Synthesis and characterization of a novel biodegradable antimicrobial polymer
Bacterial infection is a frequent complication associated with the use of medical devices. In an effort to address this problem, antibacterial agents have been incorporated or applied directly onto the surfaces of numerous types of medical devices. This study assessed the feasibility of using a nove...
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Published in: | Biomaterials 2000-06, Vol.21 (12), p.1235-1246 |
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description | Bacterial infection is a frequent complication associated with the use of medical devices. In an effort to address this problem, antibacterial agents have been incorporated or applied directly onto the surfaces of numerous types of medical devices. This study assessed the feasibility of using a novel biodegradable polymer to release antibiotic drugs in response to inflammatory related enzymes. A model drug polymer was synthesized using 1,6-hexane diisocyanate (HDI), polycaprolactone diol (PCL), and a fluoroquinolone antibiotic, ciprofloxacin. Polymers were characterized by size-exclusion chromatography (SEC), and elemental analysis. Biodegradation studies were carried out by incubating the polymers with solutions of cholesterol esterase (CE) or phosphate buffer (pH 7.0) for 30 days at 37°C. The degradation was assessed by high-performance liquid chromatography (HPLC), mass spectrometry (MS) and
14
C
radiolabel release. Subsequently, the activity of the released antibiotic was assessed against a clinical isolate of
Pseudomonas aeruginosa. HPLC analysis showed the release of multiple degradation products which were identified, by tandem MS, to include ciprofloxacin and derivatives of ciprofloxacin. The microbiological assessment showed that the released ciprofloxacin possessed antimicrobial activity; 1
μg/ml was measured after 10 days. The results of this study suggest that these novel bioresponsive antimicrobial polymers or similar analogs show promise for use in the control of medical device associated infections. |
doi_str_mv | 10.1016/S0142-9612(00)00003-X |
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14
C
radiolabel release. Subsequently, the activity of the released antibiotic was assessed against a clinical isolate of
Pseudomonas aeruginosa. HPLC analysis showed the release of multiple degradation products which were identified, by tandem MS, to include ciprofloxacin and derivatives of ciprofloxacin. The microbiological assessment showed that the released ciprofloxacin possessed antimicrobial activity; 1
μg/ml was measured after 10 days. The results of this study suggest that these novel bioresponsive antimicrobial polymers or similar analogs show promise for use in the control of medical device associated infections.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/S0142-9612(00)00003-X</identifier><identifier>PMID: 10811305</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Absorbable Implants ; Antibiotics ; Antimicrobial ; Aromatic compounds ; Biocompatible Materials - chemical synthesis ; Biodegradable polymers ; Biodegradation ; Biological and medical sciences ; Biosynthesis ; Chromatography, Gel ; Chromatography, High Pressure Liquid ; Ciprofloxacin ; Ciprofloxacin - administration & dosage ; Ciprofloxacin - analogs & derivatives ; Ciprofloxacin - chemical synthesis ; Ciprofloxacin - chemistry ; Ciprofloxacin - pharmacokinetics ; Ciprofloxacin - pharmacology ; Delayed-Action Preparations ; Diffusion ; Drug Carriers ; Enzymes ; Feasibility Studies ; Infection ; Mass Spectrometry ; Materials Testing ; Medical sciences ; Microbial Sensitivity Tests ; Microbiology ; Molecular Weight ; Phosphates ; Polyesters ; Polyesters - chemical synthesis ; Polyesters - chemistry ; Polyurethanes ; Pseudomonas aeruginosa - drug effects ; Quinolones ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Sterol Esterase - metabolism ; Technology. Biomaterials. Equipments. Material. Instrumentation</subject><ispartof>Biomaterials, 2000-06, Vol.21 (12), p.1235-1246</ispartof><rights>2000 Elsevier Science Ltd</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-d3c090ffdaa39d953d406199d658f0721d275641495b7086494dde2c27bf0f5d3</citedby><cites>FETCH-LOGICAL-c524t-d3c090ffdaa39d953d406199d658f0721d275641495b7086494dde2c27bf0f5d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27898,27899</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1346331$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10811305$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Woo, G.L.Y.</creatorcontrib><creatorcontrib>Mittelman, M.W.</creatorcontrib><creatorcontrib>Santerre, J.P.