Search results for "Urine"

showing 10 items of 924 documents

Sensitive determination of parabens in human urine and serum using methacrylate monoliths and reversed-phase capillary liquid chromatography-mass spe…

2014

A method for the determination of parabens in human urine and serum by capillary liquid chromatography (cLC) with UV-Vis and mass spectrometry (MS) detection using methacrylate ester-based monolithic columns has been developed. The influence of composition of polymerization mixture was studied. The optimum monolith was obtained with butyl methacrylate monomer at 60/40% (wt/wt) butyl methacrylate/ethylene dimethacrylate ratio and 50wt% porogens (composed of 36wt% of 1,4-butanediol, 54wt% 1-propanol and 10wt% water). Baseline resolution of analytes was achieved through a mobile phase of acetonitrile/water in gradient elution mode. Additionally, dispersive liquid-liquid microextraction (DLLME)…

Detection limitAnalytegeographyChromatography Reverse-PhaseChromatographygeography.geographical_feature_categoryResolution (mass spectrometry)ChemistryOrganic ChemistryParabensGeneral MedicineUrineUrinalysisMethacrylateMass spectrometryBiochemistryMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometryLimit of DetectionHumansMethacrylatesMonolithBlood Chemical AnalysisJournal of chromatography. A
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Improved Solid Phase Extraction Procedure for Assay of Cephalosporins in Human Urine Samples

1998

Abstract Solid phase extraction technique has been evaluated for the treatment of urine samples in the analysis of cephalosporins before injection into an HP-Hypersil ODS-C18 column. Cephalexin, cefotaxime, cefazolin, cefuroxime, and cefoxitin were tested with seven different reversed-phase extraction column cartridges and the obtained urine extracts were not clean. However, 3M Empore extraction disk cartridges packed with octadecyl (C18) bonded silica provided clean extracts with a single extraction. The recoveries of the five cephalosporins ranged from 56 to 60 % in the 1.25–500 g/mL concentration range. The assay was accurate, precise, and adequate for testing the drug content in urine s…

Detection limitChromatographyChemistryClinical BiochemistryExtraction (chemistry)Pharmaceutical ScienceUrineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryCefalexinmedicineSolid phase extractionCefuroximeAntibacterial agentmedicine.drugJournal of Liquid Chromatography & Related Technologies
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A solid-phase extraction and size-exclusion liquid chromatographic method for polyethylene glycol 25 p-aminobenzoic acid determination in urine: Vali…

2007

No previous publications about percutaneous absorption of polyethylene glycol 25 p-aminobenzoic acid (PEG-25 PABA) have been found in the literature and the expected levels to be found in human urine after sunscreens use are unknown. The method proposed here is suitable to determine PEG-25 PABA in the urine of sunscreens users in order to carry out studies on body accumulation/excretion. It is based on solid-phase extraction (SPE) with size-exclusion liquid chromatography determination. Solid-phase extraction allows the analyte to be retained and subsequently eluted for a clean-up, using a silica-based cartridge. The size-exclusion liquid chromatography of the eluted allows the rest of matr…

Detection limitChromatographyChemistryElutionExtraction (chemistry)Fluorescence spectrometryReproducibility of ResultsUrineBiochemistryPolyethylene GlycolsAnalytical ChemistryMatrix (chemical analysis)ExcretionSpectrometry FluorescenceChromatography GelHumansEnvironmental ChemistrySolid phase extraction4-Aminobenzoic AcidSunscreening AgentsSpectroscopyAnalytica Chimica Acta
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Simultaneous detection of three antiviral and four antibiotic compounds in source-separated urine with liquid chromatography

2013

An analytical method for the simultaneous screening of three antiviral agents (nevirapine, zidovudine, lamivudine), four antibiotics (sulfamethoxazole, trimethoprim, ciprofloxacin, rifampicin) and one reference compound (carbamazepine) in human urine was developed. Separation was achieved with a Kinetex XB-C18 (75 × 4.6 mm, 2.6 μm) column after the extraction of pharmaceuticals from urine with SPE. Gradient elution with a mobile phase consisting of acetonitrile and 10 mM KH2 PO4 (pH 2.5), and diode array detection with monitoring at 210 and 264 nm was applied. The developed method was validated in terms of selectivity, linearity, stability and sensitivity. Repeatability (n = 3) and between-…

Detection limitChromatographyChemistryExtraction (chemistry)Filtration and SeparationRepeatabilityUrineHigh-performance liquid chromatographyTrimethoprimAnalytical ChemistryWastewatermedicineSolid phase extractionmedicine.drugJournal of Separation Science
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Selective determination of clenbuterol residues in urine by molecular imprinted polymer—Ion mobility spectrometry

2017

Abstract Clenbuterol is banned for sports use and strictly regulated in livestock industry. In this study, a procedure for the determination of clenbuterol residues in water and urine has been developed using selective supports combined with ion mobility spectrometry (IMS) determination. A molecular imprinted polymer (MIP) was used for efficient clean-up and preconcentration of clenbuterol followed to a dispersive liquid-liquid microextraction (DLLME) in order to improve selectivity and sensitivity of IMS determinations. Quantitative recoveries from 81 to 99% were obtained for water and spiked urine samples using MIP-DLLME-IMS method. A precision of 4.5%, established as the relative standar…

Detection limitChromatographyChemistryIon-mobility spectrometry010401 analytical chemistryRelative standard deviationMolecularly imprinted polymer02 engineering and technologyUrine021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryLiquid chromatography–mass spectrometryClenbuterolmedicine0210 nano-technologySpectroscopymedicine.drugMicrochemical Journal
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Sensitive determination of probenecid in urine samples by reversed-phase liquid chromatography and UV-visible detection using solid-phase extraction …

1993

This study describes a rapid method for the determination of probenecid in human urine by liquid chromatography with UV detection at 254 nm, after clean-up through a C8 solid-phase extraction column. Liquid chromatography was carried out on a C18-bonded phase using an acetonitrile-acetate buffer (pH=4) gradient elution. Ethacrynic acid was used as internal standard. The system has been applied to the determination of probenecid in the 0.10–100.0 μg/ml concentration range; the limit of detection was 5 ng/mL.

