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Development of a new assay for the screening of hypochlorous acid scavengers based on reversed-phase high-performance liquid chromatography
A new assay for the screening of hypochlorite/hypochlorous acid (XOCl) scavengers, based on the reversed‐phase high performance liquid chromatographic analysis of human serum albumin (HSA, 0.2% in 100 mM sodium phosphate, pH 7), before and after oxidation by XOCl (1.6 mM), was developed. XOCl induce...
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Published in: | Biomedical chromatography 2002-09, Vol.16 (6), p.404-411 |
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creator | Gatto, Maria Teresa Firuzi, Omidreza Agostino, Roberta Grippa, Eleonora Borsò, Angela Spinelli, Francesca Pavan, Lucia Petrolati, Marzia Petrucci, Rita Marrosu, Giancarlo Saso, Luciano |
description | A new assay for the screening of hypochlorite/hypochlorous acid (XOCl) scavengers, based on the reversed‐phase high performance liquid chromatographic analysis of human serum albumin (HSA, 0.2% in 100 mM sodium phosphate, pH 7), before and after oxidation by XOCl (1.6 mM), was developed. XOCl induced a significant decrease of the area under the chromatographic peak of HSA at 280 nm due to the oxidation of the aromatic amino acids tryptophan and tyrosine, as suggested by the literature and by the chromatographic analyses and the electrochemical study performed here. The assay was validated by testing known XOCl scavengers such as ascorbic acid, cysteine, glutathione, S‐methylglutathione and α‐lipoic acid and other antioxidants such as carnosine and chlorogenic acid, which inhibited the oxidation of HSA. Quantitative activities were calculated using an original formula based on the changes of the area of the albumin peak. Electrochemical data collected here in a homogeneous medium showed that the anodic potentials of the antioxidants tested are less positive (ascorbic acid, chlorogenic acid and cysteine) or similar (α‐lipoic acid) compared with those of the aromatic residues (tryptophan and tyrosine) of HSA oxidized by XOCl. However, as expected, carnosine, glutathione and S‐methylglutathione were inactive at a glassy‐carbon, gold or platinum electrode. Copyright © 2002 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/bmc.174 |
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XOCl induced a significant decrease of the area under the chromatographic peak of HSA at 280 nm due to the oxidation of the aromatic amino acids tryptophan and tyrosine, as suggested by the literature and by the chromatographic analyses and the electrochemical study performed here. The assay was validated by testing known XOCl scavengers such as ascorbic acid, cysteine, glutathione, S‐methylglutathione and α‐lipoic acid and other antioxidants such as carnosine and chlorogenic acid, which inhibited the oxidation of HSA. Quantitative activities were calculated using an original formula based on the changes of the area of the albumin peak. Electrochemical data collected here in a homogeneous medium showed that the anodic potentials of the antioxidants tested are less positive (ascorbic acid, chlorogenic acid and cysteine) or similar (α‐lipoic acid) compared with those of the aromatic residues (tryptophan and tyrosine) of HSA oxidized by XOCl. However, as expected, carnosine, glutathione and S‐methylglutathione were inactive at a glassy‐carbon, gold or platinum electrode. Copyright © 2002 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.174</identifier><identifier>PMID: 12228898</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Antioxidants - analysis ; Chromatography, High Pressure Liquid - methods ; Electrochemistry ; Hypochlorous Acid - chemistry ; Reproducibility of Results ; Serum Albumin - chemistry</subject><ispartof>Biomedical chromatography, 2002-09, Vol.16 (6), p.404-411</ispartof><rights>Copyright © 2002 John Wiley & Sons, Ltd.