Search results for "testing."

showing 10 items of 1654 documents

Computational Fluid Dynamics Simulation of Hydrodynamics and Stresses in the PhEur/USP Disintegration Tester Under Fed and Fasted Fluid Characteristi…

2015

ABSTRACT: Disintegration of oral solid dosage forms is a prerequisite for drug dissolution and absorption and is to a large extent dependent on the pressures and hydrodynamic conditions in the solution that the dosage form is exposed to. In this work, the hydrodynamics in the PhEur/USP disintegration tester were investigated using computational fluid dynamics (CFD). Particle image velocimetry was used to validate the CFD predictions. The CFD simulations were performed with different Newtonian and non-Newtonian fluids, representing fasted and fed states. The results indicate that the current design and operating conditions of the disintegration test device, given by the pharmacopoeias, are n…

Pharmaceutical ScienceComputational fluid dynamicsDosage formsymbols.namesakeNewtonian fluidShear stressPressureTechnology PharmaceuticalDissolution testingComputer SimulationDosage FormsChemistrybusiness.industryViscosityReynolds numberMechanicsFastingModels TheoreticalBody FluidsParticle image velocimetrySolubilitysymbolsHydrodynamicsCurrent (fluid)businessRheologyShear StrengthTabletsJournal of pharmaceutical sciences
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Preparation and Biological Evaluation of Ethylcellulose Microspheres Containing Tolmetin

1992

AbstractTolmetin microspheres were prepared by the coacervation process from the ethylcellulose. Microspheres were obtained both in presence and without protecting colloids, such as polyisobutilene (PIB) or ethyl-vinylacetate copolimers (EVA). The effect of these agents on the preparation, drug content, wall thickness, surface morphology, drug dissolution arid release from microspheres, were evaluated. The dissolution rate analysis was carried out also in the presence of a surfactant (Tween 80) at different pH values.In addition, microspheres containing Tolmetin as a core material were submitted to biological tests, in comparison with the free drug, to evaluate upon experimental models the …

PharmacologyActive ingredientChromatographyCoacervateChemistryOrganic ChemistryPharmaceutical SciencePharmacologyDosage formPulmonary surfactantDrug DiscoverymedicineTolmetinDissolution testingAntipyreticDissolutionmedicine.drugDrug Development and Industrial Pharmacy
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Statistical inference in abstracts of 3 influential clinical pharmacology journals analysed using a text‐mining algorithm

2021

Aim To describe the trend in the prevalence of statistical inference in three influential clinical pharmacology journals METHODS: We applied a computer-based algorithm to abstracts of three clinical pharmacology journals published in 1976 to 2016 to identify statistical inference and its subtypes. Furthermore, we manually reviewed a random sample of 300 articles to access algorithm's performance in finding statistical inference in abstracts and as a screening tool for presence and absence of statistical inference in full text. Result The algorithm identified 59% (13,375/22,516 [mid p 95% CI, 59%-60%]) article abstracts with statistical inference. The percentage of abstracts with statistical…

PharmacologyClinical pharmacologybusiness.industryData interpretation030226 pharmacology & pharmacyPredictive valuelaw.invention03 medical and health sciences0302 clinical medicineText mininglawSignificance testingStatistical inferencePharmacology (medical)Screening tool030212 general & internal medicinebusinessAlgorithmMathematicsBritish Journal of Clinical Pharmacology
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In silicoprediction of drug dissolution and absorption with variation in intestinal pH for BCS class II weak acid drugs: ibuprofen and ketoprofen

2012

The FDA Biopharmaceutical Classification System guidance allows waivers for in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms only for BCS class I. Extensions of the in vivo biowaiver for a number of drugs in BCS class III and BCS class II have been proposed, in particular, BCS class II weak acids. However, a discrepancy between the in vivo BE results and in vitro dissolution results for BCS class II acids was recently observed. The objectives of this study were to determine the oral absorption of BCS class II weak acids via simulation software and to determine if the in vitro dissolution test with various dissolution media could be sufficient …

PharmacologyKetoprofenChromatographyChemistryPharmaceutical ScienceGeneral MedicineBioequivalenceIbuprofenDosage formBioavailabilitymedicinePharmacology (medical)Dissolution testingSolubilityDissolutionmedicine.drugBiopharmaceutics & Drug Disposition
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Two-stage adaptive designs with correlated test statistics.

2005

When performing a trial using an adaptive sequential design, it is usually assumed that the data for each stage come from different units; for example, patients. However, sometimes it is not possible to satisfy this condition or to check whether it is satisfied. In these cases, the test statistics and p-values of each stage may be dependent. In this paper we investigate the type I error of two-stage adaptive designs when the test statistics from the stages are assumed to be bivariate normal. Analytical considerations are performed under the restriction that the conditional error function is constant in the continuation region. We show that the decisions can become conservative as well as an…

PharmacologyStatistics and ProbabilityAnalysis of VarianceClinical Trials as TopicCorrelation coefficientMultivariate normal distributionError functionContinuationSequential analysisResearch DesignData Interpretation StatisticalStatisticsPharmacology (medical)Constant (mathematics)AlgorithmsMathematicsStatistical hypothesis testingType I and type II errorsJournal of biopharmaceutical statistics
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Multivariate equivalence tests for use in pharmaceutical development.

