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Synthesis and characterization of thiazolium chitosan derivative with enhanced antimicrobial properties and its use as component of chitosan based films
In this work, chemical modification of chitosan using cationic thiazolium groups was investigated with the aim to improve water solubility and antimicrobial properties of chitosan. Enzymatic synthesis and ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS) chemistry were empl...
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Published in: | Carbohydrate polymers 2023-02, Vol.302, p.120438-120438, Article 120438 |
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description | In this work, chemical modification of chitosan using cationic thiazolium groups was investigated with the aim to improve water solubility and antimicrobial properties of chitosan. Enzymatic synthesis and ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS) chemistry were employed to synthesize and attach to chitosan through the amine groups the molecule bearing thiazolium moieties, quaternized 4-(2-(4-methylthiazol-5-yl) ethoxy)-4-oxobutanoic acid (MTBAQ). On the basis of Fourier transform infrared spectroscopy (FTIR), elemental analysis and solid state nuclear magnetic resonance (ssNMR), around 95 % of the available amine groups of chitosan (of 25 % degree of acetylation) reacted. The resulting derivative was water soluble at physiological pH and exhibit excellent antimicrobial activity against Listeria innocua, Staphylococcus epidermidis, Staphylococcus aureus and Methicillin Resistant S. aureus Gram-positive bacteria (MIC = 8–32 μg/ mL), whereas its efficiency decreases against fungi Candida albicans and Eschericia coli Gram-negative bacterium. Subsequently, the thiazolium chitosan derivative was employed as antimicrobial component (up to 7 wt%) of chitosan/glycerol based films. The incorporation of the chitosan derivative does not modify significantly the characteristics of the film in terms of thermal and mechanical properties, while enhances considerably the antimicrobial activity.
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doi_str_mv | 10.1016/j.carbpol.2022.120438 |
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[Display omitted]</description><identifier>ISSN: 0144-8617</identifier><identifier>EISSN: 1879-1344</identifier><identifier>DOI: 10.1016/j.carbpol.2022.120438</identifier><identifier>PMID: 36604094</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>acetylation ; Amines ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; Anti-Infective Agents - chemistry ; Anti-Infective Agents - pharmacology ; Antimicrobial ; antimicrobial properties ; Candida albicans ; Chitosan ; Chitosan - chemistry ; Chitosan films ; Fourier transform infrared spectroscopy ; glycerol ; Gram-negative bacteria ; Listeria innocua ; Methicillin-Resistant Staphylococcus aureus ; nuclear magnetic resonance spectroscopy ; Spectroscopy, Fourier Transform Infrared ; Staphylococcus epidermidis ; Thiazolium ; Water ; water solubility</subject><ispartof>Carbohydrate polymers, 2023-02, Vol.302, p.120438-120438, Article 120438</ispartof><rights>2022 The Authors</rights><rights>Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-c93ac19ce24212b24fa345a659773f1f2121324cad08dc5d69fcb06729cb04e43</citedby><cites>FETCH-LOGICAL-c375t-c93ac19ce24212b24fa345a659773f1f2121324cad08dc5d69fcb06729cb04e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36604094$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Muñoz-Nuñez, C.</creatorcontrib><creatorcontrib>Cuervo-Rodríguez, R.</creatorcontrib><creatorcontrib>Echeverría, C.</creatorcontrib><creatorcontrib>Fernández-García, M.</creatorcontrib><creatorcontrib>Muñoz-Bonilla, A.</creatorcontrib><title>Synthesis and characterization of thiazolium chitosan derivative with enhanced antimicrobial properties and its use as component of chitosan based films</title><title>Carbohydrate polymers</title><addtitle>Carbohydr Polym</addtitle><description>In this work, chemical modification of chitosan using cationic thiazolium groups was investigated with the aim to improve water solubility and antimicrobial properties of chitosan. Enzymatic synthesis and ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS) chemistry were employed to synthesize and attach to chitosan through the amine groups the molecule bearing thiazolium moieties, quaternized 4-(2-(4-methylthiazol-5-yl) ethoxy)-4-oxobutanoic acid (MTBAQ). On the basis of Fourier transform infrared spectroscopy (FTIR), elemental analysis and solid state nuclear magnetic resonance (ssNMR), around 95 % of the available amine groups of chitosan (of 25 % degree of acetylation) reacted. The resulting derivative was water soluble at physiological pH and exhibit excellent antimicrobial activity against Listeria innocua, Staphylococcus epidermidis, Staphylococcus aureus and Methicillin Resistant S. aureus Gram-positive bacteria (MIC = 8–32 μg/ mL), whereas its efficiency decreases against fungi Candida albicans and Eschericia coli Gram-negative bacterium. Subsequently, the thiazolium chitosan derivative was employed as antimicrobial component (up to 7 wt%) of chitosan/glycerol based films. The incorporation of the chitosan derivative does not modify significantly the characteristics of the film in terms of thermal and mechanical properties, while enhances considerably the antimicrobial activity.
