Search results for "Chromatography-mass spectrometry"

showing 10 items of 332 documents

Polish Yellow Sweet Clover (Melilotus officinalis L.) Honey, Chromatographic Fingerprints, and Chemical Markers

2017

A case study of Polish Melilotus officinalis honey was presented for the first time. Gas chromatography–mass spectrometry (GC-MS) (after steam distillation, Soxhlet extraction, ultrasonic solvent extraction, and solid phase extraction (SPE)) and targeted high performance liquid chromatography with a photodiode array detector (HPLC-PAD) were applied to determine the characteristic components of honey. While ubiquitous in most honeys, carbohydrates, terpene derivatives, and phenylacetic acid dominated in the Soxhlet extracts (25.54%) and in the application of SPE (13.04%). In addition, lumichrome (1.85%) was found, and may be considered as a marker of this honey. Due to the presence of these …

DPPHFlavonoidPharmaceutical Science01 natural sciencesHigh-performance liquid chromatographyvolatileAntioxidantsCatechinGas Chromatography-Mass SpectrometryArticleAnalytical Chemistrylaw.inventionlcsh:QD241-441Steam distillationchemistry.chemical_compound0404 agricultural biotechnologyPhenolslcsh:Organic chemistryMelilotus officinalislawGallic AcidDrug DiscoveryMedicagoHumansGallic acidSolid phase extractionPhysical and Theoretical ChemistryChromatography High Pressure LiquidFlavonoidschemistry.chemical_classificationChromatographybiology010401 analytical chemistryOrganic ChemistryExtraction (chemistry)honey markersHoney04 agricultural and veterinary sciencesbiology.organism_classificationMelilotus officinalis040401 food science0104 chemical sciencesyellow sweet cloverchemistryChemistry (miscellaneous)yellow sweet clover; <i>Melilotus officinalis</i>; phenolic; volatile; honey markersMolecular MedicinephenolicMolecules; Volume 22; Issue 1; Pages: 138
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Chemical analysis and antioxidant activity of the essential oils of three Piperaceae species growing in the central region of Cuba.

2013

The present study describes the phytochemical profile and antioxidant activity of the essential oils of three Piperaceae species collected in the central region of Cuba. The essential oils of Piper aduncum, P. auritum and P. umbellatum leaves, obtained by hydrodistillation, were analyzed by gas chromatography-mass spectrometry. The main components of P. aduncum oil were piperitone (34%), camphor (17.1%), camphene (10.9%), 1,8-cineol (8.7%) and viridiflorol (7.4%), whereas that of P. auritum and P. umbellatum was safrole (71.8 and 26.4%, respectively). The antioxidant properties of the essential oils were also evaluated using several assays for radical scavenging ability (DPPH test and redu…

DPPHPlant ScienceAntioxidantsGas Chromatography-Mass Spectrometrylaw.inventionchemistry.chemical_compoundlawDrug DiscoveryBotanyOils VolatileFood sciencePiper auritumPropyl gallateEssential oilPharmacologyPiper aduncumbiologyCubaGeneral MedicinePiperaceaebiology.organism_classificationComplementary and alternative medicinechemistryCamphenePiperPiperitoneNatural product communications
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Influence of15N enrichment on the net isotopic fractionation factor during the reduction of nitrate to nitrous oxide in soil

2007

5 pages; International audience; Nitrous oxide, a greenhouse gas, is mainly emitted from soils during the denitrification process. Nitrogen stable-isotope investigations can help to characterise the N(2)O source and N(2)O production mechanisms. The stable-isotope approach is increasingly used with (15)N natural abundance or relatively low (15)N enrichment levels and requires a good knowledge of the isotopic fractionation effect inherent to this biological mechanism. This paper reports the measurement of the net and instantaneous isotopic fractionation factor (alpha(s/p) (i)) during the denitrification of NO(3) (-) to N(2)O over a range of (15)N substrate enrichments (0.37 to 1.00 atom% (15)…

