1,2-Dicarbonyl Compounds in Commonly Consumed Foods
1,2-Dicarbonyl compounds, formed from carbohydrates during thermal processing in the course of caramelization and Maillard reactions, are intensively discussed as precursors for advanced glycation endproducts in foods and in vivo. To obtain information about the uptake of individual compounds with c...
Gespeichert in:
Veröffentlicht in: | Journal of agricultural and food chemistry 2012-07, Vol.60 (28), p.7071-7079 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 7079 |
---|---|
container_issue | 28 |
container_start_page | 7071 |
container_title | Journal of agricultural and food chemistry |
container_volume | 60 |
creator | Degen, Julia Hellwig, Michael Henle, Thomas |
description | 1,2-Dicarbonyl compounds, formed from carbohydrates during thermal processing in the course of caramelization and Maillard reactions, are intensively discussed as precursors for advanced glycation endproducts in foods and in vivo. To obtain information about the uptake of individual compounds with commonly consumed foods, a comprehensive analysis of the content of 3-deoxyglucosone (3-DG), 3-deoxygalactosone (3-DGal), and methylglyoxal (MGO) together with 5-hydroxymethylfurfural (HMF) in 173 food items like bakery products, pasta, nonalcoholic and alcoholic beverages, sweet spreads, and condiments was performed. Following suitable cleanup procedures, 1,2-dicarbonyl compounds were quantitated after derivatization with o-phenylenediamine via RP-HPLC with UV detection. 3-DG proved to be the predominant 1,2-dicarbonyl compound with concentrations up to 410 mg/L in fruit juices, 2622 mg/L in balsamic vinegars, and 385 mg/kg in cookies, thus exceeding the corresponding concentrations of HMF. 3-DGal was found to be of relevance in many foods even in the absence of galactose. MGO was only of minor quantitative importance in all foods studied, except for manuka honey. Dietary intake was estimated to range between 20 and 160 mg/day for 3-DG and 5 and 20 mg/day for MGO, respectively. |
doi_str_mv | 10.1021/jf301306g |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1027038353</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1027038353</sourcerecordid><originalsourceid>FETCH-LOGICAL-a369t-5cfdc9982f3e04049b648ffa3d334a851f566223042ccf16d509d08e017afee53</originalsourceid><addsrcrecordid>eNpt0MtKAzEUBuAgitbqwhfQbgQFR8_JbTJLqVcouNCuhzSTlCkzk5p0Fn17U1rrxlUS8vFzzk_IBcI9AsWHhWOADOT8gAxQUMgEojokA0ifmRIST8hpjAsAUCKHY3JCaU65KnBAGN7R7Kk2Osx8t25GY98ufd9VcVR3m0fru2adLl3sW1uNXryv4hk5crqJ9nx3Dsn05flr_JZNPl7fx4-TTDNZrDJhXGWKQlHHLHDgxUxy5ZxmFWNcK4FOSEkpA06NcSgrAUUFygLm2lkr2JDcbHOXwX_3Nq7Kto7GNo3urO9jmXbPgSkmWKK3W2qCjzFYVy5D3eqwTmjjsNx3lOzlLrafpZ328reUBK53QEejGxd0Z-r45yRKlvPNfFdb57Qv9TwkM_2kgBwAsYBc_SVpE8uF70OX-vpnpB9dS4Cl</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1027038353</pqid></control><display><type>article</type><title>1,2-Dicarbonyl Compounds in Commonly Consumed Foods</title><source>MEDLINE</source><source>ACS Publications</source><creator>Degen, Julia ; Hellwig, Michael ; Henle, Thomas</creator><creatorcontrib>Degen, Julia ; Hellwig, Michael ; Henle, Thomas</creatorcontrib><description>1,2-Dicarbonyl compounds, formed from carbohydrates during thermal processing in the course of caramelization and Maillard reactions, are intensively discussed as precursors for advanced glycation endproducts in foods and in vivo. To obtain information about the uptake of individual compounds with commonly consumed foods, a comprehensive analysis of the content of 3-deoxyglucosone (3-DG), 3-deoxygalactosone (3-DGal), and methylglyoxal (MGO) together with 5-hydroxymethylfurfural (HMF) in 173 food items like bakery products, pasta, nonalcoholic and alcoholic beverages, sweet spreads, and condiments was performed. Following suitable cleanup procedures, 1,2-dicarbonyl compounds were quantitated after derivatization with o-phenylenediamine via RP-HPLC with UV detection. 3-DG proved to be the predominant 1,2-dicarbonyl compound with concentrations up to 410 mg/L in fruit juices, 2622 mg/L in balsamic vinegars, and 385 mg/kg in cookies, thus exceeding the corresponding concentrations of HMF. 3-DGal was found to be of relevance in many foods even in the absence of galactose. MGO was only of minor quantitative importance in all foods studied, except for manuka honey. Dietary intake was estimated to range between 20 and 160 mg/day for 3-DG and 5 and 20 mg/day for MGO, respectively.