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Biomedical subjects

Roger M Smith

Publications and source records attributed to Roger M Smith.

13 recordsLinked to original sources

Superheated water extraction and phase transfer methylation of phenoxy acid herbicides from solid matrices.

Phase transfer catalytic methylation was applied to directly derivatise chlorophenoxy acid herbicides in superheated water extracts from sand and soil samples. The extractions were carried out at 120 degrees C statically for 5 min and then dynamically for 10 min at 1.0 mL min(-1) using water at pH 11.0 for a sand matrix and a flow rate of 0.5 mL min(-1) at pH 7.0 for soil samples. The methylation was carried out on-line on the extraction solution with ultrasonication at 80 degrees C, using either 0.05 mmol tetrabutylammonium bromide (TBAB) or 0.0125 mmol cetyltrimethylammonium bromide (CTAB) as phase transfer catalysts with 0.20 mmol methyl iodide in 2.0 mL dichloromethane trapping solvent. The former catalyst provided a higher yield but the latter gave fewer interfering peaks. The recoveries of most chlorophenoxy acids using the TBAB catalyst ranged from 67 to 105% for sand and from 82 to 114% for soil sample, except phenoxyacetic acid, 2-(2, 4-dichlorophenoxy)propanoic acid and 1-naphthaleneacetic acid, while those by using CTAB were slightly lower. Detection limits of all the analytes extracted from sand using TBAB catalyst were in a range of 5.3-16 microg g(-1) analysed by using gas chromatography with flame ionization detection (GC-FID).

Acetates↗

Comparison of in-tube sorptive extraction techniques for non-polar volatile organic compounds by gas chromatography with mass spectrometric detection.

A commercial in-tube sorptive extraction device, known as solid-phase dynamic extraction (SPDE), has been evaluated for the extraction of non-polar volatile aromatic analytes from aqueous solutions in both headspace and liquid injection modes. An automated sampler is used with a gas-tight 2.5 ml syringe equipped with a special needle that is coated on the inside with a non-polar extraction phase. After absorption onto the phase, the analytes were thermally desorbed directly into a GC-MS system. The technique was evaluated for the determination of furan, benzene and toluene. The sensitivity for toluene was greatly improved on using SPDE compared to static headspace. A slight increase in sensitivity was observed for benzene but none for determination of furan. Estimated limits of detection ranged from 0.2 to 2 microg/l.

Calibration↗

On-line coupled extraction and separation using superheated water for the analysis of triazine herbicides in spiked compost samples.

An on-line method, with a purely aqueous mobile phase, has employed linked superheated water extraction and superheated water separation for the analysis of triazine herbicides in spiked compost samples. After the superheated water extraction, a X-Terra solid-phase trap was used to collect and focus the extracted analytes. The trapped analytes were then released by thermal desorption and passed directly to a superheated water chromatographic separation using a PGC column. Two clean-up steps (prior to extraction and separation) were included to remove most of the interfering matrix components. The effects of the sample matrix and the extraction temperatures on the recovery of the triazines were investigated. Despite some thermal degradation of the chloro-triazines during the SWE, the on-line SWE-SWC method was sensitive and rapid. The coupled method could potentially reduce costs and labour and by using only water in every stage is compatible with the concepts of green chemistry.

Chemical Fractionation↗

The GC-MS detection and characterization of neopine resulting from opium use and codeine metabolism and its potential as an opiate-product-use marker.

Neopine, a minor opium alkaloid and an isomer of codeine (also known as beta-codeine), has been detected in both the urine of opium users and pharmaceutical codeine users. The characterization of neopine was achieved by comparison of the mass spectra and GC retention times of the trimethylsilyl derivative. The presence of neopine in the urine of pharmaceutical codeine users was attributed to the metabolism of codeine through a double bond migration in ring C, from the 7-8 to the 8-14 position. The potential use of the alkaloid as a confirmation marker of opium and/or pharmaceutical codeine use and the ability to differentiate these from heroin use has been discussed.

Biomarkers↗

Monitoring effective column temperature by using shape selectivity and hydrophobicity and the effects of mobile phase temperature.

