Alanazy Eman A, Ali Daoud, Almarzoug Mohammed H A, Yaseen Khadijah N, Almutairi Bader O, Alkahtani Saad, Aldahmash Badr A, Alarifi Saud
Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Dose Response. 2025 Jul 11;23(3):15593258251360056. doi: 10.1177/15593258251360056. eCollection 2025 Jul-Sep.
In this study we used biosynthesis methods to create bimetallic nickel cobalt nanoparticles (Ni-Co NPs) utilizing seaweed. Before exposure to target cells, the characterization of Ni-Co NPs is done by UV-Vis spectrophotometry, EDX, SEM, TEM, the shape of g Ni-Co NPs are polygonal form and its size is measured 38.27 ± 3 nm. The cytotoxic effect of g Ni-Co NPs on HuH7 and HCT cells were determined by MTT and NRU assays. The cytotoxicity of NPs increased in a concentration dependent manner and it showed high cytotoxic effect on HCT-116 cells than HuH-7 cells. We determined IC 24 h for HuH-7 and HCT -116 cells at 24 h, it was 65.84 and 24.73 μg/mL, respectively. ROS was elevated at higher concentration of Ni-Co NPs. LPO was increased at 16 μg/mL in HuH-7 cells and 19 μg/mL in HCT-116 cells. CAT was reduced in HCT-116 cells than HuH-7 cells high concentration of NPs. JC-1 staining, the loss of MMP in control, Ni-Co NPs exposed cell were evaluated. In HuH-7 and HCT-116 cells, maximum apoptotic cells were observed at high concentration. Apoptotic genes were expressed in both type cells. The above findings highlight the significance of Ni-Co NPs and useful in a number of cancer treatments.
在本研究中,我们使用生物合成方法利用海藻制备双金属镍钴纳米颗粒(Ni-Co NPs)。在将其暴露于靶细胞之前,通过紫外可见分光光度法、能谱仪、扫描电子显微镜、透射电子显微镜对Ni-Co NPs进行表征,发现其形状为多边形,尺寸为38.27±3纳米。通过MTT和NRU测定法确定了Ni-Co NPs对HuH7和HCT细胞的细胞毒性作用。NPs的细胞毒性呈浓度依赖性增加,并且对HCT-116细胞的细胞毒性作用高于HuH-7细胞。我们测定了HuH-7和HCT -116细胞在24小时时的IC 24 h,分别为65.84和24.73μg/mL。在较高浓度的Ni-Co NPs下ROS升高。在HuH-7细胞中,16μg/mL时LPO增加,在HCT-116细胞中,19μg/mL时LPO增加。在高浓度NPs下,HCT-116细胞中的CAT比HuH-7细胞减少。通过JC-1染色评估了对照细胞、暴露于Ni-Co NPs的细胞中膜电位的丧失情况。在HuH-7和HCT-116细胞中,在高浓度下观察到最大数量的凋亡细胞。两种类型的细胞中均表达了凋亡基因。上述发现突出了Ni-Co NPs的重要性,并且在多种癌症治疗中具有应用价值。