Details

Autor(en) / Beteiligte

• Suzuki, Toshinari
• Kosugi, Yuki
• Hosaka, Mitsugu
• Nishimura, Tetsuji
• Nakae, Dai

Titel

Occurrence and behavior of the chiral anti-inflammatory drug naproxen in an aquatic environment

Ist Teil von

• Environmental toxicology and chemistry, 2014-12, Vol.33 (12), p.2671-2678

Ort / Verlag

Pensacola, FL: Blackwell Publishing Ltd

Erscheinungsjahr

2014

Quelle

Wiley-Blackwell Journals

Beschreibungen/Notizen

• The present study reports on the occurrence and chiral behavior of the anti‐inflammatory drug (S)‐naproxen (NAP)—(S)‐2‐(6‐methoxynaphthalen‐2‐yl)propionic acid—in an aquatic environment under both field and laboratory conditions. In influents and effluents of sewage treatment plants (STPs) in the Tama River basin (Tokyo), (S)‐NAP was detected at concentrations of 0.03 µg L−1 to 0.43 µg L−1 and 0.01 µg L−1 to 0.11 µg L−1, respectively. The concentrations of a major metabolite, 6‐O‐desmethyl NAP (DM‐NAP) were up to 0.47 µg L−1 and 0.56 µg L−1 in influents and effluents, respectively. (R)‐naproxen was not detected in STP influents, although it was present in effluents, and the enantiomeric faction (= S/[S + R]) of NAP ranged from 0.88 to 0.91. Under laboratory conditions with activated sludge from STPs, rapid degradation of (S)‐NAP to DM‐NAP and chiral inversion of (S)‐NAP to (R)‐NAP were observed. During river die‐away experiments, degradation and chiral inversion of NAP were extremely slow. In addition, chiral inversion of (S)‐NAP to (R)‐NAP was not observed during photodegradation experiments. In the river receiving STP discharge, NAP and DM‐NAP concentrations reached 0.08 µg L−1 and 0.16 µg L−1, respectively. The enantiomeric faction of NAP in the river ranged from 0.84 to 0.98 and remained almost unchanged with the increasing contribution of rainfall to the river water. These results suggest that the absence and decrease of (R)‐NAP in river waters could indicate the inflow of untreated sewage. Environ Toxicol Chem 2014;33:2671–2678. © 2014 SETAC