6533b7cefe1ef96bd1257ac0
RESEARCH PRODUCT
Biopartitioning micellar separation methods: modelling drug absorption
J.j. Martínez-plaLaura Escuder-gilabertRosa María Villanueva-camañasM.j. Medina-hernándezSalvador Sagradosubject
DrugQuantitative structure–activity relationshipCell Membrane PermeabilityChromatographyChemistryDrug discoverymedia_common.quotation_subjectClinical BiochemistryQuantitative Structure-Activity RelationshipCell BiologyGeneral MedicineHealth economyBiochemistryAnalytical ChemistryPassive permeabilityBiopharmaceuticalDrug developmentSeparation methodPharmacokineticsMicellesmedia_commondescription
The search for new pharmacologically active compounds in drug discovery programmes often neglects biopharmaceutical properties as drug absorption. As a result, poor biopharmaceutical characteristics constitute a major reason for the low success rate for candidates in clinical development. Since the cost of drug development is many times larger than the cost of drug discovery, predictive methodologies aiding the selection of bioavailable drug candidates are of profound significance. This paper has been focussed on recent developments and applications of chromatographic systems, particularly those systems based on amphiphilic structures, in the frame of alternative approaches for estimating the transport properties of new drugs. The aim of this review is to take a critical look at the separations methods proposed for describing and predicting drug passive permeability across gastrointestinal tract and the skin.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2003-11-25 | Journal of Chromatography B |