Kumar Amit, Lahiri Sitanshu S, Singh Harpal
Centre for Biomedical Engineering, Indian Institute of Technology, Delhi 110016, India.
Int J Pharm. 2006 Oct 12;323(1-2):117-24. doi: 10.1016/j.ijpharm.2006.05.050. Epub 2006 Jun 2.
An oral insulin delivery system based on copolymers of poly(ethylene glycol) dimethacrylate and methacrylic acid was developed and its functional activity was tested in non-obese diabetic rats. Poly(ethylene glycol) dimethacrylates (PEGDMA) were synthesized by esterification reaction of different molecular weight poly(ethylene glycol) with methacrylic acid (MAA) in presence of acid catalyst. PEG dimethacrylates of molecular weight ranging from 400 to 4000 and methacrylic acid were further copolymerized by suspension polymerization to obtain pH sensitive hydrogel microparticles. The diameter of poly(PEGDMA:MAA) microparticles increased with increasing the molecular weight of the poly(ethylene glycol) dimethacrylate used for respective microparticle synthesis. Insulin was loaded into the hydrogel microparticles by partitioning from concentrated insulin solution. In vitro release studies of insulin loaded microparticles were performed by simulating the condition of gastrointestinal tract, which showed the minimal insulin leakage (18-25%) at acidic pH (2.5) and significantly higher release at basic pH (7.4). Animal studies were carried out to investigate the abilities of the insulin loaded hydrogel microparticles to influence the blood glucose levels of the diabetic rats. In studies with diabetic rats, the blood glucose level reduced for animals that received the insulin loaded hydrogel microparticles and the effect lasted for 8-10h. It was also observed, two capsules per day of poly(PEGDMA4000:MAA) hydrogel microparticles containing 80 I.U./kg of insulin dose were sufficient to control the blood glucose level of fed diabetic rats between 100 and 300 mg/dl.
基于聚乙二醇二甲基丙烯酸酯和甲基丙烯酸共聚物的口服胰岛素递送系统被研发出来,并在非肥胖糖尿病大鼠中测试了其功能活性。聚乙二醇二甲基丙烯酸酯(PEGDMA)通过不同分子量的聚乙二醇与甲基丙烯酸(MAA)在酸催化剂存在下的酯化反应合成。分子量范围为400至4000的聚乙二醇二甲基丙烯酸酯和甲基丙烯酸通过悬浮聚合进一步共聚以获得pH敏感水凝胶微粒。聚(PEGDMA:MAA)微粒的直径随着用于各自微粒合成的聚乙二醇二甲基丙烯酸酯分子量增加而增大。胰岛素通过从浓缩胰岛素溶液中分配而被载入水凝胶微粒中。通过模拟胃肠道条件对载胰岛素微粒进行体外释放研究,结果显示在酸性pH(2.5)下胰岛素泄漏极少(18 - 25%),而在碱性pH(7.4)下释放显著更高。进行动物研究以考察载胰岛素水凝胶微粒影响糖尿病大鼠血糖水平的能力。在糖尿病大鼠研究中,接受载胰岛素水凝胶微粒的动物血糖水平降低,且效果持续8至10小时。还观察到,每天两粒含有80国际单位/千克胰岛素剂量的聚(PEGDMA4000:MAA)水凝胶微粒足以将喂食的糖尿病大鼠血糖水平控制在100至300毫克/分升之间。