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Determination of volatile aliphatic amines in air by solid-phase microextraction coupled with gas chromatography with flame ionization detection.

Practical aspects of the application of solid-phase microextraction (SPME) to the determination of volatile aliphatic amines in air are described. Analytes included methylamine (MA), ethylamine (EA), dimethylamine (DMA), diethylamine (DEA), trimethylamine (TMA) and triethylamine (TEA). New SPME stationary phases were examined. The effects of relative humidity and temperature on analytes uptake were taken into account in analysis. Gas chromatography (GC) with flame ionization detector (FID) was used for the final analysis.

Air↗

Headspace solid-phase microextraction and gas chromatographic determination of dinitroaniline herbicides in human blood, urine and environmental water.

Solid-phase microextraction (SPME) is a unique extraction and sampling technique, and it has been used for separation of volatile organics from water or other simple matrices. In this study, we have used SPME to separate dinitroaniline herbicides from complicated matrices of human urine and blood in order to broaden its application to biomedical analysis. The SPME conditions were optimized for water, urine and blood samples, in terms of pH, salt additives, extraction temperature, and fiber exposure time. Urine or water (1.0 ml) spiked with herbicides and 0.28 g of anhydrous sodium sulfate was preheated at 70 degrees C for 10 min, and a polydimethylsiloxane-coated fiber for SPME was exposed to the headspace at 70 degrees C for another 30 min; while spiked blood (0.5 ml) diluted with water (0.5 ml) was treated at 90 degrees C in the same way. The herbicides were extractable under these conditions, and could be determined by gas chromatography-electron capture detector (GC-ECD). The recoveries of the herbicides, measured at the concentrations of 0.50 and 1.0 ng/ml urine or water, or 6.0 and 20 ng/0.5 ml blood, ranged from 35 to 64% for different herbicides from water or urine, and from 3.2 to 7.2% from blood. The headspace SPME yielded clean extracts of dinitroaniline herbicides from urine, blood or water, which could be directly analyzed by GC-ECD without further purification. The peak areas of the extracted herbicides were proportional to their concentrations in the range 0.1-10 ng/ml in water or urine, or 1-60 ng/0.5 ml in blood. The lowest detectable concentration of the herbicides lay in 0.1 ng/ml water or urine, or in 0.5 ng/0.5 ml blood. The intra- and inter-day coefficients of variation were within 14% for most of the analytes. Although the recoveries of the herbicides were rather low, the linearity of calibration curve and the precision were good. The developed method is more sensitive and much simpler in sample preparation than previously reported ones. With the established SPME method, a dosed herbicide was successfully separated and determined in rats' blood.

Aniline Compounds↗

Solid-phase microextraction gas chromatographic-mass spectrometric method for the determination of inhalation anesthetics in urine.

Solid-phase microextraction (SPME) has been applied to the headspace sampling of inhalation anesthetics (i.e. nitrous oxide, isoflurane and halothane) in human urine. Analysis was carried out by gas chromatography-mass spectrometry using a capillary column with a divinylbenzene porous polymeric stationary phase. A SPME divinylbenzene-Carboxen-polydimethylsiloxane coated fiber, 2 cm long, was used, and its performances were compared with those of a Carboxen-PDMS in terms of sensitivity, extraction efficiency, extraction time, fiber coating-urine distribution coefficient. For both fibers, linearity was established over four orders of magnitude, limits of detection were below 100 ng/l for nitrous oxide and below 30 ng/l for halogenated. Precision calculated as %RSD was within 3-13% for all intra- and inter-day determinations. The method was applied to the quantitative analysis of anesthetics in the urine of occupationally exposed people (operating room personnel).

Anesthetics, Inhalation↗

Anodized aluminum wire as a solid-phase microextraction fiber.

The efficiency of anodized aluminum wire was investigated as a new fiber for solid-phase microextraction (SPME). Aluminum wires were anodized by direct current in a solution of sulfuric acid at room temperature and were conditioned at 300 degrees C for 30 min. These fibers were used for the extraction of some aliphatic alcohols, BTEX, and petroleum products from gaseous samples. The extracted analytes were transferred to a GC injector using an (inhouse-designed) SPME syringe that also allowed for an easy change of SPME fibers. The results obtained prove the ability of anodized aluminum wire as a new fiber for sampling of organic compounds from gaseous samples. This behavior is due most probably to the porous layer of aluminum oxide, which is formed on the metal surfaces. In this work, the optimum conditions for the preparation and conditioning of fibers and the extraction of analytes from gaseous samples were obtained. In the optimum conditions, one fiber was used in several equal analyses and the relative standard deviations were below 5% (n = 5). However, fiber-to-fiber reproducibility was 8% (n = 5). This fiber is firm, inexpensive, and durable and can be prepared simply.

