Siderophore-Mimetic hydrogel for iron chelation therapy
Two, three dihydroxybenzoic acid (DHBA), a portion of the metal chelating domain of enterobactin, was immobilized on crosslinked organic polymer polyallylamine (PAAm) and used as a chelating agent for iron removal from aqueous solutions. The swelling behavior of PAAm and PAAm hydrogels conjugated wi...
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Veröffentlicht in: | Journal of applied polymer science 2011-08, Vol.121 (3), p.1384-1392 |
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creator | Mohammadi, Zahra Xie, Sheng-Xue Golub, Allison L. Gehrke, Stevin H. Berkland, Cory |
description | Two, three dihydroxybenzoic acid (DHBA), a portion of the metal chelating domain of enterobactin, was immobilized on crosslinked organic polymer polyallylamine (PAAm) and used as a chelating agent for iron removal from aqueous solutions. The swelling behavior of PAAm and PAAm hydrogels conjugated with dihydroxybenzoic acid and the effect of contact time on the swelling and binding capacity of the hydrogel was investigated at several pH values to define the absorption mechanism. Iron uptake kinetics followed the pseudosecond order Ho model and equilibrium was described by either Temkin or Freundlich isotherms. Maximum chelating capacities of the hydrogels were found to be 500–1500 mg Fe3+ g−1 and 1500–2500 mg Fe2+ g−1 for PAAm and PAAm/DHBA hydrogels, respectively, depending on the pH of the media. The selectivity of the conjugate hydrogel toward ferric ions was studied at several different pH values. At every pH ranging from 2 to 7.5, the conjugate hydrogel showed relatively high binding affinity for ferric ions. The selective and rapid, high affinity binding of iron by this siderophore‐mimetic hydrogel offers potential application as a nonabsorbed chelator for iron in the gastrointestinal tract of patients suffering from iron overload diseases. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 |
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The swelling behavior of PAAm and PAAm hydrogels conjugated with dihydroxybenzoic acid and the effect of contact time on the swelling and binding capacity of the hydrogel was investigated at several pH values to define the absorption mechanism. Iron uptake kinetics followed the pseudosecond order Ho model and equilibrium was described by either Temkin or Freundlich isotherms. Maximum chelating capacities of the hydrogels were found to be 500–1500 mg Fe3+ g−1 and 1500–2500 mg Fe2+ g−1 for PAAm and PAAm/DHBA hydrogels, respectively, depending on the pH of the media. The selectivity of the conjugate hydrogel toward ferric ions was studied at several different pH values. At every pH ranging from 2 to 7.5, the conjugate hydrogel showed relatively high binding affinity for ferric ions. The selective and rapid, high affinity binding of iron by this siderophore‐mimetic hydrogel offers potential application as a nonabsorbed chelator for iron in the gastrointestinal tract of patients suffering from iron overload diseases. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011</description><identifier>ISSN: 0021-8995</identifier><identifier>ISSN: 1097-4628</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.33562</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Affinity ; Applied sciences ; Binding ; Chelating ; Dihydroxybenzoic acid ; Exact sciences and technology ; hydrogel ; Hydrogels ; Iron ; Materials science ; Mathematical models ; Organic polymers ; Physicochemistry of polymers ; Polymers ; Properties and characterization ; selectivity ; siderophore-mimetic ; Solution and gel properties</subject><ispartof>Journal of applied polymer science, 2011-08, Vol.121 (3), p.1384-1392</ispartof><rights>Copyright © 2011 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3972-8a3559a45f0f750ca09dd98277087c06f92aacac3040f1d340365b43bd72cf3a3</citedby><cites>FETCH-LOGICAL-c3972-8a3559a45f0f750ca09dd98277087c06f92aacac3040f1d340365b43bd72cf3a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fapp.33562$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fapp.33562$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24223854$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Mohammadi, Zahra</creatorcontrib><creatorcontrib>Xie, Sheng-Xue</creatorcontrib><creatorcontrib>Golub, Allison L.</creatorcontrib><creatorcontrib>Gehrke, Stevin H.