High throughput determination log Po/w/pKa/log Do/w of drugs by combination of UHPLC and CE methods

dc.contributor.authorCabot Canyelles, Joan Marc
dc.contributor.authorSubirats i Vila, Xavier
dc.contributor.authorFuguet i Jordà, Elisabet
dc.contributor.authorRosés Pascual, Martí
dc.date.accessioned2016-06-17T10:58:56Z
dc.date.available2016-06-17T10:58:56Z
dc.date.issued2014-07-18
dc.date.updated2016-06-17T10:59:01Z
dc.description.abstractn 1997Valkó et al. developed a generic fast gradient HPLC method, based on the calculation of the Chromatographic Hydrophobicity Index (CHI) from the gradient retention times, in order to measure lipophilicity. We have employedthe correlations between CHI and log Po/wand adapted the rapid gradient HPLC method to UHPLC obtaining excellent resolution and repeatability in a short analysis time (<4min). log Po/wvalues can be easily obtained from these CHI measurementsbut, unfortunately, these correlations are only valid for non-ionized compounds. Consequently, in order to determine the effective log Po/wvalue at a particular pH, afast high-throughput method for pKadeterminationwas required. The IS-CE method, based on the use of internal standards (IS) and capillaryelectrophoresis(CE),is a fast and attractive alternative to other methods for pKadetermination,since itoffers multiple advantages compared to them: low amounts of test compounds and reagents are needed, high purity is not required, specific interactions between test compounds and buffers are corrected, etc. In addition, it allows the determination of a pKavalue in less than 5 minutes. Both CHI and IS-CE have beencombined in order to describe a high throughput alternative in thedetermination ofthe lipophilicity profiles of bioactive compounds.
dc.format.extent9 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec642657
dc.identifier.issn1848-7718
dc.identifier.urihttps://hdl.handle.net/2445/99599
dc.language.isoeng
dc.publisherIAPC Publishing
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.5599/admet.2.2.44
dc.relation.ispartofADMET & DMPK, 2014, vol. 2, num. 2, p. 98-106
dc.relation.urihttp://dx.doi.org/10.5599/admet.2.2.44
dc.rightscc-by (c) Cabot Canyelles, Joan Marc et al., 2014
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Enginyeria Química i Química Analítica)
dc.subject.classificationDisseny de medicaments
dc.subject.classificationFunció d'acidesa
dc.subject.classificationMedicaments
dc.subject.otherDrug design
dc.subject.otherAcidity function
dc.subject.otherDrugs
dc.titleHigh throughput determination log Po/w/pKa/log Do/w of drugs by combination of UHPLC and CE methods
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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