Journal Article↗

Application of low-temperature glassy carbon films in solid-phase microextraction.

Low-temperature glassy carbon (LTGC) films were investigated as a sorbent coating for solid-phase microextraction because of its uniquely selective adsorptive characteristics. The selectivity of these coatings is primarily controlled by shape characteristics of the solute molecule and the final processing temperature used to form the LTGC, demonstrating unique adsorptive characteristics compared to commercial phases. The LTGC films were prepared by first coating porous silica particles with a diethylnyl oligomer precursor and then heat curing at temperatures between 300 and 1000 degrees C to form the LTGC. Then, using a sol-gel process, the LTGC-coated silica particles were immobilized onto stainless steel fibers and subsequently used for headspace and liquid extractions followed by GC-FID analysis. The selectivity of the LTGC is demonstrated by the extraction of a variety of aromatic hydrocarbons as well as the taste and odor contaminants geosmin, 2-methylisoborneol, and 2,4,6-trichloroanisole commonly found in water supplies. The data show that the LTGC coating has the highest affinity for molecules with the greatest cross-sectional surface area and polarizability and that this selective mechanism increases as a function of LTGC processing temperature.

Journal Article↗

Solid-phase microextraction coupled to gas chromatography/mass spectrometry for determining polycyclic aromatic hydrocarbon-micelle partition coefficients.

Solid-phase microextraction (SPME) coupled to gas chromatography with MS detection has been employed to study the partition coefficients of PAHs to ionic and nonionic micelles. The results obtained in this work for seven PAHs, using 85-microm polyacrylate- and 100-microm poly(dimethylsiloxane)-coated fibers and anionic (sodium dodecyl sulfate), cationic (cetyltrimethylammonium bromide), and nonionic (polyoxyethylene-10-lauryl ether) surfactants, indicate that SPME is a viable method for estimating the partition coefficients of PAHs to micelle. The procedure could also be potentially extended to the measurement of partition coefficients between a wide variety of semi- or nonvolatile compounds and micellar media.

Anions↗

Nondestructive, minimal-disturbance, direct-burial solid-phase microextraction fiber technique for measuring TNT in sediment.

We explored a novel technique to deploy solid-phase microextraction (SPME) fibers to nondestructively measure the explosive compound 2,4,6-trinitrotoluene (TNT) and its nitroaromatic (NA) degradation products in laboratory sediment toxicity tests and field sediments in situ. SPME fibers within steel mesh envelopes were exposed statically via direct burial within sediment. Six fiber types (polymer coatings) were tested. Polyacrylate (PA) SPME fiber was sufficiently durable for this application, yielded the lowest detection limits, and exhibited a linear uptake relationship across toxicologically relevant sediment NA concentrations (100-2000 nmol/g dw (20-500 microg/g dw)). Temperature greatly influenced SPME absorption kinetics. Via evaluation of absorption at different temperatures, recommended sampling times needed to achieve steady-state equilibrium were 48 h for room temperatures (23-25 degrees C) and up to 7 d for cold (5 degrees C) temperatures. Although a comparison of TNT residues by SPMEs and TNT bioavailability and toxicity in sediments has not been completed, differences in SPME availability of TNT and its degradation products were found between two different TNT-spiked sediments. Our disposable SPME technique was slightly less expensive and as precise as the conventional extraction for total NAs and may prove to be a powerful exposure evaluation tool for assessing the ecological risk of these compounds.

Absorption↗

Solid phase microextraction as a tool to determine membrane/water partition coefficients and bioavailable concentrations in in vitro systems.

