| Title: | Antiviral Activity of the Propylamylatin(TM) Formula against the Novel Coronavirus SARS-CoV-2 In Vitro Using Direct Injection and Gas Assays in Virus Suspensions |
| Author(s): | Brown AN; Strobel G; Hanrahan KC; Sears J; |
| Address: | "Institute for Therapeutic Innovation, Department of Medicine, College of Medicine, University of Florida, Orlando, FL 32827, USA. Department of Plant Sciences, Montana State University, Bozeman, MT 59715, USA. Center for Lab Services/RJ Lee Group, Pasco, WA 99301, USA" |
| ISSN/ISBN: | 1999-4915 (Electronic) 1999-4915 (Linking) |
| Abstract: | "Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of novel coronavirus disease 2019 (COVID-19), has become a severe threat to global public health. There are currently no antiviral therapies approved for the treatment or prevention of mild to moderate COVID-19 as remdesivir is only approved for severe COVID-19 cases. Here, we evaluated the antiviral potential of a Propylamylatin formula, which is a mixture of propionic acid and isoamyl hexanoates. The Propylamylatin formula was investigated in gaseous and liquid phases against 1 mL viral suspensions containing 10(5) PFU of SARS-CoV-2. Viral suspensions were sampled at various times post-exposure and infectious virus was quantified by plaque assay on Vero E6 cells. Propylamylatin formula vapors were effective at inactivating infectious SARS-CoV-2 to undetectable levels at room temperature and body temperature, but the decline in virus was substantially faster at the higher temperature (15 min versus 24 h). The direct injection of liquid Propylamylatin formula into viral suspensions also completely inactivated SARS-CoV-2 and the rapidity of inactivation occurred in an exposure dependent manner. The overall volume that resulted in 90% viral inactivation over the course of the direct injection experiment (EC(90)) was 4.28 microls. Further investigation revealed that the majority of the antiviral effect was attributed to the propionic acid which yielded an overall EC(90) value of 11.50 microls whereas the isoamyl hexanoates provided at most a 10-fold reduction in infectious virus. The combination of propionic acid and isoamyl hexanoates was much more potent than the individual components alone, suggesting synergy between these components. These findings illustrate the therapeutic promise of the Propylamylatin formula as a potential treatment strategy for COVID-19 and future studies are warranted" |
| Keywords: | "Animals Antiviral Agents/*pharmacology COVID-19/virology Caproates/*pharmacology Chlorocebus aethiops Drug Compounding Drug Evaluation, Preclinical Humans Propionates/*pharmacology SARS-CoV-2/*drug effects/genetics/physiology Vero Cells Virus Replication/;" |
| Notes: | "MedlineBrown, Ashley N Strobel, Gary Hanrahan, Kaley C Sears, Joe eng NA/EcoPlanet Environmental LLC/ Research Support, Non-U.S. Gov't Switzerland 2021/04/04 Viruses. 2021 Mar 5; 13(3):415. doi: 10.3390/v13030415" |
