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Analyses of pesticides and their metabolites in foods and drinks 总被引:10,自引:0,他引:10
Farid E. Ahmed 《Trends in analytical chemistry : TRAC》2001,20(11):649-661
The importance of matrix pretreatment, sample extraction and clean-up in multiresidue methods for pesticide analyses is discussed, with emphasis on alternative new techniques attempted worldwide such as accelerated solvent extraction, microwave-assisted extraction, solid-phase extraction, solid-phase micro-extraction, matrix solid-phase dispersion, supercritical fluid chromatography, ultrasonic extraction and gel permeation chromatography. Detection employing capillary gas chromatography and high-performance liquid chromatography in conjunction with mass spectrometry, capillary electrophoresis, immunoassay techniques and others is summarized. 相似文献
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Pesticides are applied widely to protect plants from disease, weeds and insect damage, and usually come into contact with soil, where they undergo a variety of transformations that provide a complex pattern of metabolites. This article reviews the most relevant analytical methods for determining pesticides and their transformation products in soils. We address some recent advances in sampling and sample-preparation technologies for soil analysis. We discuss and critically evaluate procedures, such as liquid extraction methods (pressurized liquid extraction or microwave-assisted extraction) and solid-phase based methods (headspace solid-phase microextraction, solid-phase microextraction or matrix-solid-phase dispersion). Analysis of pesticides is generally carried out by gas chromatography (GC) or liquid chromatography (LC) coupled to different detectors, especially to mass spectrometers (MSs). However, alternative and/or complementary methods, using capillary electrophoresis (CE), biosensors and bioassays have emerged recently. We also consider the advantages and the disadvantages of the various methodologies. 相似文献
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Leonardo G. GagliardiAuthor Vitae Marcos TasconAuthor VitaeCecilia B. Castells 《Analytica chimica acta》2015
Studies on the theoretical principles of acid–base equilibria are reviewed and the influence of temperature on secondary chemical equilibria within the context of separation techniques, in water and also in aqueous-organic solvent mixtures, is discussed. In order to define the relationships between the retention in liquid chromatography or the migration velocity in capillary electrophoresis and temperature, the main properties of acid–base equilibria have to be taken into account for both, the analytes and the conjugate pairs chosen to control the solution pH. The focus of this review is based on liquid–liquid extraction (LLE), liquid chromatography (LC) and capillary electrophoresis (CE), with emphasis on the use of temperature as a useful variable to modify selectivity on a predictable basis. Simpli?ed models were evaluated to achieve practical optimizations involving pH and temperature (in LLE and CE) as well as solvent composition in reversed-phase LC. 相似文献
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A high-performance capillary electrophoresis (HPCE) method for determining vasoactive intestinal peptide (VIP) in rat brain was developed. Cerebral cortex was first extracted by solid-phase extraction and purified by reversed-phase high-performance liquid chromatography. The VIP-rich fraction was further analysed by capillary zone electrophoresis (CZE) and micellar electrokinetic chromatography using a commercial HPCE instrument with UV detection. The identity of the peak of endogenous VIP was confirmed by performing multiple CZE analyses at different pH values. This HPCE method allows VIP to be detected and measured with good molecular specificity and could represent a reference method to validate data obtained by radioimmunoassay. 相似文献
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O. A. Shevlyakova A. A. Ichalaynen A. M. Antochin V. F. Taranchenko V. M. Goncharov A. V. Aksenov D. A. Mitrofanov E. I. Berizovskaya I. A. Rodin O. A. Shpigun 《Moscow University Chemistry Bulletin》2016,71(3):182-192
The modern methods of analysis of the main active substances barrenwort (Epimedium)—flavonoids—are considered. Various types of extraction are used to isolate these components from plant raw materials. Flavonoids are separated by capillary electrophoresis, thin layer chromatography, and high performance liquid chromatography (HPLC) in combination with UV and mass spectrometric detection. 相似文献
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J C Waterval H Krabbe J Teeuwsen A Bult H Lingeman W J Underberg 《Electrophoresis》1999,20(14):2909-2916
