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
Hauptverfasser: Wang, Fenrong, Wu, Yun, Ai, Yu, Bian, Qiaoxia, Ma, Wen, Lee, David Y.-W., Dai, Ronghua
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container_issue 3
container_start_page 396
container_title Biomedical chromatography
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creator Wang, Fenrong
Wu, Yun
Ai, Yu
Bian, Qiaoxia
Ma, Wen
Lee, David Y.-W.
Dai, Ronghua
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. 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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 &amp; 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 &amp; 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 &amp; 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. 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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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