Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10137720 | Regulatory Toxicology and Pharmacology | 2018 | 68 Pages |
Abstract
The European Partnership for Alternative Approaches to Animal Testing (EPAA) convened a Partners' Forum Toxicokinetics and Read-Across to provide an overview on research activities to develop in vitro toxicokinetics methods and physiologically-based kinetic (PBK) models and to find synergies to enhance use of toxicokinetic data to strengthen read-across. Currently, lacking toxicokinetic data often prevent the application of read-across. Preferably, toxicokinetic data should be generated using in vitro and in silico tools and anchored towards human relevance. In certain sectors, PBK modelling is being used for risk assessment, but less so in others. Specific activities were identified to facilitate the use of in vitro and in silico toxicokinetic data to support read-across: The collation of available tools indicating the parameters and applicability domains covered; endpoint-specific guidance on toxicokinetics parameters required for read-across; case studies exemplifying how toxicokinetic data help support read-across. Activities to enhance the scientific robustness of read-across include the further user-friendly combination of read-across tools and formal guidance by the authorities specifying the minimum information requirements to justify read-across for a given toxicity endpoint. The EPAA was invited to continue dissemination activities and to explore possibilities to collate a contemporaneous list of open toxicokinetics tools that assist risk assessment.
Keywords
EFPIAENVOECDIMIRFCSCCsMOAECHACHMPCeficEuropean Chemical Industry CouncilEURL ECVAMNOAELWOEIVIVEJRCWeight-of-evidence (WoE)Threshold of toxicological concern (TTC)CSAFHazard and risk assessmentITTCSEURAT-1LRSSSMEPPPADMEEMARTDCLPAOPTTCEFSALRIiFRaEuropean Union Reference Laboratory for Alternatives to Animal TestingThreshold of toxicological concernEuropean Medicines agencyEuropean Chemicals Agencyinnovative medicines initiativeEuropean Food Safety AuthorityTimesQSARR&DResearch and developmentDistributionRegistration, Evaluation, Authorisation and Restriction of ChemicalsAbsorptionMode-of-actionIn vitrotest guidelineQuantitative Structure Activity RelationshipREACHgrowOrganisation for Economic Co-operation and DevelopmentSmall and medium-sized enterprisesClassificationUncertainty factorMetabolismplant protection productadverse outcome pathwaybiomonitoring equivalentICHThe Netherlandsno-observed-adverse-effect levelWeight-of-evidenceEuropean parliamentScientific Committee on Consumer SafetyEuropean CommissionInternational Conference on HarmonisationIATA
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Authors
Charles Laroche, Manoj Aggarwal, Hans Bender, Paul Benndorf, Barbara Birk, Jonathan Crozier, Gianni Dal Negro, Federica De Gaetano, Christian Desaintes, Iain Gardner, Bruno Hubesch, Amaia Irizar, David John, Vikas Kumar, Alfonso Lostia, Irene Manou,