Search results for "Reference"

showing 10 items of 2491 documents

Standardization of reagents and methods used in cytological and histological practice with emphasis on dyes, stains and chromogenic reagents

1994

The need for the standardization of reagents and methods used in the histology laboratory is demonstrated. After definitions of dyes, stains, and chromogenic reagents, existing standards and standards organizations are discussed. This is followed by practical instructions on how to standardize dyes and stains through the preparation of reference materials and the development of chromatographic methods. An overview is presented of the problems concerned with standardization of the Romanowsky-Giemsa stain for cytological and histological application. Finally, the problem of how to convince routine dye and stain users of the need for standardization in their histology laboratories is discussed.

Quality ControlChromatographyStaining and LabelingStandardizationChemistryChromogenicCytological TechniquesHistological TechniquesCell BiologyReference StandardsStainStainingInvestigation methodsChromogenic CompoundsAnimalsHumansAnatomyColoring AgentsReference standardsThe Histochemical Journal
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Determination of sugars in depilatory formulations: a green analytical method employing infrared detection and partial least squares regression.

2011

A green analytical method was developed for the analysis of sugar-based depilatories. Three independent partial least squares (PLS) regression models were built for the direct determination of glucose, fructose and maltose without any sample pretreatment based on their attenuated total reflectance - Fourier transform infrared (ATR-FTIR) spectra. The models showed adequate prediction capabilities with root-mean-square-errors of prediction ranging from 7.04 to 12.55 mg sugar g(-1) sample. As a reference procedure, gradient liquid chromatography with on-line infrared detection, employing background correction based on cubic smoothing splines, was used. The analysis revealed changes in the suga…

Quality ControlChromatographySucroseChemistry PharmaceuticalAnalytical chemistryCarbohydratesFructoseGreen Chemistry TechnologyMaltoseHair RemovalAnalytical ChemistrySolventchemistry.chemical_compoundchemistryReference ValuesAttenuated total reflectionPartial least squares regressionSpectroscopy Fourier Transform InfraredLeast-Squares AnalysisSugarGlucose syrupTalanta
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Quality control Fourier transform infrared determination of diazepam in pharmaceuticals

2007

A quality control procedure has been developed for the determination of diazepam in pharmaceuticals using Fourier transform infrared (FTIR) spectroscopy. The method involves the off-line extraction of diazepam with chloroform by sonication and direct determination in the extracts through peak area measurement in the interval between 1672 and 1682 cm(-1) using a baseline correction defined between 1850 and 1524 cm(-1). For standardization it was used an external calibration line established from standard solutions of diazepam in chloroform. The method provides a limit of detection of 0.04 mg per tablet (n=5), a relative standard deviation (R.S.D.) of 0.5% for 5 independent measurements of a …

Quality ControlClinical BiochemistryAnalytical chemistryPharmaceutical ScienceInfrared spectroscopyStandard solutionAnalytical Chemistrysymbols.namesakechemistry.chemical_compoundSpectrophotometrySpectroscopy Fourier Transform InfraredDrug DiscoveryCalibrationmedicineFourier transform infrared spectroscopySpectroscopyDetection limitDiazepamChromatographyChloroformmedicine.diagnostic_testChemistryReference StandardsFourier transformAnti-Anxiety AgentsPharmaceutical PreparationsCalibrationsymbolsSpectrophotometry UltravioletTabletsJournal of Pharmaceutical and Biomedical Analysis
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Toward a Quality Guide to Facilitate the Transference of Analytical Methods from Research to Testing Laboratories: A Case Study

2009

Abstract At present, there is no single viewpoint that defines QA strategies in analytical chemistry. On the other hand, there are no unique protocols defining a set of analytical tasks and decision criteria to be performed during the method development phase (e.g., by a single research laboratory) in order to facilitate the transference to the testing laboratories intending to adapt, validate, and routinely use this method. This study proposes general criteria, a priori valid for any developed method, recommended as a provisional quality guide containing the minimum internal tasks necessary to publish new analytical method results. As an application, the selection of some basic internal qu…

