Search results for "asma"

showing 10 items of 4204 documents

Derivatives not first return integrable on a fractal set

2018

We extend to s-dimensional fractal sets the notion of first return integral (Definition 5) and we prove that there are s-derivatives not s-first return integrable.

Pure mathematicss-dimensional Hausdorff measureIntegrable systemApplied MathematicsGeneral MathematicsNumerical analysis010102 general mathematicss-setFirst return integrals-derivative01 natural sciences010305 fluids & plasmasSettore MAT/05 - Analisi Matematica0103 physical sciencesFractal set0101 mathematicsAlgebra over a fieldHenstock–Kurzweil integralMathematics
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Plasmon mass scale and quantum fluctuations of classical fields on a real time lattice

2018

Classical real-time lattice simulations play an important role in understanding non-equilibrium phenomena in gauge theories and are used in particular to model the prethermal evolution of heavy-ion collisions. Above the Debye scale the classical Yang-Mills (CYM) theory can be matched smoothly to kinetic theory. First we study the limits of the quasiparticle picture of the CYM fields by determining the plasmon mass of the system using 3 different methods. Then we argue that one needs a numerical calculation of a system of classical gauge fields and small linearized fluctuations which correspond to quantum fluctuations, in a way that keeps the separation between the two manifest. We demonstra…

QC1-999hep-latFOS: Physical sciencesplasmafysiikka114 Physical sciences01 natural sciencessymbols.namesakeHigh Energy Physics - LatticeHigh Energy Physics - Phenomenology (hep-ph)LinearizationLattice (order)0103 physical sciencesGauge theory010306 general physicsQuantum fluctuationPlasmonplasmaParticle Physics - PhenomenologyDebyePhysicsta114010308 nuclear & particles physicsplasma physicsPhysicsGaussHigh Energy Physics - Lattice (hep-lat)hep-phParticle Physics - LatticeoscillationHigh Energy Physics - PhenomenologyClassical mechanicsQuasiparticlesymbols
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Quantum walk on the line through potential barriers

2015

Quantum walks are well-known for their ballistic dispersion, traveling $\Theta(t)$ away in $t$ steps, which is quadratically faster than a classical random walk's diffusive spreading. In physical implementations of the walk, however, the particle may need to tunnel through a potential barrier to hop, and a naive calculation suggests this could eliminate the ballistic transport. We show by explicit calculation, however, that such a loss does not occur. Rather, the $\Theta(t)$ dispersion is retained, with only the coefficient changing, which additionally gives a way to detect and quantify the hopping errors in experiments.

Quadratic growthPhysicsQuantum PhysicsFOS: Physical sciencesStatistical and Nonlinear PhysicsCondensed Matter::Mesoscopic Systems and Quantum Hall EffectRandom walk01 natural sciences010305 fluids & plasmasTheoretical Computer ScienceElectronic Optical and Magnetic MaterialsModeling and SimulationBallistic conduction0103 physical sciencesSignal ProcessingLine (geometry)Dispersion (optics)Rectangular potential barrierQuantum walkStatistical physicsElectrical and Electronic EngineeringQuantum Physics (quant-ph)010306 general physicsQuantum Information Processing
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Setting the Scene: Element Determination and its Quality Control in Fractions of Refractory Organic Substances and the Corresponding Original Water S…

2007

Quality (physics)ChromatographyChemistryEnvironmental chemistryInductively coupled plasma mass spectrometryRefractory (planetary science)
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Fit-for-purpose chromatographic method for the determination of amikacin in human plasma for the dosage control of patients

2015

In this paper, a simple, rapid and sensitive method based on liquid chromatography with fluorimetric detection (HPLC-FLD) for the determination of amikacin (AMK) in human plasma is developed. Determination is performed by pre-column derivatization of AMK with ortho-phtalaldehyde (OPA) in presence of N-acetyl-L-cysteine (NAC) at pH 9.5 for 5 min at 80 °C. In our knowledge, this is the first time that NAC has been used in AMK derivatization. Derivatization conditions (pH, AMK/OPA/NAC molar ratios, temperature and reaction time) are optimized to obtain a single and stable, at room temperature, derivative. Separation of the derivative is achieved on a reversed phase LC column (Kromasil C18, 5 μ…

Quality ControlCorrelation coefficientAnalytical chemistryDerivative01 natural sciencesFluorescence spectroscopyAnalytical Chemistrychemistry.chemical_compoundmedicineHumansFluorometryDerivatizationAcetonitrileAmikacinChromatography High Pressure LiquidChromatographyDose-Response Relationship DrugPlasma samples010405 organic chemistry010401 analytical chemistryBacterial InfectionsAnti-Bacterial Agents0104 chemical scienceschemistryHuman plasmaAmikacinSpectrophotometry Ultravioletmedicine.drug
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Evaluation of the Physicochemical Properties of the Iron Nanoparticle Drug Products: Brand and Generic Sodium Ferric Gluconate

2021

Complex iron nanoparticle-based drugs are one of the oldest and most frequently administered classes of nanomedicines. In the US, there are seven FDA-approved iron nanoparticle reference drug products, of which one also has an approved generic drug product (i.e., sodium ferric gluconate (SFG)). These products are indicated for the treatment of iron deficiency anemia and are administered intravenously. On the molecular level, iron nanomedicines are colloids composed of an iron oxide core with a carbohydrate coating. This formulation makes nanomedicines more complex than conventional small molecule drugs. As such, these products are often referred to as nonbiological complex drugs (e.g., by t…

