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. 2012 Apr 23;62(4):309–316. doi: 10.4097/kjae.2012.62.4.309

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Copyright © the Korean Society of Anesthesiologists, 2012

This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 6 — Simulation was separately investigated with one pharmacokinetic (PK) parameter (V_C, V₂, V₃, Cl₁, Cl₂, and Cl₃) replaced of the PK model with the corresponding value of the other model and each curve shows the time course of the percentage differences of predictions. Each parameter of Marsh PK was replaced with that of Schnider PK (upper curves), and each parameter of Schider PK was replaced with that of Marsh PK (lower curves).