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Table 2 Effect on worm burden of single oral doses of three selected organometallic CQ derivatives administered to mice harboring a 49-day-old adult S. mansoni infection, stratified by sex and worm distribution

From: In vitro and in vivo antischistosomal activity of ferroquine derivatives

Drug

Dose (mg/kg)

No. of mice investigated

No. of mice cured

Mean number of worms (SD)

Total worm burden reduction (%)

p-value

Female worm burden reduction (%)

p-value

    

Liver

Mesenteric veins

Total

Males

Females

    

Control1

-

8

-

0.4 (0.7)

33.8 (10.2)

34.1 (10.3)

19.9 (7.7)

14.3 (4.2)

-

-

-

-

Control2

-

8

-

0.6 (1.2)

25.8 (16.7)

26.4 (16.7)

14.5 (9.3)

11.9 (7.7)

-

-

-

-

FQa

200

4

0

1.8 (2.4)

25.8 (7.3)

27.5 (7.3)

16.3 (4.9)

11.3 (4.0)

19.4

>0.05

21.0

>0.05

FQb

800

4*

0

0.7 (1.2)

16.3 (4.2)

17.0 (5.3)

10.3 (5.8)

6.7 (1.2)

35.6

>0.05

43.7

0.018

FQ-OHa,b

200

3

0

3.7 (5.5)

21.3 (26.6)

25.0 (24.4)

16.3 (14.3)

8.7 (10.8)

17.3

>0.05

33.6

>0.05

RQa

200

4

0

0.25 (0.5)

36.5 (10.7)

36.8 (10.4)

18.8 (5.3)

18.0 (5.3)

0

>0.05

0

>0.05

MQ

200

5

0

     

72.3 [8]

 

100

 

CQ

200

5

0

     

11.7 [8]

 

93.0

 
  1. *one mouse died within 24 hours post-treatment, aworm burden reduction calculated versus control 1;bworm burden reduction calculated versus control 2SD= standard deviation.