Simultaneous determination of base/neutral and acid herbicides in natural water at the part per trillion level

Summary A new method for the simultaneous identification and quantification of base/neutral and acidic pesticides at a low nanogram per liter concentration level in natural waters is presented. The method includes enrichment of the compounds by solid phase extraction on graphitized carbon black, followed by sequential elution of the base/neutral and acidic pesticides. Identification and quantification of the compounds is performed with HPLC-ESI-MS. This procedure involves passing 1 L of ground water and 2 L of drinking water samples through a 0.5 g graphitized carbon black (GCB) extraction cartridge. A conventional 4.6-mm-i.d. reversed phase LC C-18 operating with a 1 mL min⁻¹ flow of the mobile phase was used to chromatograph the analytes. A flow of 100 μL min⁻¹ of the column effluent was diverted to the ESI source. The ESI source was operated in positive ion mode for base/neutral pesticides and in negative-ion mode for acid pesticides. For the analyte considered, the response of the mass detector was linearly related to the amount of the analytes injected between 5 and 250 ng. In all cases, recoveries of the analytes were better than 90%. The limit of detection (signal-to-noise ratio=3) of the method for the pesticides considered in drinking water samples was estimated to be about 3–10 ng L⁻¹.     

Simultaneous solid-phase extraction of acidic, neutral and basic pharmaceuticals from aqueous samples at ambient (neutral) pH and their determination by gas chromatography-mass spectrometry

Seven polymeric solid-phase extraction (SPE) sorbents were evaluated with regard to their ability to extract acidic, neutral and basic pharmaceuticals and estrogens simultaneously from water at neutral pH. Highest recoveries (70-100%) for the majority of the analytes were obtained with styrene-methacrylate and styrene-N-vinylpyrrolidone co-polymers. The latter one (Oasis HLB) was chosen for further refinement of an extraction method for the quantitative determination of acidic and neutral drugs in surface water samples at detection limits below 1 ng/l. A sequential elution protocol was applied for clean-up and separation of the extracted analytes into fractions suitable for further compound specific processing. The neutral analytes as well as the acidic compounds after derivatisation were quantified by GC-MS. Caffeine, ibuprofen, its metabolites and diclofenac were detected in river water samples in the 1-100 ng/l range.     

Simultaneous determination of acidic,neutral and basic pharmaceuticals in urban wastewater by ultra high-pressure liquid chromatography-tandem mass spectrometry

In this work, an ultra high-pressure liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method has been developed for the simultaneous quantification and confirmation of the 20 most consumed pharmaceuticals in Spain in urban wastewater and surface water samples. The scope of the method included acidic, neutral and basic compounds belonging to different therapeutic classes and allows their simultaneous determination in just a single injection, giving realistic information of the most widely consumed pharmaceuticals in only one analysis. An enrichment step based on solid-phase extraction using Oasis HLB cartridges was carried out, followed by UHPLC-MS/MS measurement with a fast-acquisition triple quadrupole mass analyzer. It allowed working with short dwell times and made possible to acquire three simultaneous SRM transitions per compound to assure a reliable identification. Several isotope-labelled internal standards were used as surrogates to correct SPE losses, as well as matrix effects that notably affect quantification of analytes. The method was validated in surface water and effluent and influent urban wastewater at different concentrations from 0.005 μg/L (surface water) to 1.25 μg/L (influent wastewater). The optimized method was applied to the analysis of 84 urban wastewater samples (influent and effluent), with the result that 17 out of 20 compounds monitored were detected in the samples. Analgesics and anti-inflamatories, cholesterol lowering statin drugs and lipid regulators were the major groups found, with diclofenac, ketoprofen, naproxen, 4-aminoantipyrine, bezafibrate, gemfibrozil and venlafaxine being the most frequently detected. The highest concentration level reached was 277 μg/L for salicylic acid in influent wastewater.     

