首页> 外文期刊>European journal of drug metabolism and pharmacokinetics >Glucose-Responsive Microspheres as a Smart Drug Delivery System for Controlled Release of Insulin
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Glucose-Responsive Microspheres as a Smart Drug Delivery System for Controlled Release of Insulin

机译:葡萄糖响应的微球作为胰岛素控制释放的智能药物递送系统

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Background and Objectives Diabetes mellitus, a disease of glucose regulation, has become one of the most common medical problems in the world. At present, alternative therapy for diabetes has, to a large extent, been widely concerned with the improvement of treatment efficacy. The aims of this study were to characterize and evaluate the surface morphology of the novel glucose-responsive injectable microspheres containing insulin, along with their in vitro release and in vivo efficacy. Methods In this study, glucose-responsive microspheres as an emerging smart drug delivery system for controlled release of insulin were developed by an improved water-in-oil-in-water (W/O/W) double emulsion preparation method. Here, methoxypolyethylene glycol-hydrazone-4-methoxypolyethylene glycol benzoate (mPEG-Hz-mPEG4AB) was synthesized as a pH-responsive carrier. Results The microspheres had a good spherical structure with a particle size of 5 similar to 10 mu m. Approximately 61% of insulin was released in 15 h under a high glucose environment but was barely released within the normal glucose range in in vitro studies. After a subcutaneous injection of insulin microspheres in rats, blood glucose levels rapidly decreased within 2 h and could be maintained for 2 days in the normal range. Histopathological evaluation indicated that the microspheres were almost non-irritating. Conclusions The pH-responsive mPEG-Hz-mPEG4AB could be used as an efficient insulin microsphere carrier, and the optimized microspheres had good morphology and sustained hypoglycemic effect.
机译:背景和目标糖尿病,一种葡萄糖调节疾病,已成为世界上最常见的医学问题之一。目前,糖尿病的替代治疗在很大程度上被广泛关注治疗效能的提高。本研究的目的是表征和评估含有胰岛素的新型葡萄糖响应可注射微球的表面形态以及其体外释放和体内疗效。本研究中的方法,通过改进的水包内水(W / O / W)双乳液制备方法,开发了该研究的葡萄糖响应性微球作为胰岛素的受控释放的新出现的智能药物输送系统。这里,将甲氧基聚乙二醇 - 腙-4-甲氧基聚乙二醇苯甲酸酯(MPEG-HZ-MPEG4AB)作为pH响应载体合成。结果微球具有良好的球形结构,其粒径为5〜10μm。大约61%的胰岛素在高葡萄糖环境下在15小时内释放,但在体外研究的正常葡萄糖范围内几乎没有释放。在大鼠中皮下注射胰岛素微球后,血糖水平在2小时内快速降低,可以在正常范围内保持2天。组织病理学评估表明,微球几乎是非刺激性的。结论PH-响应物MPEG-HZ-MPEG4AB可用作有效的胰岛素微球载体,优化的微球具有良好的形态和持续的降血糖作用。

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