Low levels of peptide drugs in human plasma can be determined employing off-line solid-phase extraction, followed by capillary zone electrophoresis with UV detection. A bioanalytical procedure is presented, using gonadorelin and angiotensin II in human plasma as model compounds. The solid-phase extraction method, based on a weak cation exchange mechanism, is able to remove interfering endogenous components from the plasma sample, extract the model peptides quantitatively, and give a possibility of concentrating the sample at the same time. Transient isotachophoretic conditions were kept to increase the sample loadability by about two orders of magnitude. Up to about 70% of the capillary was filled with the reconstituted extract, whereafter the peptides were selectively concentrated during the first 15 min. Subsequently, the concentrated sample zones were separated under capillary zone electrophoresis conditions, showing the technique's high resolution. For the model cationic peptides (gonadorelin, angiotensin II) good linearity and reproducibility was observed in the 20-100 ng/mL concentration range. A more extensive washing procedure permits quantitation of gonadorelin at the 5 ng/mL level. In comparison with a liquid chromatography analysis, superior mass sensitivity and separation are obtained with the transient isotachophoretic capillary zone electrophoresis method. Moreover, in this case equivalent sensitivity is achieved when it is directly compared with a liquid chromatography method with UV detection, keeping in mind that 60 times more sample is needed for the latter method. A further gain in sensitivity can be obtained when the analysis is combined with native fluorescence detection, as is demonstrated by combining liquid chromatography separation with fluorescence detection. 相似文献
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Gómez Caravaca AM Carrasco Pancorbo A Cañabate Díaz B Segura Carretero A Fernández Gutiérrez A 《Electrophoresis》2005,26(18):3538-3551
A capillary zone electrophoresis method has been carried out to determine and quantitate some compounds of the polyphenolic fraction of virgin olive oil which have never previously been determined before using capillary electrophoresis, such as elenolic acid, ligstroside aglycon, oleuropein aglycon, and (+)-pinoresinol. The compounds were identified using standards obtained by semipreparative high-performance liquid chromatography (HPLC). A detailed method optimization was performed to separate the phenolic compounds present in olive oil using a methanol-water extract of Picual extra-virgin olive oil, and different extraction systems were compared (C18-solid phase extraction (SPE), Diol-SPE, Sax-SPE and liquid-liquid extraction). The optimized parameters were 30 mM sodium tetraborate buffer (pH 9.3) at 25 kV with 8 s hydrodynamic injection, and the quantitation was carried out by the use of two reference compounds at two different wavelengths. 相似文献
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A single enzyme treatment with alpha-amylase, prior to the quantification of added folic acid (FA) in fortified instant fried Asian noodles with analysis performed by capillary zone electrophoresis (CZE) and reversed-phase high performance liquid chromatography (RP-HPLC) with UV detection, is described. The method was validated and optimized for capillary electrophoresis (CE) with separation achieved using a 8 mM phosphate-12 mM borate run buffer with 5% MeOH at pH 9.5. FA was well separated from matrix components with nicotinic acid (NA) employed as an internal standard. In a comparative study, separation of FA was performed using HPLC with a mobile phase consisting of 27% MeOH (v/v) in aqueous potassium phosphate buffer (3.5 mM KH(2)PO(4) and 3.2 mM K(2)HPO(4)), pH 8.5, and containing 5 mM tetrabutylammonium dihydrogen phosphate as an ion-pairing agent. For both methods, excellent results were obtained for various analytical parameters including linearity, accuracy and precision. The limit of detection was calculated to be 2.2 mg/L for CE without sample stacking and 0.10 mg/L with high performance liquid chromatography (HPLC). Sample extraction involved homogenization and enzymatic extraction with alpha-amylase. Results indicated that FA was stable during four main stages of instant fried noodle manufacturing (dough crumbs, cut sheets, steaming and frying). 相似文献
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《Journal of separation science》2018,41(1):373-384
Ionic liquids have been functionalized for modern applications. The functional ionic liquids are also called task‐specific ionic liquids. Various task‐specific ionic liquids with certain groups have been constructed and exploited widely in the field of separation. To take advantage of their properties in separation science, task‐specific ionic liquids are generally used in techniques such as liquid–liquid extraction, solid‐phase extraction, gas chromatography, high‐performance liquid chromatography, and capillary electrophoresis. This review mainly covers original research papers published in the last five years, and we will focus on task‐specific ionic liquids as the chiral selectors in chiral resolution and as extractant or sensor for biological samples and metal ion purification. 相似文献
