Modernizing persistence-bioaccumulation-toxicity (PBT) assessment with high throughput animal-free methods

Abstract

The assessment of persistence (P), bioaccumulation (B), and toxicity (T) of a chemical is a crucial first step at ensuring chemical safety and is a cornerstone of the European Union's chemicals regulation REACH (Registration, Evaluation, Authorization, and Restriction of Chemicals). Existing methods for PBT assessment are overly complex and cumbersome, have produced incorrect conclusions, and rely heavily on animal-intensive testing. We explore how new-approach methodologies (NAMs) can overcome the limitations of current PBT assessment. We propose two innovative hazard indicators, termed cumulative toxicity equivalents (CTE) and persistent toxicity equivalents (PTE). Together they are intended to replace existing PBT indicators and can also accommodate the emerging concept of PMT (where M stands for mobility). The proposed "toxicity equivalents" can be measured with high throughput in vitro bioassays. CTE refers to the toxic effects measured directly in any given sample, including single chemicals, substitution products, or mixtures. PTE is the equivalent measure of cumulative toxicity equivalents measured after simulated environmental degradation of the sample. With an appropriate panel of animal-free or alternative in vitro bioassays, CTE and PTE comprise key environmental and human health hazard indicators. CTE and PTE do not require analytical identification of transformation products and mixture components but instead prompt two key questions: is the chemical or mixture toxic, and is this toxicity persistent or can it be attenuated by environmental degradation? Taken together, the proposed hazard indicators CTE and PTE have the potential to integrate P, B/M and T assessment into one high-throughput experimental workflow that sidesteps the need for analytical measurements and will support the Chemicals Strategy for Sustainability of the European Union.

Keywords: Biodegradation; Hazard assessment; In vitro bioassay; Mobility; New approach methodologies (NAMs); Persistence; Toxicity.

Fig. 1

Proposed shift from the traditional PBT indicators implemented in REACH today to our vision of modern high throughput screening indicators that integrate B and M in T and have a joint measure of P and T: cumulative toxicity equivalents (CTE) and persistent toxicity equivalents (PTE). HT  high throughput, CMR carcinogenic, mutagenic, reproduction toxic, EDC endocrine disrupting compounds

Fig. 2

Theoretical application of CTE/PTE hazard indicators for comparative assessment of a chemical and its substitution products