DenitrificationAbundance (chemistry)[SDE.MCG]Environmental Sciences/Global ChangesNitrous Oxidechemistry.chemical_elementFractionationChemical FractionationGas Chromatography-Mass SpectrometryAnalytical ChemistrySoilchemistry.chemical_compoundNitrate[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/Geochemistry[ SDU.ENVI ] Sciences of the Universe [physics]/Continental interfaces environmentSoil Pollutants[SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces environmentSpectroscopyNitratesNitrogen IsotopesChemistryOrganic ChemistrySubstrate (chemistry)Nitrous oxide[ SDU.STU.GC ] Sciences of the Universe [physics]/Earth Sciences/GeochemistryNitrogen[ SDE.MCG ] Environmental Sciences/Global ChangesEnvironmental chemistrySoil waterOxidation-ReductionRapid Communications in Mass Spectrometry
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Analysis of drugs including illicit and new psychoactive substances in oral fluids by gas chromatography-drift tube ion mobility spectrometry

2021

Abstract In this study, a gas chromatograph (GC) has been coupled to a drift tube ion mobility spectrometer (IMS) in order to develop an analytical procedure for the determination of psychoactive substances in oral fluids. Working parameters, including the GC-IMS interface ones, were adjusted in order to obtain sensitive and robust signals. A volume of 500 μL of oral fluid was extracted with 250 μL chloroform and, after centrifugation, were injected into the GC-IMS system. Amphetamine, methylone, α-PVP, ketamine, lidocaine, MPHP, cocaine, THJ-2201, and 5F-ADB were employed as model compounds, providing limits of detection from 6 to 15 μg L−1 and recoveries from 70 to 115% for field oral flu…

Detection limitAnalyteChloroformChromatographyIon-mobility spectrometryMethyloneGas Chromatography-Mass SpectrometryAnalytical ChemistryAmphetaminechemistry.chemical_compoundCertified reference materialsCocainePharmaceutical PreparationschemistryLiquid–liquid extractionIon Mobility SpectrometrymedicineGas chromatographymedicine.drugTalanta
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Determination of UV filters in both soluble and particulate fractions of seawaters by dispersive liquid–liquid microextraction followed by gas chroma…

2014

An analytical method to determine the total content (i.e., not only in the soluble fraction but also in the particulate one) of eight commonly used UV filters in seawater samples is presented for the first time. Dispersive liquid-liquid microextraction (DLLME) is used as microextraction technique to pre-concentrate the target analytes before their determination by gas chromatography-mass spectrometry (GC-MS). In order to release the UV filters from the suspended particles an ultrasound treatment is performed before DLLME. The ultrasound treatment time was studied in order to achieve a quantitative lixiviation of the target analytes. The type and volume of both disperser and extraction solve…

Detection limitAnalyteChromatographyLiquid Phase MicroextractionUltraviolet RaysChemistryOsmolar ConcentrationExtraction (chemistry)Analytical chemistryRepeatabilityHydrogen-Ion ConcentrationMass spectrometryBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistrySolventIonic strengthSolventsEnvironmental ChemistrySeawaterGas chromatography–mass spectrometrySpectroscopyAnalytica Chimica Acta
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Determination of atranol and chloroatranol in perfumes using simultaneous derivatization and dispersive liquid-liquid microextraction followed by gas…

2013

Abstract A new analytical method based on simultaneous derivatization and dispersive liquid–liquid microextraction (DLLME) followed by gas chromatography–mass spectrometry (GC–MS), for the determination of the allergenic compounds atranol and chloroatranol in perfumes, is presented. Derivatization of the target analytes by means of acetylation with anhydride acetic in carbonate buffer was carried out. Thereby volatility and detectability were increased for improved GC–MS sensitivity. In addition, extractability by DLLME was also enhanced due to a less polar character of the solutes. A liquid–liquid extraction was performed before DLLME to clean up the sample and to obtain an aqueous sample …

