Simultaneous determination of five main active constituents of Erigeron multiradiatus by HPLC-DAD–MS

An HPLC-DAD–MS method was developed for simultaneous determination of the five major active constituents in Erigeron multiradiatus (Wall.) Benth, namely 6′- O-cafferylerigeroside (1), scutellarin (2), apigenin-7- O-β- d-glucuronide (3), apigenin (4) and kaempferol (5), respectively. They were identi...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2008-11, Vol.48 (3), p.980-985
Hauptverfasser: Zhang, Zhifeng, Sun, Wenxia, Luo, Pei, Wu, Liping, Ye, Limin, Zhang, Hao
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container_issue 3
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creator Zhang, Zhifeng
Sun, Wenxia
Luo, Pei
Wu, Liping
Ye, Limin
Zhang, Hao
description An HPLC-DAD–MS method was developed for simultaneous determination of the five major active constituents in Erigeron multiradiatus (Wall.) Benth, namely 6′- O-cafferylerigeroside (1), scutellarin (2), apigenin-7- O-β- d-glucuronide (3), apigenin (4) and kaempferol (5), respectively. They were identified by ESI-MS and comparisons with literature. A comprehensive validation of the method included tests of sensitivity, linearity, precision and accuracy. The linear regressions were acquired with r > 0.999. The precision was evaluated by intra- and inter-day assays, and relative standard deviation (R.S.D.) values were reported within 2.7%. The recovery studies for the quantified compounds were observed in the range of 95.3–102.4% with R.S.D. values less than 2.3%. The overall procedure may be suitable for the qualitative and quantitative analyses of a large number of E. multiradiatus samples. Hierarchical clustering analysis based on the characteristics of the 5 investigated compound peaks in HPLC profiles showed that 18 samples were divided into 2 main clusters. The clusters corresponded to their content. The five constituents in E. multiradiatus are generally regarded as an index for the quality assessment of this herb.
doi_str_mv 10.1016/j.jpba.2008.06.010
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Benth, namely 6′- O-cafferylerigeroside (1), scutellarin (2), apigenin-7- O-β- d-glucuronide (3), apigenin (4) and kaempferol (5), respectively. They were identified by ESI-MS and comparisons with literature. A comprehensive validation of the method included tests of sensitivity, linearity, precision and accuracy. The linear regressions were acquired with r &gt; 0.999. The precision was evaluated by intra- and inter-day assays, and relative standard deviation (R.S.D.) values were reported within 2.7%. The recovery studies for the quantified compounds were observed in the range of 95.3–102.4% with R.S.D. values less than 2.3%. The overall procedure may be suitable for the qualitative and quantitative analyses of a large number of E. multiradiatus samples. Hierarchical clustering analysis based on the characteristics of the 5 investigated compound peaks in HPLC profiles showed that 18 samples were divided into 2 main clusters. The clusters corresponded to their content. 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Psychology ; General pharmacology ; Glucuronates - analysis ; Glucuronates - chemistry ; Hot Temperature ; HPLC-DAD–MS ; Kaempferols - analysis ; Kaempferols - chemistry ; Linear Models ; Mass Spectrometry - methods ; Medical sciences ; Molecular Structure ; Pharmacology. 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Benth, namely 6′- O-cafferylerigeroside (1), scutellarin (2), apigenin-7- O-β- d-glucuronide (3), apigenin (4) and kaempferol (5), respectively. They were identified by ESI-MS and comparisons with literature. A comprehensive validation of the method included tests of sensitivity, linearity, precision and accuracy. The linear regressions were acquired with r &gt; 0.999. The precision was evaluated by intra- and inter-day assays, and relative standard deviation (R.S.D.) values were reported within 2.7%. The recovery studies for the quantified compounds were observed in the range of 95.3–102.4% with R.S.D. values less than 2.3%. The overall procedure may be suitable for the qualitative and quantitative analyses of a large number of E. multiradiatus samples. Hierarchical clustering analysis based on the characteristics of the 5 investigated compound peaks in HPLC profiles showed that 18 samples were divided into 2 main clusters. The clusters corresponded to their content. 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Psychology</subject><subject>General pharmacology</subject><subject>Glucuronates - analysis</subject><subject>Glucuronates - chemistry</subject><subject>Hot Temperature</subject><subject>HPLC-DAD–MS</subject><subject>Kaempferols - analysis</subject><subject>Kaempferols - chemistry</subject><subject>Linear Models</subject><subject>Mass Spectrometry - methods</subject><subject>Medical sciences</subject><subject>Molecular Structure</subject><subject>Pharmacology. Drug treatments</subject><subject>Plant Extracts - chemistry</subject><subject>Pyrones - analysis</subject><subject>Pyrones - chemistry</subject><subject>Quality assessment</subject><subject>Reference Standards</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><subject>Time