[Display omitted]</description><subject>acetylation</subject><subject>Amines</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-Infective Agents - chemistry</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>Antimicrobial</subject><subject>antimicrobial properties</subject><subject>Candida albicans</subject><subject>Chitosan</subject><subject>Chitosan - chemistry</subject><subject>Chitosan films</subject><subject>Fourier transform infrared spectroscopy</subject><subject>glycerol</subject><subject>Gram-negative bacteria</subject><subject>Listeria innocua</subject><subject>Methicillin-Resistant Staphylococcus aureus</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><subject>Staphylococcus epidermidis</subject><subject>Thiazolium</subject><subject>Water</subject><subject>water solubility</subject><issn>0144-8617</issn><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAUhS0EokPLI4C8ZJPBf3GSFUJV-ZEqsShdW45zo9xREgfbGdQ-SR8XjzJ0W2-uZH_3HOscQj5wtueM68-HvbOhXfy4F0yIPRdMyfoV2fG6agoulXpNdowrVdSaVxfkXYwHlo_m7C25kFozxRq1I093D3MaIGKkdu6oG2ywLkHAR5vQz9T3NA1oH_2I65SfMfloZ9pl4piJI9C_mAYK82BnB10WSTihC75FO9Il-AVCQtjUMUW6RqA2Uuenxc8wp5PDs2xrY9bocZziFXnT2zHC-_O8JPffbn5f_yhuf33_ef31tnCyKlPhGmkdbxwIJbhoheqtVKXVZVNVsud9vuRSKGc7Vneu7HTTu5bpSjR5KFDyknzadPNf_6wQk5kwOhhHO4Nfo5G8VFxzofWLqKg0byqt6iqj5YbmJGIM0Jsl4GTDg-HMnPozB3Puz5z6M1t_ee_j2WJtJ-iet_4XloEvGwA5kyNCMNEhnKLHAC6ZzuMLFv8Af1Wx5A</recordid><startdate>20230215</startdate><enddate>20230215</enddate><creator>Muñoz-Nuñez, C.</creator><creator>Cuervo-Rodríguez, R.</creator><creator>Echeverría, C.</creator><creator>Fernández-García, M.</creator><creator>Muñoz-Bonilla, A.</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</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><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20230215</creationdate><title>Synthesis and characterization of thiazolium chitosan derivative with enhanced antimicrobial properties and its use as component of chitosan based films</title><author>Muñoz-Nuñez, C. ; Cuervo-Rodríguez, R. ; Echeverría, C. ; Fernández-García, M. ; Muñoz-Bonilla, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-c93ac19ce24212b24fa345a659773f1f2121324cad08dc5d69fcb06729cb04e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>acetylation</topic><topic>Amines</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-Infective Agents - chemistry</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>Antimicrobial</topic><topic>antimicrobial properties</topic><topic>Candida albicans</topic><topic>Chitosan</topic><topic>Chitosan - chemistry</topic><topic>Chitosan films</topic><topic>Fourier transform infrared spectroscopy</topic><topic>glycerol</topic><topic>Gram-negative bacteria</topic><topic>Listeria innocua</topic><topic>Methicillin-Resistant Staphylococcus aureus</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><topic>Staphylococcus epidermidis</topic><topic>Thiazolium</topic><topic>Water</topic><topic>water solubility</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Muñoz-Nuñez, C.</creatorcontrib><creatorcontrib>Cuervo-Rodríguez, R.</creatorcontrib><creatorcontrib>Echeverría, C.</creatorcontrib><creatorcontrib>Fernández-García, M.</creatorcontrib><creatorcontrib>Muñoz-Bonilla, A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Muñoz-Nuñez, C.</au><au>Cuervo-Rodríguez, R.</au><au>Echeverría, C.</au><au>Fernández-García, M.</au><au>Muñoz-Bonilla, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and characterization of thiazolium chitosan derivative with enhanced antimicrobial properties and its use as component of chitosan based films</atitle><jtitle>Carbohydrate polymers</jtitle><addtitle>Carbohydr Polym</addtitle><date>2023-02-15</date><risdate>2023</risdate><volume>302</volume><spage>120438</spage><epage>120438</epage><pages>120438-120438</pages><artnum>120438</artnum><issn>0144-8617</issn><eissn>1879-1344</eissn><abstract>In this work, chemical modification of chitosan using cationic thiazolium groups was investigated with the aim to improve water solubility and antimicrobial properties of chitosan. Enzymatic synthesis and ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS) chemistry were employed to synthesize and attach to chitosan through the amine groups the molecule bearing thiazolium moieties, quaternized 4-(2-(4-methylthiazol-5-yl) ethoxy)-4-oxobutanoic acid (MTBAQ). On the basis of Fourier transform infrared spectroscopy (FTIR), elemental analysis and solid state nuclear magnetic resonance (ssNMR), around 95 % of the available amine groups of chitosan (of 25 % degree of acetylation) reacted. The resulting derivative was water soluble at physiological pH and exhibit excellent antimicrobial activity against Listeria innocua, Staphylococcus epidermidis, Staphylococcus aureus and Methicillin Resistant S. aureus Gram-positive bacteria (MIC = 8–32 μg/ mL), whereas its efficiency decreases against fungi Candida albicans and Eschericia coli Gram-negative bacterium. Subsequently, the thiazolium chitosan derivative was employed as antimicrobial component (up to 7 wt%) of chitosan/glycerol based films. The incorporation of the chitosan derivative does not modify significantly the characteristics of the film in terms of thermal and mechanical properties, while enhances considerably the antimicrobial activity.
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subjects | acetylation Amines Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Anti-Infective Agents - chemistry Anti-Infective Agents - pharmacology Antimicrobial antimicrobial properties Candida albicans Chitosan Chitosan - chemistry Chitosan films Fourier transform infrared spectroscopy glycerol Gram-negative bacteria Listeria innocua Methicillin-Resistant Staphylococcus aureus nuclear magnetic resonance spectroscopy Spectroscopy, Fourier Transform Infrared Staphylococcus epidermidis Thiazolium Water water solubility |
title | Synthesis and characterization of thiazolium chitosan derivative with enhanced antimicrobial properties and its use as component of chitosan based films |
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