Search results for "Detection limit"

showing 10 items of 810 documents

Photo-induced chemiluminescence-based determination of diphenamid by using a multicommuted flow system

2007

This manuscript deals with the application of molecular connectivity calculations to predict the photo-induced chemiluminescent behaviour of the family of herbicides grouped as amides. Several compounds of this group were theoretically studied by means of a general discriminant equation formerly obtained, being 18 of them (plus eight from the chloroacetanilide sub-group) predicted with a high probability as photo-induced chemiluminescent. Empirical confirmation of the chemiluminometric behaviour was performed with some few commercially available amide herbicides. On the basis of these results, a new multicommutation-photo-chemiluminescent method is proposed for the determination of the diph…

Detection limitReproducibilityChromatographyChemistryAnalytical chemistryRepeatabilityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundSodium hydroxidelawAmideCalibrationPhotodegradationChemiluminescenceTalanta
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Automated determination of amisulpride by liquid chromatography with column switching and spectrophotometric detection.

2003

A fully automated chromatographic method including on-line blood serum or plasma clean-up, isocratic high-performance liquid chromatography (HPLC) and spectrophotometric detection was developed for quantitative analysis of the new antipsychotic drug amisulpride. After injection of serum or plasma onto the HPLC system and clean-up on a pre-column (10x4.0 mm I.D.) filled with Silica CN 20 micrometer (pore size 10 nm) by an eluent consisting of 8% acetonitrile in deionized water, the chromatographic separation was performed on Lichrospher CN (5 micrometer; 250x4.6 mm I.D.) by an eluent consisting of 50% acetonitrile and 50% aqueous potassium phosphate buffer (0.008 M, pH 6.4). The UV detector …

Detection limitReproducibilityChromatographyClinical BiochemistryAnalytical chemistryCell BiologyGeneral MedicineReference StandardsBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyBlood serumchemistryPotassium phosphateSpectrophotometryHumansAmisulprideSulpirideAcetonitrileQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Multimycotoxin LC-MS/MS Analysis in Tea Beverages after Dispersive Liquid-Liquid Microextraction (DLLME).

2017

The aim of the present study was to develop a multimycotoxin liquid chromatography tandem mass spectrometry (LC-MS/MS) method with a dispersive liquid-liquid microextraction procedure (DLLME) for the analysis of AFs, 3aDON, 15aDON, NIV, HT-2, T-2, ZEA, OTA, ENNs, and BEA in tea beverages and to evaluate their mycotoxin contents. The proposed method was characterized in terms of linearity, limits of detection (LODs), limits of quantification (LOQs), recoveries, repeatability (intraday precision), reproducibility (interday precision), and matrix effects to check suitability. The results show LODs in the range of 0.05-10 μg/L, LOQs in the range of 0.2-33 μg/L, and recoveries in the range of 65…

Detection limitReproducibilityChromatographyTeaChemistryLiquid Phase Microextraction010401 analytical chemistryFood Contamination04 agricultural and veterinary sciencesGeneral ChemistryRepeatabilityMycotoxinsGreen tea040401 food science01 natural sciences0104 chemical scienceschemistry.chemical_compound0404 agricultural biotechnologyLiquid chromatography–mass spectrometryLimit of DetectionTandem Mass SpectrometryLc ms msLiquid liquidGeneral Agricultural and Biological SciencesMycotoxinJournal of agricultural and food chemistry
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Simultaneous homogeneous immunoassay of phenytoin and phenobarbital using a Nafion-loaded carbon paste electrode and two redox cationic labels

1997

Abstract The dual-analyte homogeneous immunoassay of two antiepileptic drugs was carried out simultaneously at physiological pH by square-wave voltammetry at a Nafion-loaded carbon paste electrode. Phenobarbital (PB) and phenytoin (DPH) were labeled by a cobaltocenium salt (Cc+) and a ferroceneammonium salt (N+Fc), respectively, and the corresponding standard redox potentials were −1.05 V and 0.26 V. Detection limits of 0.25 and 0.2 μM were achieved for PB-Cc+ and DPH-N+Fc (S/N = 3) after a 5-minute accumulation step, with linear responses over the 0.25–5 and 0.2–5 μM ranges, respectively. The relative standard deviation was evaluated to be ≥ 11% for 1 μM of each labeled drug. The separate,…

Detection limitReproducibilityChromatographymedicine.diagnostic_testCationic polymerizationBiochemistryRedoxAnalytical ChemistryCarbon paste electrodechemistry.chemical_compoundchemistryNafionImmunoassaymedicineEnvironmental ChemistryVoltammetrySpectroscopyAnalytica Chimica Acta
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Thermal Lens Spectrometric Detection of Catecholamines after Oxidation to Aminochromes

1992

Abstract Experimental conditions for the spectrophotometric and thermal lens spectrometry (TLS) detection of catecholamines after oxidation to aminochromes with hexacyanoferrate (III) are optimized. At the low concentrations used in TLS, and in a 0.07 M citrate buffer, catecholamine oxidation can be performed at pH 7 and is immediate, whereas a lower pH value is required in spectrophotometry to avoid aminochrome polymerisation, the oxidation reactions being much slower. Similar TLS sensitivities are obtained for all catecholamines which facilitates HPLC evaluation. Sensitivity can be enhanced using a 50% ethanol-water medium. The linear dynamic range extends over two orders of magnitude, th…

