Cui Fuying, Qian Feng, Zhao Ziming, Yin Lichen, Tang Cui, Yin Chunhua
State Key Laboratory of Genetic Engineering, Department of Pharmaceutical Sciences, School of Life Sciences, Fudan University, Shanghai 200433, China.
Biomacromolecules. 2009 May 11;10(5):1253-8. doi: 10.1021/bm900035u.
To improve the efficiency of insulin via oral administration, pH-sensitive carboxylated chitosan grafted poly(methyl methacrylate) nanoparticles (CCGN) were prepared. CCGN were characterized by (1)H NMR, dynamic light scattering, zeta potential, and transmission electron microscopy, and the hypoglycemic effect of insulin loaded CCGN via the oral route was evaluated in normal and diabetic rats. CCGN exhibited a homogeneous morphology and a spherical shape with core-shell structure. They were aggregated in simulated gastric fluid while separated in simulated intestinal fluid. Insulin was mainly located in the shell of the CCGN via hydrogen bonding, electrostatic interaction, and Van der Waals force. Insulin release from the CCGN exhibited a pH-sensitive property in that it had a slow release rate at pH 2.0 and a fast release rate at pH 6.8 and 7.4. The pharmacological bioavailability after oral administration of insulin loaded CCGN at a dose of 25 IU/kg was found to be 9.7%. Besides, CCGN showed desirable tissue and blood compatibility. Therefore, the CCGN would be a promising delivery carrier for protein drugs via the oral route.
为提高胰岛素口服给药的效率,制备了pH敏感的羧化壳聚糖接枝聚甲基丙烯酸甲酯纳米粒(CCGN)。通过核磁共振氢谱(¹H NMR)、动态光散射、ζ电位和透射电子显微镜对CCGN进行了表征,并在正常大鼠和糖尿病大鼠中评估了口服载胰岛素CCGN的降血糖效果。CCGN呈现出均匀的形态和具有核壳结构的球形。它们在模拟胃液中聚集,而在模拟肠液中分离。胰岛素主要通过氢键、静电相互作用和范德华力位于CCGN的壳层中。CCGN释放胰岛素具有pH敏感性,即在pH 2.0时释放速率缓慢,在pH 6.8和7.4时释放速率较快。口服剂量为25 IU/kg的载胰岛素CCGN后的药理生物利用度为9.7%。此外,CCGN表现出良好的组织和血液相容性。因此,CCGN有望成为蛋白质药物口服给药的载体。