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High-performance liquid chromatography with ultraviolet detection HPLC

Residue analytical methods for neonicotinoids in crops, soil and water samples have been developed. The basic principle of these methods consists of the following steps extraction of the crop and/or soil samples with acetone or the other organic solvent, cleanup by liquid-liquid partition or column chromatography, and quantitative analysis by high-performance liquid chromatography with ultraviolet detection (HPLC/UV). Simple column cleanup procedures are used to improve the accuracy and sensitivity of these methods. [Pg.1128]

These authors noted the potential for the assay to underestimate the concentration of TSR due to decreased binding of metabolites relative to parent spinosad. However, the major residue found was parent spinosad, so underestimation of residues is not likely to be problematic. Overall, this method was validated in 34 matrices and showed excellent agreement with results obtained with a high-performance liquid chromatography/ultraviolet detection (HPLC/UV) method. ... [Pg.724]

High-performance liquid chromatography (HPLC) with a micellar mobile phase or with a selective pre-column or reaction detection system has also been used to determine alkylenebis(dithiocarbamaes). ° Zineb and mancozeb residues in feed were determined by ion-pair HPLC with ultraviolet (UV) detection at 272 nm. These compounds were converted to water-soluble sodium salts with ethylenediaminetetra-acetic acid (EDTA) and sodium hydroxide. The extracts were ion-pair methylated with tetrabuthylammonium hydrogensulfate (ion-pair reagent) in a chloroform-hexane solvent mixture at pH 6.5-8.S. The use of an electrochemical detector has also been reported. ... [Pg.1091]

V-Nitrosodiethanolamine can be determined in air and bulk process samples. Air samples are collected on glass fibre filters, extracted with 2-propanol and analysed by gas chromatography with thermal energy analyser detection. The limit of detection is 200 ng per sample (0.42 pg/m ). Bulk samples can be screened for 7V-nitrosodiethanol-amine by high-performance liquid chromatography (HPLC) with ultraviolet detection (Occupational Safety and Health Administration, 1990). [Pg.404]

Direct determination of urea pesticides by high-performance liquid chromatography has been widely reported in the literature (10,32-36,127-130). Ultraviolet detection has often been used (32,33,35,36,60,127) with usually acceptable sensitivity, although this detector is nonspecific and the sensibility is, in general, low. To overcome this problem, several techniques have been assayed, such as precolumn enrichment (60), postcolumn derivatization (34,10), and the use of other detection techniques such as the electrochemical (129), photoconductivity (128,130), and fluorescence detectors (9,10,34). Table 9 summarizes representative papers using these techniques in HPLC analysis. [Pg.706]

No analytical methods specifically used for the determination of tetryl in biological fluids and tissues were located. One attempt to develop a method for detecting tetryl in animal tissues using high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection was unsuccessful because of suspected metabolism and binding of the parent compound and/or metabolites to macromolecules (Army 1981a). However, methods were located for the detection of the tetryl metabolites, picric acid and picramic acid, in urine and for the analysis of tetryl in hand swabs. Table 6-1 is a summary of methods used to determine tetryl metabolites in urine and tetryl in hand swabs. [Pg.63]

Methods are also available for determining metabolites of benzene in urine. A summary of available methods is shown in Table 6-2. Both GC/FID or GC/MS and high-performance liquid chromatography (HPLC) with ultraviolet detection (UV) have been used to measure urinary metabolites. [Pg.320]

Reversed-phase high-performance liquid chromatography (RP-HPLC) is the usual method of choice for the separation of anthocyanins combined with an ultraviolet-visible (UV-Vis) or diode-array detector (DAD)(Hebrero et al., 1988 Hong et ah, 1990). With reversed-phase columns the elution pattern of anthocyanins is mainly dependent on the partition coefficients between the mobile phase and the Cjg stationary phase, and on the polarity of the analytes. The mobile phase consists normally of an aqueous solvent (water/carboxylic acid) and an organic solvent (methanol or acetonitrile/carboxylic acid). Typically the amount of carboxylic acid has been up to 10%, but with the addition of a mass spectrometer as a detector, the amount of acid has been decreased to as low as 1 % with a shift from trifluoroacetic acid to formic acid to prevent quenching of the ionization process that may occur with trifluoroacetic acid. The acidic media allows for the complete displacement of the equilibrium to the fiavylium cation, resulting in better resolution and a characteristic absorbance between 515 and 540 nm. HPLC separation methods, combined with electrochemical or DAD, are effective tools for anthocyanin analysis. The weakness of these detection methods is a lack of structural information and some nonspecificity leading to misattribution of peaks, particularly with electrochemical... [Pg.165]

API-related organic impurities usually involves high performance liquid chromatography (HPLC)-based analytical methods, with relatively non-specific detection techniques such as Ultraviolet/Visible (UV/Vis) Spectrophotometry. Residual solvents analysis usually involves gas chromatography (GC)-based analytical methods, again with relatively non-specific detection techniques such as flame ionization (FID). GC-based methods are most appropriate for volatile analytes such as residual solvents, whereas HPLC-based methods are more appropriate for the relatively non-volatile and polar API-related analytes. [Pg.3799]

Analysis is an integral part of research, clinical, and industrial laboratory methodology. The determination of the components of a substance or the sample in question can be qualitative, quantitative, or both. Techniques that are available to the analyst for such determinations are abundant. In absorption spectroscopy, the molecular absorption properties of the analyte are measured with laboratory instruments that function as detectors. Those that provide absorbance readings over the ultraviolet-visible (UV-vis) light spectrum are commonly used in high-performance liquid chromatography (HPLC). The above method is sufficiently sensitive for quantitative analysis and it has a broader application than other modes of detection. [Pg.1195]

The evaporative light-scattering detector (ELSD) was originally developed for use with high-performance liquid chromatography (HPLC) to detect nonvolatile compounds by mass rather than ultraviolet (UV) absorbance detection [1], The response is dependent on the light scattered from particles of the solute remaining after the mobile phase has evaporated and is proportional to the total amount of the solute. Because no chromophore is necessary, a response can be measured for any solute less volatile than the mobile phase. [Pg.1540]


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