| Literature DB >> 28069485 |
Jon Hamm1, Kristie Sullivan2, Amy J Clippinger3, Judy Strickland4, Shannon Bell4, Barun Bhhatarai5, Bas Blaauboer6, Warren Casey7, David Dorman8, Anna Forsby9, Natàlia Garcia-Reyero10, Sean Gehen11, Rabea Graepel12, Jon Hotchkiss5, Anna Lowit13, Joanna Matheson14, Elissa Reaves13, Louis Scarano15, Catherine Sprankle4, Jay Tunkel16, Dan Wilson5, Menghang Xia17, Hao Zhu18, David Allen4.
Abstract
Acute systemic toxicity testing provides the basis for hazard labeling and risk management of chemicals. A number of international efforts have been directed at identifying non-animal alternatives for in vivo acute systemic toxicity tests. A September 2015 workshop, Alternative Approaches for Identifying Acute Systemic Toxicity: Moving from Research to Regulatory Testing, reviewed the state-of-the-science of non-animal alternatives for this testing and explored ways to facilitate implementation of alternatives. Workshop attendees included representatives from international regulatory agencies, academia, nongovernmental organizations, and industry. Resources identified as necessary for meaningful progress in implementing alternatives included compiling and making available high-quality reference data, training on use and interpretation of in vitro and in silico approaches, and global harmonization of testing requirements. Attendees particularly noted the need to characterize variability in reference data to evaluate new approaches. They also noted the importance of understanding the mechanisms of acute toxicity, which could be facilitated by the development of adverse outcome pathways. Workshop breakout groups explored different approaches to reducing or replacing animal use for acute toxicity testing, with each group crafting a roadmap and strategy to accomplish near-term progress. The workshop steering committee has organized efforts to implement the recommendations of the workshop participants.Entities:
Keywords: 3Rs; Acute systemic toxicity; Alternatives; Dermal; In silico; In vitro; Inhalation; LD(50); Oral
Mesh:
Year: 2017 PMID: 28069485 PMCID: PMC5479748 DOI: 10.1016/j.tiv.2017.01.004
Source DB: PubMed Journal: Toxicol In Vitro ISSN: 0887-2333 Impact factor: 3.500