Search results for "monitor"

showing 10 items of 3841 documents

Multiple-stage mass spectrometric analysis of six pesticides in oranges by liquid chromatography–atmospheric pressure chemical ionization–ion trap ma…

2004

Abstract Six pesticides were determined by liquid chromatography (LC) with positive ion (PI) atmospheric pressure chemical ionization quadrupole ion-trap tandem mass spectrometry (APCI–MS–MS). Ion fragmentation was studied by MS, MS 2 and MS 3 . Fragmentation of the pesticides produced ions formed by various losses from the side-chains and through heterocyclic ring opening, but without any common fragmentation pathway. Multiple reaction monitoring (MRM) of MS, MS 2 and MS 3 was used to identify and quantify the pesticides. The samples were extracted with ethyl acetate and dried over anhydrous sodium sulfate. Comparison of the three MS modes showed that MS 3 is slightly less sensitive but mu…

Detection limitChemical ionizationChromatographyChemistryOrganic ChemistrySelected reaction monitoringAnalytical chemistryReproducibility of ResultsAtmospheric-pressure chemical ionizationGeneral MedicineTandem mass spectrometryMass spectrometrySensitivity and SpecificityBiochemistryMass SpectrometryAnalytical ChemistryAtmospheric PressureIon trapPesticidesQuadrupole ion trapChromatography LiquidCitrus sinensisJournal of Chromatography A
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Analysis of organophosphorus pesticides in honeybee by liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry.

2001

Pesticides applied in extended agricultural fields may be controlled by means of bioindicators, such as honeybees, in which are the pesticides bioaccumulate. Liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry (LC-APCI-MS) experiments with positive (PI) and negative (NI) ion modes were optimized for the analysis of 22 organophosphorus pesticides in honeybee samples. The extraction required 3 g of sample, which was extracted with acetone. The extract was purified with coagulating solution and reextracted with Cl(2)CH(2). Pesticides studied could be detected by both ionization modes except for parathion, parathion-methyl, and bromophos, which did not give signals …

Detection limitChemical ionizationInsecticidesChromatographyExtraction (chemistry)Analytical chemistryPesticide ResiduesAtmospheric-pressure chemical ionizationGeneral ChemistryPesticideBeesMass spectrometrySensitivity and SpecificityMass Spectrometrychemistry.chemical_compoundParathionOrganophosphorus CompoundschemistryAnimalsSelected ion monitoringGeneral Agricultural and Biological SciencesChromatography LiquidJournal of agricultural and food chemistry
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Fishing for a drug: solid-phase microextraction for the assay of clozapine in human plasma

1999

Solid-phase microextraction (SPME) was investigated as a sample preparation method for assaying the neuroleptic drug clozapine in human plasma. A mixture of human plasma, water, loxapine (as internal standard) and aqueous NaOH was extracted with a 100-micron polydimethylsiloxane (PDMS) fiber (Supelco). Desorption of the fiber was performed in the injection port of a gas chromatograph at 260 degrees C (HP 5890; 30 m x 0.53 mm I.D., 1 micron film capillary; nitrogen-phosphorous selective detection). Fibers were used repeatedly in up to about 75 analyses. The recovery was found to be 3% for clozapine from plasma after 30 min of extraction. However, in spite of the low recovery, the analyte was…

Detection limitChromatography GasChromatographymedicine.diagnostic_testChemistryReproducibility of ResultsLoxapineGeneral ChemistryReference StandardsSolid-phase microextractionSensitivity and SpecificityHigh-performance liquid chromatographyMatrix (chemical analysis)Therapeutic drug monitoringmedicineHumansSample preparationSolid phase extractionGas chromatographyClozapineJournal of Chromatography B: Biomedical Sciences and Applications
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Determination of amitraz and its transformation products in pears by ethyl acetate extraction and liquid chromatography-tandem mass spectrometry.

2008

A method has been developed for identification and quantification of the acaricide amitraz and its transformation products, 2,4-dimethylaniline (DMA), 2,4-dimethylformamidine (DMF) and N-2,4-dimethylphenyl-N-methylformamidine (DMPF) in pears. The analytes were extracted using ethyl acetate and anhydrous sodium sulphate. Analysis was performed by liquid chromatography-electrospray tandem mass spectrometry (LC-ESI-MS/MS) in the positive ion mode using a triple quadrupole (QqQ) instrument. Two precursor-product ion transitions were monitored for each compound in the selected reaction monitoring (SRM) mode. The method was validated with pears taken from the orchard before the amitraz treatment …

Detection limitChromatographyMaximum Residue LimitAniline CompoundsToluidinesSulfatesOrganic ChemistrySelected reaction monitoringEthyl acetatePesticide ResiduesReproducibility of ResultsGeneral MedicineAcetatesBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryTriple quadrupole mass spectrometerPyruschemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryAmitrazChromatography LiquidJournal of chromatography. A
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Automated Determination of Trimipramine and N-Desmethyl-Trimipramine in Human Plasma or Serum by HPLC With On-Line Solid Phase Extraction

1995

A fully automated method including column-switching and isocratic high performance liquid chromatography (HPLC) was developed for determination of the tricyclic antidepressant trimipramine (T) and its N-demethylated metabolite N-desmethyltrimipramine (DT). The limit of quantification was below 10 ng/ml for T and DT. The assay revealed linearity between detector response and drug concentration in a therapeutically relevant range of 10 to 500 ng/ml. The mean intra- and interassay variabilities were 6.2 and 12.3%, respectively, for T and 4.7 and 8.7% respectively, for DT. The method can be applied to therapeutic drug monitoring of patients under T therapy and may be useful for pharmacokinetic …

