LC–MS/MS determination and pharmacokinetic study of seven flavonoids in rat plasma after oral administration of Cirsium japonicum DC. extract

Cirsium japonicum DC., a Traditional Chinese Medicine, has the curative effect of antihemorrhagic and antitumor. Pharmacological studies prove that the curative effect may relate to the flavonoids. A simple and rapid resolution liquid chromatography–tandem mass spectrometry (LC–MS/MS) method was fir...

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Veröffentlicht in:Journal of ethnopharmacology 2014-12, Vol.158, p.66-75
Hauptverfasser: Zhang, Zhiyong, Jia, Peipei, Zhang, Xiaoxu, Zhang, Qiaoyue, Yang, Haotian, Shi, He, Zhang, Lantong
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container_title Journal of ethnopharmacology
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creator Zhang, Zhiyong
Jia, Peipei
Zhang, Xiaoxu
Zhang, Qiaoyue
Yang, Haotian
Shi, He
Zhang, Lantong
description Cirsium japonicum DC., a Traditional Chinese Medicine, has the curative effect of antihemorrhagic and antitumor. Pharmacological studies prove that the curative effect may relate to the flavonoids. A simple and rapid resolution liquid chromatography–tandem mass spectrometry (LC–MS/MS) method was first developed and validated for the quantification of seven flavonoids including pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and apigenin in rat plasma after oral administration of Cirsium japonicum DC. extract. The chromatographic separation was achieved on a C18 column with gradient elution by using a mixture of 0.1% formic acid aqueous solution and methanol as the mobile phase at a flow rate of 0.8mL/min. A tandem mass spectrometric detection was conducted using multiple-reaction monitoring (MRM) via an electrospray ionization (ESI) source in positive and negative ionization mode simultaneously. Samples were pre-treated by a single-step protein precipitation with methanol, and sulfamethoxazole was used as internal standard (IS). The optimized mass transition ion-pairs (m/z) for quantization were 623.4/315.2 for pectolinarin, 593.3/285.1 for linarin, 315.3/300.2 for pectolinarigenin, 301.2/286.2 for hispidulin, 301.2/258.2 for diosmetin, 283.0/267.9 for acacetin, 269.0/117.0 for apigenin and 252.2/155.8 for IS. After oral administration of 6mL/kg Cirsium japonicum DC. extract in rats, the maximum plasma concentration (Cmax) of pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and apigenin were 876.77±97.34ng/mL, 86.79±1.70ng/mL, 6.13±0.12ng/mL, 32.85±2.50ng/mL, 37.2±2.04ng/mL, 19.02±1.29ng/mL and 148.26±20.63ng/mL, respectively. The time to reach the maximum plasma concentration (Tmax) was 5min for pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and 360min for apigenin. The intra-day and inter-day precisions (RSD%) for seven compounds were less than 13.16% and 7.77% and the accuracy (RE%) range from −7.92% to 14.77%. This is the first research on the pharmacokinetic study of bioactive components in rat plasma after oral administration of Cirsium japonicum DC. extract. The results provided a meaningful basis for better understanding the absorption mechanism of Cirsium japonicum DC. and evaluating the clinical application of this herb medicine. [Display omitted]
doi_str_mv 10.1016/j.jep.2014.10.022
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Pharmacological studies prove that the curative effect may relate to the flavonoids. A simple and rapid resolution liquid chromatography–tandem mass spectrometry (LC–MS/MS) method was first developed and validated for the quantification of seven flavonoids including pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and apigenin in rat plasma after oral administration of Cirsium japonicum DC. extract. The chromatographic separation was achieved on a C18 column with gradient elution by using a mixture of 0.1% formic acid aqueous solution and methanol as the