posted on 2016-01-05, 00:00authored byBozo Zonja, Sandra Pérez, Damià Barceló
Wastewater and surface water samples,
extracted with four solid-phase
extraction cartridges of different chemistries, were suspect-screened
for the anticonvulsant lamotrigine (LMG), its metabolites, and related
compounds. LMG, three human metabolites, and a LMG synthetic impurity
(OXO-LMG) were detected. Preliminary results showed significantly
higher concentrations of OXO-LMG in wastewater effluent, suggesting
its formation in the wastewater treatment plants (WWTPs). However,
biodegradation experiments with activated sludge demonstrated that
LMG is resistant to degradation and that its human metabolite lamotrigine-N2-glucuronide (LMG-N2-G) is the actual source
of OXO-LMG in WWTPs. In batch reactors, LMG-N2-G was transformed,
following pseudo-first-order kinetics to OXO-LMG and LMG, but kinetic
experiments suggested an incomplete mass balance. A fragment ion search
applied to batch-reactor and environmental samples revealed another
transformation product (TP), formed by LMG-N2-G oxidation, which was
identified by high-resolution mass spectrometry. Accounting for all
TPs detected, a total mass balance at two concentration levels in
batch reactors was closed at 86% and 102%, respectively. In three
WWTPs, the total mass balance of LMG-N2-G ranged from 71 to 102%.
Finally, LMG-N2-G and its TPs were detected in surface water samples
with median concentration ranges of 23–139 ng L–1. The results of this study suggest that glucuronides of pharmaceuticals
might also be sources of yet undiscovered, but environmentally relevant,
transformation products.