Design, syntheses and evaluation of hemocompatible pegylated-antimicrobial polymers with well-controlled molecular structures
Abstract In this paper, we have designed and synthesized well-defined pegylated-polymers with tertiary amines from readily available commodity monomers 2-(dimethylamino)ethyl methacrylate (DMAEMA) and oligo(ethylene glycol) methyl ether methacrylate (OEGMA, Mn ∼ 475 Da) by reversible addition–fragm...
Gespeichert in:
Veröffentlicht in: | Biomaterials 2010-03, Vol.31 (7), p.1751-1756 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1756 |
---|---|
container_issue | 7 |
container_start_page | 1751 |
container_title | Biomaterials |
container_volume | 31 |
creator | Venkataraman, Shrinivas Zhang, Ying Liu, Lihong Yang, Yi-Yan |
description | Abstract In this paper, we have designed and synthesized well-defined pegylated-polymers with tertiary amines from readily available commodity monomers 2-(dimethylamino)ethyl methacrylate (DMAEMA) and oligo(ethylene glycol) methyl ether methacrylate (OEGMA, Mn ∼ 475 Da) by reversible addition–fragmentation chain transfer (RAFT) polymerisation. By employing a simple and efficient post-polymerisation functionalization strategy, tertiary amines were quaternized to result in cationic polymers. By the careful selection of the functional halide, X–(CH2 ) q –R, (where in X = halide; R = the chemical functionality; q = the number of alkyl spacer between the quaternary ammonium group and R), a series of polymers with well-controlled molecular weight, different amphiphilic balance and chemical functionalities (such as alkyl, primary alcohol, primary amine and carboxylic acid) were readily synthesized. The antimicrobial activities of these cationic polymers were determined against Gram-positive bacteria Bacillus subtilis . Minimum inhibitory concentration (MIC), the polymer concentration to completely inhibit the bacterial growth, was found to be dependent both on the nature of functional group and the hydrophobicity of the polymer. Amongst the functional groups, both the alkyl and the alcohol groups were found to be effective, with MIC values in the range of 20–80 mg/L. The haemolytic properties of polymers were analyzed against mouse red blood cells. The poymers with a short alkyl or hydroxyl group demonstrated little haemolysis, yet retained strong antimicrobial activity. The overall hydrophobicity of the polymer influenced its haemolytic behavior. These polymers can be promising antimicrobial agents. In addition, the approach proposed in this study to atom-efficient design and synthesis of antimicrobial polymers from the commercially available monomers can also be applied to develop well-defined functional cationic polymers for various biomedical applications. |
doi_str_mv | 10.1016/j.biomaterials.2009.11.030 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_877574800</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0142961209012587</els_id><sourcerecordid>877574800</sourcerecordid><originalsourceid>FETCH-LOGICAL-c466t-9e657d838d60b405d6c88c2aed3c772824df961d4827e70eb3a99e68c5dcbaa23</originalsourceid><addsrcrecordid>eNqNUk2PFSEQJEbjPlf_giFevDgjMB8wHkzMrl_JJh7UM2Gg3z6eDIzA7GYO_neZvNUYL3oiTaqqu7oaoWeU1JTQ_uWxHm2YVIZolUs1I2SoKa1JQ-6hHRVcVN1AuvtoR2jLqqGn7Aw9SulISk1a9hCdFQppS7VDPy4h2Wv_AqfV5wMkSFh5g-FGuUVlGzwOe3yAKegwzeVjdIBnuF5daW8q5bOdrI5hLJPgObh1gpjwrc0HfAvOVTr4HINzYPAUHOjFqYhTjovOS4T0GD3YFwvw5O49R1_fvf1y8aG6-vT-48Wbq0q3fZ-rAfqOG9EI05OxJZ3ptRCaKTCN5pwJ1pp9sWlawThwAmOjhsIRujN6VIo15-j5SXeO4fsCKcvJJl0GVB7CkqTgvOOtIOSfSN40omdNv2m-OiGL_ZQi7OUc7aTiKimRW07yKP_MSW45SUplyamQn961WcYJzG_qr2AK4PIEgLKWGwtRJm3BazA2gs7SBPt_fV7_JaOd9VYr9w1WSMewRL9xqExMEvl5u5jtYMhAKOsEb34CNHfDoA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733862362</pqid></control><display><type>article</type><title>Design, syntheses and evaluation of hemocompatible pegylated-antimicrobial polymers with well-controlled molecular structures</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Venkataraman, Shrinivas ; Zhang, Ying ; Liu, Lihong ; Yang, Yi-Yan</creator><creatorcontrib>Venkataraman, Shrinivas ; Zhang, Ying ; Liu, Lihong ; Yang, Yi-Yan</creatorcontrib><description>Abstract In this paper, we have designed and synthesized well-defined pegylated-polymers with tertiary amines from readily available commodity monomers 2-(dimethylamino)ethyl methacrylate (DMAEMA) and oligo(ethylene glycol) methyl ether methacrylate (OEGMA, Mn ∼ 475 Da) by reversible addition–fragmentation