Mol Pharm. 2021 Feb 1;18(2):522-538. doi: 10.1021/acs.molpharmaceut.0c00287. Epub 2020 Jun 25.
Acute brain injuries such as traumatic brain injury and stroke affect 85 million people a year worldwide, and many survivors suffer from long-term physical, cognitive, or psychosocial impairments. There are few FDA-approved therapies that are effective at preventing, halting, or ameliorating the state of disease in the brain after acute brain injury. To address this unmet need, one potential strategy is to leverage the unique physical and biological properties of nanomaterials. Decades of cancer nanomedicine research can serve as a blueprint for innovation in brain injury nanomedicines, both to emulate the successes and also to avoid potential pitfalls. In this review, we discuss how shared disease physiology between cancer and acute brain injuries can inform the design of novel nanomedicines for acute brain injuries. These disease hallmarks include dysregulated vasculature, an altered microenvironment, and changes in the immune system. We discuss several nanomaterial strategies that can be engineered to exploit these disease hallmarks, for example, passive accumulation, active targeting of disease-associated signals, bioresponsive designs that are "smart", and immune interactions.
急性脑损伤,如创伤性脑损伤和中风,每年在全球影响 8500 万人,许多幸存者长期存在身体、认知或社会心理障碍。目前仅有少数经 FDA 批准的疗法可有效预防、阻止或改善急性脑损伤后大脑的疾病状态。为了解决这一未满足的需求,一种潜在的策略是利用纳米材料的独特物理和生物学特性。几十年来的癌症纳米医学研究可以为脑损伤纳米医学的创新提供蓝图,既要借鉴成功经验,也要避免潜在的陷阱。在这篇综述中,我们讨论了癌症和急性脑损伤之间共同的疾病生理学如何为急性脑损伤的新型纳米药物设计提供信息。这些疾病特征包括血管失调、微环境改变和免疫系统变化。我们讨论了几种可以被设计用来利用这些疾病特征的纳米材料策略,例如被动积累、针对疾病相关信号的主动靶向、具有“智能”的生物响应设计以及免疫相互作用。