Differential coulometric oxidation following post column-switching high pressure liquid chromatography for fluorescence measurement of unmetabolized folic acid in human plasma
•Coulometric oxidation can generate fluorescent products for enhanced sensitivity.•Differential oxidation near the analyte half-potential increases specificity.•The specificity of EC/FL detection permits simple sample prep without SPE.•Coulometric EC/FL allows subnanomolar detection of plasma unmeta...
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description | •Coulometric oxidation can generate fluorescent products for enhanced sensitivity.•Differential oxidation near the analyte half-potential increases specificity.•The specificity of EC/FL detection permits simple sample prep without SPE.•Coulometric EC/FL allows subnanomolar detection of plasma unmetabolized folic acid.•The coulometric EC/FL method was validated by comparison to SPE/LC/MS/MS.
Although many countries have fortified their grain supplies with folic acid (FA) to decrease the incidence of neural tube defects, others have not due to concerns that this synthetic folate might have some adverse effects. Persistent unmetabolized FA has been found even in plasma from fasted subjects. To facilitate measurement of low levels of folic acid in human plasma, post-column coulometric oxidative cleavage was used to convert poorly fluorescent FA into a highly fluorescent compound determined to be 6-formyl-pterin. To minimize sample work-up and maximize recovery, column-switching HPLC transferred a window of eluate containing the FA from the first column (C8) onto a second column (phenyl-hexyl). The pH of two mobile phases were adjusted to be above and then below a pK of the FA α-carboxyl group, thus promoting separation from compounds coeluting from the C8-column. This permitted sample preparation using only a simple high recovery protein precipitation. Definitive identification of FA in human plasma was accomplished by duplicate injections of sample with the electrochemical voltage set above and below its half-potential. The LOD (S/N=3) was 0.10nM. The intra- and inter-assay CV's were 2.3% and 5%, respectively. Comparison of these results with those obtained by HPLC/MS/MS with stable isotope internal standard showed a slope of 1.00±0.019. This simple, sensitive, and repeatable assay facilitates a more thorough investigation of the response of various human populations to folic acid intake. Post-column differential coulometric electrochemistry can expand the variety of compounds amenable to fluorescence detection. |
doi_str_mv | 10.1016/j.chroma.2013.09.027 |
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Although many countries have fortified their grain supplies with folic acid (FA) to decrease the incidence of neural tube defects, others have not due to concerns that this synthetic folate might have some adverse effects. Persistent unmetabolized FA has been found even in plasma from fasted subjects. To facilitate measurement of low levels of folic acid in human plasma, post-column coulometric oxidative cleavage was used to convert poorly fluorescent FA into a highly fluorescent compound determined to be 6-formyl-pterin. To minimize sample work-up and maximize recovery, column-switching HPLC transferred a window of eluate containing the FA from the first column (C8) onto a second column (phenyl-hexyl). The pH of two mobile phases were adjusted to be above and then below a pK of the FA α-carboxyl group, thus promoting separation from compounds coeluting from the C8-column. This permitted sample preparation using only a simple high recovery protein precipitation. Definitive identification of FA in human plasma was accomplished by duplicate injections of sample with the electrochemical voltage set above and below its half-potential. The LOD (S/N=3) was 0.10nM. The intra- and inter-assay CV's were 2.3% and 5%, respectively. Comparison of these results with those obtained by HPLC/MS/MS with stable isotope internal standard showed a slope of 1.00±0.019. This simple, sensitive, and repeatable assay facilitates a more thorough investigation of the response of various human populations to folic acid intake. Post-column differential coulometric electrochemistry can expand the variety of compounds amenable to fluorescence detection.</description><identifier>ISSN: 0021-9673</identifier><identifier>EISSN: 1873-3778</identifier><identifier>DOI: 10.1016/j.chroma.2013.09.027</identifier><identifier>PMID: 24094483</identifier><identifier>CODEN: JOCRAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Analysis ; Biological and medical sciences ; Chromatography, High Pressure Liquid - methods ; Colorimetry - methods ; Column-switching HPLC ; Coulometers ; Coulometric electrochemical oxidation ; Fluorescence ; Fluorescence detection ; Folate ; Folic acid ; Folic Acid - blood ; Folic Acid - chemistry ; General pharmacology ; High performance liquid chromatography ; Human ; Humans ; Limit of Detection ; Liquid chromatography ; Medical sciences ; Oxidation-Reduction ; Pharmacology. Drug treatments ; Recovery ; Reproducibility of Results ; Reproduction ; Spectrometry, Fluorescence - methods ; Unmetabolized folic acid</subject><ispartof>Journal of Chromatography A, 2013-11, Vol.1315, p.86-91</ispartof><rights>2013 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-68541887d1495ad51a1b41fc0337e46784233068c6667b973d87f99248f54a63</citedby><cites>FETCH-LOGICAL-c458t-68541887d1495ad51a1b41fc0337e46784233068c6667b973d87f99248f54a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021967313014556$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27868622$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24094483$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bailey, Steven W.</creatorcontrib><creatorcontrib>Ayling, June E.</creatorcontrib><title>Differential coulometric oxidation following post column-switching high pressure liquid chromatography for fluorescence measurement of unmetabolized folic acid in human plasma</title><title>Journal of Chromatography A</title><addtitle>J Chromatogr A</addtitle><description>•Coulometric oxidation can generate fluorescent products for enhanced sensitivity.•Differential oxidation near the analyte half-potential increases specificity.•The specificity of EC/FL detection permits simple sample prep without SPE.•Coulometric EC/FL allows subnanomolar detection of plasma unmetabolized folic acid.•The coulometric EC/FL method was validated by comparison to SPE/LC/MS/MS.
