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PubMed2000

[From medicolegal toxicology to forensic toxicology].

The importance of forensic toxicology has been increasing until now, because of the increasing numbers of toxic substances and poisoning incidents. In Japan, a special translational word "houi-chudoku-gaku" has been used for the forensic toxicology especially in the field of legal medicine. The Japanese word, however, does not seem appropriate for translation of forensic toxicology, because it covers medicine, pharmacy and police sciences interdisciplinary. In 1980, Emeritus Prof. Hidetoshi Yoshimura created an appropriate word "hochudoku-gaku" for translation of forensic toxicology. In 1982, Prof. Yoshimura and his friends established the Japanese Association of Forensic Toxicology, consisting of people from legal medicine, pharmacy and police institutes. This Association enabled lively discussions among different fields and greatly contributed to advances of forensic toxicology in Japan. We started studies of forensic toxicology using gas chromatography (GC)/mass spectrometry (MS) in 1979. Until now, we delt with solid-phase extraction (1987-1994), surface ionization GC (1989-1997), negative ion chemical ionization MS (1981-now), solid-phase microextraction (1994-now), cryogenic oven trapping GC (1997-now), surface ionization organic MS (1998-now) and high-performance liquid chromatography/tandem MS (1998-now). In this review, the author presents some details of solid-phase microextraction, negative ion chemical ionization MS, cryogenic oven trapping GC and surface ionization organic MS. Unprecedented poisoning terrorism by use of sarin took place in Matsumoto and Tokyo in 1994 and 1995, respectively. On July 25, 1998, a curry poisoning incident using arsenious acid occurred in Wakayama, resulting in the death of 4 people and injury of 63 people. Since then, more than 30 imitative poisoning cases have been reported by mass communication within 1 year. In spite of the above continuing poisoning cases, almost no effective measures have been taken by the administration of our country and local governments. Many serious problems concerning poisoning and drug abuse are accumulating in Japan. In this review, the problems are also made manifest, and some proposals are presented to solve the problems.

Forensic Medicine↗
PubMedDate not supplied

Volatile organic compounds produced during irradiation of mail.

In 2001, Bacillus anthracis spores were delivered through the United States postal system in a series of bioterrorist acts. Controls proposed for this threat included sanitization with high-energy electrons. Solid phase microextraction was used with gas chromatography/mass spectrometry for field sampling and analysis of volatile compounds apparently produced from polymeric materials such as cellulose and plastics, immediately following processing of mail at a commercial irradiation facility. Solid phase microextraction and direct sampling of air into a cryogenically cooled temperature programmable inlet were used in the laboratory for gas chromatography/mass spectrometry analysis of air in contact with irradiated mail, envelopes only (packaged identically to mail), and air inside irradiated plastic mail packaging bags (with neither mail nor envelopes). Irradiated mail or envelope systems produced hydrocarbons such as propane, butane, pentane, hexane, heptane, methylpentanes, and benzene; and oxygen-containing compounds such as acetaldehyde, acrolein, propionaldehyde, furan, 2-methylfuran, methanol, acetone, 2-butanone, and ethanol. In addition to hydrocarbons, methyl and ethyl nitrate were detected in irradiated bags that contained only air, suggesting reactive nitrogen species formed from air irradiation reacted with hydroxy-containing compounds to give nitro esters. The similarities of volatile compounds in irradiated systems containing paper to those observed by researchers studying cellulose pyrolysis suggests common depolymerization and degradation mechanisms in each case. These similarities should guide additional work to examine irradiated mail for chemical compounds not detectable by methods used here.

Air Pollution, Indoor↗
PubMedDate not supplied

Matrix solid-phase dispersion microextraction and determination of pesticide residues in medicinal herbs by gas chromatography with a nitrogen-phosphorus detector.

A gas chromatography method for the determination of residues of 6 pesticides in Isatis indigotica Fort and Paeonia lactiflora Pall is described. Optimizations of different parameters were performed. The method used 0.5 g herb sample, silica gel as the matrix solid-phase dispersion sorbent, and acetone as the eluting solvent. Recoveries at spiked concentrations between 0.1 and 5 mg/kg were between 80.63 and 110.12%, with relative standard deviations ranging from 0.43 to 17.67%. The limits of quantitation were 0.01 mg/kg for metalaxyl, triadimefon, and paclobutrazol and 0.05 mg/kg for vinclozolin, tebuconazole, and fenarimol. The method may be useful as a screening protocol for the determination of these pesticides in medicinal herb samples.

