Search results for "Analyte"

showing 10 items of 303 documents

Oligonucleotides in Sensing and Diagnostic Applications

2015

AnalyteChemistryOligonucleotideNucleic Acid ConformationsNucleic acidOrganic chemistryG-quadruplexG-QuartetsChemical reactionNucleobase
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FT-IR quantitative analysis of solvent mixtures by the constant ratio method

1999

Abstract An analytical methodology to quantify compounds in complex mixtures by FTIR spectroscopy is proposed and the “Constant Ratio Method” (CRM) was developed. The addition of a standard to the sample allows us to establish a constant KMS characteristic of the Analyte/Standard system which can be employed as a quantification factor of the analyte in different samples . In the proposed method the measurements are independent of optical path length. This method has been successfully applied to quantify butylacetate and toluene in binary and tertiary samples and tertiary mixtures. Butylacetate/toluene/nujol have been resolved employing valeronitrile as standard, obtaining values for relativ…

AnalyteChemistryOrganic ChemistryAnalytical chemistryTolueneAnalytical ChemistryInorganic ChemistrySolventchemistry.chemical_compoundNujolFourier transform infrared spectroscopyConstant (mathematics)Quantitative analysis (chemistry)SpectroscopyOptical path lengthJournal of Molecular Structure
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Principal component analysis for the selection of variables in the application of the H-point and generalised H-point standard addition method

2000

The present paper deals with the selection of variables for the H-point and generalised H-point standard additions methods (HPSAM and GHPSAM, respectively). Both methods are applied for the resolution of spectroscopic interfered signals in the UV-vis range. The HPSAM is a suitable method for the resolution of binary and ternary mixtures when the interferent is known. The GHPSAM is applied for the resolution of samples that contain unknown interferents. In this paper, a method based on the study of a principal components analysis (PCA) for the selection of variables for the HPSAM and GHPSAM is proposed. The PCA results show the isolation of the analyte signal from the sample signal, achieved…

AnalyteChemistryStandard additionPrincipal component analysisStatisticsRange (statistics)A priori and a posterioriBinary numberBiological systemTernary operationSelection (genetic algorithm)Analytical ChemistryTalanta
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Gold Nanorods as Plasmonic Sensors for Particle Diffusion.

2016

Plasmonic gold nanoparticles are normally used as sensor to detect analytes permanently bound to their surface. If the interaction between the analyte and the nanosensor surface is negligible, it only diffuses through the sensor’s sensing volume, causing a small temporal shift of the plasmon resonance position. By using a very sensitive and fast detection scheme, we are able to detect these small fluctuations in the plasmon resonance. With the help of a theoretical model consistent with our detection geometry, we determine the analyte’s diffusion coefficient. The method is verified by observing the trends upon changing diffusor size and medium viscosity, and the diffusion coefficients obtai…

AnalyteChemistrybusiness.industryPhysics::OpticsNanoparticleNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesNanosensorColloidal goldOptoelectronicsGeneral Materials SciencePhysical and Theoretical ChemistrySurface plasmon resonanceDiffusion (business)0210 nano-technologybusinessPlasmonLocalized surface plasmonThe journal of physical chemistry letters
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Sub- and supercritical fluid extraction of trichloropyridinol from soil prior to immunoassay

1997

A comparative study on the extraction of TCP (3,5,6-trichloro-2-pyridinol, a metabolite of chlorpyrifos) from soil with CO2 and H2O is reported. The polarity of the analyte requires the presence of both a cosolvent (methanol) and an ion-pair reagent [(1R)-(-)-10-camphorsulfonic acid ammonium salt] for 95% extraction in 30 min when supercritical CO2 at 40 degrees C and 383 bar is used as extractant. Subcritical water (250 degrees C and 200 bar) enables complete extraction within 15 min without additives. Quantitation of the target analyte is performed by specific immunoassay using a non-commercial monoclonal antibody which provides a linear determination range between 0.005 and 5 micrograms/…

AnalyteChromatography GasHot TemperatureChromatographymedicine.diagnostic_testPyridonesOrganic ChemistryExtraction (chemistry)Supercritical fluid extractionReproducibility of ResultsEnzyme-Linked Immunosorbent AssayGeneral MedicineBiochemistrySupercritical fluidAnalytical Chemistrychemistry.chemical_compoundchemistryImmunoassayReagentPressuremedicineSoil PollutantsAmmoniumMethanolJournal of Chromatography A
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The determination of trace element concentrations in fly ash samples using ultrasound-assisted digestion followed with inductively coupled plasma opt…