</creatorcontrib><title>Synthesis and characterization of a novel biodegradable antimicrobial polymer</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>Bacterial infection is a frequent complication associated with the use of medical devices. In an effort to address this problem, antibacterial agents have been incorporated or applied directly onto the surfaces of numerous types of medical devices. This study assessed the feasibility of using a novel biodegradable polymer to release antibiotic drugs in response to inflammatory related enzymes. A model drug polymer was synthesized using 1,6-hexane diisocyanate (HDI), polycaprolactone diol (PCL), and a fluoroquinolone antibiotic, ciprofloxacin. Polymers were characterized by size-exclusion chromatography (SEC), and elemental analysis. Biodegradation studies were carried out by incubating the polymers with solutions of cholesterol esterase (CE) or phosphate buffer (pH 7.0) for 30 days at 37°C. The degradation was assessed by high-performance liquid chromatography (HPLC), mass spectrometry (MS) and
14
C
radiolabel release. Subsequently, the activity of the released antibiotic was assessed against a clinical isolate of
Pseudomonas aeruginosa. HPLC analysis showed the release of multiple degradation products which were identified, by tandem MS, to include ciprofloxacin and derivatives of ciprofloxacin. The microbiological assessment showed that the released ciprofloxacin possessed antimicrobial activity; 1
μg/ml was measured after 10 days. The results of this study suggest that these novel bioresponsive antimicrobial polymers or similar analogs show promise for use in the control of medical device associated infections.</description><subject>Absorbable Implants</subject><subject>Antibiotics</subject><subject>Antimicrobial</subject><subject>Aromatic compounds</subject><subject>Biocompatible Materials - chemical synthesis</subject><subject>Biodegradable polymers</subject><subject>Biodegradation</subject><subject>Biological and medical sciences</subject><subject>Biosynthesis</subject><subject>Chromatography, Gel</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Ciprofloxacin</subject><subject>Ciprofloxacin - administration & dosage</subject><subject>Ciprofloxacin - analogs & derivatives</subject><subject>Ciprofloxacin - chemical synthesis</subject><subject>Ciprofloxacin - chemistry</subject><subject>Ciprofloxacin - pharmacokinetics</subject><subject>Ciprofloxacin - pharmacology</subject><subject>Delayed-Action Preparations</subject><subject>Diffusion</subject><subject>Drug Carriers</subject><subject>Enzymes</subject><subject>Feasibility Studies</subject><subject>Infection</subject><subject>Mass Spectrometry</subject><subject>Materials Testing</subject><subject>Medical sciences</subject><subject>Microbial Sensitivity Tests</subject><subject>Microbiology</subject><subject>Molecular Weight</subject><subject>Phosphates</subject><subject>Polyesters</subject><subject>Polyesters - chemical synthesis</subject><subject>Polyesters - chemistry</subject><subject>Polyurethanes</subject><subject>Pseudomonas aeruginosa - drug effects</subject><subject>Quinolones</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Sterol Esterase - metabolism</subject><subject>Technology. Biomaterials. Equipments. Material. Instrumentation</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqN0c9rFDEUB_Agit1W_wRlDiJ6GH0vvyY5FSlWhYqHKvQWMknGRmYmazJbWP96s91Fva25hMDnvTzel5BnCG8QUL69BuS01RLpK4DXUA9rbx6QFapOtUKDeEhWf8gJOS3lB9Q3cPqYnCAoRAZiRT5fb-flNpRYGjv7xt3abN0Scvxll5jmJg2NbeZ0F8amj8mH79l624-h6iVO0eXURzs26zRup5CfkEeDHUt4erjPyLfL918vPrZXXz58unh31TpB-dJ65kDDMHhrmfZaMM9BotZeCjVAR9HTTkiOXIu-AyW55t4H6mjXDzAIz87Iy33fdU4_N6EsZorFhXG0c0ibYjpEjh2Fo5B2nVDqf2BdJVdSHoWoOFIldx3FHtYdlZLDYNY5TjZvDYLZRWjuIzS7fAyAuY_Q3NS654cPNv0U_D9V-8wqeHEAtjg7DtnOLpa_jnHJGFZ2vmehBnEXQzbFxTC74GMObjE-xSOT_AazDbbj</recordid><startdate>20000601</startdate><enddate>20000601</enddate><creator>Woo, G.L.Y.</creator><creator>Mittelman, M.W.</creator><creator>Santerre, J.P.</creator><general>Elsevier Ltd</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>F28</scope><scope>7X8</scope></search><sort><creationdate>20000601</creationdate><title>Synthesis and characterization of a novel biodegradable antimicrobial polymer</title><author>Woo, G.L.Y. ; Mittelman, M.W. ; Santerre, J.P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-d3c090ffdaa39d953d406199d658f0721d275641495b7086494dde2c27bf0f5d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Absorbable Implants</topic><topic>Antibiotics</topic><topic>Antimicrobial</topic><topic>Aromatic compounds</topic><topic>Biocompatible Materials - chemical synthesis</topic><topic>Biodegradable polymers</topic><topic>Biodegradation</topic><topic>Biological and medical