Comparative pharmacokinetics and metabolites study of seven major bioactive components of Shaoyao‐Gancao decoction in normal and polycystic ovary syndrome rats by ultra high pressure liquid chromatography with tandem mass spectrometry
A simple and sensitive liquid chromatography with tandem mass spectrometry method was developed for simultaneous quantification of paeoniflorin, albiflorin, oxypaeoniflorin, liquiritin, liquiritigenin, glycyrrhetinic acid, and glycyrrhizin in rat plasma after oral administration of Shaoyao‐Gancao de...
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creator | Liu, Jun‐jin Cheng, Yao Shao, Yun‐yun Chang, Zhuang‐peng Guo, Yi‐ting Feng, Xiao‐juan Xu, Ding Zhang, Jing‐ping Song, Yan Hou, Rui‐gang |
description | A simple and sensitive liquid chromatography with tandem mass spectrometry method was developed for simultaneous quantification of paeoniflorin, albiflorin, oxypaeoniflorin, liquiritin, liquiritigenin, glycyrrhetinic acid, and glycyrrhizin in rat plasma after oral administration of Shaoyao‐Gancao decoction, which is traditionally used in the treatment of polycystic ovary syndrome. The plasma samples were pretreated with methanol as precipitant. The method exhibited good linearity (correlation coefficient (R2) > 0.99) with lower quantification limits of 0.595–4.69 ng/mL for all analytes. Intra‐ and interbatch precision, accuracy, recovery, and stability of the method were all within accepted criteria. The results showed that the pharmacokinetic behaviors of the seven compounds were altered in the pathological status of polycystic ovary syndrome. Furthermore, a total of 36 metabolites were structurally identified based on their accurate masses and fragment ions. The major metabolic pathway involves phase I metabolic reactions (such as hydroxylation), phase II metabolic reactions (such as sulfation and glucuronidation conjugation) as well as the combined multiple‐step metabolism. This study is the first report on the pharmacokinetic and metabolic information of Shaoyao‐Gancao decoction in both normal and model rats, which would provide scientific evidences for the bioactive chemical basis of herbal medicines and also promote the clinical application of Shaoyao‐Gancao decoction for treating polycystic ovary syndrome. |
doi_str_mv | 10.1002/jssc.201900002 |
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The plasma samples were pretreated with methanol as precipitant. The method exhibited good linearity (correlation coefficient (R2) > 0.99) with lower quantification limits of 0.595–4.69 ng/mL for all analytes. Intra‐ and interbatch precision, accuracy, recovery, and stability of the method were all within accepted criteria. The results showed that the pharmacokinetic behaviors of the seven compounds were altered in the pathological status of polycystic ovary syndrome. Furthermore, a total of 36 metabolites were structurally identified based on their accurate masses and fragment ions. The major metabolic pathway involves phase I metabolic reactions (such as hydroxylation), phase II metabolic reactions (such as sulfation and glucuronidation conjugation) as well as the combined multiple‐step metabolism. This study is the first report on the pharmacokinetic and metabolic information of Shaoyao‐Gancao decoction in both normal and model rats, which would provide scientific evidences for the bioactive chemical basis of herbal medicines and also promote the clinical application of Shaoyao‐Gancao decoction for treating polycystic ovary syndrome.