</rights><rights>Copyright 2002 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4504-454a4659bebcc447d79b13f1698d73ae3f565eaf89b0af881ae31f6bf0ccce643</citedby><cites>FETCH-LOGICAL-c4504-454a4659bebcc447d79b13f1698d73ae3f565eaf89b0af881ae31f6bf0ccce643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12228898$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gatto, Maria Teresa</creatorcontrib><creatorcontrib>Firuzi, Omidreza</creatorcontrib><creatorcontrib>Agostino, Roberta</creatorcontrib><creatorcontrib>Grippa, Eleonora</creatorcontrib><creatorcontrib>Borsò, Angela</creatorcontrib><creatorcontrib>Spinelli, Francesca</creatorcontrib><creatorcontrib>Pavan, Lucia</creatorcontrib><creatorcontrib>Petrolati, Marzia</creatorcontrib><creatorcontrib>Petrucci, Rita</creatorcontrib><creatorcontrib>Marrosu, Giancarlo</creatorcontrib><creatorcontrib>Saso, Luciano</creatorcontrib><title>Development of a new assay for the screening of hypochlorous acid scavengers based on reversed-phase high-performance liquid chromatography</title><title>Biomedical chromatography</title><addtitle>Biomed. Chromatogr</addtitle><description>A new assay for the screening of hypochlorite/hypochlorous acid (XOCl) scavengers, based on the reversed‐phase high performance liquid chromatographic analysis of human serum albumin (HSA, 0.2% in 100 mM sodium phosphate, pH 7), before and after oxidation by XOCl (1.6 mM), was developed. XOCl induced a significant decrease of the area under the chromatographic peak of HSA at 280 nm due to the oxidation of the aromatic amino acids tryptophan and tyrosine, as suggested by the literature and by the chromatographic analyses and the electrochemical study performed here. The assay was validated by testing known XOCl scavengers such as ascorbic acid, cysteine, glutathione, S‐methylglutathione and α‐lipoic acid and other antioxidants such as carnosine and chlorogenic acid, which inhibited the oxidation of HSA. Quantitative activities were calculated using an original formula based on the changes of the area of the albumin peak. Electrochemical data collected here in a homogeneous medium showed that the anodic potentials of the antioxidants tested are less positive (ascorbic acid, chlorogenic acid and cysteine) or similar (α‐lipoic acid) compared with those of the aromatic residues (tryptophan and tyrosine) of HSA oxidized by XOCl. However, as expected, carnosine, glutathione and S‐methylglutathione were inactive at a glassy‐carbon, gold or platinum electrode. Copyright © 2002 John Wiley & Sons, Ltd.</description><subject>Antioxidants - analysis</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Electrochemistry</subject><subject>Hypochlorous Acid - chemistry</subject><subject>Reproducibility of Results</subject><subject>Serum Albumin - chemistry</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp1kMFu1DAURS1URKcD6h9UXrWLKsVOnNhetgMU1BYQUHVpOc7zJJDEGTvTId_AT-MqI7pi8_x0fXwkX4SOKbmghKRvy85cUM5eoAUlUiZEEHqAFiQtZJIJLg_RUQg_CSGySPkrdEjTNBVCigX68w4eoXVDB_2IncUa97DDOgQ9Yes8HmvAwXiAvunXT0A9Dc7UrfNuG7A2TRWv9SP0a_ABlzpAhV2PfbT6uCdDHSNcN-s6GcBHY6d7A7htNtv41NTedXp0a6-HenqNXlrdBnizP5fo_sP7H6uPye2X60-ry9vEsJywhOVMsyKXJZTGMMYrLkuaWVpIUfFMQ2bzIgdthSxJnILGiNqitMQYAwXLluh09g7ebbYQRtU1wUDb6h7irxRPicg5oxE8m0HjXQgerBp802k_KUrUU-8q9q5i75E82Su3ZQfVM7cvOgLnM7BrWpj-51FXd6tZl8x0E0b4_Y_W_pcqeMZz9fD5WqXk5vvXb3dC3WR_AQwEnnA</recordid><startdate>200209</startdate><enddate>200209</enddate><creator>Gatto, Maria Teresa</creator><creator>Firuzi, Omidreza</creator><creator>Agostino, Roberta</creator><creator>Grippa, Eleonora</creator><creator>Borsò, Angela</creator><creator>Spinelli, Francesca</creator><creator>Pavan, Lucia</creator><creator>Petrolati, Marzia</creator><creator>Petrucci, Rita</creator><creator>Marrosu, Giancarlo</creator><creator>Saso, Luciano</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</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>200209</creationdate><title>Development of a new assay for the screening of hypochlorous acid scavengers based on