Quality ControlDrugChemistry Pharmaceuticalmedia_common.quotation_subjectIron oxidePharmaceutical ScienceEquivalence Trials as Topic02 engineering and technologyFerric Compounds030226 pharmacology & pharmacyGel permeation chromatography03 medical and health scienceschemistry.chemical_compound0302 clinical medicinePharmacokineticsDynamic light scatteringGeneric drugDrug DiscoveryDrugs GenericHumansInductively coupled plasma mass spectrometrymedia_commonAnemia Iron-Deficiency021001 nanoscience & nanotechnologySmall moleculeDynamic Light ScatteringchemistryChromatography GelNanoparticlesMolecular Medicine0210 nano-technologyUltracentrifugationNuclear chemistryMolecular Pharmaceutics
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Detection of batch effects in liquid chromatography-mass spectrometry metabolomic data using guided principal component analysis.

2014

Metabolomics based on liquid chromatography-mass spectrometry (LC-MS) is a powerful tool for studying dynamic responses of biological systems to different physiological or pathological conditions. Differences in the instrumental response within and between batches introduce unwanted and uncontrolled data variation that should be removed to extract useful information. This work exploits a recently developed method for the identification of batch effects in high throughput genomic data based on the calculation of a delta statistic through principal component analysis (PCA) and guided PCA. Its applicability to LC-MS metabolomic data was tested on two real examples. The first example involved t…

Quality ControlPrincipal Component AnalysisChromatographyChemistryGenomic dataGuided principal component analysisMass spectrometryBatch effectMass SpectrometryAnalytical ChemistryData setPlasmaMetabolomicsLiquid chromatography–mass spectrometryPeak intensityPrincipal component analysisCalibrationLiquid chromatography-mass spectrometry (LC-MS)HumansMetabolomicsBiological systemStatisticChromatography LiquidTalanta
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Are analysts doing method validation in liquid chromatography?

2014

International audience; Method validation is being applied in the reported analytical methods for decades. Even before this protocol was defined, authors already somehow validated their methods without full awareness. They wished to assure the quality of their work. Validation is an applied approach to verify that a method is suitable and rugged enough to function as a quality control tool in different locations and times. The performance parameters and statistical protocols followed throughout a validation study vary with the source of guidelines. Before single laboratory validation, an analytical method should be fully developed and optimized. The purpose of the validation is to confirm p…

Quality ControlValidation studyDIODE-ARRAY DETECTIONMethod validationmedia_common.quotation_subjectLiquid chromatographyValidation Studies as TopicGuidelinesBiochemistryField (computer science)Analytical Chemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistrySIMPLE HPLC METHODHumansQuality (business)HUMAN PLASMATANDEM MASS-SPECTROMETRYRAT PLASMAFunction (engineering)SurveyRP-LC METHODmedia_commonProtocol (science)AnalystsChromatographyPoint (typography)ChemistryData CollectionOrganic ChemistryGeneral MedicineEvaluated validation parametersMethod developmentFully developedSOLID-PHASE EXTRACTIONESI-MS/MS METHODPHARMACEUTICAL DOSAGE FORMChromatography LiquidTHIN-LAYER-CHROMATOGRAPHY
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Use of molecular topology for the prediction of physico-chemical, pharmacokinetic and toxicological properties of a group of antihistaminic drugs

2002

We used molecular connectivity to search mathematical models for predicting physico-chemical (e.g. the partition coefficient, P), pharmacokinetic (e.g. the time of maximum plasma level, and toxicological properties (lethal dose, LD) for a group of antihistaminic drugs. The results obtained clearly reveal the high efficiency of molecular topology for the prediction of these properties. Randomization and cross-validation by use of leave-one-out tests were also performed in order to assess the stability and the prediction ability of the connectivity functions selected.

Quantitative structure–activity relationshipChemistryQuantitative Structure-Activity RelationshipPharmaceutical SciencePlasma levelsPharmacologyModels BiologicalLethal Dose 50Structure-Activity RelationshipPharmacokineticsPredictive Value of TestsHistamine H1 AntagonistsRegression AnalysisAntihistaminic drugsMolecular topologyBiological systemInternational Journal of Pharmaceutics
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A Possible Time-Dependent Generalization of the Bipartite Quantum Marginal Problem

2018

In this work we study an inverse dynamical problem for a bipartite quantum system governed by the time local master equation: to find the class of generators which give rise to a certain time evolution with the constraint of fixed reduced states (marginals). The compatibility of such choice with a global unitary evolution is considered. For the non unitary case we propose a systematic method to reconstruct examples of master equations and address them to different physical scenarios.

Quantum PhysicsAtomic and Molecular Physics and OpticTime evolutionInverseFOS: Physical sciencespure quantum state01 natural sciencesMultipartite entanglementAtomic and Molecular Physics and Optics010305 fluids & plasmasQuantum statemultipartite entanglement0103 physical sciencesMaster equationBipartite graphQuantum systemApplied mathematicsbipartite quantum system010306 general physicsQuantum Physics (quant-ph)quantum controlQuantumEngineering (miscellaneous)Mathematics
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