Focused Ultrasound Solid-liquid Extraction Research Articles

Determination of polycyclic aromatic hydrocarbons, phthalate esters, alkylphenols and alkyphenol ethoxylates in sediment using simultaneous focused ultrasound solid–liquid extraction and dispersive solid-phase extraction clean-up followed by liquid chromatography

The study presents a simple and non-laborious method for the determination of 16 polycyclic aromatic hydrocarbons (PAHs), 2 phthalate esters (PEs), 2 alkylphenols (APs) and 4 alkylphenol ethoxylates (APEOs) in sediment. The method employs sample preparation combining focused ultrasound solid–liquid extraction (FUSLE) and in situ clean-up followed by liquid chromatography with fluorescence and ultraviolet detection. Extraction of 0.5 g sediment samples with 7 mL acetone in the presence of activated silica (0.5 g) and powdered copper (0.2 g) using an ultrasonic probe for 1 min resulted in recoveries of target analytes ≥ 78 %. The analytical method was classified as “acceptable green analysis” by the analytical Eco-Scale assessment (AESA) and scored 0.54 in the AGREEprep greenness assessment for sample preparation. Matrix-matched calibration was used to quantify analytes with a linear range for PAHs 2–1000 ng g–1, for PEs 100–5000 ng g–1 and for APs and APEOs 40–2000 ng g–1 dry weight. The reached limits of quantification (LOQ) for PAHs ranged from 1.1 to 3.1 ng g−1, for PEs from 122 to 124 ng g−1, for APs from 40 to 51 ng g−1 and for APEOs from 36 to 53 ng g−1. The applicability of the method was demonstrated by the analysis of real sediment samples and natural matrix certified reference material.

Multitarget and suspect screening of antimicrobials in soil and manure by means of QuEChERS — liquid chromatography tandem mass spectrometry

The present work aimed to develop an accurate analytical method for the simultaneous analysis of twenty-four antimicrobials in soil:compost and animal manure samples by means of ultra-high performance liquid chromatography coupled to a triple-quadrupole mass spectrometer (UHPLC-QqQ). For this purpose, the effectiveness of two extraction techniques (i.e. focused ultrasound solid–liquid extraction (FUSLE) and QuEChERS (quick, easy, cheap, effective, rugged and safe)) was evaluated, and the clean-up step using solid-phase extraction (SPE) was also thoroughly studied. The method was successfully validated at 10 μg·kg−1, 25 μg·kg−1, and 50 μg·kg−1 showing adequate trueness (70–130%) and repeatability (RSD < 30%), with few exceptions. Procedural limits of quantification (LOQPRO) were determined for soil:compost (0.45 to 7.50 μg·kg−1) and manure (0.31 to 5.53 μg·kg−1) samples. Pefloxacin could not be validated at the lowest level since LOQPRO ≥ 10 μg·kg−1. Sulfamethazine (7.9 ± 0.8 µg·kg−1), danofloxacin (27.1 ± 1.4 µg·kg−1) and trimethoprim (4.9 ± 0.5 µg·kg−1) were detected in soil samples; and tetracycline (56.8 ± 2.8 µg·kg−1), among other antimicrobials, in the plants grown on the surface of the studied soil samples. Similarly, sulfonamides (SAs), tetracyclines (TCs) and fluoroquinolones (FQs) were detected in sheep manure in a range of 1.7 ± 0.3 to 93.3 ± 6.8 µg·kg−1. Soil and manure samples were also analysed through UHPLC coupled to a high-resolution mass-spectrometer (UHPLC-qOrbitrap) in order to extend the multitarget method to suspect screening of more than 22,281 suspects. A specific transformation product (TP) of sulfamethazine (formyl-sulfamethazine) was annotated at 2a level in manure samples, among others. This work contributes to the efforts that have been made in the last decade to develop analytical methods that allow multitarget analysis of a wide variety of antimicrobials, including TPs, which is a complex task due to the diverse physicochemical properties of the antimicrobials.

Determination of endocrine disrupting compounds in fish liver, brain, and muscle using focused ultrasound solid-liquid extraction and dispersive solid phase extraction as clean-up strategy.