Detection limitChromatographymedicine.diagnostic_testMetaboliteDesmethylTrimipramineHigh-performance liquid chromatographychemistry.chemical_compoundPharmacokineticschemistryTherapeutic drug monitoringmedicineMolecular MedicineSolid phase extractionmedicine.drugJournal of Liquid Chromatography
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Analysis of Polycyclic Aromatic Hydrocarbons and Their Oxygen-Containing Derivatives and Metabolites in Soils

2010

Although polycyclic aromatic hydrocarbons (PAHs) have been extensively studied, the knowledge of their oxygen-containing derivatives and metabolites (OPAHs) in soils is limited. We modified and tested an existing analytical protocol involving pressurized liquid extraction of soil followed by fractionation of target compounds into PAHs and OPAHs on a silica gel column and gas chromatography/ mass spectrometry-based separation and quantification. Polycyclic aromatic hydrocarbons and carbonyl-OPAHs were quantified directly after separation on silica gel columns, and hydroxyl/carboxyl-OPAHs were quantified after silylation with N,O-bis(trimethylsilyl)trifluoroacetamide. Recoveries between 78 an…

Detection limitEnvironmental EngineeringChromatographyOpahbiologySilylationChemistrySilica gelExtraction (chemistry)Industrial WasteFractionationManagement Monitoring Policy and Lawbiology.organism_classificationPollutionOxygenSoilchemistry.chemical_compoundEnvironmental chemistrySoil PollutantsSample preparationGas chromatographyPolycyclic Aromatic HydrocarbonsWaste Management and DisposalEnvironmental MonitoringWater Science and TechnologyJournal of Environmental Quality
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Comparison of different methods for extraction of polycyclic aromatic hydrocarbons (PAHs) from Sicilian (Italy) coastal area sediments.

2012

This paper describes a work aimed at improving the conditions of an extraction method, coupling GC-MS determination, for the analysis without cleanup phase, of polycyclic aromatic hydrocarbons (PAHs) from sediment samples. The automatic Soxhlet extraction in warm mode (using Extraction System B-811 Standard, Buchi) has demonstrated advantages for automation, reduced extraction time, and lower solvent use than for conventional Soxhlet extraction. Under these conditions, the recoveries are very good as they resulted greater than 85 % and, in most of the cases, near 100 %. The repeatability is also satisfactory (relative standard deviation less than 15 %). The detection limits are also accepta…

Detection limitGeologic SedimentsExtraction (chemistry)SedimentGeneral MedicineRepeatabilityChemical FractionationManagement Monitoring Policy and LawPollutionGas Chromatography-Mass SpectrometrySettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliMatrix (chemical analysis)Dry weightEnvironmental chemistryEnvironmental scienceEcotoxicologySeawaterSettore CHIM/01 - Chimica AnaliticaPolycyclic Aromatic HydrocarbonsGas chromatography–mass spectrometryAutomatic extraction .CRM . PAHs . Sediments . GC-MSSicilyWater Pollutants ChemicalEnvironmental MonitoringGeneral Environmental Science
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Quantitation of talinolol in rat plasma by LC-MS-MS.

2010

The aim of this study was to develop and validate an assay based on liquid chromatography-tandem mass spectrometry to quantitate talinolol in rat plasma. After a simple protein precipitation step, separation was performed by reversed-phase liquid chromatography using gradient elution with acetonitrile-water-formic acid. Electrospray ionization in the positive ion mode with multiple reaction monitoring was used to analyze talinolol employing propranolol as internal standard. The calibration curve for talinolol was linear over the concentration range 1-250 ng/mL with a correlation coefficient0.995. The method was sensitive (limit of quantitation, 1 ng/mL) and had acceptable accuracy (85-115% …

Detection limitMaleSpectrometry Mass Electrospray IonizationChromatographyElectrospray ionizationSelected reaction monitoringAnalytical chemistryGeneral MedicineReversed-phase chromatographyMass spectrometryHigh-performance liquid chromatographyAnalytical ChemistryRatsPropanolamineschemistry.chemical_compoundchemistryProtein precipitationAnimalsRats WistarAntihypertensive AgentsChromatography High Pressure LiquidTalinololChromatography LiquidJournal of chromatographic science
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Automated determination of reboxetine by high-performance liquid chromatography with column-switching and ultraviolet detection.

2000

A fully automated method including column-switching and isocratic high-performance liquid chromatography (HPLC) was developed for quantitative analysis of the new antidepressant reboxetine, a noradrenaline reuptake inhibitor. After serum injection into the HPLC system and on-line sample clean-up on a silica C8 (10x4.0 mm I.D.) clean-up column with an eluent consisting of 2.5% acetonitrile in deionized water, the chromatographic separation was performed on an analytical column (Lichrospher CN; 250x4.6 mm I.D.) with an eluent of acetonitrile-aqueous potassium phosphate buffer (0.008 M, pH 6.4) (50:50). The UV detector was set at 273 or 226 nm. The limit of quantification was about 15 ng/ml at…

Detection limitQuality ControlChromatographymedicine.diagnostic_testAdrenergic Uptake InhibitorsReboxetineMorpholinesAnalytical chemistryGeneral ChemistryHigh-performance liquid chromatographychemistry.chemical_compoundAutomationReboxetineColumn chromatographychemistryPotassium phosphateTherapeutic drug monitoringSpectrophotometrymedicineHumansSpectrophotometry UltravioletQuantitative analysis (chemistry)Chromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical sciences and applications
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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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