Search results for "Metabolite"

showing 10 items of 551 documents

Optimization of LC–MS/MS using triple quadrupole mass analyzer for the simultaneous analysis of carbosulfan and its main metabolites in oranges

2006

This paper describes an analytical method involving a simple solvent extraction for the simultaneous liquid chromatography coupled to quadrupole tandem mass spectrometry (LC-MS/MS) determination of carbosulfan, its most toxic metabolite--carbofuran--, and its other main metabolites--3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenolcarbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran and dibutylamine--in oranges. Chromatography was performed on a Zorbax Bonus-RP (150 mm x 2.1 mm, 5 microm). The mobile phase was a ternary gradient water-methanol-acetonitrile with 1.0 mM ammonium acetate at flow rate of 0.2 ml min(-1). The LC separation and MS/MS optimization were studied to selec…

Detection limitChromatographyMetaboliteAnalytical chemistryTandem mass spectrometryBiochemistryAnalytical ChemistryTriple quadrupole mass spectrometerStandard curvechemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryEnvironmental ChemistrySample preparationCarbosulfanSpectroscopyAnalytica Chimica Acta
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Quantification of Imidacloprid in Honeybees: Development of a Chemiluminescent ELISA

2010

A Chemiluminescente Enzyme-Linked Immuno-Sorbent Assay (CL-ELISA) for determination and quantification of the fungicide imidacloprid in honeybees was developed in an indirect competitive format. The assay was optimized by determining: the optimal coating conjugate concentration and anti-imidacloprid antiserum dilution, the effect of the incubation time on the competitive step, the tolerance to organic solvents. The IC50 and the limit of detection (LOD) values were 14.8 ng mL-1 and 0.11 ng mL -1, respectively, similar to those of colorimetric ELISA with a calibration range of 0.1 – 2600 ng mL-1. Cross reactivity of some related compounds such as three imidacloprid metabolites, 6-chloro nicot…

Detection limitChromatographyMetaboliteBiochemistry (medical)Clinical BiochemistryIMIDACLOPRIDBiochemistryAcetamipridCHEMILUMINESCENCEAnalytical Chemistrylaw.inventionStandard curvechemistry.chemical_compoundchemistrylawImidaclopridparasitic diseasesElectrochemistrySample preparationELISAHONEYBEESColorimetrySpectroscopyChemiluminescence
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Determination of furosemide in urine samples by direct injection in a micellar liquid chromatographic system.

2002

A sensitive, selective and efficient micellar liquid chromatographic (MLC) procedure was developed for the determination of furosemide (4-chloro-N-furfuryl-5-sulfamoylanthranilic acid) in urine samples by direct injection and UV detection. The procedure makes use of a C18 reversed-phase column and a micellar mobile phase of 0.05 mol l(-1) sodium dodecyl sulfate-6% v/v propanol and phosphate buffer at pH 3 to resolve furosemide from its photochemical degradation products. The importance of protecting the standards and urine samples to be analysed from light in the assay of furosemide, avoiding its degradation, was verified. The limit of quantification was 0.15 microg ml(-1) and the relative …

Detection limitChromatographyMetabolitemedicine.medical_treatmentSodiumchemistry.chemical_elementFurosemideReversed-phase chromatographyUrineBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryFurosemideElectrochemistrymedicineEnvironmental ChemistryHumansDiureticDiureticsQuantitative analysis (chemistry)SpectroscopyChromatography High Pressure Liquidmedicine.drugChromatography Micellar Electrokinetic CapillaryThe Analyst
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Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry Analysis of Carbosulfan, Carbofuran, 3-Hydroxycarbofuran, and Other Metabolites in …

2007

The potential of liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QqTOF-MS) to identify and confirm carbosulfan and seven of its main metabolites (carbofuran, 3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenol carbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran, dibutylamine) at trace levels from food is explored for the first time. The analytical method developed consists of pressurized liquid extraction (PLE) and LC-QqTOF-MS in positive ion mode, which attains unequivocal identification and quantification of the studied compounds in food, at levels well below of those of concern (0.05 mg/kg for the sum of carbosulfan, carbofuran, and 3-hydroxycarbofuran).…

Detection limitChromatographyMolecular StructureMetaboliteRepeatabilityButylaminesMass spectrometrySensitivity and SpecificityAnalytical ChemistryDibutylamineCarbofuranchemistry.chemical_compoundchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationCarbosulfanCarbamatesQuantitative analysis (chemistry)CarbofuranFood AnalysisChromatography LiquidAnalytical Chemistry
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Spectrophotometric flow injection determination of formetanate and m-aminophenol in water after reaction with p-aminophenol

1992

Abstract An automated procedure has been developed for the determination of formetanate and its metabolite m -aminophenol (MAP) in water samples. MAP can be selectively determined in the presence of formetanate by direct on-line reaction with p -aminophenol and spectrophotometric measurement of the absorbance at 576 nm in the presence of KIO 4 , as oxidizing agent. The method has a limit of detection of 5 × 10 −7 M , it provides a recovery percentage from 95 to 104% and permits one to carry out 120 measurements/hr. The spectrophotometric determination of formetanate must be carried out after a previous hydrolysis to MAP. To determine formetanate in the presence of MAP, two steps are necessa…

Detection limitChromatographymedicine.diagnostic_testHydrochlorideMetaboliteAnalytical ChemistryAbsorbancechemistry.chemical_compoundHydrolysischemistryFormetanateSpectrophotometrymedicineDerivatizationTalanta
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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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Optimization of sample preparation conditions for detecting trace amounts of β-tegafur in α- and β-tegafur mixture.