Chromatography, Gas↗
PubMed2006

Comparative study of two chromatographic methods for quantifying 2,4,6-trichloranisole in wines.

Here we present the validation and the comparative study of two chromatographic methods for quantifying 2,4,6-trichloroanisole (TCA) in wines (red, rosé and white wines). The first method involves headspace solid-phase microextraction and gas chromatography with electron-capture detection (ECD). The evaluation of the performance parameters shows limit of detection of 0.3 ng l(-1), limit of quantification of 1.0 ng l(-1), recoveries around 100% and repeatability of 10%. The second one implies a headspace solid-phase microextraction and gas chromatography with mass spectrometric detection. The performance parameters of this second method are limit of detection of 0.2 ng l(-1), limit of quantification of 0.8 ng l(-1) and repeatability of 10.1%. From the comparative study we can state that both methods provide similar results and the differences between them are the better sensitivity of the GC-ECD method and the very shorter chromatogram running time of the GC-MS method. The two methods are able to quantify TCA below the sensorial threshold in red, rosé and white wines using just a calibration graph, thus they could be a very good tool for quality control in wineries.

Anisoles↗
PubMed2000

Determination of organophosphorus insecticides in natural waters using SPE-disks and SPME followed by GC/FTD and GC/MS.

Two methods for the analysis of ten organophosphorus insecticides in natural waters using solid phase extraction disks containing C18 and SDB and solid phase microextraction fibers containing polyacrylate (PA) are developed. Bromophos ethyl, bromophos methyl, dichlofenthion, ethion, fenamiphos, fenitrothion, fenthion, malathion, parathion ethyl and parathion methyl were determined by GC/MS and GC/FTD. The SPE-disks require only 1000 mL of sample and provide a method limit of detection in the range of 0.01-0.07 microgram/L and recovery rates from 60.7 to 104.1%. The solid phase microextraction (SPME) technique requires 2-5 mL of water sample and provides a method limit of detection in the range of 0.01 to 0.05 microgram/L for all detectors and the recoveries compared to distilled water ranged from 86.2 to 119.7%. The proposed methods were applied to the trace level screening determination of insecticides in river water samples originating from different Greek regions.

Calibration↗
PubMed2001

[Determination of organic acids in cigarette smoke].

Solid phase microextraction (SPME) is a simple, cost-effective, time-saving extraction technique. It is rapid and highly sensitive. In this study, organic acids in cigarette smoke were extracted with 85 microns polyacrylate coated fiber. Volatile and semi-volatile organic acids, such as butanoic acid, hexanoic acid, 2-furancarboxylic acid, octanoic acid, nonanoic acid, benzoic acid, phenylacetic acid, tetradecanoic acid, and hexadecanoic acid from cigarette smoke were converted to their esters by using methanolic derivatization agent. The esters were extracted by using headspace solid phase microextraction and determined quantitatively by gas chromatography with selected ion monitoring mode mass spectrometry. Qualitative analysis of 4 brands cigarette smoke demonstrated the usefulness of this analytical technique of volatile and semi-volatile acids in cigarette smoke. More than sixty organic acids were detected by using this method.

Benzoic Acid↗
PubMed2005

Volatile profiling of Arabidopsis thaliana - putative olfactory compounds in plant communication.

