Loading…
Conjugated bisphenol S metabolites in human serum and whole blood
Studies have shown that bisphenol S (BPS) is mainly present as its conjugated metabolites in human blood. However, the distribution of conjugated BPS metabolites in different human blood matrices has not been characterized. In this study, paired human serum and whole blood samples (n = 79) were coll...
Saved in:
Published in: | Chemosphere (Oxford) 2024-06, Vol.357, p.142082-142082, Article 142082 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c236t-f604f770516df07dc89129d5acb4dc1064f4d17248249890e4a93112c1a4a6e93 |
container_end_page | 142082 |
container_issue | |
container_start_page | 142082 |
container_title | Chemosphere (Oxford) |
container_volume | 357 |
creator | Fu, Zhenling Jin, Hangbiao Mao, Weili Hu, Zefu |
description | Studies have shown that bisphenol S (BPS) is mainly present as its conjugated metabolites in human blood. However, the distribution of conjugated BPS metabolites in different human blood matrices has not been characterized. In this study, paired human serum and whole blood samples (n = 79) were collected from Chinese participants, and were measured for the occurrence of BPS and 4 BPS metabolites. BPS was detectable in 49% of human serum ( |
doi_str_mv | 10.1016/j.chemosphere.2024.142082 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3043069040</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0045653524009755</els_id><sourcerecordid>3043069040</sourcerecordid><originalsourceid>FETCH-LOGICAL-c236t-f604f770516df07dc89129d5acb4dc1064f4d17248249890e4a93112c1a4a6e93</originalsourceid><addsrcrecordid>eNqNkD1PwzAQhi0EglL4C8hsLClnx3HiEVV8SUgMwGw59oW6SuJiJyD-PakKiJHplud97-4h5JzBggGTl-uFXWEX0maFERccuFgwwaHie2TGqlJljKtqn8wARJHJIi-OyHFKa4ApXKhDcpRXUvCylDNytQz9enw1Azpa-21jH1r6RDscTB1aP2CivqersTM9TRjHjpre0Y9VaJHWbQjuhBw0pk14-j3n5OXm-nl5lz083t4vrx4yy3M5ZI0E0ZQlFEy6BkpnKzVd6Qpja-EsAyka4VjJRcWFqhSgMCpnjFtmhJGo8jm52PVuYngbMQ2688li25oew5h0DiIHqUDAhKodamNIKWKjN9F3Jn5qBnprUK_1H4N6a1DvDE7Zs-81Y92h-03-KJuA5Q7A6dl3j1En67G36HxEO2gX_D_WfAGQ-YbM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3043069040</pqid></control><display><type>article</type><title>Conjugated bisphenol S metabolites in human serum and whole blood</title><source>Elsevier</source><creator>Fu, Zhenling ; Jin, Hangbiao ; Mao, Weili ; Hu, Zefu</creator><creatorcontrib>Fu, Zhenling ; Jin, Hangbiao ; Mao, Weili ; Hu, Zefu</creatorcontrib><description>Studies have shown that bisphenol S (BPS) is mainly present as its conjugated metabolites in human blood. However, the distribution of conjugated BPS metabolites in different human blood matrices has not been characterized. In this study, paired human serum and whole blood samples (n = 79) were collected from Chinese participants, and were measured for the occurrence of BPS and 4 BPS metabolites. BPS was detectable in 49% of human serum (<LOD–1.7 ng/mL) and 78% of whole blood (<LOD–2.1 ng/mL) samples. In both human serum and whole blood, BPS-sulfate (BPS–S; 74% and 86%, respectively) and BPS-glucuronide (BPS-G; 68% and 84%, respectively) had higher detection frequency than BPS. Consistently, BPS-S was the predominant BPS metabolite in human serum (mean 0.39 ng/mL) and whole blood (0.41 ng/mL), significantly higher than BPS-G (mean 0.13 and 0.13 ng/mL, respectively). This is contrary to the data from controlled oral exposure studies on model animals and humans, in which BPS-G was the dominant BPS metabolite in serum. BPS-S (mean ± SD, 0.99 ± 0.35) had the highest partitioning coefficient between human serum and whole blood, followed by BPS-G (0.89 ± 0.27) and BPS (0.81 ± 0.28), suggesting their preferential accumulation in the red blood cell fraction. These results represent the first human data on conjugated BPS metabolites in paired human serum and whole blood, which help to elucidate of the occurrence of conjugated BPS metabolites in humans.
