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Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro

Archives of Toxicology 2021 21 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Mawien Karaca, Mawien Karaca, Benjamin Christian Fischer, Christian Tobias Willenbockel, Christian Tobias Willenbockel, Tewes Tralau, Philip Marx‐Stoelting, Denise Bloch

Summary

Researchers found that surfactants added to agricultural pesticide formulations significantly increase the toxicity of the active ingredients by making it easier for them to cross cell membranes and blocking the body's normal chemical removal pathways. This suggests that pesticide safety testing should evaluate the complete formulation — not just the active ingredient — since the added chemicals can amplify harm in ways not currently captured by regulators.

Currently, the authorisation process for plant protection products (PPPs) relies on the testing of acute and topological toxicity only. Contrastingly, the evaluation of active substances includes a more comprehensive set of toxicity studies. Nevertheless, mixture effects of active ingredients and co-formulants may result in increased toxicity. Therefore, we investigated effects of surface active co-formulants on the toxicity of two PPPs focussing on qualitative and quantitative toxicokinetic effects on absorption and secretion. The respective products are based on the active substances abamectin and fluroxypyr-meptyl and were tested for cytotoxicity in the presence or absence of the corresponding surfactants and co-formulants using Caco-2 cells. In addition, the effect of co-formulants on increased cellular permeation was quantified using LC-MS/MS, while potential kinetic mixture effects were addressed by fluorescence anisotropy measurements and ATPase assays. The results show that surface active co-formulants significantly increase the cytotoxicity of the investigated PPPs, leading to more than additive mixture effects. Moreover, analytical investigations show higher efflux ratios of both active substances and the metabolite fluroxypyr upon combination with certain concentrations of the surfactants. The results further point to a significant and concentration-dependent inhibition of Pgp transporters by most of the surfactants as well as to increased membrane fluidity. Altogether, these findings strongly support the hypothesis that surfactants contribute to increased cytotoxicity of PPPs and do so by increasing the bioavailability of the respective active substances.

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