Off-line Solid-phase Extraction Research Articles

Exploration of novel solid-phase extraction modes for analysis of multiclass emerging contaminants

Solid-phase extraction (SPE) has gained an essential role in environmental analytical chemistry. Classic off-line SPE coupled with LC-MS/MS systems creates powerful analytical procedures for ultratrace analysis of contaminants of emerging concern (CECs) in water. But, being associated with tedious work and large consumption of materials, alternative SPE modes are becoming interesting. As so, the study focuses on development, evaluation, and overall comparison of established and novel SPE modes. Off-line SPE, dispersive micro SPE (DMSPE), and ‘fast’ single-pump on-line SPE were explored, using commercially available sorbents. Their efficiency was evaluated on their performance in water analysis of 20 multiclass CECs.Hydrophilic-lipophilic sorbent and mixture of C18/C8 sorbents were the best choice for off-line and DMSPE, respectively. All optimized SPE modes coupled with UHPLC-MS/MS reached environmentally-relevant limits of detection (LODs 0.1−12 ng L‒1), acceptable repeatability (< 20% RSD), and exhibited less than ±30% matrix effects in real river water sample. Among all, on-line SPE showed a potential to fully replace the well-established off-line SPE and even improve analytical performance. This was due to the best repeatability (< 10% RSD), automatization, simplicity, the highest multiplexing capacity, as well as com-parable LODs of < 2 ng L‒1. DMSPE is, on the other hand, the most innovative and could be seen as a quick and green alternative to off-line SPE for determination of semi- to non-polar CECs, but within sub-10 ng L‒1 range.Overall, the study shows workflow for the exploration of important and promising sample pretreatment techniques in water analysis. Comparison of the developed three SPE-UHPLC-MS/MS methods suggests that alternative SPE modes can compete with the well-established off-line SPE and can even improve the analysis quality if properly applied.

Performance critical comparison of offline SPE, online SPE, and direct injection for the determination of CECs in complex liquid environmental matrices

Sample preparation for the analysis of organic micropollutants in wastewater samples is commonly carried out by solid-phase extraction (SPE) procedures, which involve different manual laboratory operations. This conventional approach requires several hours of counter labour and entail the use of a lot of disposable material, and the subsequent contaminated non-recyclable plastic-residue production. In contrast, by coupling and automatizing the pre-treatment to the instrumental analysis most of that burden erases, sample size gets miniaturized and, thus, storage becomes freed-up. Even lab counters get cleared off from sample pre-treatment apparatus. However, method performance could get alter as a trade-off. This paper presents the results from a study in which methodology, including SPE online-coupled to UHPLC-MS/MS chromatography, was developed for multi-residue (58) determination of veterinary and pharmaceutical drugs in urban and piggery wastewater (influent and effluent to wastewater treatment plants (WWTPs)). Similarly, the direct injection (DI) of large volumes (hundreds of µL) of same matrix samples into the chromatographic system was optimized too. The performance of both automated methods was statistically compared with the classical off-line SPE. As dealing with trace analysis, suitable injection volumes for the alternative approaches were selected on the premise of low limits of quantification (MLQs). Under the selected conditions, validation parameters such as linearity range, method quantification limits, peak shape and carry over were determined. Usually more than 50 % of the analytes showed MLQs below 50 ng/L, for all matrices and methodologies, especially for DI. Real wastewater samples from a local urban WWTP and farm were analysed with all three tested methodologies. Determined concentrations and removal rates were statistically compared and turned out being quite similar. However, analysis under offline SPE and DI approaches provided a larger amount of information as they reached lower MLQs. Offline-SPE provided the worst precision among all.

Design and Validation of a Sensitive Multisteroid LC-MS/MS Assay for the Routine Clinical Use: One-Step Sample Preparation with Phospholipid Removal and Comparison to Immunoassays.

