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Updated: May 1, 2026

High-throughput Screening for Broad-spectrum Chemical Inhibitors of RNA Viruses
Published on: May 5, 2014
Development of a general anti-viral therapeutic using cholestosome technology to exploit inhibition of intracellular
Lawrence Mielnicki1,2, Julie Hughes1, Mary Irving1
1Department of Chemistry, Biochemistry and Physics, Niagara University, Lewiston, NY, 14109, USA.
Abstract:
The recent events of the worldwide Covid-19 pandemic showed the need for a general anti-viral therapeutic, independent of the specific characteristics of the virus, that targets intracellular mechanisms of viral production to prevent the rapid, overwhelming spread of infection and its devastating consequences. The development of the Cholestosome technology, a drug delivery system made exclusively of cholesteryl esters, is a solution for intracellular targeting of viral replication. It is well known that Zn2+ is capable of inhibiting viral replication but the control of intracellular Zn2+ concentration is tightly regulated. Cholestosome technology can encapsulate Zn2+ and deliver it to cells to inhibit viral replication. The human betacoronavirus OC43 (OC43) model system was used to infect cells and infected cells were treated with Zn2+ encapsulated in Cholestosomes as well as appropriate controls. Viral production was measured using CPE as well as PCR methods to determine inhibition of infection. Experimental results indicated a 55 % reduction in viral load for those cells treated with Zn2+ encapsulated in cholestosomes versus Zn2+ alone.
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