Rachel Neita, Sophie Kiefte, Haley Adams, Grace V. Mercer, Céline M. Schneider and Lindsay S. Cahill
{"title":"19F固态核磁共振作为研究全氟烷基和多氟烷基物质在小鼠组织样品中的生物积累的工具","authors":"Rachel Neita, Sophie Kiefte, Haley Adams, Grace V. Mercer, Céline M. Schneider and Lindsay S. Cahill","doi":"10.1039/D5VA00220F","DOIUrl":null,"url":null,"abstract":"<p >Many per- and polyfluoroalkyl substances (PFAS) are known to be persistent in the environment and are associated with adverse health effects including kidney and liver disease and developmental toxicity. While PFAS are also known to have high bioaccumulation potential, whether these compounds can be detected in biological tissue using nuclear magnetic resonance (NMR) has not been established. In this study, we used <small><sup>19</sup></small>F solid-state magic angle spinning (MAS) NMR to investigate the accumulation of a legacy PFAS, perfluorooctanoic acid (PFOA), in murine tissue samples including the adult brain, intestine, kidney, liver, uterus, adipose tissue, placenta and fetal brain. Healthy pregnant (<em>n</em> = 4) and non-pregnant (<em>n</em> = 5) female CD-1 mice were exposed to 50 ppm of PFOA through their drinking water for 17 days. PFOA was detected above the limit of detection (10 μg g<small><sup>−1</sup></small>) in all of the liver samples (<em>n</em> = 9/9), 25% (<em>n</em> = 2/8) of the adipose tissue samples, 33.3% (<em>n</em> = 4/12) of the male placenta samples, and 16.7% (<em>n</em> = 2/12) of the female placenta samples. The detection of PFOA in adipose tissue challenges the current understanding about the behaviour of PFAS in the human body. These results demonstrate that <small><sup>19</sup></small>F solid-state MAS NMR is a promising tool for detection and quantification of PFAS in tissue samples and motivate further work to evaluate accumulation of unregulated, emerging PFAS that have different chain lengths and head groups.</p>","PeriodicalId":72941,"journal":{"name":"Environmental science. Advances","volume":" 10","pages":" 1612-1621"},"PeriodicalIF":4.4000,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/va/d5va00220f?page=search","citationCount":"0","resultStr":"{\"title\":\"19F solid-state nuclear magnetic resonance as a tool to study the bioaccumulation of per- and polyfluoroalkyl substances in murine tissue samples\",\"authors\":\"Rachel Neita, Sophie Kiefte, Haley Adams, Grace V. Mercer, Céline M. Schneider and Lindsay S. Cahill\",\"doi\":\"10.1039/D5VA00220F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Many per- and polyfluoroalkyl substances (PFAS) are known to be persistent in the environment and are associated with adverse health effects including kidney and liver disease and developmental toxicity. While PFAS are also known to have high bioaccumulation potential, whether these compounds can be detected in biological tissue using nuclear magnetic resonance (NMR) has not been established. In this study, we used <small><sup>19</sup></small>F solid-state magic angle spinning (MAS) NMR to investigate the accumulation of a legacy PFAS, perfluorooctanoic acid (PFOA), in murine tissue samples including the adult brain, intestine, kidney, liver, uterus, adipose tissue, placenta and fetal brain. Healthy pregnant (<em>n</em> = 4) and non-pregnant (<em>n</em> = 5) female CD-1 mice were exposed to 50 ppm of PFOA through their drinking water for 17 days. PFOA was detected above the limit of detection (10 μg g<small><sup>−1</sup></small>) in all of the liver samples (<em>n</em> = 9/9), 25% (<em>n</em> = 2/8) of the adipose tissue samples, 33.3% (<em>n</em> = 4/12) of the male placenta samples, and 16.7% (<em>n</em> = 2/12) of the female placenta samples. The detection of PFOA in adipose tissue challenges the current understanding about the behaviour of PFAS in the human body. These results demonstrate that <small><sup>19</sup></small>F solid-state MAS NMR is a promising tool for detection and quantification of PFAS in tissue samples and motivate further work to evaluate accumulation of unregulated, emerging PFAS that have different chain lengths and head groups.</p>\",\"PeriodicalId\":72941,\"journal\":{\"name\":\"Environmental science. Advances\",\"volume\":\" 10\",\"pages\":\" 1612-1621\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2025-08-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/va/d5va00220f?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental science. 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19F solid-state nuclear magnetic resonance as a tool to study the bioaccumulation of per- and polyfluoroalkyl substances in murine tissue samples
Many per- and polyfluoroalkyl substances (PFAS) are known to be persistent in the environment and are associated with adverse health effects including kidney and liver disease and developmental toxicity. While PFAS are also known to have high bioaccumulation potential, whether these compounds can be detected in biological tissue using nuclear magnetic resonance (NMR) has not been established. In this study, we used 19F solid-state magic angle spinning (MAS) NMR to investigate the accumulation of a legacy PFAS, perfluorooctanoic acid (PFOA), in murine tissue samples including the adult brain, intestine, kidney, liver, uterus, adipose tissue, placenta and fetal brain. Healthy pregnant (n = 4) and non-pregnant (n = 5) female CD-1 mice were exposed to 50 ppm of PFOA through their drinking water for 17 days. PFOA was detected above the limit of detection (10 μg g−1) in all of the liver samples (n = 9/9), 25% (n = 2/8) of the adipose tissue samples, 33.3% (n = 4/12) of the male placenta samples, and 16.7% (n = 2/12) of the female placenta samples. The detection of PFOA in adipose tissue challenges the current understanding about the behaviour of PFAS in the human body. These results demonstrate that 19F solid-state MAS NMR is a promising tool for detection and quantification of PFAS in tissue samples and motivate further work to evaluate accumulation of unregulated, emerging PFAS that have different chain lengths and head groups.