A Alsubeie Moodi S, Ibrahim Nasir A, Alghamdi Ahmed A, Basher Nosiba S, Al-Ammari B S, Dafaallah Awadallah B, Veettil Vajid Nettoor
Department of Biology, Faculty of Science, Imam Mohammed Ibn Saud Islamic University, Riyadh, Saudi Arabia.
National Center for Vegetation Cover Development and Combating Desertification (NCVC), Ministry of Environment, Water and Agriculture, Riyadh, Kingdom of Saudi Arabia.
Bioinformation. 2024 May 31;20(5):487-494. doi: 10.6026/973206300200487. eCollection 2024.
The cytotoxic, antioxidant, anticancer, and antibacterial properties of ethanolic extracts from is of interest. Plants of were gathered from the southern Saudi Arabian region of Albaha. extract was assessed using DPPH (2, 2-diphenyl-1-picrylhydrazyl). The German Collection of Microorganisms and Cell Cultures (DSMZ) cancer cell lines used in this investigation. The cytotoxic activity of extract was explored against MCF-7 breast and A549 lung cancer cell lines, along with doxorubicin as a positive control. In both treated cells, showed a remarkable activity suppressing the cell's survival. In terms of IC50 (concentration equivalent to a survival rate of 50%), MCF-7 breast cancer cells were more sensitive to extract.) DPPH colorimetric assay was employed to assess the antioxidant properties of extract, the antioxidant activity was increased along with increment of extract concentrations. The leaves aqueous extract of inhibited the growth of by 6.3±0.12 mm and 24±0.43 mm and 15±0.56 mm respectively for seed, leaf and stem at concentrations 50 µl. However, the same concentrations inhibited the growth of by 25±0.75, 0.00 mm and 24±0.18 mm, following the same order. Different superscript letters indicate means that are significantly different at level (p<0.05). Minimal inhibitory concentrations (MIC) of ethanolic extracts against the tested microorganisms were 1.5, 1.6 and 1.5, respectively for seed, leaf and stem against and were 1.2, 0.00 and 1.2, respectively for seed, leaf and stem against .
来自[植物名称未提及]的乙醇提取物的细胞毒性、抗氧化、抗癌和抗菌特性备受关注。[植物名称未提及]的植物采集自沙特阿拉伯南部的阿尔巴哈地区。使用DPPH(2,2 - 二苯基 - 1 - 苦基肼)评估提取物。本研究使用了德国微生物和细胞培养物保藏中心(DSMZ)的癌细胞系。研究了[植物名称未提及]提取物对MCF - 7乳腺癌细胞系和A549肺癌细胞系的细胞毒性活性,同时以阿霉素作为阳性对照。在两种处理的细胞中,[植物名称未提及]提取物均显示出显著的抑制细胞存活的活性。就IC50(相当于50%存活率的浓度)而言,MCF - 7乳腺癌细胞对[植物名称未提及]提取物更敏感。采用DPPH比色法评估[植物名称未提及]提取物的抗氧化特性,抗氧化活性随提取物浓度的增加而增强。在50微升浓度下,[植物名称未提及]的叶水提取物对种子、叶和茎的抑制生长分别为6.3±0.12毫米、24±0.43毫米和15±0.56毫米。然而,相同浓度下对[细菌名称未提及]的生长抑制分别为25±0.75毫米、0.00毫米和24±0.18毫米,顺序相同。不同的上标字母表示在水平(p<0.05)上有显著差异的均值。[植物名称未提及]乙醇提取物对受试微生物的最低抑菌浓度(MIC),对[细菌名称未提及]而言,种子、叶和茎分别为1.5、1.6和1.5,对[细菌名称未提及]而言,种子、叶和茎分别为1.2、0.00和1.2。