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. Author manuscript; available in PMC: 2019 Oct 1.
Published in final edited form as: Biochem Pharmacol. 2018 Aug 17;156:147–156. doi: 10.1016/j.bcp.2018.08.018

Table 3.

Pharmacokinetic Parameters of Valacyclovir and Acyclovir in Wildtype and Bphl Knockout Mice after the Oral and Intravenous Administrations of 25 nmoL/g Valacyclovir

Oral Cmax
(μM)
Tmax
(min)
AUC0–180
(μM·min)
T1/2
(min)
Wildtype
VACV 1.3 ± 0.6 5 ± 0 22.1 ± 6.5 48.9 ± 18.4
ACV 7.6 ± 0.6 15 ± 0 402 ± 126 47.5 ± 10.1
VACV/ACV (%) 17 ± 6 33 ± 0 5.5 ± 2.4 103 ± 1
Bphl Knockout
VACV 2.0 ± 0.5 5 ± 0 38.3 ± 10.3 37.2 ± 2.6
ACV 9.4 ± 0.2* 12 ± 3 419 ± 81 37.0 ± 6.6
VACV/ACV(%) 22 ± 2 43 ± 2* 9.1 ± 3.0 100 ± 1

Intravenous Cmax
(μM)
Tmax
(min)
AUC0–180
(μM·min)
T1/2
(min)
Wildtype
VACV 9.1 ± 0.4 2 ± 0 109 ± 8 50.2 ± 15.4
ACV 6.8 ± 0.3 5 ± 0 259 ± 18 45.9 ± 6.0
VACV/ACV(%) 134 ± 1 40 ± 0 37.3 ± 3.9 109 ± 1
Bphl Knockout
VACV 11.6 ± 0.5* 2 ± 0 145 ± 11 53.7 ± 19.8
ACV 8.8 ± 2.6 12 ± 3 373 ± 97 37.3 ± 6.2
VACV/ACV(%) 131 ± 3 17 ± 2*** 34.2 ± 9.3 144 ± 1***
*

p ≤ 0.05

***

p ≤ 0.001, as compared to wildtype mice for tde same route of administration, using an unpaired t-test.