Steroid analysis in clinical laboratories is dominated by immunoassays (IAs) that have a high sample turnover but are inherently limited in trueness, precision, and sensitivity. Liquid chromatography coupled to mass spectrometry (LC-MS/MS) has proved to be a far more capable tool, delivering better sensitivity, specificity, and the possibility of parallel analysis of multiple steroids and metabolites, providing the endocrinologist with more reliable and comprehensive diagnostic information. An LC-MS/MS assay with gradient elution over less than eight minutes and a one-step sample preparation combining protein precipitation with phospholipid removal of off-line solid-phase extraction was developed and validated. It allowed the quantification of 11-deoxycorticosterone (11-DOC), 11-deoxycortisol (11-DF), 17-OH-progesterone (17P), 21-deoxycortisol (21-DF), androstenedione (ANDRO), aldosterone (ALDO), corticosterone (CC), cortisol (CL), cortisone (CN), dehydroepiandrosterone (DHEA), dehydroepiandrosterone sulfate (DHEAS), dihydrotestosterone (DHT), estradiol (E2), progesterone (PROG), and testosterone (TES) in human serum. Interday imprecision was generally better than 15%, trueness was proven by recovery experiments with ISO 17034-certified reference materials, proficiency testing (UK NEQAS), and measuring serum reference standards. In-house comparison against IVD-CE-certified immunoassays (IA) for 17P, ANDRO, CL, DHEAS, E2, PROG, and TES was conducted by assessing leftover routine patient samples and purpose-built patient serum pools. None of the compared routine IAs were meeting the standards of the LC-MS/MS. Insufficient overall comparability was found for ANDRO and 17P (mean bias > +65%). Accuracy limitations at lower concentrations were present in IAs for PROG, E2, and TES.

Detection, occurrence, influencing factors and environmental risks of paralytic shellfish toxins in seawater in a typical mariculture bay

Paralytic shellfish toxins (PSTs) producing algae are widely distributed in the global coastal aquatic environment, posing a threat to coastal ecosystem health and mariculture safety. However, the levels and potential environmental risks of PSTs frequently detected in shellfish remain largely unexplored in seawater of mariculture zones. In this study, a new method for trace detection of 13 common PSTs (<1.0 ng/L) in seawater was established based on off-line solid phase extraction (SPE) and on-line SPE-liquid chromatography-tandem mass spectrometry (on-line SPE-LC-MS/MS), and a systematic investigation of PSTs in seawater of the Laizhou Bay, a typical aquaculture bay in China, was conducted to understand their pollution status, environmental impact factors and ecological risks for the first time. Eleven PSTs were detected in the seawater of Laizhou Bay with total concentrations ranging from 0.75 to 349.47 ng/L (mean, 176.27 ng/L), which indicates the rich diversity of PSTs in the mariculture bay and demonstrates the reliability of the proposed analytical method. C1, C2, GTX2, GTX3, dcGTX2, and dcGTX3 were found to be the predominant PSTs, which refreshed the knowledge of PST contamination in the coastal aquatic environment. PST levels in seawater exhibited the highest levels in the southeastern mouth of Laizhou Bay and decreased toward the inner bay. Correlation analyses showed that climatic factors, nutrient status and hydrological conditions had significant effects on the distribution of PST in mariculture bay. Preliminary environmental risk assessments revealed that aquatic organisms throughout the waters of Laizhou Bay are at risk of chronic PST toxicity. These findings imply that the risk of PST in seawater of mariculture bay has previously been grossly underestimated, and that the coastal aquatic environment in North China and even the world may be at more serious risk of PST pollution, which should be taken seriously.

Off-Line SPE LC-LRMS Polyphenolic Fingerprinting and Chemometrics to Classify and Authenticate Spanish Honey.

