Research on Influence of Formulation Type on Stability and Acute Toxicity of Fluazinam Formulations
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Abstract
Fluazinam is a contact fungicide widely used for the control of various plant diseases due to its broad spectrum of activity and multi-site mode of action. However, its extremely low water solubility and potential environmental toxicity require careful formulation design to ensure effective performance and safety during practical application. In this study, fluazinam was formulated into three different formulation types, including suspension concentrate (SC), wettable powder (WP), and water-dispersible granule (WDG), at laboratory scale. Selected co-formulants were applied to improve formulation performance and stability. The prepared formulations were evaluated for physicochemical stability, including active ingredient content and suspensibility, under room temperature and accelerated storage conditions. Acute toxicity was assessed according to OECD guidelines and classified based on GHS 2019 criteria. Although all formulations exhibited low acute toxicity, formulation-dependent differences in toxicological responses were observed. In particular, the SC formulation showed milder and more rapidly reversible effects in inhalation and irritation studies. These results demonstrate that formulation design influences practical exposure characteristics and toxicological behavior beyond the intrinsic properties of the active ingredient.
Keywords
Fluazinam, formulation type, suspension concentrate, wettable powder, water-dispersible granule, stability, toxicity.
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References
[2] C. D. S. Tomlin, Ed., The Pesticide Manual: A World Compendium, 14th ed., British Crop Production Council, Alton, Hampshire, UK, 2006, pp. 1–1344.
[3] World Health Organization, Fluazinam: Pesticide Residues in Food – Evaluations, WHO Press, Geneva, Switzerland, Aug. 2008, pp. 1–64.
[4] H. Mollet and A. Grubenmann, Formulation technology: Emulsions, suspensions, solid forms, Wiley-VCH, Weinheim, Germany, Dec. 2000, pp. 1–433. https://doi.org/10.1002/9783527612925
[5] European Food Safety Authority (EFSA), Conclusion regarding the peer review of the pesticide risk assessment of the active substance fluazinam, European Food Safety Authority, 6(7):137r, Jul. 2008.
https://doi.org/10.2903/j.efsa.2008.137r
[6] K. Nagy, R. C. Duca, S. Lovas, M. Creta, P. T. J. Scheepers, L. Godderis, and B. Ádám, "Systematic review of comparative studies assessing the toxicity of pesticide active ingredients and their product formulations," Environmental Research, vol. 181, p. 108926, Feb. 2020. https://doi.org/10.1016/j.envres.2019.108926
[7] A. Knowles, Recent developments of safer formulations of agrochemicals, Environmentalist, vol. 28, pp. 35–44, Mar. 2008. https://doi.org/10.1007/s10669-007-9045-4
[8] S. Mukhopadhyay, J. Mandal, B. Kanrar, D. Chatterjee, A. Bhattacharyya, and S. Majumder, Degradation and residue dynamics of fluazinam in diverse Indian soil types and water pH conditions: A comprehensive study using kinetic models, Frontiers in Environmental Science, vol. 12, Jun. 2024, Art. no. 1394847. https://doi.org/10.3389/fenvs.2024.1394847
[9] Food and Agriculture Organization (FAO), Fluazinam: FAO Specifications and Evaluations for Agricultural Pesticides, Rome, Italy: FAO, 2025, https://www.fao.org/agriculture/crops/thematic-sitemap/theme/pests/jmps/en, [Online]. Available: FAO Open Knowledge, Accessed on: Feb. 26, 2026.
[10] T. F. Tadros, Suspension Concentrates: Theory and Practice, Wiley-VCH, Weinheim, Germany,
pp. 1–328, 2004.
[11] D. A. Knowles, Chemistry and technology of agrochemical formulations, Kluwer Academic Publishers, Dordrecht, The Netherlands, pp. 1–356, 1998. https://doi.org/10.1007/978-94-011-4956-3
[12] T. F. Tadros, Formulation of Disperse Systems: Science and Technology. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. https://doi.org/10.1002/9783527678297
[13] Collaborative International Pesticides Analytical Council, CIPAC Handbook, vol. F, CIPAC, Harpenden, Hertfordshire, UK, 2016, pp. 1–642.
[14] Organisation for Economic Co-operation and Development, OECD Guidelines for the Testing of Chemicals, Section 4: Health Effects, OECD Publishing, Paris, France, 2019.
https://www.oecd.org/chemicalsafety/testing/
[15] Organisation for Economic Co-operation and Development, Test No. 403: Acute Inhalation Toxicity, OECD Publishing, Paris, France, 2018. https://doi.org/10.1787/9789264070608-en
[16] Organisation for Economic Co-operation and Development, Test no. 404: Acute dermal irritation/corrosion, OECD Publishing, Paris, France, Jul. 2015. https://doi.org/10.1787/9789264242678-en
[17] Organisation for Economic Co-operation and Development, Test no. 405: Acute eye Irritation/Corrosion, OECD Publishing, Paris, France, 2017.
https://doi.org/10.1787/9789264185333-en
[18] Organisation for Economic Co-operation and Development, Test no. 406: Skin sensitisation, OECD Publishing, Paris, France, 2018. https://doi.org/10.1787/9789264070660-en
[19] United Nations, Globally Harmonized System of Classification and Labelling of Chemicals (GHS), 7th rev. ed., United Nations, New York, NY, USA, 2017, pp. 1–534.