Search results for "Liquid Phase Microextraction"

showing 10 items of 25 documents

Sample Preparation to Determine Pharmaceutical and Personal Care Products in an All-Water Matrix: Solid Phase Extraction

2020

© 2020 by the authors.

ConcentrationWater samplesPharmaceuticals and personal care productsPharmaceutical ScienceSewageReviewCosmeticsWastewater010501 environmental sciences01 natural sciencesEnvironmental impact of pharmaceuticals and personal care productsAnalytical ChemistryAigua AnàlisiTandem Mass SpectrometryDrug DiscoverySample preparationOnlineSolid phase extractionProcess engineeringGroundwaterChromatography High Pressure LiquidSewageDispersive liquid-liquid microextractionSolid Phase ExtractionDisksPharmaceutical PreparationsWastewaterChemistry (miscellaneous)Molecular MedicineEnvironmental MonitoringFarmacologiaLiquid Phase MicroextractionCartridgesSensitivity and SpecificityWater PurificationIsolationlcsh:QD241-441lcsh:Organic chemistryPhysical and Theoretical Chemistry0105 earth and related environmental sciencesSolid-phase extractionbusiness.industry010401 analytical chemistryOrganic ChemistryAnalytical techniqueExtraction (chemistry)Water0104 chemical sciencesEnvironmental sciencebusinessSurface waterWater Pollutants Chemical
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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 N-nitrosodiethanolamine in cosmetic products by reversed-phase dispersive liquid-liquid microextraction followed by liquid chromatog…

2016

A new analytical method for the determination of N-nitrosodiethanolamine (NDELA), a very harmful compound not allowed in cosmetic products, is presented. The method is based on a new approach of dispersive liquid-liquid microextraction (DLLME) useful for extraction of highly polar compounds, called reversed-phase DLLME (RP-DLLME), followed by liquid chromatography-ultraviolet/visible (LC-UV/Vis) determination. The variables involved in the RP-DLLME process were studied to provide the best enrichment factors. Under the optimized conditions, a mixture of 750µL of acetone (disperser solvent) and 125µL of water (extraction solvent) was rapidly injected into 5mL of toluene sample solution. The e…

Detection limitChromatographyElutionLiquid Phase Microextraction010401 analytical chemistryExtraction (chemistry)02 engineering and technologyCosmetics021001 nanoscience & nanotechnology01 natural sciencesToluene0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundchemistryGriess testLimit of DetectionSolventsDiethylnitrosamine0210 nano-technologyEnrichment factorAmmonium acetateChromatography LiquidTalanta
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Determination of N -nitrosamines in cosmetic products by vortex-assisted reversed-phase dispersive liquid-liquid microextraction and liquid chromatog…

2018

A new analytical method for the simultaneous determination of trace levels of seven prohibited N-nitrosamines (N-nitrosodimethylamine, N-nitrosoethylmethylamine, N-nitrosopyrrolidine, N-nitrosodiethylamine, N-nitrosopiperidine, N-nitrosomorpholine, and N-nitrosodiethanolamine) in cosmetic products has been developed. The method is based on vortex-assisted reversed-phase dispersive liquid-liquid microextraction, which allows the extraction of highly polar compounds, followed by liquid chromatography with mass spectrometry. The variables involved in the extraction process were studied to obtain the highest enrichment factor. Under the selected conditions, 75 μL of water as extraction solvent …

Detection limitNitrosaminesMaterials scienceChromatographyMolecular StructureLiquid Phase Microextraction010401 analytical chemistryExtraction (chemistry)Mixing (process engineering)Filtration and SeparationCosmetics02 engineering and technologyRepeatability021001 nanoscience & nanotechnologyMass spectrometry01 natural sciencesMass Spectrometry0104 chemical sciencesAnalytical ChemistrySolventPhase (matter)0210 nano-technologyEnrichment factorChromatography LiquidJournal of Separation Science
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Multimycotoxin LC-MS/MS Analysis in Tea Beverages after Dispersive Liquid-Liquid Microextraction (DLLME).

2017

The aim of the present study was to develop a multimycotoxin liquid chromatography tandem mass spectrometry (LC-MS/MS) method with a dispersive liquid-liquid microextraction procedure (DLLME) for the analysis of AFs, 3aDON, 15aDON, NIV, HT-2, T-2, ZEA, OTA, ENNs, and BEA in tea beverages and to evaluate their mycotoxin contents. The proposed method was characterized in terms of linearity, limits of detection (LODs), limits of quantification (LOQs), recoveries, repeatability (intraday precision), reproducibility (interday precision), and matrix effects to check suitability. The results show LODs in the range of 0.05-10 μg/L, LOQs in the range of 0.2-33 μg/L, and recoveries in the range of 65…

Detection limitReproducibilityChromatographyTeaChemistryLiquid Phase Microextraction010401 analytical chemistryFood Contamination04 agricultural and veterinary sciencesGeneral ChemistryRepeatabilityMycotoxinsGreen tea040401 food science01 natural sciences0104 chemical scienceschemistry.chemical_compound0404 agricultural biotechnologyLiquid chromatography–mass spectrometryLimit of DetectionTandem Mass SpectrometryLc ms msLiquid liquidGeneral Agricultural and Biological SciencesMycotoxinJournal of agricultural and food chemistry
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Current trends on the determination of organic UV filters in environmental water samples based on microextraction techniques – A review