The feasibility of non-targeted off-line SPE LC-LRMS polyphenolic fingerprints to address the classification and authentication of Spanish honey samples based on both botanical origin (blossom and honeydew honeys) and geographical production region was evaluated. With this aim, 136 honey samples belonging to different botanical varieties (multifloral and monofloral) obtained from different Spanish geographical regions with specific climatic conditions were analyzed. Polyphenolic compounds were extracted by off-line solid-phase extraction (SPE) using HLB (3 mL, 60 mg) cartridges. The obtained extracts were then analyzed by C18 reversed-phase LC coupled to low-resolution mass spectrometry in a hybrid quadrupole-linear ion trap mass analyzer and using electrospray in negative ionization mode. Principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA) were employed to assess the pattern recognition capabilities of the obtained fingerprints to address honey classification and authentication. In general, a good sample discrimination was accomplished by PLS-DA, being able to differentiate both blossom-honey and honeydew-honey samples according to botanical varieties. Multiclass predictions by cross-validation for the set of blossom-honey samples showed sensitivity, specificity, and classification ratios higher than 60%, 85%, and 87%, respectively. Better results were obtained for the set of honeydew-honey samples, exhibiting 100% sensitivity, specificity, and classification ratio values. The proposed fingerprints also demonstrated that they were good honey chemical descriptors to deal with climatic and geographical issues. Characteristic polyphenols of each botanical variety were tentatively identified by LC-MS/MS in multiple-reaction monitoring mode to propose possible honey markers for future experiments (i.e., naringin for orange/lemon blossom honeys, syringic acid in thyme honeys, or galangin in rosemary honeys).

Composite Nanofibers as Novel Sorbents for On-Line and Off-Line Solid-Phase Extraction in Chromatographic System: A Comparison for Detection of Free Biogenic Monoamines and Their Metabolites in Plasma.

Two different pretreatment approaches have been used for the enrichment and separation of biogenic monoamines and metabolites in plasma for high performance liquid chromatography (HPLC) determination. The first approach, based on on-line packed-fiber solid-phase extraction (PFSPE) coupled with HPLC, allows for the simultaneous detection of epinephrine (E), norepinephrine (NE), dopamine (DA), 3-methoxyl epinephrine (MN), norepinephrine (NMN), 3-methoxytyramine (3-MT), and 5-hydroxytryptamin (5-HT). Using this developed on-line PFSPE–HPLC method, the limit of detections (LODs) of the seven analytes ranged from 1 ng/mL (NMN and MN) to 2 ng/mL (NE, E, DA, 3-MT and 5-HT). The reportable ranges were 5–300 ng/mL for NE and DA, 5–100 ng/mL for E, and 5–200 ng/mL for NMN, MN, 3-MT and 5-HT. The off-line PFSPE–HPLC was employed in the second approach and could provide simultaneous detection of NE, E, DA, NMN, and MN. The linearity was verified in the range of 0.5–20 ng/mL (NE, E, and DA) and 20–250 ng/mL (NMN and MN). The LODs of the five analytes ranged from 0.2 ng/mL (NE, E, and DA) to 5 ng/mL (NMN and MN). This study verified the possibility of using nanofibers as an adsorbent in an on-line PFSPE–HPLC system for the determination of biogenic monoamines and their metabolites in human plasma. Compared with the off-line PFSPE approach, the on-line PFSPE method deserves attention mainly due to its greener character, derived from the automation of the process and high-throughput with less operators’ handling.

Trace determination of multiple hydrophilic cyanotoxins in freshwater by off- and on-line solid phase extraction coupled to liquid chromatography-tandem mass spectrometry

