Search results for "Cosmetics"

showing 10 items of 81 documents

Near-critical carbon dioxide extraction and liquid chromatography determination of UV filters in solid cosmetic samples: A green analytical procedure

2005

Near-critical carbon dioxide extraction of four UV filters used as sunscreens in lipsticks and makeup formulations is reported. Extraction parameters were optimized. Efficient recoveries were obtained after 15 min of dynamic extraction with a 80:20 CO2/ethanol mixture at 300 atm and 54 degrees C, using a 1.8 mL/min flow rate. Extracts were collected in ethanol, and appropriately diluted with ethanol and 1% acetic acid to obtain a 70:30 v/v ethanol/1% acetic acid solution. The four UV filters were determined by LC with gradient elution using ethanol/1% acetic acid as mobile phase. The accuracy of the analytical procedure was estimated by comparing the results with those obtained by methods b…

ChromatographyChemistryElutionExtraction (chemistry)Supercritical fluid extractionUV filterFiltration and SeparationCosmeticsCarbon DioxideHigh-performance liquid chromatographySupercritical fluidAnalytical ChemistryAcetic acidchemistry.chemical_compoundSample preparationSunscreening AgentsChromatography LiquidJournal of Separation Science
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Sunscreen analysis

2005

Although there are no official analytical methods for UV filters determination in sunscreen cosmetics, their maximum content are regulated by legislation, and then analytical methods to control these products are necessary. In this paper, analytical methods for UV filters determination in cosmetics, which can be found in the literature, are reviewed. The usefulness of the analytical methods, techniques and sample preparation is discussed. The analytical methods used for the determination of UV filters in other type of samples are commented upon. Moreover, a brief overview of the European Union legislation concerning UV filters is included.

ChromatographyChemistrybusiness.industrymedia_common.quotation_subjectUV filterBiochemistryCosmeticsAnalytical ChemistryEnvironmental Chemistrymedia_common.cataloged_instanceCritical surveySample preparationEuropean unionProcess engineeringbusinessSpectroscopyControl methodsmedia_commonAnalytica Chimica Acta
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Stopped-flow Fourier-transform infra-red spectrometric speciation of glycolic and lactic acids in cosmetic formulations

2001

The dermatological activity of cosmetic formulations containing alpha-hydroxyacids depends on their different chemical forms, and it is therefore useful to determine these species in the finished products. In the present report a new procedure for studying the protonation equilibria of glycolic and lactic acids by stopped-flow Fourier-transform infra-red (FTIR) spectrometry is described. The procedure was validated for use in the speciation of glycolic and lactic acids in cosmetic formulations, with preferential attention given to glycolic acid, which is the most widely used. Species of these alpha-hydroxyacids can be approximately determined at different pHs and the total content of each a…

ChromatographySpectrophotometry Infraredmedia_common.quotation_subjectAnalytical chemistryInfrared spectroscopyProtonationCosmeticsMass spectrometryBiochemistryGlycolatesAnalytical ChemistryLactic acidchemistry.chemical_compoundSpeciationchemistryElectrochemistryEnvironmental ChemistryLactic AcidFourier transform infrared spectroscopyQuantitative analysis (chemistry)SpectroscopyGlycolic acidmedia_commonThe Analyst
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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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Green determination of eight water-soluble B vitamins in cosmetic products by liquid chromatography with ultraviolet detection.

2021

Abstract B vitamins are a group of compounds with beneficious properties for dermatologic care, and therefore they are included in the cosmetic formulations as high added-value ingredients. In this paper, an analytical method for the simultaneous determination of eight water-soluble B vitamins in cosmetic products is reported for the first time. This method is based on liquid chromatography with ultraviolet detection (LC-UV) analysis after simple water leaching of the analytes from the cosmetic matrix. No organic solvents are required, beyond the ethanol used in the chromatographic mobile phase. The proposed method has been successfully validated showing good linearity, limits of detection …

Detection limitAnalyteChromatographyChemistryClinical BiochemistryPharmaceutical ScienceReproducibility of ResultsWaterRepeatabilityCosmeticsmedicine.disease_causeAnalytical ChemistryMatrix (chemical analysis)B vitaminsWater solubleLeaching (chemistry)Drug DiscoveryVitamin B ComplexmedicineSolventsSpectroscopyUltravioletChromatography High Pressure LiquidChromatography LiquidJournal of pharmaceutical and biomedical analysis
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Determination of hydroxytyrosol and tyrosol by liquid chromatography for the quality control of cosmetic products based on olive extracts

