Search results for "In vitro dissolution"

showing 4 items of 4 documents

Exploring Bioequivalence of Dexketoprofen Trometamol Drug Products with the Gastrointestinal Simulator (GIS) and Precipitation Pathways Analyses

2019

The present work aimed to explain the differences in oral performance in fasted humans who were categorized into groups based on the three different drug product formulations of dexketoprofen trometamol (DKT) salt&mdash

liquid–liquid phase separationSALT DISPROPORTIONATIONgastrointestinal absorptionSodiumlcsh:RS1-441Pharmaceutical ScienceExcipientchemistry.chemical_elementSalt (chemistry)Hydrochloric acidSOLUBILITYCalciumBioequivalenceArticlelcsh:Pharmacy and materia medicachemistry.chemical_compoundFLUIDSEMAoral absorptionABSORPTIONmedicinePharmacology & PharmacySUPERSATURATED SOLUTIONSdexketoprofenSimulationchemistry.chemical_classificationScience & TechnologyChemistryliquid-liquid phase separationPhosphateDexketoprofenSIMILARITIESgastrointestinal simulatorin vitro dissolutionIN-VITRO DISSOLUTIONLife Sciences & BiomedicineVIVO DISSOLUTIONMETHODOLOGYmicroscopy imagingmedicine.drugPharmaceutics
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Defining level A IVIVC dissolution specifications based on individual in vitro dissolution profiles of a controlled release formulation.

2018

Regulatory guidelines recommend that, when a level A IVIVC is established, dissolution specification should be established using averaged data and the maximum difference between AUC and Cmax between the reference and test formulations cannot be greater than 20%. However, averaging data assumes a loss of information and may reflect a bias in the results. The objective of the current work is to present a new approach to establish dissolution specifications using a new methodology (individual approach) instead of average data (classical approach). Different scenarios were established based on the relationship between in vitro-in vivo dissolution rate coefficient using a level A IVIVC of a cont…

In vitro dissolutionCmaxPharmaceutical Science02 engineering and technologyBioequivalence021001 nanoscience & nanotechnology030226 pharmacology & pharmacyControlled releaseModels Biological03 medical and health sciencesDrug Liberation0302 clinical medicineIVIVCTherapeutic EquivalencyDelayed-Action PreparationsMaximum differenceRange (statistics)Computer Simulation0210 nano-technologyBiological systemDissolutionMonte Carlo MethodMathematicsTabletsEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
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Predicting Pharmacokinetics of Multisource Acyclovir Oral Products Through Physiologically Based Biopharmaceutics Modeling.

2021

Abstract Highly variable disposition after oral ingestion of acyclovir has been reported, although little is known regarding the underlying mechanisms. Different studies using the same reference product (Zovirax ®) showed that Cmax and AUC were respectively 44 and 35% lower in Saudi Arabians than Europeans, consistent with higher frequencies of reduced-activity polymorphs of the organic cation transporter (OCT1) in Europeans. In this study, the contribution of physiology (i.e., OCT1 activity) to the oral disposition of acyclovir immediate release (IR) tablets was hypothesized to be greater than dissolution. The potential role of OCT1 was studied in a validated physiologically-based biopharm…

Physiologically based pharmacokinetic modellingIn vitro dissolutionChemistryBiopharmaceuticsCmaxPharmaceutical ScienceAcyclovirBioequivalencePharmacologyBiopharmaceuticsOral ingestionPharmacokineticsSolubilityTherapeutic EquivalencyImmediate releaseTabletsJournal of pharmaceutical sciences
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Integrating theoretical and experimental permeability estimations for provisional biopharmaceutical classification: Application to the WHO essential …

2018

The accuracy of the provisional estimation of the Biopharmaceutics Classification System (BCS) is heavily influenced by the permeability measurement. In this study, several theoretical and experimental models currently employed for BCS permeability classification have been analysed. The experimental models included the in situ rat intestinal perfusion, the ex vivo rat intestinal tissue in an Ussing chamber, the MDCK and Caco-2 cell monolayers, and the parallel artificial membrane (PAMPA). The theoretical models included the octanol-water partition coefficient and the QSPeR (Quantitative Structure-Permeability Relationship) model recently developed. For model validation, a dataset of 43 comp…

In vitro dissolutionTheoretical modelsPharmaceutical Science02 engineering and technologyBioequivalenceIn Vitro TechniquesWorld Health Organization030226 pharmacology & pharmacyModels BiologicalDosage formPermeabilityBiopharmaceuticsMadin Darby Canine Kidney Cells03 medical and health sciences0302 clinical medicineDogsAnimalsHumansPharmacology (medical)Intestinal MucosaMathematicsPharmacologyGeneral Medicine021001 nanoscience & nanotechnologyBiopharmaceutics Classification SystemBioavailabilityRatsPermeability (earth sciences)BiopharmaceuticalCaco-2 Cells0210 nano-technologyBiological systemDrugs EssentialBiopharmaceuticsdrug disposition
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