Department of Biochemistry, the George W. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
J Control Release. 2010 Apr 2;143(1):128-35. doi: 10.1016/j.jconrel.2009.12.018. Epub 2010 Jan 5.
The advantages of oral insulin are well-recognized, yet such formulations are still unavailable. Towards that goal we developed, and evaluated in diabetic ICR mice, two novel insulin microparticles for oral delivery. Although different in structure and shape, both microparticle formulations share: (i) hyaluronan on their surface (ii) fibrillar insulin, loaded at 50-100% efficiency over the insulin range of 1-10mg/ml and (iii) high retention of insulin loads in simulated gastro-intestinal environments. BGL values in diabetic ICR mice were tested over a time span of 8h, following a single oral dose of each formulation, using two protocols: the conventional (12h pre-fasting and 8h fasting); our revised protocol (no pre-fasting, meal at t=4h). In both protocols, initial blood glucose levels (BGL) were 400-600 mg/dL and the novel formulations generated a continuous reduction of BGL. Results in the revised protocol, that mimics human eating habits, were more pronounced, providing stable (over several hours) glucose reductions approaching non-diabetic BGL values. These two fibrillar insulin formulations, and the fibrillar form for therapeutic proteins, merit further studies.
口服胰岛素的优势已得到广泛认可,但此类制剂仍未面世。为此,我们开发了两种新型胰岛素微粒制剂,并在糖尿病 ICR 小鼠中进行了评估,用于口服递送。尽管这两种微粒制剂在结构和形状上有所不同,但它们都具有以下特点:(i)表面有透明质酸;(ii)纤维状胰岛素,在 1-10mg/ml 的胰岛素范围内以 50-100%的效率负载;(iii)在模拟的胃肠环境中,胰岛素负载的保留率很高。在两种方案中,使用两种方案(常规方案:12h 禁食前和 8h 禁食;我们的修订方案:无禁食前,在 t=4h 时进餐),在单次口服每种制剂后,在 8h 的时间跨度内测试糖尿病 ICR 小鼠的 BGL 值。在这两种方案中,初始血糖水平(BGL)为 400-600mg/dL,新型制剂可连续降低 BGL。在模拟人类饮食习惯的修订方案中的结果更为显著,可提供稳定(数小时内)的葡萄糖降低,接近非糖尿病 BGL 值。这两种纤维状胰岛素制剂以及纤维状形式的治疗性蛋白质值得进一步研究。