Arabidopsis thaliana from the Brassicaceae family has arisen as the model organism in plant biology research. The plant's genome has been characterized and worldwide studies are conducted at the genetic, protein and metabolic level to unravell the function of genes involved in growth, reproduction, biosynthesis, and plant communication. As part of the multidisciplinary project BIOEMIT at NTNU, metabolomic studies of Arabidopsis T-DNA knock-out mutants and ecotypes have been carried out. Volatile profiles of autolyzed, intact plants and single plant organs were obtained by solid-phase microextraction coupled with gas chromatography-mass spectrometry. The studies were aimed at the diversity of defense-related compounds from the glucosinolate-myrosinase system - the isothiocyanates and nitriles. Metabolites from methionine, leucine and phenylalanine-derived glucosinolates were most abundant (4-methylthiobutyl, 4-methylpentyl, 2-phenylethyl). In addition, 24 monoterpenes, 26 sesquiterpenes and 12 aromatic structures, predominantly observed in inflorescenses, are described. Excluding the vast group of straight chain aliphatic structures, a total of 102 volatile compounds were detected, of which 59 are reported in Arabidopsis thaliana for the first time, thus emphasizing the sensitivity and applicability of solid-phase microextraction for volatile profiling of plant secondary metabolites.

Arabidopsis↗
PubMed2006

Comparison of volatile concentrations in hand-squeezed juices of four different lemon varieties.

Fresh juices of four Italian cultivars of lemons (Citrus limon Burm) have been analyzed by headspace solid phase microextraction coupled to gas chromatography and gas chromatography-mass spectrometry (GC-MS). The best results have been obtained with the 2 cm 50/30 microm divinylbenzene/carboxen on poly(dimethylsiloxane) fiber, using a homogenization time of 1 h at 40 degrees C and a sampling period of 30 min. A total of 35 volatile compounds have been identified by GC-MS, and their relative amounts have been calculated by adding internal standard to the samples. Differences in composition of lemon juices volatile components have been observed. Verdello Siracusano lemon juice has the highest amount of volatile compounds (50.28 mg/L), followed by Interdonato (8.39 mg/L), Primo Fiore Capo d'Orlando (5.75 mg/L), and Femminello Siracusano (2.62 mg/L) juices. Volatile compounds mainly consist of mono- and sesquiterpene hydrocarbons and oxygenated molecules (aldheydes, monoterpene alcohols, and monoterpene esters). Headspace solid phase microextraction coupled to a gas chromatograph equipped with a specific sulfur detector, a sulfur chemiluminescence detector, let us detect and quantify dimethyl sulfide compound at the microgram/liter level in lemon juices.

Alcohols↗
PubMed2006

Solid phase microextraction-gas chromatographic-mass spectrometric determination of nitrous oxide evolution to measure denitrification in estuarine soils and sediments.

A SPME-GC-MS method was developed to quantify nitrous oxide (N(2)O) to evaluate denitrification rates. There is a need for this sensitive and definitive N(2)O detection method to accurately measure the soil and sediment ability to convert anthropogenic mineral nitrogen loads to N(2) through denitrification hence decreasing estuarine waterway pollution loading. This method is applied to measure denitrification, which is a major pathway for inorganic nitrogen removal, by incorporating the acetylene (C(2)H(2)) block method on anaerobic assays. Currently, denitrification is largely measured using GCs fitted with TCD or ECD detectors. With a mean R(2) value of 0.996, the calibration curve spanned over three orders of magnitude (4.1-2030 nM) with a limit of detection (LOD) of 4.1 nM N(2)O (18 ppb) and a limit of quantification (LOQ) of 16 nM N(2)O (72 ppb). This detection method was valid with less than 15% relative standard deviation (RSD) and error for middle and high quality control (QC) points and less than 20% for low QC points on three experimental days. Measuring N(2)O using SPME-GC-MS technology allows for confidence in identification, high sensitivity, reproducibility, and short run times.

Chemical Fractionation↗
PubMed2004

Assessment of strawberry aroma through solid-phase microextraction-gas chromatography and artificial neuron network methods. Variety classification versus growing years.

In a previous work, the SPME-GC-MS method (chemical analysis) coupled with KSOM-ANN treatment of the results (statistical algorithm) has proved to be efficient to classify 70 strawberry samples harvested in the same year, through the 17 varieties to which they belonged, in a two-dimensional map. As an extension, the present study confirms that these results were not dependent on the year of strawberry production and discusses what effects were observed between results obtained in different years. Samples of different strawberry varieties were harvested during the three campaigns of 2000, 2001, and 2002 and analyzed independently. The chemical data matrix obtained in each case allowed the verification of the proposal that the same discriminative effect could be obtained independently of the year of production by using maps of different sizes. Therefore, 30 measures obtained from samples of 9 varieties in 2000, 54 measures from 13 varieties in 2001, and 80 measures from 20 varieties in 2002 were correctly classified by using 20, 35, and 56 hexagon maps, respectively. In a second analysis based on the 2002 production, the chemical differences between variety aromatic features were noted through the increasing size of the map used. Finally, results relative to 7 varieties cultivated in 2001 and 2002 and stored under exactly the same conditions were computed together for elaborating a single map. An interesting effect of double classification according to the year and the varieties was observed.