mobile phase at a flow rate of 0.8mL/min. A tandem mass spectrometric detection was conducted using multiple-reaction monitoring (MRM) via an electrospray ionization (ESI) source in positive and negative ionization mode simultaneously. Samples were pre-treated by a single-step protein precipitation with methanol, and sulfamethoxazole was used as internal standard (IS). The optimized mass transition ion-pairs (m/z) for quantization were 623.4/315.2 for pectolinarin, 593.3/285.1 for linarin, 315.3/300.2 for pectolinarigenin, 301.2/286.2 for hispidulin, 301.2/258.2 for diosmetin, 283.0/267.9 for acacetin, 269.0/117.0 for apigenin and 252.2/155.8 for IS. After oral administration of 6mL/kg Cirsium japonicum DC. extract in rats, the maximum plasma concentration (Cmax) of pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and apigenin were 876.77±97.34ng/mL, 86.79±1.70ng/mL, 6.13±0.12ng/mL, 32.85±2.50ng/mL, 37.2±2.04ng/mL, 19.02±1.29ng/mL and 148.26±20.63ng/mL, respectively. The time to reach the maximum plasma concentration (Tmax) was 5min for pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and 360min for apigenin. The intra-day and inter-day precisions (RSD%) for seven compounds were less than 13.16% and 7.77% and the accuracy (RE%) range from −7.92% to 14.77%. This is the first research on the pharmacokinetic study of bioactive components in rat plasma after oral administration of Cirsium japonicum DC. extract. The results provided a meaningful basis for better understanding the absorption mechanism of Cirsium japonicum DC. and evaluating the clinical application of this herb medicine. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-c24bb067d12a4db670550c0af75de171df23bb9a9ba57a1c50031440bdfbbd2e3</citedby><cites>FETCH-LOGICAL-c353t-c24bb067d12a4db670550c0af75de171df23bb9a9ba57a1c50031440bdfbbd2e3</cites><orcidid>0000-0002-7340-559X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378874114007326$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25456423$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Zhiyong</creatorcontrib><creatorcontrib>Jia, Peipei</creatorcontrib><creatorcontrib>Zhang, Xiaoxu</creatorcontrib><creatorcontrib>Zhang, Qiaoyue</creatorcontrib><creatorcontrib>Yang, Haotian</creatorcontrib><creatorcontrib>Shi, He</creatorcontrib><creatorcontrib>Zhang, Lantong</creatorcontrib><title>LC–MS/MS determination and pharmacokinetic study of seven flavonoids in rat plasma after oral administration of Cirsium japonicum DC. extract</title><title>Journal of ethnopharmacology</title><addtitle>J Ethnopharmacol</addtitle><description>Cirsium japonicum DC., a Traditional Chinese Medicine, has the curative effect of antihemorrhagic and antitumor. Pharmacological studies prove that the curative effect may relate to the flavonoids. A simple and rapid resolution liquid chromatography–tandem mass spectrometry (LC–MS/MS) method was first developed and validated for the quantification of seven flavonoids including pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and apigenin in rat plasma after oral administration of Cirsium japonicum DC. extract. The chromatographic separation was achieved on a C18 column with gradient elution by using a mixture of 0.1% formic acid aqueous solution and methanol as the mobile phase at a flow rate of 0.8mL/min. A tandem mass spectrometric detection was conducted using multiple-reaction monitoring (MRM) via an electrospray ionization (ESI) source in positive and negative ionization mode simultaneously. Samples were pre-treated by a single-step protein precipitation with methanol, and sulfamethoxazole was used as internal standard (IS). The optimized mass transition ion-pairs (m/z) for quantization were 623.4/315.2 for pectolinarin, 593.3/285.1 for linarin, 315.3/300.2 for pectolinarigenin, 301.2/286.2 for hispidulin, 301.2/258.2 for diosmetin, 283.0/267.9 for acacetin, 269.0/117.0 for apigenin and 