chain transfer (RAFT) polymerisation. By employing a simple and efficient post-polymerisation functionalization strategy, tertiary amines were quaternized to result in cationic polymers. By the careful selection of the functional halide, X–(CH2 ) q –R, (where in X = halide; R = the chemical functionality; q = the number of alkyl spacer between the quaternary ammonium group and R), a series of polymers with well-controlled molecular weight, different amphiphilic balance and chemical functionalities (such as alkyl, primary alcohol, primary amine and carboxylic acid) were readily synthesized. The antimicrobial activities of these cationic polymers were determined against Gram-positive bacteria Bacillus subtilis . Minimum inhibitory concentration (MIC), the polymer concentration to completely inhibit the bacterial growth, was found to be dependent both on the nature of functional group and the hydrophobicity of the polymer. Amongst the functional groups, both the alkyl and the alcohol groups were found to be effective, with MIC values in the range of 20–80 mg/L. The haemolytic properties of polymers were analyzed against mouse red blood cells. The poymers with a short alkyl or hydroxyl group demonstrated little haemolysis, yet retained strong antimicrobial activity. The overall hydrophobicity of the polymer influenced its haemolytic behavior. These polymers can be promising antimicrobial agents. In addition, the approach proposed in this study to atom-efficient design and synthesis of antimicrobial polymers from the commercially available monomers can also be applied to develop well-defined functional cationic polymers for various biomedical applications.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2009.11.030</identifier><identifier>PMID: 20004014</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Advanced Basic Science ; Animals ; Anti-Infective Agents - chemical synthesis ; Anti-Infective Agents - chemistry ; Anti-Infective Agents - pharmacology ; Antimicrobial ; Bacillus subtilis ; Biocompatible Materials - chemical synthesis ; Biocompatible Materials - chemistry ; Biocompatible Materials - pharmacology ; Cationic polymers ; Dentistry ; Drug Design ; Haemolysis ; Hemolysis - drug effects ; Hydrophobic and Hydrophilic Interactions ; Methacrylates - chemical synthesis ; Methacrylates - chemistry ; Methacrylates - pharmacology ; Mice ; Microbial Sensitivity Tests ; Molecular Structure ; Polyethylene Glycols - chemical synthesis ; Polyethylene Glycols - chemistry ; Polyethylene Glycols - pharmacology ; RAFT</subject><ispartof>Biomaterials, 2010-03, Vol.31 (7), p.1751-1756</ispartof><rights>Elsevier Ltd</rights><rights>2009 Elsevier Ltd</rights><rights>(c) 2009 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-9e657d838d60b405d6c88c2aed3c772824df961d4827e70eb3a99e68c5dcbaa23</citedby><cites>FETCH-LOGICAL-c466t-9e657d838d60b405d6c88c2aed3c772824df961d4827e70eb3a99e68c5dcbaa23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.biomaterials.2009.11.030$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20004014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Venkataraman, Shrinivas</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Liu, Lihong</creatorcontrib><creatorcontrib>Yang, Yi-Yan</creatorcontrib><title>Design, syntheses and evaluation of hemocompatible pegylated-antimicrobial polymers with well-controlled molecular structures</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>Abstract In this paper, we have designed and synthesized well-defined pegylated-polymers with tertiary amines from readily available commodity monomers 2-(dimethylamino)ethyl methacrylate (DMAEMA) and oligo(ethylene glycol) methyl ether methacrylate (OEGMA, Mn ∼ 475 Da) by reversible addition–fragmentation chain transfer (RAFT) polymerisation. By employing a simple and efficient post-polymerisation functionalization strategy, tertiary amines were quaternized to result in cationic polymers. By the careful selection of the functional halide, X–(CH2 ) q –R, (where in X = halide; R = the chemical functionality; q = the number of alkyl spacer between the quaternary ammonium group and R), a series of polymers with well-controlled molecular weight, different amphiphilic balance and chemical functionalities (such as alkyl, primary alcohol, primary amine and carboxylic acid) were readily synthesized. The antimicrobial activities of these cationic polymers were determined against Gram-positive bacteria