</description><identifier>ISSN: 1615-9306</identifier><identifier>EISSN: 1615-9314</identifier><identifier>DOI: 10.1002/jssc.201900002</identifier><identifier>PMID: 31144455</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>acokinetics ; Administration, Oral ; Analytical chemistry ; Animals ; Biological activity ; Bridged-Ring Compounds - blood ; Bridged-Ring Compounds - metabolism ; Bridged-Ring Compounds - pharmacokinetics ; Chromatography ; Chromatography, High Pressure Liquid ; Conjugation ; Correlation coefficients ; Drugs, Chinese Herbal - administration & dosage ; Drugs, Chinese Herbal - analysis ; Drugs, Chinese Herbal - metabolism ; Drugs, Chinese Herbal - pharmacokinetics ; Drugs, Chinese Herbal - therapeutic use ; Female ; Flavanones - blood ; Flavanones - metabolism ; Flavanones - pharmacokinetics ; Glucosides - blood ; Glucosides - metabolism ; Glucosides - pharmacokinetics ; Glycyrrhetinic Acid - blood ; Glycyrrhetinic Acid - metabolism ; Glycyrrhetinic Acid - pharmacokinetics ; Glycyrrhizic Acid - blood ; Glycyrrhizic Acid - metabolism ; Glycyrrhizic Acid - pharmacokinetics ; High performance liquid chromatography ; Hydroxylation ; Linearity ; Mass spectrometry ; Metabolism ; Metabolites ; Monoterpenes - blood ; Monoterpenes - metabolism ; Monoterpenes - pharmacokinetics ; Organic chemistry ; Pharmacokinetics ; Pharmacology ; Polycystic ovary syndrome ; Polycystic Ovary Syndrome - drug therapy ; Rats ; Rats, Sprague-Dawley ; Scientific imaging ; Spectroscopy ; Stability analysis ; Sulfation ; Tandem Mass Spectrometry ; traditional Chinese medicine</subject><ispartof>Journal of separation science, 2019-08, Vol.42 (15), p.2534-2549</ispartof><rights>2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4050-48cd21fd59884a41fa96a6db089364982bdfea8eb3e646a00f9f0db9b0a1a3063</citedby><cites>FETCH-LOGICAL-c4050-48cd21fd59884a41fa96a6db089364982bdfea8eb3e646a00f9f0db9b0a1a3063</cites><orcidid>0000-0003-4245-8012</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjssc.201900002$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjssc.201900002$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31144455$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Jun‐jin</creatorcontrib><creatorcontrib>Cheng, Yao</creatorcontrib><creatorcontrib>Shao, Yun‐yun</creatorcontrib><creatorcontrib>Chang, Zhuang‐peng</creatorcontrib><creatorcontrib>Guo, Yi‐ting</creatorcontrib><creatorcontrib>Feng, Xiao‐juan</creatorcontrib><creatorcontrib>Xu, Ding</creatorcontrib><creatorcontrib>Zhang, Jing‐ping</creatorcontrib><creatorcontrib>Song, Yan</creatorcontrib><creatorcontrib>Hou, Rui‐gang</creatorcontrib><title>Comparative pharmacokinetics and metabolites study of seven major bioactive components of Shaoyao‐Gancao decoction in normal and polycystic ovary syndrome rats by ultra high pressure liquid chromatography with tandem mass spectrometry</title><title>Journal of separation science</title><addtitle>J Sep Sci</addtitle><description>A simple and sensitive liquid chromatography with tandem mass spectrometry method was developed for simultaneous quantification of paeoniflorin, albiflorin, oxypaeoniflorin, liquiritin, liquiritigenin, glycyrrhetinic acid, and glycyrrhizin in rat plasma after oral administration of Shaoyao‐Gancao decoction, which is traditionally used in the treatment of polycystic ovary syndrome. The plasma samples were pretreated with methanol as precipitant. The method exhibited good linearity (correlation coefficient (R2) > 0.99) with lower quantification limits of 0.595–4.69 ng/mL for all analytes. Intra‐ and interbatch precision, accuracy, recovery, and stability of the method were all within accepted criteria. The results showed that the pharmacokinetic behaviors of the seven compounds were altered in the pathological status of polycystic ovary syndrome. Furthermore, a total of 36 metabolites were structurally identified based on their accurate masses