Gao Xiaoling, Wu Bingxian, Zhang Qizhi, Chen Jun, Zhu Jianhua, Zhang Weiwei, Rong Zhengxin, Chen Hongzhuan, Jiang Xinguo
Department of Pharmaceutics, School of Pharmacy, Fudan University, Shanghai, PR China.
J Control Release. 2007 Aug 28;121(3):156-67. doi: 10.1016/j.jconrel.2007.05.026. Epub 2007 Jun 2.
The development of biotech drugs such as peptides and proteins that act in the central nervous system has been significantly impeded by the difficulty of delivering them across the blood-brain barrier. The surface engineering of nanoparticles with lectins opened a novel pathway to the absorption of drugs loaded by biodegradable poly (ethylene glycol)-poly (lactic acid) nanoparticles in the brain following intranasal administration. In the present study, vasoactive intestinal peptide, a neuroprotective peptide, was efficiently incorporated into the poly (ethylene glycol)-poly (lactic acid) nanoparticles modified with wheat germ agglutinin and the biodistribution, brain uptake and neuroprotective effect of the formulation were assessed. The area under the concentration-time curve of intact 125I-vasoactive intestinal peptide in brain of mice following the intranasal administration of 125I-vasoactive intestinal peptide carried by nanoparticles and wheat germ agglutinin-conjugated ones was significantly enlarged by 3.5 approximately 4.7 folds and 5.6 approximately 7.7 folds, respectively, compared with that after intranasal application of 125I-vasoactive intestinal peptide solution. The same improvements in spatial memory in ethylcholine aziridium-treated rats were observed following intranasal administration of 25 microg/kg and 12.5 microg/kg of vasoactive intestinal peptide loaded by unmodified nanoparticles and wheat germ agglutinin-modified nanoparticles, respectively. Distribution profiles of wheat germ agglutinin-conjugated nanoparticles in the nasal cavity presented their higher affinity to the olfactory mucosa than to the respiratory one. Inhibition experiment with specific sugars suggested that the interaction between the nasal mucosa and the wheat germ agglutinin-functionalized nanoparticles were due to the immobilization of carbohydrate-binding pockets on the surface of the nanoparticles. The results clearly indicated wheat germ agglutinin-modified nanoparticles might serve as promising carriers especially for biotech drugs such as peptides and proteins.
作用于中枢神经系统的肽和蛋白质等生物技术药物的研发,因难以透过血脑屏障而受到显著阻碍。用凝集素对纳米颗粒进行表面工程处理,为经鼻给药后可生物降解的聚(乙二醇)-聚(乳酸)纳米颗粒所载药物在脑内的吸收开辟了一条新途径。在本研究中,将具有神经保护作用的血管活性肠肽高效载入经小麦胚凝集素修饰的聚(乙二醇)-聚(乳酸)纳米颗粒中,并评估了该制剂的生物分布、脑摄取及神经保护作用。与经鼻给予125I-血管活性肠肽溶液后相比,经纳米颗粒和小麦胚凝集素偶联物携带的125I-血管活性肠肽经鼻给药后,小鼠脑内完整的125I-血管活性肠肽浓度-时间曲线下面积分别显著增大了约3.5至4.7倍和5.6至7.7倍。分别经鼻给予25μg/kg和12.5μg/kg未修饰纳米颗粒和小麦胚凝集素修饰纳米颗粒所载血管活性肠肽后,在乙胆碱氮丙啶处理的大鼠中观察到了空间记忆方面同样的改善。小麦胚凝集素偶联纳米颗粒在鼻腔中的分布情况表明,它们对嗅黏膜的亲和力高于对呼吸黏膜的亲和力。用特定糖类进行的抑制实验表明,鼻黏膜与小麦胚凝集素功能化纳米颗粒之间的相互作用是由于纳米颗粒表面碳水化合物结合位点的固定化。结果清楚地表明,小麦胚凝集素修饰的纳米颗粒可能是很有前景的载体,尤其适用于肽和蛋白质等生物技术药物。