Use of novel picolinoyl derivatization for simultaneous quantification of six corticosteroids by liquid chromatography-electrospray ionization tandem mass spectrometry
Simultaneous quantification method of six corticosteroids, cortisone, cortisol, cortexolone, corticosterone, dehydrocorticosterone and deoxycorticosterone, by LC–electrospray ionization (ESI)-MS in a positive mode using novel picolinoyl derivatization was investigated. Conversion of each corticoster...
Gespeichert in:
Veröffentlicht in: | Journal of Chromatography A 2007-11, Vol.1173 (1), p.120-128 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 128 |
---|---|
container_issue | 1 |
container_start_page | 120 |
container_title | Journal of Chromatography A |
container_volume | 1173 |
creator | Yamashita, Kouwa Takahashi, Madoka Tsukamoto, Satoshi Numazawa, Mitsuteru Okuyama, Mitsunobu Honma, Seijiro |
description | Simultaneous quantification method of six corticosteroids, cortisone, cortisol, cortexolone, corticosterone, dehydrocorticosterone and deoxycorticosterone, by LC–electrospray ionization (ESI)-MS in a positive mode using novel picolinoyl derivatization was investigated. Conversion of each corticosteroid into the corresponding picolinoyl derivative was performed by mixed anhydride method using picolinic acids and 2-methyl-6-nitrobenzoic anhydride. Derivatization proceeded smoothly to afford the corresponding 21-monopicolinoyl derivatives. Positive ion-ESI mass spectra of the picolinoyl derivatives were dominated by the appearance of [
M
+
H]
+ as base peaks. The picolinoyl derivatives provided 5–10 times higher ESI response in the LC–ESI-MS-selected reaction monitoring (SRM) when compared to those of underivatized molecules in a positive LC–ESI-MS mode. The use of the picolinoyl ester, solid-phase extraction, and deuterium labeled internal standards enabled to determine the concentrations of these corticosteroids in human saliva simultaneously by LC–ESI-MS-SRM. |
doi_str_mv | 10.1016/j.chroma.2007.10.023 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68495086</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S002196730701744X</els_id><sourcerecordid>68495086</sourcerecordid><originalsourceid>FETCH-LOGICAL-c456t-2606fae40f24c67faa28d3cf7b5dc4cc8c7f53c554e8951a2cf9a66864ef38f73</originalsourceid><addsrcrecordid>eNp9kU2O1DAQhbMAMcPADRDyBnZpnMSxkw0SGvEnjcSGWVvuSplxy4nTLqdFuBDXxE0azY6FZan81fOrekXxquK7ilfy3WEHDzGMZldzrnJpx-vmSXHNeV2VvVTNVfGc6MB5pbiqnxVXleqlaDtxXfy-J2TBsimc0LPZQfBuCqtnA0Z3Msn9yidMzIbIyI2LT2bCsBA7LmZKzjrY3rMEuZ8MQkxZgxLG4AZi-5V5d1zcwDaDKfyIZn5YS_QIKQaao1lZFvj3T5YfcGSjIWI0_2VGTHF9UTy1xhO-vNw3xf2nj99vv5R33z5_vf1wV4JoZSpryaU1KLitBUhljam7oQGr9u0AAqADZdsG2lZg17eVqcH2RspOCrRNZ1VzU7zddOcYjgtS0qMjQO-3sbXsRN_yTmZQbCDkKSii1XN0o4mrrrg-h6IPeptZn0M5V3Moue31RX_Zjzg8Nl0SycCbC2AIjLfRTODoketrwVV1Nvp-4zBv4-QwagKHE-DgYl6bHoL7v5M_LJu2Mg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68495086</pqid></control><display><type>article</type><title>Use of novel picolinoyl derivatization for simultaneous quantification of six corticosteroids by liquid chromatography-electrospray ionization tandem mass spectrometry</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Yamashita, Kouwa ; Takahashi, Madoka ; Tsukamoto, Satoshi ; Numazawa, Mitsuteru ; Okuyama, Mitsunobu ; Honma, Seijiro</creator><creatorcontrib>Yamashita, Kouwa ; Takahashi, Madoka ; Tsukamoto, Satoshi ; Numazawa, Mitsuteru ; Okuyama, Mitsunobu ; Honma, Seijiro</creatorcontrib><description>Simultaneous quantification method of six corticosteroids, cortisone, cortisol, cortexolone, corticosterone, dehydrocorticosterone and deoxycorticosterone, by LC–electrospray ionization (ESI)-MS in a positive mode using novel picolinoyl derivatization was investigated. Conversion of each corticosteroid into the corresponding picolinoyl derivative was performed by mixed anhydride method using picolinic acids and 2-methyl-6-nitrobenzoic anhydride. Derivatization proceeded smoothly to afford the corresponding 21-monopicolinoyl derivatives. Positive ion-ESI mass spectra of the picolinoyl derivatives were dominated by the appearance of [
