Search results for "PREP"

showing 10 items of 1334 documents

Extraction and Sample Preparation

2015

As everyone knows, the role played by extraction and sample preparation in the analytical sciences cannot be overemphasized. Despite tremendous advances in chromatography, detection, and other aspects of analysis, extraction and sample preparation remain a preanalysis ritual of critical importance. It has been estimated that around 50% to 70% possibly even more of the time and effort that goes into an analytical process comprises extraction and sample preparation. Sample preparation procedure can vary in the degree of selectivity, speed, and convenience, depending on the approach and conditions used, as well as on the geometric configurations of the extraction phase and conditions. Proper d…

AnalyteBioanalysisChromatographylcsh:QD71-142Article SubjectChemistryElectrospray ionizationlcsh:Analytical chemistryAtmospheric-pressure chemical ionizationQuechersMass spectrometryBioinformaticsAnalytical ChemistryEditorialSample preparationSolid phase extractionInternational Journal of Analytical Chemistry
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Isotope dilution mass spectrometry as a calibration method for the analysis of trace elements in powder samples by LA-ICP-MS

2003

The applicability of the isotope dilution (ID) technique for trace element determinations in powdered solid samples by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is demonstrated. LA-ICP-IDMS combines the advantage of the isotope dilution technique as a definitive method with the powerful capability of LA-ICP-MS for a fast and direct multi-element analysis of solid samples. LA-ICP-IDMS therefore allows matrix-matched quantification of element concentrations without any external standard, which is not possible by other calibration strategies used in LA-ICP-MS, up to now. The sample preparation effort is kept minimal and consists of an addition of the corresponding…

AnalyteCertified reference materialsChromatographyIsotopeChemistrySample (material)Trace elementCalibrationAnalytical chemistrySample preparationIsotope dilutionSpectroscopyAnalytical ChemistryJ. Anal. At. Spectrom.
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Automated Photo-Induced Fluorescence Determination of Flumetsulam

2009

The present article deals with a new procedure for determination of the herbicide flumetsulam. The fluorimetric procedure is performed on the basis of photo-increased fluorimetric emission of the pesticide solution and by means of a multicommutation continuous-flow assembly. The alkaline solution containing the analyte is irradiated online and then directly forced through the fluorimeter flow cell. The analysis of different samples is completely automated, as the analyte separation was performed online by including a separation cartridge in the manifold. When dealing with solid samples (such as soil samples), the automation was completed by adding to the manifold the corresponding device fo…

AnalyteChromatographyAqueous solutionChemistryBiochemistry (medical)Clinical BiochemistryExtraction (chemistry)Fluorescence spectrometryAnalytical chemistryBiochemistryFluorescenceAnalytical ChemistryCartridgeFluorometerElectrochemistrySample preparationSpectroscopyAnalytical Letters
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In-tube solid-phase microextraction-capillary liquid chromatography as a solution for the screening analysis of organophosphorus pesticides in untrea…

2006

This paper describes a method for the selective screening of organophosphorus pesticides in water. In-tube solid-phase microextraction (SPME) in an open capillary column coupled to capillary liquid chromatography (LC) with UV detection has been used to effect preconcentration, separation and detection of the analytes in the same assembly. For in-tube SPME two capillary columns of the same length and different internal diameters and coating thicknesses have been tested and compared, a 30 cm x 0.25 mm I.D., 0.25 micro m thickness coating column, and a 30 cm x 0.1 mm I.D., 0.1 micro m of coating thickness column. In both columns the coating was 95% dimethylpolysiloxane (PDMS)-5% diphenylpolysi…

AnalyteChromatographyChemistryCapillary actionOrganic ChemistryAnalytical chemistryWaterGeneral Medicineengineering.materialEnvironmentSolid-phase microextractionBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryNonylphenolchemistry.chemical_compoundPolybrominated diphenyl ethersOrganophosphorus CompoundsCoatingengineeringSample preparationPesticidesSolid Phase MicroextractionWater Pollutants ChemicalChromatography LiquidJournal of chromatography. A
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Validation of a confirmatory method for the determination of macrolides in liver and kidney animal tissues in accordance with the European Union regu…

2006

Abstract This study proposes a simple multiresidue liquid chromatography–diode array detector (LC–DAD) method capable of determining seven macrolide antibiotics in samples of liver and kidney animals at concentrations lower than those allowed by current legislation. Samples were prepared by homogenizing the tissue with EDTA–McIlvaine's buffer and extracted with an Oasis HLB cartridge. The consumption of organic solvent during extraction was minimum. The analytes were detected by LC–DAD and also by liquid chromatography–mass spectrometry with electrospray ionization (LC–(ESI)MS). The method was specific, stable and robust enough for the required purposes. The DAD method was validated in acco…

AnalyteChromatographyChemistryElectrospray ionizationOrganic ChemistryReproducibility of ResultsGeneral MedicineKidneySensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnti-Bacterial AgentsAnalytical ChemistryLiverCalibrationAnimalsmedia_common.cataloged_instanceSample preparationEuropean UnionMacrolidesSolid phase extractionEuropean unionQuantitative analysis (chemistry)Antibacterial agentmedia_commonJournal of Chromatography A
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Column-switching techniques for high-performance liquid chromatography of drugs in biological samples.

