Octenidine in combination with polymethylmethacrylate: a new option for preventing infection?
Background Orthopedic implant infections represent a serious complication for both patient and surgeon. In order to minimize this risk, it has become standard practice in surgery and orthopedics to add antimicrobial substances to the polymethylmethacrylate (PMMA) bone cement. The aim of this study i...
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Veröffentlicht in: | Archives of orthopaedic and trauma surgery 2012, Vol.132 (1), p.15-20 |
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description | Background
Orthopedic implant infections represent a serious complication for both patient and surgeon. In order to minimize this risk, it has become standard practice in surgery and orthopedics to add antimicrobial substances to the polymethylmethacrylate (PMMA) bone cement. The aim of this study is to find new options for preventing infection by using alternative adjuvants in combination with PMMA. We hypothesized, that Octenidine, after being combined with PMMA, can be released in vitro and an antimicrobial efficacy of discharged Octenidine can be shown
.
Methods
The release of Octenidine from PMMA was assessed in high pressure liquid chromatography of the supernatant. In order to assess the efficacy of Octenidine on
Staphylococcus aureus
and
Pseudomonas aeruginosa
in vitro, a nutrient solution for these bacteria was incubated with a defined number of these bacteria (10
6
colony forming units) and cement pellets containing the antiseptic Octenidine for 24 h. After the incubation the number of bacteria in the solution was determined by counting the colony forming units on blood agar plates.
Results
Octenidine was shown to be released in a concentration-dependent manner from PMMA in the elution experiment. The experimental procedure using
S. aureus
demonstrated a bactericidal effect for bone cement containing Octenidine. For
P. aeruginosa,
bone cement containing 5–8% Octenidine was associated with tenfold reduction in bacterial count.
Conclusion
These results suggest that Octenidine is released after combining it with PMMA and reaches working concentrations in vitro. These findings suggest a new and effective alternative for prevention of infection in cemented implants. Further investigations on the biocompatibility of this combination is needed. |
doi_str_mv | 10.1007/s00402-011-1386-2 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_913441124</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>913441124</sourcerecordid><originalsourceid>FETCH-LOGICAL-c371t-59f2080415cae3e578f681ba4fd4bf956683ec548e55c46c393520cb5f7531cc3</originalsourceid><addsrcrecordid>eNp1kM9rFTEQx4NY7Gv1D_AiCx48rc3k93qRUqwKhV70KCGbN2lTdpM12dfy_nt3-6qC4GXmMJ_5zvAh5DXQ90CpPquUCspaCtACN6plz8gGBBct70A9JxvacdUaKuGYnNR6Rykw09EX5JiB0RqY2pAf137GFLcxYRNT4_PYx-TmmFPzEOfbZsrDfsT5dj-s1fmyH9yMHxrXJHxo8vRIhlyaqeA9pjmmmyUnoF8HH1-So-CGiq-e-in5fvnp28WX9ur689eL86vWcw1zK7vAqKECpHfIUWoTlIHeibAVfeikUoajl8KglF4ozzsuGfW9DFpy8J6fkneH3Knknzussx1j9TgMLmHeVdsBFwKAiYV8-w95l3clLc9ZxhR0WmvDFgoOlC-51oLBTiWOruwtULuqtwf1dlFvV_V23XnzlLzrR9z-2fjtegHYAajLKN1g-Xv6_6m_AJJzjrs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2261977782</pqid></control><display><type>article</type><title>Octenidine in combination with polymethylmethacrylate: a new option for preventing infection?</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Weckbach, Sebastian ; Möricke, Angelika ; Braunwarth, Horst ; Goroncy-Bermes, Peter ; Bischoff, Mark ; Gebhard, Florian</creator><creatorcontrib>Weckbach, Sebastian ; Möricke, Angelika ; Braunwarth, Horst ; Goroncy-Bermes, Peter ; Bischoff, Mark ; Gebhard, Florian</creatorcontrib><description>Background
Orthopedic implant infections represent a serious complication for both patient and surgeon. In order to minimize this risk, it has become standard practice in surgery and orthopedics to add antimicrobial substances to the polymethylmethacrylate (PMMA) bone cement. The aim of this study is to find new options for preventing infection by using alternative adjuvants in combination with PMMA. We hypothesized, that Octenidine, after being combined with PMMA, can be released in vitro and an antimicrobial efficacy of discharged Octenidine can be shown
.
