Search results for "Simulation."

showing 10 items of 4779 documents

Effect of cultivation techniques on the hydrodynamic and mechanical behaviour of the "Lauragais-terreforts"

1993

The effect of various seed bed preparations on hydrodynamic and mechanical parameters was studied experimentally by simulated rainfall on clayeyloamy soils Lauragais, which had developed on chalky molasse on a slope greater than 12 %. The level of soaked up rain ("pluie d'imbibition", Pi) is closely connected to the inital degree of saturation of the soil ; it varies from 10 to 24 mm when the soil is humid and increases when the soil is dry (14 to 47 mm). But when the soil surface is crusted the Pi is less and seems to be no longer controlled by the degree of water in the soil. Treatments with fine structural elements show the fewest possibilities of infiltration during the soaking up stage…

Drop (liquid)Degree of saturationSoil scienceSoil surfaceSoil saturationMolasseInfiltration (hydrology)EVOLUTION DES SOLS SOUS CULTUREINFILTRATIONSTRUCTURE DU SOLSoil waterEnvironmental scienceEROSION HYDRIQUESIMULATION DE PLUIESurface runoff
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Simulated raindrop's characteristic measurements. A new approach of image processing tested under laboratory rainfall simulation

2018

Abstract The size of the drops determines soil erosion and runoff rates, and then the fate of ecosystems. Various raindrop measurement techniques and tools have been developed to determine natural and simulated raindrop size distributions and mean drop size. There is a need to improve the procedure to determine the raindrop properties, and this is why we develop a new technique to analyze drop size distribution and fall velocity. For this purpose a rainfall simulator with two oscillating Veejet 80100 nozzles in laboratory condition, and high speed imaging technique and edge detection approach in image processing was applied to identify and measure drop size and calculate drop velocity. The …

Drop size010504 meteorology & atmospheric sciencesHigh abilityDrop (liquid)NozzleImage processing04 agricultural and veterinary sciences01 natural sciencesEdge detectionRainfall simulation040103 agronomy & agriculture0401 agriculture forestry and fisheriesEnvironmental scienceSurface runoff0105 earth and related environmental sciencesEarth-Surface ProcessesRemote sensingCATENA
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Protocol for rational design of covalently interacting inhibitors.

2014

The inhibition potencies of covalent inhibitors mainly result from the formation of a covalent bond to the enzyme during the inhibition mechanism. This class of inhibitors has essentially been ignored in previous target-directed drug discovery projects because of concerns about possible side effects. However, their advantages, such as higher binding energies and longer drug-target residence times moved them into the focus of recent investigations. While the rational design of non-covalent inhibitors became standard the corresponding design of covalent inhibitors is still in its early stages. Potent covalent inhibitors can be retrieved from large compound libraries by covalent docking approa…

Drug discoveryChemistryRational designHybrid approachCombinatorial chemistryAtomic and Molecular Physics and OpticsEnzymesQM/MMMolecular Docking SimulationNitrophenolsHIV ProteaseDocking (molecular)Covalent bondCatalytic DomainDrug DesignEpoxy CompoundsHumansQuantum TheoryPhysical and Theoretical ChemistryBinding siteEnzyme InhibitorsChemphyschem : a European journal of chemical physics and physical chemistry
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Pharmacogenomic and molecular docking studies on the cytotoxicity of the natural steroid wortmannin against multidrug-resistant tumor cells

2014

Wortmannin is a cytotoxic compound derived from the endophytic fungi Fusarium oxysporum, Penicillium wortmannii and Penicillium funiculosum that occurs in many plants, including medicinal herbs. The rationale to develop novel anticancer drugs is the frequent development of tumor resistance to the existing antineoplasic agents. Therefore, it is mandatory to analyze resistance mechanisms of novel drug candidates such as wortmannin as well to bring effective drugs into the clinic that have the potential to bypass or overcome resistance to established drugs and to substantially increase life span of cancer patients. In the present project, we found that P-glycoprotein-overexpressing tumor cells…

