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用于口服给药的载胰岛素邻苯二甲酸壳聚糖微球的研制及体内评价

Development and in-vivo evaluation of insulin-loaded chitosan phthalate microspheres for oral delivery.

作者信息

Ubaidulla Udhumansha, Khar Roop Kishan, Ahmed Farhan Jalees, Panda Amulya Kumar

机构信息

Department of Pharmaceutics, Faculty of Pharmacy, Hamdard University, New Delhi, India.

出版信息

J Pharm Pharmacol. 2007 Oct;59(10):1345-51. doi: 10.1211/jpp.59.10.0003.

Abstract

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.

摘要

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。

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