Search results for "Extraction"

showing 10 items of 2072 documents

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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Fast extraction of cannabinoids in marijuana samples by using hard-cap espresso machines

2018

Abstract A simple, quick and low cost procedure was developed for the extraction of Δ9-tetrahydrocannabinol, cannabidiol, and cannabinol from marijuana samples, based on the use of a hard-cap espresso extraction with 2-propanol. After extraction, cannabinoids were directly determined after appropriate dilution by gas-chromatography-mass spectrometry, reaching a limit of detection from 0.03 to 0.05 mg g−1. Extraction efficiency was evaluated by the comparison of results obtained for seized samples by the proposed method and a reference methodology based on ultrasound-assisted extraction. Moreover, ion mobility was proposed for the rapid and sensitive determination of Δ9-tetrahydrocannabinol …

Detection limitTime FactorsChromatographyCannabinoidsIon-mobility spectrometry010401 analytical chemistryExtraction (chemistry)Chemical FractionationCoffee01 natural sciencesGas Chromatography-Mass Spectrometry0104 chemical sciencesAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundEspresso0302 clinical medicinechemistryδ 9 tetrahydrocannabinolCannabinolHumans030216 legal & forensic medicineGas chromatography–mass spectrometryCannabisTalanta
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Simple and sensitive reversed-phase liquid chromatographic assay for analysis of chlorthalidone in urine

1993

Abstract This study describes a rapid method for the determination of chlorthalidone in human urine by reversed-phase liquid chromatography and UV detection at 230 nm, after clean-up over a C8 solid-phase extraction column. Liquid chromatography was carried out on a C18-bonded phase using acetonitrile-phosphate buffer (pH=3) gradient elution. Triamterene was used as internal standard. The system has been applied to the determination of chlorthalidone in the 0.10–10.0 μg/mL concentration interval; the limit of detection was 6 ng/mL.

Detection limitTriamtereneChromatographyChemistryExtraction (chemistry)medicineMolecular MedicineChlorthalidoneSolid phase extractionReversed-phase chromatographyHigh-performance liquid chromatographyQuantitative analysis (chemistry)medicine.drug
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Comparison of different sorbents for on-line liquid-solid extraction followed by high-performance liquid chromatographic determination of nitrogen-co…

1998

Abstract LiChrolut EN [poly(styrene-divinylbenzene), PSDVB], Carbograph (graphitized carbon black, GCB), Isolute CN (cyanopropylsilica), Isolute C 2 (ethylsilica), and LiChrospher RP18 (octadecylsilica) were studied for on-line solid-phase extraction of twelve nitrogen containing pesticides from water. Determination (UV 210 nm) was performed with a Spherisorb C 8 analytical column and an acetonitrile-water gradient. The mean recoveries from 50 ml ranged from 83% for RP18 to 44% for GCB, and decreased in the following order: RP18, CN, LiChrolut EN, C 2 , and GCB. GCB showed poor recoveries due to incomplete desorption with the acetonitrile-water gradient used, and memory effects were detecte…

Detection limitVinyl CompoundsChromatographyNitrogenChemistryElutionOrganic ChemistryExtraction (chemistry)General MedicineReversed-phase chromatographySilicon DioxideBiochemistryHigh-performance liquid chromatographyBackflush accountingCarbonAnalytical ChemistryPolystyrenesIndicators and ReagentsSpectrophotometry UltravioletSample preparationSolid phase extractionPesticidesChromatography High Pressure LiquidJournal of Chromatography A
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Bio-metal-organic frameworks for molecular recognition and sorbent extraction of hydrophilic vitamins followed by their determination using HPLC-UV

2020

A bio-metal-organic framework (bio-MOF) derived from the amino acid L-serine has been prepared in bulk form and evaluated as sorbent for the molecular recognition and extraction of B-vitamins. The functional pores of bio-MOF exhibit high amounts of hydroxyl groups jointly directing other supramolecular host-guest interactions thus providing the recognition of B-vitamins in fruit juices and energy drinks. Single-crystal X-ray diffraction studies reveal the specific B-vitamin binding sites and the existence of multiple hydrogen bonds between these target molecules and the framework. It offered unique snapshots to accomplish an efficient capture of these solutes in complex aqueous matrices. Fo…

Detection limitVitaminesSorbentChromatographySurface PropertiesUltraviolet RaysElutionChemistryHydrophilic interaction chromatography010401 analytical chemistryExtraction (chemistry)Supramolecular chemistryQuímica analítica010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryBegudesMolecular recognitionVitamin B ComplexAdsorptionSolid phase extractionParticle SizeHydrophobic and Hydrophilic InteractionsMetal-Organic FrameworksMicrochimica Acta
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Online Solid-Phase Extraction LC-MS/MS: A Rapid and Valid Method for the Determination of Perfluorinated Compounds at Sub ng·L-1Level in Natural Water