2009

Abstract A method of ultrasound-assisted digestion followed by inductively coupled plasma optical emission spectrometry (ICP-OES) used for the determination of trace element (chromium, copper, lead, nickel, vanadium and zinc) concentrations in fly ash samples was developed. All the measurements were performed in robust plasma conditions. Ultrasound-assisted digestion procedures using digestion solutions of aqua regia and hydrofluoric acid (HF) resulted in recovery rates of over 80% for all the analyte elements. Ultrasound-assisted two-step digestion with digestion solutions of 6 mL of HNO3 (Step 1) and 3 mL of HNO3 + 3 mL of HF (Step 2) resulted in recovery rates of over 92% for all the ana…

AnalyteChromatographyAcoustics and UltrasonicsOrganic ChemistryAnalytical chemistrychemistry.chemical_elementZincInorganic Chemistrychemistry.chemical_compoundChromiumDigestion (alchemy)chemistryFly ashChemical Engineering (miscellaneous)Environmental ChemistryAqua regiaRadiology Nuclear Medicine and imagingInductively coupled plasmaMicrowave digestionUltrasonics sonochemistry
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On-Line Derivatization into Precolumns for the Determination of Drugs by Liquid Chromatography and Column Switching:  Determination of Amphetamines i…

1996

A chromatographic system for the on-line derivatization of drugs using column switching is described. The system uses a 20 mm × 2.1 mm i.d. precolumn packed with a unmodified ODS stationary phase. This column is used for sample cleanup and enrichment of the analytes. Next, the trapped analytes are derivatized by injection of the derivatization reagent into the precolumn. Finally, the derivatives are transferred to the analytical column for their separation under reversed-phase conditions. The influence of several parameters such as the reaction time, the amount of derivatization reagent, or the system design has been studied using some amphetamines as model compounds and three derivatizatio…

AnalyteChromatographyAmphetaminesUrineChloroformateMethamphetamineAnalytical ChemistrySubstance Abuse Detectionchemistry.chemical_compoundColumn chromatographychemistryReagentIndicators and ReagentsColumn switchingDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidAnalytical Chemistry
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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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Analytical capabilities of high performance liquid chromatography – Atmospheric pressure photoionization – Orbitrap mass spectrometry (HPLC-APPI-Orbi…

2015

A new analytical method was established and validated for the analysis of 27 brominated flame retardants (BFRs), including so called "emerging" and "novel" BFRs (EBFRs and NBFRs) in fish samples. High performance liquid chromatography (HPLC) coupled to Orbitrap mass spectrometry (Orbitrap-MS) employing atmospheric pressure photoionization (APPI) interface operated in negative mode was used for the identification/quantitation of contaminants. HPLC-Orbitrap-MS analysis provided a fast separation of selected analytes within 14 min, thus demonstrating a high throughput processing of samples. The developed methodology was tested by intralaboratory validation in terms of recovery, repeatability, …

AnalyteChromatographyAtmospheric pressureChemistryAnalytical chemistryRepeatabilityMass spectrometryOrbitrapBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionPolybrominated diphenyl ethersCertified reference materialslawEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Adsorbent phases with nanomaterials for in-tube solid-phase microextraction coupled on-line to liquid nanochromatography

2015

Following the present trends in miniaturization, a methodology that combines on-line In-Tube Solid-Phase Microextraction (IT-SPME) with Liquid Nanochromatography (nano-LC) and UV-vis diode array detection (DAD) was developed. This coupling was achieved by using two interconnected valves (i.e. conventional and micro-automatic valves) in the system of injection. As for IT-SPME, different materials, containing in some cases nanostructures or nanoparticles and in other cases polymeric adsorbent phases immobilized on capillary columns, were tested in order to improve extraction efficiencies of organic compounds; diclofenac was selected as the target analyte. Additionally, the transfer time of th…

AnalyteChromatographyCapillary actionChemistry010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Analytical chemistryNanoparticle02 engineering and technologyGeneral Medicine021001 nanoscience & nanotechnologySolid-phase microextraction01 natural sciencesBiochemistryNanostructures0104 chemical sciencesAnalytical ChemistryNanomaterialsAdsorptionMiniaturizationAdsorption0210 nano-technologySolid Phase MicroextractionChromatography LiquidJournal of Chromatography A
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