ι-CG type V |
ICR mice infected with MCMV |
0.5 mg |
PFU |
Intraperitoneal |
Decreased mortality and titer and increased PFU/LD50
|
[63] |
ι-CG type V |
ICR mice infected with MCMV |
0.5 mg |
PFU |
Intraperitoneal |
Inhibition of viral spread from the peritoneal cavity to the plasma |
[62] |
λ/κ/ι-CG |
BALB/c mice infected with HSV-2 |
0.05–1% |
PFU in vaginal secretion |
Vaginal |
Inhibition of infection |
[89] |
κ-CG |
C57B1/6 mice infected with HSV-2 |
0.1–100 mg/mL |
Shedding of virus, visible lesions, and CPE |
Vaginal |
Inhibition of infection |
[81] |
CG-based nonoxynol-9 |
BALB/c mice infected with HSV-2 |
20 ul of 3% |
Symptom of infection |
Vaginal |
Inhibition of infection |
[90] |
λ-CG type IV (1T1), ι-CG type V |
Swiss Webster mice infected with HSV-2 |
10 mg/mL |
Sign of disease |
Vaginal |
Inhibition of infection |
[82] |
λ-CG |
BALB/c mice infected with HSV-2 |
2 and 3% |
Survival |
Vaginal |
100% survival |
[87] |
λ-CG 1T1 |
BALB/c mice infected with HSV-2 |
10 mg/mL |
PFU and survival |
Vaginal |
90% survival and no virus shedding |
[84] |
κι/ν-CG C2 |
BALB/c mice infected with HSV-2 |
8 mg/mL |
PFU and survival |
Vaginal |
70% survival |
[40] |
λ-CG type IV |
FHV-1 induced conjunctivitis in cats |
250 µg/mL |
PFU |
Topical |
Reduction of virus titers but no alteration in the clinical course |
[88] |
λ/κ-CG + ZA |
BALB/c mice infected with HSV-2 |
20 µL of 3% |
Survival |
Vaginal and rectal |
Inhibition of infection |
[85] |
λ/κ-CG + ZA |
BALB/c mice infected with HSV-2 |
20 µL of 3% |
Survival |
Vaginal and rectal |
Inhibition of infection |
[8] |
CG + griffithsin |
BALB/c mice infected with HSV-2 |
50 µL of griffithsin solution (19.1 mg/mL) |
Infection rate |
Vaginal |
Inhibition of infection |
[86] |
CG + MIV-150 + ZA |
BALB/c mice infected with HSV-2 |
10 µL of stock |
qPCR |
Vaginal |
Inhibition of infection |
[7] |
CG + griffithsin |
BALB/c mice infected with HSV-2 |
10 µL of 0.1% stock |
qPCR |
Vaginal |
Inhibition of infection |
[80] |