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In this study, an innovative and high-throughput parallel-single-drop microextraction (Pa-SDME) using the [P6,6,6,14+]2[MnCl42−] magnetic ionic liquid (MIL) as extraction phase is demonstrated, for the first time, in the determination of methylparaben, ethylparaben, propylparaben, bisphenol A, butylparaben, benzophenone and triclocarban from environmental aqueous samples. This experimental setup comprised of a 96-well plate system containing a set of magnetic pins which aided in stabilizing the MIL drops and enabled the simultaneous extraction of up to 96 samples. Using this low-cost experimental apparatus, the sample throughput was lower than 1 min per sample. This novel approach exhibits a number of advantages over classical SDME approaches, particularly in maintaining a stable solvent microdrop and facilitating highthroughput analysis. Experimental conditions were carefully optimized using one-factor-at-a-time and multivariate designs. The optimal conditions employed 5.38 ± 0.55 mg (n = 10) of MIL, a sample volume of 1.5 mL at pH 6, and dilution in 20 μL of acetonitrile. The analytical parameters of merit were determined under the optimized conditions and highly satisfactory results were achieved, with LODs ranging from 1.5 to 3 μg L−1 and coefficients of determination higher than 0.994. Intraday and interday precision ranged from 0.6 to 21.3% (n = 3) and 10.4-20.2% (n = 9), respectively, with analyte relative recovery in three aqueous samples ranging between 63% and 126%.

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A novel in vivo design was used in combination with solid-phase microextraction (SPME) and gas chromatography/mass spectrometry (GC/MS) to characterize the volatile compounds from the skin secretion of two species of tree frogs. Conventional SPME-GC/MS also was used for the analysis of volatiles present in skin samples and for the analysis of volatiles present in the diet and terraria. In total, 40 and 37 compounds were identified in the secretion of Hypsiboas pulchellus and H. riojanus, respectively, of which, 35 were common to both species. Aliphatic aldehydes, a low molecular weight alkadiene, an aromatic alcohol, and other aromatics, ketones, a methoxy pyrazine, sulfur containing compounds, and hemiterpenes are reported here for the first time in anurans. Most of the aliphatic compounds seem to be biosynthesized by the frogs following different metabolic pathways, whereas aromatics and monoterpenes are most likely sequestered from environmental sources. The characteristic smell of the secretion of H. pulchellus described by herpetologists as skunk-like or herbaceous is explained by a complex blend of different odoriferous components. The possible role of the volatiles found in H. pulchellus and H. riojanus is discussed in the context of previous hypotheses about the biological function of volatile secretions in frogs (e.g., sex pheromones, defense secretions against predators, mosquito repellents).

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In this study, a rapid and straightforward approach based on magnetic ionic liquids (MIL) as extraction phases and dispersive liquid-liquid microextraction (DLLME) was developed to analyze the hormones estriol, 17-β-estradiol, 17-α-ethynylestradiol, and estrone in human urine samples. This is the first report of an application of manganese-based MILs compatible with HPLC to extract compounds of biological interest from urine samples. The hydrophobic MILs trihexyltetradecylphosphonium tetrachloromanganate (II) ([P][MnCl]) and aliquat tetrachloromanganate (II) ([Aliquat][MnCl]) were employed and the optimized extraction conditions were comprised of 5 mg of MIL ([P][MnCl]), 5 μL of methanol (MeOH) as disperser solvent, and an extraction time of 90 s at sample pH 6. The analytical parameters of merit were determined under optimized conditions and very satisfactory results were achieved, with LODs of 2 ng mL for all analytes, determination coefficients (R) ranging from 0.9949 for 17-β-estradiol to 0.9998 for estrone. In addition, good results of method precision were achieved with the intraday (n = 3) varying from 4.7% for 17-β-estradiol to 19.5% for estriol (both at 5 ng mL) and interday precision (evaluated at 100 ng mL) ranging from 11.4% for estrone to 17.7% for 17-α-ethynylestradiol and analyte relative recovery evaluated in three real samples ranged from 67.5 to 115.6%. The proposed DLLME/MIL-based approach allowed for a reliable, environmentally friendly and high-throughput methodology with no need for a centrifugation step. Graphical abstract An overview of the rapid and straightforward extraction procedure using DLLME/MIL-based approach.