and fragment ions. The major metabolic pathway involves phase I metabolic reactions (such as hydroxylation), phase II metabolic reactions (such as sulfation and glucuronidation conjugation) as well as the combined multiple‐step metabolism. This study is the first report on the pharmacokinetic and metabolic information of Shaoyao‐Gancao decoction in both normal and model rats, which would provide scientific evidences for the bioactive chemical basis of herbal medicines and also promote the clinical application of Shaoyao‐Gancao decoction for treating polycystic ovary syndrome.</description><subject>acokinetics</subject><subject>Administration, Oral</subject><subject>Analytical chemistry</subject><subject>Animals</subject><subject>Biological activity</subject><subject>Bridged-Ring Compounds - blood</subject><subject>Bridged-Ring Compounds - metabolism</subject><subject>Bridged-Ring Compounds - pharmacokinetics</subject><subject>Chromatography</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Conjugation</subject><subject>Correlation coefficients</subject><subject>Drugs, Chinese Herbal - administration & dosage</subject><subject>Drugs, Chinese Herbal - analysis</subject><subject>Drugs, Chinese Herbal - metabolism</subject><subject>Drugs, Chinese Herbal - pharmacokinetics</subject><subject>Drugs, Chinese Herbal - therapeutic use</subject><subject>Female</subject><subject>Flavanones - blood</subject><subject>Flavanones - metabolism</subject><subject>Flavanones - pharmacokinetics</subject><subject>Glucosides - blood</subject><subject>Glucosides - metabolism</subject><subject>Glucosides - pharmacokinetics</subject><subject>Glycyrrhetinic Acid - blood</subject><subject>Glycyrrhetinic Acid - metabolism</subject><subject>Glycyrrhetinic Acid - pharmacokinetics</subject><subject>Glycyrrhizic Acid - blood</subject><subject>Glycyrrhizic Acid - metabolism</subject><subject>Glycyrrhizic Acid - pharmacokinetics</subject><subject>High performance liquid chromatography</subject><subject>Hydroxylation</subject><subject>Linearity</subject><subject>Mass spectrometry</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Monoterpenes - blood</subject><subject>Monoterpenes - metabolism</subject><subject>Monoterpenes - pharmacokinetics</subject><subject>Organic chemistry</subject><subject>Pharmacokinetics</subject><subject>Pharmacology</subject><subject>Polycystic ovary syndrome</subject><subject>Polycystic Ovary Syndrome - drug therapy</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Scientific imaging</subject><subject>Spectroscopy</subject><subject>Stability analysis</subject><subject>Sulfation</subject><subject>Tandem Mass Spectrometry</subject><subject>traditional Chinese medicine</subject><issn>1615-9306</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhSMEoqVw5YhG4ryLnThpckQraEGVOCyco4k9abwkdmo7W_nGT-A3cu6PwNste8UX-_DNe2_8suwtZ2vOWP5h571c54w3LJ38WXbOK16umoKL56c3q86yV97vGOOXdcNeZmcF50KIsjzPHjZ2mtFh0HuCeUA3obQ_taGgpQc0CiYK2NlRB_Lgw6Ii2B487cnAhDvroNMW5eO8TFrWkAn-wGwHtBHtn1-_r9BItKBI2gRaA9qAsclqfHSY7Rhl9MkR7B5dBB-NcnYiSLk8dBGWMTiEQd8OMDvyfnEEo75btAI5JBKDvXU4DxHudRggJFWaUjyfIs8kw0EsuPg6e9Hj6OnN032R_fj86fvmenXz7erL5uPNSgpWspWopcp5r8qmrgUK3mNTYaU6VjdFJZo671RPWFNXUCUqZKxveqa6pmPIMf12cZG9P-rOzt4t5EO7s4szybLN8-qyKPO6rBO1PlLSWe8d9e3s9JT2bzlrD-W2h3LbU7lp4N2T7NJNpE74vzYTII7AvR4p_keu_brdbipRs-Ivk_653Q</recordid><startdate>201908</startdate><enddate>201908</enddate><creator>Liu, Jun‐jin</creator><creator>Cheng, Yao</creator><creator>Shao, Yun‐yun</creator><creator>Chang, Zhuang‐peng</creator><creator>Guo, Yi‐ting</creator><creator>Feng, Xiao‐juan</creator><creator>Xu, Ding</creator><creator>Zhang, Jing‐ping</creator><creator>Song, Yan</creator><creator>Hou, Rui‐gang</creator><general>Wiley