Cooling assisted headspace microextraction by packed sorbent coupled to HPLC for the determination of volatile polycyclic aromatic hydrocarbons in soil.

A headspace microextraction by packed sorbent technique (HS-MEPS) was developed that is assisted by cooling the extraction phase and, in the same time, heating the sample matrix. The innovated cooling assisted HS-MEPS system was optimized for the extraction and HPLC determination of volatile polycyclic aromatic hydrocarbons (PAHs) in solid samples. Amino ethyl-functionalized SBA-15 was used as a nanoporous sorbent for packing the conical hub of the MEPS syringe. For efficient extraction of PAHs, several parameters such as the nature and mass of sorbent, eluent type, elution volume, extraction temperature and number of draw-eject cycles of the syringe were studied and optimized. Under the optimal experimental conditions, only 2 mg of the sorbent was sufficient by applying a temperature of 0 °C to the sorbent while the sample was heated up to 150 °C. Linear calibration curves (R2 > 0.95) were obtained for all the studied PAHs and their quantitation limits were in the range of 0.042-0.25 ng g-1. The method was successfully applied to the extraction and HPLC analysis of PAHs in some polluted soil samples.

Synthesis and characterization of MIL-101(Cr) intercalated by polyaniline composite, doped with silica nanoparticles and its evaluation as an efficient solid-phase extraction sorbent.

A metal-organic framework/polyaniline composite was synthesized and doped with silica nanoparticles. The structure and morphology of the composite were characterized using Fourier transform infrared spectroscopy and scanning electron microscopy. It was packed inside a cartridge and evaluated for the solid-phase extraction of thymol and carvacrol, followed by gas chromatography with flame ionization detection measurement. The influence of the important experimental variables on the efficiency of the proposed method, including pH, ionic strength, volume of sample solution and type, and volume of eluent were studied and optimized. Under the optimal conditions, the relative standard deviations were found to be 3.8 and 9.8% for thymol and carvacrol, respectively, and the corresponding limits of detection were 0.1 and 1.0 ng/mL. The linear dynamic ranges for the calibration curves of the analytes were 10-10000 ng/mL, with determination coefficients (R2 ) > 0.993. The limits of quantifications were found to be 0.01 and 0.5 µg/mL, for thymol and carvacrol, respectively. The prepared nanocomposite sorbent was applied successfully to the extraction and determination of thymol and carvacrol in Lamiaceae plant extracts and a honey sample, with relative recoveries in the range of 90.28-122.0%.

A Needle Trap Device Packed with Nanoporous Silica Sorbents for Separation and Gas Chromatographic Determination of Polycyclic Aromatic Hydrocarbons in Contaminated Soils.

SBA-15 and MCM-41 nanoporous silica sorbents were synthesized and functionalized by amine groups and used, for the first time, for packing a needle trap device (NTD). The characteristics of the synthesized SBA-15 and MCM-41 sorbents were investigated by X-ray diffraction, scanning electron microscopy and Fourier transfer infrared spectroscopy. The NTD coupling to gas chromatography with a flame ionization detector (GC-FID) was carried out to extract and determine polycyclic aromatic hydrocarbons (PAHs) in contaminated soil samples. The performances of the sorbents for the extraction of PAHs were compared under identical conditions and the NH2-SBA-15 sorbent showed superior results. Extraction temperature, extraction time, recycling gas flow rate, sample moisture, desorption time and desorption temperature were evaluated and optimized for the system. Under the optimum conditions, detection limits of 0.0004-0.0035 µg g-1, quantitation limits of 0.001-0.01 µg g-1 and relative standard deviations of 7.4-14.9% were obtained for the PAHs. The results showed the more effectiveness of this sorbent for the extraction of the PAHs compared to that of a commercial sorbent. The method was successfully applied for the extraction and determination of PAHs in polluted soil samples collected from gas stations, with recoveries ranging from 64 to 112%.

Comparison of the Conventional and Electroenhanced Direct-Immersion Solid-Phase Microextraction for Sampling of Nicotine in Biological Fluids of the Human Body.

