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. Author manuscript; available in PMC: 2018 Sep 28.
Published in final edited form as: Environ Toxicol Chem. 2016 Aug 25;36(2):463–471. doi: 10.1002/etc.3572

Table 1.

Intrinsic clearance of 6 polycyclic aromatic hydrocarbons by cryopreserved trout hepatocytes and trout liver S9 fractions

Chemical log Kowa Substrate conc. (μΜ) CLin vitro, int,hep (mL/h/106 cells) CLin vivo,int,hep (mL/h/g liver) CLin vivo, int,s9 (mL/h/g liver)b
Naphthalene 3.30 2.7 ± 0.2 0.018 ± 0.009 9.4 ± 4.6 22.4 ± 2.5
Fluorene 4.18 0.93 ± 0.18 0.30 ± 0.11 151 ± 55 58.1 ± 2.3
Anthracene 4.45 0.14 ± 0.01 0.32 ± 0.10 162 ± 51 80.5 ± 5.8
Phenanthrene 4.47 1.5 ± 0.2 0.21 ± 0.04 109 ± 20 94.0 ± 2.7
Pyrene 4.88 0.25 ± 0.02 3.1 ± 1.0 1580± 500 1610 ± 160
Benzo[a]pyrene 6.13 0.16 ± 0.01 0.54 ± 0.10 273 ± 52 2660 ± 250

Kow = log10 octanol-water partition coefficient; CLin vitro, int,hep = in vitro intrinsic clearance measured using hepatocytes; CLin vivo,int,hep = in vivo intrinsic clearance calculated using data from hepatocytes; CLin vivo, int,s9 = in vivo intrinsic clearance calculated using data from liver S9 fractions; all data reported as mean ± SD

a

log Kow values are based on MLogP estimates (with preference given to measured values) in Bio-Loom for Windows

b

Data provided in Nichols et al. [19]