Cavitation-Control Technology Inc, Farmington, CT, USA. D'Arrigo is now with Cav-Con, Inc, Bellevue, WA, USA.
Am J Alzheimers Dis Other Demen. 2020 Jan-Dec;35:1533317520976761. doi: 10.1177/1533317520976761.
By incorporating appropriate drug(s) into lipid (biobased) nanocarriers, one obtains a combination therapeutic for dementia treatment that targets certain cell-surface scavenger receptors (mainly class B type I, or "SR-BI") and thereby crosses the blood-brain barrier. The cardiovascular risk factors for dementia trigger widespread inflammation -- which lead to neurodegeneration, gradual cognitive/memory decline, and eventually (late-onset) dementia. Accordingly, one useful strategy to delay dementia could be based upon nanotargeting drug(s), using lipid nanocarriers, toward a major receptor class responsible for inflammation-associated (cytokine-mediated) cell signaling events. At the same time, the immune response and excessive inflammation, commonly observed in the very recent human coronavirus (COVID-19) pandemic, may accelerate the progression of brain inflammatory neurodegeneration-which increases the probability of post-infection memory impairment and accelerating progression of Alzheimer's disease. Hence, the proposed multitasking combination therapeutic, using a (biobased) lipid nanocarrier, may also display greater effectiveness at different stages of dementia.
通过将适当的药物(物)纳入脂质(生物基)纳米载体中,获得针对痴呆治疗的联合治疗方法,该方法针对某些细胞表面清道夫受体(主要是 B 类 I 型或“SR-BI”),从而穿过血脑屏障。痴呆症的心血管危险因素会引发广泛的炎症——导致神经退行性变、逐渐的认知/记忆下降,最终(迟发性)痴呆。因此,一种有用的延迟痴呆策略可能基于纳米靶向药物(物),使用脂质纳米载体,针对负责炎症相关(细胞因子介导)细胞信号事件的主要受体类。同时,在最近的人类冠状病毒(COVID-19)大流行中常见的免疫反应和过度炎症,可能会加速大脑炎症性神经退行性变的进展——增加感染后记忆障碍的可能性,并加速阿尔茨海默病的进展。因此,拟议的使用(生物基)脂质纳米载体的多任务联合治疗方法,在痴呆症的不同阶段可能也具有更大的效果。