Phytochemical Profiling and In vivo Antimalarial Evaluation of the Stem Bark of Enantia chlorantha in Plasmodium berghei infected mice

Main Article Content

Vincent O. Imieje
Chidimma B. Onyia

Abstract

Background: Malaria is one of the significant public health diseases in Sub-Saharan Africa with a high mortality rate, especially among underage children and pregnant women. The rate of development of resistance to the current drugs in clinical use to treat the disease is alarming, especially strains resistant to ACTs. This study aimed to investigate the in vivo potential of Enantia chlorantha, a medicinal plant used to treat malaria in Nigeria and other African countries.


 


Methods: Plasmodium berghei (NK65) infected mice were treated with methanol extract and fractions of Enantia chlorantha using the curative assay method (Rane's test). The antioxidant activity of the extract and fractions was determined using the DPPH and FRAP assays and the total phenolic and flavonoid contents.


 


Results: The extract showed the presence of alkaloids, phenolic compounds, flavonoids, saponins, terpenoids, etc., but no tannins and anthraquinones. The total phenolic and flavonoid contents were 86.2±22.42 and 146±5.1 for the extract. The extract showed percentage inhibition in the antioxidant assay with an IC50 value of 43 µg/mL compared to the standard ascorbic acid (IC50=0.1 µg/mL). In vivo, antimalarial screening revealed that on day 7 post-inoculation, the untreated mice had a 27.6 % percentage parasitaemia, artesunate (0.6%), and ACT showed complete parasitaemia clearance.


 


Conclusion: The findings of this study revealed the extract of Enantia chlorantha exhibited a suppressive parasitaemia effect in Plasmodium berghei-infected mice after 14 days of treatment post-inoculation, suggesting its potential use in suppressive malaria treatment only.

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How to Cite
Imieje , V. O., & Onyia, C. B. (2025). Phytochemical Profiling and In vivo Antimalarial Evaluation of the Stem Bark of Enantia chlorantha in Plasmodium berghei infected mice. Nigerian Journal of Pharmaceutical and Applied Science Research, 14(2). https://doi.org/10.60787/nijophasr-v14-i2-609
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