Multiple non-animal-based test methods have never been formally validated. In order to use such new approach methods (NAMs) in a regulatory context, criteria to define their readiness are necessary. The field of developmental neurotoxicity (DNT) testing is used to exemplify the application of readiness criteria. The costs and number of untested chemicals are overwhelming for in vivo DNT testing. Thus, there is a need for inexpensive, high-throughput NAMs, to obtain initial information on potential hazards, and to allow prioritization for further testing. A background on the regulatory and scientific status of DNT testing is provided showing different types of test readiness levels, depending on the intended use of data from NAMs. Readiness criteria, compiled during a stakeholder workshop, uniting scientists from academia, industry and regulatory authorities are presented. An important step beyond the listing of criteria, was the suggestion for a preliminary scoring scheme. On this basis a (semi)-quantitative analysis process was assembled on test readiness of 17 NAMs with respect to various uses (e.g. prioritization/screening, risk assessment). The scoring results suggest that several assays are currently at high readiness levels. Therefore, suggestions are made on how DNT NAMs may be assembled into an integrated approach to testing and assessment (IATA). In parallel, the testing state in these assays was compiled for more than 1000 compounds. Finally, a vision is presented on how further NAM development may be guided by knowledge of signaling pathways necessary for brain development, DNT pathophysiology, and relevant adverse outcome pathways (AOP).

Recommendation on test readiness criteria for new approach methods in toxicology : exemplified for developmental neurotoxicity / A. Bal-Price, H.T. Hogberg, K.M. Crofton, M. Daneshian, R.E. Fitzgerald, E. Fritsche, T. Heinonen, S. Hougaard Bennekou, S. Klima, A.H. Piersma, M. Sachana, T.J. Shafer, A. Terron, F. Monnet-Tschudi, B. Viviani, T. Waldmann, R.H.S. Westerink, M.F. Wilks, H. Witters, M.-. Zurich, M. Leist. - In: ALTERNATIVES TO ANIMAL EXPERIMENTATION. - ISSN 1868-596X. - 35:3(2018), pp. 306-352. [10.14573/altex.1712081]

Recommendation on test readiness criteria for new approach methods in toxicology : exemplified for developmental neurotoxicity

B. Viviani;
2018

Abstract

Multiple non-animal-based test methods have never been formally validated. In order to use such new approach methods (NAMs) in a regulatory context, criteria to define their readiness are necessary. The field of developmental neurotoxicity (DNT) testing is used to exemplify the application of readiness criteria. The costs and number of untested chemicals are overwhelming for in vivo DNT testing. Thus, there is a need for inexpensive, high-throughput NAMs, to obtain initial information on potential hazards, and to allow prioritization for further testing. A background on the regulatory and scientific status of DNT testing is provided showing different types of test readiness levels, depending on the intended use of data from NAMs. Readiness criteria, compiled during a stakeholder workshop, uniting scientists from academia, industry and regulatory authorities are presented. An important step beyond the listing of criteria, was the suggestion for a preliminary scoring scheme. On this basis a (semi)-quantitative analysis process was assembled on test readiness of 17 NAMs with respect to various uses (e.g. prioritization/screening, risk assessment). The scoring results suggest that several assays are currently at high readiness levels. Therefore, suggestions are made on how DNT NAMs may be assembled into an integrated approach to testing and assessment (IATA). In parallel, the testing state in these assays was compiled for more than 1000 compounds. Finally, a vision is presented on how further NAM development may be guided by knowledge of signaling pathways necessary for brain development, DNT pathophysiology, and relevant adverse outcome pathways (AOP).
developmental in vitro neurotoxicity testing; quality assurance; regulatory toxicology; toxicity screening; Animals; Education; Humans; Neurotoxicity Syndromes; Risk Assessment; Toxicity Tests; Animal Testing Alternatives; Guidelines as Topic
Settore BIO/14 - Farmacologia
2018
Article (author)
File in questo prodotto:
File Dimensione Formato  
ALTEX 2018.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 6.46 MB
Formato Adobe PDF
6.46 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/732146
Citazioni
  • ???jsp.display-item.citation.pmc??? 59
  • Scopus 124
  • ???jsp.display-item.citation.isi??? 124
social impact