Search results for "Urine"

showing 10 items of 924 documents

Preliminary Estimation of Deoxynivalenol Excretion through a 24 h Pilot Study

2015

A duplicate diet study was designed to explore the occurrence of 15 Fusarium mycotoxins in the 24 h-diet consumed by one volunteer as well as the levels of mycotoxins in his 24 h-collected urine. The employed methodology involved solvent extraction at high ionic strength followed by dispersive solid phase extraction and gas chromatography determination coupled to mass spectrometry in tandem. Satisfactory results in method performance were achieved. The method"s accuracy was in a range of 68%108%, with intra-day relative standard deviation and inter-day relative standard deviation lower than 12% and 15%, respectively. The limits of quantitation ranged from 0.1 to 8 μg/Kg. The matrix effect w…

Tolerable daily intakeAdultMaleChromatography GasHealth Toxicology and Mutagenesisdeoxynivalenollcsh:MedicineFood ContaminationPilot ProjectsUrineToxicologyArticleExcretionFusariumGC-MS/MSTandem Mass Spectrometryduplicate diet studyHumansSolid phase extractionCookingToxicologiaVolunteerChromatographyChemistrylcsh:RSolid Phase ExtractionBeerrisk characterizationEnvironmental exposureEnvironmental ExposureurineDietCreatinineFood MicrobiologyLinear ModelsDietaGas chromatographyTrichothecenesFood AnalysisFood contaminant
researchProduct

The repair of oxidized purines in the DNA of human lymphocytes requires an activation involving NF-YA-mediated upregulation of OGG1.

2014

8-Oxoguanine DNA glycosylase (OGG1), which initiates the repair of DNA purine modifications such as 8-oxo-7,8-dihydroguanine (8-oxoG), is often regarded as a house keeping protein ubiquitously active in mammalian cells. We have analysed the repair rates of oxidized purines generated by photosensitization in peripheral human lymphocytes and observed that the cells were virtually unable to remove these lesions (less than 10% removal within 24h). However, stimulation of the lymphocytes with phytohemagglutinin (PHA) strongly accelerated the repair so that ∼30% of the lesions were repaired within 4h. Within 24h following PHA stimulation and preceding the induction of cell proliferation, Western …

Transcriptional ActivationDNA RepairBiologyBiochemistryDNA Glycosylaseschemistry.chemical_compoundDownregulation and upregulationHumansLymphocytesPhytohemagglutininsMolecular BiologyGeneTranscription factorCell Line TransformedCell growthCell BiologyBase excision repairDNAMolecular biologyUp-RegulationchemistryCCAAT-Binding FactorDNA glycosylasePurinesChromatin immunoprecipitationOxidation-ReductionDNADNA DamageDNA repair
researchProduct

MO945SERUM AND URINE LEUCINE RICH ALPHA-2-GLYCOPROTEIN-1 IS ASSOCIATED WITH KIDNEY TRANSPLANT INJURY AND FAILURE

2021

Abstract Background and Aims Kidney transplantation is the treatment of choice for most of the patients with end stage chronic kidney disease. To improve patient and graft survival, early diagnostics and discovery of specific biomarkers is important. Leucine rich alpha-2-glycoprotein-1 (LRG-1) is an innovative, non-invasive biomarker that is elevated in case of angiogenesis, inflammation and kidney injury. Aim was to evaluate biomarker LRG-1 level in serum and urine in kidney transplant recipients in accordance with kidney injury markers and time period after kidney transplantation. Method In the study 35 patients were enrolled. Patients had functioning kidney grafts and they were more than…

Transplantationmedicine.medical_specialtyProteinuriabusiness.industryUrineKidney transplantEndocrinologyNephrologyInternal medicinemedicinePrednisoloneGraft survivalLeucine rich alpha 2 glycoproteinmedicine.symptombusinessmedicine.drugNephrology Dialysis Transplantation
researchProduct

MO319BEDSIDE URINE SEDIMENT EXAMINATION IN IMMUNOGLOBULIN A NEPHROPATHY PATIENTS PERFORMED BY NEPHROLOGISTS

2021

Abstract Background and Aims Urine sediment microscopy is mostly abandoned by nephrologists nowadays, however it is an important diagnostic tool in kidney and urinary tract diseases. The aim of this study is to emphasize the benefits of urine microscopy performed by a nephrologist. Method A prospective cohort study at Pauls Stradins Clinical University Hospital Nephrology center included patients with histologically confirmed diagnosis of IgA nephropathy from 1st January 2020 till December 2020. Appropriately collected urine samples were examined using manual microscopy within an hour after sample collection and by automated urinalysis. Samples were centrifuged at 4000 rpm for 4 minutes, th…