Simultaneous analysis of neutral and acidic pharmaceuticals as well as related compounds by gas chromatography-tandem mass spectrometry in wastewater

This work presents a new multi-residue analytical method based on solid phase extraction (SPE) with Oasis HLB sorbent, followed by gas chromatography tandem mass spectrometry (GC-MS/MS) for the simultaneous determination of a group of 10 acidic and neutral pharmaceuticals and related compounds in wastewaters. The typical derivation step was avoided, allowing the determination of acidic and neutral pollutants in a single analysis as well as providing a fast and easy method suitable for routine monitoring. Target pollutants include: anti-inflammatory drugs (ibuprofen, acetaminophen and diclofenac); an antiepileptic agent (carbamazepine); stimulants (caffeine and nicotine); an antiseptic (triclosan); a plasticizer (bisphenol A) and two of their more relevant metabolites (2,8-dichlorodibenzo-p-dioxin and 1,7-dimethylxanthine). Recoveries between 66 and 112% were achieved for all the target compounds (except for 2,8-dichlorodibenzo-p-dioxin). Good linearity was observed within the studied ranges (R² > 0.993). Acceptable intra and inter-day precision was obtained, with relative standard deviation between 2 and 18%. The application of the optimized MS/MS mode allowed method detection limits in the range of 0.2-16 ng/L, with the exception of ibuprofen (120 ng/L). Finally, the methodology was successfully applied to the analysis of hospital effluent samples. All target analytes were detected at concentrations between 1 ng/L and 83215 μg/L. Even in the absence of derivatization, all the analytes showed good peak shape, except acetaminophen, which exhibited peak tailing. However, the method proved to be repetitive and reproducible, and the peak shape did not represent a problem for the reliable quantification of this compound. For most of the analytes studied, the detection limits achieved compare well against values reported in previously published methods.     

Multiresidue fully automated online SPE-HPLC-MS/MS method for the quantification of endocrine-disrupting and pharmaceutical compounds at trace level in surface water

The present work describes the development and validation of a sensitive method for the determination of traces of diverse groups of pharmaceuticals and endocrine disruptors in surface water. Thirty-seven substances have been selected, including 10 pesticides, 6 hormonal steroids and assimilates, 12 pharmaceuticals, 5 alkylphenols, 1 chlorophenol and 3 other well-known human contaminants, 1 UV filter and 2 plasticisers. An automated online solid-phase extraction (SPE) is directly coupled to liquid chromatography–tandem mass spectrometry. Different SPE columns have been tested, and the injection volume has been optimised. The developed analytical methodology is based on the direct injection of 2.5 mL of water sample acidified at pH 1.6 on an Oasis HLB loading column (20 × 2.1 mm) with 5-µm particles. Then, the chromatographic separation is achieved on a Kinetex XB C18 (100 × 2.1 mm; 1.7 µm) column, and the quantification is realised in multiple-reaction monitoring mode. The online SPE step warrants minimal sample handling, low solvent consumption, high sample throughput, saving time and costs. This method allows the quantification of the target analytes in the lower ng/L concentration range, with limits of quantification (LQs) between 100 pg/L and 10 ng/L, 26 compounds having LQ lower than 1 ng/L. The monitoring of two selected MS/MS transitions for each compound allows the reliable confirmation of positive findings even at the LQ level. The developed and validated methodology has been applied to the analysis of various real samples from two French rivers. Twelve target compounds have been detected in the environmental samples, and the major pollutants are pharmaceuticals usually used by humans (paracetamol, carbamazepine, oxazepam, ketoprofen, trimethoprim). The pesticides atrazine and carbendazim have been ubiquitously detected in real samples too. Metronidazole, sulfamethoxazole and diuron were also frequently quantified in the water samples.     

Determination of polycyclic aromatic hydrocarbons in industrial waste water at the ng/ml. level

A combination of column, thin-layer and capillary gas chromatography was investigated as a quantitative method for determination of polycyclic aromatic hydrocarbons in industrial waste water at the 10-100 ng/ml level. The method gives 90-95% overall recovery. Analytical results for polycyclic aromatic hydrocarbons in waste water from a Norwegian aluminium plant are presented.     

