AI Article Synopsis

  • Fluorine is both essential and potentially toxic to humans and animals, necessitating reliable detection methods in animal feed.
  • The study measured fluorine using a fluoride-selective electrode (ISE) and a new high-resolution spectrometry method, facing challenges like chemical interferences and reagent contamination.
  • Results from both methods were consistent, confirming accuracy in measuring fluorine in its fluoride form, with findings indicating that fluoride levels in most samples were below established safety thresholds.

Article Abstract

Fluorine, depending on its concentration and chemical form, is essential or toxic to humans and animals. Therefore, it is crucial to be able to determine it reliably. In this study, fluorine was determined in animal feed after extraction with HCl (gastric juice simulation). The standard potentiometric method with a fluoride-selective electrode (ISE) and newly developed high-resolution continuum source graphite furnace molecular absorption spectrometry (HR-CS GFMAS) method was applied. Feed samples turned out to be a challenge for HR-CS GFMAS. Chemical interferences (formation of competing molecules, CaF, GaCl, and GaP, instead of the target GaF molecule) and spectral effects (including a phosphorous molecule spectrum and atomic lines) were identified. An additional difficulty was caused by reagent contamination with F and memory effects. Difficulties were eliminated/reduced. The quality of ISE analysis was multi-directionally verified (including comprehensive proficiency testing). A risk of inaccuracy at low F concentration, where the calibration relationship is nonlinear, was investigated. The results of both methods were consistent, which confirms the accuracy of the methods and informs that the extracted fluorine is in fluoride form. The results of extensive ISE tests conducted in Poland in 2021-2023 have shown that, in most cases, the fluoride content is significantly lower than the threshold values.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11204728PMC
http://dx.doi.org/10.3390/ma17122812DOI Listing

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