Comparing PMMA and calcium sulfate as carriers for the local delivery of antibiotics to infected surgical sites
Antibiotic-loaded bone cement is a primary option for treatment of orthopedic infections. Poly(methyl methacrylate) (PMMA) is a widely used cement that, when loaded with antibiotics in spacer or bead form, has been shown to reduce infection rates. However, PMMA is not resorbable and requires a secon...
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Veröffentlicht in: | Journal of biomedical materials research. Part B, Applied biomaterials Applied biomaterials, 2015-05, Vol.103 (4), p.870-877 |
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creator | McConoughey, Stephen J. Howlin, Robert P. Wiseman, Jessica Stoodley, Paul Calhoun, Jason H. |
description | Antibiotic-loaded bone cement is a primary option for treatment of orthopedic infections. Poly(methyl methacrylate) (PMMA) is a widely used cement that, when loaded with antibiotics in spacer or bead form, has been shown to reduce infection rates. However, PMMA is not resorbable and requires a second surgery for removal, while also acting as a potential foreign body for bacterial colonization. Alternatively, resorbable bone cements, such as calcium sulfate, have been proposed and present the advantage of being completely reabsorbed. It is unknown whether the antibiotic elution characteristics of absorbable bone cements are similar to PMMA. This study (1) characterized antibiotic elution from synthetic, highly purified calcium sulfate cement beads of varying sizes against pathogenic bacteria both in liquid culture and seeded on agar plates, (2) tested calcium sulfate beads against PMMA beads loaded with the same antibiotics, and (3) analyzed the structural differences between how PMMA and calcium sulfate bind to antibiotics. In every assay, the calcium sulfate beads performed as well as, or better than, the PMMA beads in inhibition of bacterial growth and elution of vancomycin in vitro with complete elution observed from calcium sulfate within three days. These data suggest that calcium sulfate, functions, as well as PMMA in the patient setting for infection control. |
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Poly(methyl methacrylate) (PMMA) is a widely used cement that, when loaded with antibiotics in spacer or bead form, has been shown to reduce infection rates. However, PMMA is not resorbable and requires a second surgery for removal, while also acting as a potential foreign body for bacterial colonization. Alternatively, resorbable bone cements, such as calcium sulfate, have been proposed and present the advantage of being completely reabsorbed. It is unknown whether the antibiotic elution characteristics of absorbable bone cements are similar to PMMA. This study (1) characterized antibiotic elution from synthetic, highly purified calcium sulfate cement beads of varying sizes against pathogenic bacteria both in liquid culture and seeded on agar plates, (2) tested calcium sulfate beads against PMMA beads loaded with the same antibiotics, and (3) analyzed the structural differences between how PMMA and calcium sulfate bind to antibiotics. In every assay, the calcium sulfate beads performed as well as, or better than, the PMMA beads in inhibition of bacterial growth and elution of vancomycin in vitro with complete elution observed from calcium sulfate within three days. These data suggest that calcium sulfate, functions, as well as PMMA in the patient setting for infection control.</description><identifier>ISSN: 1552-4973</identifier><identifier>EISSN: 1552-4981</identifier><identifier>DOI: 10.1002/jbm.b.33247</identifier><identifier>PMID: 25142105</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; bacteria ; bioabsorption ; Biomedical materials ; Bone Substitutes - chemistry ; Bone Substitutes - pharmacology ; calcium sulfate ; Calcium Sulfate - chemistry ; Calcium Sulfate - pharmacology ; Drug Carriers ; infection ; Materials research ; Materials science ; Methicillin-Resistant Staphylococcus aureus - growth & development ; PMMA ; Polymethyl Methacrylate - chemistry ; Polymethyl Methacrylate - pharmacology ; Staphylococcus epidermidis - growth & development ; Surgical Wound Infection - drug therapy</subject><ispartof>Journal of biomedical materials research. 