Search results for "ROMA"

showing 10 items of 13919 documents

Identification and determination of synthetic cannabinoids in herbal products by dry film attenuated total reflectance-infrared spectroscopy.

2017

A new procedure has been developed for the identification and quantitative determination of synthetic cannabinoids in illicit herbal preparations. The methodology is based on the use of attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) measurement of sample extracts with 2-propanol drying 5µL of the extracts onto the ATR crystal. The qualitative identification was carried out on the 2-propanol extract after identification of the herbal matrix, followed by its subtraction and using a cut-off criterion of 75%. Quantitative determination was made by univariate calibration using the absorbance of the band located at 1520cm-1 of the spectrum. Four different cannabin…

AnalyteChromatographyChemistryCannabinoidsPlant Extracts010401 analytical chemistryInfrared spectroscopy01 natural sciences0104 chemical sciencesAnalytical ChemistryMatrix (chemical analysis)Absorbance03 medical and health sciences0302 clinical medicineAttenuated total reflectionSynthetic cannabinoidsCalibrationSpectroscopy Fourier Transform InfraredmedicineCalibration030216 legal & forensic medicineFourier transform infrared spectroscopymedicine.drugTalanta
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In-tube solid-phase microextraction-capillary liquid chromatography as a solution for the screening analysis of organophosphorus pesticides in untrea…

2006

This paper describes a method for the selective screening of organophosphorus pesticides in water. In-tube solid-phase microextraction (SPME) in an open capillary column coupled to capillary liquid chromatography (LC) with UV detection has been used to effect preconcentration, separation and detection of the analytes in the same assembly. For in-tube SPME two capillary columns of the same length and different internal diameters and coating thicknesses have been tested and compared, a 30 cm x 0.25 mm I.D., 0.25 micro m thickness coating column, and a 30 cm x 0.1 mm I.D., 0.1 micro m of coating thickness column. In both columns the coating was 95% dimethylpolysiloxane (PDMS)-5% diphenylpolysi…

AnalyteChromatographyChemistryCapillary actionOrganic ChemistryAnalytical chemistryWaterGeneral Medicineengineering.materialEnvironmentSolid-phase microextractionBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryNonylphenolchemistry.chemical_compoundPolybrominated diphenyl ethersOrganophosphorus CompoundsCoatingengineeringSample preparationPesticidesSolid Phase MicroextractionWater Pollutants ChemicalChromatography LiquidJournal of chromatography. A
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Validation of a confirmatory method for the determination of macrolides in liver and kidney animal tissues in accordance with the European Union regu…

2006

Abstract This study proposes a simple multiresidue liquid chromatography–diode array detector (LC–DAD) method capable of determining seven macrolide antibiotics in samples of liver and kidney animals at concentrations lower than those allowed by current legislation. Samples were prepared by homogenizing the tissue with EDTA–McIlvaine's buffer and extracted with an Oasis HLB cartridge. The consumption of organic solvent during extraction was minimum. The analytes were detected by LC–DAD and also by liquid chromatography–mass spectrometry with electrospray ionization (LC–(ESI)MS). The method was specific, stable and robust enough for the required purposes. The DAD method was validated in acco…

AnalyteChromatographyChemistryElectrospray ionizationOrganic ChemistryReproducibility of ResultsGeneral MedicineKidneySensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnti-Bacterial AgentsAnalytical ChemistryLiverCalibrationAnimalsmedia_common.cataloged_instanceSample preparationEuropean UnionMacrolidesSolid phase extractionEuropean unionQuantitative analysis (chemistry)Antibacterial agentmedia_commonJournal of Chromatography A
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o-Phthalaldehyde–N-acetylcysteine polyamine derivatives: formation and stability in solution and in C18 supports

2001

A comparative study of different derivatization procedures has been performed in order to improve the stability of the reaction products o-phthalaldehyde-N-acetylcysteine (OPA-NAC) polyamines. Procedures such as solution derivatization, solution derivatization followed by retention on a packing support, derivatization on different packing supports and on-column derivatization, have been optimized and compared. The degradation rate constant (k) of the derivative was dependent on the procedure used and on the analyte. For the spermine (the most unstable isoindol tested) k was 8 +/- 2 x 10(-2) min(-1) in solution versus 7.7 +/- 1.1 x 10(-4) min(-1) on the (C18) solid support. The results obtai…

AnalyteChromatographyChemistryElutionGeneral ChemistryStandard solutionSensitivity and SpecificityAcetylcysteineMatrix (chemical analysis)O-Phthalaldehydechemistry.chemical_compoundDrug StabilityReagentPolyaminesSpectrophotometry UltravioletSolid phase extractionDerivatizationChromatography High Pressure Liquido-PhthalaldehydeJournal of Chromatography B: Biomedical Sciences and Applications
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Column-switching techniques for high-performance liquid chromatography of drugs in biological samples.

1993

In recent years, an increasing number of publications have demonstrated the potential of column-switching techniques for the chromatographic separation, determination and preparative isolation of analytes from biological matrices. Column-switching systems greatly facilitate drug analysis, by on-line sample clean-up and trace enrichment, or by improving the analytical separative process. In this paper, the main applications of column-switching techniques to drug analysis in biological samples, are reviewed.