A stainless steel fiber was made porous and adhesive by platinization and then coated by nanostructured polypyrrole (PPy), using an appropriate electrophoretic deposition (EPD) method. The morphological surface structure and functional groups of the PPy-coated fiber were studied using SEM (Scanning electron microscope) instrument. The prepared fiber was used for comparison of direct immersion (DI) and electroenhanced direct immersion solid-phase microextraction (EE-DI-SPME) of nicotine in human plasma and urine samples followed by gas chromatography flame ionization detector (GC-FID) determination. The effects of the influential experimental parameters on the efficiency of the DI-SPME and EE-DI-SPME methods, including the pH and ionic strength of the sample solution, applied Direct current (DC) voltage, extraction temperature and time and stirring rate, were optimized. Under the optimal conditions, the calibration curves for the DI-SPME-GC-FID and EE-DI-SPME-GC-FID methods were linear over the ranges of 0.1⁻10.0 µg mL-1 and 0.001⁻10.0 µg mL-1, respectively. The relative standard deviations (RSDs, n = 6) were found to be 6.1% and 4.6% for the DI and EE strategies, respectively. The LODs (limit of detection) of the DI-SPME-GC-FID and EE-DI-SPME-GC-FID methods were found to be 10 and 0.3 ng mL-1, respectively. The relative recovery values (for the analysis of 1 µg mL-1 nicotine) were found to be 91⁻110% for EE-DI-SPME and 75⁻105% for DI-SPME. The enrichment factors for DI-SPME and EE-DI-SPME sampling were obtained as 38,734 and 50,597, respectively. The results indicated that EE-SPME was more efficient for quantitation of nicotine in biological fluids. The developed procedure was successfully carried out for the extraction and measurement of nicotine in real plasma and urine samples.

Chemometrics-assisted investigation of interactions of Tasmar with human serum albumin at a glassy carbon disk: Application to electrochemical biosensing of electro-inactive serum albumin.

In this work, voltammetric data recorded by a glassy carbon electrode (GCE) was used to investigate the interactions of tolcapone (Tasmar, TAS) with human serum albumin (HSA) at the electrode surface. The recorded voltammetric data was also combined with spectroscopic data to construct an augmented data matrix which was analysed by multivariate curve resolution-alternating least squares (MCR-ALS) as an efficient chemometric tool to obtain more information about TAS-HSA interactions. The results of MCR-ALS confirmed formation of one complex species (HSA-TAS2) and application of MCR-BANDS to the results of MCR-ALS confirmed the absence of rotational ambiguities and existing unambiguous and reliable results. Binding of TAS to HSA was also modeled by molecular docking and the results showed that the TAS was bound to sub-domain IIA of HSA which were compatible with the ones obtained by recording experimental data. Hard-modeling of combined voltammetric and spectroscopic data by EQUISPEC helped us to compute binding constant of HSA-TAS2 complex species which was compatible with the binding constant value obtained by direct analysis of experimental data. Finally, a new electroanalytical method was developed based on TAS-HSA interactions for determination of HSA in two ranges of 0-541 nM and 541-1200 nM with a limit of detection of 0.04 nM and a sensitivity of 0.02 µA nM-1.

Comparison of the atmospheric- and reduced-pressure HS-SPME strategies for analysis of residual solvents in commercial antibiotics using a steel fiber coated with a multiwalled carbon nanotube/polyaniline nanocomposite.

A low-cost, sensitive and reliable reduced-pressure headspace solid-phase microextraction (HS-SPME) setup was developed and evaluated for direct extraction of residual solvents in commercial antibiotics, followed by determination by gas chromatography with flame ionization detection (GC-FID). A stainless steel narrow wire was made porous and adhesive by platinization by a modified electrophoretic deposition method and coated with a polyaniline/multiwalled carbon nanotube nanocomposite. All experimental variables affecting the extraction efficiency were investigated for both atmospheric-pressure and reduced-pressure conditions. Comparison of the optimal experimental conditions and the results demonstrated that the reduced-pressure strategy leads to a remarkable increase in the extraction efficiency and reduction of the extraction time and temperature (10 min, 25 °Ï¹ vs 20 min, 40 °Ï¹). Additionally, the reduced-pressure strategy showed better analytical performances compared with those obtained by the conventional HS-SPME-GC-FID method. Limit of detections, linear dynamic ranges, and relative standard deviations of the reduced-pressure HS-SPME procedure for benzene, toluene, ethylbenzene, and xylene (BTEX) in injectable solid drugs were obtained over the ranges of 20-100 pg g-1, 0.02-40 µg g-1, and 2.8-10.2%, respectively. The procedure developed was successful for the analysis of BTEX in commercial containers of penicillin, ampicillin, ceftriaxone, and cefazolin. Graphical abstract Schematic representation of the developed RP-HS-SPME setup.