This study describes a new method for the simultaneous extraction of several endocrine disrupting compounds, including alkylphenols (APs), estrogen, bisphenol-A (BPA) and one phthalate metabolite (mono-2-ethylhexyl ester, MEHP) in fish liver, brain, and muscle. Parameters affecting the extraction (extraction solvent and temperature) and the clean-up (dispersive phase nature and amount) steps were evaluated. The extraction was performed by means of focused ultrasound solid-liquid extraction (FUSLE) using 10mL of n-hexane:acetone (50:50, v/v) for 5min at ~0°C, and the clean-up was done by means of dispersive solid phase extraction (dSPE) using 100mg of ENVI-CARB and 100mg of MgSO4 for the cleaning of brain and muscle extracts together with 100mg of PSA in the case of liver extracts. Good apparent recoveries were obtained in the case of liver (62-132%), brain (66-120%), and muscle (74-129%), relative standard deviation (RSD%) was always below 26%, and the method detection limits (MDLs) were at low ng/g level. The developed method was applied to fish captured in Urdaibai estuary (Bay of Biscay) in December 2015, and the concentrations obtained were in the range MDL-1115ng/g in brain, MDL-962ng/g in muscle, and MDL-672ng/g in liver. In general, the highest concentrations were measured in liver, followed by brain and muscle. In addition, diethylstilbestrol was only detected in fish brain. Graphical Abstract MS method scheme for the/MS method scheme for the determination of EDCs in fish liver, brain and muscle.

Determination of humic substances in sediments by focused ultrasound extraction and ultraviolet visible spectroscopy

The development of a new/fast methodology in order to determine the amount of organic matter (HSs) present in sediment samples was deeply optimized in this work. Emphasis was performed on alkaline extraction because traditional methods required high volumes and long extraction times. Focused ultrasound solid liquid extraction (FUSLE) followed by separation of HSs in acidic media and determination by means of UV–Vis turned out to be a very suitable analytical procedure to speed up HSs extraction, specifically humic acid (HA) and fulvic acid (FA). All variables affecting the extraction process (sodium hydroxide concentration and volume, ultrasound power, cycles and time) were screened by using the analysis of variance and multivariate design. These variables led optimum values of 29min, continuous application power of 95% (10cycles) and 15ml of NaOH 1moll−1. This methodology was found precise (RSD of 3.3% for HA and 3.7% for FA, for 5 determinations in 3 different days) and sensitive (LODs were 0.1μgg−1 and 0.3μgg−1 for HA and FA, respectively). Finally, the addition of Mn(II) was proven to be a good alternative to prevent the degradation of HSs in the extraction step.

Determination of plastic additives in packaging by liquid chromatography coupled to high resolution mass spectrometry

A simple and sensitive analytical method for the determination of several plastic additives in multilayer packaging based on solid-liquid extraction (SLE) and ultra-high performance liquid chromatography (UHPLC) coupled to variable wavelength (VWD) and time of flight mass spectrometry (TOF-MS) detectors is presented.The proposed method allows the simultaneous determination of fourteen additives belonging to different families such as antioxidants, slip agents and light stabilizers, as well as two oxidation products in only 9min. The developed method was validated in terms of linearity, matrix effect error, detection and quantification limits, repeatability and intermediate precision. The instrumental method showed satisfactory repeatability and intermediate precision at concentrations closed to LOQ with RSDs less than 7 and 20%, respectively, and LODs until 5000 times more sensitive than other GC-FID and HPLC-VWD methods previously reported. Also, focused ultrasound solid-liquid extraction (FUSLE) was optimized and evaluated to extract plastic additives from packaging. Extraction results obtained by FUSLE and SLE were compared to those obtained by pressurized liquid extraction (PLE). All extraction methods showed excellent extraction efficiency for slip agents, however quantitative recovery of all analytes was achieved only by SLE with just 5ml of hexane for 10h. Finally, the selected method was applied to the analysis of packaging samples where erucamide, Irgafos 168, oxidized Irgafos 168, Irganox 1076 and Irganox 1010 were detected and quantified.