AnalyteChromatographyChemistryGeneral ChemistryHigh-performance liquid chromatographyBiological materialsChromatographic separationColumn chromatographyPharmaceutical PreparationsAnimalsHumansColumn switchingDrug analysisQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography
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Comparison of Three Techniques for Lipid Removal from Seal Blubber: Gel Permeation, Acid Treatment, and Dialysis with Semipermeable Membrane

2000

Abstract Harbor seal blubber samples were analyzed for PCDD/Fs and PCBs by splitting the initial extract into three aliquots and applying three different techniques for lipid removal (the first step of sample cleanup methodology for GC-HRMS analysis): gel permeation chromatography (GPC), sulfuric acid treatment, and dialysis through semipermeable membrane. Correlation coefficients of analyte concentrations obtained from three sets of replicate samples ranged from 0.965 to 0.994. In addition, a number of seal blubber samples were processed without pre-extraction using only the dialysis technique. The analyte concentrations in these samples correlated well with the analyte concentrations obta…

AnalyteChromatographyChemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthSoil ScienceSulfuric acidPermeationPollutionSeal (mechanical)Analytical ChemistryGel permeation chromatographychemistry.chemical_compoundBlubberEnvironmental ChemistrySemipermeable membraneDialysis (biochemistry)Waste Management and DisposalWater Science and TechnologyInternational Journal of Environmental Analytical Chemistry
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Green aspects, developments and perspectives of liquid phase microextraction techniques.

2014

Determination of analytes at trace levels in complex samples (e.g. biological or contaminated water or soils) are often required for the environmental assessment and monitoring as well as for scientific research in the field of environmental pollution. A limited number of analytical techniques are sensitive enough for the direct determination of trace components in samples and, because of that, a preliminary step of the analyte isolation/enrichment prior to analysis is required in many cases. In this work the newest trends and innovations in liquid phase microextraction, like: single-drop microextraction (SDME), hollow fiber liquid-phase microextraction (HF-LPME), and dispersive liquid-liqu…

AnalyteChromatographyChemistryLiquid Phase MicroextractionEnvironmental pollutionSolid-phase microextractionAnalytical ChemistrySolutionschemistry.chemical_compoundCapillary electrophoresisLiquid–liquid extractionIonic liquidSolventsSample preparationGas chromatographyTalanta
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Environmentally friendly LC for the simultaneous determination of ascorbic acid and its derivatives in skin-whitening cosmetics

2008

Ascorbic acid (AA), also known as vitamin C, is a very popular skin-whitening agent used in cosmetics. However, the use of AA (and also its sodium or magnesium salts) in cosmetic products is limited owing to its labile oxidative properties. In order to avoid its early degradation, different derivatives have been designed, such as ascorbyl phosphate (APH; as magnesium or sodium salts) and ascorbyl palmitate (AP), and more recently the ascorbyl glucoside (AG). Bearing in mind that all these chemicals in skin-whitening cosmetic products must be determined in order to control the efficacy of such products, this paper focuses on developing a wide-ranging LC analytical method able to determine th…

AnalyteChromatographyChemistryMagnesiumSodiummedia_common.quotation_subjectAscorbyl palmitatechemistry.chemical_elementFiltration and SeparationAscorbic AcidCosmeticsReversed-phase chromatographyReference StandardsAscorbic acidSensitivity and SpecificityCosmeticsHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundSpectrophotometry UltravioletChromatography Liquidmedia_commonJournal of Separation Science
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Flow-injection spectrofluorimetric determination of paracetamol

1990

Abstract A flow-injection spectrofluorimetric determination of paracetamol is reported, based on the oxidation of the analyte with potassium hexacyanoferrate(III) immobilized on an anion-exchange resin, the fluorescence being enhanced with N,N′-dimethylformamide. Concentrations of paracetamol in the range 0.04–17.60 mg l−1 are determined with a relative standard deviation of 1.5%. The injection rate is 25 samples h−1. The influence of foreign species and the determination of paracetamol in several pharamaceutical formulations are also reported.

AnalyteChromatographyChemistryPotassiumdigestive oral and skin physiologyRelative standard deviationFluorescence spectrometrychemistry.chemical_elementInjection rateBiochemistryAnalytical ChemistryEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Sensitive and selective plasmonic assay for spermine as biomarker in human urine.

2014

A simple, fast, and highly selective and sensitive colorimetric assay to detect nanomolar levels of spermine in human urine (healthy donors, cancer patients) is reported. This assay is based on the absence of a competitive organic capping on the gold nanoparticles together with the high affinity of the amine groups of the analyte for the nanoparticle surface.

AnalyteChromatographyChemistrySpermineMetal NanoparticlesUrineUrinalysisHighly selective3. Good healthAnalytical Chemistrychemistry.chemical_compoundBiomarkerBiochemistryColloidal goldLimit of DetectionHumansAmine gas treatingColorimetrySpermineGoldBiomarkersAnalytical chemistry
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