GHS additivity formula: A true replacement method for acute systemic toxicity testing of agrochemical formulations

被引:19
作者
Corvaro, M. [1 ]
Gehen, S. [2 ]
Andrews, K. [1 ]
Chatfield, R. [1 ]
Arasti, C. [1 ]
Mehta, J. [1 ]
机构
[1] Dow AgroSci Ltd, European Dev Ctr, Milton Pk, Abingdon OX14 4RN, Oxon, England
[2] Dow AgroSci LLC, 9330 Zionsville Rd, Indianapolis, IN 46268 USA
关键词
Acute toxicity; GHS; Theory of additivity; Replacement; Global policy change; 3Rs; DRUG-DELIVERY;
D O I
10.1016/j.yrtph.2016.10.007
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Acute systemic (oral, dermal, inhalation) toxicity testing of agrochemical formulations (end-use products) is mainly needed for Classification and Labelling (C&L) and definition of personal protection equipment (PPE). A retrospective analysis of 225 formulations with available in vivo data showed that: A) LD50/LC50 values were above limit doses in <20.2% via oral route but only in <1% and <2.4% of cases via dermal and inhalation route, respectively; B) for each formulation the acute oral toxicity is always equal or greater than the Acute Toxicity Estimate (ATE) via the other two routes; C) the GHS (Global Harmonised System) computational method based on ATE, currently of limited acceptance, has very high accuracy and specificity for prediction of agrochemical mixture toxicity according to the internationally established classification thresholds. By integrating this evidence, an exposure- and data-based waiving strategy is proposed to determine classification and adequate PPE and to ensure only triggered animal testing is used. Safety characterisation above 2000 mg/kg body weight or 1.0 mg/L air should not be recommended, based on the agrochemical exposure scenarios. The global implementation of these tools would allow a remarkable reduction (up to 95%) in in vivo testing, often inducing lethality and/or severe toxicity, for agrochemical formulations. (C) 2016 Published by Elsevier Inc.
引用
收藏
页码:99 / 110
页数:12
相关论文
共 46 条
  • [1] [Anonymous], OECD GUID TEST CHEM
  • [2] [Anonymous], LAB REV MAN
  • [3] [Anonymous], 2009, ICH HARMONISED TRIPA
  • [4] [Anonymous], OECD SER TEST ASS
  • [5] [Anonymous], FIN GUID PROC EV IMP
  • [6] APMVA, 2015, REG AGR PROD DAT GUI
  • [7] Acute Toxicity Prediction in Multiple Species by Leveraging Mechanistic ToxCast Mitochondrial Inhibition Data and Simulation of Oral Bioavailability
    Bhhatarai, Barun
    Wilson, Daniel M.
    Bartels, Michael J.
    Chaudhuri, Shubhra
    Price, Paul S.
    Carney, Edward W.
    [J]. TOXICOLOGICAL SCIENCES, 2015, 147 (02) : 386 - 396
  • [8] CIB, 2014, GUID DOC TOX REG PES
  • [9] CLI, 2008, TECHN MON
  • [10] DESCRIBING THE VALIDITY OF CARCINOGEN SCREENING-TESTS
    COOPER, JA
    SARACCI, R
    COLE, P
    [J]. BRITISH JOURNAL OF CANCER, 1979, 39 (01) : 87 - 89