Search results for "Detection limit"

showing 10 items of 810 documents

Exploring hand-portable nano-liquid chromatography for in place water analysis: Determination of trimethylxanthines as a use case.

2020

Abstract Analytical performance and optimization of figures of merit of a portable nano liquid chromatograph (NanoLC) with UV detection at 255 nm have been established for in place analysis. Methylxanthines: caffeine, theophylline and theobromine were selected as target analytes. A fast lab method based on IT-SPME coupled on line with capillary liquid chromatograph (CapLC) with diode array detection (DAD) was employed for comparative studies. IT-SPME and solid phase extraction were coupled off-line to NanoLC for improving instrumental parameters, mainly detection capacity and selectivity. IT-SPME or SPE/portable NanoLC based methods were superior in terms of chromatographic resolution and o…

Detection limitAnalyteEnvironmental EngineeringChromatographyMaterials science010504 meteorology & atmospheric sciencesResolution (mass spectrometry)Capillary action010501 environmental sciences01 natural sciencesPollutionDiode arrayNano liquid chromatographyTheophyllineLimit of DetectionCaffeineEnvironmental ChemistryFigure of meritSolid phase extractionWaste Management and DisposalChromatography High Pressure LiquidSolid Phase MicroextractionWater Pollutants Chemical0105 earth and related environmental sciencesChromatography LiquidThe Science of the total environment
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Selection of calibration set samples in determination of olive oil acidity by partial least squares–attenuated total reflectance–Fourier transform in…

2003

Abstract A chemometric method has been applied for the determination of the free fatty acid (FFA) concentration in commercial olive oil samples of different types an origins by using Fourier transform infrared spectroscopy (FTIR) attenuated total reflectance (ATR) measurements. Different methods for selecting the training set, including hierarchical cluster analysis, were applied and compared. The prediction capabilities of partial least squares (PLS) multivariate calibration methods, net analyte signal (NAS) preprocessing followed by PLS or classical least squares (CLS) regression method of ATR–FTIR data were evaluated. Several aspects, like spectral range to be considered, different prepr…

Detection limitAnalyteMean squared errorChemistryAnalytical chemistryBiochemistryFourier transform spectroscopyStandard deviationAnalytical ChemistryChemometricsPartial least squares regressionCalibrationEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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SiPM as miniaturised optical biosensor for DNA-microarray applications

2015

A miniaturized optical biosensor for low-level fluorescence emitted by DNA strands labelled with CY5 is showed. Aim of this work is to demonstrate that a Si-based photodetector, having a low noise and a high sensitivity, can replace traditional detection systems in DNA-microarray applications. The photodetector used is a photomultiplier (SiPM), with 25 pixels. It exhibits a higher sensitivity than commercial optical readers and we experimentally found a detection limit for spotted dried samples of ∼1 nM. We measured the fluorescence signal in different operating conditions (angle of analysis, fluorophores concentrations, solution volumes and support). Once fixed the angle of analysis, for s…

Detection limitAnalytePhotomultiplierMaterials scienceoptical biosensorbusiness.industrySiPMDNA microarrayPhotodetectorLinearityDNA-microarraySignalSettore ING-INF/01 - ElettronicaElectronic Optical and Magnetic MaterialsSilicon photomultiplierOpticslcsh:TA1-2040DNA microarray; Fluorophore detection; Optical Biosensor; SiPMSignal ProcessingElectrical and Electronic Engineeringbusinesslcsh:Engineering (General). Civil engineering (General)Sensitivity (electronics)Fluorophore detectionBiotechnologySensing and Bio-Sensing Research
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Determination of alternative preservatives in cosmetic products by chromophoric derivatization followed by vortex-assisted liquid-liquid semimicroext…

2016

An analytical method for the simultaneous determination of phenethyl alcohol, methylpropanediol, phenylpropanol, caprylyl glycol, and ethylhexylglycerin, which are used as alternative preservatives in cosmetic products, has been developed. The method is based on liquid chromatography with UV spectrophotometric detection after chromophoric derivatization with benzoyl chloride and vortex-assisted liquid-liquid semimicroextraction. Different chromatographic parameters, derivatization conditions, and sample preparation variables were studied. Under optimized conditions, the limits of detection values for the analytes ranged from 0.02 to 0.06µgmL(-1). The method was validated with good recovery …

Detection limitAnalytePreservativeChromatographymedia_common.quotation_subject010401 analytical chemistryPreservatives Pharmaceutical02 engineering and technologyCosmeticsPhenylethyl Alcohol021001 nanoscience & nanotechnology01 natural sciencesCosmetics0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundBenzoyl chloridechemistryPhenethyl alcoholSample preparation0210 nano-technologyDerivatizationmedia_commonChromatography LiquidTalanta
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Stir bar sorptive-dispersive microextraction mediated by magnetic nanoparticles-nylon 6 composite for the extraction of hydrophilic organic compounds…

2016

A new and sensitive analytical method based on the recently developed approach termed stir bar-sorptive dispersive microextraction (SBSDME) using a magnetic CoFe2O4@SiO2-nylon 6 composite as sorbent material is presented for the extraction of hydrophilic organic compounds. The simultaneous determination of four hydrophilic UV filters in environmental water samples has been chosen as a model analytical application due to the increasing awareness regarding the occurrence of sunscreen residuals in natural waters. The developed SBSDME approach combines the principles and benefits of stir bar sorptive extraction (SBSE) and dispersive solid phase extraction (DSPE) but allows for lower extraction …

