Ullah Ata, Qazi Javaria, Rahman Lutfur, Kanaras Antonios G, Khan Waheed S, Hussain Irshad, Rehman Asma
National Institute for Biotechnology and Genetic Engineering Faisalabad Pakistan.
Department of Biotechnology Quaid-i-Azam University Islamabad Pakistan.
Nano Sel. 2020 Dec;1(6):612-621. doi: 10.1002/nano.202000125. Epub 2020 Oct 12.
The current pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has challenged healthcare structures across the globe. Although a few therapies are approved by FDA, the search for better treatment options is continuously on rise. Clinical management includes infection prevention and supportive care such as supplemental oxygen and mechanical ventilatory support. Given the urgent nature of the pandemic and the number of companies and researchers developing COVID-19 related therapies, FDA has created an emergency program to move potential treatments with already approved drugs to patients as quickly as possible in parallel to the development of new drugs that must first pass the clinical trials. In this manuscript, we have reviewed the available literature on the use of sequence-specific degradation of viral genome using short-interfering RNA (siRNA) suggesting it as a possible treatment against SARS-CoV-2. Delivery of siRNA can be promoted by the use of FDA approved lipids, polymers or lipid-polymer hybrids. These nanoparticulate systems can be engineered to exhibit increased targetability and formulated as inhalable aerosols.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019年冠状病毒病(COVID-19)大流行给全球医疗结构带来了挑战。尽管美国食品药品监督管理局(FDA)批准了一些疗法,但对更好治疗方案的探索仍在不断增加。临床管理包括感染预防和支持性护理,如补充氧气和机械通气支持。鉴于大流行的紧迫性以及开发COVID-19相关疗法的公司和研究人员数量众多,FDA制定了一项紧急计划,以便在开发必须首先通过临床试验的新药的同时,尽快将已批准药物的潜在治疗方法应用于患者。在本手稿中,我们回顾了有关使用短干扰RNA(siRNA)对病毒基因组进行序列特异性降解的现有文献,表明其可能是一种对抗SARS-CoV-2的治疗方法。使用FDA批准的脂质、聚合物或脂质-聚合物杂化物可以促进siRNA的递送。这些纳米颗粒系统可以设计成具有更高的靶向性,并制成可吸入气雾剂。