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Biomedical subjects

J Pawliszyn

Publications and source records attributed to J Pawliszyn.

At least 19 recordsLinked to original sources
PubMed2000

Dynamics of capillary isoelectric focusing in the absence of fluid flow: high-resolution computer simulation and experimental validation with whole column optical imaging.

A 150-component, dynamic electrophoresis simulator was developed and applied to the description of capillary isoelectric focusing (CIEF) of amphoteric substances in quiescent solution. The simulator is shown to be capable of producing high-resolution pH 3-10 focusing data with 140 individual carrier ampholytes (20/pH unit) and at current densities that are used in CIEF, i.e., under conditions that were hitherto unaccessible by dynamic computer simulation. Having a focusing capillary of 5-cm length, the predicted focusing dynamics for amphoteric dyes obtained at a constant voltage of 1500 V (300 V/cm) are shown to qualitatively agree with data obtained by whole-column optical imaging. The simulation data provide detailed insight into the dynamics of the focusing process for the cases with the focusing column being sandwiched between 40 mM NaOH (catholyte) and 100 mM phosphoric acid (anolyte) or having the column ends only permeable for OH- and H+ at cathode and anode, respectively. Simulation data reveal that the number of sample boundaries migrating from the two ends of the column to the focusing positions is always equal to the number of sample components. The number of detectable migrating sample boundaries, however, can be lower. Whole-column optical imaging is demonstrated to be the method of choice for following the approach to equilibrium. With that detection format, transient sample peaks can be recognized and properly identified. This would also be possible with a scanning detector moving rapidly and repeatedly along the column but cannot be accomplished by a stationary detector placed at a specified location. The data presented demonstrate that the model together with imaging monitoring can be used to optimize the CIEF separation conditions.

Coloring Agents↗
PubMed2000

Air sampling with porous solid-phase microextraction fibers

A new, rapid air sampling/sample preparation methodology was investigated using adsorptive solid-phase microextraction (SPME) fiber coatings and nonequilibrium conditions for volatile organic compounds (VOCs). This method is the fastest extraction technique for air sampling at typical airborne VOC concentrations. A theoretical model for the extraction was formulated based on the diffusion through the interface between the sampled (bulk) air and the SPME coating. Parameters that affect the extraction process including sampling time, air velocity, air temperature, and relative humidity were investigated with the porous (solid) PDMS/DVB and Carboxen/PDMS coatings. Very short sampling times from 5 s to 1 min were used to minimize the effects of competitive adsorption and to calibrate the extraction process in the initial linear extraction region. The predicted amounts of extracted mass compared well with the measured amounts of target VOCs. Findings presented in this study extend the existing fundamental knowledge related to sampling/sample preparation with SPME, thereby enabling the development of new sampling devices for the rapid sampling of air, headspace, water, and soil.

Journal Article↗
PubMed2000

Time-weighted average sampling of volatile and semi-volatile airborne organic compounds by the solid-phase microextraction device.

The ultimate goal of the chemist is to perform sample preparation, and analysis, if possible at the place where a sample is located rather than moving the sample to laboratory, as is common practice in many cases at the present time. This approach eliminates errors and time associated with sample transport and storage and therefore it would result in more accurate, precise and faster analytical data. In addition to portability, two other important features of ideal field sample preparation technique are elimination of solvent use and integration with a sampling step. A method is developed which addresses these requirements for the determination of time-weighted average concentration of gas phase compounds using a solid-phase microextraction device. Quantification of target analytes in air using this method can be carried out without external calibration. The volatile and semi-volatile organic compounds in air diffuse into the fiber coating which is retracted a known distance into its needle housing during the sampling period. The coatings used are poly(dimethylsiloxane) and poly(dimethylsiloxane)-divinylbenzene. The sampling rate at which gas phase analytes load onto the fiber is determined for a wide range of hydrocarbons. There is a good agreement between the theoretical and experimental sampling rates. Sampling time ranges from 1 min to 24 h depending on the coating used and its retraction distance. Effect of the flow-rate on the uptake rate by the fiber is studied. The method is tested in the field and compared with National Institute of Occupational Health and Safety Method 1550. Good agreement between the results is obtained.

