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. 2006 May;50(5):1649–1655. doi: 10.1128/AAC.50.5.1649-1655.2006

TABLE 1.

Mean efficacy parameters for PQD-A4, PQD-BE, PQD, and AS following daily intragastric or intravenous administrations for 3 days in rats infected with P. berghei ANKAa

Parametera Result obtained with the following drug at the indicated daily dose (mg/kg [μmol/kg])a:
Oral PQD-A4
Oral PQD-BE
Oral PQD
Intravenous AS
Control (0) VC (0) 0.625 (1.2) 1.25 (2.4) 2.5 (4.8) 5 (9.5) 10 (19.0) 20 (38.1) 100 (190.0) 200 (381.0) VC (0) 0.6 (1.2) 1.2 (2.4) 2.4 (4.8) 4.8 (9.5) 9.6 (19.0) 19.2 (38.1) 38.4 (76.2) 76.8 (153.0) Control (0) VC (0) 0.43 (1.2) 0.86 (2.4) 1.71 (4.8) 3.42 (9.5) 8.6 (24.0) 17.1 (48.0) 34.2 (95.0) Control (0) VC (0) 2.3 (6.0) 4.6 (12.0) 9.2 (23.9) 18.4 (47.8) 30.0 (95.6) 60.0 (156.3) 240 (625.0) 480 (1,250)
No. of rats 4 5 5 5 5 4 7 6 5 4 5 5 5 5 4 5 5 5 4 5 5 5 5 5 5 4 4 4 5 4 4 6 6 6 6 6 6 5
Parasitemia (%) on day 6 4.8 5.1 5.2 4.9 6.0 4.3 6.4 4.7 4.2 5.0 5.1 5.2 4.9 5.0 4.3 6.1 4.5 4.8 5.1 5.0 5.1 6.2 4.7 5.8 5.3 4.9 5.2 5.0 3.9 2.5 3.3 7.6 4.6 4.5 5.4 6.5 6.7 3.9
Suppression (%) 87.2 0 77.3 0 0 91.4 0 0 23.3 80.7 89.5
No. of rats with clearance/total no. 0/4 0/5 0/5 5/5 5/5 5/5 7/7 6/6 0/5 0/5 5/5 5/5 5/5 5/5 5/5 5/5 0/5 0/5 0/5 5/5 5/5 5/5 4/4 0/5 0/4 0/4 0/6 0/6 3/6 4/6 6/6 6/6
PCT (h) 49.8 46.8 58.5 49.5 52.4 59.4 69.6 43.5 48.0 40.8 36.5 49.2 68.4 49.5 47.4 48.0 59.5 62.6 49.0 54.0
No. of days to clearance 3.1 5.5 9.8 Cured Cured 2.3 4.7 11.0 Cured Cured Cured 4.6 9.1 Cured Cured 3.5 7.8
No. of rats in recrudescence/total 5/5 5/5 4/4 0/7 0/6 5/5 5/5 2/4 0/5 0/5 0/5 5/5 5/5 0/5 0/4 3/2 4/4 6/6 6/6
No. of rats cured/total no. 0/4 0/5 0/5 0/5 0/5 0/5 7/7 6/6 0/5 0/5 0/5 0/5 2/4 5/5 5/5 5/5 0/3 0/5 0/5 0/5 0/5 5/5 4/4 0 0 0 0 0 0
Mortality rate (%) 0 20.0 0 0 0 0 0 0 0 100 20 0 0 0 0 0 0 0 75 20 0 0 0 0 0 0 50 100 20 25 0 0 0 0 0 0 0 80
a

VC, vehicle control; −, no application. The administration times of the oral and intravenous doses are days 6, 7, and 8 after infection. Recrudescence has been calculated with the first day of oral or intravenous administration as day 0.