Hydrophilic cyanotoxins (HCTs), such as paralytic shellfish toxins (PSTs), anatoxin-a (ATX-a), and cylindrospermopsin (CYN) are highly toxic and toxin-producing algae are widely distributed worldwide. However, HCTs, especially PSTs, are rarely reported in freshwater due to analytical limitations. This may result in an underestimation of the ecological risks and health risks. This study developed a new method to detect ATX-a, CYN, and thirteen common PSTs in freshwater simultaneously by using off-line solid phase extraction (SPE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS). The limits of detection (LODs) of all targets were lower than 0.05 μg/L, which could meet the regulatory requirements for monitoring of HCTs in drinking water in different countries and regions. To improve the detection sensitivities for trace PSTs, a method based on off-line SPE and on-line SPE-LC-MS/MS was established with LOD around 0.001 μg/L. GTX1&4, GTX2&3, and GTX5 were detected in freshwater in China for the first time, highlighting that overall communities are facing potential risks of exposure to various PSTs in China. High concentrations of ATX-a and CYN were also detected in freshwater from Northern China. The proposed method helps to understand the pollution status of HCT in water bodies, especially during the non-algal bloom period.

Simultaneous determination of selected pesticides and/or their metabolites in urine by off-line solid phase extraction and ultra high performance liquid chromatography/hybrid quadrupole time-of-flight mass spectrometry

An innovative method for the determination of pesticides of different uses and from different chemical families and/or their known metabolites in human urine was developed. The protocol includes an enzymatic hydrolysis followed by an off-line solid phase extraction (SPE) step and then a targeted quantitative analysis by ultra-high performance liquid chromatography coupled with hybrid quadrupole time-of-flight mass spectrometry (UHPLC/QTOFMS). Still rarely used for this purpose, this technique nevertheless offers excellent quantitative performance with high selectivity, but requires two separate injections for the same sample, one in the negative electrospray ionization mode (ESI-), and the other in the positive mode (ESI+). Two analytical methods were thus developed to cover 40 substances corresponding to 23 different pesticides plus nicotine and cotinine. The first method allows the determination of 15 biomarkers (SPE on a weak anion exchange polymeric support; ESI- mode) and the second 27 (SPE on a reverse phase polymeric support; ESI+ mode) with detection limits for a 2-mL urine sample varying from 0.02 to 25 μg.L−1. Replicate analysis of three pools of urine non-spiked and spiked at an intermediate level on about 20 different days showed most often excellent performance in terms of inter-day precision (<30%) and accuracy (between 80 and 125%), confirming that the UHPLC/QTOFMS coupling is perfectly adapted to a targeted quantitative analysis. The proposed methods were then applied to fifteen real urine samples, demonstrating the presence of pesticides, predominantly in metabolized form, in the urine of French pregnant women, and the capabilities of the proposed methods to detect them. They were finally applied to a study of the impact of thawing/freezing cycles on the conservation of the target substances, showing for the first time to our knowledge that the thawing/freezing cycles and the composition of urine samples could have an influence on the stability of some of the target substances.

Assessment of automated off-line solid-phase extraction LC-MS/MS to monitor EPA priority endocrine disruptors in tap water, surface water, and wastewater.

EPA method 539.1 recently introduced an expanded list of priority endocrine-disrupting compounds (EDCs), some of which were also included in the Unregulated Contaminant Monitoring Rule 3 (UCMR3). Though standardized methods are available for drinking water, analysis of steroid hormones and bisphenol A (BPA) at the ultra-trace level remains challenging. This study set out to evaluate the suitability of automated off-line solid-phase extraction (SPE) liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) for the determination of EPA-priority EDCs in environmental water matrixes (tap water, surface water, and wastewater influents and effluents). The target molecules included 14 steroid hormones (altrenogest, androstenedione, equilenin, equilin, α-estradiol, β-estradiol, estriol, estrone, ethinylestradiol, levonorgestrel, medroxyprogesterone, norethindrone, progesterone, testosterone) and BPA. Factors that may influence the analytical performance were assessed. This involved, for instance, testing combinations of SPE materials from different brands and protocol variations. Several materials presented absolute extraction efficiencies in acceptable ranges. Initial sample pH, nature of reconstitution medium, and mobile phase salt concentration were among the potential factors affecting analyte signal. Storage conditions (different preservative agents) possibly exerted the strongest influence, in agreement with the literature. Limits of detection were in the range of 0.03-0.5ng/L in drinking water, 0.1-0.5ng/L in surface water, and 0.16-1ng/L in wastewater. Method validation also involved testing linearity, accuracy, and precision in reagent water and matrix-matched extracted calibrants. The method was applied to field-collected water samples in Eastern Canada. Summed EDC concentrations remained low in tap water (<LOQ-0.92ng/L), while higher detection frequencies and contamination levels were reported in riverine surface waters (2.6-37ng/L) and municipal wastewaters (10-424ng/L).