Chromatography↗
PubMed2000

Determination of distribution constants between a liquid polymeric coating and water by a solid-phase microextraction technique with a flow-through standard water system

This paper describes an optimized experimental system for determining water/polymer coating distribution constants and discusses the mechanism of extraction of high molecular weight compounds by poly(dimethylsiloxane) (PDMS). The proposed flow-through standard water generator eliminates errors associated with both losses of analytes to the system surfaces and limited sample volume. In addition, the errors caused by partial precipitation or poor dissolution of highly hydrophobic analytes during spiking of water when producing calibration standards are also eliminated. The target analytes are a range of polycyclic aromatic hydrocarbons (PAHs). The results demonstrate that absorption partitioning is the predominant mechanism of extraction of analytes into PDMS-coated fibers for all PAHs investigated regardless of molecular weight. There is a strong correlation between determined PDMS/water distribution constants (K(fw)) and literature K(ow) values for all PAHs.

Journal Article↗
PubMed2000

Evolution of solid-phase microextraction technology.

The main objective of this contribution is to describe the development of the concepts, techniques and devices associated with solid-phase microextraction, as a response to the evolution of understanding of the fundamental principles behind this technique. The discussion begins with an historical perspective on the very early work conduced almost a decade ago. As new fundamental understanding about the functioning of the technology developed, new ways of constructing and using the SPME devices evolved.

Chromatography, Liquid↗
PubMed2000

In-tube solid-phase microextraction coupled to capillary LC for carbamate analysis in water samples.

Recently, the on-line sample preparation technique, intube solid-phase microextraction (SPME), was successfully implemented with a Hewlett-Packard 1100 HPLC system for analysis of carbamates in water samples. This paper describes the coupling of in-tube SPME to capillary LC and explores its utility as a sample preparation method in that format, relative to conventional LC. The Hewlett-Packard HPLC system was upgraded to a capillary LC system using commercially available accessories from LC Packings. The combination of in-tube SPME with a capillary LC system was expected to build on the merits of both in-tube SPME and the capillary LC to generate a sensitive method with an easy, effective, and efficient sample preparation. Due to the relatively large effective injection volume of the in-tube SPME technique (30-45 microL), on-column focusing was employed in order to achieve good chromatographic efficiency. Excellent sensitivity was achieved with very good method precision. For all carbamates studied, the RSD of retention time was between 0.5 and 0.8% under 4 microL/min microgradient conditions. The RSD of peak area counts was between 1.5 and 4.6%. The detection limits for all carbamates studied were less than 0.3 microg/L and, for carbaryl, just 0.02 microg/L (20 ppt). Compared with the conventional in-tube SPME/LC method, the LODs were lowered for carbaryl, propham, methiocarb, promecarb, chlorpropham, and barban, by factors of 24, 45, 42, 81, 62, and 56, respectively. The optimized method was successfully applied to the analysis of carbamates in surface water samples.

Carbamates↗
PubMed2000

Applications of solid-phase microextraction in food analysis.

Food analysis is important for the evaluation of the nutritional value and quality of fresh and processed products, and for monitoring food additives and other toxic contaminants. Sample preparation, such as extraction, concentration and isolation of analytes, greatly influences the reliable and accurate analysis of food. Solid-phase microextraction (SPME) is a new sample preparation technique using a fused-silica fiber that is coated on the outside with an appropriate stationary phase. Analyte in the sample is directly extracted to the fiber coating. The SPME technique can be used routinely in combination with gas chromatography (GC), GC-mass spectrometry (GC-MS), high-performance liquid chromatography (HPLC) or LC-MS. Furthermore, another SPME technique known as in-tube SPME has also been developed for combination with LC or LC-MS using an open tubular fused-silica capillary column as an SPME device instead of SPME fiber. These methods using SPME techniques save preparation time, solvent purchase and disposal costs, and can improve the detection limits. This review summarizes the SPME techniques for coupling with various analytical instruments and the applications of these techniques to food analysis.