Detection limitAnalyteSorbentChromatographyChemistry010401 analytical chemistryComposite numberExtraction (chemistry)02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistryDesorptionEnvironmental ChemistryMagnetic nanoparticlesSolid phase extraction0210 nano-technologySpectroscopyAnalytica chimica acta
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A new selective method for dimethylamine in water analysis by liquid chromatography using solid-phase microextraction and two-stage derivatization wi…

2005

Abstract A new method is presented for the determination of DMA in water as its 9-fluorenylmethyl chloroformate (FMOC) derivative using solid-phase microextraction (SPME) and liquid chromatography. The method is based on the employment of SPME fibres coated with carbowax-templated resin (CW-TR) for analyte extraction and derivatization. The fibres were successively immersed in the samples, in a solution of o -phthalaldialdehyde and N -acethyl- l -cysteine (OPA–NAC) and finally, in a solution of FMOC. OPA–NAC reacted on the fibre with possible primary aliphatic amines present in the samples, particularly with PA which is a direct interferent in the determination of DMA with FMOC. In such a w…

Detection limitAnalytechemistry.chemical_compoundChromatographychemistryExtraction (chemistry)Sample preparationChloroformateDerivatizationSolid-phase microextractionDimethylamineAnalytical Chemistry
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Method and apparatus using selected superparamagnetic labels for rapid quantification of immunochromatographic tests

2009

Mika PA Laitinen1, Jari Salmela2, Leona Gilbert1, Risto Kaivola1, Topi Tikkala2, Christian Oker-Blom1, Jukka Pekola3, Matti Vuento11Department of Biological and Environmental Science; 2Department of Physics, University of Jyväskylä, Jyväskylä, Finland; 3Low Temperature Laboratory, Helsinki University of Technology, Helsinki, FinlandAbstract: A rapid method and instrumentation for quantification of immunochromatographic tests (ICT) are described. The principle and performance of the method was demonstrated by measuring the levels of human chorionic gonadotropin (hCG) present in urine. The test format was a sandwich assay using two distinct monoclonal antib…

Detection limitAnalyteendocrine systemChromatographyChemistryCapillary actionmedicine.drug_classBiomedical EngineeringBioengineeringBioinformaticsMonoclonal antibodyLinear rangemedicineUrine sampleBiosensorhormones hormone substitutes and hormone antagonistsSuperparamagnetismOriginal ResearchNanotechnology Science and ApplicationsNanotechnology, Science and Applications
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Sensitive determination of parabens in human urine and serum using methacrylate monoliths and reversed-phase capillary liquid chromatography-mass spe…

2014

A method for the determination of parabens in human urine and serum by capillary liquid chromatography (cLC) with UV-Vis and mass spectrometry (MS) detection using methacrylate ester-based monolithic columns has been developed. The influence of composition of polymerization mixture was studied. The optimum monolith was obtained with butyl methacrylate monomer at 60/40% (wt/wt) butyl methacrylate/ethylene dimethacrylate ratio and 50wt% porogens (composed of 36wt% of 1,4-butanediol, 54wt% 1-propanol and 10wt% water). Baseline resolution of analytes was achieved through a mobile phase of acetonitrile/water in gradient elution mode. Additionally, dispersive liquid-liquid microextraction (DLLME)…

Detection limitAnalytegeographyChromatography Reverse-PhaseChromatographygeography.geographical_feature_categoryResolution (mass spectrometry)ChemistryOrganic ChemistryParabensGeneral MedicineUrineUrinalysisMethacrylateMass spectrometryBiochemistryMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometryLimit of DetectionHumansMethacrylatesMonolithBlood Chemical AnalysisJournal of chromatography. A
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Flow-injection determination of water in organic solvents by near-infrared spectrometry

1993

Abstract A flow-injection (FI) procedure was developed for the direct determination of water in organic solvents by using the O-H stretch absorbance band of water in the near-infrared (NIR) region. Dichloromethane was employed as a test solvent to study the influence of the flow parameters (carrier flow and sample injection volume) and time interval on the sensitivity and repeatability of the FI-NIR measurements. The developed procedure permits the determination of water in dichloromethane and isobutyl methyl ketone samples with limits of detection of 0.01 and 0.005% (v/v), respectively. Real and spiked samples of solvents were analysed by FI-NIR and accurate results were found. The method …

Detection limitAnalytical chemistryInfrared spectroscopyRepeatabilityContaminationBiochemistryAnalytical ChemistrySolventAbsorbancechemistry.chemical_compoundchemistryEnvironmental ChemistryWater contentSpectroscopyDichloromethaneAnalytica Chimica Acta
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On-line bidirectional electrostacking of chromium(III) and chromium(VI) for flame atomic absorption spectrometry determination

2000

Abstract An on-line bidirectional electrostacking-flow injection-flame atomic absorption spectrometry method has been developed for the simultaneous separation, pre-concentration and determination of Cr(III) and Cr(VI). The electrostacking-flow injection unit was established, the pH and components of the support buffer and sample medium were investigated. Results indicated that the ionic mobility, electric field strength and sample area cross-section are the main influence factors on the electrostacking. The calibration range for both, Cr(III) and Cr(VI), was from 20 to 400 μg l −1 . The limit of detection was 7 μg l −1 for three-times the standard deviation of blank values using a electros…

Detection limitAnalytical chemistrychemistry.chemical_elementIonic bondingBiochemistryAnalytical Chemistrylaw.inventionChromiumchemistryFlame atomic absorption spectrometrylawEnvironmental ChemistrySample areaAtomic absorption spectroscopyQuantitative analysis (chemistry)SpectroscopyLine (formation)Analytica Chimica Acta
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