Lalatsa Aikaterini, Schatzlein Andreas G, Uchegbu Ijeoma F
Department of Pharmaceutics, School of Pharmacy and Biomedical Sciences, University of Portsmouth , St Michael's Building 5.05, White Swan Road, Portsmouth, PO1 2DT, U.K.
Mol Pharm. 2014 Apr 7;11(4):1081-93. doi: 10.1021/mp400680d. Epub 2014 Mar 21.
Neurological diseases such as neurodegeneration, pain, psychiatric disorders, stroke, and brain cancers would greatly benefit from the use of highly potent and specific peptide pharmaceuticals. Peptides are especially desirable because of their low inherent toxicity. The presence of the blood brain barrier (BBB), their short duration of action, and their need for parenteral administration limits their clinical use. However, over the past decade there have been significant advances in delivering peptides to the central nervous system. Angiopep peptides developed by Angiochem (Montreal, Canada), transferrin antibodies developed by ArmaGen (Santa Monica, USA), and cell penetrating peptides have all shown promise in delivering therapeutic peptides across the BBB after intravenous administration. Noninvasive methods of delivering peptides to the brain include the use of chitosan amphiphile nanoparticles for oral delivery and nose to brain strategies. The uptake of the chitosan amphiphile nanoparticles by the gastrointestinal epithelium is important for oral peptide delivery. Finally protecting peptides from plasma degradation is integral to the success of most of these peptide delivery strategies.
神经退行性疾病、疼痛、精神疾病、中风和脑癌等神经系统疾病将极大地受益于高效且特异性的肽类药物。肽类因其固有的低毒性而特别受青睐。血脑屏障(BBB)的存在、其作用持续时间短以及需要肠胃外给药限制了它们的临床应用。然而,在过去十年中,将肽类递送至中枢神经系统方面取得了重大进展。由加拿大蒙特利尔的Angiochem公司研发的Angiopep肽、美国圣莫尼卡的ArmaGen公司研发的转铁蛋白抗体以及细胞穿透肽在静脉给药后将治疗性肽类穿过血脑屏障方面均显示出前景。将肽类递送至大脑的非侵入性方法包括使用壳聚糖两亲性纳米颗粒进行口服给药以及鼻至脑策略。壳聚糖两亲性纳米颗粒被胃肠道上皮细胞摄取对于口服肽类给药很重要。最后,保护肽类免受血浆降解是大多数这些肽类递送策略成功的关键。