Search results for "Analyte"
showing 10 items of 303 documents
Multivariate optimization of the hollow fibre liquid phase microextraction of muscimol in human urine samples.
2016
Abstract A liquid phase microextraction based on hollow fibre followed by liquid chromatographic determination was developed for the extraction and quantitation of the hallucinogenic muscimol from urine samples. Method applicability on polar hallucinogens was also tested on two alkaloids, a psychedelic hallucinogen, tryptamine and a polar amino acid, tryptophan which exists in its charged state in the entire pH range. A multivariate design of experiments was used in which a half fractional factorial approach was applied to screen six factors (donor phase pH, acceptor phase HCl concentration, carrier composition, stirring rate, extraction time and salt content) for their extent of vitality i…
FIA-fluorimetric determination of thiamine.
1990
A flow injection-fluorimetric determination of thiamine is reported. The procedure is based on the oxidation of the analyte with potassium hexacyanoferrate(III) immobilized on an anionic exchange resin; the fluorescence is monitored in aqueous basic solution. Concentrations of the vitamin of 0.1-4 ppm have been determined; the relative standard deviation was 1.8%. The injection rate was 28 samples/h. The influence of other substances and the determination of the drug in a pharmaceutical formulation are also reported.
Partial least squares-near infrared determination of pesticides in commercial formulations
2007
Abstract A solvent free, fast and environmentally friendly near infrared-based methodology (NIR) was developed for pesticide determination in commercially available formulations. This methodology was based on the direct measurement of the diffuse reflectance spectra of solid samples and a multivariate calibration model (partial least squares, PLS) to determine the active principle concentration in commercial formulations. The PLS calibration set was built on using the spiked samples by mixing different amounts of pesticide standards and powdered samples. Buprofezin, Diuron and Daminozide were used as test analytes. Concentration of Buprofezin in the samples was calculated employing a 4-fact…
Determination of total and free sulphur dioxide in wine with a continuous-flow microdistillation system
1993
Abstract A continuous-flow microdistillation system for the determination of SO2 (free and total) in wine samples is described. The assembly permits the successive addition of discrete volumes of sample to the microdistillation module with the aid of a nitrogen carrier stream. The nitrogen carrier also transports the volatilized SO2, after the distillation step, to the absorption module, where the analyte reacts with a solution of 2,2′-dinitro-5,5′-dithiodibenzoic acid in phosphate buffer (pH 6) to give a yellow derivative, which is monitored spectrophotometrically at 410 nm. Free and total so2 signals are obtained by operating the microdistillation module at room temperature (ca. 20°C) and…
The use of core-shell high-performance liquid chromatography column technology to improve biogenic amine quantification in wine
2015
BACKGROUND HPLC column technology has been improved, providing better resolution of closely eluting compounds, better analyte sensitivity, and shorter analysis times. The core-shell technology columns offer a faster analysis through the use of shorter columns without compromising resolution. The aim of this work was to improve the methods for determination of biogenic amines (BAs) in wine using the new HPLC PFP core-shell column technology. RESULTS Two different elution programs were designed to quantify BAs with the core-shell PFP column. Program I flow rate was 2 mL min−1. The total elution time was 10 min. In elution program II, the flow rate was 0.8 mL min−1 and the total elution time w…
Gradient design for liquid chromatography using multi-scale optimization.
2017
Abstract In reversed phase-liquid chromatography, the usual solution to the “general elution problem” is the application of gradient elution with programmed changes of organic solvent (or other properties). A correct quantification of chromatographic peaks in liquid chromatography requires well resolved signals in a proper analysis time. When the complexity of the sample is high, the gradient program should be accommodated to the local resolution needs of each analyte. This makes the optimization of such situations rather troublesome, since enhancing the resolution for a given analyte may imply a collateral worsening of the resolution of other analytes. The aim of this work is to design mul…
Specificity and Sensitivity Characterization of a Gallium Arsenide Resonant Bio-Sensor
2018
International audience; The characterization of the performances of a Gallium Arsenide (GaAs) based biosensor, in terms of sensitivity and specificity, is reported. The design of the sensor consists in a resonant membrane fabricated in GaAs crystal that operates at shear modes of bulk acoustic waves generated by lateral field excitation. The transducer element was fabricated by using typical clean room microfabrication techniques. The backside of the membrane is functionalized by a self-assembled monolayer (SAM) of alkanethiols to immobilize bio-receptors, which will allow the specific capture of the analyte of interest. The theoretical sensitivity of the sensor had been determined by model…
Evaluation and comparison of tailor-made stationary phases based on spherical silica-based beads for capillary electrochromatography via peptide sepa…
2004
Small cyclic peptides have been employed to elucidate the performance of novel sorbents as stationary phases in capillary electrochromatography (CEC). In this paper chain length dependencies for ordinary liquid chromatographic sorbents are reported together with findings acquired on beads specifically designed to suit CEC. The latter, tailor-made, spherical, porous silica exhibits a distinguished surface modification to meet the criteria anticipated to enhance performance profiles in CEC. With well-characterised peptides resembling the analytes, probing of the CEC system in a systematic manner (predominantly via the organic modifier content of the background electrolyte (BE)) reveals insigh…
Chromatographic peak profile of ionogenic analytes upon elution with unbuffered eluents
1998
Experimental proof of the model was carried out for the separation of benzoic acid on a LiChrospher RP-18 column. The observed chromatographic peak profile coincides with the peak profile predicted by the model. The retention times of the dissociated and non-dissociated species determined by using an appropriate fitting procedure were 2.2 and 4.3 min, respectively. Based on these values, a theoretical peak profile was calculated, demonstrating a close agreement with the experimentally observed peak profile. An unexpectedly large difference was found for the retention times of the dissociated and non-dissociated species calculated by a fitting procedure and those experimentally measured on t…
Transport mechanism of peptides through supported liquid membranes
2007
Abstract The transport of selected dipeptides through supported liquid membranes impregnated with di(2-ethylhexyl) phosphoric acid in n-dihexylether has been investigated. The fluxes depend on the side chain of amino acids, presence in the peptide structure. The highest fluxes were obtained for the peptides extracted with the highest efficiency. It has been found that the hydrophobicity of investigated peptides, was not the major factor, influences their SLM permeation. In the conditions studied, it has been observed that the transport of peptide–carrier complex was depending on the acidic–basic properties of the analyte. The linearly least-square fittings of log {K1 + [H+]D} and log[(HR)2]…