Food Analysis↗
PubMed2000

Speciation of alkyllead and inorganic lead by derivatization with deuterium-labeled sodium tetraethylborate and SPME-GC/MS.

A method for full speciation and determination of alkyllead and inorganic lead(II) in aqueous samples was developed. This was accomplished by in situ derivatization with deuterium-labeled sodium tetraethylborate NaB(C2D5)4 (DSTEB). The derivatization was carried out directly in the aqueous sample and the derivatives were extracted from the headspace by a solid-phase microextraction (SPME) fiber. The extracted analytes were then transferred to a GC/MS or a GC/FID for separation and detection. The research presented demonstrates that SPME and the derivatization reagent DSTEB can be used successfully for the speciation of Pb2+, Pb(CH3)3+, Pb(C2H5)3+, and Pb(C2H5)4 in water samples. All derivatives, Pb(C2D5)4, (CH3)3Pb(C2D5), (C2H5)3Pb(C2D5), and Pb(C2H5)4, are separated using an SBP-5 column. This method was applied to monitor degradation of tetraethyllead in water. This is the first report of ethylation by DSTEB for full speciation of methyllead, ethyllead, and inorganic lead compounds. This approach can be extended to other organometallic compounds as demonstrated for ethyltin speciation. This full speciation method will aid in monitoring occurrence, pathways, toxicity, and biological effects of these compounds in the environment. It is easily adopted for field analysis.

Borates↗
PubMed2000

Determination of butyltin species in water and sediment by solid-phase microextraction-gas chromatography-flame ionization detection.

A procedure for determination of tetraethyltin (TeET) and tetrabutyltin (TeBT) in water by solid-phase microextraction (SPME) using the headspace approach has been developed. The method has been adapted for the simultaneous determination of mono-, di- and tributyltin species (MBT, DBT and TBT) after derivatization with sodium tetraethylborate in water and sediment samples. The analytical procedures were optimized with respect to stirring conditions, extraction time and extraction temperature. The pH and the amount of derivatizing reagent were also considered in derivatization reaction procedures. The analysis was carried out using gas chromatography equipped with flame ionization detection. The detection limits obtained for TeET and TeBT, in equilibrium conditions (room temperature for TeET and 40 degrees C for TeBT) were 28 and 20 ng/l (as Sn), respectively. The detection limit for butyltin species in water, which was limited by signals which are non-specific for the tin compounds and the sensitivity of the FID system, was found ca. 1 microg/l (as Sn). The SPME method was validated for analysis of sediments by analyzing the certified reference material PACS-2 finding a good agreement with the certified values.

Calibration↗
PubMed2000

Automated in-tube solid-phase microextraction-high-performance liquid chromatography for carbamate pesticide analysis.

In-tube solid-phase microextraction (SPME) is an automated version of SPME that can be easily coupled to a conventional HPLC autosampler for on-line sample preparation, separation and quantitation. It has been termed "in-tube" SPME because the extraction phase is coated inside a section of fused-silica tubing rather than coated on the surface of a fused-silica rod as in the conventional syringe-like SPME device. The new in-tube SPME technique has been demonstrated as a very efficient extraction method for the analysis of polar and thermally labile analytes. The in-tube SPME-HPLC method used with the FAMOS autosampler from LC Packings was developed for detecting polar carbamate pesticides in clean water samples. The main parameters relating to the extraction and desorption processes of in-tube SPME (selection of coatings, aspirate/dispense steps, selection of the desorption solvents, and the efficiency of desorption solvent, etc.) were investigated. The method was evaluated according to the reproducibility, linear range and limit of detection. This method is simple, effective, reproducible and sensitive. The relative standard deviation for all the carbamates investigated was between 1.7 and 5.3%. The method showed good linearity between 5 and 10000 microg/l with correlation coefficients between 0.9824 and 0.9995. For the carbamates studied, the limits of detection observed are lower than or similar to that of US Environmental Protection Agency or National Pesticide Survey methods. Detection of carbaryl present in clean water samples at 1 microg/l is possible.

