SEURAT: Safety Evaluation Ultimately Replacing Animal Testing-Recommendations for future research in the field of predictive toxicology

被引:33
作者
Daston, George [1 ]
Knight, Derek J. [2 ]
Schwarz, Michael [3 ]
Gocht, Tilman [3 ]
Thomas, Russell S. [4 ]
Mahony, Catherine [5 ]
Whelan, Maurice [6 ]
机构
[1] Procter & Gamble Co, Cent Prod Safety Dept, Mason, OH 45040 USA
[2] European Chem Agcy, Helsinki 00121, Finland
[3] Univ Tubingen, Dept Toxicol, Inst Expt & Clin Pharmacol & Toxicol, D-72074 Tubingen, Germany
[4] US EPA, Natl Ctr Computat Toxicol, Res Triangle Pk, NC 27711 USA
[5] Procter & Gamble Tech Ctr Ltd, Egham TW20 9NW, Surrey, England
[6] Commiss European Communities, Joint Res Ctr, IHCP, I-21027 Ispra, VA, Italy
关键词
Critical biological targets; Adverse outcome pathways; Safety assessment; Read-across; Ab initio prediction; HEALTH-RISK ASSESSMENT; TOXCAST PROGRAM; FRAMEWORK; CHEMICALS; UPDATE; READ;
D O I
10.1007/s00204-014-1421-5
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The development of non-animal methodology to evaluate the potential for a chemical to cause systemic toxicity is one of the grand challenges of modern science. The European research programme SEURAT is active in this field and will conclude its first phase, SEURAT-1, in December 2015. Drawing on the experience gained in SEURAT-1 and appreciating international advancement in both basic and regulatory science, we reflect here on how SEURAT should evolve and propose that further research and development should be directed along two complementary and interconnecting work streams. The first work stream would focus on developing new 'paradigm' approaches for regulatory science. The goal here is the identification of 'critical biological targets' relevant for toxicity and to test their suitability to be used as anchors for predicting toxicity. The second work stream would focus on integration and application of new approach methods for hazard (and risk) assessment within the current regulatory 'paradigm', aiming for acceptance of animal-free testing strategies by regulatory authorities (i.e. translating scientific achievements into regulation). Components for both work streams are discussed and may provide a structure for a future research programme in the field of predictive toxicology.
引用
收藏
页码:15 / 23
页数:9
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