DART isotope dilution high resolution mass spectrometry and <sup>19</sup> F-NMR detection of fluorotelomeric alcohols in hydrolyzed food contact paper

Fluorotelomer-based acrylate polymers and surfactants used to grease-proof food contact paper (FCP) are potential sources of dietary exposure to perfluoroalkyl substances (PFAS). Food contact substances (FCS) containing polyfluorinated long-chains (≥C8) were voluntarily removed by their manufacturers from the U.S. market in 2011 due to health concerns and largely replaced with FCSs containing short-chain (≤C7) PFAS. In 2020, FDA findings of potential biopersistence of 6:2 FTOH (CF<sub>3</sub>(CF<sub>2</sub>)<sub>5</sub>CH<sub>2</sub>CH<sub>2</sub>OH) similarly prompted an additional voluntarily phase-out of FCSs containing 6:2 FTOH by their manufacturers that was completed by the end of 2023. To monitor the phase-out process, a screening method was developed to detect FCPs containing ester-linked polyfluorinated pendant chains. Direct Analysis in Real Time-Isotope Dilution-High Resolution Mass Spectrometry (DART-ID-HRMS) enabled rapid semi-quantitative detection of 6:2 FTOH in FCP saponification reaction headspace without requiring sample concentration or chromatography. <sup>19</sup>F-NMR analysis confirmed 6:2 FTOH pendant chain identity and detection dependence on saponification. The speed and specificity of this approach arise from ester saponification in the presence of stable isotopically labeled 6:2 FTOH; high FTOH differential volatility relative to nonfluorinated matrix, and the facile production of FTOH gas-phase anions (<i>e</i>.<i>g</i>., [M + O<sub>2</sub>]<sup>·-</sup>, [M-H + CO<sub>2</sub>]<sup>-</sup>) under ambient ionization conditions. The efficiency of this simple workflow makes it well-suited for monitoring the phase-out of FCS containing ester-linked polyfluorinated chains from the U.S. marketplace.

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Publication Details

Journal
Food Additives & Contaminants Part A
Published
2024-11-11
DOI
https://doi.org/10.1080/19440049.2024.2423868
Citations
1
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
0.25
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article

DART isotope dilution high resolution mass spectrometry and 19 F-NMR detection of fluorotelomeric alcohols in hydrolyzed food contact paper

Sharon Koh-Fallet, Peter F. Scholl, Luke K. Ackerman, Clark D. Ridge et al.
1 citations
Food Additives & Contaminants Part A
Per- and polyfluoroalkyl substances research
0.25
article

DART isotope dilution high resolution mass spectrometry and 19 F-NMR detection of fluorotelomeric alcohols in hydrolyzed food contact paper

Sharon Koh-Fallet, Peter F. Scholl, Luke K. Ackerman, Clark D. Ridge, Katherine Carlos
article en
1 citations

Abstract

Fluorotelomer-based acrylate polymers and surfactants used to grease-proof food contact paper (FCP) are potential sources of dietary exposure to perfluoroalkyl substances (PFAS). Food contact substances (FCS) containing polyfluorinated long-chains (≥C8) were voluntarily removed by their manufacturers from the U.S. market in 2011 due to health concerns and largely replaced with FCSs containing short-chain (≤C7) PFAS. In 2020, FDA findings of potential biopersistence of 6:2 FTOH (CF<sub>3</sub>(CF<sub>2</sub>)<sub>5</sub>CH<sub>2</sub>CH<sub>2</sub>OH) similarly prompted an additional voluntarily phase-out of FCSs containing 6:2 FTOH by their manufacturers that was completed by the end of 2023. To monitor the phase-out process, a screening method was developed to detect FCPs containing ester-linked polyfluorinated pendant chains. Direct Analysis in Real Time-Isotope Dilution-High Resolution Mass Spectrometry (DART-ID-HRMS) enabled rapid semi-quantitative detection of 6:2 FTOH in FCP saponification reaction headspace without requiring sample concentration or chromatography. <sup>19</sup>F-NMR analysis confirmed 6:2 FTOH pendant chain identity and detection dependence on saponification. The speed and specificity of this approach arise from ester saponification in the presence of stable isotopically labeled 6:2 FTOH; high FTOH differential volatility relative to nonfluorinated matrix, and the facile production of FTOH gas-phase anions (<i>e</i>.<i>g</i>., [M + O<sub>2</sub>]<sup>·-</sup>, [M-H + CO<sub>2</sub>]<sup>-</sup>) under ambient ionization conditions. The efficiency of this simple workflow makes it well-suited for monitoring the phase-out of FCS containing ester-linked polyfluorinated chains from the U.S. marketplace.

Food Additives & Contaminants Part AVol. 42(1)
Center for Food Safety and Applied Nutrition (US), United States Food and Drug Administration (US), Food Safety and Inspection Service (US)
Zero hunger
Openalex Percentile: Top 42%
Per- and polyfluoroalkyl substances research
0.25
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