Abstract

A rapid sample preparation fabric phase sorptive extraction (FPSE) methodology followed by gas chromatography coupled to tandem mass spectrometry is proposed for the first time to determine 12 synthetic musks including nitro-, polycyclic and macrocyclic musk in environmental water and wastewater. An asymmetric screening design of experiments was used to evaluate the influence of nine parameters affecting FPSE in only 16 experiments. The factors included the sol–gel sorbent coating, stirring mode (both extraction and desorption), extraction and desorption time, salting-out effect, sample volume, type of solvent, and desorption solvent volume. The selected conditions imply the use of the sol–gel PDMS sorbent coating, 15 min extraction by ultrasound energy employing 10 mL of sample and 0.5 mL of ethanol as desorption solvent during 5 min. Accuracy and precision were assessed in different real water samples. Matrix effects were evaluated performing recovery studies in several aqueous matrices: river, sea, spring, laundry washing place, and wastewater at different concentration levels (0.1, 2, 10 µg L−1) demonstrating method accuracy (results ranged between 82 and 110%) and good precision (relative standard deviation, RSD < 12% in all cases). Limits of detection (LODs) were below 8 ng L−1 for the analyzed synthetic musks. As extraction was quantitative (exhaustive extraction), calibration was carried out using solvent standards without the need of repeating the extraction step, which is required in most microextraction methods, improving sample throughput, and reducing costs. Finally, the analysis of real contaminated samples revealed the presence of 11 out of the 12 target synthetic musks at concentrations up to 30 µg L−1, three of them banned in cosmetic regulation (musk tibetene, ambrette, and moskene). The developed FPSE based methodology uses low volume (0.5 mL) of a Generally Recognized as Safe (GRAS) solvent (ethanol), as well as minimum energy and time consumption, demonstrating to be a sustainable alternative to detect these microcontaminants in environmental waters and wastewaters.

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