Simultaneous extraction of acidic and basic drugs at neutral sample pH: A novel electro-mediated microextraction approach

The simultaneous extraction of acidic and basic analytes from a particular sample is a challenging task. In this work, electromembrane extraction (EME) of acidic non-steroidal anti-inflammatory drugs and basic β-blockers in a single step was carried out for the first time. It was shown that by designing an appropriate compartmentalized membrane envelope, the two classes of drugs could be electrokinetically extracted by a 300 V direct current electrical potential. This method required only a very short 10-min extraction time from a pH-neutral sample, with a small amount (50 μL) of organic solvent (1-octanol) as the acceptor phase. Analysis was carried out using gas chromatography–mass spectrometry after derivatization of the analytes. Extraction parameters such as extraction time, applied voltage, pH range, and concentration of salt added were optimized. The proposed EME technique provided good linearity with correlation coefficients from 0.982 to 0.997 over a concentration range of 1–200 μg L⁻¹. Detection limits of the drugs ranged between 0.0081 and 0.26 μg L⁻¹, while reproducibility ranged from 6 to 13% (n = 6). Finally, the application of the new method to wastewater samples was demonstrated.     

Simultaneous determination of acidic and non-acidic pesticides in natural waters by liquid chromatography-mass spectrometry

There is increasing interest and demand for real multi-residue methods able to simultaneously determine pesticides with a broad spectrum of chemical characteristics in environmental and biological matrices. A method based on solid-phase extraction with a Carbograph 4 cartridge and liquid chromatography with electrospray mass spectrometry (LC-ES-MS) enabling simultaneous determination of non-acidic and acidic pesticides in real water samples is described. On repeatedly (n=5) extracting 4 l of drinking water (spike level 50 ng/l), 2 l of ground water (spike level 100 ng/l) and 1 l of river water (spike level 200 ng/l), recovery of 26 base/neutral pesticides and 13 acidic pesticides were equal to or better than 80%, except for carbendazim (67%), butocarboxim (73%), aldicarb (75%) and molinate (77%). Relative standard deviations ranged between 4 and 15%. Final extracts containing acidic and non-acidic pesticides were analyzed in a single chromatographic run while the ES-MS system was operated in both positive and negative ion modes. With the aim of finding the best operating conditions, in terms of sensitivity, the pH of the LC eluent was varied in the 2.9-8.4 range. Altogether, the best results were obtained by using an LC eluent containing 1 mmol/l formic acid. Over the entire pH range considered, well shaped peaks for both basic and acidic analytes were achieved by the use of a new generation LC column. By extracting selected ion current profiles from the total ion current mass chromatogram relative to analysis of 4 l of drinking water spiked with 50 ng/l of each of the 39 analytes, estimated limits of detection ranged between 0.05 and 1.5 ng/l, except for propyzamide (8 ng/l) and 2,4-DB (3 ng/l).     

Suspect screening and target quantification of multi-class pharmaceuticals in surface water based on large-volume injection liquid chromatography and time-of-flight mass spectrometry

The ever-growing number of emerging micropollutants such as pharmaceuticals requests rapid and sensitive full-spectrum analytical techniques. Time-of-flight high-resolution mass spectrometry (TOF-HRMS) is a promising alternative for the state-of-the-art tandem mass spectrometry instruments because of its ability to simultaneously screen for a virtually unlimited number of suspect analytes and to perform target quantification. The challenge for such suspect screening is to develop a strategy, which minimizes the false-negative rate without restraining numerous false-positives. At the same time, omitting laborious sample enrichment through large-volume injection ultra-performance liquid chromatography (LVI-UPLC) avoids selective preconcentration. A suspect screening strategy was developed using LVI-UPLC-TOF-MS aiming the detection of 69 multi-class pharmaceuticals in surface water without the a priori availability of analytical standards. As a novel approach, the screening takes into account the signal-intensity-dependent accurate mass error of TOF-MS, hereby restraining 95 % of the measured suspect pharmaceuticals present in surface water. Application on five Belgian river water samples showed the potential of the suspect screening approach, as exemplified by a false-positive rate not higher than 15 % and given that 30 out of 37 restrained suspect compounds were confirmed by the retention time of analytical standards. Subsequently, this paper discusses the validation and applicability of the LVI-UPLC full-spectrum HRMS method for target quantification of the 69 pharmaceuticals in surface water. Analysis of five Belgian river water samples revealed the occurrence of 17 pharmaceuticals in a concentration range of 17 ng L^?1 up to 3.1 μg L^?1.