Reinforced microextraction of polycyclic aromatic hydrocarbons from polluted soil samples using an in-needle coated fiber with polypyrrole/graphene oxide nanocomposite.

The surface of a stainless-steel wire was platinized using electrophoretic deposition method to create a high-surface-area with porous and cohesive substrate. The platinized fiber was coated by the polypyrrole/graphene oxide nanocomposite by electropolymerization and accommodated into a stainless-steel needle to fabricate an in-needle coated fiber. The developed setup was coupled to gas chromatography with flame ionization detection and applied to extract and determine polycyclic aromatic hydrocarbons (naphthalene, fluorene, phenanthrene, fluoranthene, and pyrene) in complicated solid matrices, along with reinforcement of the extraction by cooling the sorbent, using liquid carbon dioxide. To obtain the best extraction efficiency, the important experimental variables including extraction temperature and time, temperature of cooled sorbent, sampling flow rate, and desorption condition were studied. Under the optimal condition, limits of detection for five studied analytes were in the range of 0.2-0.8 pg/g. Linear dynamic ranges for the calibration curves were found to be in the range of 0.001-1000 ng/g. Relative standard deviations obtained for six replicated analyses of 1 ng/g of analytes were 4.9-13.5%. The reinforced in-needle coated fiber method was successfully applied for the analysis of polycyclic aromatic hydrocarbons in contaminated soil samples.

Single-step reinforced microextraction of polycyclic aromatic hydrocarbons from soil samples using an inside needle capillary adsorption trap with electropolymerized aniline/multi-walled carbon nanotube sorbent.

A polyaniline/multi-wall carbon nanotubes (PANI/MWCNT) composite was electrodeposited on the interior surface of a platinized stainless steel capillary needle and used to prepare an inside needle capillary adsorption trap (INCAT) device. The platinization expanded the interior adsorbing surface of the needle and made it more porous and cohesive for nanocomposite film. The nanocomposite was characterized using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR). The fabricated INCAT was fixed into a cooling capsule to fabricate a cooling-assisted INCAT (CA-INCAT) system. The CA-INCAT device was used to extract polycyclic aromatic hydrocarbons (PAHs) from solid samples followed by gas chromatography-flame ionization detection (GC-FID) determination. To obtain the best extraction efficiency, the important experimental variables were studied and optimized. Under the optimal conditions, the limits of detection (LODs) for the studied PAHs were in the range of 0.002-0.02ngg-1. Linear dynamic ranges (LDRs) for the calibration curves were found to be 0.1-30,000ngg-1. Relative standard deviations (RSDs%) for six replicated analysis of 1ngg-1 PAHs were obtained 7.7-11%. The CA-INCAT-GC-FID method was successfully applied for the extraction and determination of PAHs in contaminated soil samples. The results were in agreement with those obtained by a validated ultrasound-assisted solvent extraction (UA-SE) method.

Use of volatile organic solvents in headspace liquid-phase microextraction by direct cooling of the organic drop using a simple cooling capsule.