sciences</topic><topic>Biosynthesis</topic><topic>Chromatography, Gel</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Ciprofloxacin</topic><topic>Ciprofloxacin - administration & dosage</topic><topic>Ciprofloxacin - analogs & derivatives</topic><topic>Ciprofloxacin - chemical synthesis</topic><topic>Ciprofloxacin - chemistry</topic><topic>Ciprofloxacin - pharmacokinetics</topic><topic>Ciprofloxacin - pharmacology</topic><topic>Delayed-Action Preparations</topic><topic>Diffusion</topic><topic>Drug Carriers</topic><topic>Enzymes</topic><topic>Feasibility Studies</topic><topic>Infection</topic><topic>Mass Spectrometry</topic><topic>Materials Testing</topic><topic>Medical sciences</topic><topic>Microbial Sensitivity Tests</topic><topic>Microbiology</topic><topic>Molecular Weight</topic><topic>Phosphates</topic><topic>Polyesters</topic><topic>Polyesters - chemical synthesis</topic><topic>Polyesters - chemistry</topic><topic>Polyurethanes</topic><topic>Pseudomonas aeruginosa - drug effects</topic><topic>Quinolones</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>Sterol Esterase - metabolism</topic><topic>Technology. Biomaterials. Equipments. Material. Instrumentation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woo, G.L.Y.</creatorcontrib><creatorcontrib>Mittelman, M.W.</creatorcontrib><creatorcontrib>Santerre, J.P.</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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>MEDLINE - Academic</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woo, G.L.Y.</au><au>Mittelman, M.W.</au><au>Santerre, J.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and characterization of a novel biodegradable antimicrobial polymer</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2000-06-01</date><risdate>2000</risdate><volume>21</volume><issue>12</issue><spage>1235</spage><epage>1246</epage><pages>1235-1246</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Bacterial infection is a frequent complication associated with the use of medical devices. In an effort to address this problem, antibacterial agents have been incorporated or applied directly onto the surfaces of numerous types of medical devices. This study assessed the feasibility of using a novel biodegradable polymer to release antibiotic drugs in response to inflammatory related enzymes. A model drug polymer was synthesized using 1,6-hexane diisocyanate (HDI), polycaprolactone diol (PCL), and a fluoroquinolone antibiotic, ciprofloxacin. Polymers were characterized by size-exclusion chromatography (SEC), and elemental analysis. Biodegradation studies were carried out by incubating the polymers with solutions of cholesterol esterase (CE) or phosphate buffer (pH 7.0) for 30 days at 37°C. The degradation was assessed by high-performance liquid chromatography (HPLC), mass spectrometry (MS) and
14
C
radiolabel release. Subsequently, the activity of the released antibiotic was assessed against a clinical isolate of
Pseudomonas aeruginosa. HPLC analysis showed the release of multiple degradation products which were identified, by tandem MS, to include ciprofloxacin and derivatives of ciprofloxacin. The microbiological assessment showed that the released ciprofloxacin possessed antimicrobial activity; 1
μg/ml was measured after 10 days. The results of this study suggest that these novel bioresponsive antimicrobial polymers or similar analogs show promise for use in the control of medical device associated infections.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>10811305</pmid><doi>10.1016/S0142-9612(00)00003-X</doi><tpages>12</tpages></addata></record> |
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subjects | Absorbable Implants Antibiotics Antimicrobial Aromatic compounds Biocompatible Materials - chemical synthesis Biodegradable polymers Biodegradation Biological and medical sciences Biosynthesis Chromatography, Gel Chromatography, High Pressure Liquid Ciprofloxacin Ciprofloxacin - administration & dosage Ciprofloxacin - analogs & derivatives Ciprofloxacin - chemical synthesis Ciprofloxacin - chemistry Ciprofloxacin - pharmacokinetics Ciprofloxacin - pharmacology Delayed-Action Preparations Diffusion Drug Carriers Enzymes Feasibility Studies Infection Mass Spectrometry Materials Testing Medical sciences Microbial Sensitivity Tests Microbiology Molecular Weight Phosphates Polyesters Polyesters - chemical synthesis Polyesters - chemistry Polyurethanes Pseudomonas aeruginosa - drug effects Quinolones Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) Sterol Esterase - metabolism Technology. Biomaterials. Equipments. Material. Instrumentation |
title | Synthesis and characterization of a novel biodegradable antimicrobial polymer |
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