A UHPLC method for the rapid separation and quantification of anthocyanins in acai berry and dry blueberry extracts
[Display omitted] •A fast method for quantification of six anthocyanins in acai berry and dry blueberry extracts was developed.•The method shows short time (5min) of analysis, all peaks were separated in less than 1min of gradient runtime.•The method shows unique selectivity of pentafluorophenyl (F5...
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Veröffentlicht in: | Journal of pharmaceutical and biomedical analysis 2017-09, Vol.143, p.204-213 |
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creator | Fibigr, Jakub Šatínský, Dalibor Solich, Petr |
description | [Display omitted]
•A fast method for quantification of six anthocyanins in acai berry and dry blueberry extracts was developed.•The method shows short time (5min) of analysis, all peaks were separated in less than 1min of gradient runtime.•The method shows unique selectivity of pentafluorophenyl (F5) stationary phase for separation of desired anthocyanins.•The F5 stationary phase provided better efficiency than two tested C18 stationary phases (PS and Polar).
The presented work describes the development and validation of a rapid UHPLC-UV method using a core-shell particle column with a pentafluorophenyl stationary phase for the separation and quantitative analysis of the six anthocyanins in acai berry and dry blueberry extracts. The anthocyanins (cyanidin-3-glucoside, cyanidin-3-rutenoside, delphinidin-3-galactoside, delphinidin-3-glucoside, delphinidin-3-rutenoside, and peonidin-3-glucoside) were separated and analyzed in 5min. The chromatographic separation was performed on a Kinetex PFP (150×2.1mm) core-shell column with a particle size of 1.7μm at a temperature of 50°C. Acetonitrile was used as mobile phase B and 5% formic acid, filtrated through a 0.22μm filter, as mobile phase A. They were delivered at a flow rate of 0.55mLmin−1 according to the elution gradient program. The detection wavelength was set at 520nm. A solid-liquid extraction with a solution of methanol and a 5% water solution of formic acid (25+75v/v) using an ultrasonic bath was chosen for the preparation of the available commercial samples of food supplements with a content of acai berry extract and blueberry extract. Under optimal chromatographic conditions, the method was validated. Recoveries for all analyzed anthocyanins were 97.8–102.6% and the relative standard deviation ranged from 0.4% to 3.0% for within-day and from 0.6% to 3.1% for between-day repeatability. The limits of detection were in the range of 0.11–0.14μgmL−1. |
doi_str_mv | 10.1016/j.jpba.2017.05.045 |
format | Article |
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•A fast method for quantification of six anthocyanins in acai berry and dry blueberry extracts was developed.•The method shows short time (5min) of analysis, all peaks were separated in less than 1min of gradient runtime.•The method shows unique selectivity of pentafluorophenyl (F5) stationary phase for separation of desired anthocyanins.•The F5 stationary phase provided better efficiency than two tested C18 stationary phases (PS and Polar).