reversed-phase high-performance liquid chromatography</title><author>Gatto, Maria Teresa ; Firuzi, Omidreza ; Agostino, Roberta ; Grippa, Eleonora ; Borsò, Angela ; Spinelli, Francesca ; Pavan, Lucia ; Petrolati, Marzia ; Petrucci, Rita ; Marrosu, Giancarlo ; Saso, Luciano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4504-454a4659bebcc447d79b13f1698d73ae3f565eaf89b0af881ae31f6bf0ccce643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Antioxidants - analysis</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Electrochemistry</topic><topic>Hypochlorous Acid - chemistry</topic><topic>Reproducibility of Results</topic><topic>Serum Albumin - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gatto, Maria Teresa</creatorcontrib><creatorcontrib>Firuzi, Omidreza</creatorcontrib><creatorcontrib>Agostino, Roberta</creatorcontrib><creatorcontrib>Grippa, Eleonora</creatorcontrib><creatorcontrib>Borsò, Angela</creatorcontrib><creatorcontrib>Spinelli, Francesca</creatorcontrib><creatorcontrib>Pavan, Lucia</creatorcontrib><creatorcontrib>Petrolati, Marzia</creatorcontrib><creatorcontrib>Petrucci, Rita</creatorcontrib><creatorcontrib>Marrosu, Giancarlo</creatorcontrib><creatorcontrib>Saso, Luciano</creatorcontrib><collection>Istex</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>Biomedical chromatography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gatto, Maria Teresa</au><au>Firuzi, Omidreza</au><au>Agostino, Roberta</au><au>Grippa, Eleonora</au><au>Borsò, Angela</au><au>Spinelli, Francesca</au><au>Pavan, Lucia</au><au>Petrolati, Marzia</au><au>Petrucci, Rita</au><au>Marrosu, Giancarlo</au><au>Saso, Luciano</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a new assay for the screening of hypochlorous acid scavengers based on reversed-phase high-performance liquid chromatography</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed. Chromatogr</addtitle><date>2002-09</date><risdate>2002</risdate><volume>16</volume><issue>6</issue><spage>404</spage><epage>411</epage><pages>404-411</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>A new assay for the screening of hypochlorite/hypochlorous acid (XOCl) scavengers, based on the reversed‐phase high performance liquid chromatographic analysis of human serum albumin (HSA, 0.2% in 100 mM sodium phosphate, pH 7), before and after oxidation by XOCl (1.6 mM), was developed. XOCl induced a significant decrease of the area under the chromatographic peak of HSA at 280 nm due to the oxidation of the aromatic amino acids tryptophan and tyrosine, as suggested by the literature and by the chromatographic analyses and the electrochemical study performed here. The assay was validated by testing known XOCl scavengers such as ascorbic acid, cysteine, glutathione, S‐methylglutathione and α‐lipoic acid and other antioxidants such as carnosine and chlorogenic acid, which inhibited the oxidation of HSA. Quantitative activities were calculated using an original formula based on the changes of the area of the albumin peak. Electrochemical data collected here in a homogeneous medium showed that the anodic potentials of the antioxidants tested are less positive (ascorbic acid, chlorogenic acid and cysteine) or similar (α‐lipoic acid) compared with those of the aromatic residues (tryptophan and tyrosine) of HSA oxidized by XOCl. However, as expected, carnosine, glutathione and S‐methylglutathione were inactive at a glassy‐carbon, gold or platinum electrode. Copyright © 2002 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>12228898</pmid><doi>10.1002/bmc.174</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antioxidants - analysis Chromatography, High Pressure Liquid - methods Electrochemistry Hypochlorous Acid - chemistry Reproducibility of Results Serum Albumin - chemistry |
title | Development of a new assay for the screening of hypochlorous acid scavengers based on reversed-phase high-performance liquid chromatography |
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