Martin Allen, Joignant Alena N, Farrell Matt, Planchart Antonio, Muddiman David C
FTMS Laboratory for Human Health Research, Department of Chemistry, North Carolina State University, Raleigh, North Carolina, USA.
Department of Biological Sciences, North Carolina State University, Raleigh, North Carolina, USA.
J Mass Spectrom. 2025 Feb;60(2):e5112. doi: 10.1002/jms.5112.
Perfluoroalkyl and polyfluoroalkyl substances (PFAS) are a class of emerging contaminants that have been in use industrially since the 1940s. Their long-term and extensive commercial use has led to their ubiquitous presence in the environment. The ability to measure the bioconcentration and distribution of PFAS in the tissue of aquatic organisms helps elucidate the persistence of PFAS as well as environmental impacts. Traditional analysis by LC-MS/MS can measure total PFAS concentrations within an organism but cannot provide comprehensive spatial information regarding PFAS concentrations within the organism. In the current study, we used infrared matrix-assisted laser desorption electrospray ionization (IR-MALDESI) to determine the limit of detection (LOD) of several PFAS utilizing a commercial standard mix spotted on mouse liver tissue. The traditional ice matrix and an alternative matrix, 1,8-bis (tetramethylguanidino)naphthalene (TMGN), were explored when determining the limits of detection for various PFAS by IR-MALDESI. The ice matrix alone resulted in a higher response than the combination of TMGN and ice. The resulting LOD for perfluorooctane sulfonic acid (PFOS) on a per voxel basis was 0.16 fmol/voxel. For comparison, zebrafish that were exposed to perfluorooctanoic acid (PFOA), PFOS, and perfluorohexanesulfonic acid (PFHxS) at different concentrations were homogenized, and PFAS were extracted by solid-liquid extraction, purified by solid phase extraction, and analyzed by LC-MS/MS to determine the level of bioaccumulation in the zebrafish. PFOS resulted in the highest level of bioaccumulation (731.9 μg/kg, or 234.2 fg/voxel). A zebrafish that had been exposed to a PFAS mixture of PFOA (250 ng/L), PFOS (250 ng/L), and PFHxS (125 ng/L) was cryosectioned and analyzed by IR-MALDESI. Images could not be generated as the accumulation of PFAS in the sectioned tissue was below detection limit of the technique.
全氟烷基和多氟烷基物质(PFAS)是一类自20世纪40年代以来一直在工业上使用的新兴污染物。它们长期广泛的商业用途导致其在环境中普遍存在。测量PFAS在水生生物组织中的生物富集和分布能力有助于阐明PFAS的持久性以及环境影响。传统的液相色谱-串联质谱(LC-MS/MS)分析可以测量生物体中的总PFAS浓度,但无法提供关于生物体中PFAS浓度的全面空间信息。在本研究中,我们使用红外基质辅助激光解吸电喷雾电离(IR-MALDESI),通过在小鼠肝脏组织上点样的商业标准混合物来确定几种PFAS的检测限(LOD)。在通过IR-MALDESI确定各种PFAS的检测限时,探索了传统的冰基质和另一种基质1,8-双(四甲基胍基)萘(TMGN)。单独的冰基质比TMGN和冰的组合产生更高的响应。基于每个体素,全氟辛烷磺酸(PFOS)的所得检测限为0.16 fmol/体素。作为比较,将暴露于不同浓度全氟辛酸(PFOA)、PFOS和全氟己烷磺酸(PFHxS)的斑马鱼匀浆,通过固液萃取提取PFAS,通过固相萃取纯化,并通过LC-MS/MS分析以确定斑马鱼中的生物累积水平。PFOS导致最高水平的生物累积(731.9μg/kg,或234.2 fg/体素)。将暴露于PFOA(250 ng/L)、PFOS(250 ng/L)和PFHxS(125 ng/L)的PFAS混合物的斑马鱼进行冷冻切片,并通过IR-MALDESI分析。由于切片组织中PFAS的积累低于该技术的检测限,因此无法生成图像。