2018

In this research paper, we report a method able to detect perfluorinated compound at pg·L−1 levels in superficial and underground water samples. An online solid phase extraction HPLC-MS/MS method was developed for the analysis of 12 perfluoroalkyl acids (PFASs). The method is based on injection of 5000 µL of water sample in SPE online WAX column followed by chromatography separation and mass spectrometry determination. SPE online elution was performed by water + 0.05% NH4OH and methanol + 0.05% NH4OH, while separation of target compounds was achieved within 10 min by Gemini chromatographic column operating from 1 to 12 pH range and using a mixture of water-methanol + 0.05% NH4OH. Sub ng·L−1…

Detection limitWaxChromatographyArticle SubjectElution010401 analytical chemistryChemistry (all)Perfluorinated compoundGeneral Chemistry010501 environmental sciencesMass spectrometry01 natural sciences0104 chemical scienceslcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999visual_artLc ms msvisual_art.visual_art_mediumSolid phase extractionQuantitative analysis (chemistry)0105 earth and related environmental sciences
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Derivative Fourier transform infrared spectrometric determination of ethanol in alcoholic beverages

1994

Abstract A derivative Fourier transform infrared (FT-TR) spectrometric procedure was developed for the direct determination of ethanol in alcoholic beverages, from beers to spirit samples. The method is based on first-order derivative FT-IR measurements between the peak at 1052 cm −1 and the valley at 1040 cm −1 , which are present in aqueous solutions and alcoholic beverages, by using a micro flow transmittance cell with ZnSe windows and a spacer of 0.029 mm. The method involves the accumulation of ten scans and provides accurate results in the determination of ethanol in alcoholic beverages without requiring any previous chemical treatment of the sample or a previous separation or extract…

Detection limitWineAqueous solutionChromatographyEthanolExtraction (chemistry)Analytical chemistryInfrared spectroscopyDerivativeBiochemistryAnalytical Chemistrysymbols.namesakechemistry.chemical_compoundFourier transformchemistrysymbolsEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Supercritical fluid extraction of resveratrol from grape skin of Vitis vinifera and determination by HPLC

2000

Supercritical fluid extraction of resveratrol from grape skin of Vitis vinifera was studied. Extraction variables such pressure, modifier concentration (ethanol), and extraction time were optimised. Final extraction conditions were: 40 degrees C, 150 bar, 7.5% ethanol and extraction time 15 min. Extraction recovery and precision (variation coefficient between 0.2 and 1.0%) were calculated. The resveratrol content in the ethanolic extract was determined by HPLC with UV detection at 306 nm. Acetic acid-methanol-water was used as the mobile phase, and C-18 and C-8 columns were tested, instrumental parameters were optimised, and analytical parameters were calculated (lineal interval 0-75 mg l(-…

Detection limitWinechemistry.chemical_compoundChromatographychemistryCoefficient of variationExtraction (chemistry)Supercritical fluid extractionResveratrolHigh-performance liquid chromatographyQuantitative analysis (chemistry)Analytical ChemistryTalanta
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Determination of inorganic species of Sb and Te in cereals by hydride generation atomic fluorescence spectrometry

2011

A non-chromatographic fast, sensitive and easy method has been developed for the determination of Sb(III), Sb(V), Te(IV) and Te(VI) in cereal samples. The procedure is based on ultrasound assisted extraction and determination by hydride generation atomic fluorescence spectrometry (HG AFS). Preliminary studies were made in order to get the best extraction efficiency using 1 mol L-1 phosphoric acid, 1 mol L-1 nitric acid, aqua regia, 1 mol L-1 sulfuric acid and 6 mol L-1 hydrochloric acid. The extraction with aquaregia showed a clear interconversion of the species during the process, being H2SO4 the best extractant with efficiencies greater than 90% from the total content of Sb and Te quantif…

Detection limitcerealshydride generation atomic fluorescence spectrometryChemistryHydrideantimonyExtraction (chemistry)Hydrochloric acidSulfuric acidGeneral Chemistrychemistry.chemical_compoundspeciationNitric acidtelluriumAqua regiaPhosphoric acidNuclear chemistry
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Determination of carbonyl compounds in particulate matter PM2.5 by in-tube solid-phase microextraction coupled to capillary liquid chromatography/mas…

2013

Abstract In this paper, a new procedure based on in-tube solid phase microextraction (IT-SPME)-capillary liquid chromatography hyphenated to mass spectrometry detection by using microelectrospray ionisation (CapLC–MS), has been reported. The device was proposed to quantify 12 carbonyl compounds (10 aliphatic aldehydes, an unsaturated aldehyde and a ketone) derivatized with 2,4-dinitrophenylhidrazine (DNPH) reagent in aqueous extracts of PM 2.5 . This methodology involves the on-line preconcentration of DNPH-carbonyl compounds derivatives coupled to the CapLC–MS system, efficiently providing appropriate sensitivity for the determination of the target analytes. Detection limits for the analyt…

Detection limitchemistry.chemical_classificationAnalyteAldehydesChromatographyKetoneAnalytical chemistryKetonesMass spectrometrySolid-phase microextractionAldehydeMass SpectrometryAnalytical ChemistryPhenylhydrazineschemistryLiquid chromatography–mass spectrometryLimit of DetectionReagentParticulate MatterSolid Phase MicroextractionWater Pollutants ChemicalChromatography LiquidTalanta
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