Methods
The release of Octenidine from PMMA was assessed in high pressure liquid chromatography of the supernatant. In order to assess the efficacy of Octenidine on
Staphylococcus aureus
and
Pseudomonas aeruginosa
in vitro, a nutrient solution for these bacteria was incubated with a defined number of these bacteria (10
6
colony forming units) and cement pellets containing the antiseptic Octenidine for 24 h. After the incubation the number of bacteria in the solution was determined by counting the colony forming units on blood agar plates.
Results
Octenidine was shown to be released in a concentration-dependent manner from PMMA in the elution experiment. The experimental procedure using
S. aureus
demonstrated a bactericidal effect for bone cement containing Octenidine. For
P. aeruginosa,
bone cement containing 5–8% Octenidine was associated with tenfold reduction in bacterial count.
Conclusion
These results suggest that Octenidine is released after combining it with PMMA and reaches working concentrations in vitro. These findings suggest a new and effective alternative for prevention of infection in cemented implants. Further investigations on the biocompatibility of this combination is needed.</description><identifier>ISSN: 0936-8051</identifier><identifier>EISSN: 1434-3916</identifier><identifier>DOI: 10.1007/s00402-011-1386-2</identifier><identifier>PMID: 21877126</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Anti-Bacterial Agents - pharmacokinetics ; Anti-Bacterial Agents - pharmacology ; Bacteria ; Bone Cements ; Cement ; Chromatography, High Pressure Liquid ; Colony Count, Microbial ; Humans ; Infections ; Medicine ; Medicine & Public Health ; Orthopaedic Surgery ; Orthopedics ; Polymethyl Methacrylate ; Prosthesis-Related Infections - prevention & control ; Pseudomonas aeruginosa - drug effects ; Pseudomonas aeruginosa - growth & development ; Pyridines - pharmacokinetics ; Pyridines - pharmacology ; Staphylococcus aureus - drug effects ; Staphylococcus aureus - growth & development ; Transplants & implants</subject><ispartof>Archives of orthopaedic and trauma surgery, 2012, Vol.132 (1), p.15-20</ispartof><rights>Springer-Verlag 2011</rights><rights>Archives of Orthopaedic and Trauma Surgery is a copyright of Springer, (2011). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-59f2080415cae3e578f681ba4fd4bf956683ec548e55c46c393520cb5f7531cc3</citedby><cites>FETCH-LOGICAL-c371t-59f2080415cae3e578f681ba4fd4bf956683ec548e55c46c393520cb5f7531cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00402-011-1386-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00402-011-1386-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27911,27912,41475,42544,51306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21877126$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weckbach, Sebastian</creatorcontrib><creatorcontrib>Möricke, Angelika</creatorcontrib><creatorcontrib>Braunwarth, Horst</creatorcontrib><creatorcontrib>Goroncy-Bermes, Peter</creatorcontrib><creatorcontrib>Bischoff, Mark</creatorcontrib><creatorcontrib>Gebhard, Florian</creatorcontrib><title>Octenidine in combination with polymethylmethacrylate: a new option for preventing infection?</title><title>Archives of orthopaedic and trauma surgery</title><addtitle>Arch Orthop Trauma Surg</addtitle><addtitle>Arch Orthop Trauma Surg</addtitle><description>Background
Orthopedic implant infections represent a serious complication for both patient and surgeon. In order to minimize this risk, it has become standard practice in surgery and orthopedics to add antimicrobial substances to the polymethylmethacrylate (PMMA) bone cement. The aim of this study is to find new options for preventing infection by using alternative adjuvants in combination with PMMA. We hypothesized, that Octenidine, after being combined with PMMA, can be released in vitro and an antimicrobial efficacy of discharged Octenidine can be shown
.