M
+
H]
+ as base peaks. The picolinoyl derivatives provided 5–10 times higher ESI response in the LC–ESI-MS-selected reaction monitoring (SRM) when compared to those of underivatized molecules in a positive LC–ESI-MS mode. The use of the picolinoyl ester, solid-phase extraction, and deuterium labeled internal standards enabled to determine the concentrations of these corticosteroids in human saliva simultaneously by LC–ESI-MS-SRM.</description><identifier>ISSN: 0021-9673</identifier><identifier>DOI: 10.1016/j.chroma.2007.10.023</identifier><identifier>PMID: 17964584</identifier><identifier>CODEN: JOCRAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adrenal Cortex Hormones - analysis ; Adrenal Cortex Hormones - chemistry ; Analysis ; Biological and medical sciences ; Chromatography, High Pressure Liquid - methods ; Electrospray ionization ; General pharmacology ; Humans ; Liquid chromatography-tandem mass spectrometry ; Medical sciences ; Molecular Structure ; Pharmacology. Drug treatments ; Picolinic Acids - chemistry ; Picolinoyl derivative ; Reproducibility of Results ; Saliva - chemistry ; Salivary corticosteroids ; Spectrometry, Mass, Electrospray Ionization - methods ; Tandem Mass Spectrometry - methods</subject><ispartof>Journal of Chromatography A, 2007-11, Vol.1173 (1), p.120-128</ispartof><rights>2007 Elsevier B.V.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-2606fae40f24c67faa28d3cf7b5dc4cc8c7f53c554e8951a2cf9a66864ef38f73</citedby><cites>FETCH-LOGICAL-c456t-2606fae40f24c67faa28d3cf7b5dc4cc8c7f53c554e8951a2cf9a66864ef38f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S002196730701744X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19240717$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17964584$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamashita, Kouwa</creatorcontrib><creatorcontrib>Takahashi, Madoka</creatorcontrib><creatorcontrib>Tsukamoto, Satoshi</creatorcontrib><creatorcontrib>Numazawa, Mitsuteru</creatorcontrib><creatorcontrib>Okuyama, Mitsunobu</creatorcontrib><creatorcontrib>Honma, Seijiro</creatorcontrib><title>Use of novel picolinoyl derivatization for simultaneous quantification of six corticosteroids by liquid chromatography-electrospray ionization tandem mass spectrometry</title><title>Journal of Chromatography A</title><addtitle>J Chromatogr A</addtitle><description>Simultaneous quantification method of six corticosteroids, cortisone, cortisol, cortexolone, corticosterone, dehydrocorticosterone and deoxycorticosterone, by LC–electrospray ionization (ESI)-MS in a positive mode using novel picolinoyl derivatization was investigated. Conversion of each corticosteroid into the corresponding picolinoyl derivative was performed by mixed anhydride method using picolinic acids and 2-methyl-6-nitrobenzoic anhydride. Derivatization proceeded smoothly to afford the corresponding 21-monopicolinoyl derivatives. Positive ion-ESI mass spectra of the picolinoyl derivatives were dominated by the appearance of [
M
+
H]