Bacillus subtilis . Minimum inhibitory concentration (MIC), the polymer concentration to completely inhibit the bacterial growth, was found to be dependent both on the nature of functional group and the hydrophobicity of the polymer. Amongst the functional groups, both the alkyl and the alcohol groups were found to be effective, with MIC values in the range of 20–80 mg/L. The haemolytic properties of polymers were analyzed against mouse red blood cells. The poymers with a short alkyl or hydroxyl group demonstrated little haemolysis, yet retained strong antimicrobial activity. The overall hydrophobicity of the polymer influenced its haemolytic behavior. These polymers can be promising antimicrobial agents. In addition, the approach proposed in this study to atom-efficient design and synthesis of antimicrobial polymers from the commercially available monomers can also be applied to develop well-defined functional cationic polymers for various biomedical applications.</description><subject>Advanced Basic Science</subject><subject>Animals</subject><subject>Anti-Infective Agents - chemical synthesis</subject><subject>Anti-Infective Agents - chemistry</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>Antimicrobial</subject><subject>Bacillus subtilis</subject><subject>Biocompatible Materials - chemical synthesis</subject><subject>Biocompatible Materials - chemistry</subject><subject>Biocompatible Materials - pharmacology</subject><subject>Cationic polymers</subject><subject>Dentistry</subject><subject>Drug Design</subject><subject>Haemolysis</subject><subject>Hemolysis - drug effects</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Methacrylates - chemical synthesis</subject><subject>Methacrylates - chemistry</subject><subject>Methacrylates - pharmacology</subject><subject>Mice</subject><subject>Microbial Sensitivity Tests</subject><subject>Molecular Structure</subject><subject>Polyethylene Glycols - chemical synthesis</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Polyethylene Glycols - pharmacology</subject><subject>RAFT</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUk2PFSEQJEbjPlf_giFevDgjMB8wHkzMrl_JJh7UM2Gg3z6eDIzA7GYO_neZvNUYL3oiTaqqu7oaoWeU1JTQ_uWxHm2YVIZolUs1I2SoKa1JQ-6hHRVcVN1AuvtoR2jLqqGn7Aw9SulISk1a9hCdFQppS7VDPy4h2Wv_AqfV5wMkSFh5g-FGuUVlGzwOe3yAKegwzeVjdIBnuF5daW8q5bOdrI5hLJPgObh1gpjwrc0HfAvOVTr4HINzYPAUHOjFqYhTjovOS4T0GD3YFwvw5O49R1_fvf1y8aG6-vT-48Wbq0q3fZ-rAfqOG9EI05OxJZ3ptRCaKTCN5pwJ1pp9sWlawThwAmOjhsIRujN6VIo15-j5SXeO4fsCKcvJJl0GVB7CkqTgvOOtIOSfSN40omdNv2m-OiGL_ZQi7OUc7aTiKimRW07yKP_MSW45SUplyamQn961WcYJzG_qr2AK4PIEgLKWGwtRJm3BazA2gs7SBPt_fV7_JaOd9VYr9w1WSMewRL9xqExMEvl5u5jtYMhAKOsEb34CNHfDoA</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Venkataraman, Shrinivas</creator><creator>Zhang, Ying</creator><creator>Liu, Lihong</creator><creator>Yang, Yi-Yan</creator><general>Elsevier Ltd</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20100301</creationdate><title>Design, syntheses and evaluation of hemocompatible pegylated-antimicrobial polymers with well-controlled molecular structures</title><author>Venkataraman, Shrinivas ; Zhang, Ying ; Liu, Lihong ; Yang, Yi-Yan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-9e657d838d60b405d6c88c2aed3c772824df961d4827e70eb3a99e68c5dcbaa23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Advanced Basic Science</topic><topic>Animals</topic><topic>Anti-Infective Agents - chemical synthesis</topic><topic>Anti-Infective Agents - chemistry</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>Antimicrobial</topic><topic>Bacillus subtilis</topic><topic>Biocompatible Materials - chemical synthesis</topic><topic>Biocompatible Materials - chemistry</topic><topic>Biocompatible Materials - pharmacology</topic><topic>Cationic polymers</topic><topic>Dentistry</topic><topic>Drug Design</topic><topic>Haemolysis</topic><topic>Hemolysis - drug effects</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Methacrylates - chemical synthesis</topic><topic>Methacrylates - chemistry</topic><topic>Methacrylates - pharmacology</topic><topic>Mice</topic><topic>Microbial Sensitivity Tests</topic><topic>Molecular Structure</topic><topic>Polyethylene Glycols - chemical synthesis</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Polyethylene Glycols - pharmacology</topic><topic>RAFT</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Venkataraman, Shrinivas</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Liu, Lihong</creatorcontrib><creatorcontrib>Yang, Yi-Yan</creatorcontrib><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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Venkataraman, Shrinivas</au><au>Zhang, Ying</au><au>Liu, Lihong</au><au>Yang, Yi-Yan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design, syntheses and evaluation of hemocompatible pegylated-antimicrobial polymers with well-controlled molecular structures</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>31</volume><issue>7</issue><spage>1751</spage><epage>1756</epage><pages>1751-1756</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Abstract In this paper, we have designed and synthesized well-defined pegylated-polymers with tertiary amines from readily available commodity monomers 2-(dimethylamino)ethyl methacrylate (DMAEMA) and oligo(ethylene glycol) methyl ether methacrylate (OEGMA, Mn ∼ 475 Da) by reversible addition–fragmentation chain transfer (RAFT) polymerisation. By employing a simple and efficient post-polymerisation functionalization strategy, tertiary amines were quaternized to result in cationic polymers. By the careful selection of the functional halide, X–(CH2 ) q –R, (where in X = halide; R = the chemical functionality; q = the number of alkyl spacer between the quaternary ammonium group and R), a series of polymers with well-controlled molecular weight, different amphiphilic balance and chemical functionalities (such as alkyl, primary alcohol, primary amine and carboxylic acid) were readily synthesized. The antimicrobial activities of these cationic polymers were determined against Gram-positive bacteria Bacillus subtilis . Minimum inhibitory concentration (MIC), the polymer concentration to completely inhibit the bacterial growth, was found to be dependent both on the nature of functional group and the hydrophobicity of the polymer. Amongst the functional groups, both the alkyl and the alcohol groups were found to be effective, with MIC values in the range of 20–80 mg/L. The haemolytic properties of polymers were analyzed against mouse red blood cells. The poymers with a short alkyl or hydroxyl group demonstrated little haemolysis, yet retained strong antimicrobial activity. The overall hydrophobicity of the polymer influenced its haemolytic behavior. These polymers can be promising antimicrobial agents. In addition, the approach proposed in this study to atom-efficient design and synthesis of antimicrobial polymers from the commercially available monomers can also be applied to develop well-defined functional cationic polymers for various biomedical applications.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>20004014</pmid><doi>10.1016/j.biomaterials.2009.11.030</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0142-9612 |
ispartof | Biomaterials, 2010-03, Vol.31 (7), p.1751-1756 |
issn | 0142-9612 1878-5905 |
language | eng |
recordid | cdi_proquest_miscellaneous_877574800 |
source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Advanced Basic Science Animals Anti-Infective Agents - chemical synthesis Anti-Infective Agents - chemistry Anti-Infective Agents - pharmacology Antimicrobial Bacillus subtilis Biocompatible Materials - chemical synthesis Biocompatible Materials - chemistry Biocompatible Materials - pharmacology Cationic polymers Dentistry Drug Design Haemolysis Hemolysis - drug effects Hydrophobic and Hydrophilic Interactions Methacrylates - chemical synthesis Methacrylates - chemistry Methacrylates - pharmacology Mice Microbial Sensitivity Tests Molecular Structure Polyethylene Glycols - chemical synthesis Polyethylene Glycols - chemistry Polyethylene Glycols - pharmacology RAFT |
title | Design, syntheses and evaluation of hemocompatible pegylated-antimicrobial polymers with well-controlled molecular structures |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T21%3A14%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Design,%20syntheses%20and%20evaluation%20of%20hemocompatible%20pegylated-antimicrobial%20polymers%20with%20well-controlled%20molecular%20structures&rft.jtitle=Biomaterials&rft.au=Venkataraman,%20Shrinivas&rft.date=2010-03-01&rft.volume=31&rft.issue=7&rft.spage=1751&rft.epage=1756&rft.pages=1751-1756&rft.issn=0142-9612&rft.eissn=1878-5905&rft_id=info:doi/10.1016/j.biomaterials.2009.11.030&rft_dat=%3Cproquest_cross%3E877574800%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=733862362&rft_id=info:pmid/20004014&rft_els_id=1_s2_0_S0142961209012587&rfr_iscdi=true |