Metabolites identification of Huo Luo Xiao Ling Dan in rat urine by UPLC coupled with electrospray ionization time-of-flight mass spectrometry
Huo Luo Xiao Ling Dan (HLXLD), a Chinese herbal formula, is used in folk medicine for the treatment of arthritis and other chronic inflammatory diseases. However, the in vivo integrated metabolism of its multiple components remains unknown. In this paper, an ultra‐performance liquid chromatography c...
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Veröffentlicht in: | Biomedical chromatography 2016-03, Vol.30 (3), p.396-409 |
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description | Huo Luo Xiao Ling Dan (HLXLD), a Chinese herbal formula, is used in folk medicine for the treatment of arthritis and other chronic inflammatory diseases. However, the in vivo integrated metabolism of its multiple components remains unknown. In this paper, an ultra‐performance liquid chromatography coupled with quadrupole time‐of‐flight tandem mass spectrometry (UPLC‐Q‐TOF‐MS) method was developed for detection and identification of HLXLD metabolites in rat urine at high and normal clinical dosages. The prototype constituents and their metabolites in urine were analyzed. The mass measurements were accurate within 8 ppm, and subsequent fragment ions offered higher quality structural information for interpretation of the fragmentation pathways of various compounds. A total of 85 compounds were detected in high dosages urine samples by a highly sensitive extracted ion chromatograms method, including 31 parent compounds and 54 metabolites. Our results indicated that phase 2 reactions (e.g. glucuronidation, glutathionidation and sulfation) were the main metabolic pathways of lactones, alkaloids and flavones, while phase I reactions (e.g. hydrogenation and hydroxylation) were the major metabolic reaction for coumarins, paeoniflorin and iridoids. This investigation provided important structural information on the metabolism of HLXLD and provided scientific evidence to obtain a more comprehensive metabolic profile. Copyright © 2015 John Wiley & Sons, Ltd. |
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However, the in vivo integrated metabolism of its multiple components remains unknown. In this paper, an ultra‐performance liquid chromatography coupled with quadrupole time‐of‐flight tandem mass spectrometry (UPLC‐Q‐TOF‐MS) method was developed for detection and identification of HLXLD metabolites in rat urine at high and normal clinical dosages. The prototype constituents and their metabolites in urine were analyzed. The mass measurements were accurate within 8 ppm, and subsequent fragment ions offered higher quality structural information for interpretation of the fragmentation pathways of various compounds. A total of 85 compounds were detected in high dosages urine samples by a highly sensitive extracted ion chromatograms method, including 31 parent compounds and 54 metabolites. Our results indicated that phase 2 reactions (e.g. glucuronidation, glutathionidation and sulfation) were the main metabolic pathways of lactones, alkaloids and flavones, while phase I reactions (e.g. hydrogenation and hydroxylation) were the major metabolic reaction for coumarins, paeoniflorin and iridoids. This investigation provided important structural information on the metabolism of HLXLD and provided scientific evidence to obtain a more comprehensive metabolic profile. Copyright © 2015 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.3561</identifier><identifier>PMID: 26174205</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Alkaloids - metabolism ; Alkaloids - urine ; Animals ; Benzopyrans - metabolism ; Benzopyrans - urine ; Chromatography, High Pressure Liquid - methods ; Drugs, Chinese Herbal - administration & dosage ; Drugs, Chinese Herbal - metabolism ; Drugs, Chinese Herbal - pharmacokinetics ; Huo Luo Xiao Ling Dan ; Lactones - metabolism ; Lactones - urine ; Male ; metabolites in vivo ; Rats ; Rats, Sprague-Dawley ; Spectrometry, Mass, Electrospray Ionization - methods ; UPLC-ESI-Q-TOF-MS ; urine</subject><ispartof>Biomedical chromatography, 2016-03, Vol.30 (3), p.396-409</ispartof><rights>Copyright © 2015 