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Release of Vancomycin and Teicoplanin from a Plasticized and Resorbable Gelatin Sponge: in Vitro Investigation of a New Antibiotic Delivery System with Glycopeptides
Authors:O Drognitz  D Thorn  T Krüger  S G Gatermann  H Iven  H-P Bruch  E Muhl
Institution:1. Universit?tsklinikum Freiburg, Klinik und Poliklinik für Chirurgie, Abteilung für Allgemein- und Viszeralchirurgie, Hugstetter Str. 55, 79106, Freiburg i. Brsg., Germany
2. University of Lausanne, Thoracic Surgery Unit, Lausanne, Switzerland
3. University of Bochum, Dept. of Medical Microbiology and Hygiene, Bochum, Germany
4. University Hospital Schleswig-Holstein, Campus Luebeck, Dept. of Experimental and Clinical Pharmacology and Toxicology, Luebeck, Germany
5. University Hospital Schleswig-Holstein, Campus Luebeck, Dept. of Surgery, Luebeck, Germany
Abstract:Abstract Background: The aim of this study was to evaluate the efficacy of sustained release of vancomycin and teicoplanin from a resorbable gelatin glycerol sponge, in order to establish a new delivery system for local anti-infective therapy. Materials and Methods: 60 plasticized glycerol gelatin sponges containing either 10 or 20% gelatin (w/v) were incubated in vancomycin or teicoplanin solution at 20 °C for either 1 or 24 h. In vitro release properties of the sponges were investigated over a period of 1 week by determining the levels of vancomycin and teicoplanin eluted in plasma using fluorescent polarization immunoassay. The rate constant and the half-life for the antibiotic release of each group were calculated by linear regression assuming first order kinetics. Results: Presoaking for 24 h was associated with a significant increase in the total antibiotic release in all groups opposed to 1 h of incubation, except for the 10% sponges presoaked in teicoplanin. Doubling the gelatin content of the sponges from 10 to 20% significantly increased the total release of antibiotic load only in teicoplanin-containing sponges after 24 h incubation. In all corresponding groups investigated, release of vancomycin was more prolonged compared to teicoplanin, which allowed a gradual release beyond 5 days. The half-life (h ± SEM) of both types of vancomycin-containing sponges was significantly prolonged by 24 h incubation in comparison to 1 h incubation (29.1 ± 5.9 vs 5.9 ± 1.0; p < 0.001, 30.0 ± 2.1 vs 11.1 ± 1.9; p < 0.001). However, neither doubling the gelatin content of the sponges nor a prolonged incubation was associated with a significantly prolonged delivery of teicoplanin. Conclusion: This study demonstrated a better diffusion-controlled release of vancomycin-impregnated glycerol gelatin sponges compared to those pretreated with teicoplanin. The plasticized glycerol gelatin sponge may be a promising carrier for the application of vancomycin to infected wounds for local anti-infective therapy.
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