2014

An analytical method for the simultaneous determination of hydroxytyrosol and tyrosol in different types of olive extract raw materials and cosmetic cream samples has been developed. The determination was performed by liquid chromatography with UV spectrophotometric detection. Different chromatographic parameters, such as mobile phase pH and composition, oven temperature and different sample preparation variables were studied. The best chromatographic separation was obtained under the following conditions: C18 column set at 35°C and isocratic elution of a mixture ethanol: 1% acetic acid solution at pH 5 (5:95, v/v) as mobile phase pumped at 1 mL min(-1). The detection wavelength was set at …

Detection limitAnalyteChromatographyIsocratic elutionPlant ExtractsClinical BiochemistryPharmaceutical ScienceCosmeticsRepeatabilityPhenylethyl AlcoholRaw materialAnalytical ChemistryTyrosolchemistry.chemical_compoundchemistryLimit of DetectionOleaDrug DiscoveryHydroxytyrosolSpectrophotometry UltravioletSample preparationSpectroscopyChromatography LiquidJournal of Pharmaceutical and Biomedical Analysis
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Determination of alternative preservatives in cosmetic products by chromophoric derivatization followed by vortex-assisted liquid-liquid semimicroext…

2016

An analytical method for the simultaneous determination of phenethyl alcohol, methylpropanediol, phenylpropanol, caprylyl glycol, and ethylhexylglycerin, which are used as alternative preservatives in cosmetic products, has been developed. The method is based on liquid chromatography with UV spectrophotometric detection after chromophoric derivatization with benzoyl chloride and vortex-assisted liquid-liquid semimicroextraction. Different chromatographic parameters, derivatization conditions, and sample preparation variables were studied. Under optimized conditions, the limits of detection values for the analytes ranged from 0.02 to 0.06µgmL(-1). The method was validated with good recovery …

Detection limitAnalytePreservativeChromatographymedia_common.quotation_subject010401 analytical chemistryPreservatives Pharmaceutical02 engineering and technologyCosmeticsPhenylethyl Alcohol021001 nanoscience & nanotechnology01 natural sciencesCosmetics0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundBenzoyl chloridechemistryPhenethyl alcoholSample preparation0210 nano-technologyDerivatizationmedia_commonChromatography LiquidTalanta
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Sequential injection spectrophotometric determination of oxybenzone in lipsticks

2001

A sequential injection (SI) procedure for the spectrophotometric determination of oxybenzone in lipsticks is reported. The colorimetric reaction between nickel and oxybenzone was used. SI parameters such as sample solution volume, reagent solution volume, propulsion flow rate and reaction coil length were studied. The limit of detection was 3 microg ml(-1). The sensitivity was 0.0108+/-0.0002 ml microg(-1). The relative standard deviations of the results were between 6 and 12%. The real concentrations of samples and the values obtained by HPLC were comparable. Microwave sample pre-treatment allowed the extraction of oxybenzone with ethanol, thus avoiding the use of toxic organic solvents. E…

Detection limitChromatographyChemistryExtraction (chemistry)CosmeticsBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryVolumetric flow rateBenzophenoneschemistry.chemical_compoundVolume (thermodynamics)SpectrophotometryReagentElectrochemistryEnvironmental ChemistryOxybenzoneQuantitative analysis (chemistry)SpectroscopyThe Analyst
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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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A reliable and environmentally-friendly liquid-chromatographic method for multi-class determination of fat-soluble UV filters in cosmetic products.

2013

An environmentally-friendly analytical method for the simultaneous determination of 15 fat-soluble ultraviolet (UV) filters currently authorized by the European Union regulation on cosmetic products has been developed. The determination was performed by liquid chromatography with UV spectrophotometric detection. Different parameters, such as type of column, oven temperature, mobile phase composition and flow rate were studied. The best chromatographic separation was obtained under the following conditions: C18 column set at 60°C and gradient ethanol:water (containing 1% formic acid and 20mM of 2-hydroxypropyl-β-cyclodextrin) as mobile phase pumped at 1mL min(-1). 2-Hydroxypropyl-β-cyclodext…

Detection limitChromatographyFormic acidmedia_common.quotation_subjectAnalytical chemistrymedicine.disease_causeBiochemistryCosmeticsEnvironmentally friendlyAnalytical Chemistrychemistry.chemical_compoundchemistryPhase (matter)Phase compositionmedicineEnvironmental Chemistrymedia_common.cataloged_instanceEuropean unionSpectroscopyUltravioletmedia_commonAnalytica chimica acta
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