Detection limitChromatographyAqueous solutionTime FactorsMolecular StructureLiquid Phase MicroextractionOsmolar ConcentrationHydrogen-Ion ConcentrationBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryPerfumeSolventMatrix (chemical analysis)chemistry.chemical_compoundchemistryReagentStandard additionBenzaldehydesSolventsEnvironmental ChemistryGas chromatography–mass spectrometryDerivatizationSpectroscopyAnalytica chimica acta
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Determination of hydroxylated benzophenone UV filters in sea water samples by dispersive liquid-liquid microextraction followed by gas chromatography…

2010

A new analytical method for the determination of four hydroxylated benzophenone UV filters (i.e. 2-hydroxy-4-methoxybenzophenone (HMB), 2,4-dihydroxybenzophenone (DHB), 2,2'-dihydroxy-4-methoxybenzophenone (DHMB) and 2,3,4-trihydroxybenzophenone (THB)) in sea water samples is presented. The method is based on dispersive liquid-liquid microextraction (DLLME) followed by gas chromatography-mass spectrometry (GC-MS) determination. The variables involved in the DLLME process were studied. Under optimized conditions, 1000 microL of acetone (disperser solvent) containing 60 microL of chloroform (extraction solvent) were injected into 5 mL of aqueous sample adjusted to pH 4 and containing 10% NaCl…

Detection limitChromatographySilylationOrganic ChemistryGeneral MedicineBSTFAChemical FractionationBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundBenzophenoneschemistryStandard additionSample preparationSeawaterGas chromatographyGas chromatography–mass spectrometryDerivatizationWater Pollutants ChemicalJournal of chromatography. A
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Implementing the contamination prevention programs in the pesticide industry by infrared spectroscopy.

2014

Abstract An infrared spectroscopy based methodology has been successfully developed to implement contamination prevention programs in the pesticide industry. Sensitivity of the IR procedure, traditionally considered the Achilles Hell of the technique, has been improved by using a transmission cell with an open upper side, an internal volume of 35 µL and an optical pathlength of 0.5 mm, providing detection limits of 32 mg L−1 for folpet and 48 mg L−1 for cymoxanil. The manufacturing of folpet and cymoxanil was employed as an example and the IR methodology was validated for the implementation of contamination prevention programs in the pesticide industry. The swab test and rinsate method were…

Detection limitChromatographySpectrophotometry InfraredChemistryChlorpyrifos-methylAnalytical chemistryInfrared spectroscopyContaminationPesticideOptical pathlengthGas Chromatography-Mass SpectrometryAnalytical ChemistryLimit of DetectionChemical IndustryEnvironmental PollutantsPesticidesTalanta
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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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Validated, non-destructive and environmentally friendly determination of cocaine in euro bank notes.

2005

A non-destructive, fast and environmentally friendly procedure has been developed for cocaine determination in euro bank notes. Cocaine was extracted with 15 ml methanol by vortex agitation during 5 min. The extract was evaporated and reconstituted in 0.5 ml methanol. GC-MS-MS analysis was performed using as precursor ion m/z 182.2, with an excitation energy voltage of 1.60 eV, being the product ions measured m/z 150.2 and 82.0. A limit of detection of 0.15 ng per note and a repeatability of 6%, established from the relative standard deviation, of a 1 ng ml(-1) level, were achieved. Recoveries of 101+/-2 and 98+/-3% were obtained for samples spiked with 100 and 10 microg respectively. Resul…

Detection limitPaperChromatographyOrganic ChemistryForensic SciencesAnalytical chemistryReproducibility of ResultsGeneral MedicineRepeatabilityBiochemistryEnvironmentally friendlySensitivity and SpecificityGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryCocaineSample preparationMethanolGas chromatographyGas chromatography–mass spectrometryQuantitative analysis (chemistry)Journal of chromatography. A
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