Fragaria↗
PubMed2004

Preliminary studies for the differentiation of apple juice samples by chemometric analysis of solid-phase microextraction-gas chromatographic data.

A combination of gas chromatography (GC) and chemometrics was evaluated for its ability to differentiate between apple juice samples on the basis of apple variety and applied heat treatment. The heat treatment involved exposure of 15 mL juice samples for 30 s in a 900 W domestic microwave oven. The chromatographic results were subjected to two chemometric procedures: (1) partial least squares (PLS) regression and (2) linear discriminant analysis (LDA) applied to principal component (PC) scores. The percent correct classification of samples were obtained from PLS and LDA in terms of separation on the basis of apple variety and applied heat treatment. PLS gave the highest level of correct classification of the apple juice samples according to both variety and heat treatment, 92.5% correct classification in each case. When LDA was performed on the PC scores obtained from GC analysis, 87.5% and 80% of samples were correctly classified according to apple variety used and applied heat treatment, respectively.

Beverages↗
PubMed2006

Analytical microextraction: current status and future trends.

Analytical microextractions, defined as nonexhaustive sample preparation with a very small volume of extracting phase (microliter range or smaller) relative to the sample volume, represent an important development in the field of analytical chemistry. Analytes are extracted by a small volume of a solid or semi-solid polymeric material, as in solid-phase microextraction (SPME), or alternatively by a small volume of a liquid, as in liquid-phase microextraction (LPME). This paper gives an overview of the SPME and LPME techniques and discusses future trends. This includes a discussion of the different extraction formats available, commercial equipment, method transfer from traditional sample preparation methods to microextraction, and performance as well as robustness for the latter type of systems. In addition, the paper contains a unified approach to the understanding of extraction thermodynamics and kinetics applicable to both SPME and LPME.

Chemical Fractionation↗
PubMed2006

On-site polymer-coated hollow fiber membrane microextraction and gas chromatography--mass spectrometry of polychlorinated biphenyls and polybrominated diphenyl ethers.

Porous polypropylene hollow fiber membrane coated with a conjugated polymer was used as an on-site sampling device for the extraction of polychlorinated biphenyls and polybrominated biphenyl ethers from coastal sea water samples. The coated hollow fiber membrane was placed in a vial containing the sample, and the target compounds extracted via manual shaking of the vials at the site of sample collection. For each extraction, two fibers were used. After extraction, the fibers with the adsorbed analytes were brought back to the laboratory for further processing. Care was taken to preserve the integrity of the analytes and to avoid contamination during transport; after extraction, the fibers were carefully removed and placed in air-tight crimper vials which were stored in an ice-box. The analytes were desorbed by solvent in the laboratory and analyses were carried out using gas chromatography/mass spectrometry. This method was highly reproducible with relative standard deviations in the range of 1-9%. Recoveries from spiked water samples ranged from 83% to 98%. Low limits of detections between 0.04 and 0.21ngl(-1) were achieved. The extraction efficiency was compared with solid-phase microextraction.

Gas Chromatography-Mass Spectrometry↗
PubMed2006

Developments in multiple headspace extraction.

This paper reviews new developments in multiple headspace extraction (MHE), especially its combination with two miniaturized extraction techniques, solid-phase microextraction (SPME) and single-drop microextraction (SDME). The combination of the techniques broadens the applicability of SPME and SDME to quantitative determination of analytes in complex liquid and solid matrixes. These new methods offer several advantages over traditional liquid-solid, liquid-liquid and headspace extraction techniques. The potential applications include extraction of volatiles and semivolatiles from environmental and physiological samples and from different polymer products such as medical and biomedical materials, food packaging and building materials. The theoretical principals of the techniques are also briefly reviewed.

