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Table 1 Extraction yield and biological activities of crude extracts

From: Identification of 3,3′-O-dimethylellagic acid and apigenin as the main antiplasmodial constituents of Endodesmia calophylloides Benth and Hymenostegia afzelii (Oliver.) Harms

Plant species

Part

Solvent

Code

Yield (%)

EC50 (μg/mL)

RI

CC50 (μg/mL)

SI

  

Vero

Raw

  

Pf3D7

PfDd2

Vero

Raw

Pf3D7 (PfDd2)

Pf3D7 (PfDd2)

H. afzelii

Stem bark

Hydroethanol

HasbHE

19.50

3.32 ± 0.15

3.08 ± 0.21

0.93

> 200

> 200

> 60.24 (> 64.94)

> 60.24 (> 64.94)a

Stem bark

Methanol

HasbM

12.50

> 100

> 100

E. calophylloides

Stem bark

Hydroethanol

EcsbHE

07.40

5.32 ± 0.03

8.72 ± 1.02

1.63

66.85 ± 4.45

31.72 ± 6.27

12.57 (7.67)

5.96 (3.63)

Stem bark

Methanol

EcsbM

08.20

7.40 ± 0.19

7.48 ± 0.07

1.01

> 200

99.09 ± 1.42

> 27.02 (> 26.74)

13.40 (13.24)a

Reference drugs (μM)

Artemisinin

   

0.014 ± 0.001

0.018 ± 0.003

1.28

NA

NA

Chloroquine

   

0.018 ± 0.002

0.449 ± 0.065

24.94

NA

NA

 

Podophyllotoxin

   

NA

NA

 

1.89 ± 0.38

0.76 ± 0.09

  1. Results are expressed as Means ± standard deviation of duplicate experiments
  2. HasbHE hydroethanolic extract of Hymenostegia afzelii stem bark, HasbM methanolic extract of Hymenostegia afzelii stem bark, EcsbHE hydroethanolic extract of Endodesmia calophylloides stem bark, EcsbM methanolic extract of Endodesmia calophylloides stem bark, Pf Plasmodium falciparum, NA not applicable, EC50 50% effective concentration, CC50 50% cytotoxicity concentration, RI resistance index, SI selectivity index; aCrude extracts of interest