A low-cost and simple cooling-assisted headspace liquid-phase microextraction device for the extraction and determination of 2,6,6-trimethyl-1,3 cyclohexadiene-1-carboxaldehyde (safranal) in Saffron samples, using volatile organic solvents, was fabricated and evaluated. The main part of the cooling-assisted headspace liquid-phase microextraction system was a cooling capsule, with a Teflon microcup to hold the extracting organic solvent, which is able to directly cool down the extraction phase while the sample matrix is simultaneously heated. Different experimental factors such as type of organic extraction solvent, sample temperature, extraction solvent temperature, and extraction time were optimized. The optimal conditions were obtained as: extraction solvent, methanol (10 µL); extraction temperature, 60°C; extraction solvent temperature, 0°C; and extraction time, 20 min. Good linearity of the calibration curve (R(2) = 0.995) was obtained in the concentration range of 0.01-50.0 µg/mL. The limit of detection was 0.001 µg/mL. The relative standard deviation for 1.0 µg/mL of safranal was 10.7% (n = 6). The proposed cooling-assisted headspace liquid-phase microextraction device was coupled (off-line) to high-performance liquid chromatography and used for the determination of safranal in Saffron samples. Reasonable agreement was observed between the results of the cooling-assisted headspace liquid-phase microextraction high-performance liquid chromatography method and those obtained by a validated ultrasound-assisted solvent extraction procedure.

Direct determination of acrylamide in potato chips by using headspace solid-phase microextraction coupled with gas chromatography-flame ionization detection.

Acrylamide is a potentially toxic and carcinogenic substance present in many high-consumption foods. Recently, this matter has been placed in category of "reasonably anticipated to be a human carcinogen" by National Toxicology Program (NTP). Therefore, simple and cost-effective determination of acrylamide in food samples has attracted intense interest. The most reported techniques for this purpose are GC-MS and LC-MS, which are very expensive and available in few laboratories. In this research, for the first time, a rapid, easy and low-cost method is introduced for sensitive and precise determination of acrylamide in foodstuffs, using gas chromatography-flame ionization detection (GC-FID) system after its direct trapping in the upper atmosphere of samples by headspace solid-phase microextraction (HS-SPME). The effects of main experimental variables were studied and the optimized parameters were obtained as the type of fiber, carboxen/divinylbenzene/polydimethylsiloxane (CAR/DVB/PDMS); extraction time, 30 min; extraction temperature, 60°C; moisture content, 10 µL water per 1g of sample; desorption time, 2 min; and desorption temperature, 230°C. The linear calibration graph was obtained in the range of 0.77-50 µg g(-1), with regression coefficient of 0.998. The detection and quantification limits of the proposed method were 0.22 and 0.77 µg g(-1), respectively. The recoveries, for different food samples, were 79.6-95.7%. The repeatability of measurements, expressed as relative standard deviation (RSD), were found to be 4.1-8.0% (n=9). The proposed HS-SPME-GC-FID method was successfully carried out for quantifying of trace levels of acrylamide in some processed food products (chips and French fries), sold in open local markets.

Cooling/heating-assisted headspace solid-phase microextraction of polycyclic aromatic hydrocarbons from contaminated soils.

A simple, low-cost, and effective cooling/heating-assisted headspace solid-phase microextraction (CHA-HS-SPME) device, capable of direct cooling the fiber to low temperatures and simultaneous heating the sample matrix to high temperatures, was fabricated and evaluated. It was able to cool down the commercial and handmade fibers for the effective tapping of volatile and semi-volatile species in the headspace of complex solid matrices, with minimal manipulation compared with conventional SPME. The CHA-HS-SPME system can create large temperature gaps (up to 200 °C) between the fiber and the sample matrix, because the cooling process is directly applied onto the fiber. Different effective experimental parameters for the fabrication of the CHA-HS-SPME device as well as for the extraction and determination of polycyclic aromatic hydrocarbons (PAHs) from solid samples were evaluated and optimized. The proposed device coupled to GC-FID was successfully applied for the extraction and determination of PAHs in contaminated soils without any sample pretreatment step. Good agreement was observed between the results obtained by the proposed CHA-HS-SPME-GC-FID method and those achieved by validated method.

Application of graphene nanoplatelets silica composite, prepared by sol-gel technology, as a novel sorbent in two microextraction techniques.

