The Integral Method, a new approach to quantify bactericidal activity

Abstract The bactericidal activity (BA) of antimicrobial agents is generally derived from the results of killing assays. A reliable quantitative characterization and particularly a comparison of these substances, however, are impossible with this information. We here propose a new method that takes into account the course of the complete killing curve for assaying BA and that allows a clear-cut quantitative comparison of antimicrobial agents with only one number. The new Integral Method, based on the reciprocal area below the killing curve, reliably calculates an average BA [log 10  CFU/min] and, by implementation of the agent's concentration C, the average specific bactericidal activity SBA = BA / C [log 10  CFU/min/mM]. Based on experimental killing data, the pertaining BA and SBA values of exemplary active halogen compounds were established, allowing quantitative assertions. N -chlorotaurine (NCT), chloramine T (CAT), monochloramine (NH 2 Cl), and iodine (I 2 ) showed extremely diverging SBA values of 0.0020 ± 0.0005, 1.11 ± 0.15, 3.49 ± 0.22, and 291 ± 137 log 10  CFU/min/mM, respectively, against Staphylococcus aureus . This immediately demonstrates an approximately 550-fold stronger activity of CAT, 1730-fold of NH 2 Cl, and 150,000-fold of I 2 compared to NCT. The inferred quantitative assertions and conclusions prove the new method suitable for characterizing bactericidal activity. Its application comprises the effect of defined agents on various bacteria, the consequence of temperature shifts, the influence of varying drug structure, dose–effect relationships, ranking of isosteric agents, comparison of competing commercial antimicrobial formulations, and the effect of additives.