Transplantationmedicine.medical_specialtyUrinalysismedicine.diagnostic_testNephrologybusiness.industryUrinary sedimentmedicineUrologyUrine sedimentImmunoglobulin A NephropathybusinessNephrology Dialysis Transplantation
researchProduct

S. haematobium as a Common Cause of Genital Morbidity in Girls: A Cross-sectional Study of Children in South Africa

2013

Background Schistosoma (S.) haematobium infection is a common cause of genital morbidity in adult women. Ova in the genital mucosal lining may cause lesions, bleeding, pain, discharge, and the damaged surfaces may pose a risk for HIV. In a heterogeneous schistosomiasis endemic area in South Africa, we sought to investigate if young girls had genital symptoms and if this was associated with urinary S. haematobium. Methodology In a cross-sectional study of 18 randomly chosen primary schools, we included 1057 schoolgirls between the age of 10 and 12 years. We interviewed assenting girls, whose parents had consented to their participation and examined three urines from each of them for schistos…

Travel-Associated Diseasesmedicine.medical_specialtylcsh:Arctic medicine. Tropical medicineInfectious Disease ControlEpidemiologylcsh:RC955-962Cross-sectional studyUrologyGynecologic InfectionsVDP::Medical disciplines: 700::Clinical medical disciplines: 750::Tropical medicine: 761SCHISTOSOMIASIS HAEMATOBIASexually Transmitted DiseasesHelminth InfectionUrineGlobal HealthPediatricsReproductive Tract InfectionsInfectious Disease EpidemiologySchistosomiasis haematobiaSouth AfricaParasitic DiseasesPrevalencemedicineSchistosomiasisAnimalsHumansSex organChildSchistosoma haematobiumSchoolsbiologyGenitourinary Infectionsbusiness.industrylcsh:Public aspects of medicinePublic Health Environmental and Occupational Healthlcsh:RA1-1270biology.organism_classificationSurgeryCross-Sectional StudiesInfectious DiseasesSchistosoma haematobiumNeglected tropical diseasesMedicineWomen's HealthFemalebusinessResearch ArticleNeglected Tropical DiseasesDemographyPLoS Neglected Tropical Diseases
researchProduct

Analysis of Diuretics in Urine by Column-Switching Chromatography and Fluorescence Detection

1997

The potential of column-switching chromatography and fluorescence detection for the analysis of diuretics in urine is evaluated. Sample cleanup and chromatographic parameters have been optimized to achieve maximum sensitivity for the detection and quantification of some relevant diuretics. On the basis of these studies, an on-line procedure for the simultaneous determination of amiloride, furosemide, bumetanide and triamterene is presented. The linearity, precision, accuracy and sensitivity of the method are discussed. The utility of the described approach has been tested by analysing urine samples obtained after administration of bumetanide.

TriamtereneChromatographyChemistrymedicine.drug_classmedicine.medical_treatmentClinical BiochemistryPharmaceutical ScienceUrineBiochemistryHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical ChemistryPotassium-sparing diureticmedicineDiureticQuantitative analysis (chemistry)Bumetanidemedicine.drugJournal of Liquid Chromatography & Related Technologies
researchProduct

Determination of triamterene in urine by HPLC using fluorescence detection and column-switching

1994

A liquid chromatographic method incorporating column-switching and fluorimetric detection for the determination of triamterene in untreated urine, is described. The urine samples (5 μL) were directly introduced onto an Hypersil ODS-C18, 30 μm (20 mm×2.1 mm I.D.) pre-column. Polar urinary compounds were removed by flushing the pre-column with water for 1 min, and the analyte was then switched onto an HP-LiChrospher RP C18,5 μm (125 mm×4mm ID) analytical column using an acetonitrile/phosphate buffer gradient elution. Fluorescence detection was performed at 230 nm excitation and 430 nm emission wavelengths. The recovery of drug was 102±2% in the 0.10–20.0 μg/mL concentration range, the limit o…