252.2/155.8 for IS. After oral administration of 6mL/kg Cirsium japonicum DC. extract in rats, the maximum plasma concentration (Cmax) of pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and apigenin were 876.77±97.34ng/mL, 86.79±1.70ng/mL, 6.13±0.12ng/mL, 32.85±2.50ng/mL, 37.2±2.04ng/mL, 19.02±1.29ng/mL and 148.26±20.63ng/mL, respectively. The time to reach the maximum plasma concentration (Tmax) was 5min for pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and 360min for apigenin. The intra-day and inter-day precisions (RSD%) for seven compounds were less than 13.16% and 7.77% and the accuracy (RE%) range from −7.92% to 14.77%. This is the first research on the pharmacokinetic study of bioactive components in rat plasma after oral administration of Cirsium japonicum DC. extract. The results provided a meaningful basis for better understanding the absorption mechanism of Cirsium japonicum DC. and evaluating the clinical application of this herb medicine. [Display omitted]</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Chromatography, Liquid - methods</subject><subject>Cirsium - chemistry</subject><subject>Cirsium japonicum DC</subject><subject>Flavonoids</subject><subject>Flavonoids - isolation &amp; purification</subject><subject>Flavonoids - pharmacokinetics</subject><subject>HPLC–MS/MS</subject><subject>Male</subject><subject>Medicine, Chinese Traditional</subject><subject>Pharmacokinetics</subject><subject>Plant Extracts - administration &amp; dosage</subject><subject>Plant Extracts - pharmacokinetics</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Tandem Mass Spectrometry - methods</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1DAURiMEotPCA7BBXrJJajt2nIoVSqEgTcWisLb8cyMcEjvYzojueAMWvCFPgkdTWLLy9dX5jmR_VfWC4IZg0l1OzQRrQzFh5d5gSh9VO9ILWgsu2sfVDreir3vByFl1ntKEMRaE4afVGeWMd4y2u-rnfvj949ft3eXtHbKQIS7Oq-yCR8pbtH5RcVEmfHUesjMo5c3eozCiBAfwaJzVIfjgbELOo6gyWmeVFoXUWEwoRDUjZYvRpRxP1pIdXExuW9Ck1uCdKdP10CD4XhCTn1VPRjUneP5wXlSf3739NLyv9x9vPgxv9rVpeZtrQ5nWuBOWUMWs7gTmHBusRsEtEEHsSFutr9SVVlwoYjjGLWEMaztqbSm0F9Wrk3eN4dsGKcvFJQPzrDyELUnSccrantK-oOSEmhhSijDKNbpFxXtJsDz2ICdZepDHHo6r0kPJvHzQb3oB-y_x9-ML8PoEQHnkwUGUyTjwBqyLYLK0wf1H_wcEWpv8</recordid><startdate>20141202</startdate><enddate>20141202</enddate><creator>Zhang, Zhiyong</creator><creator>Jia, Peipei</creator><creator>Zhang, Xiaoxu</creator><creator>Zhang, Qiaoyue</creator><creator>Yang, Haotian</creator><creator>Shi, He</creator><creator>Zhang, Lantong</creator><general>Elsevier Ireland Ltd</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>7X8</scope><orcidid>https://orcid.org/0000-0002-7340-559X</orcidid></search><sort><creationdate>20141202</creationdate><title>LC–MS/MS determination and pharmacokinetic study of seven flavonoids in rat plasma after oral administration of Cirsium japonicum DC. extract</title><author>Zhang, Zhiyong ; Jia, Peipei ; Zhang, Xiaoxu ; Zhang, Qiaoyue ; Yang, Haotian ; Shi, He ; Zhang, Lantong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-c24bb067d12a4db670550c0af75de171df23bb9a9ba57a1c50031440bdfbbd2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Chromatography, Liquid - methods</topic><topic>Cirsium - chemistry</topic><topic>Cirsium japonicum DC</topic><topic>Flavonoids</topic><topic>Flavonoids - isolation &amp; purification</topic><topic>Flavonoids - pharmacokinetics</topic><topic>HPLC–MS/MS</topic><topic>Male</topic><topic>Medicine, Chinese Traditional</topic><topic>Pharmacokinetics</topic><topic>Plant Extracts - administration &amp; dosage</topic><topic>Plant Extracts - pharmacokinetics</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Tandem Mass Spectrometry - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Zhiyong</creatorcontrib><creatorcontrib>Jia, Peipei</creatorcontrib><creatorcontrib>Zhang, Xiaoxu</creatorcontrib><creatorcontrib>Zhang, Qiaoyue</creatorcontrib><creatorcontrib>Yang, Haotian</creatorcontrib><creatorcontrib>Shi, He</creatorcontrib><creatorcontrib>Zhang, Lantong</creatorcontrib><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 ethnopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Zhiyong</au><au>Jia, Peipei</au><au>Zhang, Xiaoxu</au><au>Zhang, Qiaoyue</au><au>Yang, Haotian</au><au>Shi, He</au><au>Zhang, Lantong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LC–MS/MS determination and pharmacokinetic study of seven flavonoids in rat plasma after oral administration of Cirsium japonicum DC. extract</atitle><jtitle>Journal of ethnopharmacology</jtitle><addtitle>J Ethnopharmacol</addtitle><date>2014-12-02</date><risdate>2014</risdate><volume>158</volume><spage>66</spage><epage>75</epage><pages>66-75</pages><issn>0378-8741</issn><eissn>1872-7573</eissn><abstract>Cirsium japonicum DC., a Traditional Chinese Medicine, has the curative effect of antihemorrhagic and antitumor. Pharmacological studies prove that the curative effect may relate to the flavonoids. A simple and rapid resolution liquid chromatography–tandem mass spectrometry (LC–MS/MS) method was first developed and validated for the quantification of seven flavonoids including pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and apigenin in rat plasma after oral administration of Cirsium japonicum DC. extract. The chromatographic separation was achieved on a C18 column with gradient elution by using a mixture of 0.1% formic acid aqueous solution and methanol as the mobile phase at a flow rate of 0.8mL/min. A tandem mass spectrometric detection was conducted using multiple-reaction monitoring (MRM) via an electrospray ionization (ESI) source in positive and negative ionization mode simultaneously. Samples were pre-treated by a single-step protein precipitation with methanol, and sulfamethoxazole was used as internal standard (IS). The optimized mass transition ion-pairs (m/z) for quantization were 623.4/315.2 for pectolinarin, 593.3/285.1 for linarin, 315.3/300.2 for pectolinarigenin, 301.2/286.2 for hispidulin, 301.2/258.2 for diosmetin, 283.0/267.9 for acacetin, 269.0/117.0 for apigenin and 252.2/155.8 for IS. After oral administration of 6mL/kg Cirsium japonicum DC. extract in rats, the maximum plasma concentration (Cmax) of pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and apigenin were 876.77±97.34ng/mL, 86.79±1.70ng/mL, 6.13±0.12ng/mL, 32.85±2.50ng/mL, 37.2±2.04ng/mL, 19.02±1.29ng/mL and 148.26±20.63ng/mL, respectively. The time to reach the maximum plasma concentration (Tmax) was 5min for pectolinarin, linarin, pectolinarigenin, hispidulin, diosmetin, acacetin and 360min for apigenin. The intra-day and inter-day precisions (RSD%) for seven compounds were less than 13.16% and 7.77% and the accuracy (RE%) range from −7.92% to 14.77%. This is the first research on the pharmacokinetic study of bioactive components in rat plasma after oral administration of Cirsium japonicum DC. extract. The results provided a meaningful basis for better understanding the absorption mechanism of Cirsium japonicum DC. and evaluating the clinical application of this herb medicine. [Display omitted]</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>25456423</pmid><doi>10.1016/j.jep.2014.10.022</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-7340-559X</orcidid></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Administration, Oral
Animals
Chromatography, Liquid - methods
Cirsium - chemistry
Cirsium japonicum DC
Flavonoids
Flavonoids - isolation & purification
Flavonoids - pharmacokinetics
HPLC–MS/MS
Male
Medicine, Chinese Traditional
Pharmacokinetics
Plant Extracts - administration & dosage
Plant Extracts - pharmacokinetics
Rats
Rats, Sprague-Dawley
Tandem Mass Spectrometry - methods
title LC–MS/MS determination and pharmacokinetic study of seven flavonoids in rat plasma after oral administration of Cirsium japonicum DC. extract
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