Subscription Services, Inc</general><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>7U5</scope><scope>8FD</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0003-4245-8012</orcidid></search><sort><creationdate>201908</creationdate><title>Comparative pharmacokinetics and metabolites study of seven major bioactive components of Shaoyao‐Gancao decoction in normal and polycystic ovary syndrome rats by ultra high pressure liquid chromatography with tandem mass spectrometry</title><author>Liu, Jun‐jin ; Cheng, Yao ; Shao, Yun‐yun ; Chang, Zhuang‐peng ; Guo, Yi‐ting ; Feng, Xiao‐juan ; Xu, Ding ; Zhang, Jing‐ping ; Song, Yan ; Hou, Rui‐gang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4050-48cd21fd59884a41fa96a6db089364982bdfea8eb3e646a00f9f0db9b0a1a3063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>acokinetics</topic><topic>Administration, Oral</topic><topic>Analytical chemistry</topic><topic>Animals</topic><topic>Biological activity</topic><topic>Bridged-Ring Compounds - blood</topic><topic>Bridged-Ring Compounds - metabolism</topic><topic>Bridged-Ring Compounds - pharmacokinetics</topic><topic>Chromatography</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Conjugation</topic><topic>Correlation coefficients</topic><topic>Drugs, Chinese Herbal - administration & dosage</topic><topic>Drugs, Chinese Herbal - analysis</topic><topic>Drugs, Chinese Herbal - metabolism</topic><topic>Drugs, Chinese Herbal - pharmacokinetics</topic><topic>Drugs, Chinese Herbal - therapeutic use</topic><topic>Female</topic><topic>Flavanones - blood</topic><topic>Flavanones - metabolism</topic><topic>Flavanones - pharmacokinetics</topic><topic>Glucosides - blood</topic><topic>Glucosides - metabolism</topic><topic>Glucosides - pharmacokinetics</topic><topic>Glycyrrhetinic Acid - blood</topic><topic>Glycyrrhetinic Acid - metabolism</topic><topic>Glycyrrhetinic Acid - pharmacokinetics</topic><topic>Glycyrrhizic Acid - blood</topic><topic>Glycyrrhizic Acid - metabolism</topic><topic>Glycyrrhizic Acid - pharmacokinetics</topic><topic>High performance liquid chromatography</topic><topic>Hydroxylation</topic><topic>Linearity</topic><topic>Mass spectrometry</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Monoterpenes - blood</topic><topic>Monoterpenes - metabolism</topic><topic>Monoterpenes - pharmacokinetics</topic><topic>Organic chemistry</topic><topic>Pharmacokinetics</topic><topic>Pharmacology</topic><topic>Polycystic ovary syndrome</topic><topic>Polycystic Ovary Syndrome - drug therapy</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Scientific imaging</topic><topic>Spectroscopy</topic><topic>Stability analysis</topic><topic>Sulfation</topic><topic>Tandem Mass Spectrometry</topic><topic>traditional Chinese medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Jun‐jin</creatorcontrib><creatorcontrib>Cheng, Yao</creatorcontrib><creatorcontrib>Shao, Yun‐yun</creatorcontrib><creatorcontrib>Chang, Zhuang‐peng</creatorcontrib><creatorcontrib>Guo, Yi‐ting</creatorcontrib><creatorcontrib>Feng, Xiao‐juan</creatorcontrib><creatorcontrib>Xu, Ding</creatorcontrib><creatorcontrib>Zhang, Jing‐ping</creatorcontrib><creatorcontrib>Song, Yan</creatorcontrib><creatorcontrib>Hou, Rui‐gang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of separation science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Jun‐jin</au><au>Cheng, Yao</au><au>Shao, Yun‐yun</au><au>Chang, Zhuang‐peng</au><au>Guo, Yi‐ting</au><au>Feng, Xiao‐juan</au><au>Xu, Ding</au><au>Zhang, Jing‐ping</au><au>Song, Yan</au><au>Hou, Rui‐gang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative pharmacokinetics and metabolites study of seven major bioactive components of Shaoyao‐Gancao decoction in normal