In this study, the application of a novel nanomaterial composite was investigated in two microextraction techniques of solid-phase microextraction and a needle trap device in a variety of sampling conditions. The optimum sampling temperature and relative humidity were 10°C and 20%, respectively, for both techniques with two sorbents of graphene/silica composite and polydimethyl siloxane. The two microextraction techniques with the proposed sorbent showed recoveries of 95.2 and 94.6% after 7 days. For the needle trap device the optimums desorption time and temperature were 3 min at 290°C and for SPME these measures were 1 and 1.5 min at 240-250°C for the graphene/silica composite and polydimethyl siloxane, respectively. The relative standard division obtained in inter- and intra-day comparative studies were 3.3-14.3 and 5.1-25.4, respectively. For four sample the limit of detection was 0.021-0.25 ng/mL, and the limit of quantitation was 0.08-0.75 ng/mL. The results show that the graphene/silica composite is an appropriate extraction media for both techniques. Combining an appropriate sorbent with microextraction techniques, and using these in conjunction with a sensitive analytical instrument can introduce a strong method for sampling and analysis of occupational and environmental pollutants in air.

Graphene packed needle trap device as a novel field sampler for determination of perchloroethylene in the air of dry cleaning establishments.

In this paper we describe the application of a needle trap microextraction device packed with graphene nanoplatelets for the sampling and analysis of perchloroethylene in dry cleaning. The study was carried out in two phases. First the parameters for the sampling and analysis of perchloroethylene by NTD were evaluated and optimized in the laboratory. Then the sampler was used to determine the levels of perchloroethylene in a dry-cleaning shop. In the laboratory phase of the study the performance of the NTD packed with the proposed sorbent was examined in a variety of sampling conditions to evaluate the technique. The technique was also compared with NTDs packed with PDMS as well as SPME with Carboxen/PDMS-coated fibers. Both the NTDs and SPME performed better at lower sampling temperatures and relative humidity levels. The post-sampling storage times for a 95% recovery of the analyte were 5, 5 and 3 days for NTD-graphene, NTD-PDMS and SPME-CAR/PDMS respectively. The optimum desorption time was 3 min for NTDs packed with either graphene or PDMS and 1 min for SPME-CAR/PDMS. The limits of detection for the GC/MS detection system were 0.023 and 0.25 ng mL(-1) for NTDs packed with graphene and PDMS and 0.014 ng mL(-1) for SPME coated with CAR/PDMS. In the second stage of the study the evaluated technique was applied to the sampling and analysis of perchloroethylene in dry cleaning. In this environment the performance of the NTD-graphene as a field sampler for PCE was similar to that of the SPME-CA/PDMS, and better than the NIOSH 1003 method which had greater measurement variations. The results show that a NTD packed with carbonic graphene nanoplatelets and used as an active exhaustive sampling technique is effective for determination of VOC and HVOC occupational/environmental pollutants in air.

A needle trap device packed with a sol-gel derived, multi-walled carbon nanotubes/silica composite for sampling and analysis of volatile organohalogen compounds in air.

A needle trap device (NTD) packed with silica composite of multi-walled carbon nanotubes (MWCNTs) prepared based on sol-gel technique was utilized for sampling and analysis of volatile organohalogen compounds (HVOCs) in air. The performance of the NTD packed with MWCNTs/silica composite as sorbent was examined in a variety of sampling conditions and was compared with NTDs packed with PDMS as well as SPME with Carboxen/PDMS-coated fibers. The limit of detection of NTDs for the GC/MS detection system was 0.01-0.05 ng mL(-1) and the limit of quantitation was 0.04-0.18 ng mL(-1). The RSD were 1.1-7.8% for intra-NTD comparison intended for repeatability of technique. The NTD-MWCNTs/silica composite showed better analytical performances compared to the NTD-PDMS composite and had the same analytical performances when compared to the SPME-Carboxen/PDMS fibers. The results show that NTD-MWCNTs-GC/MS is a powerful technique for active sampling of occupational/environmental pollutants in air.

A novel needle trap device with single wall carbon nanotubes sol-gel sorbent packed for sampling and analysis of volatile organohalogen compounds in air.

