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Formulation of Chitosan Nanoparticles Loaded with Metronidazole for the Treatment of Infectious Diseases

机译:甲硝唑负载壳聚糖纳米粒的治疗感染性疾病

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Conventional chemotherapy of intracellular infections often fails due to the low uptake of commonly used antibiotics or to their reduced activity at the acidic pH of lysosomes. With the aim of improving the therapeutic action of metronidazole against intracellular infections along with an overcome of their important drawbacks, we investigated its incorporation into a drug delivery nanosystem based on the biodegradable polymer chitosan. The formulation of this polymeric colloid assured a high electric surface charge and a great hydrophobicity, which are known to be two important characteristics determining an intense and non-specific recognition by the mononuclear phagocyte system (i.e., rapid uptake by infected phagocytes). Two metronidazole loading procedures were investigated: i) drug surface deposition or adsorption method onto already formed nanoparticles; and ii) drug absorption or entrapment into the polymeric matrix: incorporation of metronidazole prior to the coacervation process that leads to the formation of chitosan nanoparticles. Such polymeric colloid hold very significant characteristics (high drug loading and little burst release, hydrophobicity and high surface charge), suggesting its potential application for an efficient metronidazole delivery to intracellular infections.
机译:传统的细胞内感染化学疗法通常由于常用抗生素的摄取量低或在溶酶体的酸性pH下活性降低而失败。为了改善甲硝唑对细胞内感染的治疗作用并克服其重要缺点,我们研究了将甲硝唑掺入基于可生物降解的聚合物壳聚糖的药物递送纳米系统中的方法。该聚合物胶体的配方确保了高的表面电荷和很大的疏水性,这是确定单核吞噬细胞系统强烈和非特异性识别(即被感染的吞噬细胞快速吸收)的两个重要特征。研究了两种甲硝唑加载程序:i)在已经形成的纳米颗粒上进行药物表面沉积或吸附; ii)药物吸收或截留到聚合物基质中:在凝聚过程之前并入甲硝唑,导致形成壳聚糖纳米颗粒。这种聚合物胶体具有非常重要的特性(高载药量和极少的突发释放,疏水性和高表面电荷),表明其潜在的应用将甲硝唑有效地递送至细胞内感染。

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