Focused ultrasound solid–liquid extraction for the determination of organic biomarkers in beachrocks

Beachrocks are consolidated coastal sedimentary formations resulting mainly from the relative rapid cementation of beach sediments by different calcium carbonate polymorphs. Although previous works have already studied the elemental composition and the mineral phases composing these cements, few of them have focused their attention on the organic matter present therein. This work describes an extraction methodology based on focused ultrasound solid–liquid extraction (FUSLE), followed by analysis using large volume injection (LVI) in a programmable temperature vaporizer (PTV) combined with gas chromatography–mass spectrometry (GC–MS) in order to determine organics such as polycyclic aromatic hydrocarbons (PAHs) and biomarkers (hopanes), which can increase and confirm the information obtained so far. This goal has been achieved after the optimization of the main parameters affecting the extraction procedure, such as, extraction solvent, FUSLE variables (amplitude, extraction time and pulse time) and also variables affecting the LVI–PTV (vent time, injection speed and cryo-focusing temperature). The developed method rendered results comparable to traditional extraction methods in terms of accuracy (77–109%) and repeatability (RSD<23%). Finally, the analyses performed over real beachrock samples from the Bay of Biscay (Northern Spain) revealed the presence of the 16 EPA priority PAHs, as well as some organic biomarkers which could increase the knowledge about such beachrock formation.

Determination of caffeoylquinic acids in feed and related products by focused ultrasound solid–liquid extraction and ultra-high performance liquid chromatography–mass spectrometry

A method to determine caffeoylquinic acids (CQAs) in three sources (herbal extract, feed additive and finished feed) using for the first time focused ultrasound solid–liquid extraction (FUSLE) followed by ultra-high performance liquid chromatography (UPLC) coupled to quadrupole-time of flight mass spectrometry is presented. Pressurized liquid extraction (PLE) was also tested as extraction technique but it was discarded because cynarin was not stable under temperature values used in PLE. The separation of the CQAs isomers was carried out in only seven minutes. FUSLE variables such as extraction solvent, power and time were optimized by a central composite design. Under optimal conditions, FUSLE extraction was performed with 8mL of an 83:17 methanol–water mixture for 30s at a power of 60%. Only two extraction steps were found necessary to recover analytes quantitatively. Sensitivity, linearity, accuracy and precision were established. Matrix effect was studied for each type of sample. It was not detected for mono-CQAs, whereas the cynarin signal was strongly decreased due to ionization suppression in presence of matrix components; so the quantification by standard addition was mandatory for the determination of di-caffeoylquinic acids. Finally, the method was applied to the analysis of herbal extracts, feed additives and finished feed. In all samples, chlorogenic acid was the predominant CQA, followed by criptochlorogenic acid, neochlorogenic acid and cynarin. The method allows an efficient determination of chlorogenic acid with good recovery rates. Therefore, it may be used for screening of raw material and for process and quality control in feed manufacture.

Determination of perfluorinated alkyl acids in corn, popcorn and popcorn bags before and after cooking by focused ultrasound solid–liquid extraction, liquid chromatography and quadrupole-time of flight mass spectrometry

An analytical method is proposed to determine ten perfluorinated alkyl acids (PFAAs) [nine perfluorocarboxylic acids (PFCAs) and perfluorooctane sulfonate (PFOS)] in corn, popcorn and microwave popcorn packaging by focused ultrasound solid–liquid extraction (FUSLE) and ultra high performance liquid chromatography (UHPLC) coupled to quadrupole-time of flight mass spectrometry (QTOF-MS/MS). Selected PFAAs were extracted efficiently in only one 10-s cycle by FUSLE, a simple, safe and inexpensive technique. The developed method was validated for microwave popcorn bags matrix as well as corn and popcorn matrices in terms of linearity, matrix effect error, detection and quantification limits, repeatability and recovery values. The method showed good accuracy with recovery values around 100% except for the lowest chain length PFAAs, satisfactory reproducibility with RSDs under 16%, and sensitivity with limits of detection in the order of hundreds picograms per gram of sample (between 0.2 and 0.7ng/g). This method was also applied to the analysis of six microwave popcorn bags and the popcorn inside before and after cooking. PFCAs contents between 3.50ng/g and 750ng/g were found in bags, being PFHxA (perfluorohexanoic acid) the most abundant of them. However, no PFAAs were detected either corn or popcorn, therefore no migration was assumed.