Solid phase microextraction (SPME) is an extraction technique that uses a polymer-coated fiber as the extraction device. After extraction, the compound of interest can be desorbed from the fiber and subsequently analyzed by GC or HPLC. One of the properties of SPME is that only the freely dissolved fraction of a chemical is available for partitioning to the extraction device. The method can be applied in a way that small amounts are extracted from the sample, which allows negligible depletion extraction. These two properties make SPME devices particularly suitable for measurements of free concentrations. In toxicological studies the free concentration is considered to be a more relevant parameter, concerning toxic effects, than the nominal concentration that is used most frequently. In the current study, the usefulness of this method to measure phospholipid/water partition coefficients and free concentrations in three different in vitro test systems (rat hepatocytes in primary culture, 9000 g and 100,000 g homogenate fractions of rainbow trout liver) was demonstrated. Results show separate relationships between phospholipid/water and n-octanol/water partition coefficients for a set of polar and nonpolar organic chemicals, respectively. These observations suggest that phospholipid/water partition coefficients may be a more suitable parameter in modeling the kinetic behavior of organic chemicals. Additionally, differences between the nominal and the actual free concentration in in vitro systems are more pronounced for more hydrophobic compounds, as was expected based on theoretical considerations. To our knowledge, the approach presented here is the first analytical method to measure toxicologically relevant concentrations in in vitro test systems in a fast and efficient way.

Animals↗

Theory of solid-phase microextraction

The main objective of this contribution is to describe the fundamental concepts associated with solid-phase microextraction (SPME). Theory provides insight when developing SPME methods and identifies parameters for rigorous control and optimization. A mathematical model has been developed to understand the principal processes of SPME by applying basic fundamental principles of thermodynamics and diffusion theory. The model assumes idealized conditions and is limited to air, liquid, or headspace above liquid sampling. Theory for ideal cases can be quite accurate for trace concentrations in simple matrices such as air or drinking water at ambient conditions when secondary factors such as thermal expansion of polymers and changes in diffusion coefficients because of solutes in polymers can be neglected. When conditions are more complex, theory for ideal cases still efficiently estimates general relationships between parameters.

Journal Article↗

Headspace-solid-phase microextraction in the analysis of the volatile fraction of aromatic and medicinal plants.

Headspace (HS)-solid-phase microextraction (SPME) has assumed an ever increasing importance as a technique for HS sampling to study the composition of the HS of medicinal and aromatic plants. HS-SPME has mainly been applied for (a) studying the composition of the volatile fraction, including in addition to or as an alternative to other sampling techniques; (b) monitoring the biological phenomena involved with the volatile fraction of a plant; (c) discriminating between species, subspecies, varieties, cultivars, or chemotypes; and (d) quality control of plant samples. A review of 108 articles published during 2000-2005 is presented covering the use of HS-SPME in the field of aromatic and medicinal plants, selection of the most effective fiber and sampling conditions, comparison of HS-SPME and other volatile fraction sample preparation techniques, and the advantages and limits of HS-SPME when applied to medicinal and aromatic plants.

Chromatography, Liquid↗

Solid-phase microextraction in the determination of methadone in human saliva by gas chromatography-mass spectrometry.

Solid-phase microextraction (SPME) with a 100-microm polydimethylsiloxane film fiber was applied to the determination of methadone and 2-ethylidine-3,3-diphenylpyrrolidine (EDDP) by GC-MS in human saliva and compared with liquid-liquid extraction. A shorter extraction time of 30 min with the fiber was obtained, speeding up the total analysis time. Linearity was found for SPME from 0.05 to 2.0 microg/mL (r = 0.9976 for methadone; r = 0.9988 for EDDP) with precision between 0.7 and 4.3% for saliva spiked with 0.2 and 1.5 microg/mL of methadone and EDDP. The limit of detection using SPME was 0.04 microg/mL for methadone and 0.008 microg/mL for EDDP. Analytical recoveries of SPME and liquid-liquid extraction ranged from 98.8 to 103.6%. The use of deuterated internal standard by both methods have yielded comparable results. Thus, the SPME method is highly accurate, precise, and useful for determination of methadone and EDDP in saliva.

Dimethylpolysiloxanes↗

Extraction of chloroform and methylene chloride in human whole blood and urine by headspace solid phase microextraction (SPME).