Relative changes in the hydrophobicity and shape selectivity of standard analytes are shown to be a valuable method to monitor the reproducibility of the effective temperature experienced by the analytes in a chromatographic column in different ovens. Significant differences were observed between ovens with the same nominal temperature and could be a major cause of problems encountered in transferring methods between instruments or laboratories. By using two parameters, changes due to the column temperature can be distinguished from those caused by mobile phase composition differences. In addition marked increases in column efficiency were noted as the mobile phase temperature was reduced below the column temperature in contrast to claims that thermal equilibration is essential.

Chromatography, Liquid↗

Superheated water chromatography-nuclear magnetic resonance spectroscopy and mass spectrometry of vitamins.

The water-soluble vitamins, pyridoxine, riboflavin, and thiamine, were separated by reversed-phase liquid chromatography using hot or superheated water as the mobile phase and were detected using a range of detectors, including ultraviolet and fluorescence spectroscopy and mass spectrometry. By using deuterium oxide as the eluent, direct on-line nuclear magnetic resonance spectra could be obtained with minimal spectral interference from the mobile phase. Some of the compounds showed deuterium exchange of alkyl-protons when separated at high temperatures.

Hot Temperature↗

Before the injection--modern methods of sample preparation for separation techniques.

The importance of sample preparation methods as the first stage in an analytical procedure is emphasised and examined. Examples are given of the extraction and concentration of analytes from solid, liquid and gas phase matrices, including solvent phase extractions, such as supercritical fluids and superheated water extraction, solid-phase extraction and solid-phase microextraction, headspace analysis and vapour trapping. The potential role of selective extraction methods, including molecular imprinted phases and affinity columns, are considered. For problem samples alternative approaches, such as derivatisation are discussed, and potential new approaches minimising sample preparation are noted.

Chromatography↗

Analysis of a ginger extract by high-performance liquid chromatography coupled to nuclear magnetic resonance spectroscopy using superheated deuterium oxide as the mobile phase.

A methanolic extract of powdered ginger was separated on a Xterra RP 18 column using deuterium oxide as the eluent and a temperature gradient from 50 to 130 degrees C at 4 degrees C/min. On-line and off-line HPLC-NMR analysis yielded spectra for vanillin, dihydroferulic acid, zingerone and ferulic acid. The identification of dihydroferulic acid and zingerone were confirmed by mass spectroscopy.

Analysis of Variance↗

Extractions with superheated water.

As the temperature of liquid water is raised under pressure, between 100 and 374 degrees C, the polarity decreases markedly and it can be used as an extraction solvent for a wide range of analytes. Most interest has been in its application for the determination of PAHs, PCBs, and pesticides from environmental samples, where it gives comparable results to Soxhlet extraction but more rapidly and without the use of significant volumes of organic solvents. Unlike SPE, n-alkanes are not extracted unless the pressure is reduced and steam is used. Other applications have included the extraction of essential oils from plant material where it preferentially extracts the economically more important oxygenated components compared to steam distillation. The aqueous extract has been concentrated in a number of different methods (solvent extraction, SPE, SPME, extraction disc) or the extraction can be linked on-line to LC or GC. In many cases the superheated water extraction is cleaner, faster and cheaper than the conventional extraction methods.

Environmental Pollutants↗

On-line coupled superheated water extraction (SWE) and superheated water chromatography (SWC).

Superheated water extraction has been linked directly to a superheated water chromatographic separation so that the process of sample extraction and separation can be achieved without the need for organic solvents at any stage. A model matrix spiked with pharmaceuticals and antioxidants was extracted and the extracted components were collected on a cold polystyrene-divinylbenzene trap. The analytes were then sequentially released by raising the temperature in stages. Each fraction was passed on-line to a polystyrene divinylbenzene analytical column and was eluted with superheated water using a thermal gradient.

Journal Article↗

Superheated water chromatography-nuclear magnetic resonance spectroscopy of kava lactones.

Three kava lactone constituents of Piper methysticum, namely, kawain, methysticin and desmethoxyyangonin, have been separated and identified by reversed-phase HPLC using superheated deuterium oxide as the mobile phase and on-line 1H-NMR detection. The method avoids the use of organic solvents in the mobile phase and hence interferences in the NMR analysis are minimised.

Chromatography, High Pressure Liquid↗