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Part B, Applied biomaterials</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Antibiotic-loaded bone cement is a primary option for treatment of orthopedic infections. Poly(methyl methacrylate) (PMMA) is a widely used cement that, when loaded with antibiotics in spacer or bead form, has been shown to reduce infection rates. However, PMMA is not resorbable and requires a second surgery for removal, while also acting as a potential foreign body for bacterial colonization. Alternatively, resorbable bone cements, such as calcium sulfate, have been proposed and present the advantage of being completely reabsorbed. It is unknown whether the antibiotic elution characteristics of absorbable bone cements are similar to PMMA. This study (1) characterized antibiotic elution from synthetic, highly purified calcium sulfate cement beads of varying sizes against pathogenic bacteria both in liquid culture and seeded on agar plates, (2) tested calcium sulfate beads against PMMA beads loaded with the same antibiotics, and (3) analyzed the structural differences between how PMMA and calcium sulfate bind to antibiotics. In every assay, the calcium sulfate beads performed as well as, or better than, the PMMA beads in inhibition of bacterial growth and elution of vancomycin in vitro with complete elution observed from calcium sulfate within three days. These data suggest that calcium sulfate, functions, as well as PMMA in the patient setting for infection control.</description><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>bacteria</subject><subject>bioabsorption</subject><subject>Biomedical materials</subject><subject>Bone Substitutes - chemistry</subject><subject>Bone Substitutes - pharmacology</subject><subject>calcium sulfate</subject><subject>Calcium Sulfate - chemistry</subject><subject>Calcium Sulfate - pharmacology</subject><subject>Drug Carriers</subject><subject>infection</subject><subject>Materials research</subject><subject>Materials science</subject><subject>Methicillin-Resistant Staphylococcus aureus - growth & development</subject><subject>PMMA</subject><subject>Polymethyl Methacrylate - chemistry</subject><subject>Polymethyl Methacrylate - pharmacology</subject><subject>Staphylococcus epidermidis - growth & development</subject><subject>Surgical Wound Infection - drug therapy</subject><issn>1552-4973</issn><issn>1552-4981</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0DtPxDAMAOAIgXhP7CgSC0uPvEtHdIIDxOMGHmOVpg7kaJsjSRH8e4J4DEy27M-WZYT2KJlQQtjRouknzYRzJsoVtEmlZIWojunqX17yDbQV4yJjRSRfRxtMUsEokZvIT32_1MENT3h-fX2C9dBiozvjxh7HsbM6AdYxl0JwECK2PuD0DLjzWeEWOvcG4QN7myeTa5xPzkScPHaDBZOgzVvCk_vC0SWIO2jN6i7C7k_cRvdnp3fT8-LqdnYxPbkqjGAqFVZoTqyRLWlk01plFNhKS0KUYoIzRhQBoS0ISRlvha0aIbg1hFtqbK7zbXT4vXcZ_OsIMdW9iwa6Tg_gx1hTVUqqKs5Vpgf_6MKPYcjXfSnBWP5mldX-jxqbHtp6GVyvw0f9-8oMim_gYoL3v74OL7UqeSnrx5tZzS8rOZ8fP9R3_BNzgITY</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>McConoughey, Stephen J.</creator><creator>Howlin, Robert P.</creator><creator>Wiseman, Jessica</creator><creator>Stoodley, Paul</creator><creator>Calhoun, Jason H.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20150501</creationdate><title>Comparing PMMA and calcium sulfate as carriers for the local delivery of antibiotics to infected surgical sites</title><author>McConoughey, Stephen J. ; 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Poly(methyl methacrylate) (PMMA) is a widely used cement that, when loaded with antibiotics in spacer or bead form, has been shown to reduce infection rates. However, PMMA is not resorbable and requires a second surgery for removal, while also acting as a potential foreign body for bacterial colonization. Alternatively, resorbable bone cements, such as calcium sulfate, have been proposed and present the advantage of being completely reabsorbed. It is unknown whether the antibiotic elution characteristics of absorbable bone cements are similar to PMMA. This study (1) characterized antibiotic elution from synthetic, highly purified calcium sulfate cement beads of varying sizes against pathogenic bacteria both in liquid culture and seeded on agar plates, (2) tested calcium sulfate beads against PMMA beads loaded with the same antibiotics, and (3) analyzed the structural differences between how PMMA and calcium sulfate bind to antibiotics. In every assay, the calcium sulfate beads performed as well as, or better than, the PMMA beads in inhibition of bacterial growth and elution of vancomycin in vitro with complete elution observed from calcium sulfate within three days. These data suggest that calcium sulfate, functions, as well as PMMA in the patient setting for infection control.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25142105</pmid><doi>10.1002/jbm.b.33247</doi><tpages>8</tpages></addata></record> |
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subjects | Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology bacteria bioabsorption Biomedical materials Bone Substitutes - chemistry Bone Substitutes - pharmacology calcium sulfate Calcium Sulfate - chemistry Calcium Sulfate - pharmacology Drug Carriers infection Materials research Materials science Methicillin-Resistant Staphylococcus aureus - growth & development PMMA Polymethyl Methacrylate - chemistry Polymethyl Methacrylate - pharmacology Staphylococcus epidermidis - growth & development Surgical Wound Infection - drug therapy |
title | Comparing PMMA and calcium sulfate as carriers for the local delivery of antibiotics to infected surgical sites |
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