链脲霉素糖尿病大鼠口腔给药人胰岛素。

A al-Achi, R Greenwood
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引用次数: 0

摘要

本研究探讨了口腔给药途径在人胰岛素大鼠体内的应用。以链脲佐菌素诱导的糖尿病雌性Wistar大鼠为研究对象。口腔给予游离胰岛素(即胰岛素溶液)或与载体(即红细胞鬼(EG)和脂质体囊泡(LEV))相关的胰岛素(100 U)。在5小时的时间内从尾部采集血液样本。这些结果表明,胰岛素吸收发生了,正如血糖浓度下降所证明的那样,在游离胰岛素和红细胞-鬼胰岛素(EG-INS)的情况下。游离胰岛素组和EG-INS组的血糖下降幅度最大,分别为39.53 mg/dl(2小时)和26.23 mg/dl(4小时)。LEV或脂质体-囊泡-胰岛素(LEV- ins)治疗后血糖水平无显著差异。本研究证明,当人胰岛素以简单溶液或EG-INS悬浮液的形式注入口腔时,人胰岛素能够被吸收。这种吸收产生了明确的药理作用,但没有显著的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Buccal administration of human insulin in streptozocin-diabetic rats.

This study investigates the use of the buccal route of administration in the delivery of human insulin in rats. Streptozocin-induced diabetic female Wistar rats were used in this study. Insulin (100 U) either free (i.e., insulin solution) or associated with a carrier, namely erythrocyte-ghosts (EG) and liposomes-vesicles (LEV), was administered buccally. Blood samples were collected from the tail over a period of 5 hr. These results indicate that insulin absorption occurred, as evidenced from a decrease in blood glucose concentration, and in the case of free insulin and erythrocyte-ghosts-insulin (EG-INS). The magnitude of the blood glucose level decline was at its maximum of 39.53 mg/dl (at 2 hr) and 26.23 mg/dl (at 4 hr) for free insulin and EG-INS, respectively. No significant difference in the blood glucose level profile was observed after either LEV or liposomes-vesicles-insulin (LEV-INS). This study demonstrates the ability of human insulin to be absorbed from the mouth cavity when it is instilled in the form of a simple solution or EG-INS suspension. This absorption resulted in a definite pharmacological effect but not a significant therapeutic effect.

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