The nominal concentration
is generally used to express concentration–effect
relationships in in vitro toxicity assays. However, the nominal concentration
does not necessarily represent the exposure concentration responsible
for the observed effect. Surfactants accumulate at interphases and
likely sorb to in vitro system components such as serum protein and
well plate plastic. The extent of sorption and the consequences of
this sorption on in vitro readouts is largely unknown for these chemicals.
The aim of this study was to demonstrate the effect of sorption to
in vitro components on the observed cytotoxic potency of benzalkonium
chlorides (BAC) varying in alkyl chain length (6–18 carbon
atoms, C6–18) in a basal cytotoxicity assay with
the rainbow trout gill cell line (RTgill-W1). Cells were exposed for
48 h in 96-well plates to increasing concentration of BACs in exposure
medium containing 0, 60 μM bovine serum albumin (BSA) or 10%
fetal bovine serum (FBS). Before and after exposure, BAC concentrations
in exposure medium were analytically determined. Based on freely dissolved
concentrations at the end of the exposure, median effect concentrations
(EC50) decreased with increasing alkyl chain length up
to 14 carbons. For BAC with alkyl chains of 12 or more carbons, EC50’s based on measured concentrations after exposure
in supplement-free medium were up to 25-times lower than EC50’s calculated using nominal concentrations. When BSA or FBS
was added to the medium, a decrease in cytotoxic potency of up to
22 times was observed for BAC with alkyl chains of eight or more carbons.
The results of this study emphasize the importance of expressing the
in vitro readouts as a function of a dose metric that is least influenced
by assay setup to compare assay sensitivities and chemical potencies.