6533b857fe1ef96bd12b3b87

RESEARCH PRODUCT

Permeability and toxicological profile estimation of organochlorine compounds by biopartitioning micellar chromatography

M.j. Medina-hernándezLaura Escuder-gilabertSalvador SagradoRosa María Villanueva-camañas

subject

Clinical BiochemistryBioconcentrationAbsorption (skin)Models BiologicalBiochemistryPermeabilityAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryHydrocarbons ChlorinatedAnimalsHumansDicofolPesticidesMolecular BiologySkinPharmacologyChromatographyChromatographyGeneral MedicineHexachlorobenzeneOrganochlorideBioavailabilityPartition coefficientchemistryBlood-Brain BarrierChlorobenzeneEnvironmental chemistrySoftware

description

This paper points out the usefulness of biopartitioning micellar chromatography (BMC) as a high-throughput primary screening tool providing key information about the oral absorption, skin permeability (Kp), brain–blood distribution coefficient (BB) and ecotoxicological parameters such as median lethal concentration (LC50) and bioconcentration factors of 15 organochloride compounds. The retention data of compounds in BMC conditions were interpolated in previously developed quantitative–retention activity relationships by our research group. Results show that the compounds studied readily cross the intestinal barrier (oral absorption >ercnt;) and the blood–brain barrier (log BB >p;0.4). In addition, the organochlorines DDE, chlorobenzene, 1,3-dichlorobenzene and 1,2-dichlorobenzene are the compounds which can more quickly cross the skin barrier (log Kp >nus;0.74 cm/h). From a ecotoxicological point of view, it can be concluded that the most retained compounds, DDE, DDD, hexachlorobenzene and dicofol, are the most toxic and bioacumulative. Copyright © 2008 John Wiley & Sons, Ltd.

https://doi.org/10.1002/bmc.1126