Authors :
Rashmi Das; Ann Irene D.
Volume/Issue :
Volume 10 - 2025, Issue 8 - August
Google Scholar :
https://tinyurl.com/d2venfsu
Scribd :
https://tinyurl.com/4t3wdk3x
DOI :
https://doi.org/10.38124/ijisrt/25aug1452
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
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Abstract :
Medicinal plants are known to produce a wide array of secondary metabolites, many of which possess potent
antimicrobial properties. Continuous research into new plant species expands the potential for discovering novel
therapeutic agents. This study focuses on Parmotrema perlatum, a foliose lichen traditionally used as a spice (known as
Kalpasi), to explore its antiparasitic potential. Three protozoan pathogens—Plasmodium falciparum, Toxoplasma gondii,
and Entamoeba histolytica—remain major global health threats. P. falciparum, the causative agent of malaria, has claimed
countless lives across human history. It is transmitted by the female Anopheles mosquito and causes recurring cycles of
fever, chills, and anemia by attacking red blood cells. T. gondii, primarily hosted in cats, infects humans via contaminated
food or water, often lying dormant in the brain and muscles. While asymptomatic in healthy individuals, it poses serious
risks to fetuses and immunocompromised patients. E. histolytica spreads via contaminated food or water, invades the
intestinal wall, and causes severe gastrointestinal complications such as dysentery and liver abscesses. To address the
growing resistance to conventional drugs, this research investigates phytochemicals derived from P. perlatum as potential
antiparasitic agents. The powdered form of the plant was subjected to Gas Chromatography-Mass Spectrometry (GC-MS)
analysis to identify its active compounds. Two phytochemicals—Thujopsene and Resibufogenin—were selected based on
their potential bioactivity.Before targeting the protozoan pathogens, these compounds were initially evaluated against
Shigella flexneri using both bioinformatics (molecular docking) and in vitro antibacterial assays. Key proteins from each
pathogen were selected based on structural relevance and docking compatibility.The primary goal of this study is to assess
whether the identified compounds from P. perlatum can serve as effective drug candidates against parasitic infections,
offering a natural alternative to synthetic drugs in the fight against endemic protozoan disease.
Keywords :
Plasmodium, Entamoeba, Toxoplasma; Phytochemical Analysis, Molecular Docking, Calculated Affinity, Malaria, HSP 90, HSP70, Permotrema parlatum, GCMS, Resibufogenin, Thujopsin.
References :
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Medicinal plants are known to produce a wide array of secondary metabolites, many of which possess potent
antimicrobial properties. Continuous research into new plant species expands the potential for discovering novel
therapeutic agents. This study focuses on Parmotrema perlatum, a foliose lichen traditionally used as a spice (known as
Kalpasi), to explore its antiparasitic potential. Three protozoan pathogens—Plasmodium falciparum, Toxoplasma gondii,
and Entamoeba histolytica—remain major global health threats. P. falciparum, the causative agent of malaria, has claimed
countless lives across human history. It is transmitted by the female Anopheles mosquito and causes recurring cycles of
fever, chills, and anemia by attacking red blood cells. T. gondii, primarily hosted in cats, infects humans via contaminated
food or water, often lying dormant in the brain and muscles. While asymptomatic in healthy individuals, it poses serious
risks to fetuses and immunocompromised patients. E. histolytica spreads via contaminated food or water, invades the
intestinal wall, and causes severe gastrointestinal complications such as dysentery and liver abscesses. To address the
growing resistance to conventional drugs, this research investigates phytochemicals derived from P. perlatum as potential
antiparasitic agents. The powdered form of the plant was subjected to Gas Chromatography-Mass Spectrometry (GC-MS)
analysis to identify its active compounds. Two phytochemicals—Thujopsene and Resibufogenin—were selected based on
their potential bioactivity.Before targeting the protozoan pathogens, these compounds were initially evaluated against
Shigella flexneri using both bioinformatics (molecular docking) and in vitro antibacterial assays. Key proteins from each
pathogen were selected based on structural relevance and docking compatibility.The primary goal of this study is to assess
whether the identified compounds from P. perlatum can serve as effective drug candidates against parasitic infections,
offering a natural alternative to synthetic drugs in the fight against endemic protozoan disease.
Keywords :
Plasmodium, Entamoeba, Toxoplasma; Phytochemical Analysis, Molecular Docking, Calculated Affinity, Malaria, HSP 90, HSP70, Permotrema parlatum, GCMS, Resibufogenin, Thujopsin.