Chloroform and methylene chloride were extracted from human whole blood and urine by headspace solid phase microextraction (SPME) using a Carboxen/polydimethylsiloxane (Carboxen/PDMS) fibre before capillary gas chromatography (GC)/flame ionization detection (FID). Whole blood or urine was placed in a vial and mixed with distilled water. The vial was heated at 30 degrees C, and the solvents were extracted from the headspace by SPME. The extraction efficiencies of chloroform and methylene chloride from whole blood were 40.3% and 35.8%, respectively; those for urine were 57.0% and 43.6%, respectively. The calibration curves for chloroform were linear in the range of 1-8 micrograms/ml for blood and urine samples, and those for methylene chloride in the range of 0.5-8 micrograms/ml. The detection limits for both compounds were 0.3 microgram/ml for whole blood and 0.2 microgram/ml for urine. The headspace SPME with Carboxen/PDMS fibre coupled with GC/FID seems useful for analyses of chloroform and methylene chloride in forensic toxicology and environmental chemistry.

Blood Chemical Analysis↗

Use of headspace solid-phase microextraction to characterize odour compounds in subsurface flow constructed wetland for wastewater treatment.

A headspace solid-phase microextraction (HS-SPME) preconcentration method was applied to the analysis of some of the major odorous compounds occurring in wastewater using GC/MS or GC/NPD detection. The detection limit for volatile amines, volatile fatty acids, and volatile alkylsulphides ranged from 3 to 100, 2 to 150, and 0.0006 to 0.035 microg/L, respectively. The SPME method was used to examine the fate of odorous compounds in the subsurface flow constructed wetlands (SFCW) operated under different hydraulic loading rate (HLR), bed aspect ratio, and granular medium size. Among the experimental conditions evaluated in the SFCW beds, HLR was found to be the most important factor influencing the evolution of the studied compounds. There were also significant differences among bed types in the behaviour of ammonia (NH3), acetic acid (Ac), isovaleric acid (IsoA), propionic acid (PrA), and dimethylsulphide. Aspect ratio and medium granular size were minor factors influencing SFCW performance. The major odour compounds by mass in the effluent of SFCW with different operational conditions were NH3 and Ac. Further removal of these two compounds is considered as very important from the viewpoint of chemical composition. On the other hand, Relative Odour Intensity (ROI: ratio between the absolute concentration to the odour threshold concentration) suggested that PrA and IsoA were the two major compounds responsible for odour intensity. Thus, further removal of these two compounds is viewed as very important for the effluent deodorization, especially for PrA. From our results, this compound appears to be produced by processes occurring in the SFCW.

Biodegradation, Environmental↗

Preparation of polyaniline coating on a stainless-steel wire using electroplating and its application to the determination of six aromatic amines using headspace solid-phase microextraction.

A novel polyaniline (PANI) coating was prepared on a stainless-steel wire for solid-phase microextraction by electroplating method. For better mechanical strength, the stainless-steel wire was used instead of the fused silica fiber. The electroplating method had advantages of ease of preparation and simple equipments. The PANI fiber was evaluated by analyzing six aromatic amines (aniline, N,N-dimethylaniline, m-methylaniline, 2,4-dimethylaniline, 2-chloroaniline, 3,4-dichloroaniline) in water. After the analytical procedure was optimized, the linearity was from 4.8 to 2.75 x 10(4) microg L(-1) and the detection limits was from 0.019 to 1.06 microg L(-1). Relative standard deviations were found to be 2.02-6.00%. Good recoveries were obtained when wastewater samples were analyzed.

Amines↗

Determination of aromatic hydrocarbons in bituminous emulsion sealants using headspace solid-phase microextraction and gas chromatography-mass spectrometry.

The possibility of quantitative determination of aromatic hydrocarbons in bituminous emulsion sealants was investigated using headspace solid-phase microextraction (HS-SPME) followed by gas chromatography-mass spectrometry (GC-MS). The target analytes studied were benzene, toluene, ethylbenzene, p-, m-, and o-xylene (BTEX) as well as 1,3,5- and 1,2,4-trimethylbenzene. Experimental factors influencing HS-SPME efficiency were studied (sample-headspace equilibration time, extraction time and sample matrix effects). A HS-SPME method using surrogate matrix was developed. The detection limit was estimated as approximately 0.1 ppmw for the target analytes investigated. Good linearity was observed (R(2)>0.997) for all calibration curves obtained. The repeatability of the method (RSD, relative standard deviation) was found less than 10%. The accuracy of the method given by recovery of spiked samples was between 99 and 116%. The HS-SPME method developed was applied to two commercially available bituminous emulsion sealants. External calibration and standard addition approaches were investigated, and statistical paired t-test was performed. The contents of target aromatic hydrocarbons in the sealants studied varied from approximately 0.4 to 150 ppmw. The method developed shows potential as a tool for the determination of aromatic hydrocarbons in emulsified bituminous materials.

