Comparative Pharmacological Evaluation of Mangrove Plant Xylocarpus mekongensis Pierre and Associated Fungus
Sadia Airin,
Rahul Dev Bairagi,
Sharika Noshin,
Md. Sohanur Rahaman,
Ritu Porna Biswas,
Amit Kumar Amit Kumar Acharzo and
Md. Amirul Islam
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Sadia Airin: Khulna University, Bangladesh
Rahul Dev Bairagi: Khulna University, Bangladesh
Sharika Noshin: Khulna University, Bangladesh
Md. Sohanur Rahaman: Khulna University, Bangladesh
Ritu Porna Biswas: Khulna University, Bangladesh
Amit Kumar Amit Kumar Acharzo: Khulna University, Bangladesh
Md. Amirul Islam: Khulna University, Bangladesh
European Journal of Pharmaceutical Research, 2023, vol. 3, issue 5, 11-15
Abstract:
Xylocarpus mekongensis commonly known as Poshur, is an evergreen mangrove plant originating from Asia, Indonesia, the Southwestern Pacific Islands, and northern Australia. This study was aimed at compiling information on the comparative pharmacological properties of the methanolic bark extract of X. mekongensis and the fungal endophyte based on their antioxidant, antimicrobial, and cytotoxic activity. The plant extract showed more phenolic (277 mg GAE/g) and flavonoid (140 mg QE/g) content than the fungal extract (45 mg GAE/g and 76 mg QE/g, respectively). The bark extract exhibited better DPPH scavenging capacity (IC50 = 28.27 µg/ml) than endophyte XMSF-I (IC50 = 143.46 µg/ml) extract. Furthermore, we observed that the endophytes associated with this plant showed more significant antimicrobial activity against E. coli, S. aureus, B. subtilis, and A. brasiliensis than its bark extract. In the brine shrimp lethality bioassay, the bark extract and endophyte revealed diminutive lethality (214 and 286 µg/ml, respectively) in comparison with standard vincristine sulfate (0.44 µg/ml). Hence, methanolic bark extract showed more positive reviews than associated fungi.
Keywords: Antioxidant; Antimicrobial; Cytotoxic; Fungus; Sundarban; Xylocarpus mekongensis (search for similar items in EconPapers)
Date: 2023
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Persistent link: https://EconPapers.repec.org/RePEc:epw:pharma:v:3:y:2023:i:5:id:773
DOI: 10.24018/ejpharma.2023.3.5.73
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