Improvement on recovery and reproducibility for quantifying urinary mono-hydroxylated polycyclic aromatic hydrocarbons (OH-PAHs)

Efficient and reproducible measurements of multiple polycyclic aromatic hydrocarbon (PAH) metabolites in urinary samples are required to evaluate the complex health effects of PAH exposure. Here, we demonstrate a highly practical, automated off-line solid-phase extraction (SPE) of deconjugated hydroxylated PAHs followed by LC-MS/MS to simultaneously measure eight mono-hydroxylated PAH compounds: 1-hydroxynaphthalene, 2-hydroxynaphthalene, 2-hydroxyfluorene, 1-hydroxyphenanthrene, 2&3-hydroxyphenanthrene, 4-hydroxyphenanthrene and 1-hydroxypyrene. Initially, we observed low recovery rates (e.g., 16% for 1-hydroxypyrene) when using previously published methods. We optimized the procedure by choosing polymeric absorbent-based cartridges, automating the sample loading step by diluting samples with 15% methanol/sodium acetate, and most importantly, replacing acetonitrile with methanol as the eluting solvent. Optimized sample preparation has improved the recovery rates to more than 69% for analytes of interest. This improvement led to higher method sensitivity and detection frequency, especially for 1-hydroxypyrene, in all of 100 urine samples collected in the New York City site of the Legacy Girls Study. The limits of detection ranged from 7.6 pg/mL to 20.3 pg/mL using 1 mL of urine, compared to the 2 mL required in CDC, method 09-OD. The average coefficients of variance of quality control samples (n = 60) ranged between 7 and 21%; variance of repeated measurements (n = 45) was less than 10%. This efficient and reliable method for measuring PAH metabolites will greatly benefit epidemiology studies and biomonitoring programs.

Simultaneous Determination of Selected Pesticides And/Or Their Metabolites in Urine by Off-Line Solid Phase Extraction and Ultra-High Performance Liquid Chromatography / Hybrid Quadrupole Time-of-Flight Mass Spectrometry

Simultaneous Determination of Selected Pesticides And/Or Their Metabolites in Urine by Off-Line Solid Phase Extraction and Ultra-High Performance Liquid Chromatography / Hybrid Quadrupole Time-of-Flight Mass Spectrometry

Non-Steroidal Anti-Inflammatory Drugs Current Challenges and Future Perceptions

An analytical methodology for the simultaneous determination of seven pharmaceuticals and two metabolites belonging to the non-steroidal anti-inflammatory drugs (NSAIDs) and analgesics therapeutic groups was developed based on off-line solid-phase extraction and ultra-high performance liquid chromatography coupled to tandem mass spectrometry 1 (SPE–UHPLC–MS/MS). Extraction conditions were optimized taking into account parameters like sorbent material, sample volume and sample 1,2 PH. Method detection limits (MDLs) ranging from 0.02 to 8.18 ng/L were obtained 2,3. This methodology was successfully applied to the determination of the selected pharmaceuticals in seawater samples of Atlantic Ocean in the Northern Portuguese coast. All the pharmaceuticals have been detected in the seawater samples, with pharmaceuticals like ibuprofen, acetaminophen, ketoprofen and the metabolite hydroxy ibuprofen being the most frequently detected at concentrations that can reach some hundreds of ng/L 4.

