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A vast number of emerging pollutants is being detected in the environment. Another lingering problem are health-threatening contaminants, such as mycotoxins, that deteriorate food and feed.
Analytical methods, suitable for trace analysis, are needed that are desirably also fast, inexpensive and, if possible, robust, and portable. Immunoanalytical, i.e., anti-body-based technologies, which are available in a broad range of formats, can be profitably used here to analyze for the distribution and the concentration trends of contaminants.
Some of these formats are single-analyte but high-throughput methods. To use them wisely, indicator substances or sum parameters must be established to be used in screening approaches. Other methods are suitable to be performed on portable in-strumentation in the field (on-site), more precisely at the point-of-need. Furthermore, there are array technologies that allow for parallel analysis of several analytes of interest (multiplexing). The talk reports on methods and data for compounds con-sidered as anthropogenic contamination markers (the antiepileptic carbamazepine, the analgesic diclofenac, the anti-histaminic cetirizine, the steroid hormone estrone, the antimicrobial amoxicillin, the stimulants caffeine and cocaine, the endocrine disruptor bisphenol A, and a bile acid). Some work on mycotoxins (ochratoxin A and ergot alkaloids) is also presented. It is demonstrated that antibody-based technolo-gies have a huge potential to gain analytical insights at the point-of-need.
γ-Hydroxybutyric acid (GHB) is a natural metabolite, which is currently used as a date rape drug. Particularly, GHB is rapidly eliminated and its detection in realistic environments is only possible within 6-12 h after ingestion. Owing to the increasing use of GHB for criminal purposes, a need has arisen to develop simple and in situ efficient assays for its identification in aqueous and alcoholic drinks. Based on the above, we report herein an indicator displacement assay (IDA) for GHB detection that consists of a Cu2+ complex with a tetradentate ligand and the fluorescent dye coumarin 343 (IDA probe 1). Firstly, the tetradentate ligand was synthesized by reductive amination of a 1,2-cyclohexyl diamine with 2-quinoline carboxaldehyde. Subsequently, this ligand was reacted with Cu(CF3SO3)2 to obtain the corresponding copper complex, which generates the final sensing ensemble by coordinating with coumarin 343 (IDA probe 1). The sensing mechanism relies on a displacement of coumarin 343 from the sensing ensemble 1 thus restoring its fluorescence, as a consequence of the higher binding constant between GHB and complex, showing a high sensitivity in MES buffer (50 mM, pH 6.0) (detection limit of 0.03 μM). Likewise, system design and optimization led to a straightforward integration into a lateral-flow assay without further treatment or conditioning of the test strips while guaranteeing fast overall assay times of 1 min (Figure 1). In this way, IDA probe 1 was incorporated into a coated PEG-glass fibre (PEG-GF) membrane to obtain a highly robust and sensitive lateral flow assay for GHB detection in spiked alcoholic drinks with a detection limit of 0.1 μM in less than 1 min coupled to smartphone readout.