Katayama Ken, Kato Yoshinori, Onishi Hiraku, Nagai Tsuneji, Machida Yoshiharu
Department of Drug Delivery Research, Hoshi University, Shinagawa-ku, Tokyo, Japan.
Drug Dev Ind Pharm. 2003 Aug;29(7):725-31. doi: 10.1081/ddc-120021771.
The biopharmaceutical characteristics of double liposomes (DLs) containing insulin were examined, and the usefulness of DLs in combination with aprotinin is discussed. Encapsulation of insulin was influenced by lipid composition, and the highest efficiency was observed with positively charged liposomes. Insulin encapsulated in liposomes, especially in DLs, was protected from enzymatic proteolysis. A portion of insulin molecules was adsorbed on the surface of the membrane when liposomes were prepared using a lipid with a positive charge and was degraded by enzymes. Remarkable hypoglycemic effects were observed after intragastric administration of DLs containing insulin at a dose of 20 IU/kg to normal male Wistar rats. The highest mean relative efficacy to administration was obtained with insulin-loading DLs containing aprotinin as a protease inhibitor. These results suggest that DLs are applicable as an oral dosage form for peptide drugs such as insulin etc., especially in combination with protease inhibitors.
对含有胰岛素的双脂质体(DLs)的生物制药特性进行了研究,并探讨了DLs与抑肽酶联合使用的有效性。胰岛素的包封受脂质组成的影响,在带正电荷的脂质体中观察到最高的包封效率。包封在脂质体中的胰岛素,尤其是在DLs中,可免受酶促蛋白水解的影响。当使用带正电荷的脂质制备脂质体时,一部分胰岛素分子吸附在膜表面并被酶降解。给正常雄性Wistar大鼠胃内给予剂量为20 IU/kg的含胰岛素的DLs后,观察到显著的降血糖作用。以含有抑肽酶作为蛋白酶抑制剂的载胰岛素DLs获得了最高的平均给药相对疗效。这些结果表明,DLs可作为胰岛素等肽类药物的口服剂型,特别是与蛋白酶抑制剂联合使用时。