Construction of imine-linked covalent organic framework as advanced adsorbent for the sensitive determination of chlorophenols

Food safety is a great concern of the general public. Chlorophenols (CPs) as organic pollutant can be found in drinking water and foods, causing serious harm to human health. Herein, imine-linked covalent organic frameworks (COFs), named as TAPT-AN-COF, was synthesized by aniline modulation strategy through condensation of 1,3,5-triformylphoroglucinol and 4,4′,4′'-(1,3,5-Triazine-2,4,6-triyl)trianiline with aniline as modulator. The prepared TAPT-AN-COF possesses good crystallinity and regular morphology, displaying excellent adsorption capability towards CPs pollutants. Thus, the TAPT-AN-COF was used as novel adsorbent for off-line solid-phase extraction of four CPs (2-CP, 3-CP, 2,3-CPs, 2,4-CPs) from bottled water, tea drink and honey samples before high performance liquid chromatography-ultraviolet detection. Under optimal conditions, wide linear range, low detection limits and satisfactory extraction recovery were gained. The π-stacking and hydrophobic interactions between the TAPT-AN-COF and the analytes played an important role in the adsorption. The established method has a great potential in determining other hydrophobic aromatic compounds.

Offline Solid-Phase Extraction and Separation of Mineral Oil Saturated Hydrocarbons and Mineral Oil Aromatic Hydrocarbons in Edible Oils, and Analysis via GC with a Flame Ionization Detector.

A method was developed for the determination of mineral oil saturated hydrocarbons (MOSH) and mineral oil aromatic hydrocarbons (MOAH) in edible oils, achieving similar limits of quantification than those obtained by online extraction methodologies, i.e., 0.5 mg/kg. The isolation of MOSH and MOAH was performed in a silver nitrated silica gel stationary phase prior to their analysis by gas chromatography–flame ionization detector (GC-FID). To improve the sensitivity, the simulated on-column injection method, using a suitable liner, was optimized. The method was validated at 0.5, 10.0 and 17.9 mg/kg, and recoveries ranged from 80 to 110%. Intra and inter-day precision were evaluated at the same levels, and relative standard deviation (RSD) was lower than 20%. The method was applied to a total of 27 samples of different types of oil previously analyzed in an accredited laboratory, detecting MOSH up to 79.2 mg/kg and MOAH up to 22.4 mg/kg.

Development an automated and high-throughput analytical platform for screening 39 glucocorticoids in animal-derived food for doping control

For the purpose of doping control, increasing demand has been highlighted for the determination of glucocorticoids in animal derived foods. Although several methods have been established, the barrier of low throughput still exists for doping control. Herein, we report an on-line purification and high throughput platform for fast screening of 39 glucocorticoids in animal-derived food (pork, chicken, milk and eggs) using on-line solid-phase extraction (SPE) technology and liquid chromatography-tandem high-resolution mass spectrometry (LC-HRMS). An in-house developed, low-cost monolithic column was applied in this work which prevented the requirement of laborious and costly off-line solid-phase extraction columns. With one-step extraction and replacement of solvent, the sample can be directly and automatically injected as well as purified to screen 39 glucocorticoids in a single run time. The overall recoveries ranged from 62.0%–116.3% with intraday and inter-day relative standard deviation lower than 10.9% and 12.4%, respectively. The limits of quantitation for different matrices were between 0.84 and 4.94 μg/kg. Compared to the previous methods, the platform developed in this study shows excellent performance for rapid analysis of large numbers of samples and a wide variety of compounds with respect to short running time, analytical specificity and sensitivity as well as overall method accuracy and precision. In conclusion, this platform can function as a high-throughput tool in the field of doping analysis and contribute to a better safety assurance of animal-derived food.

