Search results for "Pipemidic Acid"

showing 4 items of 4 documents

Determination of quinolone residues in chicken and fish by capillary electrophoresis-mass spectrometry

2006

A specific pressure-assisted CE-MS method is described for the analysis of five quinolone residues. MS using a single quadrupole is compared with multiple-stage MS using a quadrupole IT (QIT-MS(n)). The procedure involves a common sample preparation by SPE on disposable cartridges. The most suitable electrolyte is 60 mM (NH(4))(2)CO(3) at pH 9.2. Single quadrupole does not provide enough fragmentation to confirm identities according to the current legislation. However, QIT-MS(n) achieves selective fragmentation. Using this method, danofloxacin, enrofloxacin, flumequine, ofloxacin, and pipemidic acid are analyzed in fortified samples of chicken and fish. Recoveries at levels of 50 ng/g were …

ChromatographyDanofloxacinChemistryClinical BiochemistryElectrophoresis CapillaryPipemidic acidQuinolonesMass spectrometryBiochemistryCapillary electrophoresis–mass spectrometryMass SpectrometryAnalytical ChemistryCapillary electrophoresisFish ProductsFlumequineEnrofloxacinmedicineAnimalsHumansSample preparationPoultry ProductsMuscle SkeletalChickensmedicine.drugELECTROPHORESIS
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Spectrophotometric determination of nalidixic and pipemidic acids in a flow injection assembly with a solid-phase reactor as a highly stable reagent …

2001

Abstract The flow-injection spectrophotometric determination of nalidixic (I) and pipemidic (II) acids were carried out by reaction with Fe(III) ions entrapped in a polymeric material and filling a packed-bed reactor; the released Fe(III) complexed with the quinolone is monitored at 426 nm. The method worked with a high reproducibility, even when using different reactors, days and solutions. Selectivity of the procedure was tested with different foreign compounds found in human urine as well as in pharmaceutical formulations containing both quinolones; no relevant interferences were observed. The calibration graph for (I) was linear over the range 1–250 μg ml −1 with a relative standard dev…

Chromatographymedicine.diagnostic_testNalidixic acidCalibration curveChemistryPipemidic acidBiochemistryDosage formAnalytical ChemistrySpectrophotometryReagentmedicineEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyAntibacterial agentmedicine.drugAnalytica Chimica Acta
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Biotransformation of methylxanthines in mammalian cell lines genetically engineered for expression of single cytochrome P450 isoforms. Allocation of …

1993

V79 Chinese hamster cells genetically engineered for stable expression of single forms of rat cytochromes P450IA1, P450IA2, P450IIB1, human P450IA2, and rat liver epithelial cells expressing murine P450IA2 were used to allocate metabolic pathways of methylxanthines to specific isoforms and to test the suitability of such cell lines for investigations on drug interactions occurring at the cytochrome expressed. The cell lines were exposed to caffeine and/or theophylline and concentrations of metabolites formed in the medium were determined by HPLC. Caffeine was metabolized by human, rat and murine P450IA2, resulting in the formation of four primary demethylated and hydroxylated metabolites. H…

CytochromeToxicologyCell Linechemistry.chemical_compoundCricetulusCytochrome P-450 Enzyme SystemIn vivoCaffeineCricetinaemedicineAnimalsHumansTheophyllineBiotransformationChromatography High Pressure LiquidbiologyCytochrome P450PefloxacinPipemidic AcidRatsIsoenzymesMetabolic pathwayBiochemistrychemistryCell cultureMicrosomebiology.proteinQuinolinesCaffeinemedicine.drugToxicology
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ComparativeIn Vitroevaluation of cumulative release of the urinary antiseptics Nalidixic acid, Pipemidic acid, Cinoxacin, and norfloxacin from white …

1994

AbstractThe in vitro diffusion of nalidixic acid (1), pipemidic acid (2), cinoxacin (3), and norfloxacin (4) was studied. The transfer rate constants (kd) from simulated gastro-intestinal juices to simulated plasma, throughout artificial wall lipid membranes, were defined. The kd values suggested that the four drugs are absorbed both in gastric and intestinal environments in similar amounts. To obtain lack of gastric unwanted effects white beeswax microspheres containing 1, 2, 3, and 4 were investigated as a vehicle for the drug intestinal release; they were prepared by the meltable dispersion process using wetting agents. Discrete, reproducible free flowing microspheres were obtained. The …

PharmacologyActive ingredientChromatographyNalidixic acidChemistryOrganic ChemistryCinoxacinPharmaceutical SciencePipemidic acidAbsorption (skin)Dosage formBiochemistryDrug DiscoverymedicineNorfloxacinmedicine.drugAntibacterial agentDrug Development and Industrial Pharmacy
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