Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Department of Inorganic and Organic Chemistry, University of Barcelona, 08028 Barcelona, Spain.
Curr Pharm Des. 2018;24(13):1366-1376. doi: 10.2174/1381612824666171201115126.
The brain is a complex, regulated organ with a highly controlled access mechanism: The Blood-Brain Barrier (BBB). The selectivity of this barrier is a double-edged sword, being both its greatest strength and weakness. This weakness is evident when trying to target therapeutics against diseases within the brain. Diseases such as metastatic brain cancer have extremely poor prognosis due to the poor permeability of many therapeutics across the BBB. Peptides can be designed to target BBB receptors and gain access to the brain by transcytosis. These peptides (known as BBB-shuttles) can carry compounds, usually excluded from the brain, across the BBB. BBB-shuttles are limited by poor loading of therapeutics and degradation of the peptide and cargo. Likewise, nano- submicro- and microparticles can be fine-tuned to limit their degradation and with high loading of therapeutics. However, most nano- and microparticles' core materials completely lack efficient targeting, with a few selected materials able to cross the BBB passively. Combining the selectivity of peptides with the high loading potential of nano-, microparticles offers an exciting strategy to develop novel, targeted therapeutics towards many brain disorders and diseases. Nevertheless, at present the field is diverse, in both scope and nomenclature, often with competing or contradictory names. In this review, we will try to address some of these issues and evaluate the current state of peptide mediated nano,-microparticle transport to the brain, analyzing delivery vehicle type and peptide design, the two key components that must act synergistically for optimal therapeutic impact.
大脑是一个复杂的、受调节的器官,具有高度受控的进入机制:血脑屏障(BBB)。这种屏障的选择性是一把双刃剑,既是其最大的优势,也是其最大的弱点。当试图针对大脑内的疾病靶向治疗时,这种弱点就变得很明显。由于许多治疗药物穿过 BBB 的通透性很差,转移性脑癌等疾病的预后非常差。肽可以被设计为靶向 BBB 受体,并通过胞吞作用进入大脑。这些肽(称为 BBB-穿梭物)可以携带化合物,通常被排除在大脑之外,穿过 BBB。BBB-穿梭物受到治疗药物负载不良和肽和货物降解的限制。同样,纳米亚微米和微米颗粒可以进行微调,以限制其降解并实现高载药量的治疗药物。然而,大多数纳米和微颗粒的核心材料完全缺乏有效的靶向性,只有少数选定的材料能够被动地穿过 BBB。将肽的选择性与纳米、微颗粒的高载药潜力相结合,为开发针对许多脑障碍和疾病的新型靶向治疗提供了令人兴奋的策略。然而,目前该领域在范围和命名方面都存在多样性,通常存在竞争或矛盾的名称。在这篇综述中,我们将尝试解决其中的一些问题,并评估肽介导的纳米、微粒向大脑运输的现状,分析输送载体类型和肽设计,这两个关键组成部分必须协同作用,以达到最佳的治疗效果。