α-Lipoic acid in dietary supplements: Development and comparison of HPLC-CEAD and HPLC-ESI-MS methods
α-Lipoic acid is an antioxidant used both in the prevention and treatment of various oxidative stress related diseases. It is an important constituent of some dietary supplements and can also be found in plant and animal sources. A rapid method for the determination of α-lipoic acid in dietary suppl...
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Veröffentlicht in: | Journal of pharmaceutical and biomedical analysis 2007-11, Vol.45 (4), p.694-699 |
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description | α-Lipoic acid is an antioxidant used both in the prevention and treatment of various oxidative stress related diseases. It is an important constituent of some dietary supplements and can also be found in plant and animal sources. A rapid method for the determination of α-lipoic acid in dietary supplements based on high performance liquid chromatography coupled with a coulometric electrode array detector (CEAD) and an electrospray ionization mass spectrometer (ESI-MS) was developed. First, α-lipoic acid was extracted with methanol by sonication, chromatographic separation was then achieved by isocratic elution [acetonitrile/methanol/50
mM potassium dihydrogen phosphate (pH 3, adjusted with phosphoric acid): 350/65/585, v/v/v] using an ACE 3-C-18 column at a flow rate of 0.45
ml/min. α-Lipoic acid was detected by means of a CEAD at +300, +400, +450, +500, +550, +600, +650, and +700
mV against palladium reference electrodes. For ESI-MS detection (negative mode), the composition of the mobile phase was changed to 0.1% acetic acid in water/acetonitrile 55:45, v/v applying a flow rate of 0.2
ml/min. The presented methods were utilized to determine the α-lipoic acid content in six dietary supplements. The results of both detection modes were in good correlation. |
doi_str_mv | 10.1016/j.jpba.2007.08.003 |
format | Article |
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mM potassium dihydrogen phosphate (pH 3, adjusted with phosphoric acid): 350/65/585, v/v/v] using an ACE 3-C-18 column at a flow rate of 0.45
ml/min. α-Lipoic acid was detected by means of a CEAD at +300, +400, +450, +500, +550, +600, +650, and +700
mV against palladium reference electrodes. For ESI-MS detection (negative mode), the composition of the mobile phase was changed to 0.1% acetic acid in water/acetonitrile 55:45, v/v applying a flow rate of 0.2
ml/min. The presented methods were utilized to determine the α-lipoic acid content in six dietary supplements. The results of both detection modes were in good correlation.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2007.08.003</identifier><identifier>PMID: 17881179</identifier><identifier>CODEN: JPBADA</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Analysis ; Analytical, structural and metabolic biochemistry ; Antioxidants - analysis ; Biological and medical sciences ; Calibration ; Chromatography, High Pressure Liquid ; Coulometric electrode array detection ; Dietary supplements ; Dietary Supplements - analysis ; Dietary Supplements - standards ; Electrodes ; Electrospray ionization mass spectrometry ; Fundamental and applied biological sciences. Psychology ; General pharmacology ; Linear Models ; Lipoic acid ; Medical sciences ; Pharmacology. Drug treatments ; Reproducibility of Results ; Reversed-phase high performance liquid chromatography ; Sensitivity and Specificity ; Spectrometry, Mass, Electrospray Ionization ; Thioctic Acid - analysis</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2007-11, Vol.45 (4), p.694-699</ispartof><rights>2007 Elsevier B.V.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-4eedf0640ec8c6b9423ef6e62b6718fa4656c0675338162285a0a930ddd4fdf73</citedby><cites>FETCH-LOGICAL-c384t-4eedf0640ec8c6b9423ef6e62b6718fa4656c0675338162285a0a930ddd4fdf73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S073170850700461X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19984591$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17881179$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Durrani, Arjumand I.</creatorcontrib><creatorcontrib>Schwartz, Heidi</creatorcontrib><creatorcontrib>Schmid, Walther</creatorcontrib><creatorcontrib>Sontag, Gerhard</creatorcontrib><title>α-Lipoic acid in dietary supplements: Development and comparison of HPLC-CEAD and HPLC-ESI-MS methods</title><title>Journal of pharmaceutical and biomedical analysis</title><addtitle>J Pharm Biomed Anal</addtitle><description>α-Lipoic acid is an antioxidant used both in the prevention and treatment of various oxidative stress related diseases. It is an important constituent of some dietary supplements and can also be found in plant and animal sources. A rapid method for the determination of α-lipoic acid in dietary supplements based on high performance liquid chromatography coupled with a coulometric electrode array detector (CEAD) and an electrospray ionization mass spectrometer (ESI-MS) was developed. First, α-lipoic acid was extracted with methanol by sonication, chromatographic separation was then achieved by isocratic elution [acetonitrile/methanol/50
mM potassium dihydrogen phosphate (pH 3, adjusted with phosphoric acid): 350/65/585, v/v/v] using an ACE 3-C-18 column at a flow rate of 0.45
ml/min. α-Lipoic acid was detected by means of a CEAD at +300, +400, +450, +500, +550, +600, +650, and +700
mV against palladium reference electrodes. For ESI-MS detection (negative mode), the composition of the mobile phase was changed to 0.1% acetic acid in water/acetonitrile 55:45, v/v applying a flow rate of 0.2