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf301306g</identifier><identifier>PMID: 22724891</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>alcoholic beverages ; Biological and medical sciences ; Chromatography, High Pressure Liquid ; condiments ; cookies ; Deoxyglucose - analogs & derivatives ; Deoxyglucose - analysis ; derivatization ; Diet ; Food Analysis ; Food industries ; fruit juices ; Fundamental and applied biological sciences. Psychology ; Furaldehyde - analogs & derivatives ; Furaldehyde - analysis ; galactose ; Galactose - analogs & derivatives ; Galactose - analysis ; glycation ; honey ; hydroxymethylfurfural ; pasta ; Pyruvaldehyde - analysis ; reversed-phase high performance liquid chromatography ; vinegars</subject><ispartof>Journal of agricultural and food chemistry, 2012-07, Vol.60 (28), p.7071-7079</ispartof><rights>Copyright © 2012 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a369t-5cfdc9982f3e04049b648ffa3d334a851f566223042ccf16d509d08e017afee53</citedby><cites>FETCH-LOGICAL-a369t-5cfdc9982f3e04049b648ffa3d334a851f566223042ccf16d509d08e017afee53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf301306g$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf301306g$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2764,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26163745$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22724891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Degen, Julia</creatorcontrib><creatorcontrib>Hellwig, Michael</creatorcontrib><creatorcontrib>Henle, Thomas</creatorcontrib><title>1,2-Dicarbonyl Compounds in Commonly Consumed Foods</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>1,2-Dicarbonyl compounds, formed from carbohydrates during thermal processing in the course of caramelization and Maillard reactions, are intensively discussed as precursors for advanced glycation endproducts in foods and in vivo. To obtain information about the uptake of individual compounds with commonly consumed foods, a comprehensive analysis of the content of 3-deoxyglucosone (3-DG), 3-deoxygalactosone (3-DGal), and methylglyoxal (MGO) together with 5-hydroxymethylfurfural (HMF) in 173 food items like bakery products, pasta, nonalcoholic and alcoholic beverages, sweet spreads, and condiments was performed. Following suitable cleanup procedures, 1,2-dicarbonyl compounds were quantitated after derivatization with o-phenylenediamine via RP-HPLC with UV detection. 3-DG proved to be the predominant 1,2-dicarbonyl compound with concentrations up to 410 mg/L in fruit juices, 2622 mg/L in balsamic vinegars, and 385 mg/kg in cookies, thus exceeding the corresponding concentrations of HMF. 3-DGal was found to be of relevance in many foods even in the absence of galactose. MGO was only of minor quantitative importance in all foods studied, except for manuka honey. Dietary intake was estimated to range between 20 and 160 mg/day for 3-DG and 5 and 20 mg/day for MGO, respectively.</description><subject>alcoholic beverages</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid</subject><subject>condiments</subject><subject>cookies</subject><subject>Deoxyglucose - analogs & derivatives</subject><subject>Deoxyglucose - analysis</subject><subject>derivatization</subject><subject>Diet</subject><subject>Food Analysis</subject><subject>Food industries</subject><subject>fruit juices</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Furaldehyde - analogs & derivatives</subject><subject>Furaldehyde - analysis</subject><subject>galactose</subject><subject>Galactose - analogs & derivatives</subject><subject>Galactose - analysis</subject><subject>glycation</subject><subject>honey</subject><subject>hydroxymethylfurfural</subject><subject>pasta</subject><subject>Pyruvaldehyde - analysis</subject><subject>reversed-phase high performance liquid chromatography</subject><subject>vinegars</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0MtKAzEUBuAgitbqwhfQbgQFR8_JbTJLqVcouNCuhzSTlCkzk5p0Fn17U1rrxlUS8vFzzk_IBcI9AsWHhWOADOT8gAxQUMgEojokA0ifmRIST8hpjAsAUCKHY3JCaU65KnBAGN7R7Kk2Osx8t25GY98ufd9VcVR3m0fru2adLl3sW1uNXryv4hk5crqJ9nx3Dsn05flr_JZNPl7fx4-TTDNZrDJhXGWKQlHHLHDgxUxy5ZxmFWNcK4FOSEkpA06NcSgrAUUFygLm2lkr2JDcbHOXwX_3Nq7Kto7GNo3urO9jmXbPgSkmWKK3W2qCjzFYVy5D3eqwTmjjsNx3lOzlLrafpZ328reUBK53QEejGxd0Z-r45yRKlvPNfFdb57Qv9TwkM_2kgBwAsYBc_SVpE8uF70OX-vpnpB9dS4Cl</recordid><startdate>20120718</startdate><enddate>20120718</enddate><creator>Degen, Julia</creator><creator>Hellwig, Michael</creator><creator>Henle, Thomas</creator><general>American Chemical Society</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120718</creationdate><title>1,2-Dicarbonyl