Pesticide pollution in water has been well described; however, little is known on pesticide accumulation by aquatic organisms, and to date, most studies in this line have been focused on persistent organochlorine pesticides. For this reason, a method based on QuEChERS extraction and subsequent liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed and validated for the determination of 52 medium to highly polar pesticides in fresh fish muscle. Target pesticides were selected on the basis of use and occurrence in surface waters. Quantification is carried out following an isotope dilution approach. The method developed is satisfactory in terms of accuracy (relative recovery between 71-120%), precision (relative standard deviation below 20.6%) and sensitivity (limits of determination in the pg/g or low ng/g f.w. range for most compounds). The application of the validated methodology to fish specimens collected from the Adige River (Italy) revealed the presence of trace levels of diazinon, dichlorvos and diuron, and measurable levels of metolachlor, quinoxyfen, irgarol, terbutryn, and acetamiprid, but in all cases at concentrations below the default maximum residue level of 10 ng/g established for pesticides not specifically regulated in fish. Metolachlor and quinoxyfen were both the most ubiquitous and abundant pesticides, in agreement with their high potential of bioaccumulation. Both are toxic to aquatic organisms, and therefore, their potential effects on aquatic ecosystems should be further explored.
The widespread use of pesticides in the last decades and their accumulation into the environment gave rise to major environmental and human health concerns. To address this topic, the scientific community pointed out the need to develop methodologies to detect and measure the presence of pesticides in different matrices. Biosensors have been recently explored as fast, easy, and sensitive methods for direct organophosphate pesticides monitoring. Thus, the present work aimed at designing and testing a 3D printed adapter useful on different equipment, and a membrane support to immobilize the esterase-2 from Alicyclobacillus acidocaldarius (EST2) bioreceptor. The latter is labelled with the IAEDANS, a bright fluorescent probe. EST2 was selected since it shows a high specificity toward paraoxon. Our results showed good stability and replicability, with an increasing linear fluorescent intensity recorded from 15 to 150 pmol of labelled EST2. Linearity of data was also observed when using the immobilized labelled EST2 to detect increasing amounts of paraoxon, with a limit of detection (LOD) of 0.09 pmol. This LOD value reveals the high sensitivity of our membrane support when mounted on the 3D adapter, comparable to modern methods using robotic workstations. Notably, the use of an independent support significantly simplified the manipulation of the membrane during experimental procedures and enabled it to match the specificities of different systems. In sum, this work emphasizes the advantages of using 3D printed accessories adapted to respond to the newest research needs.
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