Ubaidulla Udhumansha, Khar Roop Kishan, Ahmed Farhan Jalees, Panda Amulya Kumar
Department of Pharmaceutics, Faculty of Pharmacy, Hamdard University, New Delhi, India.
J Pharm Pharmacol. 2007 Oct;59(10):1345-51. doi: 10.1211/jpp.59.10.0003.
Novel chitosan phthalate microspheres containing insulin were prepared by emulsion cross-linking technique. The feasibility of these microspheres as oral insulin delivery carriers was evaluated. The pH-responsive release behaviour of insulin from microspheres was analysed. The ability of chitosan phthalate-insulin microspheres to enhance intestinal absorption and improve the relative pharmacological availability of insulin was investigated by monitoring the plasma glucose and insulin level of streptozotocin-induced diabetic rats after oral administration of microspheres at insulin dose of 20 IU kg(-1). In simulated gastric fluid (pH 2.0), insulin release from the microspheres was very slow. However, as the pH of the medium was changed to simulated intestinal fluid (pH 7.4), a rapid release of insulin occurred. The relative pharmacological efficacy for chitosan phthalate microspheres (18.66 +/- 3.84%) was almost four-fold higher than the efficacy of the chitosan phthalate-insulin solution administration (4.08 +/- 1.52%). Chitosan phthalate microspheres sustained the plasma glucose at pre-diabetic level for at least 16 h. These findings suggest that the microsphere is a promising carrier as oral insulin delivery system.
采用乳化交联技术制备了含胰岛素的新型邻苯二甲酸壳聚糖微球。评估了这些微球作为口服胰岛素递送载体的可行性。分析了胰岛素从微球中的pH响应释放行为。通过监测链脲佐菌素诱导的糖尿病大鼠在以20 IU kg(-1)的胰岛素剂量口服微球后的血糖和胰岛素水平,研究了邻苯二甲酸壳聚糖-胰岛素微球增强肠道吸收和提高胰岛素相对药理利用率的能力。在模拟胃液(pH 2.0)中,微球中胰岛素的释放非常缓慢。然而,随着介质pH值变为模拟肠液(pH 7.4),胰岛素迅速释放。邻苯二甲酸壳聚糖微球的相对药理疗效(18.66 +/- 3.84%)几乎是邻苯二甲酸壳聚糖-胰岛素溶液给药疗效(4.08 +/- 1.52%)的四倍。邻苯二甲酸壳聚糖微球可使血糖维持在糖尿病前期水平至少16小时。这些发现表明,该微球作为口服胰岛素递送系统是一种有前景的载体。