Virucidal Efficacy Testing


Introduction

In the United States, virucidal disinfectants used on environmental surfaces are regulated by the Environmental Protection Agency (EPA) under the Federal Insecticide, Fungicide, and Redenticide Act (FIFRA). EPA regulates disinfectants and sanitizers as pesticides, often referring to them as "antimicrobial pesticides." Before a disinfectant can be sold in the U.S. it must first be registered with EPA, as well as with all 50 states. Currently the U.S. EPA does not recognize "virucidal sanitizers" - all virucides must meet disinfectant-grade efficacy guidelines.

To register a virucidal disinfectant companies must submit chemical characterization, safety, and efficacy data to EPA, as well as pay registration fees. Efficacy data should be generated in compliance with Good Laboratory Practice Regulations (GLP). Test methods used should be taken from the Series 810 guidance, and companies should consult EPA's Pesticide Registration Manual.

Virucidal Efficacy Testing Is Different - Here's How:

Disinfectant Testing Basics:

EPA currently only recognizes "hard surface carrier" methods for substantiation of virucidal efficacy claims. These methods consist of a non-porous carrier (typically glass) being inoculated with the selected virus, dried, and then treated with the disinfectant. Virucidal hard surface carrier methods are quantitative, meaning that percent and log reductions are calculated by determining the TCID50 (50% Tissue Culture Infective Dose) per carrier before and after treatment with the disinfectant. The disinfectant must demonstrate complete inactivation of the virus down to the limit of detection of the assay, or (if cytotoxicity is observed) a ≥ 3.00 log10 reduction (99.9%).

Observation of Results:

Virus testing is unique within the laboratory because the presence of viruses before and after product treatment is not determined by observing growth of virus, but rather by observing the damage caused by infection to mammalian host cells. When virologists analyze individual sets of cells after a study, they use a microscope to look for where healthy cell layers become damaged. This damage is known as the cytopathic effects (CPE) of infection. The quantity and quality of CPE is used to calculate the amount of virus present.

CPE is typically observed as changes to cell appearance and monolayer (the layer host cells form when they attach to a flask or tray) disruptions. CPE can vary depending on the virus and host cell line used. Some instances of CPE are distinct, consisting of severe monolayer disruption and cell rounding. Some CPE can be subtle, consisting of gradual enlargement of host cells that is only recognizable when compared to a negative control. In cases where CPE is difficult to distinuish special confirmatory assays are used to verify the results of the assay. Some more common confirmatory assays include Hemagglutination Assays (HA) and immunofluorescent staining (IF).

Study Preparation and Timeline:

From the laboratory's perspective, a significant amount of work and time is required to grow and maintain the sterile cell cultures that are needed to propagate and detect viruses in antimicrobial efficacy studies. From our customer's point of view, the cell culture requirement means that extra time must be given to the laboratoy to prepare for and execute the study. Most studies take 1-2 weeks to complete, though some can take 3-4 weeks. The behind-the-scenes cell culture work and extraordinary expertise necessary to conduct virological assays also means that virological studies are more expensive than their related bacteriological assays.

Study Conduct and Parameters:

There are two main viral morphologies - enveloped and non-enveloped. Non-enveloped viruses consist of genetic material surrounded by a hard protein coat. Enveloped viruses have an additional lipid layer encompassing their protein coat. The limited sensitivity of non-enveloped viral components means that these viruses can persist in an infectious state even when exposed to harsh environmental conditions - including exposure to UV or relatively high temperatures. When it comes to testing, this means that you can translate almost any bacteriological study into a non-enveloped viral assay without changing too many parameters.

Enveloped viruses are another story. Their delicate lipid envelopes leave them vulnerable to environmental factors like osmotic pressure, low humidity, and high temperatures. When working with enveloped viruses certain parameters (like contact times and contact temperatures) and even general study methods may need to be modified to accomodate the unique demands of these microbes.

Viruses Tested at the Laboratory*

* Microchem Laboratory is happy to acquire additional viruses to meet your testing needs. Contact us today to discuss viral acquisition and your testing options.

Virucidal Efficacy Test Methods and Services

Preliminary Testing and Guidance

Suspension-Based Tests

  • ASTM E1052 - Standard Test Method for Efficacy of Antimicrobial Agents Against Viruses in Suspension
  • EN 14476 - Chemical Disinfectants and Antiseptics - Quantitiative Suspension Test for the Evaluation of Virucidal Activity in the Medical Area (Phase 2/Step 1)

Hard Surface Carrier Tests

Treated Surfaces and Textiles

  • AATCC 100 - Assessment of Antibacterial Finishes on Textile Materials, Modified for Viruses
  • JIS Z 2801 -  Measurement of Antimicrobial Activity of Plastic Surfaces
  • ISO 22196 - Test for Antimicrobial Activity of Treated Surfaces
  • EPA Copper Sanitization

Additional Testing