Preparative isolation and purification of antioxidative stilbene oligomers from Vitis chunganeniss using high-speed counter-current chromatography in stepwise elution mode
Preparative high-speed counter-current chromatography (HSCCC) was successfully applied to the isolation and purification of three stilbene oligomers from Vitis chunganeniss using stepwise elution with a pair of two-phase solvent systems composed of n-hexane-ethyl acetate-methanol-water at (2:5:2:5,...
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Veröffentlicht in: | Journal of separation science 2009-07, Vol.32 (14), p.2339-2345 |
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description | Preparative high-speed counter-current chromatography (HSCCC) was successfully applied to the isolation and purification of three stilbene oligomers from Vitis chunganeniss using stepwise elution with a pair of two-phase solvent systems composed of n-hexane-ethyl acetate-methanol-water at (2:5:2:5, v/v) and (1:2:1:2, v/v). The preparative HSCCC separation was performed on 800 mg of crude sample yielding hopeaphenol (21.1 mg), amurensin G (37.2 mg) and vitisin A (95.6 mg) in a one-step separation, with purities over 95% as determined by HPLC. The structures of these three compounds were identified by MS, ¹H NMR and ¹³C NMR. In addition, their antioxidant activities were screened by DPPH assay, where vitisin A showed strong antioxidant activity. Further EPR experiments with spin-trapping technique demonstrated that vitisin A is a potent and selective singlet oxygen quencher, which may be used in singlet oxygen-mediated diseases as a pharmacological agent. |
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The preparative HSCCC separation was performed on 800 mg of crude sample yielding hopeaphenol (21.1 mg), amurensin G (37.2 mg) and vitisin A (95.6 mg) in a one-step separation, with purities over 95% as determined by HPLC. The structures of these three compounds were identified by MS, ¹H NMR and ¹³C NMR. In addition, their antioxidant activities were screened by DPPH assay, where vitisin A showed strong antioxidant activity. Further EPR experiments with spin-trapping technique demonstrated that vitisin A is a potent and selective singlet oxygen quencher, which may be used in singlet oxygen-mediated diseases as a pharmacological agent.</description><identifier>ISSN: 1615-9306</identifier><identifier>EISSN: 1615-9314</identifier><identifier>DOI: 10.1002/jssc.200900033</identifier><identifier>PMID: 19557810</identifier><language>eng</language><publisher>Weinheim: Wiley-VCH Verlag</publisher><subject>Acetates - chemistry ; Antioxidant ; Antioxidants - chemistry ; Antioxidants - isolation & purification ; Biological and medical sciences ; Chromatography, High Pressure Liquid - instrumentation ; Chromatography, High Pressure Liquid - methods ; Countercurrent Distribution - instrumentation ; Countercurrent Distribution - methods ; General pharmacology ; Hexanes - chemistry ; High‐speed counter‐current chromatography ; Medical sciences ; Methanol - chemistry ; Molecular Conformation ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. Drug treatments ; Solvents - chemistry ; Stepwise ; Stilbene oligomer ; Stilbenes - chemistry ; Stilbenes - isolation & purification ; Time Factors ; Vitis - chemistry ; Vitis chunganeniss ; Water - chemistry</subject><ispartof>Journal of separation science, 2009-07, Vol.32 (14), p.2339-2345</ispartof><rights>Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. 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The preparative HSCCC separation was performed on 800 mg of crude sample yielding hopeaphenol (21.1 mg), amurensin G (37.2 mg) and vitisin A (95.6 mg) in a one-step separation, with purities over 95% as determined by HPLC. The structures of these three compounds were identified by MS, ¹H NMR and ¹³C NMR. In addition, their antioxidant activities were screened by DPPH assay, where vitisin A showed strong antioxidant activity. Further EPR experiments with spin-trapping technique demonstrated that vitisin A is a potent and selective singlet oxygen quencher, which may be used in singlet oxygen-mediated diseases as a pharmacological agent.</description><subject>Acetates - chemistry</subject><subject>Antioxidant</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - isolation & purification</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid - instrumentation</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Countercurrent Distribution - instrumentation</subject><subject>Countercurrent Distribution - methods</subject><subject>General pharmacology</subject><subject>Hexanes - chemistry</subject><subject>High‐speed counter‐current chromatography</subject><subject>Medical sciences</subject><subject>Methanol - chemistry</subject><subject>Molecular Conformation</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Solvents - chemistry</subject><subject>Stepwise</subject><subject>Stilbene oligomer</subject><subject>Stilbenes - chemistry</subject><subject>Stilbenes - isolation & purification</subject><subject>Time Factors</subject><subject>Vitis - chemistry</subject><subject>Vitis chunganeniss</subject><subject>Water - chemistry</subject><issn>1615-9306</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuP1DAQhCMEYh9w5Qi-sLcMbTtO4iMa8dRKIA3LNXKcdsarxA52wjK_iT-Jl4wGbntyqfVVdVuVZS8obCgAe3Mbo94wAAkAnD_KzmlJRS45LR6fNJRn2UWMtwC0qiU8zc6oFKKqKZxnv78GnFRQs_2JxEY_JOUdUa4j0xKssXodeJNmSf2y3crG2Q4tOiR-sL0fMURigh_JdzvbSPR-cb1y6GyMZInW9WRv-30eJ8SOaL-4GUOulxDQzYlOTjX7PqhpfyDWpXSc7mxEgsPyd__oO3yWPTFqiPj8-F5mN-_ffdt-zK-_fPi0fXud64LVPFe1pqXihe640p0Epk2thJRatYybQjCBrSiUaY3QUlGjBS0oa1ulmTQUBL_MrtbcKfgfC8a5GW3UOAzpQ36JTVkJ4CXlD4K8qCSrQSZws4I6-BgDmmYKdlTh0FBo7nts7ntsTj0mw8tj8tKO2P3Dj8Ul4PURUFGrwQTltI0njtGqAimqxMmVu7MDHh5Y23ze7bb_H_Fq9RrlG9WHlH-zY0A50FLIQhT8DxrAxts</recordid><startdate>200907</startdate><enddate>200907</enddate><creator>He, Shan</creator><creator>Lu, Yanbin</creator><creator>Jiang, Liyan</creator><creator>Wu, Bin</creator><creator>Zhang, Feiying</creator><creator>Pan, Yuanjiang</creator><general>Wiley-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley</general><scope>FBQ</scope><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>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>200907</creationdate><title>Preparative isolation and purification of antioxidative stilbene oligomers from Vitis chunganeniss using high-speed counter-current chromatography in stepwise elution mode</title><author>He, Shan ; Lu, Yanbin ; Jiang, Liyan ; Wu, Bin ; Zhang, Feiying ; Pan, Yuanjiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4283-a8c16a34cd3acd902cf8a599cab23f4525eb54afbf5c9a1fc51412bbac29f1053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acetates - chemistry</topic><topic>Antioxidant</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - isolation & purification</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid - instrumentation</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Countercurrent Distribution - instrumentation</topic><topic>Countercurrent Distribution - methods</topic><topic>General pharmacology</topic><topic>Hexanes - chemistry</topic><topic>High‐speed counter‐current chromatography</topic><topic>Medical sciences</topic><topic>Methanol - chemistry</topic><topic>Molecular Conformation</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Solvents - chemistry</topic><topic>Stepwise</topic><topic>Stilbene oligomer</topic><topic>Stilbenes - chemistry</topic><topic>Stilbenes - isolation & purification</topic><topic>Time Factors</topic><topic>Vitis - chemistry</topic><topic>Vitis chunganeniss</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Shan</creatorcontrib><creatorcontrib>Lu, Yanbin</creatorcontrib><creatorcontrib>Jiang, Liyan</creatorcontrib><creatorcontrib>Wu, Bin</creatorcontrib><creatorcontrib>Zhang, Feiying</creatorcontrib><creatorcontrib>Pan, Yuanjiang</creatorcontrib><collection>AGRIS</collection><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>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of separation science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Shan</au><au>Lu, Yanbin</au><au>Jiang, Liyan</au><au>Wu, Bin</au><au>Zhang, Feiying</au><au>Pan, Yuanjiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparative isolation and purification of antioxidative stilbene oligomers from Vitis chunganeniss using high-speed counter-current chromatography in stepwise elution mode</atitle><jtitle>Journal of separation science</jtitle><addtitle>J Sep Sci</addtitle><date>2009-07</date><risdate>2009</risdate><volume>32</volume><issue>14</issue><spage>2339</spage><epage>2345</epage><pages>2339-2345</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>Preparative high-speed counter-current chromatography (HSCCC) was successfully applied to the isolation and purification of three stilbene oligomers from Vitis chunganeniss using stepwise elution with a pair of two-phase solvent systems composed of n-hexane-ethyl acetate-methanol-water at (2:5:2:5, v/v) and (1:2:1:2, v/v). The preparative HSCCC separation was performed on 800 mg of crude sample yielding hopeaphenol (21.1 mg), amurensin G (37.2 mg) and vitisin A (95.6 mg) in a one-step separation, with purities over 95% as determined by HPLC. The structures of these three compounds were identified by MS, ¹H NMR and ¹³C NMR. In addition, their antioxidant activities were screened by DPPH assay, where vitisin A showed strong antioxidant activity. Further EPR experiments with spin-trapping technique demonstrated that vitisin A is a potent and selective singlet oxygen quencher, which may be used in singlet oxygen-mediated diseases as a pharmacological agent.</abstract><cop>Weinheim</cop><pub>Wiley-VCH Verlag</pub><pmid>19557810</pmid><doi>10.1002/jssc.200900033</doi><tpages>7</tpages></addata></record> |
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subjects | Acetates - chemistry Antioxidant Antioxidants - chemistry Antioxidants - isolation & purification Biological and medical sciences Chromatography, High Pressure Liquid - instrumentation Chromatography, High Pressure Liquid - methods Countercurrent Distribution - instrumentation Countercurrent Distribution - methods General pharmacology Hexanes - chemistry High‐speed counter‐current chromatography Medical sciences Methanol - chemistry Molecular Conformation Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Solvents - chemistry Stepwise Stilbene oligomer Stilbenes - chemistry Stilbenes - isolation & purification Time Factors Vitis - chemistry Vitis chunganeniss Water - chemistry |
title | Preparative isolation and purification of antioxidative stilbene oligomers from Vitis chunganeniss using high-speed counter-current chromatography in stepwise elution mode |
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