Source:http://linkedlifedata.com/resource/pubmed/id/12418028
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2002-11-5
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pubmed:abstractText |
The current delivery system of antibiotics for the treatment of osteomyelitis uses polymethylmethacrylate (PMMA) beads as a local drug-release agent. The nonbiodegradable nature of the PMMA, however, necessitates a second operation to remove the beads. This article explores the alternative of using biodegradable polymers as antibiotic beads for a long-term drug release in vivo. To manufacture an antibiotic bead, lactide-glycolide copolymers were mixed with vancomycin. The mixture was compressed and sintered at 55 degrees C to form beads 8 mm in diameter. An in vivo animal model was proposed to characterize the elution rate of antibiotic over a 55-day period. Biodegradable beads released high concentrations of antibiotic (well above the breakpoint sensitivity concentration) in vivo for the period of time needed to treat bone infection; that is, 4-6 weeks. A bacterial inhibition test was also carried out to determine the relative activity of the released antibiotics. The diameter of the sample inhibition zone ranged from 8 to 18 mm, which is equivalent to 9.1 to 100% of relative activity. In addition, the antibiotic concentration of systemic blood was found to be very low. Antibiotic-impregnated biodegradable beads may have a potential role in the prevention and management of surgical infections.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Bacterial Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Biocompatible Materials,
http://linkedlifedata.com/resource/pubmed/chemical/Delayed-Action Preparations,
http://linkedlifedata.com/resource/pubmed/chemical/Drug Implants,
http://linkedlifedata.com/resource/pubmed/chemical/Polymethyl Methacrylate,
http://linkedlifedata.com/resource/pubmed/chemical/Vancomycin
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pubmed:status |
MEDLINE
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pubmed:issn |
0021-9304
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2002 Wiley Periodicals, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
63
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
807-13
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12418028-Animals,
pubmed-meshheading:12418028-Anti-Bacterial Agents,
pubmed-meshheading:12418028-Biocompatible Materials,
pubmed-meshheading:12418028-Biodegradation, Environmental,
pubmed-meshheading:12418028-Delayed-Action Preparations,
pubmed-meshheading:12418028-Drug Delivery Systems,
pubmed-meshheading:12418028-Drug Implants,
pubmed-meshheading:12418028-Materials Testing,
pubmed-meshheading:12418028-Osteomyelitis,
pubmed-meshheading:12418028-Polymethyl Methacrylate,
pubmed-meshheading:12418028-Rabbits,
pubmed-meshheading:12418028-Vancomycin
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pubmed:year |
2002
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pubmed:articleTitle |
In vivo release of vancomycin from biodegradable beads.
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pubmed:affiliation |
Department of Mechanical Engineering, Chang Gung University, Tao-Yuan, Taiwan.
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pubmed:publicationType |
Journal Article
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