MEKC combined with SPE and sample stacking for multiple analysis of pesticides in water samples at the ng/L level

In this work, a new multiresidue analytical method based on MEKC with UV detection combined with SPE as off-line preconcentration strategy, and reversed-electrode polarity stacking mode (REPSM) as on-line stacking procedure, has been developed for the monitoring of 12 pesticides (carbendazim, pirimicarb, metalaxyl, pyrimethanil, procymidone, nuarimol, azoxystrobin, tebufenozide, fenarimol, benalaxyl, penconazole, and tetradifon) that are currently being used in the Canary Islands (Spain). The optimized MEKC buffer, consisting of 100 mM sodium tetraborate and 30 mM SDS at pH 8.5 with 6% v/v 1-propanol, provided baseline resolution of the 12 pesticides in less than 20 min. The developed method was applied to the analysis of mineral, stagnant, and tap water samples. The proposed SPE-REPSM-MEKC-UV method showed high extraction efficiencies with detection limits (LODs) at the low ng/L level providing LOD values down to 64 ng/L for these real samples.     

超高效液相色谱-串联质谱法同时检测地表水中18种药物与个人护理品的残留量

采用固相萃取对水样进行预处理,建立了同时检测地表水中包括抗生素、β-阻滞剂、驱蚊剂、抗癫痫药、中枢神经兴奋剂、血脂调节剂、非甾体抗炎药、杀菌消毒剂在内的18种药物与个人护理品的超高效液相色谱-串联质谱分析方法。采用中性条件萃取水样,控制上样流速为2 mL/min,用甲醇-乙腈(1:1, v/v)溶液洗脱。纯水中的平均加标回收率为53.9%～112%,相对标准偏差为2.6%～15.3%(n=6);以地表水样加标100 ng/L为样品,目标分析物平均回收率为45.1%～156.6%,相对标准偏差为2.4%～15.7%(n=6)。结果表明,本方法可同时精确检测地表水样中的18种分析物,方法验证结果表明所建立的方法可靠。用该方法分析杭州余杭塘河水,结果检出9种分析物,其中咖啡因平均质量浓度达550.7 ng/L。结果表明该方法可靠。     

Chemometric evaluation of surface water quality at regional level

Summary To reduce the volume of information needed for the evaluation of the quality of some surface waters designated for purification, data gathered in a previous study on three rivers (Simeto, Alcantara and Oreto) in Sicily have been subjected to statistical multivariate analysis. The data base comprised twentyfive variables from eight sampling points at monthly intervals for one year. Such a complex matrix cannot easily be interpreted and a statistical package have been used to put the data into a more useful form. The three adopted methods (KNN, LDA and SIMCA) gave partially different results as regarding confidence limits and basically convergent results as regarding the geographic classification of the surface waters examined. This analysis also shows that the measured variables cluster into different groups, according to their information content, and provide a reliable criterion for the choice of optimal parameters.     

Simultaneous analysis of carbamate pesticides in tap and raw water by LC/ESI/MS.

Ten carbamate pesticides including four suspected endocrine disruptors, methomyl, benomyl (carbendazim), aldicarb and carbaryl, were simultaneously analyzed by LC/ESI/MS. The influence of the matrix on the variation of the ion signal intensities of (M + H)+ and adduct ions was investigated. Although the intensities of three oxamyl ions changed depending on the matrix, the variation in the concentration calculation of oxamyl was reduced by using the sum total of the area value of two ions. The limits of the quantitation of ten pesticides without a concentration procedure were from 0.4 - 30 microg/l. The solid-phase recovery rates of ten pesticides spiked into tap water and raw water were in the range of 69-111%. Using this method, the concentrations of the pesticides in tap and raw water sampled at 14 monitoring points in Hyogo Prefecture were determined. Carbendazim in three raw water samples and carbofuran in one of these three samples were detected at low concentrations (less than 0.32 microg/l).     

