School of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Shenyang, PR China.
Department of stomatology, The Fifth Medical Center of PLA General Hospital, Beijing, PR China.
Drug Deliv. 2020 Dec;27(1):502-518. doi: 10.1080/10717544.2020.1745328.
Reactive oxygen species (ROS)-induced neuronal mitochondrial dysfunction is a key pathologic factor in sporadic Alzheimer's disease (AD). Neuronal mitochondria have been proposed to be a promising therapeutic target for AD, especially for the failures of phase III clinical trials on conventional amyloid-β (Aβ) targeted therapy. However, the efficient intravenous delivery of therapeutic agents to neuronal mitochondria in the brain remains a major challenge due to the complicated physiological environment. Recently, biomaterials-based nanomedicine has been widely investigated for the treatment of AD. Herein, we devised a strategy for functional antioxidant delivery to neuronal mitochondria by loading antioxidants into red blood cell (RBC) membrane-coated nanostructured lipid carriers (NLC) bearing rabies virus glycoprotein (RVG29) and triphenylphosphine cation (TPP) molecules attached to the RBC membrane surface (RVG/TPP NPs@RBCm). With the advantage of suitable physicochemical properties of NLC and unique biological functions of the RBC membrane, RVG/TPP NPs@RBCm are stabilized and enabled sustained drug release, providing improved biocompatibility and long-term circulation. Under the synergistic effects of RVG29 and TPP, RVG/TPP NPs@RBCm can not only penetrate the blood-brain barrier (BBB) but also target neuron cells and further localize in the mitochondria. After encapsulating Resveratrol (RSV) as the model antioxidant, the data demonstrated that RVG/TPP-RSV NPs@RBCm can relieve AD symptoms by mitigating Aβ-related mitochondrial oxidative stress both and . The memory impairment in APP/PS1 mice is significantly improved following the systemic administration of RVG/TPP-RSV NPs@RBCm. In conclusion, intravenous neuronal mitochondria-targeted dual-modified novel biomimetic nanosystems are a promising therapeutic candidate for ROS-induced mitochondrial dysfunction in AD.
活性氧(ROS)诱导的神经元线粒体功能障碍是散发性阿尔茨海默病(AD)的关键病理因素。神经元线粒体被认为是 AD 的一个有前途的治疗靶点,特别是对于传统淀粉样蛋白-β(Aβ)靶向治疗的 III 期临床试验失败。然而,由于复杂的生理环境,有效的将治疗剂递送至大脑中的神经元线粒体仍然是一个主要挑战。最近,基于生物材料的纳米医学已被广泛用于 AD 的治疗。在此,我们设计了一种通过将抗氧化剂装载到带有狂犬病病毒糖蛋白(RVG29)和三苯基膦阳离子(TPP)分子的红细胞(RBC)膜包裹的纳米结构脂质载体(NLC)中,从而将功能性抗氧化剂递送至神经元线粒体的策略,这些分子附着在 RBC 膜表面(RVG/TPP NPs@RBCm)。利用 NLC 合适的物理化学性质和 RBC 膜的独特生物学功能,RVG/TPP NPs@RBCm 得到稳定,并能够持续释放药物,提高生物相容性和延长循环时间。在 RVG29 和 TPP 的协同作用下,RVG/TPP NPs@RBCm 不仅可以穿透血脑屏障(BBB),还可以靶向神经元细胞并进一步定位于线粒体。包封白藜芦醇(RSV)作为模型抗氧化剂后,数据表明 RVG/TPP-RSV NPs@RBCm 可以通过减轻 Aβ 相关的线粒体氧化应激来缓解 AD 症状。在 APP/PS1 小鼠中,RVG/TPP-RSV NPs@RBCm 的全身给药显著改善了记忆障碍。综上所述,静脉内神经元线粒体靶向双重修饰新型仿生纳米系统是治疗 AD 中 ROS 诱导的线粒体功能障碍的一种很有前途的治疗候选物。