Automatic analytical approach for the determination of 12 illicit drugs and nicotine metabolites in wastewater using on-line SPE-UHPLC-MS/MS

In this study, we developed a novel on-line solid phase extraction (SPE)-ultra-high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS)-based analytical method for simultaneously quantifying 12 illicit drugs and metabolites (methamphetamine, amphetamine, morphine, codeine, 6-monoacetylmorphine, benzoylecgonine, 3,4-methylenedioxymethamphetamine, 3,4-methylenedioxyamphetamine, cocaine, ketamine, norketamine, and methcathinone) and cotinine (COT) in wastewater samples. The analysis was performed by loading 2 mL of the sample onto an Oasis hydrophilic-lipophilic balance cartridge and using a cleanup step (5% methanol) to eliminate interference with a total run time of 13 min. The isotope-labeled internal standard method was used to quantify the target substances and correct for unavoidable losses and matrix effects during the on-line SPE process. Typical analytical characteristics used for method validation were sensitivity, linearity, precision, repeatability, recovery, and matrix effects. The limit of detection (LOD) and limit of quantification (LOQ) of each target were set at 0.20 ng/L and 0.50 ng/L, respectively. The linearity was between 0.5 ng/L and 250 ng/L, except for that of COT. The intra- and inter-day precisions were <10.45% and 25.64%, respectively, and the relative recovery ranged from 83.74% to 162.26%. The method was used to analyze various wastewater samples from 33 cities in China, and the results were compared with the experimental results of identical samples analyzed using off-line SPE. The difference rate was between 19.91% and −20.44%, and the error range could be considered acceptable. These findings showed that on-line SPE is a suitable alternative to off-line SPE for the analysis of illicit drugs in samples.

Simple determination of six groups of lipophilic marine algal toxins in seawater by automated on-line solid phase extraction coupled to liquid chromatography-tandem mass spectrometry

Lipophilic marine algal toxins (LMATs) are highly toxic secondary metabolites produced by marine microalgae that pose a great threat to marine aquaculture organisms and human health. In this study, a novel and automated method for the simultaneous determination of six groups of LMATs in seawater was developed by on-line solid phase extraction (SPE) coupled with liquid chromatography-tandem mass spectrometry (LC-MS/MS). Condition optimization and method validation were performed, and the recoveries of all 14 target LMATs featuring different properties ranged from 83.5% to 96.0%. The limits of detection of most target compounds were within ≤3.000 ng/L with good precision (relative standard deviation ≤ 12.1%) and linearity (R2≥0.9916). Compared with off-line SPE methods, the proposed on-line SPE method has better recovery, sensitivity, repeatability, and throughput; in addition, the volume of seawater sample necessary to conduct determinations is greatly reduced in the present method. Finally, the method was applied to determine LMATs in actual seawater samples collected from the Bohai and South Yellow Seas of China in summer, and okadaic acid and pectenotoxin-2 were detected in all seawater samples. The highest concentration of ∑LMATs (22.23 ng/L) occurred in the coastal mariculture area of Shandong Province. Therefore, routine monitoring of LMATs in seawater of the coastal mariculture zone is necessary to prevent shellfish contamination especially in summer, and the proposed on-line SPE-LC-MS/MS method is a powerful way for direct and automatic detection of various LMATs in coastal mariculture area.

Improved oxytocin analysis from human serum and urine by orbitrap ESI-LC-HRAM-MS.

Native circulating oxytocin (OT) levels in non-pregnant/non-lactating/non-medicated humans are very low (≤ 8 pg/mL). The lower limit of detection (LLOD) of our previous liquid chromatography mass spectrometry (LC-MS) method (10-25 pg/mL) precluded their quantification in serum and urine. Thus, we sought to improve the LC-MS sensitivity of OT measurements in these matrices by hydrophobic tagging and solid phase extraction (SPE). In the former approach, OT was reduced then alkylated with N-alkyl acetamide (C12, C14, C16, and C18) tags or derivatized using sulfonyl chloride-based reagents. In the latter approach, native OT in serum and urine was concentrated by offline SPE using gradient acetonitrile washings after first crashing with acetonitrile. Peak urinary eluate fractions were further concentrated online then analyzed by orbitrap-based LC-MS with electrospray ionization. All hydrophobic OT derivatives had lower sensitivity than native OT. Washing with a water-acetonitrile gradient during SPE improved the LLOD of OT in spiked serum to 2.5 pg/mL, while adding a subsequent online-concentration step improved the LLOD in spiked urine to 1-5 pg/mL and allowed us to detect OT in urine from lactating women. We were unable to improve the sensitivity of OT measurements by hydrophobic tagging or by derivatization using sulfonyl chloride-based reagents. However, we were successful in improving the sensitivity of native OT measurements in serum and urine 2- and 5-fold, respectively, from our previous orbitrap-based LC-MS method. Offline SPE was mandatory for both matrices and a subsequent online-concentration step was required for urine.

