Evaluation of Gossypium merserverium as an antimalarial agent: In vitro and computational studies

Enitan Omobolanle Adesanya , Akingbolabo Daniel Ogunlakin , Gideon Ampoma Gyebi , Omobolaji Olumide Odunayo , Mariam Oyindamola Odunlami , Adeola Victoria Ogunbowale , Damilare Ogundare , Timileyin Odusanya , Abraham Oluwalana Nkumah
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Abstract

Gossypium merserverium leaves' decoction has traditionally been used in treating malaria, but no scientific data exists. Therefore, this study investigates the antiplasmodial potential of the plant extract from Gossypium merserverium. The methanol extract was obtained through in vacuo concentration of the methanol extract of G. merserverium. Thereafter, the in vitro assay of the extract was tested for its 50 % inhibitory concentration (IC50) using the β-haematin inhibition assay. The Gas Chromatography-Mass Spectrometry (GC-MS) analysis was conducted to identify compounds present in the extract, and identified compounds in G. merserverium were subjected to computational analysis focusing on ICET. Methanolic extract of G. merserverium exhibited an IC50 value of 175.8 ± 0.02 μg/mL. The GC-MS analysis result identified 38 compounds, including Bis(2-ethylhexyl)phthalate, Thymol, Neophytadiene, Hexadecanoic acid methyl ester, and Phytol. In silico study on the compounds identified in Gossypium merserverium via GC-MS analysis, the ICET_Bis(2-ethylhexyl)phthalate showed the greatest variability, ranging from 35 to 45 ns. These findings offer a basis for future research into specific compounds responsible for their antiplasmodial properties and the nature of their interaction with chloroquine and other standard antimalarial drugs. This could optimize these extracts for malaria treatment.
棉花棉作为抗疟剂的评价:体外和计算研究
棉叶煎剂传统上用于治疗疟疾,但没有科学数据。因此,本研究探讨了棉花提取物的抗疟原虫潜能。用真空浓缩法对金银花甲醇提取物进行浓缩,得到甲醇提取物。然后,用β-血红素抑制法测定提取物的体外抑制浓度(IC50)为50 %。采用气相色谱-质谱(GC-MS)分析鉴定提取物中存在的化合物,并以ICET为重点对金银花中鉴定的化合物进行计算分析。金银花甲醇提取物的IC50值为175.8 ± 0.02 μg/mL。GC-MS分析结果鉴定出38个化合物,包括邻苯二甲酸双(2-乙基己基)酯、百里香酚、新叶二烯、十六酸甲酯和叶绿醇。通过气相色谱-质谱分析对棉花中鉴定的化合物进行了硅质谱研究,发现icet_双(2-乙基己基)邻苯二甲酸酯具有最大的变异性,范围在35 ~ 45 ns之间。这些发现为今后研究具有抗疟原虫特性的特定化合物及其与氯喹和其他标准抗疟疾药物相互作用的性质提供了基础。这可以优化这些提取物用于疟疾治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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