Schipper N G, Romeijn S G, Verhoef J C, Merkus F W
Center for Bio-Pharmaceutical Sciences, Leiden University, The Netherlands.
Pharm Res. 1993 May;10(5):682-6. doi: 10.1023/a:1018999414088.
The nasal absorption of insulin using dimethyl-beta-cyclodextrin (DM beta CD) as an absorption enhancer in rabbits was studied. The nasal administration of insulin/DM beta CD liquid formulations did not result in significant changes in serum insulin and blood glucose concentrations. In contrast, previous experiments in rats showed that the addition of DM beta CD to the liquid nasal formulation resulted in an almost-complete insulin absorption, with a concomitant strong hypoglycaemic response. Apparently, the effect of the cyclodextrin derivative on insulin absorption differs between animal species following nasal delivery of insulin/DM beta CD solutions. On the other hand, nasal administration of the lyophilized insulin/DM beta CD powder dosage form in rabbits resulted in increased serum insulin concentrations, and a maximum decrease in blood glucose of about 50%. The absolute bioavailability of the nasally administered insulin/DM beta CD powder was 13 +/- 4%, compared to 1 +/- 1% for both an insulin/DM beta CD liquid and an insulin/lactose powder formulation. It is concluded that insulin powder formulations with DM beta CD as an absorption enhancer are much more effective than liquid formulations.
研究了以二甲基-β-环糊精(DMβCD)作为吸收促进剂时胰岛素在兔鼻腔中的吸收情况。胰岛素/DMβCD液体制剂经鼻腔给药后,血清胰岛素和血糖浓度未出现显著变化。相比之下,先前在大鼠身上进行的实验表明,在液体鼻腔制剂中添加DMβCD会导致胰岛素几乎完全吸收,并伴有强烈的降血糖反应。显然,在经鼻腔递送胰岛素/DMβCD溶液后,环糊精衍生物对胰岛素吸收的影响在不同动物物种之间存在差异。另一方面,兔经鼻腔给予冻干的胰岛素/DMβCD粉末剂型后,血清胰岛素浓度升高,血糖最多降低约50%。经鼻腔给药的胰岛素/DMβCD粉末的绝对生物利用度为13±4%,而胰岛素/DMβCD液体和胰岛素/乳糖粉末制剂的绝对生物利用度均为1±1%。得出的结论是,以DMβCD作为吸收促进剂的胰岛素粉末制剂比液体制剂有效得多。