+ as base peaks. The picolinoyl derivatives provided 5–10 times higher ESI response in the LC–ESI-MS-selected reaction monitoring (SRM) when compared to those of underivatized molecules in a positive LC–ESI-MS mode. The use of the picolinoyl ester, solid-phase extraction, and deuterium labeled internal standards enabled to determine the concentrations of these corticosteroids in human saliva simultaneously by LC–ESI-MS-SRM.</description><subject>Adrenal Cortex Hormones - analysis</subject><subject>Adrenal Cortex Hormones - chemistry</subject><subject>Analysis</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Electrospray ionization</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Liquid chromatography-tandem mass spectrometry</subject><subject>Medical sciences</subject><subject>Molecular Structure</subject><subject>Pharmacology. Drug treatments</subject><subject>Picolinic Acids - chemistry</subject><subject>Picolinoyl derivative</subject><subject>Reproducibility of Results</subject><subject>Saliva - chemistry</subject><subject>Salivary corticosteroids</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><subject>Tandem Mass Spectrometry - methods</subject><issn>0021-9673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2O1DAQhbMAMcPADRDyBnZpnMSxkw0SGvEnjcSGWVvuSplxy4nTLqdFuBDXxE0azY6FZan81fOrekXxquK7ilfy3WEHDzGMZldzrnJpx-vmSXHNeV2VvVTNVfGc6MB5pbiqnxVXleqlaDtxXfy-J2TBsimc0LPZQfBuCqtnA0Z3Msn9yidMzIbIyI2LT2bCsBA7LmZKzjrY3rMEuZ8MQkxZgxLG4AZi-5V5d1zcwDaDKfyIZn5YS_QIKQaao1lZFvj3T5YfcGSjIWI0_2VGTHF9UTy1xhO-vNw3xf2nj99vv5R33z5_vf1wV4JoZSpryaU1KLitBUhljam7oQGr9u0AAqADZdsG2lZg17eVqcH2RspOCrRNZ1VzU7zddOcYjgtS0qMjQO-3sbXsRN_yTmZQbCDkKSii1XN0o4mrrrg-h6IPeptZn0M5V3Moue31RX_Zjzg8Nl0SycCbC2AIjLfRTODoketrwVV1Nvp-4zBv4-QwagKHE-DgYl6bHoL7v5M_LJu2Mg</recordid><startdate>20071130</startdate><enddate>20071130</enddate><creator>Yamashita, Kouwa</creator><creator>Takahashi, Madoka</creator><creator>Tsukamoto, Satoshi</creator><creator>Numazawa, Mitsuteru</creator><creator>Okuyama, Mitsunobu</creator><creator>Honma, Seijiro</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>7X8</scope></search><sort><creationdate>20071130</creationdate><title>Use of novel picolinoyl derivatization for simultaneous quantification of six corticosteroids by liquid chromatography-electrospray ionization tandem mass spectrometry</title><author>Yamashita, Kouwa ; Takahashi, Madoka ; Tsukamoto, Satoshi ; Numazawa, Mitsuteru ; Okuyama, Mitsunobu ; Honma, Seijiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-2606fae40f24c67faa28d3cf7b5dc4cc8c7f53c554e8951a2cf9a66864ef38f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adrenal Cortex Hormones - analysis</topic><topic>Adrenal Cortex Hormones - chemistry</topic><topic>Analysis</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Electrospray ionization</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Liquid chromatography-tandem mass spectrometry</topic><topic>Medical sciences</topic><topic>Molecular Structure</topic><topic>Pharmacology. Drug treatments</topic><topic>Picolinic Acids - chemistry</topic><topic>Picolinoyl derivative</topic><topic>Reproducibility of Results</topic><topic>Saliva - chemistry</topic><topic>Salivary corticosteroids</topic><topic>Spectrometry, Mass, Electrospray Ionization - methods</topic><topic>Tandem Mass Spectrometry - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamashita, Kouwa</creatorcontrib><creatorcontrib>Takahashi, Madoka</creatorcontrib><creatorcontrib>Tsukamoto, Satoshi</creatorcontrib><creatorcontrib>Numazawa, Mitsuteru</creatorcontrib><creatorcontrib>Okuyama, Mitsunobu</creatorcontrib><creatorcontrib>Honma, Seijiro</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>MEDLINE - Academic</collection><jtitle>Journal