Focused ultrasound solid–liquid extraction for the determination of perfluorinated compounds in fish, vegetables and amended soil

In the present work a method was developed for the determination of different perfluorinated compounds (PFCs), including three perfluorinated sulfonic acids (PFSAs), seven perfluorocarboxylic acids (PFCAs), three perfluorophosphonic acids (PFPAs) and perfluorooctanesulfonamide (PFOSA) in fish, vegetables and amended soil samples based on focused ultrasound solid–liquid extraction (FUSLE) followed by solid-phase extraction (SPE) clean-up and liquid chromatography–tandem mass spectrometry (LC–MS/MS). Different variables affecting the chromatographic separation (column type and pH of the mobile phase), the electrospray ionization (capillary voltage, nebulizer pressure and drying gas flow) and mass spectrometric detection (fragmentor voltage and collision energy) were optimized in order to improve the sensitivity of the separation and detection steps. In the case of FUSLE variables such as the solvent type, the solvent volume, the extraction temperature, the sonication and extraction time and the percentage of applied irradiation power were studied. Under optimized conditions, sonication of 2.5min with pulse times on of 0.8s and pulse times off of 0.2s in 7mL of (9:1) acetonitrile (ACN): water mixture in duplicate guaranteed exhaustive extraction of the matrices analyzed. Due to the non-selective extraction using FUSLE, different SPE cartridges (200-mg Waters Oasis-HLB, 150-mg Waters Oasis-WAX and 150-mg Waters Oasis-MAX) were tested in terms of extraction efficiency and matrix effect both in the extraction and detection steps. Mix mode SPE using Waters Oasis-WAX provided the best extraction efficiencies with the lowest matrix effect. The final method was validated in terms of recovery at two fortification levels (in the 80–120% for most of the analytes and matrices), precision (relative standard deviation in the 2–15% range) and method detection limits (MDLs, 0.3–12.4ng/g for vegetables, 0.2–12.5ng/g for fish and 1–22ng/g for amended soil). Finally the method was applied for the determination of the 14 PFCs in different vegetables and fish samples from a local supermarket and in a soil amended with a compost from a local wastewater treatment plant (WWTP).

Focused ultrasound assisted extraction for the determination of PBDEs in vegetables and amended soil

Focused-ultrasound solid-liquid extraction was developed for the extraction of polybrominated diphenyl ethers in vegetables and amended soil. Firstly, solid-phase extraction clean-up using 2g and 5 g of Florisil and 2-g silica cartridges were evaluated and elution profile was also optimised. Similar recoveries were obtained for most compounds while better recoveries were obtained for 5-g Florisil in the case of the heavier PBDEs. FUSLE extraction time (2 min) guaranteed quantitative extraction of the target analytes in the four studied matrices (69-130%). Method detection limit values were in the range of 1-5 ng g(-1) for splitless injection in a gas chromatograph coupled to a mass spectrometer and no significant improvement was obtained for large volume injection. Relative standard deviation values were between 1% and 30%. Recoveries obtained using FUSLE were compared with those obtained with microwave assisted extraction and the developed method was also applied to a certify reference material of polybrominated diphenyl ethers and polychlorinared biphenyls in sediment. Similar values were obtained in the case of carrot and pepper matrices (77-130% for FUSLE and 77-112% for MAE). However, MAE provided extraction recoveries higher than 100% for most of the BDE congeners in lettuce and amended soil.

Fast determination of perfluorocompounds in packaging by focused ultrasound solid–liquid extraction and liquid chromatography coupled to quadrupole-time of flight mass spectrometry

A focused ultrasound solid–liquid extraction (FUSLE) and liquid chromatography (HPLC) coupled to quadrupole-time of flight mass spectrometry (QTOF-MS/MS) based method is proposed to determine six perfluorocarboxylic acids (PFCA) and perfluorooctane sulfonate (PFOS) in food-contact packaging. FUSLE, a simple, inexpensive and fast extraction technique, has been carried out with just 8mL of ethanol in one cycle of only 10s. The whole method presented good repeatability and intermediate precision, with RSDs below 11% and 15%, respectively; limits of detection, with values between 0.5ng/g and 2.2ng/g, and successful recovery values, around 100% in all cases. The developed method has been validated and applied to the analysis of real food-contact packaging samples. FUSLE results have been compared to those obtained with pressurized liquid extraction (PLE) and no significant differences between them have been found. PFAA were detected in all the packaging samples analyzed, in a concentration range between 4ng/g and 29ng/g, being PFHpA (perfluoroheptanoic acid) the most abundant of them.