DrugATP Binding Cassette Transporter Subfamily BClass I Phosphatidylinositol 3-Kinasesmedia_common.quotation_subjectPharmaceutical ScienceAntineoplastic AgentsATP-binding cassette transporterDrug resistancePharmacologyBiologyWortmanninPhosphatidylinositol 3-Kinaseschemistry.chemical_compoundCell Line TumorDrug DiscoveryCluster AnalysisHumansCytotoxicityProtein kinase BPI3K/AKT/mTOR pathwayOligonucleotide Array Sequence Analysismedia_commonPharmacologyDrug Resistance MultipleAndrostadienesMolecular Docking SimulationMultiple drug resistanceComplementary and alternative medicinechemistryDrug Resistance NeoplasmPharmacogeneticsMolecular MedicineWortmanninSignal TransductionPhytomedicine
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Computer simulations for bioequivalence trials: selection of analyte in BCS drugs with first-pass metabolism and two metabolic pathways.

2010

The objective of this work is to use a computer simulation approach to define the most sensitive analyte for in vivo bioequivalence studies of all types of Biopharmaceutics Classification System (BCS) drugs undergoing first-pass hepatic metabolism with two metabolic pathways. A semi-physiological model was developed in NONMEM VI to simulate bioequivalence trials. Four BCS classes (from Class I to IV) of drugs, with three possible saturation scenarios (non-saturation, saturation and saturation of only the major route of metabolism), two (high or low) dose schemes, and six types of pharmaceutical quality for the drug products were simulated. The number of investigated scenarios was 144 (4 × 3…

DrugAnalyteChemistrymedia_common.quotation_subjectMetabolitePharmaceutical SciencePharmacologyBioequivalenceBiopharmaceutics Classification SystemModels BiologicalNONMEMBiopharmaceuticschemistry.chemical_compoundPharmacokineticsPharmaceutical PreparationsTherapeutic EquivalencyArea Under CurveComputer SimulationDrug metabolismAlgorithmsMetabolic Networks and Pathwaysmedia_commonEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
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Computer simulations of bioequivalence trials: selection of design and analyte in BCS drugs with first-pass hepatic metabolism: linear kinetics (I).

2008

Modeling and simulation approaches are useful tools to assess the potential outcome of different scenarios in bioequivalence studies. The aim of this study is to propose a new and improved semi-physiological model for bioequivalence trial simulations and apply it for all BCS (Biopharmaceutic Classification System) drug classes with non-saturated first-pass hepatic metabolism. The semi-physiological model was developed in NONMEM VI to simulate bioequivalence trials. Parent drug and metabolite levels for both reference and test were simulated. Eight types of drugs (with high or low permeability and high or low solubility (class I to IV) and high or low intrinsic clearance) were considered in …

DrugAnalytemedia_common.quotation_subjectMetabolitePharmaceutical ScienceBioequivalencePharmacologychemistry.chemical_compoundFirst pass effectPharmacokineticsHumansComputer SimulationPharmacokineticsTissue Distributionmedia_commonDose-Response Relationship DrugChemistryNONMEMLiverNonlinear DynamicsPharmaceutical PreparationsTherapeutic EquivalencyArea Under CurveData Interpretation StatisticalDrug metabolismAlgorithmsEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
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A high-quality homology model for the human dopamine transporter validated for drug design purposes.

2018

The human dopamine transporter (hDAT) plays many vital functions within the central nervous system and is thus targeted by many pharmaceutical agents. Dopamine-related therapies are in current development for individuals with dopamine-related disorders including depression, Parkinson's disease, and psychostimulant addictions such as cocaine abuse. Yet, most efforts to develop new dopamine therapies are within costly structure-activity relationship studies. Through structure-based drug design techniques, the binding site of hDAT can be utilized to develop novel selective and potent dopamine therapies at reduced costs. However, no structural models of hDAT specifically validated for rational …

DrugComputer sciencemedia_common.quotation_subjectDrug designComputational biologyNortriptyline01 natural sciencesBiochemistryInhibitory Concentration 50DopamineDrug DiscoverymedicineAnimalsDrosophila ProteinsHumansHomology modelingmedia_commonDopamine transporterPharmacologyDopamine Plasma Membrane Transport ProteinsBinding Sitesbiology010405 organic chemistryAddictionOrganic Chemistry0104 chemical sciencesProtein Structure TertiaryMolecular Docking Simulation010404 medicinal & biomolecular chemistryDrug Designbiology.proteinMolecular MedicineDrosophilaCocaine abusemedicine.drugChemical biologydrug design
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From In Silico to Experimental Validation: Tailoring Peptide Substrates for a Serine Protease.