Compounds in Commonly Consumed Foods</title><author>Degen, Julia ; Hellwig, Michael ; Henle, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a369t-5cfdc9982f3e04049b648ffa3d334a851f566223042ccf16d509d08e017afee53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>alcoholic beverages</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid</topic><topic>condiments</topic><topic>cookies</topic><topic>Deoxyglucose - analogs & derivatives</topic><topic>Deoxyglucose - analysis</topic><topic>derivatization</topic><topic>Diet</topic><topic>Food Analysis</topic><topic>Food industries</topic><topic>fruit juices</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Furaldehyde - analogs & derivatives</topic><topic>Furaldehyde - analysis</topic><topic>galactose</topic><topic>Galactose - analogs & derivatives</topic><topic>Galactose - analysis</topic><topic>glycation</topic><topic>honey</topic><topic>hydroxymethylfurfural</topic><topic>pasta</topic><topic>Pyruvaldehyde - analysis</topic><topic>reversed-phase high performance liquid chromatography</topic><topic>vinegars</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Degen, Julia</creatorcontrib><creatorcontrib>Hellwig, Michael</creatorcontrib><creatorcontrib>Henle, Thomas</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Degen, Julia</au><au>Hellwig, Michael</au><au>Henle, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1,2-Dicarbonyl Compounds in Commonly Consumed Foods</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2012-07-18</date><risdate>2012</risdate><volume>60</volume><issue>28</issue><spage>7071</spage><epage>7079</epage><pages>7071-7079</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>1,2-Dicarbonyl compounds, formed from carbohydrates during thermal processing in the course of caramelization and Maillard reactions, are intensively discussed as precursors for advanced glycation endproducts in foods and in vivo. To obtain information about the uptake of individual compounds with commonly consumed foods, a comprehensive analysis of the content of 3-deoxyglucosone (3-DG), 3-deoxygalactosone (3-DGal), and methylglyoxal (MGO) together with 5-hydroxymethylfurfural (HMF) in 173 food items like bakery products, pasta, nonalcoholic and alcoholic beverages, sweet spreads, and condiments was performed. Following suitable cleanup procedures, 1,2-dicarbonyl compounds were quantitated after derivatization with o-phenylenediamine via RP-HPLC with UV detection. 3-DG proved to be the predominant 1,2-dicarbonyl compound with concentrations up to 410 mg/L in fruit juices, 2622 mg/L in balsamic vinegars, and 385 mg/kg in cookies, thus exceeding the corresponding concentrations of HMF. 3-DGal was found to be of relevance in many foods even in the absence of galactose. MGO was only of minor quantitative importance in all foods studied, except for manuka honey. Dietary intake was estimated to range between 20 and 160 mg/day for 3-DG and 5 and 20 mg/day for MGO, respectively.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>22724891</pmid><doi>10.1021/jf301306g</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-8561 |
ispartof | Journal of agricultural and food chemistry, 2012-07, Vol.60 (28), p.7071-7079 |
issn | 0021-8561 1520-5118 |
language | eng |
recordid | cdi_proquest_miscellaneous_1027038353 |
source | MEDLINE; ACS Publications |
subjects | alcoholic beverages Biological and medical sciences Chromatography, High Pressure Liquid condiments cookies Deoxyglucose - analogs & derivatives Deoxyglucose - analysis derivatization Diet Food Analysis Food industries fruit juices Fundamental and applied biological sciences. Psychology Furaldehyde - analogs & derivatives Furaldehyde - analysis galactose Galactose - analogs & derivatives Galactose - analysis glycation honey hydroxymethylfurfural pasta Pyruvaldehyde - analysis reversed-phase high performance liquid chromatography vinegars |
title | 1,2-Dicarbonyl Compounds in Commonly Consumed Foods |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T23%3A07%3A26IST&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=1,2-Dicarbonyl%20Compounds%20in%20Commonly%20Consumed%20Foods&rft.jtitle=Journal%20of%20agricultural%20and%20food%20chemistry&rft.au=Degen,%20Julia&rft.date=2012-07-18&rft.volume=60&rft.issue=28&rft.spage=7071&rft.epage=7079&rft.pages=7071-7079&rft.issn=0021-8561&rft.eissn=1520-5118&rft.coden=JAFCAU&rft_id=info:doi/10.1021/jf301306g&rft_dat=%3Cproquest_cross%3E1027038353%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1027038353&rft_id=info:pmid/22724891&rfr_iscdi=true |