[Display omitted]
•BPS was detected in 49% of human serum and 78% of whole blood samples.•BPS-S was the predominant BPS metabolite in both human serum and whole blood.•BPS-S had a higher mean blood partitioning coefficient than BPS-G and BPS.•This study first examines partitioning of conjugated BPS metabolites in human blood.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2024.142082</identifier><identifier>PMID: 38642776</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>BPS-G ; BPS-S ; Distribution ; Serum ; Whole blood</subject><ispartof>Chemosphere (Oxford), 2024-06, Vol.357, p.142082-142082, Article 142082</ispartof><rights>2024 Elsevier Ltd</rights><rights>Copyright © 2024. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c236t-f604f770516df07dc89129d5acb4dc1064f4d17248249890e4a93112c1a4a6e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38642776$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fu, Zhenling</creatorcontrib><creatorcontrib>Jin, Hangbiao</creatorcontrib><creatorcontrib>Mao, Weili</creatorcontrib><creatorcontrib>Hu, Zefu</creatorcontrib><title>Conjugated bisphenol S metabolites in human serum and whole blood</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>Studies have shown that bisphenol S (BPS) is mainly present as its conjugated metabolites in human blood. However, the distribution of conjugated BPS metabolites in different human blood matrices has not been characterized. In this study, paired human serum and whole blood samples (n = 79) were collected from Chinese participants, and were measured for the occurrence of BPS and 4 BPS metabolites. BPS was detectable in 49% of human serum (<LOD–1.7 ng/mL) and 78% of whole blood (<LOD–2.1 ng/mL) samples. In both human serum and whole blood, BPS-sulfate (BPS–S; 74% and 86%, respectively) and BPS-glucuronide (BPS-G; 68% and 84%, respectively) had higher detection frequency than BPS. Consistently, BPS-S was the predominant BPS metabolite in human serum (mean 0.39 ng/mL) and whole blood (0.41 ng/mL), significantly higher than BPS-G (mean 0.13 and 0.13 ng/mL, respectively). This is contrary to the data from controlled oral exposure studies on model animals and humans, in which BPS-G was the dominant BPS metabolite in serum. BPS-S (mean ± SD, 0.99 ± 0.35) had the highest partitioning coefficient between human serum and whole blood, followed by BPS-G (0.89 ± 0.27) and BPS (0.81 ± 0.28), suggesting their preferential accumulation in the red blood cell fraction. These results represent the first human data on conjugated BPS metabolites in paired human serum and whole blood, which help to elucidate of the occurrence of conjugated BPS metabolites in humans.
[Display omitted]
•BPS was detected in 49% of human serum and 78% of whole blood samples.•BPS-S was the predominant BPS metabolite in both human serum and whole blood.•BPS-S had a higher mean blood partitioning coefficient than BPS-G and BPS.•This study first examines partitioning of conjugated BPS metabolites in human blood.</description><subject>BPS-G</subject><subject>BPS-S</subject><subject>Distribution</subject><subject>Serum</subject><subject>Whole blood</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqNkD1PwzAQhi0EglL4C8hsLClnx3HiEVV8SUgMwGw59oW6SuJiJyD-PakKiJHplud97-4h5JzBggGTl-uFXWEX0maFERccuFgwwaHie2TGqlJljKtqn8wARJHJIi-OyHFKa4ApXKhDcpRXUvCylDNytQz9enw1Azpa-21jH1r6RDscTB1aP2CivqersTM9TRjHjpre0Y9VaJHWbQjuhBw0pk14-j3n5OXm-nl5lz083t4vrx4yy3M5ZI0E0ZQlFEy6BkpnKzVd6Qpja-EsAyka4VjJRcWFqhSgMCpnjFtmhJGo8jm52PVuYngbMQ2688li25oew5h0DiIHqUDAhKodamNIKWKjN9F3Jn5qBnprUK_1H4N6a1DvDE7Zs-81Y92h-03-KJuA5Q7A6dl3j1En67G36HxEO2gX_D_WfAGQ-YbM</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Fu, Zhenling</creator><creator>Jin, Hangbiao</creator><creator>Mao, Weili</creator><creator>Hu, Zefu</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20240601</creationdate><title>Conjugated bisphenol S metabolites in human serum and whole blood</title><author>Fu, Zhenling ; Jin, Hangbiao ; Mao, Weili ; Hu, Zefu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c236t-f604f770516df07dc89129d5acb4dc1064f4d17248249890e4a93112c1a4a6e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>BPS-G</topic><topic>BPS-S</topic><topic>Distribution</topic><topic>Serum</topic><topic>Whole blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fu, Zhenling</creatorcontrib><creatorcontrib>Jin, Hangbiao</creatorcontrib><creatorcontrib>Mao, Weili</creatorcontrib><creatorcontrib>Hu, Zefu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fu, Zhenling</au><au>Jin, Hangbiao</au><au>Mao, Weili</au><au>Hu, Zefu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conjugated bisphenol S metabolites in human serum and whole blood</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2024-06-01</date><risdate>2024</risdate><volume>357</volume><spage>142082</spage><epage>142082</epage><pages>142082-142082</pages><artnum>142082</artnum><issn>0045-6535</issn><eissn>1879-1298</eissn><abstract>Studies have shown that bisphenol S (BPS) is mainly present as its conjugated metabolites in human blood. However, the distribution of conjugated BPS metabolites in different human blood matrices has not been characterized. In this study, paired human serum and whole blood samples (n = 79) were collected from Chinese participants, and were measured for the occurrence of BPS and 4 BPS metabolites. BPS was detectable in 49% of human serum (<LOD–1.7 ng/mL) and 78% of whole blood (<LOD–2.1 ng/mL) samples. In both human serum and whole blood, BPS-sulfate (BPS–S; 74% and 86%, respectively) and BPS-glucuronide (BPS-G; 68% and 84%, respectively) had higher detection frequency than BPS. Consistently, BPS-S was the predominant BPS metabolite in human serum (mean 0.39 ng/mL) and whole blood (0.41 ng/mL), significantly higher than BPS-G (mean 0.13 and 0.13 ng/mL, respectively). This is contrary to the data from controlled oral exposure studies on model animals and humans, in which BPS-G was the dominant BPS metabolite in serum. BPS-S (mean ± SD, 0.99 ± 0.35) had the highest partitioning coefficient between human serum and whole blood, followed by BPS-G (0.89 ± 0.27) and BPS (0.81 ± 0.28), suggesting their preferential accumulation in the red blood cell fraction. These results represent the first human data on conjugated BPS metabolites in paired human serum and whole blood, which help to elucidate of the occurrence of conjugated BPS metabolites in humans.
[Display omitted]
•BPS was detected in 49% of human serum and 78% of whole blood samples.•BPS-S was the predominant BPS metabolite in both human serum and whole blood.•BPS-S had a higher mean blood partitioning coefficient than BPS-G and BPS.•This study first examines partitioning of conjugated BPS metabolites in human blood.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>38642776</pmid><doi>10.1016/j.chemosphere.2024.142082</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0045-6535 |
ispartof | Chemosphere (Oxford), 2024-06, Vol.357, p.142082-142082, Article 142082 |
issn | 0045-6535 1879-1298 |
language | eng |
recordid | cdi_proquest_miscellaneous_3043069040 |
source | Elsevier |
subjects | BPS-G BPS-S Distribution Serum Whole blood |
title | Conjugated bisphenol S metabolites in human serum and whole blood |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T02%3A02%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Conjugated%20bisphenol%20S%20metabolites%20in%20human%20serum%20and%20whole%20blood&rft.jtitle=Chemosphere%20(Oxford)&rft.au=Fu,%20Zhenling&rft.date=2024-06-01&rft.volume=357&rft.spage=142082&rft.epage=142082&rft.pages=142082-142082&rft.artnum=142082&rft.issn=0045-6535&rft.eissn=1879-1298&rft_id=info:doi/10.1016/j.chemosphere.2024.142082&rft_dat=%3Cproquest_cross%3E3043069040%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c236t-f604f770516df07dc89129d5acb4dc1064f4d17248249890e4a93112c1a4a6e93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3043069040&rft_id=info:pmid/38642776&rfr_iscdi=true |