Kanchibhotla Divya, Subramanian Saumya, Ravi Kumar Reddy M, Venkatesh Hari K R, Pathania Monika
Sri Sri Institute for Advanced Research, India.
Sri Sri Institute for Advanced Research, India.
J Ayurveda Integr Med. 2022 Jul-Sep;13(3):100581. doi: 10.1016/j.jaim.2022.100581. Epub 2022 Jun 23.
In the last two years, COVID-19 pandemic caused by SARS-CoV-2 has created a mass destruction among humanity causing a major health crisis around the world. With the emergence of new strains of the virus, lack of targeted drugs and antimicrobial resistance, there is a dire need to discover specific antiviral with minimum side effects targeted against COVID-19.
The present study evaluates the antiviral efficacy of a novel Ayurvedic polyherbal formulation, NOQ19, composed of a 13 well known herbs, in a cell-based setting.
Vero E6 (CL1008), the African green monkey kidney epithelial cell, were infected with SARS-CoV-2 virus (isolate USA-WA1/2020) in a 96 well-plate. NOQ19 test material was diluted at different concentration: 0.05 mg/ml, 0.1 mg/ml, 0.2 mg/ml, 0.3 mg/ml, 0.4 mg/ml, 0.5 mg/ml, 0.6 mg/ml, 0.7 mg/ml, 0.8 mg/ml and 0.9 mg/ml. These different concentrations of NOQ19 were added to infected cells respectively and incubated for 3 days in 5% CO incubator. Remdesivir was used as a positive control. The cells were finally fixed with formaldehyde, stained with crystal violet and plaques were visualized. The number of plaques were counted to determine the PFU(plaque forming units)/ml.
The results of the present study demonstrated an excellent an antiviral efficacy of NOQ19 at 0.9 mg/ml concentration, eliminating 100% virus. The IC of the drug was found to be 0.2 mg/ml.
There is limited data around pre-clinical efficacy of polyherbal Ayurvedic drugs. Ayurvedic and herbal formations need to be tested in a preclinical setting to support the human data. The results of the present study demonstrated viral load reduction using NOQ19 in Vero E6 cell lines infected with SARS-CoV-2 virus. These result along with other preclinical and clinical trials could further evaluate the efficacy of NOQ19 as a potential therapeutic option in the fighting the COVID-19 challenge.
在过去两年中,由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病疫情给人类带来了巨大破坏,在全球引发了重大健康危机。随着病毒新变种的出现、缺乏针对性药物以及抗菌药物耐药性问题,迫切需要研发出针对2019冠状病毒病且副作用最小的特异性抗病毒药物。
本研究在细胞水平上评估一种由13种知名草药组成的新型阿育吠陀多草药配方NOQ19的抗病毒疗效。
在96孔板中,用SARS-CoV-2病毒(分离株USA-WA1/2020)感染非洲绿猴肾上皮细胞Vero E6(CL1008)。将NOQ19测试材料稀释成不同浓度:0.05毫克/毫升、0.1毫克/毫升、0.2毫克/毫升、0.3毫克/毫升、0.4毫克/毫升、0.5毫克/毫升、0.6毫克/毫升、0.7毫克/毫升、0.8毫克/毫升和0.9毫克/毫升。将这些不同浓度的NOQ19分别加入感染的细胞中,并在5%二氧化碳培养箱中孵育3天。瑞德西韦用作阳性对照。最后用甲醛固定细胞,用结晶紫染色,观察噬斑。计算噬斑数量以确定每毫升的空斑形成单位(PFU)。
本研究结果表明,在浓度为0.9毫克/毫升时,NOQ19具有出色的抗病毒疗效,可消除100%的病毒。该药物的半数抑制浓度(IC)为0.2毫克/毫升。
关于阿育吠陀多草药药物临床前疗效的数据有限。阿育吠陀和草药配方需要在临床前环境中进行测试,以支持人体数据。本研究结果表明,在感染SARS-CoV-2病毒的Vero E6细胞系中使用NOQ19可降低病毒载量。这些结果以及其他临床前和临床试验可以进一步评估NOQ19作为对抗2019冠状病毒病挑战的潜在治疗选择的疗效。