2018

UV filters are a group of cosmetic ingredients commonly used in a wide variety of cosmetic products to protect users from UV solar radiation. They belong to different chemical families, such as benzophenones, p-aminobenzoates, salicylates, cinnamates, benzotriazoles, benzimidazoles, camphor derivatives, triazines, etc. These cosmetic ingredients are considered as emerging contaminants since they easily reach the aquatic environment, where they are accumulated causing harmful effects in the flora and fauna despite being present at the ng L-1 level. Therefore, the development of sensitive and selective analytical methods for their environmental surveillance monitoring is of high interest. In …

High interestLiquid Phase MicroextractionUltraviolet RaysChemistryEnvironmental surveillance010401 analytical chemistry02 engineering and technologyContamination021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistryEnvironmental waterAquatic environmentEnvironmental chemistryEnvironmental ChemistrySample preparationWater quality0210 nano-technologyWater pollutionSolid Phase MicroextractionWater Pollutants ChemicalSpectroscopyEnvironmental MonitoringAnalytica Chimica Acta
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Stir bar sorptive-dispersive microextraction for trace determination of triphenyl and diphenyl phosphate in urine of nail polish users

2018

Abstract This work describes a new analytical method useful for monitoring the human exposure to the endocrine-disrupting plasticizer triphenyl phosphate (TPP) via nail polish use. The method allows trace determination of this parent compound and its main metabolite, namely diphenyl phosphate (DPP), in urine samples of nail polish users. The method is based on a novel microextraction technique termed stir bar sorptive-dispersive microextraction (SBSDME) using a magnetic composite made of CoFe2O4 magnetic nanoparticles embedded into a mixed-mode weak anion exchange polymer (Strata™-X-AW), followed by liquid chromatography-tandem mass spectrometry (LC–MS/MS). The main parameters involved in t…

Liquid Phase MicroextractionCosmetics010402 general chemistryMass spectrometry01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionTandem Mass SpectrometryHumansDetection limitChromatographyIon exchangeBiphenyl Compounds010401 analytical chemistryOrganic ChemistryExtraction (chemistry)PlasticizerReproducibility of ResultsGeneral MedicineOrganophosphates0104 chemical sciencesNail polishchemistryLinear ModelsMagnetic nanoparticlesChromatography LiquidTriphenyl phosphateJournal of Chromatography A
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Determination of benzophenone-3 and its main metabolites in human serum by dispersive liquid–liquid microextraction followed by liquid chromatography…

2013

A new analytical method for the determination of benzophenone-3 (2-hydroxy-4-methoxybenzophenone), and its main metabolites (2,4-dihydroxybenzophenone and 2,2'-dihydroxy-4-methoxybenzophenone) in human serum is presented. The method is based on dispersive liquid-liquid microextraction (DLLME) as preconcentration and clean-up technique, followed by liquid chromatography tandem mass spectrometry (LC-MS/MS). Acidic hydrolysis and protein precipitation with HCl 6 M (1:1) (100 °C, 1 h) were carried out before extraction. The variables involved in the DLLME process were studied. Under the optimized conditions, 70 µL of acetone (disperser solvent) and 30 µL of chloroform (extraction solvent) were …

MaleLiquid Phase MicroextractionEndocrine DisruptorsAdministration CutaneousAnalytical ChemistryAcetoneBenzophenoneschemistry.chemical_compoundLimit of DetectionTandem Mass SpectrometryLiquid chromatography–mass spectrometryHumansProtein precipitationDetection limitAqueous solutionChloroformChromatographyChemistryHydrolysisExtraction (chemistry)Reproducibility of ResultsRepeatabilityAllergensHydrogen-Ion ConcentrationSolventSolventsFemaleChloroformSunscreening AgentsChromatography LiquidTalanta
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Occurrence of Mycotoxins in Botanical Dietary Supplement Infusion Beverages.

2019

The aim of the present work was to study the occurrence of mycotoxins [aflatoxins (1-4), 3-acetyldeoxyniavlenol (5), 15-acetyldeoxynivalenol (6), nivalenol (7), HT-2 (8), T-2 (9), ochratoxin A (10), zearalenone (11), enniatin A (12), enniatin A1 (13), enniatin B (14), enniatin B1 (15), and beauvericin (16)] present in potable products derived from herbal teas. Analysis was carried out by liquid chromatography coupled to ion-trap tandem mass spectrometry (LC-MS/MS-IT) after a dispersive liquid-liquid microextraction procedure (DLLME) was conducted. The DLLME method was applied to 52 commercial samples of chamomile, chamomile with anise, chamomile with honey, linden, pennyroyal mint, thyme, v…

Ochratoxin AAflatoxinLiquid Phase MicroextractionPharmaceutical Science01 natural sciencesRisk AssessmentAnalytical ChemistryBeverageschemistry.chemical_compoundHerbal teaTandem Mass SpectrometryDrug DiscoveryFood scienceMycotoxinZearalenonePharmacology010405 organic chemistryChemistryOrganic ChemistryMycotoxinsBeauvericin0104 chemical sciences010404 medicinal & biomolecular chemistryComplementary and alternative medicineDietary SupplementsMolecular MedicineEnniatinTeas HerbalPennyroyalChromatography LiquidJournal of natural products
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