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Novel fatty acid gentamicin salts as slow-release drug carrier systems for anti-infective protection of vascular biomaterials

机译:新型脂肪酸庆大霉素盐作为缓释药物载体系统,对血管生物材料具有抗感染保护作用

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摘要

Infections of vascular prostheses are still a major risk in surgery. The current work presents an in vitro evaluation of novel slow release antibiotic coatings based on new gentamicin fatty acid salts for polytetrafluoroeth-ylene grafts. These grafts were coated with gentamicin sodium dodecyl sulfate, gentamicin laurate and gentamicin palmitate. Drug release kinetics, anti-infective characteristics, biocompatibility and haemocompatibility of developed coatings were compared to commercially available gelatin sealed PTFE grafts (SEALPTFE™) and knitted silver coated Dacron® grafts (InterGard®). Each gentamicin fatty acid coating showed a continuous drug release in the first eight hours followed by a low continuous release. Grafts coated with gentamicin fatty acids reduced bacterial growth even beyond pathologically relevant high concentrations. Cytotoxicity levels depending on drug formulation bringing up gentamicin palmitate as the most promising biocompatible coating. Thrombelastography studies, ELISA assays and an amidolytic substrate assay confirmed haemocompatibility of developed gentamicin fatty acid coatings comparable to commercially available grafts.
机译:血管假体的感染仍然是手术中的主要风险。当前的工作提出了一种基于新型庆大霉素脂肪酸盐的新型缓释抗生素涂层的体外评估,该涂层用于聚四氟乙烯-乙烯接枝。这些移植物涂有庆大霉素十二烷基硫酸钠,月桂酸庆大霉素和棕榈酸庆大霉素。将已开发涂层的药物释放动力学,抗感染特性,生物相容性和血液相容性与市售明胶密封的PTFE移植物(SEALPTFE™)和编织的银涂层Dacron®移植物(InterGard®)进行了比较。每个庆大霉素脂肪酸涂层在开始的八小时内显示出连续的药物释放,然后是低的连续释放。庆大霉素脂肪酸涂层的接枝减少了细菌的生长,甚至超出了病理相关的高浓度。细胞毒性水平取决于药物配方,使庆大霉素棕榈酸酯成为最有前途的生物相容性涂层。血栓弹力图研究,ELISA测定法和酰胺分解底物测定法证实,所开发的庆大霉素脂肪酸涂层的血液相容性与市售移植物相当。

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  • 来源
    《Journal of materials science》 |2012年第7期|p.1675-1683|共9页
  • 作者单位

    Klinik fur Orthopadie und Sportorthopadie, Klinikum r.d. Isar,Technische Universitat Miinchen, Muskuloskelettale Forschung,Ismaninger Str. 22, 81675 Munich, Germany;

    Klinik fur Orthopadie und Sportorthopadie, Klinikum r.d. Isar,Technische Universitat Miinchen, Muskuloskelettale Forschung,Ismaninger Str. 22, 81675 Munich, Germany;

    Alfried Krupp Krankenhaus Essen-Steele, Klinik fur Unfallchirurgie und Orthopadie, Essen, Germany;

    Klinik fur Gefa'Bchirurgie, Klinikum r.d. Isar, Technische Universitat Miinchen, Munich, Germany;

    Universitatsklinik fur Orthopaedie, Medizinische Universitat Graz, Graz, Austria;

    Universitatsklinikum Giessen und Marburg GmbH, Klinik fur Orthopadie und Rheumatologie, Marburg, Germany;

    Klinik fur Orthopadie und Sportorthopadie, Klinikum r.d. Isar,Technische Universitat Miinchen, Muskuloskelettale Forschung,Ismaninger Str. 22, 81675 Munich, Germany;

    Klinik fur Orthopadie und Sportorthopadie, Klinikum r.d. Isar,Technische Universitat Miinchen, Muskuloskelettale Forschung,Ismaninger Str. 22, 81675 Munich, Germany;

    Klinik fur Orthopadie und Sportorthopadie, Klinikum r.d. Isar,Technische Universitat Miinchen, Muskuloskelettale Forschung,Ismaninger Str. 22, 81675 Munich, Germany;

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