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http://dx.doi.org/10.25673/121189Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Dahley, Carolin | - |
| dc.contributor.author | Goss, Kai-Uwe | - |
| dc.contributor.author | Ebert, Andrea | - |
| dc.date.accessioned | 2025-11-11T08:06:08Z | - |
| dc.date.available | 2025-11-11T08:06:08Z | - |
| dc.date.issued | 2025 | - |
| dc.identifier.uri | https://opendata.uni-halle.de//handle/1981185920/123142 | - |
| dc.identifier.uri | http://dx.doi.org/10.25673/121189 | - |
| dc.description.abstract | Reliable membrane permeability data are essential in early drug development. Therefore, there is a strong need for robust experimental high-throughput screening methods, or ideally, accurate predictive tools, to assess membrane permeability. In a previous study, we demonstrated that the solubility-diffusion model can successfully predict passive permeability across biological Caco-2 and MDCK membranes, provided accurate hexadecane/water partition coefficients (Khex/w) are available. In this study, we investigated the HDM-PAMPA method for determining Khex/w. We measured our own data (64 compounds) using this assay and compared the results with established methods such as black lipid membrane (BLM) experiments and classical two-phase systems. Our results show good agreement across methods, with both our data and literature values aligning closely. Using these experimentally determined Khex/w values, we achieved accurate predictions of permeability in Caco-2 and MDCK cell membranes (RMSE = 0.8, n = 29) based on a previously calibrated equation. We further evaluated the in silico prediction of Khex/w using the UFZ-LSER database and the software COSMOtherm. COSMOtherm performed nearly as well as experimental measurements (RMSE = 1.20, n = 29), while the LSER approach (RMSE = 1.63, n = 29) is best applied when experimental descriptors are available or as a complement to COSMOtherm. This work highlights the practical utility of Khex/w in high-throughput permeability estimation, which can support efficient screening and prioritization of drug candidates in pharmaceutical research. | eng |
| dc.language.iso | eng | - |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | - |
| dc.subject.ddc | 540 | - |
| dc.title | Predicting Caco-2/MDCK intrinsic membrane permeability from HDM-PAMPA-derived hexadecane/water partition coefficients | eng |
| dc.type | Article | - |
| local.versionType | publishedVersion | - |
| local.bibliographicCitation.journaltitle | European journal of pharmaceutical sciences | - |
| local.bibliographicCitation.volume | 214 | - |
| local.bibliographicCitation.pagestart | 1 | - |
| local.bibliographicCitation.pageend | 8 | - |
| local.bibliographicCitation.publishername | Elsevier | - |
| local.bibliographicCitation.publisherplace | New York, NY [u.a.] | - |
| local.bibliographicCitation.doi | 10.1016/j.ejps.2025.107280 | - |
| local.openaccess | true | - |
| dc.identifier.ppn | 194080017X | - |
| cbs.publication.displayform | 2025 | - |
| local.bibliographicCitation.year | 2025 | - |
| cbs.sru.importDate | 2025-11-11T08:05:45Z | - |
| local.bibliographicCitation | Enthalten in European journal of pharmaceutical sciences - New York, NY [u.a.] : Elsevier, 1993 | - |
| local.accessrights.dnb | free | - |
| Appears in Collections: | Open Access Publikationen der MLU | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 1-s2.0-S0928098725002787-main.pdf | 1.02 MB | Adobe PDF | ![]() View/Open |