Carbamates↗
PubMed2000

Development of a headspace solid-phase microextraction procedure for the determination of free volatile fatty acids in waste waters.

An analytical procedure based on headspace solid-phase microextraction (SPME) coupled to GC-flame ionization detection/Negative Chemical Ionization Mass Spectrometry has been developed for the determination of free volatile fatty acids (C2-C7) in waste water samples. Five different coatings have been evaluated and polydimethylsiloxane-Carboxen was the only fiber that allows a successful extraction of the shortest chain fatty acids (acetic and propionic). Several parameters such as extraction time and temperature, desorption conditions, agitation speed and sample volume have been optimized using the polydimethylsiloxane-Carboxen fiber. The linear dynamic range was over two-four orders of magnitude, depending on the acid. Procedural detection limits were in the low to medium microg/l levels and the RSDs were between 5.6% and 13.3%. To evaluate the applicability of the developed SPME procedure on real samples, fermented urban wastewaters were analysed.

Chromatography, Gas↗
PubMed2000

Development of membrane extraction with a sorbent interface-micro gas chromatography system for field analysis.

The commercially available portable gas chromatographs have a rather limited scope of applications, typically allowing analysis of gaseous samples only, and having relatively poor sensitivity. Combination of those instruments with modern sampling/sample preparation techniques can remedy these problems. A Chrompack micro-GC system equipped with a thermal conductivity detector has been coupled to membrane extraction with a sorbent interface (MESI). The sorbent trap has replaced the GC injector. The design of the trap was also modified in order to enhance the preconcentration of analytes. The use of a thin flat sheet membrane reduces the response time, and decreases the memory effect of the system. Rapid separation times were achieved, and the sensitivity was significantly improved. MESI enables semi-continuous monitoring of both gaseous and aqueous samples, owing to the selectivity of the membrane material. The system does not use moving parts, therefore being reliable. The sensitivity of the micro-GC system was increased by a factor of more than 100 by the addition of the MESI system, even with a preconcentration time as short as 1 min. Chloroform, having a concentration lower than 1 ppb, was detected in tap water. A cup system was used to allow headspace sampling of volatile organic compounds from aqueous matrices, keeping the membrane away from interfering species that could be present in water, and improving the mass transfer. A linear calibration line was obtained, and the estimated limit of detection was 60 ppt. This represents a great improvement for the sensitivity of the micro-GC system.

Chromatography, Gas↗
PubMed2000

Kinetics of solid-phase extraction and solid-phase microextraction in thin adsorbent layer with saturation sorption isotherm.

The effects of sorbent saturation in thin adsorbent layers have been much overlooked in earlier research and should be taken into account in both the theory and practice of solid-phase extraction (SPE) and solid-phase microextraction (SPME). The adsorption kinetics of a single analyte into a thin adsorptive layer was modeled for several cases of agitation conditions in the analyzed volume. The extraction process in the adsorbent layer was modeled using a Langmuir isotherm approximated by the linear isotherm at low concentrations and by a saturation plateau at concentrations exceeding the critical saturation concentration. Laplace transformations were used to estimate the equilibration time and adsorbed analyte concentration profile for no agitation, practical and perfect agitation in the analyzed volume. The equilibration time may be significantly reduced at high degrees of oversaturation and/or agitation in the analyzed volume. The resulting models indicated that the adsorbent layer becomes saturated at some critical value of the oversaturation degree parameter. The critical value of the oversaturation parameter is affected by both the concentration of the analyte in the analyzed volume and the sorbent characteristics. It was also shown that the adsorption process is carried out via the propagation of the saturation adsorption boundary toward the inner boundary of the adsorbent layer. These new adsorption models should serve as "stepping stones" for the development of competitive adsorption kinetic models for both SPE and SPME, particularly in cases where fast sampling is used.

