic matter (DOM) and model sediments were determined. The highest values were found for fluoxetine for both DOM and sediments, followed by atenolol or ibuprofen. These Koc values were comparable to those of pyrene and 17beta-estradiol, a nonpolar four-ring polycyclic aromatic hydrocarbon and a polar natural estrogen, respectively. For these four pharmaceuticals, partition coefficients between synthetic membrane vesicles (liposomes) and water (Klipw values), and removal efficiencies for a simple batch activated sludge treatment were also determined. The highest Klipw values were again found for fluoxetine followed by atenolol. The removal efficiency for a 6-hour batch activated sludge treatment was over 90% for the two NSAIDs whereas that for atenolol was as low as 10%; both agreed with the results obtained in conventional studies, which showed the concentration in the influent and effluent of sewage treatment plants. The removal efficiency for fluoxetine was also over 90%, but it was sorbed by sludge and not biodegraded.
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