1993

In recent years, an increasing number of publications have demonstrated the potential of column-switching techniques for the chromatographic separation, determination and preparative isolation of analytes from biological matrices. Column-switching systems greatly facilitate drug analysis, by on-line sample clean-up and trace enrichment, or by improving the analytical separative process. In this paper, the main applications of column-switching techniques to drug analysis in biological samples, are reviewed.

AnalyteChromatographyChemistryGeneral ChemistryHigh-performance liquid chromatographyBiological materialsChromatographic separationColumn chromatographyPharmaceutical PreparationsAnimalsHumansColumn switchingDrug analysisQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography
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Green aspects, developments and perspectives of liquid phase microextraction techniques.

2014

Determination of analytes at trace levels in complex samples (e.g. biological or contaminated water or soils) are often required for the environmental assessment and monitoring as well as for scientific research in the field of environmental pollution. A limited number of analytical techniques are sensitive enough for the direct determination of trace components in samples and, because of that, a preliminary step of the analyte isolation/enrichment prior to analysis is required in many cases. In this work the newest trends and innovations in liquid phase microextraction, like: single-drop microextraction (SDME), hollow fiber liquid-phase microextraction (HF-LPME), and dispersive liquid-liqu…

AnalyteChromatographyChemistryLiquid Phase MicroextractionEnvironmental pollutionSolid-phase microextractionAnalytical ChemistrySolutionschemistry.chemical_compoundCapillary electrophoresisLiquid–liquid extractionIonic liquidSolventsSample preparationGas chromatographyTalanta
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Development and validation of a fast and sensitive chromatographic assay for all-trans-retinol and tocopherols in human serum and plasma using liquid…

2002

A sensitive HPLC assay for all-trans-retinol, alpha-tocopherol, and gamma-tocopherols in human serum and plasma is reported. Sample preparation is performed in one step and involves precipitation of proteins and extraction of lipids with two volumes of an ethanol-chloroform mixture (3:1, v/v) without I.S. addition. After removal of the precipitated protein, 20 microl aliquots of the supernatant (equivalent to 6.7 microl of serum or plasma) were injected into the HPLC system and analyzed using fluorometric detection. RP-HPLC was performed using a C(18) S3 ODS2 column with a methanol-water step gradient (97:3 to 100) at 1.0 ml/min. The quantification limit expressed as nanograms of analyte pe…

AnalyteChromatographyClinical BiochemistryExtraction (chemistry)RetinolReproducibility of ResultsTocopherolsLiterCell BiologyGeneral MedicineBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundSpectrometry FluorescencechemistryLiquid–liquid extractionHumansSample preparationAll trans retinolVitamin AChromatography High Pressure LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Theoretical prediction of the native fluorescence of pharmaceuticals

2009

At present, to search fluorescent compounds or to increase the native fluorescence is an active research line specially and not only with analytical purposes. On some analytical areas and from the early times of applications of fluorescence (mid-fifties) the fluorimeter was defined as the suitable detector for determination of pharmaceuticals and subsequently, this detection mode has been widely applied. Therefore, it is mandatory to develop new strategies to discover or to enhance in a simple way the native fluorescence of organic compounds to increase the number of analytes to be determined by direct fluorescence. In the present paper are studied further applications of a new tool suitabl…

AnalyteChromatographyScreening testChemistryFluorescence spectrometryDiscriminant AnalysisModels TheoreticalFluorescenceFluorescenceAnalytical ChemistryPharmaceutical PreparationsFluorometerFluorometryPesticidesBiological systemTalanta
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Computer simulations for bioequivalence trials: Selection of analyte in BCS class II and IV drugs with first-pass metabolism, two metabolic pathways …

2018

A semi-physiological two compartment pharmacokinetic model with two active metabolites (primary (PM) and secondary metabolites (SM)) with saturable and non-saturable pre-systemic efflux transporter, intestinal and hepatic metabolism has been developed. The aim of this work is to explore in several scenarios which analyte (parent drug or any of the metabolites) is the most sensitive to changes in drug product performance (i.e. differences in in vivo dissolution) and to make recommendations based on the simulations outcome. A total of 128 scenarios (2 Biopharmaceutics Classification System (BCS) drug types, 2 levels of KM Pgp, in 4 metabolic scenarios at 2 dose levels in 4 quality levels of t…

AnalyteCmaxPharmaceutical ScienceAdministration Oral02 engineering and technologyEquivalence Trials as TopicPharmacologyBioequivalence030226 pharmacology & pharmacyModels Biological03 medical and health sciencesFirst pass effect0302 clinical medicinePharmacokineticsHumansComputer SimulationPharmacokineticsIntestinal MucosaBiotransformationChemistryMembrane Transport Proteins021001 nanoscience & nanotechnologyBiopharmaceutics Classification SystemNONMEMNonlinear DynamicsPharmaceutical PreparationsSolubilityTherapeutic EquivalencyResearch DesignArea Under CurveLinear Models0210 nano-technologyMonte Carlo MethodDrug metabolismEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
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