Although many countries have fortified their grain supplies with folic acid (FA) to decrease the incidence of neural tube defects, others have not due to concerns that this synthetic folate might have some adverse effects. Persistent unmetabolized FA has been found even in plasma from fasted subjects. To facilitate measurement of low levels of folic acid in human plasma, post-column coulometric oxidative cleavage was used to convert poorly fluorescent FA into a highly fluorescent compound determined to be 6-formyl-pterin. To minimize sample work-up and maximize recovery, column-switching HPLC transferred a window of eluate containing the FA from the first column (C8) onto a second column (phenyl-hexyl). The pH of two mobile phases were adjusted to be above and then below a pK of the FA α-carboxyl group, thus promoting separation from compounds coeluting from the C8-column. This permitted sample preparation using only a simple high recovery protein precipitation. Definitive identification of FA in human plasma was accomplished by duplicate injections of sample with the electrochemical voltage set above and below its half-potential. The LOD (S/N=3) was 0.10nM. The intra- and inter-assay CV's were 2.3% and 5%, respectively. Comparison of these results with those obtained by HPLC/MS/MS with stable isotope internal standard showed a slope of 1.00±0.019. This simple, sensitive, and repeatable assay facilitates a more thorough investigation of the response of various human populations to folic acid intake. Post-column differential coulometric electrochemistry can expand the variety of compounds amenable to fluorescence detection.</description><subject>Analysis</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Colorimetry - methods</subject><subject>Column-switching HPLC</subject><subject>Coulometers</subject><subject>Coulometric electrochemical oxidation</subject><subject>Fluorescence</subject><subject>Fluorescence detection</subject><subject>Folate</subject><subject>Folic acid</subject><subject>Folic Acid - blood</subject><subject>Folic Acid - chemistry</subject><subject>General pharmacology</subject><subject>High performance liquid chromatography</subject><subject>Human</subject><subject>Humans</subject><subject>Limit of Detection</subject><subject>Liquid chromatography</subject><subject>Medical sciences</subject><subject>Oxidation-Reduction</subject><subject>Pharmacology. Drug treatments</subject><subject>Recovery</subject><subject>Reproducibility of Results</subject><subject>Reproduction</subject><subject>Spectrometry, Fluorescence - methods</subject><subject>Unmetabolized folic acid</subject><issn>0021-9673</issn><issn>1873-3778</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2KFDEUhQtRnHb0DUSyEdxUm79KUhtBxl8YcDP7kE4lXWlSSU1ScWZ8KV_RFNXqTlcXLt8953BP07xEcI8gYm9Pez2mOKk9hojsYb-HmD9qdkhw0hLOxeNmByFGbc84uWie5XyCEHHI8dPmAlPYUyrIrvn5wVlrkgmLUx7oWHyczJKcBvHeDWpxMQAbvY93LhzBHPNSIV-m0OY7t-hx3Y7uOII5mZxLMsC72-IGsIVb4jGpeXyoGglYX2KltAnagMmoFZ-qM4gWlFBt1SF698MMq2NNoHTVcQGMZVIBzF7lST1vnljls3lxnpfNzaePN1df2utvn79evb9uNe3E0jLRUSQEHxDtOzV0SKEDRVZDQrihjAuKCYFMaMYYP_ScDILbvsdU2I4qRi6bN5vsnOJtMXmRk6vBvVfBxJIlEhBSzCFF_0cZ6SDGHYEVpRuqU8w5GSvn5CaVHiSCci1VnuT2N7mWKmEva6n17NXZoRwmM_w5-t1iBV6fAZW18japoF3-y3HBBMO4cu82ztTPfXcmyazd2sbgktGLHKL7d5JfKQDFnQ</recordid><startdate>20131108</startdate><enddate>20131108</enddate><creator>Bailey, Steven W.</creator><creator>Ayling, June E.</creator><general>Elsevier B.V</general><general>Elsevier</general><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>7QH</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20131108</creationdate><title>Differential coulometric oxidation following post column-switching high pressure liquid chromatography for fluorescence measurement of unmetabolized folic acid in human plasma</title><author>Bailey, Steven W. ; Ayling, June E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-68541887d1495ad51a1b41fc0337e46784233068c6667b973d87f99248f54a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analysis</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Colorimetry - methods</topic><topic>Column-switching HPLC</topic><topic>Coulometers</topic><topic>Coulometric electrochemical oxidation</topic><topic>Fluorescence</topic><topic>Fluorescence detection</topic><topic>Folate</topic><topic>Folic acid</topic><topic>Folic Acid - blood</topic><topic>Folic Acid - chemistry</topic><topic>General pharmacology</topic><topic>High performance liquid chromatography</topic><topic>Human</topic><topic>Humans</topic><topic>Limit of Detection</topic><topic>Liquid chromatography</topic><topic>Medical sciences</topic><topic>Oxidation-Reduction</topic><topic>Pharmacology. Drug treatments</topic><topic>Recovery</topic><topic>Reproducibility of Results</topic><topic>Reproduction</topic><topic>Spectrometry, Fluorescence - methods</topic><topic>Unmetabolized folic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bailey, Steven W.