This paper describes a new approach that combines needle trap devices (NTDs) with a newly synthesized silanated nano material as sorbent for sampling and analysis of HVOCs in air. The sol-gel technique was used for preparation of the single wall carbon nanotube (SWCNT)/silica composite as sorbent, packed inside a 21-gauge NTD. Application of this method as an exhaustive sampler device was investigated under different laboratory conditions in this study. Predetermined concentrations of each analyte were prepared in a home-made standard chamber, and the effects of experimental parameters, such as temperature, humidity, sampling air flow rate, breakthrough volume and storage time on NTD, and the sorbent performance were investigated. The proposed NTD was used in two different modes and two different injection methods, and an NTD with a side hole, a narrow neck glass liner and syringe pump assisted injection of carrier gas were applied. The NTD packed with SWCNTs/silica composite was compared to the NTD packed with PDMS and also SPME with CAR/PDMS. For four compounds, LOD was 0.001-0.01 ng mL(-1), LOQ was 0.007-0.03 ng mL(-1), and the relative standard division for repeatability of method was 2.5-6.7%. The results show that the incorporation of NTD and SWCNTs/silica composite is a reliable and effective approach for the sampling and analysis of HVOCs in air. Coupling this system to GC-MS make it more sensitive and powerful technique.

Comparison of headspace solid-phase microextraction, headspace single-drop microextraction and hydrodistillation for chemical screening of volatiles in Myrtus communis L.

INTRODUCTION: Headspace solid-phase microextraction (HS-SPME) and headspace single-drop microextraction (HS-SDME) methods have never been used for the extraction and analysis of the volatile compounds of Myrtus communis. For that reason, in this work, these two techniques were compared with the traditional hydrodistillation (HD) extraction technique. OBJECTIVE: To compare SPME and SDME with HD for the extraction and analysis of Myrtus communis volatiles. METHODOLOGY: Three extraction methods, i.e. SPME, SDME and HD, coupled to gas chromatography-mass spectrometry were used and optimised for the analysis of Myrtus communis volatiles. The SPME extraction was performed on a 100 µm PDMS fibre and for SDME a drop of n-octadecane containing 0.7% of menthol as internal standard was used as extracting solvent. The results were compared from different viewpoints including efficiency of extraction, different kinds of species extracted and quantity of extracted compounds with HD. RESULTS: The main analytes extracted by SPME were found to be α-pinene, limonene, 1,8-cineole, linalool, linalyl acetate, α-terpinyl acetate and geranyl acetate, whereas for SDME α-pinene, limonene, 1,8-cineole, linalool, linalyl acetate and ß-myrcene were extracted as major components. Hydrodistillation could extract α-pinene, limonene, 1,8-cineole, linalool, α-terpineol, linalyl acetate, α-terpinyl acetate, geranyl acetate and cis-isoeugenol better than other volatiles from Myrtus communis. CONCLUSION: The results demonstrated that HS-SPME and HS-SDME can be applied successfully for the extraction and separation of volatiles in aromatic plants, and these techniques are easier to perform, and more effective than HD for collection of more volatile compounds.

Reversed-phase dispersive liquid-liquid microextraction with multivariate optimization for sensitive HPLC determination of tyrosol and hydroxytyrosol in olive oil.

A reversed-phase dispersive liquid-liquid microextraction (RP-DLLME) method coupled to HPLC was developed for the extraction of hydroxytyrosol (HTy) and tyrosol (Ty) from virgin olive oil. In this first application of the RP-DLLME method to non-polar samples, the phenolic compounds were directly extracted into an aqueous micro-drop, which could be injected into a chromatography column without any further pretreatment. A glass test tube with lengthened conical bottom was fitted inside a centrifuge tube in this work for more efficient withdrawal of the sedimented phase with a microsyringe. The volumes of water and ethyl acetate, the pH of water and the centrifuge time as four effective parameters on the extraction were optimized by a central composite design (response surface) method. Five replicated analyses under the optimized conditions (i.e., 0.2 mL ethyl acetate as disperser and 100 µL water at pH 11 as the extraction solvent) resulted in recoveries of 104.3 and 97.6%, and relative standard deviations of 5.75 and 4.57 for HTy and Ty, respectively. The detection limit of the method (3σ) was 0.043 mg L(-1) for HTy and 0.032 mg L(-1) for Ty. The method was successfully applied to the determination of HTy and Ty in five olive oil samples.

