Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, Kuala Nerus, Terengganu, Malaysia.
Pharmaceutical Biotechnology Laboratory, Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Microsc Res Tech. 2024 Mar;87(3):602-615. doi: 10.1002/jemt.24437. Epub 2023 Nov 28.
This study aimed to investigate the characterization of zinc oxide nanoparticles (ZnONPs) produced from Cucurbita pepo L. (pumpkin seeds) and their selective cytotoxic effectiveness on human colon cancer cells (HCT 116) and African Green Monkey Kidney, Vero cells. The study also investigated the antioxidant activity of ZnONPs. The study also examined ZnONPs' antioxidant properties. This was motivated by the limited research on the comparative cytotoxic effects of ZnO NPs on normal and HCT116 cells. The ZnO NPs were characterized using Fourier-transform infrared spectroscopy (FTIR), Thermogravimetric Analysis (TGA), Transmission Electron Microscope/Selected Area Electron Diffraction (TEM/SAED), and Scanning Electron Microscope-Energy Dispersive X-ray (SEM-EDX) for determination of chemical fingerprinting, heat stability, size, and morphology of the elements, respectively. Based on the results, ZnO NPs from pumpkins were found to be less than 5 μm and agglomerates in nature. Furthermore, the ZnO NPs fingerprinting and SEM-EDX element analysis were similar to previous literature, suggesting the sample was proven as ZnO NPs. The ZnO NPs also stable at a temperature of 380°C indicating that the green material is quite robust at 60-400°C. The cell viability of Vero cells and HCT 116 cell line were measured at two different time points (24 and 48 h) to assess the cytotoxicity effects of ZnO NP on these cells using AlamarBlue assay. Cytotoxic results have shown that ZnO NPs did not inhibit Vero cells but were slightly toxic to cancer cells, with a dose-response curve IC50 = ~409.7 μg/mL. This green synthesis of ZnO NPs was found to be non-toxic to normal cells but has a slight cytotoxicity effect on HCT 116 cells. A theoretical study used molecular docking to investigate nanoparticle interaction with cyclin-dependent kinase 2 (CDK2), exploring its mechanism in inhibiting CDK2's role in cancer. Further study should be carried out to determine suitable concentrations for cytotoxicity studies. Additionally, DPPH has a significant antioxidant capacity, with an IC50 of 142.857 μg/mL. RESEARCH HIGHLIGHTS: Pumpkin seed extracts facilitated a rapid, high-yielding, and environmentally friendly synthesis of ZnO nanoparticles. Spectrophotometric analysis was used to investigate the optical properties, scalability, size, shape, dispersity, and stability of ZnO NPs. The cytotoxicity of ZnO NPs on Vero and HCT 116 cells was assessed, showing no inhibition of Vero cells and cytotoxicity of cancer cells. The DPPH assay was also used to investigate the antioxidant potential of biogenic nanoparticles. A molecular docking study was performed to investigate the interaction of ZnO NPs with CDK2 and to explore the mechanism by which they inhibit CDK2's role in cancer.
本研究旨在探究由南瓜(Cucurbita pepo L.)种子制备的氧化锌纳米粒子(ZnONPs)的特性及其对人结肠癌细胞(HCT 116)和非洲绿猴肾,Vero 细胞的选择性细胞毒性作用。本研究还探究了 ZnONPs 的抗氧化活性。这是因为关于 ZnO NPs 对正常细胞和 HCT116 细胞的比较细胞毒性作用的研究有限。使用傅里叶变换红外光谱(FTIR)、热重分析(TGA)、透射电子显微镜/选区电子衍射(TEM/SAED)和扫描电子显微镜-能量色散 X 射线(SEM-EDX)对 ZnO NPs 进行了表征,分别用于确定化学指纹、热稳定性、尺寸和元素形貌。基于结果,发现南瓜来源的 ZnO NPs 小于 5μm,且为自然团聚体。此外,ZnO NPs 的指纹图谱和 SEM-EDX 元素分析与先前的文献相似,表明该样品被确认为 ZnO NPs。ZnO NPs 在 380°C 的温度下也很稳定,表明该绿色材料在 60-400°C 下相当稳定。使用 AlamarBlue 测定法在两个不同的时间点(24 和 48 h)测量 Vero 细胞和 HCT 116 细胞系的细胞活力,以评估 ZnO NP 对这些细胞的细胞毒性作用。细胞毒性结果表明,ZnO NPs 对 Vero 细胞没有抑制作用,但对癌细胞有轻微毒性,半抑制浓度(IC50)约为 409.7μg/mL。这种绿色合成的 ZnO NPs 被发现对正常细胞无毒,但对 HCT 116 细胞有轻微的细胞毒性作用。理论研究使用分子对接来研究纳米颗粒与细胞周期蛋白依赖性激酶 2(CDK2)的相互作用,探索其抑制 CDK2 在癌症中作用的机制。应进一步进行研究以确定用于细胞毒性研究的合适浓度。此外,DPPH 具有显著的抗氧化能力,IC50 为 142.857μg/mL。研究亮点:南瓜籽提取物促进了 ZnO 纳米粒子的快速、高产和环保合成。分光光度分析用于研究 ZnO NPs 的光学性质、可扩展性、尺寸、形状、分散性和稳定性。评估了 ZnO NPs 对 Vero 和 HCT 116 细胞的细胞毒性,结果表明对 Vero 细胞无抑制作用,对癌细胞有细胞毒性。还使用 DPPH 测定法研究了生物纳米颗粒的抗氧化潜力。进行了分子对接研究,以研究 ZnO NPs 与 CDK2 的相互作用,并探索它们抑制 CDK2 在癌症中作用的机制。