Chromatography, Gas↗
PubMed2004

A survey on high-concentration-capability headspace sampling techniques in the analysis of flavors and fragrances.

This survey critically discusses high-concentration-capacity (HCC) headspace (HS) techniques applied to sample the volatile fraction of matrices of interest in the flavors and fragrance fields. In particular, the advantages, limits, and fields of application of HS solid-phase microextraction (SPME), high-capacity HS sorptive extraction (HSSE) and HS solid-phase dynamic extraction (SPDE) are evaluated. These techniques are discussed in view of the peculiar characteristic of HCC-HS techniques, from the standpoint that these techniques are a bridge between static (S-HS) and dynamic HS (D-HS) because they are as simple, fast, easy to automate, and reliable as S-HS, yet afford analyte concentration factors comparable to those of D-HS. Moreover, the different degree of their development is a consequence of the different times in which they were introduced into the market, because the potential of HS-SPME is now well known, having been introduced approximately 12 years ago, but that of HSSE has still to be fully explored, and HS-SPDE still has to be investigated because it is very recent.

Data Collection↗
PubMed2006

[Monitoring sulfadiazine and sulfamethazine residues in eggs using polymer monolith microextraction coupled with high performance liquid chromatography].

The method for the quantitative monitoring of sulfadiazine and sulfamethazine residues in eggs was established by coupling polymer monolith microextraction (PMME) with high performance liquid chromatography and ultra-violet detection (HPLC/UV). The PMME is an effective sample preparation technique, which has been developed on the basis of in-tube solid-phase microextraction. A poly (methacrylic acid-ethylene glycol dimethacrylate) monolithic capillary column was selected as an extraction device. To obtain the optimum extraction efficiency, several parameters related to PMME, including extraction flow-rate, extraction volume, and pH value of the sample matrix were investigated. The sample solution can be directly injected into the device for extraction after simple extraction with ethanol, dilution with phosphate buffer solution, and centrifugation. Because of the high extraction capacity of the monolith column, low detection limits (S/N=3) (8.8 ng/g for sulfamethazine and 11.2 ng/g for sulfadiazine) and quantification limits (S/N=10) (29.3 ng/g for sulfamethazine and 37.5 ng/g for sulfadiazine) were obtained. The method showed good linearity ranging from 50 to 5000 ng/g. Excellent reproducibility of the method was found by intraday and interday precisions, yielding the relative standard deviations of < or = 7.6% and < or = 8.2%, respectively. Recoveries for them were higher than 65%. Compared with the standard methods used in China, improved results were obtained using this method. The proposed method was proved to be simple, rapid, sensitive, and competent in monitoring sulfadiazine and sulfamethazine residues in eggs.

Animals↗
PubMed2006

Development of a simple, accurate SPME-based method for assay of VOCs in column breakthrough experiments.

Solid-phase microextraction (SPME) with gas chromatography is to be used for assay of effluent liquid samples from soil column experiments associated with VOC fate/transport studies. One goal of the fate/transport studies is to develop accurate, highly reproducible column breakthrough curves for 1,2-cis-dichloroethylene (cis-DCE) and trichloroethylene (TCE) to better understand interactions with selected natural solid phases. For SPME, the influences of the sample equilibration time, extraction temperature and the ratio of volume of sample bottle to that of the liquid sample (V(T)/V(w)) are the critical factors that could influence accuracy and precision of the measured results. Equilibrium between the gas phase and liquid phase was attained after 200 min of equilibration time. The temperature must be carefully controlled due to variation of both the Henry's constant (K(h)) and the fibre/gas phase distribution coefficient (K(fg)). K(h) decreases with decreasing temperature while K(fg) increases. Low V(T)/V(w) yields better sensitivity but results in analyte losses and negative bias of the resultant assay. High V(T)/V(w) ratio yields reduced sensitivity but analyte losses were found to be minimal, leading to better accuracy and reproducibility. A fast SPME method was achieved, 5 min for SPME extraction and 3.10 min for GC analysis. A linear calibration function in the gas phase was developed to analyse the breakthrough curve data, linear between a range of 0.9-236 microgl(-1), and a detection limit lower than 5 microgl(-1).

Chromatography, Gas↗