Martín-González Natalia, Vieira Gonçalves Leonam, Condezo Gabriela N, San Martín Carmen, Rubiano María, Fallis Ian, Rubino Joseph R, Ijaz M Khalid, Maillard Jean-Yves, De Pablo Pedro J
Department of Condensed Matter Physics, Universidad Autónoma de Madrid, Madrid, Spain.
School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, Wales, United Kingdom.
Front Mol Biosci. 2020 Dec 17;7:570914. doi: 10.3389/fmolb.2020.570914. eCollection 2020.
Hygiene and disinfection practices play an important role at preventing spread of viral infections in household, industrial and clinical settings. Although formulations based on >70% ethanol are virucidal, there is a currently a need to reformulate products with much lower alcohol concentrations. It has been reported that zinc can increase the virucidal activity of alcohols, although the reasons for such potentiation is unclear. One approach in developing virucidal formulations is to understand the mechanisms of action of active ingredients and formulation excipients. Here, we investigated the virucidal activity of alcohol (40% w/v) and zinc sulfate (0.1% w/v) combinations and their impact on a human adenovirus (HAdV) using, nucleic acid integrity assays, atomic force microscopy (AFM) and transmission electron microscopy (TEM). We observed no difference in virucidal activity (5 log reduction in 60 min) against between an ethanol only based formulation and a formulation combining ethanol and zinc salt. Furthermore, TEM imaging showed that the ethanol only formulation produced gross capsid damage, whilst zinc-based formulation or formulation combining both ethanol and zinc did not affect HAdV DNA. Unexpectedly, the addition of nickel salt (5 mM NiCl) to the ethanol-zinc formulation contributed to a weakening of the capsid and alteration of the capsid mechanics exemplified by AFM imaging, together with structural capsid damage. The addition of zinc sulfate to the ethanol formulation did not add the formulation efficacy, but the unexpected mechanistic synergy between NiCl and the ethanol formulation opens an interesting perspective for the possible potentiation of an alcohol-based formulation. Furthermore, we show that AFM can be an important tool for understanding the mechanistic impact of virucidal formulation.
卫生和消毒措施在家庭、工业和临床环境中预防病毒感染传播方面发挥着重要作用。尽管基于>70%乙醇的制剂具有杀病毒作用,但目前需要重新配制酒精浓度低得多的产品。据报道,锌可以提高酒精的杀病毒活性,尽管这种增强作用的原因尚不清楚。开发杀病毒制剂的一种方法是了解活性成分和制剂辅料的作用机制。在这里,我们使用核酸完整性测定、原子力显微镜(AFM)和透射电子显微镜(TEM)研究了酒精(40% w/v)和硫酸锌(0.1% w/v)组合的杀病毒活性及其对人腺病毒(HAdV)的影响。我们观察到,仅基于乙醇的制剂与乙醇和锌盐组合的制剂在杀病毒活性(60分钟内5个对数级降低)方面没有差异。此外,TEM成像显示,仅乙醇制剂会导致衣壳严重受损,而基于锌的制剂或乙醇和锌两者组合的制剂不会影响HAdV DNA。出乎意料的是,向乙醇-锌制剂中添加镍盐(5 mM NiCl)会导致衣壳减弱以及AFM成像所显示的衣壳力学改变,同时伴有衣壳结构损伤。向乙醇制剂中添加硫酸锌并没有提高制剂的效力,但NiCl与乙醇制剂之间意外的机制协同作用为基于酒精的制剂的可能增强作用开辟了一个有趣的前景。此外,我们表明AFM可以成为理解杀病毒制剂机制影响的重要工具。