Detection limitReproducibilityChromatographymedicine.diagnostic_testChemistryBiochemistry (medical)Clinical BiochemistryMass spectrometryBiochemistryRedoxHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionLens (optics)lawSpectrophotometryElectrochemistrymedicineUrine sampleSpectroscopyAnalytical Letters
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Electrochemical detection of chloride ions using Ag-based electrodes obtained from compact disc

2022

Abstract In this work electrochemical sensors fabricated from compact disc material (waste or new) are used to quantify chloride ions in different types of samples. All three electrodes, working, counter, and pseudo-reference electrodes, were fabricated from the compact disc and directly used. Different parameters were studied in order to demonstrate the possibility of using this waste material for efficient and low-cost electrochemical sensors. Chloride sensing performance was evaluated using linear scan voltammetry as the detection technique. A sensitivity of 0.174 mA mM−1 cm−2 with a limit of detection of 20 μM and excellent selectivity against many interferents was observed. Selectivity…

Detection limitReproducibilityCompact DisksChemistryAnalytical chemistryReproducibility of ResultsElectrochemical TechniquesElectrochemistryBiochemistryChlorideAnalytical ChemistryElectrochemical gas sensorSettore ING-IND/23 - Chimica Fisica ApplicataChloridesChloride ions Compact disc Cystic fibrosis Disposable sensor Electrochemical sensor Real time monitoring Water quality Wearable sensorsElectrodeSettore ING-IND/17 - Impianti Industriali MeccanicimedicineEnvironmental ChemistrySelectivityVoltammetryElectrodesSpectroscopymedicine.drug
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Vanadium and molybdenum concentrations in particulate from Palermo (Italy): analytical methods using voltammetry

2014

The main purpose of this work was to develop a reliable method for the determination of vanadium (V) and molybdenum (Mo) in atmosphere particles or aerosols because they can not be readily measured using conventional techniques. For this research, 30 particulate samples were collected from five different stations located at Palermo, Italy. We used the catalytic adsorptive stripping voltammetry and differential pulsed voltammetry to measure Vand Mo in atmospheric particulate, respectively. The represented method includes advantages of high sensitivity, high selectivity, simplicity, reproducibility, speed and low costs. The quantification limits for V and Mo are, respectively, 0.57 and 0.80 n…

Detection limitReproducibilityRelative standard deviationAnalytical chemistrychemistry.chemical_elementVanadiumParticulatesSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturalichemistryMolybdenumEnvironmental chemistryvanadium molybdenum particulate voltammetry PalermoAdsorptive stripping voltammetrySettore CHIM/01 - Chimica AnaliticaVoltammetryGeneral Environmental Science
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Selective chlorine determination by gas diffusion in a tandem flow assembly and spectrophotometric detection with o-dianisidine

2001

Abstract A fast, selective, sensitive and automated method for determination of free chlorine in industrial formulations and water samples is proposed. The automation of the flow assembly is based on the “tandem flow” approach, which uses a set of solenoid valves acting as independent switches. The operating cycle for obtaining a typical analytical transient signal can easily be programmed by means of friendly software running in the Windows environment. The manifold is provided with a gas diffusion unit which permits the removal of interfering species as well as concentrating the chlorine. The determination of chlorine is performed on the basis of the oxidation of o-dianisidine as the colo…

Detection limitReproducibilityTandemChemistryAnalytical chemistrychemistry.chemical_elementSolenoidBiochemistryAnalytical ChemistryReagentpolycyclic compoundsChlorineEnvironmental ChemistryGaseous diffusionQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Determination of benzoylurea insecticides in food by pressurized liquid extraction and LC-MS

2010

A method based on pressurized liquid extraction and LC-MS/MS has been developed for determining nine benzoylureas (BUs) in fruit, vegetable, cereals, and animal products. Samples (5 g) were homogenized with diatomaceous earth and extracted in a 22 mL cell with 22 mL of ethyl acetate at 80 degrees C and 1500 psi. After solvent concentration and exchange to methanol, BUs were analyzed by LC-MS/MS using an IT mass analyzer, which achieved several transitions of precursor ions that increase selectivity providing identification. LOQs were between 0.002 and 0.01 mg/kg, which are equal or lower than maximum residue limits established by the Codex Alimentarius. Excellent linearity was achieved over…

Detection limitResidue (complex analysis)ChromatographyBenzoylureaExtraction (chemistry)Ethyl acetateFiltration and SeparationHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometrymedicineSample preparationmedicine.drugJournal of Separation Science
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Capillary zone electrophoresis for the determination of thiabendazole, prochloraz and procymidone in grapes

2001

Capillary zone electrophoresis with UV detection was applied to the simultaneous determination of thiabendazole, prochloraz and procymidone in grapes. Electrolyte conditions such as pH, composition and concentration of the buffer, addition of organic solvent and working voltage were checked to obtain a high-performance separation of the three fungicides (by measurement of separation efficiency and resolution). The most critical parameter was the pH of the running buffer. The best separation was achieved in 4 mM phosphate solution at pH 3.5. The repeatability of the migration times, expressed as RSD, was <0.44%. The three peaks were completely resolved with a separation efficiency up to 100 …

Detection limitResidue (complex analysis)ChromatographyChemistryExtraction (chemistry)ImidazolesAnalytical chemistryElectrophoresis CapillaryRepeatabilityBiochemistryAnalytical ChemistryBridged Bicyclo Compoundschemistry.chemical_compoundCapillary electrophoresisThiabendazoleElectrochemistryEnvironmental ChemistryVitisProcymidoneTheoretical plateSolid phase extractionSpectroscopyThe Analyst
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