2012

We report a semiquantitative method for determining trace amounts (<1%) of thermodynamically stable forms in polymorphic mixtures, focusing on sample preparation ef- fects on solid phase transitions. Tegafur (5-fluoro-1-(oxolan-2-yl)-1,2,3,4-tetrahydropyrimidine- 2,4-dione) was used as a model material in this study. The amounts of the thermodynamically stable $ tegafur were increased to levels detectable by powder X-ray diffractometry by grind- ing the samples in a ball mill in the presence of water. The limit of detection for this method was as low as 0.0005% of $ tegafur in " and $ tegafur mixtures. The amount of $ tegafur after sample preparation was found to be proportional to the init…

Detection limitLangmuirAntimetabolites AntineoplasticTrace AmountsChemistryAnalytical chemistryPharmaceutical ScienceTegafurPhase TransitionPolymorphism (materials science)IsomerismX-Ray DiffractionLimit of DetectionmedicineThermodynamicsSample preparationBall millMass fractionPowder Diffractionmedicine.drugTegafurJournal of pharmaceutical sciences
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Determination of ochratoxin A in maize bread samples by LC with fluorescence detection.

2007

Ochratoxin A (OTA) is a secondary fungal metabolite produced by several moulds, mainly by Aspergillus ochraceus, A. carbonarius, A. niger and by Penicillium verrucosum. The present work shows the results of comparative studies using different procedures for the analysis of OTA in maize bread samples. The studied analytical methods involved extraction with different volumes of PBS/methanol, different extraction apparatus, and clean-up through immunoaffinity columns. The separation and identification were carried out by high-performance liquid chromatography with fluorescence detection. The optimized method for analysis of OTA in maize bread involved extraction with PBS:methanol (50:50), and …

Detection limitOchratoxin AChromatographybiologyMetaboliteExtraction (chemistry)Ochratoxin Abiology.organism_classificationHigh-performance liquid chromatographyAnalytical ChemistryMaize breadchemistry.chemical_compoundchemistryPenicillium verrucosumSample preparationAspergillus ochraceusTalanta
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Identification of the Biotransformation Products of 2-Ethylhexyl 4-(N,N-Dimethylamino)benzoate

2010

Nowadays, 2-ethylhexyl 4-(N,N-dimethylamino)benzoate (EDP) is one of the most widely used UV filters in sunscreen cosmetics and other cosmetic products. However, undesirable processes such as percutaneous absorption and biological activity have been attributed to this compound. The in vitro metabolism of EDP was elucidated in the present work. First of all, the phase I biotransformation was studied in rat liver microsomes and two metabolites, N,N-dimethyl-p-aminobenzoic acid (DMP) and N-monomethyl-p-aminobenzoic acid (MMP), were identified by GC-MS analysis. Secondly, the phase II metabolism was investigated by means of LC-MS. The investigated reactions were acetylation and glucuronidation …

Detection limitSunscreen cosmeticsChromatographyChemistryOriginalMetaboliteOrganic ChemistryClinical BiochemistryGlucuronidation2-Ethylhexyl 4-(NN-dimethylamino)benzoateHigh-performance liquid chromatographyBiochemistryAnalytical Chemistrychemistry.chemical_compoundBiotransformationLiquid chromatography–mass spectrometryMicrosomeSolid phase extractionLiquid chromatography-mass spectrometryUV filtering
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Estimation of the presence of unmetabolized dialkyl phthalates in untreated human urine by an on-line miniaturized reliable method

2015

Abstract At present, human exposure to dialkyl phthalates is assessed through urinary measurement of their metabolites due mainly to contamination in their analysis by their ubiquitous presence. An on-line miniaturized method and the processing of the untreated urine samples have been the key factors for minimizing contamination and achieving unbiased results. Di(2-ethylhexyl) (DEHP), diethyl (DEP), dibutyl (DBP) and mono-ethylhexyl (MEHP) phthalates in urine samples have been included in the study; MEHP as metabolite of the main dialkyl phthalate such as DEHP. On-line in-tube solid-phase microextraction (IT-SPME)-capillary liquid chromatography (CapLC) with diode array detection (DAD) is e…

Detection limitendocrine systemEnvironmental EngineeringChromatographyMetabolitePhthalic AcidsPhthalateEnvironmental ExposureUrineUrinalysisContaminationPollutionDiode arraychemistry.chemical_compoundKey factorschemistryHuman exposureHumansEnvironmental ChemistryEnvironmental PollutantsWaste Management and DisposalScience of The Total Environment
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