Determination of four basic pharmaceuticals and one pesticide in surface water with UPLC-ESI-MS/MS

This paper describes the optimisation and validation of an ultra performance liquid chromatography- tandem mass spectrometry (UPLC-MS/MS) method for the analysis of four pharmaceuticals (flubendazole, pipamperone, rabeprazole and domperidone) and one pesticide (propiconazole) in surface water. Sample preparation was reduced substantially as compared to a previously published high performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) method, thanks to the use of UPLC. In addition, internal standards could now be used for quantification instead of the standard addition method. Extraction was performed on a Speedisk phenyl solid-phase extraction tube. A Waters Acquity HSS T3 UPLC column (100?×?2.1?mm i.d.; 1.8-µm particles) was used for separation and an API 4000 triple quadrupole was used as a detector. Total run time was 8.59 minutes. Matrix effects were examined on different surface water samples. Limits of detection and quantification in surface water samples were between 100 and 500 pg/l. Validation was performed on surface water. The method showed good precision (<15%) and accuracy (85–120%). This method is less time-consuming and labour-intensive than a previously published HPLC-procedure without compromising validation parameters.     

The effect of signal suppression and mobile phase composition on the simultaneous analysis of multiple classes of acidic/neutral pharmaceuticals and personal care products in surface water by solid-phase extraction and ultra performance liquid chromatography-negative electrospray tandem mass spectrometry

A new multi-residue method for the determination of 25 acidic/neutral pharmaceuticals (antibiotics, anti-inflammatory/analgesics, lipid regulating agents, diuretics, triazides, H2-receptor antagonists, cardiac glicozides and angiotensin II antagonists) and personal care products (sunscreen agents and preservatives) in surface water with the usage of a new technique: ultra performance liquid chromatography–negative electrospray tandem mass spectrometry (UPLC–MS/MS) was developed and validated. The novel UPLC system with 1.7 μm particle-packed column allowed for good resolution of analytes with the application of low mobile phase flow rates (0.05 mL min⁻¹) and short retention times (from 4.7 min to 13.3 min) delivering a fast and cost-effective multi-residue method. SPE with the usage of Oasis MCX strong cation-exchange mixed-mode polymeric sorbent was chosen for sample clean-up and concentration. The influence of mobile-phase composition, matrix assisted ion suppression and SPE recovery on the sensitivity of the method was identified and quantified. The instrumental limits of quantification varied from 0.2 μg L⁻¹ to 30 μg L⁻¹. The method limits of quantification were at low nanogram per litre levels and ranged from 0.3 ng L⁻¹ to 30 ng L⁻¹. The instrumental and method intra-day and inter-day repeatabilities were on average less than 5%. The method was successfully applied for the determination of PPCPs in River Taff. Thirteen compounds were determined in river water at levels ranging from a single to a few hundred nanograms per litre. Among them were ten pharmaceuticals (aspirin, salicylic acid, ketoprofen, naproxen, diclofenac, ibuprofen, mefenamic acid, furosemide, sulfasalazine and valsartan) and three personal care products (methyl- and ethylparaben and 4-benzophenone).     

Preliminary selection of clay minerals for the removal of pharmaceuticals,bisphenol A and triclosan in acidic and neutral aqueous solutions

