Yu Jiaojiao, Wang Qiongyan, Liu Haofan, Shan Xiaosong, Pang Ziyan, Song Pengjin, Niu Feng, Hu Liandong
School of Pharmaceutical Sciences, Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Hebei University, No. 180, Wusi East Road, Baoding, 071000, Hebei, China.
Affiliated Hospital of Hebei University, Baoding, 071000, China.
Eur J Drug Metab Pharmacokinet. 2020 Feb;45(1):113-121. doi: 10.1007/s13318-019-00588-2.
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.
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.
The microspheres had a good spherical structure with a particle size of 5 ~ 10 μm. 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.
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.
糖尿病作为一种葡萄糖调节疾病,已成为全球最常见的医学问题之一。目前,糖尿病替代疗法在很大程度上已广泛关注治疗效果的改善。本研究旨在表征和评估含胰岛素的新型葡萄糖响应性可注射微球的表面形态及其体外释放和体内疗效。
在本研究中,通过改进的水包油包水(W/O/W)双乳液制备方法开发了一种作为新兴智能药物递送系统用于胰岛素控释的葡萄糖响应性微球。在此,合成了甲氧基聚乙二醇-腙-4-甲氧基聚乙二醇苯甲酸酯(mPEG-Hz-mPEG4AB)作为pH响应载体。
微球具有良好的球形结构,粒径为5~10μm。在体外研究中,在高糖环境下约61%的胰岛素在15小时内释放,但在正常血糖范围内几乎不释放。大鼠皮下注射胰岛素微球后,血糖水平在2小时内迅速下降,并可在正常范围内维持2天。组织病理学评估表明微球几乎无刺激性。
pH响应性mPEG-Hz-mPEG4AB可作为一种有效的胰岛素微球载体,优化后的微球具有良好的形态和持续的降血糖作用。