Synthesis of silica amino-functionalized microporous organic network composites for efficient on-line solid phase extraction of trace phenols from water

Microporous organic network (MON) is a promise class of functional materials in solid phase extraction (SPE). However, the previous MON-based SPE works are all focused on off-line mode. The inherent drawbacks of off-line SPE such as complicated operation steps and poor repeatability still hinder the potential applications of MON. In addition, direct use of traditional synthesized nano-sized MON in on-line SPE is impractical. To solve these issues, here we show the synthesis of silica amino-functionalized MON (SiO2@MON-NH2) microsphere as an advanced adsorbent for on-line SPE of trace phenols prior to the high performance liquid chromatography (HPLC) analysis. The SiO2 microsphere is served as the core to support the in-situ engineering of MON-NH2 to reduce the back pressure during on-line SPE. Integrating amino groups (hydrogen binding sites) with aromatic MON's networks (hydrophobic and π-π interaction sites) on SiO2@MON-NH2 provides supersensitive performance for phenols. The SiO2@MON-NH2 microsphere for on-line SPE coupled with HPLC for the analysis of five phenols offers low limit of detections (S/N = 3, 0.009–0.030 μg L−1), wide linear range (0.025–100 μg L−1), large enrichment factors (5036–5689) and good intra-day and inter-day precisions (RSDs, 0.7–1.6 and 1.0–2.7%, respectively). The proposed method is also successfully applied to analyze trace phenols in tap, lake and river water samples with good recoveries. The newly-synthesized MON composites own great potential in on-line SPE for further determination of diverse trace contaminants.

Enhanced photolytic and photooxidative treatments for removal of selected pharmaceutical ingredients and their degradation products in water matrices

Photolytic and photooxidative degradations of diclofenac (DICL), naproxen (NAPR) and carbamazepine (CARB) were compared by a conventional low-pressure mercury-vapor lamp with λmax = 254 nm and a vacuum UV (VUV) one, emitting also at 185 nm (in 11%) in ultra-pure water (UPW) and municipal wastewater (WW) spiked with 5 × 10−6 M for each drug. Almost complete photolytic and photooxidative degradations were observed by VUV irradiation for all three compounds in 2 min. About 75% decrease in the total organic carbon content was determined in UPW irradiated samples spiked at the 2–5 × 10−5 M levels in 15 min. Effective degradations of DICL, NAPR and CARB were achieved in spiked WW by photolysis and photooxidation (PhO) at 185 nm (11%) within 1, 2 and 10 min, respectively. Several aromatic degradation products of DICL, NAPR and CARB were identified by quadrupole time-of-flight mass spectrometer hyphenated to an ultra-high performance liquid chromatograph after preconcentration with off-line solid phase extraction upon irradiation of the UPW matrix spiked with the selected drugs at 254 nm. For several degradation products, chemical structures differing from those previously reported have been proposed. Moreover, acridine has not yet been reported as photodegradation product for DICL. Degradation pathways have been also proposed. Almost complete degradation of DICL, NAPR and CARB as well as their degradation products by VUV + PhO in WW took place in 5, 10 and 30 min, respectively. However, the total organic content decreased by only 25% in the WW sample.