The presented work describes the development and validation of a rapid UHPLC-UV method using a core-shell particle column with a pentafluorophenyl stationary phase for the separation and quantitative analysis of the six anthocyanins in acai berry and dry blueberry extracts. The anthocyanins (cyanidin-3-glucoside, cyanidin-3-rutenoside, delphinidin-3-galactoside, delphinidin-3-glucoside, delphinidin-3-rutenoside, and peonidin-3-glucoside) were separated and analyzed in 5min. The chromatographic separation was performed on a Kinetex PFP (150×2.1mm) core-shell column with a particle size of 1.7μm at a temperature of 50°C. Acetonitrile was used as mobile phase B and 5% formic acid, filtrated through a 0.22μm filter, as mobile phase A. They were delivered at a flow rate of 0.55mLmin−1 according to the elution gradient program. The detection wavelength was set at 520nm. A solid-liquid extraction with a solution of methanol and a 5% water solution of formic acid (25+75v/v) using an ultrasonic bath was chosen for the preparation of the available commercial samples of food supplements with a content of acai berry extract and blueberry extract. Under optimal chromatographic conditions, the method was validated. Recoveries for all analyzed anthocyanins were 97.8–102.6% and the relative standard deviation ranged from 0.4% to 3.0% for within-day and from 0.6% to 3.1% for between-day repeatability. The limits of detection were in the range of 0.11–0.14μgmL−1.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2017.05.045</identifier><identifier>PMID: 28605682</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Acai berry ; Anthocyanins ; Blueberry ; Chromatography, High Pressure Liquid ; Core-shell column ; Euterpe ; Fast separation ; Plant extracts</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2017-09, Vol.143, p.204-213</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-cc40e615f2ce2725588ab0649b927d79ae7c925dc7489b8c1358b98c63e463683</citedby><cites>FETCH-LOGICAL-c356t-cc40e615f2ce2725588ab0649b927d79ae7c925dc7489b8c1358b98c63e463683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpba.2017.05.045$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28605682$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fibigr, Jakub</creatorcontrib><creatorcontrib>Šatínský, Dalibor</creatorcontrib><creatorcontrib>Solich, Petr</creatorcontrib><title>A UHPLC method for the rapid separation and quantification of anthocyanins in acai berry and dry blueberry extracts</title><title>Journal of pharmaceutical and biomedical analysis</title><addtitle>J Pharm Biomed Anal</addtitle><description>[Display omitted]
•A fast method for quantification of six anthocyanins in acai berry and dry blueberry extracts was developed.•The method shows short time (5min) of analysis, all peaks were separated in less than 1min of gradient runtime.•The method shows unique selectivity of pentafluorophenyl (F5) stationary phase for separation of desired anthocyanins.•The F5 stationary phase provided better efficiency than two tested C18 stationary phases (PS and Polar).
The presented work describes the development and validation of a rapid UHPLC-UV method using a core-shell particle column with a pentafluorophenyl stationary phase for the separation and quantitative analysis of the six anthocyanins in acai berry and dry blueberry extracts. The anthocyanins (cyanidin-3-glucoside, cyanidin-3-rutenoside, delphinidin-3-galactoside, delphinidin-3-glucoside, delphinidin-3-rutenoside, and peonidin-3-glucoside) were separated and analyzed in 5min. The chromatographic separation was performed on a Kinetex PFP (150×2.1mm) core-shell column with a particle size of 1.7μm at a temperature of 50°C. Acetonitrile was used as mobile phase B and 5% formic acid, filtrated through a 0.22μm filter, as mobile phase A. They were delivered at a flow rate of 0.55mLmin−1 according to the elution gradient program. The detection wavelength was set at 520nm. A solid-liquid extraction with a solution of methanol and a 5% water solution of formic acid (25+75v/v) using an ultrasonic bath was chosen for the preparation of the available commercial samples of food supplements with a content of acai berry extract and blueberry extract. Under optimal chromatographic conditions, the method was validated. Recoveries for all analyzed anthocyanins were 97.8–102.6% and the relative standard deviation ranged from 0.4% to 3.0% for within-day and from 0.6% to 3.1% for between-day repeatability. The limits of detection were in the range of 0.11–0.14μgmL−1.