2014

Statistical equivalence analyses are well-established parts of many studies in the biomedical sciences. Also in pharmaceutical development and manufacturing equivalence testing methods are required in order to statistically establish similarities between machines, process components, or complete processes. This article presents a choice of multivariate equivalence testing procedures for normally distributed data as generalizations of existing univariate methods. In all derived methods, variability is interpreted as nuisance parameter. The use of the proposed methods in pharmaceutical development is demonstrated with a comparative analysis of dissolution profiles.

PharmacologyStatistics and ProbabilityMultivariate statisticsMahalanobis distanceEquivalence testingDrug Industrybusiness.industryUnivariateNormal DistributionMachine learningcomputer.software_genreDelta methodPharmaceutical PreparationsSolubilityResearch DesignData Interpretation StatisticalMultivariate AnalysisEconometricsNuisance parameterPharmacology (medical)Artificial intelligencebusinesscomputerEquivalence (measure theory)MathematicsJournal of biopharmaceutical statistics
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Relationships betweenin vitrodrug dissolution andin vivoresponse

2012

In recent years there has been an effort to relate manufacturing variables to the performance of the dosage form from a clinical point of view (in terms of safety and efficacy). Consequently any control strategy or the establishment of meaningful specifications should take into consideration the clinical impact on the patient. Since plasma levels are considered to be one of the most useful surrogates for clinical safety (in that bioequivalent plasma levels are considered therapeutically equivalent) and dissolution is the best surrogate for bioavailability, it is a natural consequence that dissolution be used to establish the design space in which all the formulations would have similar safe…

Pharmacologybusiness.industryPharmaceutical ScienceGeneral MedicinePlasma levelsPharmacologyBioequivalenceDosage formBioavailabilityIn vivoClinical safetyMedicinePharmacology (medical)Dissolution testingBiochemical engineeringbusinessDesign spaceBiopharmaceutics & Drug Disposition
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High-repetition-rate source delivering optical pulse trains with a controllable level of amplitude and temporal jitters

2020

International audience; We theoretically propose and numerically validate an all-optical scheme to generate optical pulse trains with varying peak-powers and durations. A shaping of the spectral phase thanks to discrete /2 phase shifts enables an efficient phase-to-intensity conversion of a temporal phase modulation based on a two-tone sinusoidal beating. Experiments carried out at telecommunication wavelengths and at a repetition rate of 10 GHz confirm the ability of our approach to efficiently generate a train made of pulses with properties that vary from pulse-to-pulse. The levels of jitters can be accurately controlled.

Phase (waves)FOS: Physical sciences02 engineering and technologyoptical telecommunications01 natural scienceslcsh:QA75.5-76.95010309 optics020210 optoelectronics & photonicsOptics0103 physical sciences0202 electrical engineering electronic engineering information engineeringhigh-repetition rate optical pulse trainsPhysics[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]optical component testingRepetition (rhetorical device)business.industryhigh‐repetition rate optical pulse trainsPulse (physics)WavelengthAmplitudelcsh:TA1-2040Trainlcsh:Electronic computers. Computer sciencebusinesslcsh:Engineering (General). Civil engineering (General)Phase modulationOptics (physics.optics)Physics - Optics
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Concurrent molecular dynamics simulation of spinodal phase transition on transputer arrays

1990

Abstract We describe a concurrent implementation on cost-effective transputer arrays of a molecular dynamics program to efficiently simulate physical systems consisting of thousands of mobile particles with an interaction range much shorter than the system dimensions. This program, which uses a geometric decomposition strategy and includes a distributed dynamic load balancer, has been extensively tested by simulating the two-dimensional spinodal phase separation of a large Lennard-Jones system.

Phase transitionSpinodalComputer sciencebusiness.industrySpinodal decompositionTransputerPhysical systemGeneral Physics and AstronomyDynamic load testingComputational scienceMolecular dynamicsSoftwareHardware and ArchitecturebusinessAlgorithmComputer Physics Communications
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Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanin…

1999

not available

Phenylketonuria MaternalPhenylalanine hydroxylasephenylalanine 4 monooxygenasePhenylalanineGene mutationMaternal bloodNeonatal ScreeningPregnancyPhenylketonuriasMedicineHumansMaternal phenylketonuriaGenetic TestingPhenylalanine levelGeneticsbiologybusiness.industryInfant NewbornPhenylalanine HydroxylasePedigreeItalyPediatrics Perinatology and Child HealthMutationbiology.proteinIdentification (biology)FemalebusinessEuropean journal of pediatrics
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