Factors</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1u1DAURi0EokPhBVigbOgu4TpObEdiU01LizQIpILEznKca-RRfgbbqdQd78Ab8iS1NSPYsbKle-5nf4eQ1xQqCpS_21f7Q6-rGkBWwCug8IRsqBSsrHnz_SnZgGC0FCDbM_IihD0AtLRrnpMzKrmQTdtuiL1z0zpGPeOyhmLAiH5ys45umYvFFtbdYzFpNxfaxHw3yxyiiyvOMWTg2rsf6BOcU5zXg9MxBfUPxe2X3ba8urz68-v3p7uX5JnVY8BXp_OcfPtw_XV7W-4-33zcXu5Kw2QTy8Zqga0UXc8M5alX3doOGmkHFJw1lMlWt0MvaRrlGTeph-xRGgZCWM7OycUx9-CXnyuGqCYXDI7jsaDiHe-AQwbrI2j8EoJHqw7eTdo_KAoq21V7le2qbFcBV8luWnpzSl_7CYd_KyedCXh7AnQwerRez8aFv1xNayo6ll9_f-Qwubh36FUwDmeDg_NoohoW979_PAKb3ZkD</recordid><startdate>20081104</startdate><enddate>20081104</enddate><creator>Zhang, Zhifeng</creator><creator>Sun, Wenxia</creator><creator>Luo, Pei</creator><creator>Wu, Liping</creator><creator>Ye, Limin</creator><creator>Zhang, Hao</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</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>20081104</creationdate><title>Simultaneous determination of five main active constituents of Erigeron multiradiatus by HPLC-DAD–MS</title><author>Zhang, Zhifeng ; Sun, Wenxia ; Luo, Pei ; Wu, Liping ; Ye, Limin ; Zhang, Hao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-4fa7e5879b3c1600825f9048fde76341385a5db81008825f6c6788be8c3077f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Analysis</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Apigenin - analysis</topic><topic>Apigenin - chemistry</topic><topic>Biological and medical sciences</topic><topic>Calibration</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Cluster Analysis</topic><topic>Erigeron - chemistry</topic><topic>Erigeron multiradiatus</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>Glucuronates - analysis</topic><topic>Glucuronates - chemistry</topic><topic>Hot Temperature</topic><topic>HPLC-DAD–MS</topic><topic>Kaempferols - analysis</topic><topic>Kaempferols - chemistry</topic><topic>Linear Models</topic><topic>Mass Spectrometry - methods</topic><topic>Medical sciences</topic><topic>Molecular Structure</topic><topic>Pharmacology. Drug treatments</topic><topic>Plant Extracts - chemistry</topic><topic>Pyrones - analysis</topic><topic>Pyrones - chemistry</topic><topic>Quality assessment</topic><topic>Reference Standards</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Spectrometry, Mass, Electrospray Ionization - methods</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Zhifeng</creatorcontrib><creatorcontrib>Sun, Wenxia</creatorcontrib><creatorcontrib>Luo, Pei</creatorcontrib><creatorcontrib>Wu, Liping</creatorcontrib><creatorcontrib>Ye, Limin</creatorcontrib><creatorcontrib>Zhang, Hao</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>CrossRef</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>Zhang, Zhifeng</au><au>Sun, Wenxia</au><au>Luo, Pei</au><au>Wu, Liping</au><au>Ye, Limin</au><au>Zhang, Hao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous determination of five main active constituents of Erigeron multiradiatus by HPLC-DAD–MS</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2008-11-04</date><risdate>2008</risdate><volume>48</volume><issue>3</issue><spage>980</spage><epage>985</epage><pages>980-985</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><coden>JPBADA</coden><abstract>An HPLC-DAD–MS method was developed for simultaneous determination of the five major active constituents in Erigeron multiradiatus (Wall.) Benth, namely 6′- O-cafferylerigeroside (1), scutellarin (2), apigenin-7- O-β- d-glucuronide (3), apigenin (4) and kaempferol (5), respectively. They were identified by ESI-MS and comparisons with literature. A comprehensive validation of the method included tests of sensitivity, linearity, precision and accuracy. The linear regressions were acquired with r &gt; 0.999. The precision was evaluated by intra- and inter-day assays, and relative standard deviation (R.S.D.) values were reported within 2.7%. The recovery studies for the quantified compounds were observed in the range of 95.3–102.4% with R.S.D. values less than 2.3%. The overall procedure may be suitable for the qualitative and quantitative analyses of a large number of E. multiradiatus samples. Hierarchical clustering analysis based on the characteristics of the 5 investigated compound peaks in HPLC profiles showed that 18 samples were divided into 2 main clusters. The clusters corresponded to their content. The five constituents in E. multiradiatus are generally regarded as an index for the quality assessment of this herb.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>18678455</pmid><doi>10.1016/j.jpba.2008.06.010</doi><tpages>6</tpages></addata></record>
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subjects Analysis
Analytical, structural and metabolic biochemistry
Apigenin - analysis
Apigenin - chemistry
Biological and medical sciences
Calibration
Chromatography, High Pressure Liquid - methods
Cluster Analysis
Erigeron - chemistry
Erigeron multiradiatus
Fundamental and applied biological sciences. Psychology
General pharmacology
Glucuronates - analysis
Glucuronates - chemistry
Hot Temperature
HPLC-DAD–MS
Kaempferols - analysis
Kaempferols - chemistry
Linear Models
Mass Spectrometry - methods
Medical sciences
Molecular Structure
Pharmacology. Drug treatments
Plant Extracts - chemistry
Pyrones - analysis
Pyrones - chemistry
Quality assessment
Reference Standards
Reproducibility of Results
Sensitivity and Specificity
Spectrometry, Mass, Electrospray Ionization - methods
Time Factors
title Simultaneous determination of five main active constituents of Erigeron multiradiatus by HPLC-DAD–MS
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