Empirical evaluation of sufficient similarity in dose—Response for environmental risk assessment of chemical mixtures

2008 ◽  
Vol 13 (3) ◽  
pp. 313-333 ◽  
Author(s):  
Leanna G. Stork ◽  
Chris Gennings ◽  
Walter H. Carter ◽  
Linda K. Teuschler ◽  
Edward W. Carney
2018 ◽  
Author(s):  
Virgile Baudrot ◽  
Sandrine Charles

ABSTRACTProviding reliable environmental quality standards (EQSs) is a challenging issue in environmental risk assessment (ERA). These EQSs are derived from toxicity endpoints estimated from dose-response models to identify and characterize the environmental hazard of chemical compounds such as those released by human activities. These toxicity endpoints include the classicalx% effect/lethal concentrations at a specific timet(EC/LC(x,t)) and the new multiplication factors applied to environmental exposure profiles leading tox% effect reduction at a specific timet(MF(x,t), or denotedLP(x,t) by the EFSA). However, classical dose-response models used to estimate toxicity endpoints have some weaknesses, such as their dependency on observation time points, which are likely to differ between species (e.g., experiment duration). Furthermore, real-world exposure profiles are rarely constant over time, which makes the use of classical dose-response models difficult and compromises the derivation ofMF(x,t). When dealing with survival or immobility toxicity test data, these issues can be overcome with the use of the general unified threshold model of survival (GUTS), a toxicokinetics-toxicodynamics (TKTD) model that provides an explicit framework to analyse both time- and concentration-dependent data sets as well as obtain a mechanistic derivation ofEC/LC(x,t) andMF(x,t) regardless of x and at any time t of interest. In addition, the assessment of a risk is inherently built upon probability distributions, such that the next critical step for ERA is to characterize the uncertainties of toxicity endpoints and, consequently, those of EQSs. With this perspective, we investigated the use of a Bayesian framework to obtain the uncertainties from the calibration process and to propagate them to model predictions, includingLC(x,t) andMF(x,t) derivations. We also explored the mathematical properties ofLC(x,t) andMF(x,t) as well as the impact of different experimental designs to provide some recommendations for a robust derivation of toxicity endpoints leading to reliable EQSs: avoid computingLC(x,t) andMF(x,t) for extremexvalues (0 or 100%), where uncertainty is maximal; computeMF(x,t) after a long period of time to take depuration time into account and test survival under few correlated and uncorrelated pulses of the contaminant in terms of depuration.


2015 ◽  
Vol 15 (3) ◽  
pp. 73-88 ◽  
Author(s):  
Vladimir Kirilloviсh Shitikov ◽  
Vera Alexandrovna Terekhova ◽  
Beksultan Almazovich Uzbekov ◽  
Kamila Asylbekovna Kydralieva ◽  
Bermet Merlisovna Khudaibergenova

Apidologie ◽  
2003 ◽  
Vol 34 (2) ◽  
pp. 139-145 ◽  
Author(s):  
Henrik F. Brodsgaard ◽  
Camilla J. Brodsgaard ◽  
Henrik Hansen ◽  
G�bor L. L�vei

2008 ◽  
Vol 15 (5) ◽  
pp. 394-404 ◽  
Author(s):  
Stefan Scholz ◽  
Stephan Fischer ◽  
Ulrike Gündel ◽  
Eberhard Küster ◽  
Till Luckenbach ◽  
...  

2007 ◽  
Vol preprint (2009) ◽  
pp. 1
Author(s):  
Heike Schmitt ◽  
Tatiana Boucard ◽  
Jeanne Garric ◽  
John Jensen ◽  
Joanne Parrott ◽  
...  

2016 ◽  
Vol 88 (8) ◽  
pp. 713-830
Author(s):  
John H. Duffus ◽  
Michael Schwenk ◽  
Douglas M. Templeton

Abstract The primary objective of this glossary is to give clear definitions for those who contribute to studies relevant to these disciplines, or who must interpret them, but are not themselves reproductive physiologists or physicians. This applies especially to chemists who need to understand the literature of reproductive and teratogenic effects of substances without recourse to a multiplicity of other glossaries or dictionaries. The glossary includes terms related to basic and clinical reproductive biology and teratogenesis, insofar as they are necessary for a self-contained document, particularly terms related to diagnosing, measuring, and understanding the effects of substances on the embryo, the fetus, and on the male and female reproductive systems. The glossary consists of about 1200 primary alphabetical entries and includes Annexes of common abbreviations and examples of chemicals with known effects on human reproduction and development. The authors hope that toxicologists, pharmacologists, medical practitioners, risk assessors, and regulatory authorities are among the groups who will find this glossary helpful, in addition to chemists. In particular, the glossary should facilitate the worldwide use of chemical terminology in relation to occupational and environmental risk assessment.


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