Figure 7From: Amphipathic DNA polymers exhibit antiviral activity against systemic Murine Cytomegalovirus infectionIn vivo Antiviral Dose Effect of REP 9C following Intraperitoneal or Oral Dosing. (a) Virus titer levels in the livers from mice treated with various doses of REP 9C. Three-week old mice (8 mice/group) were treated by daily i.p. administration of saline or 10 mg/kg (QD), 5 mg/kg (BID), 3 mg/kg (BID), 2 mg/kg (BID), or 0.5 mg/kg (BID) of REP 9C starting at 8 days prior to infection with MCMV and continued for 11 days. Data represents results from one of two separate experiments; Mean +/- standard deviation (n = 8). (b) Virus titer levels in the livers from mice treated orally with 100 mg sodium caprate (C10), 20 mg/kg REP 9C, 400 mg/kg REP 9C in 100 mg C10, and 400 mg/kg REP 9C in 0.25% (w/v) TDM. Five-week old mice (8 mice/group) were treated by daily oral administration of C10 or REP 9C + C10 or TDM starting 2 days prior to i.p. inoculation with 1 × 105 pfu of MCMV (K181+) and continued to 3 days post infection. Data represents results from one of two separate experiments with similar outcomes; mean +/- standard error (n = 8). The asterisk indicates groups in which mice died due to non-drug related technical difficulties with oral administration. In (a) and (b), mice with no detectable MCMV titer are indicated as x negative/8 total below each bar. P values are shown in figure.Back to article page