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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.

机译:从可塑和可吸收的明胶海绵中释放万古霉素和替考拉宁:体外研究一种新的糖肽抗生素递送系统。

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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 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. 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.
机译:背景:这项研究的目的是评估从可吸收的明胶甘油海绵中持续释放万古霉素和替考拉宁的功效,以便为局部抗感染治疗建立新的递送系统。材料与方法:将60个含有10%或20%明胶(w / v)的增塑甘油明胶海绵在万古霉素或替考拉宁溶液中于20摄氏度孵育1或24小时。通过使用荧光偏振免疫测定法测定血浆中洗脱的万古霉素和替考拉宁水平,研究了海绵在1周内的体外释放特性。通过线性回归假设一级动力学,计算每组抗生素释放的速率常数和半衰期。结果:与温育1 h相对,预浸泡24 h与所有组中抗生素释放总量的显着增加有关,除了将10%海绵预先浸泡在替考拉宁中。孵育24小时后,仅在含替考拉宁的海绵中,海绵的明胶含量从10%增至20%会显着增加抗生素负荷的总释放量。与替考拉宁相比,在所有相应的研究组中,万古霉素的释放时间更长,而替考拉宁允许5天后逐渐释放。相比于1小时孵育,两种类型的含万古霉素海绵的半衰期(h +/- SEM)显着延长了24小时孵育(29.1 +/- 5.9与5.9 +/- 1.0; p <0.001、30.0) +/- 2.1与11.1 +/- 1.9; p <0.001)。但是,海绵的明胶含量不加倍或温育时间延长都与替考拉宁的明显延长无关。结论:本研究表明,与用替考拉宁预处理的海绵相比,万古霉素浸渍的甘油明胶海绵具有更好的扩散控制释放。对于将万古霉素应用于感染的伤口进行局部抗感染治疗,增塑的甘油明胶海绵可能是一种有前途的载体。

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