TriamtereneDetection limitAnalyteChromatographyChemistryOrganic ChemistryClinical BiochemistryUrineBiochemistryHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical Chemistrychemistry.chemical_compoundmedicineAcetonitrileQuantitative analysis (chemistry)medicine.drugChromatographia
researchProduct

The quantitative determination of metabolites of 6-mercaptopurine in biological materials. VII. Chemical synthesis by phosphorylation of 6-thioguanos…

1990

Abstract A fast and reliable two-step method has been established for the chemical synthesis of 6-thioguanosine 5′-monophosphate, 6-thioguanosine 5′-diphosphate and 6-thioguanosine 5′-triphosphate starting from the ribonucleoside. In the first step, 6-thioguanosine dissolved in triethyl phosphate, at high yield reacts with phosphorus oxide trichloride to 6-thioguanosine 5′-monophosphate which is purified by anion-exchange chromatography on DEAE-Sephadex using a step gradient of hydrochloric acid. In the second step, 6-thioguanosine 5′-monophosphate dissolved in water, reacts with phosphoric acid in the presence of pyridine/dicyclohexyl carbodiimide and is converted to 6-thioguanosine 5′-dip…

Triethyl phosphateChromatographyMercaptopurineBiophysicsThionucleotidesRibonucleosideBiochemistryChemical synthesisHigh-performance liquid chromatographyGuanosine DiphosphateGuanine NucleotidesEnzymeschemistry.chemical_compoundKineticsAmmonium bicarbonatechemistryAnimalsGuanosine TriphosphateRabbitsPhosphorylationMolecular BiologyPhosphoric acidPyruvate kinaseChromatography High Pressure LiquidCarbodiimideBiochimica et biophysica acta
researchProduct

Analytical study and exposure to Fusarium mycotoxins = Estudio analítico y de exposición a micotoxinas de Fusarium

2015

Las micotoxinas son metabolitos secundarios de determinadas especies fúngicas que se encuentran habitualmente en los alimentos. El Reglamento No. 1881/2006 de la Comisión Europea, parcialmente modificado por posteriores Reglamentos, establece los contenidos máximos de micotoxinas para diferentes productos alimenticios. La introducción de estas normas pone de manifiesto el interés por el conocimiento de valores relativos a la concentración de estos tóxicos para poder evaluar riesgos y adoptar las medidas necesarias para proteger la salud de los consumidores. Los productos agrícolas contaminados, especialmente cereales y sus derivados, son la principal fuente de micotoxinas en la dieta de la …

UNESCO::QUÍMICA::Química analítica::Espectroscopía de masasUNESCO::CIENCIAS DE LA VIDA::Microbiología ::Mohosexposure assessmentgas chromatographyUNESCO::CIENCIAS MÉDICAS ::Ciencias de la Nutrición ::Toxicidad de los alimentosurine:CIENCIAS MÉDICAS ::Ciencias de la Nutrición ::Toxicidad de los alimentos [UNESCO]:CIENCIAS DE LA VIDA::Microbiología ::Mohos [UNESCO]:QUÍMICA::Química analítica::Espectroscopía de masas [UNESCO]:QUÍMICA::Química analítica::Análisis cromatográfico [UNESCO]UNESCO::CIENCIAS MÉDICAS ::Ciencias de la Nutrición ::Sustancias tóxicas naturalesfood matricesmycotoxinsbiomarkerUNESCO::QUÍMICA::Química analítica::Análisis cromatográficomethod developmentmass spectrometry:CIENCIAS MÉDICAS ::Ciencias de la Nutrición ::Sustancias tóxicas naturales [UNESCO]
researchProduct

Pharmacological characterization of Uracil nucleotide-sensitive P2Y receptors in mouse ileum

2010

Since uracil nucleotide-preferring receptors, belonging to the P2Y receptor family and responding to either uridine triphosphate (UTP) or uridine diphosphate (UDP), have been proposed to be present at different cellular level in the gut, regulating various functions, we aimed to investigate whether their activation by uracil nucleotides may modulate the contractility of the intestinal muscle. Experiments were carried out in vitro, and the contractility of the longitudinal muscle from mouse ileum was recorded as changes of the isometric tension. UDP or UTP evoked a concentrationdependent, tetrodotoxin insensitive, contractile response. UDP effect was antagonized by suramin and by PPADS, P2 r…

Uracil nucleotidesPurinergic receptors enteric neurotrasmission mouse ileum
researchProduct