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Tissue reactions to bacteria-inoculated rat lead samples. II. Effect of local gentamicin release through surface-modified polyurethane tubing
A surface modification technique was developed to achieve controlled release of gentamicin from implanted polyurethane (PU) rat lead samples. PU tubing first was provided with an acrylic acid/acrylamide copolymer surface graft and then loaded with gentamicin. This surface modification technique resu...
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Published in: | Journal of biomedical materials research 1997-05, Vol.35 (2), p.233-247 |
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container_title | Journal of biomedical materials research |
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creator | van Wachem, P. B. van Luyn, M. J. A. de Wit, A. W. Raatjes, D. Hendriks, M. Verhoeven, M. L. P. M. Cahalan, P. T. |
description | A surface modification technique was developed to achieve controlled release of gentamicin from implanted polyurethane (PU) rat lead samples. PU tubing first was provided with an acrylic acid/acrylamide copolymer surface graft and then loaded with gentamicin. This surface modification technique resulted in release of gentamicin base (GB) and was applied either to the inner luminal surface only (PU‐GB‐1x) or to both the inner and outer surfaces (PU‐GB‐2x). First we investigated whether the early tissue response was harmfully compromised when surface‐modified rat lead samples were implanted without any infectious challenge. Additionally, the efficacy of this type of local gentamicin therapy was investigated by establishing its effect on tissue response and its ability to prevent lead‐related infections after inoculation with Staphylococcus aureus. It was demonstrated that the applied surface modification(s) did not induce adverse effects although an increase in the infiltration of granulocytes and macrophages and an increase in the formation of wound fluid and fibrin were observed. This effect was stronger with PU‐GB‐2x than with PU‐GB‐1x. With bacterial inoculation the applied surface modification successfully suppressed the infectious challenge, PU‐GB‐2x more effectively than PU‐GB‐1x. PU‐GB‐2x also was more effective when compared to the gentamicin‐delivery methods discussed in the first part of this two‐part study, i.e., release through a vicinal gentamicin‐containing collagen sponge and preoperative gentamicin solution‐dipping of rat lead samples. © 1997 John Wiley & Sons, Inc. |
doi_str_mv | 10.1002/(SICI)1097-4636(199705)35:2<233::AID-JBM11>3.0.CO;2-I |
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II. Effect of local gentamicin release through surface-modified polyurethane tubing</title><source>Wiley</source><creator>van Wachem, P. B. ; van Luyn, M. J. A. ; de Wit, A. W. ; Raatjes, D. ; Hendriks, M. ; Verhoeven, M. L. P. M. ; Cahalan, P. T.</creator><creatorcontrib>van Wachem, P. B. ; van Luyn, M. J. A. ; de Wit, A. W. ; Raatjes, D. ; Hendriks, M. ; Verhoeven, M. L. P. M. ; Cahalan, P. T.</creatorcontrib><description>A surface modification technique was developed to achieve controlled release of gentamicin from implanted polyurethane (PU) rat lead samples. PU tubing first was provided with an acrylic acid/acrylamide copolymer surface graft and then loaded with gentamicin. This surface modification technique resulted in release of gentamicin base (GB) and was applied either to the inner luminal surface only (PU‐GB‐1x) or to both the inner and outer surfaces (PU‐GB‐2x). First we investigated whether the early tissue response was harmfully compromised when surface‐modified rat lead samples were implanted without any infectious challenge. Additionally, the efficacy of this type of local gentamicin therapy was investigated by establishing its effect on tissue response and its ability to prevent lead‐related infections after inoculation with Staphylococcus aureus. It was demonstrated that the applied surface modification(s) did not induce adverse effects although an increase in the infiltration of granulocytes and macrophages and an increase in the formation of wound fluid and fibrin were observed. This effect was stronger with PU‐GB‐2x than with PU‐GB‐1x. With bacterial inoculation the applied surface modification successfully suppressed the infectious challenge, PU‐GB‐2x more effectively than PU‐GB‐1x. PU‐GB‐2x also was more effective when compared to the gentamicin‐delivery methods discussed in the first part of this two‐part study, i.e., release through a vicinal gentamicin‐containing collagen sponge and preoperative gentamicin solution‐dipping of rat lead samples. © 1997 John Wiley & Sons, Inc.