“…However, according to the American Standard, of which the virucidal efficacy criterion is a 3 log 10 reduction, CHX had an ATS-D antiviral activity at 10 −3 mol L −1 and 60 min, but this activity is not really representative of field use conditions. In most studies, CHX has been shown: (i) to be inefficient against naked viruses (Bernstein et al, 1990;Kawana et al, 1997;Narang and Codd, 1983;Wood and Payne, 1998) and (ii) to be efficient at concentrations >10 −3 mol L −1 on enveloped viruses but its activity depends on viruses tested and testing conditions (Bernstein et al, 1990;Kawana et al, 1997;Platt and Bucknall, 1985;Tyler and Ayliffe, 1987;Wood and Payne, 1998). For instance, CHX reduced Herpes simplex virus viral titers of >3 log 10 in suspension tests for under 3 min (Kawana et al, 1997;Wood and Payne, 1998) and only of 1 log 10 on a dried sample of HSV in 10 min (Tyler and Ayliffe, 1987).…”