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        <datestamp>2026-09-29T07:04:09Z</datestamp>
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        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Multimatrix
Biomonitoring
and Transplacental Transfer
of Legacy and Emerging PFAS in Korean Pregnant Women</dc:title>
          <dc:creator>Hyewon Shin (7037438)</dc:creator>
          <dc:creator>Na-Youn Park (4798590)</dc:creator>
          <dc:creator>Young Ah Lee (7305380)</dc:creator>
          <dc:creator>Jong Kwan Jun (7309832)</dc:creator>
          <dc:creator>Kyungho Choi (513597)</dc:creator>
          <dc:creator>Sun Wook Cho (8911283)</dc:creator>
          <dc:creator>Younglim Kho (1928767)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Mathematical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Hematology</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Plant Biology</dc:subject>
          <dc:subject>fetal growth indicators</dc:subject>
          <dc:subject>2 dipap showed</dc:subject>
          <dc:subject>alternative pfas 9cl</dc:subject>
          <dc:subject>specific exposure profiles</dc:subject>
          <dc:subject>measured 33 legacy</dc:subject>
          <dc:subject>bound pfas detected</dc:subject>
          <dc:subject>regulated legacy pfas</dc:subject>
          <dc:subject>specific pfas detection</dc:subject>
          <dc:subject>consistently detected</dc:subject>
          <dc:subject>emerging pfas</dc:subject>
          <dc:subject>transplacental transfer</dc:subject>
          <dc:subject>pregnancy rather</dc:subject>
          <dc:subject>population level</dc:subject>
          <dc:subject>polyfluoroalkyl substances</dc:subject>
          <dc:subject>physicochemical properties</dc:subject>
          <dc:subject>neonatal factors</dc:subject>
          <dc:subject>n &lt;/</dc:subject>
          <dc:subject>multimatrix biomonitoring</dc:subject>
          <dc:subject>findings suggest</dc:subject>
          <dc:subject>elimination pathways</dc:subject>
          <dc:subject>distribution patterns</dc:subject>
          <dc:subject>cord serum</dc:subject>
          <dc:subject>blood matrices</dc:subject>
          <dc:description>Maternal–fetal exposure to
per- and polyfluoroalkyl
substances
(PFAS) cannot be adequately characterized using single biological
matrices because compound-specific distribution patterns vary according
to physicochemical properties and elimination pathways. We measured
33 legacy, precursor, and emerging PFAS in maternal serum, plasma,
urine, and cord serum from Korean singleton pregnancies (&lt;i&gt;n&lt;/i&gt; = 151) to characterize matrix-specific exposure profiles, transplacental
transfer, and associations with maternal and neonatal factors. Matrix-specific
detection patterns distinguished predominantly protein-bound PFAS
detected in blood matrices from short-chain, renally excreted PFAS
prevalent in urine at the population level. Notably, the precursor
6:2 diPAP showed a relatively high estimated maternal–cord
concentration ratio, whereas the alternative PFAS 9Cl-PF3ONS was consistently
detected in maternal blood and cord serum, suggesting compound-specific
distribution patterns compared with regulated legacy PFAS. Associations
with fetal growth indicators were modest, matrix- and sex-specific,
and interpreted as exploratory. Overall, these findings suggest that
multimatrix biomonitoring can reveal matrix-specific PFAS detection
and distribution patterns that may not be captured by single-matrix
approaches. However, maternal–cord comparisons should be interpreted
cautiously because maternal samples were collected during pregnancy
rather than at delivery.</dc:description>
          <dc:date>2026-09-29T00:00:00Z</dc:date>
          <dc:type>Text</dc:type>
          <dc:type>Journal contribution</dc:type>
          <dc:identifier>10.1021/acs.est.6c08434.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/journal_contribution/Multimatrix_Biomonitoring_and_Transplacental_Transfer_of_Legacy_and_Emerging_PFAS_in_Korean_Pregnant_Women/34021731</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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