Chromatography, Liquid↗
PubMed2000

Speciation of dimethylarsinic acid and monomethylarsonic acid by solid-phase microextraction-gas chromatography-ion trap mass spectrometry.

A solid-phase microextraction (SPME) method has been developed to determine two methylated arsenic species in human urine samples by GC-MS. The direct extraction of the methyl arsenic compounds by SPME after thioglycol methylate derivatization was studied. Direct extraction with SPME was suitable for the determination of trace levels of dimethylarsinic acid (DMA) and monomethylarsonic acid (MMA) in urine samples. Four different commercial SPME fibers were tested for the extraction of methyl arsenic compounds, and the best results were obtained using the polydimethylsiloxane coating. The extraction and desorption time profiles of DMA and MMA were determined. The detection limits for DMA and MMA using the SPME-GC-MS method were 0.12 and 0.29 ng/ml, respectively. The method is linear in the 1 to 200 ng/ml range.

Arsenicals↗
PubMed2000

Calibration of membrane extraction for air analysis

Calibration methods based on the recently developed mathematical model are proposed for air monitoring by membrane extraction. In membrane extraction, analytes permeate through the membrane at a constant rate controlled by the distribution constant and the diffusion coefficient. The principle of the proposed calibration approach is based on either theoretical or experimental determination of both constants at the extraction conditions. A group of selected compounds was employed for the experimental testing, and the results indicated practical feasibility of the approach. On-line determination of partition coefficients and distribution constants was proposed and investigated, producing very promising results. Both approaches to calibration facilitate quantitative monitoring.

Journal Article↗
PubMed2000

Membrane extraction with a sorbent interface for headspace monitoring of aqueous samples using a cap sampling device

A cap-shaped device was employed for headspace sampling. This sampling device coupled to membrane extraction with a sorbent interface (MESI) is intended to perform on-site and on-line aqueous sample monitoring. A laboratory sampling testwas performed both at the water surface and under water, and it showed some advantages in underwater monitoring. A group of volatile organic compounds (VOCs), varying in PDMS/gas and gas/water distribution constants, benzene, toluene, ethylbenzene, o-xylene, and trichloroethylene (TCE), was used for the sampling study. Magnetic stirring of the sample and circulation of the headspace air with a microfan were used for the enhancement of mass transfer between sample matrix and membrane to obtain higher extraction rate and efficiency. The agitation approaches were investigated individually and compared. The results showed that simultaneous agitation in water and air could greatly improve the extraction efficiency. Good linearity and precision and low detection limits were obtained for water-surface monitoring. The study demonstrated that Cap-MESI is a useful tool for field headspace monitoring of volatile organic compounds.

Journal Article↗
PubMed2000

On-line coupling of high performance gel filtration chromatography with imaged capillary isoelectric focusing using a membrane interface.

A high performance liquid chromatography system, a sample preparation device, and an imaged capillary IEF (CIEF) instrument are integrated and multiplexed on-line. The system is equivalent to two-dimensional polyacrylamide gel electrophoresis (2-D PAGE), by transferring the principle of 2-D separation to the capillary format. High performance liquid chromatography (HPLC) provides protein separation based on size using a gel filtration chromatography (GFC) column. Each eluted protein is sampled and directed to a novel microdialysis hollow fiber membrane device, where simultaneous desalting and carrier ampholyte mixing occurs. The sample is then driven to the separation column in an on-line fashion, where CIEF takes place. The fluidic technology used by our 2-D system leads to natural automation. The coupling of the two techniques is simple. This is attributed to high speed and efficiency of the sample preparation device that acts as an interface between the two systems, as well as the speed and simplicity of our whole column absorption imaged CIEF instrument. To demonstrate the feasibility of this approach, the separation of a mixture of two model proteins is studied. Sample preparation and CIEF were complete in just 4-5 min, for each of the eluted proteins. Total analysis time is about 24 min. Three-dimensional data representations are constructed. Challenges and methods to further improve our instrument are discussed, and the design of an improved horseshoe-shaped sample preparation sample loop membrane interface is presented and characterized.

Animals↗