</description><subject>Acai berry</subject><subject>Anthocyanins</subject><subject>Blueberry</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Core-shell column</subject><subject>Euterpe</subject><subject>Fast separation</subject><subject>Plant extracts</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1r3DAURUVpaCZp_0AWQctu7Eqy9QXdhCFpAgPNIoHshCw9Ew0ztiPJJfPvo6nTLrN6cDn3wjsIXVBSU0LFj229nTpbM0JlTXhNWv4JraiSTcVE-_QZrYhsaCWJ4qfoLKUtIYRT3X5Bp0wJwoViK5Su8OPt_WaN95CfR4_7MeL8DDjaKXicYLLR5jAO2A4ev8x2yKEPbonGvqSl5Q52CEPCoVDOBtxBjIe_BV9ut5thSeA1R-ty-opOertL8O39nqPHm-uH9W21-f3rbn21qVzDRa6cawkIynvmgEnGuVK2I6LVnWbSS21BOs24d7JVulOONlx1WjnRQCsaoZpz9H3ZneL4MkPKZh-Sg93ODjDOyVBNNCNcS1ZQtqAujilF6M0Uw97Gg6HEHGWbrTnKNkfZhnBTZJfS5fv-3O3B_6_8s1uAnwsA5cs_AaJJLsDgwIcILhs_ho_23wB7eJC-</recordid><startdate>20170905</startdate><enddate>20170905</enddate><creator>Fibigr, Jakub</creator><creator>Šatínský, Dalibor</creator><creator>Solich, Petr</creator><general>Elsevier B.V</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></search><sort><creationdate>20170905</creationdate><title>A UHPLC method for the rapid separation and quantification of anthocyanins in acai berry and dry blueberry extracts</title><author>Fibigr, Jakub ; Šatínský, Dalibor ; Solich, Petr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-cc40e615f2ce2725588ab0649b927d79ae7c925dc7489b8c1358b98c63e463683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acai berry</topic><topic>Anthocyanins</topic><topic>Blueberry</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Core-shell column</topic><topic>Euterpe</topic><topic>Fast separation</topic><topic>Plant extracts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fibigr, Jakub</creatorcontrib><creatorcontrib>Šatínský, Dalibor</creatorcontrib><creatorcontrib>Solich, Petr</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 pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fibigr, Jakub</au><au>Šatínský, Dalibor</au><au>Solich, Petr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A UHPLC method for the rapid separation and quantification of anthocyanins in acai berry and dry blueberry extracts</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2017-09-05</date><risdate>2017</risdate><volume>143</volume><spage>204</spage><epage>213</epage><pages>204-213</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><abstract>[Display omitted]
•A fast method for quantification of six anthocyanins in acai berry and dry blueberry extracts was developed.•The method shows short time (5min) of analysis, all peaks were separated in less than 1min of gradient runtime.•The method shows unique selectivity of pentafluorophenyl (F5) stationary phase for separation of desired anthocyanins.•The F5 stationary phase provided better efficiency than two tested C18 stationary phases (PS and Polar).
The presented work describes the development and validation of a rapid UHPLC-UV method using a core-shell particle column with a pentafluorophenyl stationary phase for the separation and quantitative analysis of the six anthocyanins in acai berry and dry blueberry extracts. The anthocyanins (cyanidin-3-glucoside, cyanidin-3-rutenoside, delphinidin-3-galactoside, delphinidin-3-glucoside, delphinidin-3-rutenoside, and peonidin-3-glucoside) were separated and analyzed in 5min. The chromatographic separation was performed on a Kinetex PFP (150×2.1mm) core-shell column with a particle size of 1.7μm at a temperature of 50°C. Acetonitrile was used as mobile phase B and 5% formic acid, filtrated through a 0.22μm filter, as mobile phase A. They were delivered at a flow rate of 0.55mLmin−1 according to the elution gradient program. The detection wavelength was set at 520nm. A solid-liquid extraction with a solution of methanol and a 5% water solution of formic acid (25+75v/v) using an ultrasonic bath was chosen for the preparation of the available commercial samples of food supplements with a content of acai berry extract and blueberry extract. Under optimal chromatographic conditions, the method was validated. Recoveries for all analyzed anthocyanins were 97.8–102.6% and the relative standard deviation ranged from 0.4% to 3.0% for within-day and from 0.6% to 3.1% for between-day repeatability. The limits of detection were in the range of 0.11–0.14μgmL−1.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>28605682</pmid><doi>10.1016/j.jpba.2017.05.045</doi><tpages>10</tpages></addata></record> |
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subjects | Acai berry Anthocyanins Blueberry Chromatography, High Pressure Liquid Core-shell column Euterpe Fast separation Plant extracts |
title | A UHPLC method for the rapid separation and quantification of anthocyanins in acai berry and dry blueberry extracts |
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