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in infected cells, HSV or VZV coded thymidine kinases facilitate the conversion of aciclovir to the active aciclovir monophosphate which then acts as an inhibitor of, and substrate for, the herpes specified DNA polymerase, preventing further viral DNA synthesis.
plasma half-life is ~3hrs
60-90% of aciclovir is excreted unchanged in urine where it is insoluble
adjust dose in renal impaired patients
probenecid increases the half life by ~18%
high doses are cytotoxic in animal studies
crosses the placenta readily and is excreted in breast milk
category B3 for pregnant women
use in lactating women if benefits outweigh risks