Methods
The release of Octenidine from PMMA was assessed in high pressure liquid chromatography of the supernatant. In order to assess the efficacy of Octenidine on
Staphylococcus aureus
and
Pseudomonas aeruginosa
in vitro, a nutrient solution for these bacteria was incubated with a defined number of these bacteria (10
6
colony forming units) and cement pellets containing the antiseptic Octenidine for 24 h. After the incubation the number of bacteria in the solution was determined by counting the colony forming units on blood agar plates.
Results
Octenidine was shown to be released in a concentration-dependent manner from PMMA in the elution experiment. The experimental procedure using
S. aureus
demonstrated a bactericidal effect for bone cement containing Octenidine. For
P. aeruginosa,
bone cement containing 5–8% Octenidine was associated with tenfold reduction in bacterial count.
Conclusion
These results suggest that Octenidine is released after combining it with PMMA and reaches working concentrations in vitro. These findings suggest a new and effective alternative for prevention of infection in cemented implants. Further investigations on the biocompatibility of this combination is needed.</description><subject>Anti-Bacterial Agents - pharmacokinetics</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Bacteria</subject><subject>Bone Cements</subject><subject>Cement</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Colony Count, Microbial</subject><subject>Humans</subject><subject>Infections</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Orthopaedic Surgery</subject><subject>Orthopedics</subject><subject>Polymethyl Methacrylate</subject><subject>Prosthesis-Related Infections - prevention & control</subject><subject>Pseudomonas aeruginosa - drug effects</subject><subject>Pseudomonas aeruginosa - growth & development</subject><subject>Pyridines - pharmacokinetics</subject><subject>Pyridines - pharmacology</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Staphylococcus aureus - growth & development</subject><subject>Transplants & implants</subject><issn>0936-8051</issn><issn>1434-3916</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kM9rFTEQx4NY7Gv1D_AiCx48rc3k93qRUqwKhV70KCGbN2lTdpM12dfy_nt3-6qC4GXmMJ_5zvAh5DXQ90CpPquUCspaCtACN6plz8gGBBct70A9JxvacdUaKuGYnNR6Rykw09EX5JiB0RqY2pAf137GFLcxYRNT4_PYx-TmmFPzEOfbZsrDfsT5dj-s1fmyH9yMHxrXJHxo8vRIhlyaqeA9pjmmmyUnoF8HH1-So-CGiq-e-in5fvnp28WX9ur689eL86vWcw1zK7vAqKECpHfIUWoTlIHeibAVfeikUoajl8KglF4ozzsuGfW9DFpy8J6fkneH3Knknzussx1j9TgMLmHeVdsBFwKAiYV8-w95l3clLc9ZxhR0WmvDFgoOlC-51oLBTiWOruwtULuqtwf1dlFvV_V23XnzlLzrR9z-2fjtegHYAajLKN1g-Xv6_6m_AJJzjrs</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Weckbach, Sebastian</creator><creator>Möricke, Angelika</creator><creator>Braunwarth, Horst</creator><creator>Goroncy-Bermes, Peter</creator><creator>Bischoff, Mark</creator><creator>Gebhard, Florian</creator><general>Springer-Verlag</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>2012</creationdate><title>Octenidine in combination with polymethylmethacrylate: a new option for preventing infection?</title><author>Weckbach, Sebastian ; Möricke, Angelika ; Braunwarth, Horst ; Goroncy-Bermes, Peter ; Bischoff, Mark ; Gebhard, Florian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-59f2080415cae3e578f681ba4fd4bf956683ec548e55c46c393520cb5f7531cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Anti-Bacterial Agents - pharmacokinetics</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Bacteria</topic><topic>Bone Cements</topic><topic>Cement</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Colony Count, Microbial</topic><topic>Humans</topic><topic>Infections</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Orthopaedic Surgery</topic><topic>Orthopedics</topic><topic>Polymethyl Methacrylate</topic><topic>Prosthesis-Related Infections - prevention & control</topic><topic>Pseudomonas aeruginosa - drug effects</topic><topic>Pseudomonas aeruginosa - growth & development</topic><topic>Pyridines - pharmacokinetics</topic><topic>Pyridines - pharmacology</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Staphylococcus aureus - growth & development</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weckbach, Sebastian</creatorcontrib><creatorcontrib>Möricke, Angelika</creatorcontrib><creatorcontrib>Braunwarth, Horst</creatorcontrib><creatorcontrib>Goroncy-Bermes, Peter</creatorcontrib><creatorcontrib>Bischoff, Mark</creatorcontrib><creatorcontrib>Gebhard, Florian</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of orthopaedic and trauma surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weckbach, Sebastian</au><au>Möricke, Angelika</au><au>Braunwarth, Horst</au><au>Goroncy-Bermes, Peter</au><au>Bischoff, Mark</au><au>Gebhard, Florian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Octenidine in combination with polymethylmethacrylate: a new option for preventing infection?</atitle><jtitle>Archives of orthopaedic and trauma surgery</jtitle><stitle>Arch Orthop Trauma Surg</stitle><addtitle>Arch Orthop Trauma Surg</addtitle><date>2012</date><risdate>2012</risdate><volume>132</volume><issue>1</issue><spage>15</spage><epage>20</epage><pages>15-20</pages><issn>0936-8051</issn><eissn>1434-3916</eissn><abstract>Background
Orthopedic implant infections represent a serious complication for both patient and surgeon. In order to minimize this risk, it has become standard practice in surgery and orthopedics to add antimicrobial substances to the polymethylmethacrylate (PMMA) bone cement. The aim of this study is to find new options for preventing infection by using alternative adjuvants in combination with PMMA. We hypothesized, that Octenidine, after being combined with PMMA, can be released in vitro and an antimicrobial efficacy of discharged Octenidine can be shown
.
Methods
The release of Octenidine from PMMA was assessed in high pressure liquid chromatography of the supernatant. In order to assess the efficacy of Octenidine on
Staphylococcus aureus
and
Pseudomonas aeruginosa
in vitro, a nutrient solution for these bacteria was incubated with a defined number of these bacteria (10
6
colony forming units) and cement pellets containing the antiseptic Octenidine for 24 h. After the incubation the number of bacteria in the solution was determined by counting the colony forming units on blood agar plates.
Results
Octenidine was shown to be released in a concentration-dependent manner from PMMA in the elution experiment. The experimental procedure using
S. aureus
demonstrated a bactericidal effect for bone cement containing Octenidine. For
P. aeruginosa,
bone cement containing 5–8% Octenidine was associated with tenfold reduction in bacterial count.
Conclusion
These results suggest that Octenidine is released after combining it with PMMA and reaches working concentrations in vitro. These findings suggest a new and effective alternative for prevention of infection in cemented implants. Further investigations on the biocompatibility of this combination is needed.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21877126</pmid><doi>10.1007/s00402-011-1386-2</doi><tpages>6</tpages></addata></record> |
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subjects | Anti-Bacterial Agents - pharmacokinetics Anti-Bacterial Agents - pharmacology Bacteria Bone Cements Cement Chromatography, High Pressure Liquid Colony Count, Microbial Humans Infections Medicine Medicine & Public Health Orthopaedic Surgery Orthopedics Polymethyl Methacrylate Prosthesis-Related Infections - prevention & control Pseudomonas aeruginosa - drug effects Pseudomonas aeruginosa - growth & development Pyridines - pharmacokinetics Pyridines - pharmacology Staphylococcus aureus - drug effects Staphylococcus aureus - growth & development Transplants & implants |
title | Octenidine in combination with polymethylmethacrylate: a new option for preventing infection? |
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