</creatorcontrib><creatorcontrib>Ayling, June E.</creatorcontrib><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>Aqualine</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of Chromatography A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bailey, Steven W.</au><au>Ayling, June E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential coulometric oxidation following post column-switching high pressure liquid chromatography for fluorescence measurement of unmetabolized folic acid in human plasma</atitle><jtitle>Journal of Chromatography A</jtitle><addtitle>J Chromatogr A</addtitle><date>2013-11-08</date><risdate>2013</risdate><volume>1315</volume><spage>86</spage><epage>91</epage><pages>86-91</pages><issn>0021-9673</issn><eissn>1873-3778</eissn><coden>JOCRAM</coden><abstract>•Coulometric oxidation can generate fluorescent products for enhanced sensitivity.•Differential oxidation near the analyte half-potential increases specificity.•The specificity of EC/FL detection permits simple sample prep without SPE.•Coulometric EC/FL allows subnanomolar detection of plasma unmetabolized folic acid.•The coulometric EC/FL method was validated by comparison to SPE/LC/MS/MS.
Although many countries have fortified their grain supplies with folic acid (FA) to decrease the incidence of neural tube defects, others have not due to concerns that this synthetic folate might have some adverse effects. Persistent unmetabolized FA has been found even in plasma from fasted subjects. To facilitate measurement of low levels of folic acid in human plasma, post-column coulometric oxidative cleavage was used to convert poorly fluorescent FA into a highly fluorescent compound determined to be 6-formyl-pterin. To minimize sample work-up and maximize recovery, column-switching HPLC transferred a window of eluate containing the FA from the first column (C8) onto a second column (phenyl-hexyl). The pH of two mobile phases were adjusted to be above and then below a pK of the FA α-carboxyl group, thus promoting separation from compounds coeluting from the C8-column. This permitted sample preparation using only a simple high recovery protein precipitation. Definitive identification of FA in human plasma was accomplished by duplicate injections of sample with the electrochemical voltage set above and below its half-potential. The LOD (S/N=3) was 0.10nM. The intra- and inter-assay CV's were 2.3% and 5%, respectively. Comparison of these results with those obtained by HPLC/MS/MS with stable isotope internal standard showed a slope of 1.00±0.019. This simple, sensitive, and repeatable assay facilitates a more thorough investigation of the response of various human populations to folic acid intake. Post-column differential coulometric electrochemistry can expand the variety of compounds amenable to fluorescence detection.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>24094483</pmid><doi>10.1016/j.chroma.2013.09.027</doi><tpages>6</tpages></addata></record> |
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subjects | Analysis Biological and medical sciences Chromatography, High Pressure Liquid - methods Colorimetry - methods Column-switching HPLC Coulometers Coulometric electrochemical oxidation Fluorescence Fluorescence detection Folate Folic acid Folic Acid - blood Folic Acid - chemistry General pharmacology High performance liquid chromatography Human Humans Limit of Detection Liquid chromatography Medical sciences Oxidation-Reduction Pharmacology. Drug treatments Recovery Reproducibility of Results Reproduction Spectrometry, Fluorescence - methods Unmetabolized folic acid |
title | Differential coulometric oxidation following post column-switching high pressure liquid chromatography for fluorescence measurement of unmetabolized folic acid in human plasma |
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