Invitro anti malarial potential of chrozophora senegalensis extracts on cysteine protease of plasmodium falciparum
Table Of Contents
Chapter ONE
INTRODUCTION
- 1.1Introduction
- 1.2Background of Study
- 1.3Problem Statement
- 1.4Objective of Study
- 1.5Limitation of Study
- 1.6Scope of Study
- 1.7Significance of Study
- 1.8Structure of the Research
- 1.9Definition of Terms
Chapter TWO
LITERATURE REVIEW
- 2.1Overview of Cysteine Protease
- 2.2Malarial Disease and its Impact
- 2.3Chrozophora Senegalensis: Botanical Description
- 2.4Previous Studies on Chrozophora Senegalensis
- 2.5Anti-malarial Properties of Chrozophora Senegalensis
- 2.6Cysteine Protease Inhibition in Plasmodium Falciparum
- 2.7Methods of Extracting Compounds from Chrozophora Senegalensis
- 2.8Mechanism of Action of Cysteine Protease Inhibitors
- 2.9Challenges in Developing Anti-malarial Drugs
- 2.10Future Directions in Malaria Research
Chapter THREE
RESEARCH METHODOLOGY
- 3.1Research Design and Approach
- 3.2Selection of Study Participants
- 3.3Data Collection Methods
- 3.4Data Analysis Techniques
- 3.5Ethical Considerations
- 3.6Sampling Techniques
- 3.7Experimental Setup
- 3.8Statistical Tools Used
Chapter FOUR
DATA PRESENTATION AND ANALYSIS
- 4.1Analysis of Extracts on Cysteine Protease
- 4.2Comparison of Different Extraction Methods
- 4.3Inhibition Efficiency of Chrozophora Senegalensis Extracts
- 4.4Impact of Extract Concentration on Inhibition
- 4.5Cellular Uptake of Extracts
- 4.6Toxicity Studies of Chrozophora Senegalensis Compounds
- 4.7Comparison with Standard Anti-malarial Drugs
- 4.8Discussion on Synergistic Effects
Chapter FIVE
SUMMARY, CONCLUSION AND RECOMMENDATIONS
- 5.1Summary of Findings
- 5.2Conclusion
- 5.3Recommendations for Future Research
- 5.4Implications of the Study
- 5.5Practical Applications of the Research
Project Abstract
<p> </p><div><p><em>Chrozophora senegalensis </em>is traditionally used to treat malaria. The plant extracts were prepared by cold maceration with 4 different solvents n-hexane, ethyl ether, methanol, and aqueous. Phytochemical analysis shows the presence of tannins, alkaloids, saponins, flavonoids and phenolic in the methanol and aqueous extracts while the ethyl ether and n-hexane extracts contains terpenes, tannins and phenolics. Ethylether has flavonoids and n-hexane has traces of alkaloids.The extracts were tested in vitro against cultured <em>Plasmodium</em> <em>falciparum</em>. The highest inhibition of the<em> P. falciparum </em>with an IC50 of 2.37ยตg/ml` was demonstrated by the methanol extract followed by aqueous extract with IC50 of 13.36ยตg/ml, ethylether 32.47ยตg/ml and least by n hexane 37.68ยตg/ml. Further investigation against malarial cysteine protease with the four extracts shows highest inhibitory activity of the enzyme in the methanol extract with percentage inhibition of 80% and also 76%, 29%, and 15% for aqueous, n- hexane and ethyl ether respectively. Quantitative phytochemical screening of the methanol extract shows that tannins content was highest with 3.12mg/100g followed byalkaloids 3.10mg/100g, flavonoids 2.51mg/100g, phenolics 2.24mg/100g, saponins 1.69mg/100g and then terpenes 1.61mg/100g. Fractionation of the most active extract that is the methanol extract gave rise to 50 fractions which were pooled to ten different fractions according to their similarities in Rf values. The ten fractions were also further tested against the enzyme malarial cysteine protease. Fraction 3 showed highest inhibitory activity. Characterization of fraction three that shows the best inhibitory activity through gas chromatography/mass spectroscopy revealed the presence of nitro-benzoic acid and ellagic acid alone side other fatty-acids and their derivatives. The anti- plasmodial effect of the methanol extract of the plant could be due to its cysteine protease inhibitory activity. Further work on fraction 3 will be required to characterized and isolate the active compound.</p><p></p></div><h3></h3><br> <br><p></p>
Project Overview