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. Author manuscript; available in PMC: 2013 Aug 1.
Published in final edited form as: J Pharmacokinet Pharmacodyn. 2012 May 26;39(4):313–327. doi: 10.1007/s10928-012-9252-6

Figure 6. Simulated concentration-time curves using a priori predicted partition coefficients for cotinine.

Figure 6

Adipose, brain, heart, kidney, liver, lung, muscle, and splanchnic concentration-time curves are simulated using a priori predicted partition coefficients based on the method of Poulin et al. [4] with the correction by Berezhkovskiy [24]. Well-stirred tank (solid medium gray lines) and flow-limited two-subcompartment (dashed dark gray lines) model simulations are plotted against rat pharmacokinetic data from Gabrielsson, et al. [27] (filled dark gray circles, mean; vertical bars, range). Plasma concentration-time curves are also plotted in each tissue panel (well-stirred, solid light gray lines; flow-limited two-subcompartment, dashed medium gray lines) against rat plasma time course data (filled light gray squares, mean; vertical bars, range). Partition coefficient values for cotinine are reported in Table 4, and AUC values are reported in Table 5.