CMK-3 nanoporous carbon as a new fiber coating for solid-phase microextraction coupled to gas chromatography-mass spectrometry.

CMK-3 nanoporous carbon was prepared and characterized as a highly porous fiber coating, with a highly ordered carbon framework, for solid-phase microextraction (SPME). The nanomaterial was immobilized onto platinum, stainless steel and copper metal wires for preparation of new SPME fibers. The copper-CMK-3 fiber showed superior properties and therefore was applied for extraction of some phenolic compounds in combination with GC-MS. For optimization of the extraction conditions, a simplex optimization method was used. The selected conditions were: sample volume 13 ml, extraction temperature 56°C, extraction time 7 min, ultrasonic time 5.5 min, pH 5 and salt concentration 8.9%. The selected fiber showed some selectivity towards the polar phenolic compounds and its extraction efficiency was better than a commercial PDMS fiber. Linear calibration curves with correlation coefficients better than 0.99 and detection limits in the range from 0.002 to 0.068 µg mL(-1) were obtained for the fiber. No significant change was observed in the extraction efficiency of the new SPME fiber over at least 40 extractions. The fiber was successfully used for the determination of phenolic compounds in natural water samples.

Reversed-phase dispersive liquid-liquid microextraction with central composite design optimization for preconcentration and HPLC determination of oleuropein.

A reversed-phase dispersive liquid-liquid microextraction (RP-DLLME) method was developed for the preconcentration and direct HPLC determination of oleuropein in olive's processing wastewater (OPW) and olive leaves extracts. In conventional DLLME, the sedimented phase is a micro-drop of a chlorinated organic solvent that is not compatible with RP-HPLC. Therefore, solvent evaporation and reconstitution with an appropriate solvent is often required. In RP-DLLME, this problem was overcome by overturning the solvent polarity in the ordinary DLLME and replacing the organic solvent with water. A central composite chemometrics design was used for multivariate optimization of the effects of five different parameters influencing the extraction efficiency of the method. In the optimized conditions, a mixture of 1.4 mL of an ethyl acetate extract of sample and 40 microL water (pH 5.0) was rapidly injected into 5.3 mL of cyclohexane. After centrifugation of the formed cloudy mixture, a micro-drop of the aqueous phase was sedimented at the conical bottom of the centrifuge tube. This phase, that contained the preconcentrated and partially purified analyte, was directly injected into an RP-HPLC column for analysis. A mean extraction recovery of 102.5 (+/-4.5) % with enrichment factors exceeding 38, was obtained for five replicated analysis. The detection limit of the method (3 sigma) for OE was 0.02 microg L(-1) for OPW and 2 x 10(-3) mg kg(-1) for olive leaves samples. The results showed that, RP-DLLME is a promising technique which is quick, easily operated and can be directly coupled to HPLC.

Development of a simple device for dispersive liquid-liquid microextraction with lighter than water organic solvents: isolation and enrichment of glycyrrhizic acid from licorice.

A simple device was developed that makes the use of lighter than water organic solvents feasible in dispersive liquid-liquid microextraction (DLLME) method. In the ordinary DLLME, the fact that a heavier than water organic solvent must be used, to be sedimented at the conical bottom of a centrifuge tube, limits the applications of this method in some extent. In the developed method, a glass tube with a narrow neck is inserted inside the centrifuge tube. After phase separation, the organic solvent is accumulated in the narrow neck of the device and therefore, can be simply collected by a micro-syringe. The DLLME method with the proposed device was tested for the enrichment of glycyrrhizic acid from aqueous extracts of licorice before analysis by a HPLC method. n-Hexanol and acetone were used as the organic and disperser phases, respectively. Effects of pH, salt concentration and phase volumes on the extraction of the analyte were optimized using a central composite (response surface) design. Under the optimized conditions (i.e. pH 1.3, ionic strength 0.2 mol L(-1), n-hexanol 140 microL and acetone 0.8 mL) an extraction recovery of 104.1 (+/-5.1)% and an enrichment factor of 54 were obtained. The proposed method was successfully applied for the study of glycyrrhizic acid's level of licorice roots grown in three regions of Lorestan province, Iran, with different climate conditions.