of Chromatography A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamashita, Kouwa</au><au>Takahashi, Madoka</au><au>Tsukamoto, Satoshi</au><au>Numazawa, Mitsuteru</au><au>Okuyama, Mitsunobu</au><au>Honma, Seijiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of novel picolinoyl derivatization for simultaneous quantification of six corticosteroids by liquid chromatography-electrospray ionization tandem mass spectrometry</atitle><jtitle>Journal of Chromatography A</jtitle><addtitle>J Chromatogr A</addtitle><date>2007-11-30</date><risdate>2007</risdate><volume>1173</volume><issue>1</issue><spage>120</spage><epage>128</epage><pages>120-128</pages><issn>0021-9673</issn><coden>JOCRAM</coden><abstract>Simultaneous quantification method of six corticosteroids, cortisone, cortisol, cortexolone, corticosterone, dehydrocorticosterone and deoxycorticosterone, by LC–electrospray ionization (ESI)-MS in a positive mode using novel picolinoyl derivatization was investigated. Conversion of each corticosteroid into the corresponding picolinoyl derivative was performed by mixed anhydride method using picolinic acids and 2-methyl-6-nitrobenzoic anhydride. Derivatization proceeded smoothly to afford the corresponding 21-monopicolinoyl derivatives. Positive ion-ESI mass spectra of the picolinoyl derivatives were dominated by the appearance of [
M
+
H]
+ as base peaks. The picolinoyl derivatives provided 5–10 times higher ESI response in the LC–ESI-MS-selected reaction monitoring (SRM) when compared to those of underivatized molecules in a positive LC–ESI-MS mode. The use of the picolinoyl ester, solid-phase extraction, and deuterium labeled internal standards enabled to determine the concentrations of these corticosteroids in human saliva simultaneously by LC–ESI-MS-SRM.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>17964584</pmid><doi>10.1016/j.chroma.2007.10.023</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9673 |
ispartof | Journal of Chromatography A, 2007-11, Vol.1173 (1), p.120-128 |
issn | 0021-9673 |
language | eng |
recordid | cdi_proquest_miscellaneous_68495086 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Adrenal Cortex Hormones - analysis Adrenal Cortex Hormones - chemistry Analysis Biological and medical sciences Chromatography, High Pressure Liquid - methods Electrospray ionization General pharmacology Humans Liquid chromatography-tandem mass spectrometry Medical sciences Molecular Structure Pharmacology. Drug treatments Picolinic Acids - chemistry Picolinoyl derivative Reproducibility of Results Saliva - chemistry Salivary corticosteroids Spectrometry, Mass, Electrospray Ionization - methods Tandem Mass Spectrometry - methods |
title | Use of novel picolinoyl derivatization for simultaneous quantification of six corticosteroids by liquid chromatography-electrospray ionization tandem mass spectrometry |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T06%3A30%3A00IST&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=Use%20of%20novel%20picolinoyl%20derivatization%20for%20simultaneous%20quantification%20of%20six%20corticosteroids%20by%20liquid%20chromatography-electrospray%20ionization%20tandem%20mass%20spectrometry&rft.jtitle=Journal%20of%20Chromatography%20A&rft.au=Yamashita,%20Kouwa&rft.date=2007-11-30&rft.volume=1173&rft.issue=1&rft.spage=120&rft.epage=128&rft.pages=120-128&rft.issn=0021-9673&rft.coden=JOCRAM&rft_id=info:doi/10.1016/j.chroma.2007.10.023&rft_dat=%3Cproquest_cross%3E68495086%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=68495086&rft_id=info:pmid/17964584&rft_els_id=S002196730701744X&rfr_iscdi=true |