Utility of In Vitro Bioactivity as a Lower Bound Estimate of In Vivo Adverse Effect Levels and in Risk-Based Prioritization

Friedman, KP; Gagne, M; Loo, L; Karamertzanis, P; Netzeva, T; Sobanski, T; Franzosa, JA; Richard, A; Lougee, RR; Gissi, A; Lee, J; Angrish, M; Dorne, J; Foster, S; Raffaele, K; Bahadori, T; Gwinn, MR; Lambert, J; Whelan, M; Rasenberg, M; Barton-Maclaren, T; Thomas, RS

HERO ID

7376323

Reference Type

Journal Article

Year

2020

Language

English

PMID

31532525

HERO ID 7376323
In Press No
Year 2020
Title Utility of In Vitro Bioactivity as a Lower Bound Estimate of In Vivo Adverse Effect Levels and in Risk-Based Prioritization
Authors Friedman, KP; Gagne, M; Loo, L; Karamertzanis, P; Netzeva, T; Sobanski, T; Franzosa, JA; Richard, A; Lougee, RR; Gissi, A; Lee, J; Angrish, M; Dorne, J; Foster, S; Raffaele, K; Bahadori, T; Gwinn, MR; Lambert, J; Whelan, M; Rasenberg, M; Barton-Maclaren, T; Thomas, RS
Journal Toxicological Sciences
Volume 173
Issue 1
Page Numbers 202-225
Abstract Use of high-throughput, in vitro bioactivity data in setting a point-of-departure (POD) has the potential to accelerate the pace of human health safety evaluation by informing screening-level assessments. The primary objective of this work was to compare PODs based on high-throughput predictions of bioactivity, exposure predictions, and traditional hazard information for 448 chemicals. PODs derived from new approach methodologies (NAMs) were obtained for this comparison using the 50th (PODNAM, 50) and the 95th (PODNAM, 95) percentile credible interval estimates for the steady-state plasma concentration used in in vitro to in vivo extrapolation of administered equivalent doses. Of the 448 substances, 89% had a PODNAM, 95 that was less than the traditional POD (PODtraditional) value. For the 48 substances for which PODtraditional < PODNAM, 95, the PODNAM and PODtraditional were typically within a factor of 10 of each other, and there was an enrichment of chemical structural features associated with organophosphate and carbamate insecticides. When PODtraditional < PODNAM, 95, it did not appear to result from an enrichment of PODtraditional based on a particular study type (eg, developmental, reproductive, and chronic studies). Bioactivity:exposure ratios, useful for identification of substances with potential priority, demonstrated that high-throughput exposure predictions were greater than the PODNAM, 95 for 11 substances. When compared with threshold of toxicological concern (TTC) values, the PODNAM, 95 was greater than the corresponding TTC value 90% of the time. This work demonstrates the feasibility, and continuing challenges, of using in vitro bioactivity as a protective estimate of POD in screening-level assessments via a case study.
Doi 10.1093/toxsci/kfz201
Pmid 31532525
Wosid WOS:000508116400018
Url https://academic.oup.com/toxsci/article/173/1/202/5571376
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword high-throughput screening; high-throughput toxicokinetics; threshold of toxicological concern (TTC); point-of-departure (POD); new approach methodologies