ml/min. The presented methods were utilized to determine the α-lipoic acid content in six dietary supplements. The results of both detection modes were in good correlation.</description><subject>Analysis</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Antioxidants - analysis</subject><subject>Biological and medical sciences</subject><subject>Calibration</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Coulometric electrode array detection</subject><subject>Dietary supplements</subject><subject>Dietary Supplements - analysis</subject><subject>Dietary Supplements - standards</subject><subject>Electrodes</subject><subject>Electrospray ionization mass spectrometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General pharmacology</subject><subject>Linear Models</subject><subject>Lipoic acid</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Reproducibility of Results</subject><subject>Reversed-phase high performance liquid chromatography</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Thioctic Acid - analysis</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM9q3DAQh0VpaLZpX6CHoktzszuyZEkuvYTN5g9sSCAt9Ca00ohqsS3X8gb6WH2RPlO92YXcehqG-ebHzEfIBwYlAyY_b8vtsLFlBaBK0CUAf0UWTCteVFL8eE0WoDgrFOj6lLzNeQsANWvEG3LKlNaMqWZBwt8_xToOKTpqXfQ09tRHnOz4m-bdMLTYYT_lL_QSn7BNw76jtvfUpW6wY8yppynQm4f1sliuLi6fZ8_d6vG2uHukHU4_k8_vyEmwbcb3x3pGvl-tvi1vivX99e3yYl04rsVUCEQfQApAp53cNKLiGCTKaiMV08EKWUsHUtWcayarStcWbMPBey-CD4qfkfND7jCmXzvMk-lidti2tse0y0ZqMSdVYgarA-jGlPOIwQxj7Oa3DQOzt2u2Zm_X7O0a0Ga2Oy99PKbvNh36l5Wjzhn4dARsdrYNo-1dzC9c02hRN2zmvh44nF08RRxNdhF7hz6O6CbjU_zfHf8A0q6XSA</recordid><startdate>20071130</startdate><enddate>20071130</enddate><creator>Durrani, Arjumand I.</creator><creator>Schwartz, Heidi</creator><creator>Schmid, Walther</creator><creator>Sontag, Gerhard</creator><general>Elsevier B.V</general><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>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20071130</creationdate><title>α-Lipoic acid in dietary supplements: Development and comparison of HPLC-CEAD and HPLC-ESI-MS methods</title><author>Durrani, Arjumand I. ; Schwartz, Heidi ; Schmid, Walther ; Sontag, Gerhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-4eedf0640ec8c6b9423ef6e62b6718fa4656c0675338162285a0a930ddd4fdf73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Analysis</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Antioxidants - analysis</topic><topic>Biological and medical sciences</topic><topic>Calibration</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Coulometric electrode array detection</topic><topic>Dietary supplements</topic><topic>Dietary Supplements - analysis</topic><topic>Dietary Supplements - standards</topic><topic>Electrodes</topic><topic>Electrospray ionization mass spectrometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>Linear Models</topic><topic>Lipoic acid</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Reproducibility of Results</topic><topic>Reversed-phase high performance liquid chromatography</topic><topic>Sensitivity and Specificity</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Thioctic Acid - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Durrani, Arjumand I.</creatorcontrib><creatorcontrib>Schwartz, Heidi</creatorcontrib><creatorcontrib>Schmid, Walther</creatorcontrib><creatorcontrib>Sontag, Gerhard</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>Durrani, Arjumand I.</au><au>Schwartz, Heidi</au><au>Schmid, Walther</au><au>Sontag, Gerhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>α-Lipoic acid in dietary supplements: Development and comparison of HPLC-CEAD and HPLC-ESI-MS methods</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2007-11-30</date><risdate>2007</risdate><volume>45</volume><issue>4</issue><spage>694</spage><epage>699</epage><pages>694-699</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><coden>JPBADA</coden><abstract>α-Lipoic acid is an antioxidant used both in the prevention and treatment of various oxidative stress related diseases. It is an important constituent of some dietary supplements and can also be found in plant and animal sources. A rapid method for the determination of α-lipoic acid in dietary supplements based on high performance liquid chromatography coupled with a coulometric electrode array detector (CEAD) and an electrospray ionization mass spectrometer (ESI-MS) was developed. First, α-lipoic acid was extracted with methanol by sonication, chromatographic separation was then achieved by isocratic elution [acetonitrile/methanol/50
mM potassium dihydrogen phosphate (pH 3, adjusted with phosphoric acid): 350/65/585, v/v/v] using an ACE 3-C-18 column at a flow rate of 0.45
ml/min. α-Lipoic acid was detected by means of a CEAD at +300, +400, +450, +500, +550, +600, +650, and +700
mV against palladium reference electrodes. For ESI-MS detection (negative mode), the composition of the mobile phase was changed to 0.1% acetic acid in water/acetonitrile 55:45, v/v applying a flow rate of 0.2
ml/min. The presented methods were utilized to determine the α-lipoic acid content in six dietary supplements. The results of both detection modes were in good correlation.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>17881179</pmid><doi>10.1016/j.jpba.2007.08.003</doi><tpages>6</tpages></addata></record> |
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subjects | Analysis Analytical, structural and metabolic biochemistry Antioxidants - analysis Biological and medical sciences Calibration Chromatography, High Pressure Liquid Coulometric electrode array detection Dietary supplements Dietary Supplements - analysis Dietary Supplements - standards Electrodes Electrospray ionization mass spectrometry Fundamental and applied biological sciences. Psychology General pharmacology Linear Models Lipoic acid Medical sciences Pharmacology. Drug treatments Reproducibility of Results Reversed-phase high performance liquid chromatography Sensitivity and Specificity Spectrometry, Mass, Electrospray Ionization Thioctic Acid - analysis |
title | α-Lipoic acid in dietary supplements: Development and comparison of HPLC-CEAD and HPLC-ESI-MS methods |
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