Calibration↗

Determination of microcystins in water using integrated solid-phase microextraction with microbore high-performance liquid chromatography-electrospray quadruple time-of-flight mass spectrometry.

The development of a technique combining solid-phase microextraction (SPME) with microbore high-performance liquid chromatography (micro-HPLC)-tandem quadrupole time-of-flight (QTOF) mass spectrometry (MS) for determination of dissolved microcystins in water is reported. Several important parameters affecting the efficiency of SPME extraction of microcystins are investigated. A microbore C18 column HPLC coupled with tandem QTOF-MS with information-dependent acquisition (IDA) is developed to effectively analyze microcystins in microliter volumes of SPME extracts. The micro-HPLC-QTOF-MS with IDA technique provides comprehensive information, including a survey chromatogram (total ion chromatogram), full scan mass spectrum, and product ion scan mass spectra at different collision energies for individual analytes, which allows for both identification and quantitation in the same run. Linear calibration curves of microcystin standard [microcystin (MC)-arginine (R)R] 1-100 microg/L and of microcystin standard [MC-leucine (L)R] 1-250 microg/L are obtained with a correlation coefficient of 0.996. The combination of SPME with HPLC-QTOF-MS and IDA offers limits of detection of 0.6 pg for MC-RR and 1.6 pg for MC-LR. Analysis of spiked lake-water samples shows a recovery of > 86% for MC-RR and > 70% for MC-LR. This technique requires small sample volumes, minimizes the use of organic solvents, and provides sensitive and information-rich analysis of unknown samples.

Chromatography, High Pressure Liquid↗

Simultaneous optimization by neuro-genetic approach of a multiresidue method for determination of pesticides in Passiflora alata infuses using headspace solid phase microextraction and gas chromatography.

A simultaneous optimization strategy based on neuro-genetic approach has been applied to a HS-SPME-GC-ECD (Headspace Solid Phase Microextraction coupled to Gas Chromatography with Electron Capture Detection) method for simultaneous determination of the pesticides chlorotalonil, methyl parathion, malathion, alpha-endosulfan and beta-endosulfan in herbal infusions of Passiflora alata (Dryander). Two types of extractive fibers were used: a home-made device coated by sol-gel process with polydimethylsiloxane-poly(vinyl alcohol) (PDMS/PVA) and a commercial PDMS. The effects of extraction parameters such as dilution of the infusion, extraction temperature and time, as well as sample ionic strength were evaluated through the Doehlert design. To find a model that could relate these extraction parameters with the extraction efficiency of all pesticide simultaneously, a Bayesian Regularized Artificial Neural Network (BRANN) approach was employed. Subsequently, Genetic Algorithm (GA) was applied to attain the optimum values from the model developed by the neural network. The use of the proposed approach allowed the determination of a single extraction condition that maximized the peak areas of all pesticides simultaneously, showing a promising and a suitable new procedure to the optimization process of complex analytical problems.

Algorithms↗

Rapid determination of acetone in human plasma by gas chromatography-mass spectrometry and solid-phase microextraction with on-fiber derivatization.

Acetone is an important volatile disease marker. Due to its nature of activity and volatility, it is a difficult task to measure the concentration of acetone in biological samples with accuracy. In this paper, we developed a novel method for determination of trace amount acetone in human plasma by solid-phase microextraction technique with on-fiber derivatization. In this method, the poly(dimethylsiloxane)/divinylbenzene (PDMS/DVB) fiber was used and O-2,3,4,5,6-(pentafluorobenzyl) hydroxylamine hydrochloride (PFBHA) was first loaded on the fiber. Acetone in plasma sample was agitated into headspace and extracted by solid-phase microextraction (SPME) fiber and subsequently derivatized with PFBHA on the fiber. Acetone oxime was analyzed by gas chromatography-mass spectrometry (GC-MS). Quantitative analysis of acetone in plasma was carried out by using external standard method. The SPME conditions (extraction temperature and time) and the method validation were studied. The present method was tested by determination of acetone in diabetes plasma and normal plasma. Acetone concentration in diabetes plasma was found to be higher than 1.8mM, while in normal plasma was lower than 0.017 mM. The results show that the present method is a potential tool for diagnosis of diabetes.

Acetone↗