posted on 2017-02-13, 00:00authored byHongxia Xiao, Markus Brinkmann, Beat Thalmann, Andreas Schiwy, Sigrid Große Brinkhaus, Christine Achten, Kathrin Eichbaum, Carolin Gembé, Thomas-Benjamin Seiler, Henner Hollert
Effect-directed
analysis (EDA) is a powerful strategy to identify
biologically active compounds in environmental samples. However, in
current EDA studies, fractionation and handling procedures are laborious,
consist of multiple evaporation steps, and thus bear the risk of contamination
and decreased recoveries of the target compounds. The low resulting
throughput has been one of the major bottlenecks of EDA. Here, we
propose a high-throughput EDA (HT-EDA) work-flow combining reversed
phase high-performance liquid chromatography fractionation of samples
into 96-well microplates, followed by toxicity assessment in the micro-EROD
bioassay with the wild-type rat hepatoma H4IIE cells, and chemical
analysis of bioactive fractions. The approach was evaluated using
single substances, binary mixtures, and extracts of sediment samples
collected at the Three Gorges Reservoir, Yangtze River, China, as
well as the rivers Rhine and Elbe, Germany. Selected bioactive fractions
were analyzed by highly sensitive gas chromatography–atmospheric
pressure laser ionization-time-of-flight-mass spectrometry. In addition,
we optimized the work-flow by seeding previously adapted suspension-cultured
H4IIE cells directly into the microplate used for fractionation, which
makes any transfers of fractionated samples unnecessary. The proposed
HT-EDA work-flow simplifies the procedure for wider application in
ecotoxicology and environmental routine programs.