Pharmaceuticals, personal care products and endocrine disruptors demonstrate huge potential to cause adverse ecological health effects at very low concentration in aquatic environment. There is a need to improve current purification technologies used in sewage and drinking-water treatment plants. This article aims at providing new insights into the recent development of natural and modified clay-based sorbents for the removal of aqueous contaminants such as pharmaceuticals and personal care products. The removal of six widely used pharmaceuticals: ibuprofen, diclofenac, ketoprofen, carbamazepine, as well as endocrine disrupting chemicals – bisphenol A and a bactericidal agent, triclosan – was examined by sorption onto eight adsorbents. Sorption was performed using natural and modified clay minerals – montmorillonite (Mt), vermiculite (VER), bentonite (B), kaolinite (K), commercial acid activated montmorillonites K10 and K30, and two carbonaceous-mineral nanocomposites, MtG5%T, BAlG3%C. This study showed that among the tested natural clays, vermiculite is the most promising sorbent for the removal of pharmaceuticals in purification processes. Among the modified clay minerals, the best results were achieved for carbonaceous bentonite and two acid activated montmorillonites K10 and K30. However, the removal of acidic pharmaceuticals on montomorillonite K10 and carbonaceous bentonite was strongly dependent on the pH value. In the case of vermiculite and acid-modified montmorillonite K30, the sorption of the selected compounds was not significantly affected by pH, which is crucial in wastewater treatment. The sorption constant divided by the specific surface area (K_d/A) is proposed to assess whether the surface area or chemical properties of the materials control the sorption process. K_d/A values were relatively high in the case of vermiculite, so it should be noticed that individual and specific surface properties of vermiculite were of crucial importance for sorption.     

Simultaneous determination of Cs and Sr in the high level waste by ion-chromatography

A method based on ion-chromatography has been developed for determination of Cs and Sr in high level waste (HLW) without matrix separation. The acidity of HLW (3 M HNO₃) was decreased to 0.01 M by addition of NaOH. Chromatographic separation of Cs⁺ and Sr⁺⁺ in presence of bulk Na⁺ has achieved using methane sulphonic acid as mobile phase in isocratic and gradient mode. The calibration plot was linear for the concentration range of 0.5–12 mg/L for Cs and 0.025–6 mg/L for Sr with regression coefficients close to 1. RSD obtained for Cs and Sr was 1 and 5 % respectively. Detection limit calculated as 3(S/N) was found to be 20 μg/L for Cs and 30 μg/L for Sr. The standard addition procedure was used to validate the developed method. The samples received from PREFRE, Tarapur and WIP, BARC were analyzed by the new method and the results are presented.     

Multi-residue method for the determination of basic/neutral pharmaceuticals and illicit drugs in surface water by solid-phase extraction and ultra performance liquid chromatography-positive electrospray ionisation tandem mass spectrometry

The paper presents the development and validation of a new multi-residue method for the determination of 28 basic/neutral pharmaceuticals (antiepileptics, antibacterial drugs, beta-blockers, analgesics, lipid-regulating agents, bronchodilators, histamine-2-blockers, anti-inflammatory agents, calcium channel blockers, angiotensin-II antagonists and antidepressants) and illicit drugs in surface water with the usage of a new technique: ultra performance liquid chromatography-positive electrospray tandem mass spectrometry (UPLC-MS/MS). The usage of the novel UPLC system with 1.7 microm particle size and 1mm internal diameter column allowed for low mobile phase flow rates (0.07 mL min(-1)) and short retention times (from 1.3 to 15.5 min) for all compounds analysed. As a result, a fast and cost-effective method was developed. SPE with the usage of Oasis MCX strong cation-exchange mixed-mode polymeric sorbent was chosen for pharmaceuticals extraction from environmental samples. The influence of matrix-assisted ion suppression and low SPE recovery on the sensitivity of the method was studied. The instrumental limits of quantification varied from 0.2 to 10 microg L(-1). The method limits of quantification were at low nanogram per litre levels and ranged from 0.3 to 50 ng L(-1). The instrumental and method intra- and inter-day repeatabilities were on average less than 10%. The method was applied for the determination of pharmaceuticals in Rivers Taff (UK) and Warta (Poland). Fifteen compounds were determined in river water at levels ranging from single nanograms to single micrograms per litre.     

人工神经网络-分光光度法同时测定废水中的金和钯

贵金属金和钯都能与新试剂5-（2-羟基-3,5-二甲基苯偶氮）罗丹宁（HD—PAR）形成稳定的红色络合物,由于二者吸收峰严重重叠,采用化学计量学中的人工神经网络方法实现了金和钯的同时测定,方法可用于废水中金和钯的同时测定。