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4291-5ab373bfad88588f423864f74a5e63d4a3f05474c59a7a23bfb40783c54724963</citedby><cites>FETCH-LOGICAL-c4291-5ab373bfad88588f423864f74a5e63d4a3f05474c59a7a23bfb40783c54724963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbmc.3561$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbmc.3561$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26174205$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Fenrong</creatorcontrib><creatorcontrib>Wu, Yun</creatorcontrib><creatorcontrib>Ai, Yu</creatorcontrib><creatorcontrib>Bian, Qiaoxia</creatorcontrib><creatorcontrib>Ma, Wen</creatorcontrib><creatorcontrib>Lee, David Y.-W.</creatorcontrib><creatorcontrib>Dai, Ronghua</creatorcontrib><title>Metabolites identification of Huo Luo Xiao Ling Dan in rat urine by UPLC coupled with electrospray ionization time-of-flight mass spectrometry</title><title>Biomedical chromatography</title><addtitle>Biomed. Chromatogr</addtitle><description>Huo Luo Xiao Ling Dan (HLXLD), a Chinese herbal formula, is used in folk medicine for the treatment of arthritis and other chronic inflammatory diseases. However, the in vivo integrated metabolism of its multiple components remains unknown. In this paper, an ultra‐performance liquid chromatography coupled with quadrupole time‐of‐flight tandem mass spectrometry (UPLC‐Q‐TOF‐MS) method was developed for detection and identification of HLXLD metabolites in rat urine at high and normal clinical dosages. The prototype constituents and their metabolites in urine were analyzed. The mass measurements were accurate within 8 ppm, and subsequent fragment ions offered higher quality structural information for interpretation of the fragmentation pathways of various compounds. A total of 85 compounds were detected in high dosages urine samples by a highly sensitive extracted ion chromatograms method, including 31 parent compounds and 54 metabolites. Our results indicated that phase 2 reactions (e.g. glucuronidation, glutathionidation and sulfation) were the main metabolic pathways of lactones, alkaloids and flavones, while phase I reactions (e.g. hydrogenation and hydroxylation) were the major metabolic reaction for coumarins, paeoniflorin and iridoids. This investigation provided important structural information on the metabolism of HLXLD and provided scientific evidence to obtain a more comprehensive metabolic profile. Copyright © 2015 John Wiley & Sons, Ltd.</description><subject>Alkaloids - metabolism</subject><subject>Alkaloids - urine</subject><subject>Animals</subject><subject>Benzopyrans - metabolism</subject><subject>Benzopyrans - urine</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Drugs, Chinese Herbal - administration & dosage</subject><subject>Drugs, Chinese Herbal - metabolism</subject><subject>Drugs, Chinese Herbal - pharmacokinetics</subject><subject>Huo Luo Xiao Ling Dan</subject><subject>Lactones - metabolism</subject><subject>Lactones - urine</subject><subject>Male</subject><subject>metabolites in vivo</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><subject>UPLC-ESI-Q-TOF-MS</subject><subject>urine</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtu1DAUQC0EokNB4guQl2xSHL-zhCm0oCkgRAs7y3Hs1pDEqe2opB_Rb67bGcqKhXWtq6Mj3QPAyxod1AjhN-1gDgjj9SOwqlHTVEii-jFYIcybikjR7IFnKf1CCDUci6dgD_NaUIzYCtyc2Kzb0PtsE_SdHbN33ujswwiDg8dzgJvyfnpdPn48h4d6hH6EUWc4Rz9a2C7w9OtmDU2Yp9528MrnC2h7a3IMaYp6gcXlr7fK7AdbBVe53p9fZDjolGCa7tnB5rg8B0-c7pN9sZv74PTD--_r42rz5ejj-u2mMhQ3dcV0SwRpne6kZFI6ionk1AmqmeWko5o4xKighjVaaFzIliIhiSlLTBtO9sHrrXeK4XK2KavBJ2P7Xo82zEnVgmNCCUHsH2rKPSlap6boBx0XVSN1V1-V-uqufkFf7axzO9juAfybuwDVFrjyvV3-K1LvTtY74Y73Kds_D7yOvxUXRDD14_OROvt2hg7ZJ64kuQViKp4C</recordid><startdate>201603</startdate><enddate>201603</enddate><creator>Wang, Fenrong</creator><creator>Wu, Yun</creator><creator>Ai, Yu</creator><creator>Bian, Qiaoxia</creator><creator>Ma, Wen</creator><creator>Lee, David Y.-W.</creator><creator>Dai, Ronghua</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>201603</creationdate><title>Metabolites identification of Huo Luo Xiao Ling Dan in rat urine by UPLC coupled with electrospray ionization time-of-flight mass spectrometry</title><author>Wang, Fenrong ; Wu, Yun ; Ai, Yu ; Bian, Qiaoxia ; Ma, Wen ; Lee, David Y.