Quality ControlComputer sciencemedia_common.quotation_subjectChemistry Techniques AnalyticalAnalytical ChemistrySet (abstract data type)Environmental ChemistryComputer SimulationQuality (business)Differential (infinitesimal)Publicationmedia_commonPharmacologyNitratesbusiness.industryReproducibility of ResultsReference StandardsMultiple-criteria decision analysisMethod developmentInternal qualitySystems engineeringA priori and a posterioriIndicators and ReagentsLaboratoriesbusinessMonte Carlo MethodAgronomy and Crop SciencePolarographyFood ScienceJournal of AOAC INTERNATIONAL
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Chromatographic multivariate quality control of pharmaceuticals giving strongly overlapped peaks based on the chromatogram profile

2004

In the present paper, the simultaneous quantification of two analytes showing strongly overlapped chromatographic peaks (alpha = 1.02), under the assumption that both available equipment and training of the laboratory staff are basic, is studied. A pharmaceutical preparation (Mutabase) containing two drugs of similar physicochemical properties (amitriptyline and perphenazine) is selected as case of study. The assays are carried out under realistic working conditions (i.e. routine testing laboratories). Uncertainty considerations are introduced in the study. A partial least squares model is directly applied to the chromatographic data (with no previous signal transformation) to perform quali…

Quality ControlProtocol (science)Multivariate statisticsAnalyteChromatographyChemistryOrganic ChemistryGeneral MedicineReference StandardsPharmaceutical formulationBiochemistryAnalytical ChemistryChemometricsQuality (physics)Pharmaceutical PreparationsApproximation errorMultivariate AnalysisPartial least squares regressionJournal of Chromatography A
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Plasma pharmacokinetics and tissue distribution study of cajaninstilbene acid in rats by liquid chromatography with tandem mass spectrometry

2010

Cajaninstilbene acid (CSA; 3-hydroxy-4-prenyl-5-methoxystilbene-2-carboxylic acid) is a major active constituent of pigeonpea leaves, has been proven to be effective in clinical treatment of diabetes, hepatitis, measles and dysentery. A rapid and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed and validated for the determination of CSA in rat plasma and various tissues (brain, heart, lung, liver, spleen, small intestine and kidney) of rat for the first time. Rat plasma and tissue distribution pre-treated by protein precipitation with acetoacetate was analyzed using LC-MS/MS with an electrospray ionization (ESI) interface, and isoliquiritigenin was us…

Quality ControlTime FactorsMetabolic Clearance RateFormic acidElectrospray ionizationClinical BiochemistryCarboxylic AcidsPharmaceutical ScienceTandem mass spectrometrySensitivity and SpecificityHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundCajanusDrug StabilityPharmacokineticsTandem Mass SpectrometryLiquid chromatography–mass spectrometryFreezingStilbenesDrug DiscoveryAnimalsProtein precipitationTissue DistributionSpectroscopyChromatographyMolecular StructureTemperatureReproducibility of ResultsHalf-lifeRats Inbred StrainsReference StandardsSalicylatesRatschemistryArea Under CurveCalibrationFemaleChromatography LiquidHalf-LifeJournal of Pharmaceutical and Biomedical Analysis
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Evaluation of DR and CR digital mammography systems based on phantom and breast dosimetry.

2006

Digital mammography has been progressively introduced in screening centers, since recent evolution of CR and DR detectors. However, it is questionable which exposure conditions would be more suitable when these techniques are applied, in order to reduce the glandular breast doses, as they are related with induced carcinogenesis. Several exposures have been performed in CR and DR mammography units for comparing absorbed doses during quality control assessments and during screening, diagnosis and treatment. In the first case, the CIRS11A mammographic phantom has been used with standard exposure conditions (28 kV, AEC mode with blackening +0, 50:50 glandularity and 4.5 compressed breast thickn…

