Drognitz O, Thorn D, Krüger T, Gatermann S G, Iven H, Bruch H-P, Muhl E
Universitätsklinikum Freiburg, Klinik und Poliklinik für Chirurgie, Abteilung für Allgemein- und Viszeralchirurgie, Hugstetter Str. 55, 79106 Freiburg i. Brsg., Germany.
Infection. 2006 Feb;34(1):29-34. doi: 10.1007/s15010-006-1067-1.
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.
60 plasticized glycerol gelatin sponges containing either 10 or 20% gelatin (w/v) were incubated in vancomycin or teicoplanin solution at 20 degrees 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.
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.
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.
本研究旨在评估万古霉素和替考拉宁从可吸收明胶甘油海绵中的持续释放效果,以建立一种新的局部抗感染治疗给药系统。
将60块含10%或20%明胶(w/v)的增塑甘油明胶海绵在20℃下于万古霉素或替考拉宁溶液中孵育1小时或24小时。通过使用荧光偏振免疫分析法测定血浆中洗脱的万古霉素和替考拉宁水平,在1周时间内研究海绵的体外释放特性。假设为一级动力学,通过线性回归计算每组抗生素释放的速率常数和半衰期。
与1小时孵育相比,所有组预浸泡24小时均导致总抗生素释放显著增加,但预浸泡在替考拉宁中的10%海绵除外。将海绵的明胶含量从10%加倍至20%仅在24小时孵育后含替考拉宁的海绵中显著增加了抗生素负载的总释放量。在所有研究的相应组中,与替考拉宁相比,万古霉素的释放更持久,可实现超过5天的逐渐释放。与1小时孵育相比,两种含万古霉素海绵的半衰期(h±SEM)通过24小时孵育均显著延长(29.1±5.9对5.9±1.0;p<0.001,30.0±2.1对11.1±1.9;p<0.001)。然而,海绵明胶含量加倍或延长孵育时间均未导致替考拉宁的给药显著延长。
本研究表明,与用替考拉宁预处理的海绵相比,含万古霉素的甘油明胶海绵具有更好的扩散控制释放效果。增塑甘油明胶海绵可能是将万古霉素应用于感染伤口进行局部抗感染治疗的一种有前景的载体。