The multifunctional nano-immunoliposome design: hypothesis on a therapeutic approach for COVID-19

Zahra Abpeikar, Roohollah Mohseni, M. Safaei
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Abstract

Abstract The article presents a hypothesis on a co-delivery strategy to suppress or reduce infection caused by the COVID-19 virus. Co-delivery was illustrated in many diseases, and results showed that it produced a high therapeutic efficacy against disorders. We proposed an approach to suppress or reduce infection caused by the coronavirus disease 2019 via designing an intelligent nano-liposome loaded with interferon γ, interleukin 4 and small interfering RNA against vimentin. At the surface of this nanostructure, there is a matrix metallopeptidase3 substrate to provide a platform for the enzymatic function of matrix metallopeptidase3 to destroy the extracellular matrix, angiotensin-converting enzyme 2 blocker, and antibody against vimentin for targeting, trans-activator of transcription peptide, and polyethylene glycol. Due to the increasing application of nano-liposomes commercially as a drug-delivery system, it is important to consider this effective approach for the coronavirus disease 2019 treatment. Graphical Abstract
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多功能纳米免疫脂质体设计:对COVID-19治疗方法的假设
摘要本文提出了抑制或减少COVID-19病毒感染的共同递送策略假设。在许多疾病中发现了共递送,结果表明它对疾病有很高的治疗效果。我们提出了一种通过设计一种装载干扰素γ、白细胞介素4和小干扰RNA的智能纳米脂质体来抑制或减少2019冠状病毒病引起的感染的方法。在该纳米结构的表面,存在基质金属肽酶e3底物,为基质金属肽酶e3破坏细胞外基质、血管紧张素转换酶2阻滞剂、靶向抗vimentin抗体、转录肽反式激活剂、聚乙二醇等酶促功能提供平台。由于纳米脂质体作为一种药物传递系统的商业应用越来越多,因此考虑这种有效的方法来治疗2019冠状病毒病是很重要的。图形抽象
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