2020

Smart nanocarriers for the transport of drugs to tumor cells are nowadays of great interest for treating cancer. The use of enzymatic stimuli to cleave peptide-based drug nanocapsules for the selective release of nanocapsule cargo in close proximity to tumor cells opens new possibilities in cancer research. In the present work, we demonstrate a methodology for finding and optimizing cleavable substrate sequences by the type II transmembrane serine protease hepsin, which is highly overexpressed in prostate cancer. The design and screening of combinatorial libraries in silico against the binding cavity of hepsin allow the identification of a panel of promising substrates with high-calculated …

DrugMalePolymers and PlasticsIn silicoHepsinmedia_common.quotation_subjectBioengineeringPeptide02 engineering and technology010402 general chemistry01 natural sciencesNanocapsulesBiomaterialsCleaveCell Line TumorMaterials ChemistryHumansComputer Simulationmedia_commonSerine proteasechemistry.chemical_classificationbiologyChemistryProstatic Neoplasms021001 nanoscience & nanotechnology0104 chemical sciencesBiochemistrybiology.proteinNanocarriersSerine Proteases0210 nano-technologyPeptidesBiomacromolecules
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Pharmacokinetic evaluation of oral fenofibrate nanosuspensions and SLN in comparison to conventional suspensions of micronized drug.

2007

An increasing number of newly developed drugs show bioavailability problems due to poor water solubility. Formulating the drugs as nanosuspensions may help to overcome these problems by increasing saturation solubility and dissolution velocity. In the present study the bioavailability of the poorly soluble fenofibrate following oral administration was investigated in rats. Four formulations were tested: a nanosuspension type DissoCube(R), one solid lipid nanoparticle (SLN) preparation and two suspensions of micronized fenofibrate as reference formulations, one suspension in sirupus simplex and a second in a solution of hydroxyethy-cellulose in physiological saline. Both colloidal drug deliv…

DrugMalemedia_common.quotation_subjectPharmaceutical ScienceAdministration OralBiological AvailabilityPharmacologyModels BiologicalDosage formPharmacokineticsFenofibrateSuspensionsSolid lipid nanoparticlemedicineAnimalsComputer SimulationTissue DistributionSolubilityRats Wistarmedia_commonHypolipidemic AgentsFenofibrateChemistryLipidsBioavailabilityRatsSolubilityDrug deliveryNanoparticlesmedicine.drugAdvanced drug delivery reviews
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Design and development of hyaluronan-functionalized polybenzofulvene nanoparticles as CD44 receptor mediated drug delivery system

2017

A tri-component polymer brush (TCPB), composed of a polybenzofulvene copolymer bearing low molecular weight hyaluronic acid (HA) on the surface of its cylindrical brush-like backbone and oligo-PEG fractions, was employed in the preparation of 350 nm nanostructured drug delivery systems capable of delivering the anticancer drug doxorubicin. The obtained drug delivery systems were characterized on the basis of drug loading and release, dimensions and zeta potential, morphology and in vitro cell activity, and uptake on three different human cell lines, namely the bronchial epithelial 16HBE, the breast adenocarcinoma MCF-7, and the colon cancer HCT116 cells. Finally, the ability of doxorubicin…

DrugMaterials scienceAtomic and Molecular Physics and Opticmedia_common.quotation_subjectHyaluronic acidCD44 receptorBioengineering02 engineering and technologyPharmacology010402 general chemistry01 natural sciencesCD44 receptor; Doxorubicin; Hyaluronic acid; Nanomedicine; Polybenzofulvene; Tri-component polymer brush TCPB; Bioengineering; Chemistry (all); Atomic and Molecular Physics and Optics; Modeling and Simulation; Materials Science (all); Condensed Matter Physicschemistry.chemical_compoundAtomic and Molecular PhysicsHyaluronic acidTri-component polymer brush TCPBmedicineGeneral Materials ScienceDoxorubicinmedia_commonbiologyCD44Chemistry (all)General Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesNanomedicinechemistryTargeted drug deliveryDoxorubicinModeling and SimulationDrug deliveryCancer cellbiology.proteinBiophysicsNanomedicineMaterials Science (all)Polybenzofulveneand Optics0210 nano-technologymedicine.drug
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