Quality Controlmedicine.medical_specialtyDigital mammographyImage qualityBreast NeoplasmsRadiation DosageImaging phantommedicineMammographyDosimetryHumansMedical physicsRadiometrymedicine.diagnostic_testbusiness.industryComputersPhantoms ImagingEquipment DesignRadiographic Image EnhancementClinical diagnosisReference valuesRadiographic Image EnhancementFemaleNuclear medicinebusinessSoftwareMammographyConference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference
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Heterogeneity in general practitioners’ preferences for quality improvement programs: a choice experiment and policy simulation in France

2016

International audience; Despite increasing popularity, quality improvement programs (QIP) have had modest and variable impacts on enhancing the quality of physician practice. We investigate the heterogeneity of physicians’ preferences as a potential explanation of these mixed results in France, where the national voluntary QIP – the CAPI – has been cancelled due to its unpopularity. We rely on a discrete choice experiment to elicit heterogeneity in physicians’ preferences for the financial and non-financial components of QIP. Using mixed and latent class logit models, results show that the two models should be used in concert to shed light on different aspects of the heterogeneity in prefer…

Quality managementmedia_common.quotation_subjectLogit03 medical and health sciences0302 clinical medicineMixed logitGeneral practitionersddc:330Economics[ SHS.ECO ] Humanities and Social Sciences/Economies and financesQuality (business)030212 general & internal medicineLatent class logitPreference (economics)media_commonActuarial scienceI18I11030503 health policy & servicesHealth PolicyResearchUnpopularityPolicy simulation[SHS.ECO]Humanities and Social Sciences/Economics and FinancePopularityLatent class modelDiscrete choice experimentC25Mixed logit0305 other medical scienceQuality improvement programsHealth Economics Review
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The course of fatigue in patients with gynecologic and breast cancer

2013

Objective: The objective of this study is to examine the course of fatigue in female cancer patients during the first months after treatment. Methods: We examined a sample of 110 patients suffering from gynecological or breast cancer. Fatigue was assessed with two questionnaires, the Multidimensional Fatigue Inventory (MFI) and the fatigue scale of the quality of life questionnaire European Organisation for Research and Treatment of Cancer (EORTC QLQ-C30). Participants were tested during their stay in the hospital (t1), two weeks after discharge (t2), and three months after discharge (t3). Results: Fatigue in the patients’ sample was markedly higher than the general population reference val…

Quality of lifemedicine.medical_specialtyPopulationChangePsycho-oncologyBreast cancerObstetrics and gynaecologyQuality of lifeTumor stagemedicineIn patienteducationFatigueeducation.field_of_studybusiness.industryObstetrics and GynecologyCancerQuality-of-LifeGeneral Medicinemedicine.diseasehumanitiesOncologyReference valuesPhysical therapyOriginal ArticlePsychological wellbeingbusinessJournal of Gynecologic Oncology
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Vanilloid Derivatives as Tyrosinase Inhibitors Driven by Virtual Screening-Based QSAR Models

2010

A number of vanilloids have been tested as tyrosinase inhibitors using Ligand-Based Virtual Screening (LBVS) driven by QSAR (Quantitative Structure-Activity Relationship) models as the multi-agent classification system. A total of 81 models were used to screen this family. Then, a preliminary cluster analysis of the selected chemicals was carried out based on their bioactivity to detect possible similar substructural features among these compounds and the active database used in the QSAR model construction. The compounds identified were tested in vitro to corroborate the results obtained in silico. Among them, two chemicals, isovanillin (K(M) (app) = 1.08 mM) near to kojic acid (reference d…

Quantitative structure–activity relationshipStereochemistryTyrosinaseIn silicoQuantitative Structure-Activity RelationshipPharmaceutical ScienceIsovanillinModels BiologicalSkin DiseasesVanilloidsAnalytical Chemistrychemistry.chemical_compoundCluster AnalysisHumansEnvironmental ChemistryComputer SimulationEnzyme InhibitorsSpectroscopyVirtual screeningMonophenol MonooxygenaseReference drugCombinatorial chemistrychemistryBenzaldehydesDrug DesignKojic acidAlgorithmsDrug Testing and Analysis
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