</description><identifier>ISSN: 0021-9304</identifier><identifier>EISSN: 1097-4636</identifier><identifier>DOI: 10.1002/(SICI)1097-4636(199705)35:2<233::AID-JBM11>3.0.CO;2-I</identifier><identifier>PMID: 9135172</identifier><identifier>CODEN: JBMRBG</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Animals ; Anti-Bacterial Agents - administration & dosage ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - therapeutic use ; Biological and medical sciences ; Drug Implants ; Electrodes, Implanted ; Gentamicins - administration & dosage ; Gentamicins - adverse effects ; Gentamicins - therapeutic use ; Male ; Medical sciences ; Muscle, Skeletal - pathology ; Polyurethanes ; Prosthesis-Related Infections - pathology ; Prosthesis-Related Infections - prevention & control ; Rats ; Skin - pathology ; Staphylococcal Infections - microbiology ; Staphylococcal Infections - prevention & control ; Surface Properties ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Technology. Biomaterials. Equipments</subject><ispartof>Journal of biomedical materials research, 1997-05, Vol.35 (2), p.233-247</ispartof><rights>Copyright © 1997 John Wiley & Sons, Inc.</rights><rights>1997 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4381-6fbc5b6c533032e433e8b182a467f7e1bf0b29f80d35814b25cc7167c58f8d303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2651331$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9135172$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van Wachem, P. B.</creatorcontrib><creatorcontrib>van Luyn, M. J. A.</creatorcontrib><creatorcontrib>de Wit, A. W.</creatorcontrib><creatorcontrib>Raatjes, D.</creatorcontrib><creatorcontrib>Hendriks, M.</creatorcontrib><creatorcontrib>Verhoeven, M. L. P. M.</creatorcontrib><creatorcontrib>Cahalan, P. T.</creatorcontrib><title>Tissue reactions to bacteria-inoculated rat lead samples. II. Effect of local gentamicin release through surface-modified polyurethane tubing</title><title>Journal of biomedical materials research</title><addtitle>J. Biomed. Mater. Res</addtitle><description>A surface modification technique was developed to achieve controlled release of gentamicin from implanted polyurethane (PU) rat lead samples. PU tubing first was provided with an acrylic acid/acrylamide copolymer surface graft and then loaded with gentamicin. This surface modification technique resulted in release of gentamicin base (GB) and was applied either to the inner luminal surface only (PU‐GB‐1x) or to both the inner and outer surfaces (PU‐GB‐2x). First we investigated whether the early tissue response was harmfully compromised when surface‐modified rat lead samples were implanted without any infectious challenge. Additionally, the efficacy of this type of local gentamicin therapy was investigated by establishing its effect on tissue response and its ability to prevent lead‐related infections after inoculation with Staphylococcus aureus. It was demonstrated that the applied surface modification(s) did not induce adverse effects although an increase in the infiltration of granulocytes and macrophages and an increase in the formation of wound fluid and fibrin were observed. This effect was stronger with PU‐GB‐2x than with PU‐GB‐1x. With bacterial inoculation the applied surface modification successfully suppressed the infectious challenge, PU‐GB‐2x more effectively than PU‐GB‐1x. PU‐GB‐2x also was more effective when compared to the gentamicin‐delivery methods discussed in the first part of this two‐part study, i.e., release through a vicinal gentamicin‐containing collagen sponge and preoperative gentamicin solution‐dipping of rat lead samples. © 1997 John Wiley & Sons, Inc.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Anti-Bacterial Agents - adverse effects</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Drug Implants</subject><subject>Electrodes, Implanted</subject><subject>Gentamicins - administration & dosage</subject><subject>Gentamicins - adverse effects</subject><subject>Gentamicins - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Muscle, Skeletal - pathology</subject><subject>Polyurethanes</subject><subject>Prosthesis-Related Infections - pathology</subject><subject>Prosthesis-Related Infections - prevention & control</subject><subject>Rats</subject><subject>Skin - pathology</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcal Infections - prevention & control</subject><subject>Surface Properties</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Technology. Biomaterials. 