and polycystic ovary syndrome rats by ultra high pressure liquid chromatography with tandem mass spectrometry</atitle><jtitle>Journal of separation science</jtitle><addtitle>J Sep Sci</addtitle><date>2019-08</date><risdate>2019</risdate><volume>42</volume><issue>15</issue><spage>2534</spage><epage>2549</epage><pages>2534-2549</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>A simple and sensitive liquid chromatography with tandem mass spectrometry method was developed for simultaneous quantification of paeoniflorin, albiflorin, oxypaeoniflorin, liquiritin, liquiritigenin, glycyrrhetinic acid, and glycyrrhizin in rat plasma after oral administration of Shaoyao‐Gancao decoction, which is traditionally used in the treatment of polycystic ovary syndrome. The plasma samples were pretreated with methanol as precipitant. The method exhibited good linearity (correlation coefficient (R2) > 0.99) with lower quantification limits of 0.595–4.69 ng/mL for all analytes. Intra‐ and interbatch precision, accuracy, recovery, and stability of the method were all within accepted criteria. The results showed that the pharmacokinetic behaviors of the seven compounds were altered in the pathological status of polycystic ovary syndrome. Furthermore, a total of 36 metabolites were structurally identified based on their accurate masses and fragment ions. The major metabolic pathway involves phase I metabolic reactions (such as hydroxylation), phase II metabolic reactions (such as sulfation and glucuronidation conjugation) as well as the combined multiple‐step metabolism. This study is the first report on the pharmacokinetic and metabolic information of Shaoyao‐Gancao decoction in both normal and model rats, which would provide scientific evidences for the bioactive chemical basis of herbal medicines and also promote the clinical application of Shaoyao‐Gancao decoction for treating polycystic ovary syndrome.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31144455</pmid><doi>10.1002/jssc.201900002</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-4245-8012</orcidid></addata></record> |
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subjects | acokinetics Administration, Oral Analytical chemistry Animals Biological activity Bridged-Ring Compounds - blood Bridged-Ring Compounds - metabolism Bridged-Ring Compounds - pharmacokinetics Chromatography Chromatography, High Pressure Liquid Conjugation Correlation coefficients Drugs, Chinese Herbal - administration & dosage Drugs, Chinese Herbal - analysis Drugs, Chinese Herbal - metabolism Drugs, Chinese Herbal - pharmacokinetics Drugs, Chinese Herbal - therapeutic use Female Flavanones - blood Flavanones - metabolism Flavanones - pharmacokinetics Glucosides - blood Glucosides - metabolism Glucosides - pharmacokinetics Glycyrrhetinic Acid - blood Glycyrrhetinic Acid - metabolism Glycyrrhetinic Acid - pharmacokinetics Glycyrrhizic Acid - blood Glycyrrhizic Acid - metabolism Glycyrrhizic Acid - pharmacokinetics High performance liquid chromatography Hydroxylation Linearity Mass spectrometry Metabolism Metabolites Monoterpenes - blood Monoterpenes - metabolism Monoterpenes - pharmacokinetics Organic chemistry Pharmacokinetics Pharmacology Polycystic ovary syndrome Polycystic Ovary Syndrome - drug therapy Rats Rats, Sprague-Dawley Scientific imaging Spectroscopy Stability analysis Sulfation Tandem Mass Spectrometry traditional Chinese medicine |
title | Comparative pharmacokinetics and metabolites study of seven major bioactive components of Shaoyao‐Gancao decoction in normal and polycystic ovary syndrome rats by ultra high pressure liquid chromatography with tandem mass spectrometry |
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