</creatorcontrib><creatorcontrib>Berkland, Cory</creatorcontrib><title>Siderophore-Mimetic hydrogel for iron chelation therapy</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>Two, three dihydroxybenzoic acid (DHBA), a portion of the metal chelating domain of enterobactin, was immobilized on crosslinked organic polymer polyallylamine (PAAm) and used as a chelating agent for iron removal from aqueous solutions. The swelling behavior of PAAm and PAAm hydrogels conjugated with dihydroxybenzoic acid and the effect of contact time on the swelling and binding capacity of the hydrogel was investigated at several pH values to define the absorption mechanism. Iron uptake kinetics followed the pseudosecond order Ho model and equilibrium was described by either Temkin or Freundlich isotherms. Maximum chelating capacities of the hydrogels were found to be 500–1500 mg Fe3+ g−1 and 1500–2500 mg Fe2+ g−1 for PAAm and PAAm/DHBA hydrogels, respectively, depending on the pH of the media. The selectivity of the conjugate hydrogel toward ferric ions was studied at several different pH values. At every pH ranging from 2 to 7.5, the conjugate hydrogel showed relatively high binding affinity for ferric ions. The selective and rapid, high affinity binding of iron by this siderophore‐mimetic hydrogel offers potential application as a nonabsorbed chelator for iron in the gastrointestinal tract of patients suffering from iron overload diseases. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011</description><subject>Affinity</subject><subject>Applied sciences</subject><subject>Binding</subject><subject>Chelating</subject><subject>Dihydroxybenzoic acid</subject><subject>Exact sciences and technology</subject><subject>hydrogel</subject><subject>Hydrogels</subject><subject>Iron</subject><subject>Materials science</subject><subject>Mathematical models</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polymers</subject><subject>Properties and characterization</subject><subject>selectivity</subject><subject>siderophore-mimetic</subject><subject>Solution and gel properties</subject><issn>0021-8995</issn><issn>1097-4628</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp1kF1LHDEUhoNYcN32wn-wICK9GD35mkwuZbEqbNsF-wHehGMmcaOzmzGZRfffm3atF0KvciDP-5zDS8gBhRMKwE6x7084lzXbISMKWlWiZs0uGZU_WjVayz2yn_M9AKUS6hFR16F1KfaLmFz1NSzdEOxksWlTvHPdxMc0CSmuJnbhOhxCmYaFS9hvPpIPHrvsPr2-Y_Lzy_mP6WU1-35xNT2bVZZrxaoGuZQahfTglQSLoNtWN0wpaJSF2muGaNFyEOBpywXwWt4KftsqZj1HPibHW2-f4uPa5cEsQ7au63Dl4jobDbSWQlBVyMN35H1cp1U5zlBJ6wKWlYX6vKVsijkn502fwhLTxlAwfxo0pUHzt8HCHr0aMVvsfMKVDfktwARjvJGicKdb7il0bvN_oTmbz_-Zq20i5ME9vyUwPZhacSXN728Xhv2acpjfKMP4C-70jEs</recordid><startdate>20110805</startdate><enddate>20110805</enddate><creator>Mohammadi, Zahra</creator><creator>Xie, Sheng-Xue</creator><creator>Golub, Allison L.</creator><creator>Gehrke, Stevin H.</creator><creator>Berkland, Cory</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20110805</creationdate><title>Siderophore-Mimetic hydrogel for iron chelation therapy</title><author>Mohammadi, Zahra ; Xie, Sheng-Xue ; Golub, Allison L. ; Gehrke, Stevin H. ; Berkland, Cory</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3972-8a3559a45f0f750ca09dd98277087c06f92aacac3040f1d340365b43bd72cf3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Affinity</topic><topic>Applied sciences</topic><topic>Binding</topic><topic>Chelating</topic><topic>Dihydroxybenzoic acid</topic><topic>Exact sciences and technology</topic><topic>hydrogel</topic><topic>Hydrogels</topic><topic>Iron</topic><topic>Materials science</topic><topic>Mathematical models</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polymers</topic><topic>Properties and characterization</topic><topic>selectivity</topic><topic>siderophore-mimetic</topic><topic>Solution and gel properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohammadi, Zahra</creatorcontrib><creatorcontrib>Xie, Sheng-Xue</creatorcontrib><creatorcontrib>Golub, Allison L.</creatorcontrib><creatorcontrib>Gehrke, Stevin H.</creatorcontrib><creatorcontrib>Berkland, Cory</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohammadi, Zahra</au><au>Xie, Sheng-Xue</au><au>Golub, Allison L.</au><au>Gehrke, Stevin H.</au><au>Berkland, Cory</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Siderophore-Mimetic hydrogel for iron chelation therapy</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2011-08-05</date><risdate>2011</risdate><volume>121</volume><issue>3</issue><spage>1384</spage><epage>1392</epage><pages>1384-1392</pages><issn>0021-8995</issn><issn>1097-4628</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>Two, three dihydroxybenzoic acid (DHBA), a portion of the metal chelating domain of enterobactin, was immobilized on crosslinked organic polymer polyallylamine (PAAm) and used as a chelating agent for iron removal from aqueous solutions. The swelling behavior of PAAm and PAAm hydrogels conjugated with dihydroxybenzoic acid and the effect of contact time on the swelling and binding capacity of the hydrogel was investigated at several pH values to define the absorption mechanism. Iron uptake kinetics followed the pseudosecond order Ho model and equilibrium was described by either Temkin or Freundlich isotherms. 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subjects | Affinity Applied sciences Binding Chelating Dihydroxybenzoic acid Exact sciences and technology hydrogel Hydrogels Iron Materials science Mathematical models Organic polymers Physicochemistry of polymers Polymers Properties and characterization selectivity siderophore-mimetic Solution and gel properties |
title | Siderophore-Mimetic hydrogel for iron chelation therapy |
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