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W.</creator><creator>Raatjes, D.</creator><creator>Hendriks, M.</creator><creator>Verhoeven, M. L. P. M.</creator><creator>Cahalan, P. T.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley & Sons</general><scope>BSCLL</scope><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>7QL</scope><scope>C1K</scope><scope>7SR</scope><scope>JG9</scope></search><sort><creationdate>199705</creationdate><title>Tissue reactions to bacteria-inoculated rat lead samples. II. Effect of local gentamicin release through surface-modified polyurethane tubing</title><author>van Wachem, P. B. ; van Luyn, M. J. A. ; de Wit, A. W. ; Raatjes, D. ; Hendriks, M. ; Verhoeven, M. L. P. M. ; Cahalan, P. 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B.</au><au>van Luyn, M. J. A.</au><au>de Wit, A. W.</au><au>Raatjes, D.</au><au>Hendriks, M.</au><au>Verhoeven, M. L. P. M.</au><au>Cahalan, P. T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tissue reactions to bacteria-inoculated rat lead samples. II. Effect of local gentamicin release through surface-modified polyurethane tubing</atitle><jtitle>Journal of biomedical materials research</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>1997-05</date><risdate>1997</risdate><volume>35</volume><issue>2</issue><spage>233</spage><epage>247</epage><pages>233-247</pages><issn>0021-9304</issn><eissn>1097-4636</eissn><coden>JBMRBG</coden><abstract>A surface modification technique was developed to achieve controlled release of gentamicin from implanted polyurethane (PU) rat lead samples. PU tubing first was provided with an acrylic acid/acrylamide copolymer surface graft and then loaded with gentamicin. This surface modification technique resulted in release of gentamicin base (GB) and was applied either to the inner luminal surface only (PU‐GB‐1x) or to both the inner and outer surfaces (PU‐GB‐2x). First we investigated whether the early tissue response was harmfully compromised when surface‐modified rat lead samples were implanted without any infectious challenge. Additionally, the efficacy of this type of local gentamicin therapy was investigated by establishing its effect on tissue response and its ability to prevent lead‐related infections after inoculation with Staphylococcus aureus. It was demonstrated that the applied surface modification(s) did not induce adverse effects although an increase in the infiltration of granulocytes and macrophages and an increase in the formation of wound fluid and fibrin were observed. This effect was stronger with PU‐GB‐2x than with PU‐GB‐1x. With bacterial inoculation the applied surface modification successfully suppressed the infectious challenge, PU‐GB‐2x more effectively than PU‐GB‐1x. PU‐GB‐2x also was more effective when compared to the gentamicin‐delivery methods discussed in the first part of this two‐part study, i.e., release through a vicinal gentamicin‐containing collagen sponge and preoperative gentamicin solution‐dipping of rat lead samples. © 1997 John Wiley & Sons, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>9135172</pmid><doi>10.1002/(SICI)1097-4636(199705)35:2<233::AID-JBM11>3.0.CO;2-I</doi><tpages>15</tpages></addata></record> |
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subjects | Animals Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - adverse effects Anti-Bacterial Agents - therapeutic use Biological and medical sciences Drug Implants Electrodes, Implanted Gentamicins - administration & dosage Gentamicins - adverse effects Gentamicins - therapeutic use Male Medical sciences Muscle, Skeletal - pathology Polyurethanes Prosthesis-Related Infections - pathology Prosthesis-Related Infections - prevention & control Rats Skin - pathology Staphylococcal Infections - microbiology Staphylococcal Infections - prevention & control Surface Properties Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Technology. Biomaterials. Equipments |
title | Tissue reactions to bacteria-inoculated rat lead samples. II. Effect of local gentamicin release through surface-modified polyurethane tubing |
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