TY - JOUR
T1 - New Approach Methodologies (NAMs) for Human-Relevant Biokinetics Predictions
T2 - Meeting the Paradigm Shift in Toxicology Towards an Animal-Free Chemical Risk Assessment
AU - Punt, Ans
AU - Bouwmeester, Hans
AU - Blaauboer, Bas J.
AU - Coecke, Sandra
AU - Hakkert, Betty
AU - Hendriks, Delilah F.G.
AU - Jennings, Paul
AU - Kramer, Nynke I.
AU - Neuhoff, Sibylle
AU - Masereeuw, Rosalinde
AU - Paini, Alicia
AU - Peijnenburg, Ad A.C.M.
AU - Rooseboom, Martijn
AU - Shuler, Michael L.
AU - Sorrell, Ian
AU - Spee, Bart
AU - Strikwold, Marije
AU - van der Meer, Andries D.
AU - van der Zande, Meike
AU - Vinken, Mathieu
AU - Yang, Huan
AU - Bos, Peter M.J.
AU - Heringa, Minne B.
N1 - Publisher Copyright:
© The Authors, 2020.
PY - 2020
Y1 - 2020
N2 - For almost fifteen years, the availability and regulatory acceptance of new approach methodologies (NAMs) to assess the absorption, distribution, metabolism and excretion (ADME/biokinetics) in chemical risk evaluations are a bottleneck. To enhance the field, a team of 24 experts from science, industry, and regulatory bodies, including new generation toxicologists, met at the Lorentz Centre in Leiden, The Netherlands. A range of possibilities for the use of NAMs for biokinetics in risk evaluations were formulated (for example to define species differences and human variation or to perform quantitative in vitro-in vivo extrapolations). To increase the regulatory use and acceptance of NAMs for biokinetics for these ADME considerations within risk evaluations, the development of test guidelines (protocols) and of overarching guidance documents is considered a critical step. To this end, a need for an expert group on biokinetics within the Organisation of Economic Cooperation and Development (OECD) to supervise this process was formulated. The workshop discussions revealed that method development is still required, particularly to adequately capture transporter mediated processes as well as to obtain cell models that reflect the physiology and kinetic characteristics of relevant organs. Developments in the fields of stem cells, organoids and organ-on-a-chip models provide promising tools to meet these research needs in the future.
AB - For almost fifteen years, the availability and regulatory acceptance of new approach methodologies (NAMs) to assess the absorption, distribution, metabolism and excretion (ADME/biokinetics) in chemical risk evaluations are a bottleneck. To enhance the field, a team of 24 experts from science, industry, and regulatory bodies, including new generation toxicologists, met at the Lorentz Centre in Leiden, The Netherlands. A range of possibilities for the use of NAMs for biokinetics in risk evaluations were formulated (for example to define species differences and human variation or to perform quantitative in vitro-in vivo extrapolations). To increase the regulatory use and acceptance of NAMs for biokinetics for these ADME considerations within risk evaluations, the development of test guidelines (protocols) and of overarching guidance documents is considered a critical step. To this end, a need for an expert group on biokinetics within the Organisation of Economic Cooperation and Development (OECD) to supervise this process was formulated. The workshop discussions revealed that method development is still required, particularly to adequately capture transporter mediated processes as well as to obtain cell models that reflect the physiology and kinetic characteristics of relevant organs. Developments in the fields of stem cells, organoids and organ-on-a-chip models provide promising tools to meet these research needs in the future.
UR - http://www.scopus.com/inward/record.url?scp=85092380042&partnerID=8YFLogxK
U2 - 10.14573/altex.2003242
DO - 10.14573/altex.2003242
M3 - Article
C2 - 32521035
AN - SCOPUS:85092380042
SN - 1868-596X
VL - 37
SP - 607
EP - 622
JO - Altex
JF - Altex
IS - 4
ER -