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. Author manuscript; available in PMC: 2010 Jul 1.
Published in final edited form as: Toxicol Appl Pharmacol. 2009 May 3;238(1):90–99. doi: 10.1016/j.taap.2009.04.019

Table 4.

Kinetic parameter estimates of the best-fit model (model D).

Parameter Notes Final Value Clearance, L/hr Half-life, hr
k01 TCE (GI) → TCE (blood) 104 - -
k1e TCE (blood) elimination 0.393 0.0742 1.77
k12 TCE (blood) → TCE (peripheral) 0.384 - -
k21 TCE (peripheral) → TCE (blood) 0.33 - -
V1 Volume of distribution for TCE 0.189 - -

k1fT TCE → TCA formation 0.0303 - -
kTe TCA elimination 0.0578 0.00381 12.0
VmT Volume of distribution for TCA 0.0660 - -
k1fD TCE → DCA formation 1.46×10−7 - -
kD12 DCA: central → peripheral 10.9 - -
kD21 DCA: peripheral → central 0.500 - -
kDe DCA elimination 1.16 8.07×10−5 0.598
VmD Volume of distribution for DCA 6.96×10−5 - -
k1fG TCE → DCVG formation 4.16×10−6 - -
kGfC DCVG → DCVC formation 0.490 0.0168 1.41
VmG Volume of distribution for DCVG 0.0342 - -
kCe DCVC elimination 0.600 0.176 1.16
VmC Volume of distribution for DCVC 0.293 - -

Clearance is the product between elimination constant and volume of distribution of TCE or each metabolite, reflecting systemic clearance. Units of the reaction constants and volume of distributions are hr−1 and liter, respectively.