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Since 1999, substantial research has been devoted to the development of liquid-phase microextraction (LPME) based on porous hollow fibers. With this technology, target analytes are extracted from aqueous samples, through a thin supported liquid membrane (SLM) sustained in the pores in the wall of a porous hollow fiber, and further into a microL volume of acceptor solution placed inside the lumen of the hollow fiber. After extraction, the acceptor solution is directly subjected to a final chemical analysis by liquid chromatography (HPLC), gas chromatography (GC), capillary electrophoresis (CE), or mass spectrometry (MS). In this review, LPME will be discussed with focus on extraction principles, historical development, fundamental theory, and performance. Also, major applications have been compiled, and recent forefront developments will be discussed. 相似文献
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Imran Ali Chakresh Kumar Jain 《International journal of environmental analytical chemistry》2013,93(12):947-964
The present review describes the speciation techniques of arsenic. The principal advanced techniques discussed are gas chromatography, reversed-phase liquid chromatography, ion chromatography, capillary electrophoresis. Some other techniques are also mentioned. The extraction procedures of arsenic species from unknown samples are also discussed. Arsenic speciation is summarized in tabular form and optimizing parameters are also discussed. 相似文献
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In this work, using benzo(a)pyrene (BaP) as marker, the analytical merits of on-line flow-injection cloud-point extraction (FI CPE), including preconcentration
factor, extraction efficiency, sample throughput, and analysis time were evaluated by use of peroxyoxalate chemiluminescence
(CL) detection. Moreover, by detailed discussion of several preconcentration conditions for traditional and on-line FI CPE
the advantages of on-line FI CPE became conspicuously apparent. When coupled with separation techniques such as high-performance
liquid chromatography (HPLC) or capillary electrophoresis (CE), on-line FI CPE–CL has much potential for analysis of low concentrations
of polycyclic aromatic hydrocarbons (PAH) in environmental samples. 相似文献
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Analysis at trace levels, an ideal area of application for hyphenated techniques, is steadily gaining importance. Many sample pre-concentration and clean-up methods have been hyphenated with core analytical techniques to accomplish the task of low level detection. The present article describes the state of the art of hyphenation of various techniques such as solid phase extraction, micro-solid phase extraction, dialysis, and chromatographic modalities etc. with liquid chromatography, gas chromatography, capillary electrophoresis, and spectroscopic methods. Besides, attempts have been made to address the hyphenation approach in microfluidic devices. 相似文献
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In hollow fiber membrane liquid-phase microextraction (LPME), target analytes are extracted from aqueous samples and into a supported liquid membrane (SLM) sustained in the pores in the wall of a small porous hollow fiber, and further into an acceptor phase present inside the lumen of the hollow fiber. The acceptor phase can be organic, providing a two-phase extraction system compatible with capillary gas chromatography, or the acceptor phase can be aqueous resulting in a three-phase system compatible with high-performance liquid chromatography or capillary electrophoresis. Due to high enrichment, efficient sample clean-up, and the low consumption of organic solvent, substantial interest has been devoted to LPME in recent years. This paper reviews important applications of LPME with special focus on bioanalytical and environmental chemistry, and also covers a new possible direction for LPME namely electromembrane extraction, where analytes are extracted through the SLM and into the acceptor phase by the application of electrical potentials. 相似文献
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William C. Brumley Cynthia M. Brownrigg Andrew H. Grange 《Journal of chromatography. A》1994,680(2):635-644
Applications of capillary electrophoresis (CE) and capillary liquid chromatography (LC) to environmental analysis have been limited. In this work we present applications of micellar electrokinetic chromatography (MEKC) to the analysis of environmental matrices for synthetic dyes. Separations obtained by capillary LC are compared with those obtained under MEKC for seven selected dyes. Both techniques are capable of resolving the subject compounds at high efficiency. Recovery data for spiked water and soil matrices were obtained for four dyes using solid-phase extraction cartridges and disks with determination by MEKC-UV detection. Both pH adjustment via acid and ion-pairing via a cationic surfactant were investigated for isolating dyes. Capillary LC detection was by continuous-flow liquid secondary ion mass spectrometry (CF-LSI-MS) whereas MEKC used UV detection (214 nm). Application of peak-profiling at high mass resolution is illustrated with the capillary LC-MS technique. Interfacing capillary LC under CF-LSI-MS using the coaxial arrangement is easier than interfacing CE with this arrangement. MEKC provides a powerful screening and determinative technique, while capillary LC-MS provides a confirmatory tool. 相似文献