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胰岛素粉末制剂的鼻腔生物利用度:渗透促进剂与蛋白质比例的影响。

Intranasal bioavailability of insulin powder formulations: effect of permeation enhancer-to-protein ratio.

作者信息

Lee W A, Narog B A, Patapoff T W, Wang Y J

机构信息

California Biotechnology Inc., Mountain View 94043.

出版信息

J Pharm Sci. 1991 Aug;80(8):725-9. doi: 10.1002/jps.2600800803.

Abstract

The intranasal administration of powder formulations containing insulin and the permeation enhancer sodium tauro-24,25-dihydrofusidate (STDHF) were investigated in the sheep model. Both the hypoglycemic response and the serum insulin levels increased as the mole ratio of STDHF to insulin was increased from 0 to 16.8. In vitro dissolution rates of the powders and the rapid tmax (approximately 5 min) observed after intranasal administration suggest that the absorption of insulin is not dissolution limited. The bioavailabilities (F) of the powder formulations ranged from 2.9 to 37.8%. In comparison, the F values for a solution formulation with a STDHF:insulin ratio of 8.4 administered as either drops or spray were 15.7 and 37.4%, respectively. The permeation enhancer STDHF increases mucosal permeability and reduces the average molecular weight of the insulin species.

摘要

在绵羊模型中研究了含胰岛素和渗透促进剂牛磺-24,25-二氢fusidate钠(STDHF)的粉末制剂的鼻内给药。随着STDHF与胰岛素的摩尔比从0增加到16.8,降糖反应和血清胰岛素水平均升高。粉末的体外溶解速率以及鼻内给药后观察到的快速达峰时间(约5分钟)表明胰岛素的吸收不受溶解限制。粉末制剂的生物利用度(F)范围为2.9%至37.8%。相比之下,STDHF与胰岛素比例为8.4的溶液制剂以滴剂或喷雾剂给药时的F值分别为15.7%和37.4%。渗透促进剂STDHF可增加粘膜通透性并降低胰岛素种类的平均分子量。

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