The AUC24 was calculated by means of the trapezoidal rule using concentration values as predicted by the pharmacokinetic model (individual post-hoc concentration time course).
For estimating the elimination efficiency for the different analytes, we used the concentration values of the corresponding influent and effluent samples.
Using the relation between used concentrations and neutral red intensity value, IC50 of the barberry ethanolic extract and standard berberine chloride was calculated.
Data were modeled using real concentration values, and both concentration values and cell viability output data were transformed using the z score function in MATLAB.
Using the concentration values obtained from the quantitative PCR, a 500 pM aliquot was prepared from the stock library and titrated to 0.9 1.0 pM for input into ABI 1.0 pM-scale emulsion reactions.
Three dominant approximations can be glued, using the concentration values at the times of the switching of dominant approximation as initial values for the next stage.
We evaluated the quality of the predicted values from kriging using cross-validation, a technique with which each monitoring station is removed, one at a time, and the concentration at each omitted station is predicted using the concentration values observed at the other monitors.
The income inequalities are explored using concentration index (CI) with CI values below zero indicating pro-poor inequality whereas CI values above zero indicating pro-rich inequality.
To estimate MeHg intake from less commonly-consumed other finfish and shellfish we used average FDA MeHg concentration values for all finfish and all shellfish, respectively.
Using concentrations close to their IC10 IC20 values, combination of the three drugs showed strong synergistic cytotoxicity.