Focused ultrasound solid–liquid extraction of perfluorinated compounds from sewage sludge

A method for the determination of perfluorocarboxylic acids (PFCAs) and perfluorooctanesulfonic acid (PFOS) in sewage sludge based on focused ultrasound solid–liquid extraction (FUSLE) and reverse-phase ultra-performance liquid chromatography (UPLC) coupled to quadrupole-time of flight mass spectrometry (QTOFMS) has been developed. FUSLE is a fast, low-cost and efficient extraction technique based on the application of high power focused ultrasonic waves using a micro-tip immersed directly in the extraction mixture.For the method development, the extraction solvent was studied and afterwards the factors affecting the extraction efficiency were optimised by means of a central composite design. Optimal FUSLE conditions were: 8mL of acetonitrile as extraction solvent and an ultrasonic irradiation power of 65% for only 20s. Two extraction cycles were enough for the quantitative extraction of PFCs from sewage sludge. Limits of detection below 0.2ngg−1 (dry sewage sludge), relative standard deviation values less than 8% and recovery values between 69 and 104% were found for the target analytes. Finally, the method was applied to the analysis of sewage sludge samples from several wastewater treatment plants of La Rioja.

Focused ultrasound solid–liquid extraction and gas chromatography tandem mass spectrometry determination of brominated flame retardants in indoor dust

This study presents a focused ultrasound solid-liquid extraction (FUSLE) and gas chromatography tandem mass spectrometry method for the determination of brominated diphenyl ethers (BDEs), from mono- to hexa-congeners, in indoor dust. This approach provided a simple, fast, and economical method. After the solvent extraction selection, the FUSLE conditions were studied using a central composite design. Finally, the number of extraction cycles was studied. The selected conditions were 8mL of 3:1 n-hexane-acetone mixture as extraction solvent, at a power of 65% for 20s. The proposed method allowed accurate determination of BDEs, with recovery values around 100% and detection limits between 0.05 and 0.8ngg(-1). It also has advantages over other existing methods in terms of simplicity, analysis time, and solvent consumption. The analysis of several indoor dust samples showed high concentration values of BDEs 47, 99, 100, 153, and 154 in some of the samples, moreover, BDEs 47 and 99 were found in all samples.

Focused ultrasound solid–liquid extraction and selective pressurised liquid extraction to determine bisphenol A and alkylphenols in sewage sludge by gas chromatography–mass spectrometry

A new method for determining endocrine disrupter compounds (EDCs) in sewage sludge is described in this paper. EDCs studied were bisphenol A (BPA) and alkylphenols (APs). In order to obtain a fast and simple method, selective pressurised liquid extraction (SPLE) and focused ultrasound solid-liquid extraction (FUSLE) were tested. Best results for SPLE were obtained using Florisil as clean-up sorbent and dichloromethane as extraction solvent, while temperature was the only significant variable. Analyte extraction by SPLE was completed in only one extraction cycle of 1 min at 130 °C. FUSLE was carried out in one step of 20 s at 75% power (0.5 cycles) and with 8 mL of ethyl acetate. Although the optimised FUSLE process was faster, simpler and cheaper, SPLE provided higher recovery values (ranging from 81 to 105%) and therefore SPLE-based method was selected and validated. The SPLE and GC-MS method showed an LOD of 10.7 ng/g for BPA and LODs between 1.2 and 41.6 ng/g for APs. Relative standard deviation values lower than 6% were obtained for all analytes. As a result, an efficient, fast and simple method based on SPLE and GC-MS for the determination of BPA and APs in sewage sludge is proposed.