Detection limitChromatographyChemistryOrganic ChemistryClinical BiochemistryExtraction (chemistry)Reversed-phase chromatographyUrineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryProbenecidPhase (matter)medicineSolid phase extractionmedicine.drugChromatographia
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A rapid procedure for the determination of caffeine, theophylline and theobromine in urine by micellar liquid chromatography and direct sample inject…

1995

Abstract A liquid chromatographic procedure for the determination of caffeine, theophylline and theobromine in urine samples is described. The proposed system uses a Spherisorb octadecyl-silane ODS-2 C18 analytical column and a guard column of similar characteristics. The UV detector was set at 273 nm. A study to adequately select the composition of the micellar mobile phase for the separation of these compounds in urine samples is performed. Maximum resolution was achieved with a 0.075 M sodium dodecylsulphate-1.5% propanol eluent. Limits of detection at 273 nm ranged between 0.4 μg/ml for theobromine and theophylline and 1.2 μg/ml for caffeine. The procedure allows the determination of th…

Detection limitChromatographyChemistryUrineBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyMicellar liquid chromatographymedicineEnvironmental ChemistryTheophyllineCaffeineTheobromineSpectroscopymedicine.drugAnalytica Chimica Acta
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Electrochemical detection of uric acid and ascorbic acid using r-GO/NPs based sensors

2021

Abstract A sensitive and selective electrochemical sensor, based on reduced graphene oxide and gold nanoparticles obtained by simple co-electrodeposition, was developed for the detection of uric acid and ascorbic acid. Because of the electrochemical oxidation of both uric and ascorbic acid depending on the pH, the sensor performances were studied at different pH values. Excellent results were obtained for uric acid detection in a linear range from 10 to 500 µmol dm−3 with a sensitivity of 0.31 µA cm−2 µM−1. A limit of detection and quantification of 3.6 µM and 10.95 µmol dm−3, respectively, was calculated. Sensors showed good selectivity toward different interfering species present in the m…

Detection limitChromatographyGeneral Chemical Engineering02 engineering and technologyUrineUric acid Food010402 general chemistry021001 nanoscience & nanotechnologyAscorbic acid01 natural sciences0104 chemical sciencesElectrochemical gas sensorMatrix (chemical analysis)chemistry.chemical_compoundBody fluidsSettore ING-IND/23 - Chimica Fisica ApplicatachemistryLinear rangeElectrochemical sensorColloidal goldSettore ING-IND/17 - Impianti Industriali MeccaniciElectrochemistryUric acidAscorbic acid0210 nano-technology
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Determination of furosemide in urine samples by direct injection in a micellar liquid chromatographic system.

2002

A sensitive, selective and efficient micellar liquid chromatographic (MLC) procedure was developed for the determination of furosemide (4-chloro-N-furfuryl-5-sulfamoylanthranilic acid) in urine samples by direct injection and UV detection. The procedure makes use of a C18 reversed-phase column and a micellar mobile phase of 0.05 mol l(-1) sodium dodecyl sulfate-6% v/v propanol and phosphate buffer at pH 3 to resolve furosemide from its photochemical degradation products. The importance of protecting the standards and urine samples to be analysed from light in the assay of furosemide, avoiding its degradation, was verified. The limit of quantification was 0.15 microg ml(-1) and the relative …

Detection limitChromatographyMetabolitemedicine.medical_treatmentSodiumchemistry.chemical_elementFurosemideReversed-phase chromatographyUrineBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryFurosemideElectrochemistrymedicineEnvironmental ChemistryHumansDiureticDiureticsQuantitative analysis (chemistry)SpectroscopyChromatography High Pressure Liquidmedicine.drugChromatography Micellar Electrokinetic CapillaryThe Analyst
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Extractive-spectrophotometric determination of amphetamine in urine samples with sodium 1,2-naphthoquinone 4-sulphonate

1993

Abstract Sodium 1,2-naphthoquinone 4-sulphonate (NQS) was tested as a reagent for amphetamine in order to develop an extractive-spectrophotometric method for the drug in urine samples. The standard additions method showed the absence of proportional bias error whereas the Youden method and the two standard addition plots method showed the presence of a constant bias error [total Youden blank (TYB)]. Acceptable results were obtained by evaluating the TYB error or by using a placebo (urine sample from a normal subject). The dynamic range of concentrations was 1.4–50 mg 1−1 in urine samples and the detection limit was 0.6 mg 1−1 when 10 ml of urine sample were taken.

Detection limitChromatographymedicine.diagnostic_testSodiumExtraction (chemistry)NQSchemistry.chemical_elementUrineBiochemistryAnalytical ChemistrychemistryStandard additionReagentSpectrophotometrymedicineEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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