Abstract
The biodegradability of the anticonvulsant pregabalin (PGB) was studied in laboratory incubation experiments in contact with water/sediment systems under different redox conditions. PGB was degraded by biological processes under aerobic conditions reaching half-lives of 8 to 10 d, while inactivated and anaerobic control experiments revealed no significant decrease of PGB concentrations. Within experiments spiked with elevated PGB concentrations, 12 TPs were formed and tentative chemical structures could be proposed by accurate masses and fragmentation pathways detected via measurements with high resolution mass spectrometry (LC-QToF-MS). Four of the proposed TPs were finally confirmed either by authentic reference standards (PGB-Lactam, ISA, TP 157-A (II)) or a self-synthesized standard (NA-PGB). PGB-Lactam was identified as the quantitatively most relevant TP formed via intramolecular cyclization under aerobic conditions, reaching up to 33% of the initial PGB concentration. Incubation experiments spiked with PGB-Lactam revealed three times higher half-lives compared to the parent compound, indicating that PGB-Lactam is more stable than PGB. A comparison with results gained from water/sediment incubation experiments with the structurally related compound gabapentin (GBP) revealed, that the transformation behaviour can be mainly extrapolated to PGB. Most of the observed transformation reactions found for PGB were comparable to the ones found for GBP. The TPs PGB-Lactam and NA-PGB as well as three GBP TPs (GBP-Lactam, NA-GBP and CCHA) have been detected in German wastewater treatment plants (WWTPs) effluents and the river Rhine including some of its tributaries such as Main, Neckar, Moselle and Aare. Moreover, GBP and PGB as well as some of their TPs were detected in German bank filtrates and finished drinking waters up to 260 ng L-1. For that reason these compounds should be monitored in drinking water in the future.
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