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Quality control of Chinese medicinal preparations LC/ESI(+)/MS/MS analyses of saikosaponins-a and -c as markers of bupleuri radix samples
We have used LC/ion trap tandem MS analysis to determine saikosaponin-a and -c as target markers in crude 70% methanol extracts from three different species of Bupleuri radix and the 10 most-popular Chinese medicinal preparations containing "Chaihu" (B. radix) without any clean-up. The opt...
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Published in: | Journal of pharmaceutical and biomedical analysis 2007-02, Vol.43 (3), p.1174-1178 |
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creator | LIAU, Bing-Chung HSIAO, Shun-Sheng LEE, Maw-Rong JONG, Ting-Ting CHIANG, Shu-Tuan |
description | We have used LC/ion trap tandem MS analysis to determine saikosaponin-a and -c as target markers in crude 70% methanol extracts from three different species of Bupleuri radix and the 10 most-popular Chinese medicinal preparations containing "Chaihu" (B. radix) without any clean-up. The optimal ionization characteristics were obtained when using positive-ion electrospray ionization (ESI) with 50 microM sodium acetate as an additive in the mobile phase. We observed good linearity over the range from 0.02 to 2 microg/ml for saikosaponin-a and from 0.02 to 1 microg/ml for saikosaponin-c. The intra-day precisions varied between 3.3 and 8.8% for saikosaponin-a and 0.3 and 11.1% for saikosaponin-c. The limits of detection were 0.01 microg/ml for both markers. The recoveries of saikosaponin-a and -c from the extract of a medicinal preparation sample (Chai-Hu-Ching-Gan-Tang, No. 13 in the table of section Analysis on actual samples) were 97 and 100%, respectively, at a 1 microg/ml spiking concentration of each marker. The highest concentrations of saikosaponin-a and -c among the three B. radixes were found in B. kaoi Liu Chao & Chuang (10.1 mg/g) and in B. falcatum (3.4 mg/g), respectively. The amounts of these saikosaponins in the 10 Chinese medicinal preparations ranged between 0.11 and 1.22 mg/g for saikosaponin-a and between 0.01 and 0.33 mg/g for saikosaponin-c. |
doi_str_mv | 10.1016/j.jpba.2006.10.002 |
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The optimal ionization characteristics were obtained when using positive-ion electrospray ionization (ESI) with 50 microM sodium acetate as an additive in the mobile phase. We observed good linearity over the range from 0.02 to 2 microg/ml for saikosaponin-a and from 0.02 to 1 microg/ml for saikosaponin-c. The intra-day precisions varied between 3.3 and 8.8% for saikosaponin-a and 0.3 and 11.1% for saikosaponin-c. The limits of detection were 0.01 microg/ml for both markers. The recoveries of saikosaponin-a and -c from the extract of a medicinal preparation sample (Chai-Hu-Ching-Gan-Tang, No. 13 in the table of section Analysis on actual samples) were 97 and 100%, respectively, at a 1 microg/ml spiking concentration of each marker. The highest concentrations of saikosaponin-a and -c among the three B. radixes were found in B. kaoi Liu Chao & Chuang (10.1 mg/g) and in B. falcatum (3.4 mg/g), respectively. The amounts of these saikosaponins in the 10 Chinese medicinal preparations ranged between 0.11 and 1.22 mg/g for saikosaponin-a and between 0.01 and 0.33 mg/g for saikosaponin-c.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2006.10.002</identifier><identifier>PMID: 17118609</identifier><identifier>CODEN: JPBADA</identifier><language>eng</language><publisher>Amsterdam: Elsevier Science</publisher><subject>Analysis ; Analytical, structural and metabolic biochemistry ; Biological and medical sciences ; Calibration ; Chromatography, High Pressure Liquid ; Drugs, Chinese Herbal - analysis ; Drugs, Chinese Herbal - standards ; Fundamental and applied biological sciences. Psychology ; General pharmacology ; Medical sciences ; Oleanolic Acid - analogs & derivatives ; Oleanolic Acid - analysis ; Pharmacology. Drug treatments ; Quality Control ; Reference Standards ; Saponins - analysis ; Spectrometry, Mass, Electrospray Ionization</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2007-02, Vol.43 (3), p.1174-1178</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18521672$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17118609$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LIAU, Bing-Chung</creatorcontrib><creatorcontrib>HSIAO, Shun-Sheng</creatorcontrib><creatorcontrib>LEE, Maw-Rong</creatorcontrib><creatorcontrib>JONG, Ting-Ting</creatorcontrib><creatorcontrib>CHIANG, Shu-Tuan</creatorcontrib><title>Quality control of Chinese medicinal preparations LC/ESI(+)/MS/MS analyses of saikosaponins-a and -c as markers of bupleuri radix samples</title><title>Journal of pharmaceutical and biomedical analysis</title><addtitle>J Pharm Biomed Anal</addtitle><description>We have used LC/ion trap tandem MS analysis to determine saikosaponin-a and -c as target markers in crude 70% methanol extracts from three different species of Bupleuri radix and the 10 most-popular Chinese medicinal preparations containing "Chaihu" (B. radix) without any clean-up. The optimal ionization characteristics were obtained when using positive-ion electrospray ionization (ESI) with 50 microM sodium acetate as an additive in the mobile phase. We observed good linearity over the range from 0.02 to 2 microg/ml for saikosaponin-a and from 0.02 to 1 microg/ml for saikosaponin-c. The intra-day precisions varied between 3.3 and 8.8% for saikosaponin-a and 0.3 and 11.1% for saikosaponin-c. The limits of detection were 0.01 microg/ml for both markers. The recoveries of saikosaponin-a and -c from the extract of a medicinal preparation sample (Chai-Hu-Ching-Gan-Tang, No. 13 in the table of section Analysis on actual samples) were 97 and 100%, respectively, at a 1 microg/ml spiking concentration of each marker. The highest concentrations of saikosaponin-a and -c among the three B. radixes were found in B. kaoi Liu Chao & Chuang (10.1 mg/g) and in B. falcatum (3.4 mg/g), respectively. The amounts of these saikosaponins in the 10 Chinese medicinal preparations ranged between 0.11 and 1.22 mg/g for saikosaponin-a and between 0.01 and 0.33 mg/g for saikosaponin-c.</description><subject>Analysis</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Biological and medical sciences</subject><subject>Calibration</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Drugs, Chinese Herbal - analysis</subject><subject>Drugs, Chinese Herbal - standards</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Oleanolic Acid - analogs & derivatives</subject><subject>Oleanolic Acid - analysis</subject><subject>Pharmacology. Drug treatments</subject><subject>Quality Control</subject><subject>Reference Standards</subject><subject>Saponins - analysis</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpFkG9LwzAQxoMobv75Ar6QvFEU6ZakTdK-lDF1MBGZgu_GNU0xs2trrgX3EfzWRp0IB8fd_Z4H7iHkhLMRZ1yNV6NVm8NIMKbCYsSY2CFDnuo4Eip52SVDpmMeaZbKATlAXDHGJM-SfTLgmvNUsWxIPh97qFy3oaapO99UtCnp5NXVFi1d28IZV0NFW29b8NC5pkY6n4yni9nF1eX4fhGKQiA2aPFbiuDeGoS2qV2NEYRbQSNDAeka_Jv1P1Det5XtvaMeCvcRNOsw4xHZK6FCe7zth-T5Zvo0uYvmD7ezyfU8akWcdVEhcq2lScHKMhfSFEzkJitEAiBTXgiVycTEgksrbGa1SGJhSpCykIZDInl8SM5_fVvfvPcWu-XaobFVBbVtelyqNNM6VSqAp1uwz0MUy9a78MRm-RdeAM62AKCBqvRQG4f_XCoFV1rEX3yyf_s</recordid><startdate>20070219</startdate><enddate>20070219</enddate><creator>LIAU, Bing-Chung</creator><creator>HSIAO, Shun-Sheng</creator><creator>LEE, Maw-Rong</creator><creator>JONG, Ting-Ting</creator><creator>CHIANG, Shu-Tuan</creator><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20070219</creationdate><title>Quality control of Chinese medicinal preparations LC/ESI(+)/MS/MS analyses of saikosaponins-a and -c as markers of bupleuri radix samples</title><author>LIAU, Bing-Chung ; HSIAO, Shun-Sheng ; LEE, Maw-Rong ; JONG, Ting-Ting ; CHIANG, Shu-Tuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p239t-d2b775c8ae5fb25cd02bc9d24aa581d26954c3215e2e9e72432cfa55d5c1a4513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Analysis</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Biological and medical sciences</topic><topic>Calibration</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Drugs, Chinese Herbal - analysis</topic><topic>Drugs, Chinese Herbal - standards</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>Medical sciences</topic><topic>Oleanolic Acid - analogs & derivatives</topic><topic>Oleanolic Acid - analysis</topic><topic>Pharmacology. Drug treatments</topic><topic>Quality Control</topic><topic>Reference Standards</topic><topic>Saponins - analysis</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LIAU, Bing-Chung</creatorcontrib><creatorcontrib>HSIAO, Shun-Sheng</creatorcontrib><creatorcontrib>LEE, Maw-Rong</creatorcontrib><creatorcontrib>JONG, Ting-Ting</creatorcontrib><creatorcontrib>CHIANG, Shu-Tuan</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>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LIAU, Bing-Chung</au><au>HSIAO, Shun-Sheng</au><au>LEE, Maw-Rong</au><au>JONG, Ting-Ting</au><au>CHIANG, Shu-Tuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quality control of Chinese medicinal preparations LC/ESI(+)/MS/MS analyses of saikosaponins-a and -c as markers of bupleuri radix samples</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2007-02-19</date><risdate>2007</risdate><volume>43</volume><issue>3</issue><spage>1174</spage><epage>1178</epage><pages>1174-1178</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><coden>JPBADA</coden><abstract>We have used LC/ion trap tandem MS analysis to determine saikosaponin-a and -c as target markers in crude 70% methanol extracts from three different species of Bupleuri radix and the 10 most-popular Chinese medicinal preparations containing "Chaihu" (B. radix) without any clean-up. The optimal ionization characteristics were obtained when using positive-ion electrospray ionization (ESI) with 50 microM sodium acetate as an additive in the mobile phase. We observed good linearity over the range from 0.02 to 2 microg/ml for saikosaponin-a and from 0.02 to 1 microg/ml for saikosaponin-c. The intra-day precisions varied between 3.3 and 8.8% for saikosaponin-a and 0.3 and 11.1% for saikosaponin-c. The limits of detection were 0.01 microg/ml for both markers. The recoveries of saikosaponin-a and -c from the extract of a medicinal preparation sample (Chai-Hu-Ching-Gan-Tang, No. 13 in the table of section Analysis on actual samples) were 97 and 100%, respectively, at a 1 microg/ml spiking concentration of each marker. The highest concentrations of saikosaponin-a and -c among the three B. radixes were found in B. kaoi Liu Chao & Chuang (10.1 mg/g) and in B. falcatum (3.4 mg/g), respectively. The amounts of these saikosaponins in the 10 Chinese medicinal preparations ranged between 0.11 and 1.22 mg/g for saikosaponin-a and between 0.01 and 0.33 mg/g for saikosaponin-c.</abstract><cop>Amsterdam</cop><pub>Elsevier Science</pub><pmid>17118609</pmid><doi>10.1016/j.jpba.2006.10.002</doi><tpages>5</tpages></addata></record> |
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subjects | Analysis Analytical, structural and metabolic biochemistry Biological and medical sciences Calibration Chromatography, High Pressure Liquid Drugs, Chinese Herbal - analysis Drugs, Chinese Herbal - standards Fundamental and applied biological sciences. Psychology General pharmacology Medical sciences Oleanolic Acid - analogs & derivatives Oleanolic Acid - analysis Pharmacology. Drug treatments Quality Control Reference Standards Saponins - analysis Spectrometry, Mass, Electrospray Ionization |
title | Quality control of Chinese medicinal preparations LC/ESI(+)/MS/MS analyses of saikosaponins-a and -c as markers of bupleuri radix samples |
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