Bioindustrial Technology Program, Faculty of Agro-Based Industry, Universiti Malaysia Kelantan, Campus Jeli, 17600 Jeli, Malaysia.
Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
Biomed Res Int. 2021 Sep 29;2021:5125681. doi: 10.1155/2021/5125681. eCollection 2021.
Studies on green biosynthesis of newly engineered nanoparticles for their prominent medicinal applications are being the torch-bearing concerns of the state-of-the-art research strategies. In this concern, we have engineered the biosynthesized silver nanoparticles of flavonoid -glycosides in the anisotropic form isolated from aqueous leave extracts of , a popular traditional and ayurvedic plant in south-east Asian countries. These were structurally confirmed by Ultraviolet-visible (UV-Vis), Fourier transform infrared spectroscopy accessed with attenuated total reflection (FTIR-ATR) spectral analyses followed by the scanning electron microscopic (SEM) and the X-ray diffraction (XRD) crystallographic studies and found them with the face-centered cubic () structure. Medicinally, we have explored their significant antioxidant (DPPH and ABTS assays), antibacterial (disc diffusion assay on , , , , and ), and anticancer (MTT assay on MCF-7, MDA-MB-231, U87, and DBTRG cell lines) potentialities which augmented the present investigation. The molecular docking analysis of title compounds against 3NM8 (DPPH) and 1DNU (ABTS) proteins for antioxidant activity; 5FGK (Gram-Positive Bacteria) and 1AB4 (Gram-Negative Bacteria) proteins for antibacterial activity; and 4GBD (MCF-7), 5FI2 (MDA-MB-231), 1D5R (U87), and 5TIJ (DBTRG) proteins for anticancer activity has affirmed the promising ligand-protein binding interactions among the hydroxy groups of the title compounds and aspartic acid of the concerned enzymatic proteins. The binding energy varying from -9.1645 to -7.7955 for Cosmosioside (1, Apigenin-7-glucoside) and from -9.2690 to -7.8306 for Cynaroside (2, Luteolin-7-glucoside) implies the isolated compounds as potential bioactive compounds. In addition, the performed studies like QSAR, ADMET, bioactivity properties, drug scores, and toxicity risks confirmed them as potential drug candidates and aspartic acid receptor antagonists. This research auxiliary augmented the existing array of phytological nanomedicines with new drug candidates that are credible with multiple bioactivities.
关于新工程纳米粒子的绿色生物合成及其在医学上的突出应用的研究,是当前最先进的研究策略的关注焦点。在这方面的研究中,我们已经成功地在各向异性形式下合成了黄酮苷类生物合成的银纳米粒子,这些纳米粒子是从东南亚国家流行的传统和阿育吠陀植物 的水提物中分离出来的。这些纳米粒子的结构通过紫外可见(UV-Vis)、傅里叶变换红外光谱(FTIR-ATR)光谱分析得到了证实,并通过扫描电子显微镜(SEM)和X 射线衍射(XRD)晶体学研究得到了进一步的确认,结果表明这些纳米粒子具有面心立方(fcc)结构。在医学上,我们探索了它们显著的抗氧化(DPPH 和 ABTS 测定)、抗菌(在 、 、 、 和 上进行的圆盘扩散测定)和抗癌(在 MCF-7、MDA-MB-231、U87 和 DBTRG 细胞系上进行的 MTT 测定)潜力,这增强了本研究。标题化合物对 3NM8(DPPH)和 1DNU(ABTS)蛋白的抗氧化活性的分子对接分析;对 5FGK(革兰氏阳性菌)和 1AB4(革兰氏阴性菌)蛋白的抗菌活性的分子对接分析;以及对 4GBD(MCF-7)、5FI2(MDA-MB-231)、1D5R(U87)和 5TIJ(DBTRG)蛋白的抗癌活性的分子对接分析,证实了标题化合物的羟基与相关酶蛋白的天冬氨酸之间存在有前途的配体-蛋白结合相互作用。Cosmosioside(1,芹菜素-7-葡萄糖苷)的结合能从-9.1645 到-7.7955,而 Cynaroside(2,木樨草素-7-葡萄糖苷)的结合能从-9.2690 到-7.8306,这表明分离得到的化合物具有潜在的生物活性。此外,QSAR、ADMET、生物活性特性、药物评分和毒性风险等研究也证实了它们作为潜在药物候选物和天冬氨酸受体拮抗剂的可能性。这项研究辅助增加了新的药物候选物,使现有的植物纳米药物具有更多的生物活性。