-W. ; Dai, Ronghua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4291-5ab373bfad88588f423864f74a5e63d4a3f05474c59a7a23bfb40783c54724963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Alkaloids - metabolism</topic><topic>Alkaloids - urine</topic><topic>Animals</topic><topic>Benzopyrans - metabolism</topic><topic>Benzopyrans - urine</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Drugs, Chinese Herbal - administration & dosage</topic><topic>Drugs, Chinese Herbal - metabolism</topic><topic>Drugs, Chinese Herbal - pharmacokinetics</topic><topic>Huo Luo Xiao Ling Dan</topic><topic>Lactones - metabolism</topic><topic>Lactones - urine</topic><topic>Male</topic><topic>metabolites in vivo</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Spectrometry, Mass, Electrospray Ionization - methods</topic><topic>UPLC-ESI-Q-TOF-MS</topic><topic>urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Fenrong</creatorcontrib><creatorcontrib>Wu, Yun</creatorcontrib><creatorcontrib>Ai, Yu</creatorcontrib><creatorcontrib>Bian, Qiaoxia</creatorcontrib><creatorcontrib>Ma, Wen</creatorcontrib><creatorcontrib>Lee, David Y.-W.</creatorcontrib><creatorcontrib>Dai, Ronghua</creatorcontrib><collection>Istex</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>Biomedical chromatography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Fenrong</au><au>Wu, Yun</au><au>Ai, Yu</au><au>Bian, Qiaoxia</au><au>Ma, Wen</au><au>Lee, David Y.-W.</au><au>Dai, Ronghua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolites identification of Huo Luo Xiao Ling Dan in rat urine by UPLC coupled with electrospray ionization time-of-flight mass spectrometry</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed. Chromatogr</addtitle><date>2016-03</date><risdate>2016</risdate><volume>30</volume><issue>3</issue><spage>396</spage><epage>409</epage><pages>396-409</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>Huo Luo Xiao Ling Dan (HLXLD), a Chinese herbal formula, is used in folk medicine for the treatment of arthritis and other chronic inflammatory diseases. However, the in vivo integrated metabolism of its multiple components remains unknown. In this paper, an ultra‐performance liquid chromatography coupled with quadrupole time‐of‐flight tandem mass spectrometry (UPLC‐Q‐TOF‐MS) method was developed for detection and identification of HLXLD metabolites in rat urine at high and normal clinical dosages. The prototype constituents and their metabolites in urine were analyzed. The mass measurements were accurate within 8 ppm, and subsequent fragment ions offered higher quality structural information for interpretation of the fragmentation pathways of various compounds. A total of 85 compounds were detected in high dosages urine samples by a highly sensitive extracted ion chromatograms method, including 31 parent compounds and 54 metabolites. Our results indicated that phase 2 reactions (e.g. glucuronidation, glutathionidation and sulfation) were the main metabolic pathways of lactones, alkaloids and flavones, while phase I reactions (e.g. hydrogenation and hydroxylation) were the major metabolic reaction for coumarins, paeoniflorin and iridoids. This investigation provided important structural information on the metabolism of HLXLD and provided scientific evidence to obtain a more comprehensive metabolic profile. Copyright © 2015 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26174205</pmid><doi>10.1002/bmc.3561</doi><tpages>14</tpages></addata></record> |
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subjects | Alkaloids - metabolism Alkaloids - urine Animals Benzopyrans - metabolism Benzopyrans - urine Chromatography, High Pressure Liquid - methods Drugs, Chinese Herbal - administration & dosage Drugs, Chinese Herbal - metabolism Drugs, Chinese Herbal - pharmacokinetics Huo Luo Xiao Ling Dan Lactones - metabolism Lactones - urine Male metabolites in vivo Rats Rats, Sprague-Dawley Spectrometry, Mass, Electrospray Ionization - methods UPLC-ESI-Q-TOF-MS urine |
title | Metabolites identification of Huo Luo Xiao Ling Dan in rat urine by UPLC coupled with electrospray ionization time-of-flight mass spectrometry |
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