Department of Nanotechnology, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
J Biomol Struct Dyn. 2020 Jul;38(10):2945-2954. doi: 10.1080/07391102.2019.1650114. Epub 2019 Aug 8.
Studies on the anti-cancer effects of nanomaterials are a very important step in the clinical practice and treatment of cancerous tissues. Since IONPs have a high potential for cancer treatment, their anti-cancer properties can help us to resolve some of the therapeutic problems. For this purpose, in addition to synthesizing two types of IONPs including MN and MHN, Lf coating was used to increase their anti-cancer activity. MN and MHN were synthesized by hydrothermal and thermal methods, respectively, and their physicochemical properties were examined by SEM, zeta-potential, DLS, FTIR, TGA, and magnetism saturation. Molecular modelling was also done to model two steps of functionalization on the IONPs surface. In order to prove the biological activity of fabricated NPs experimental assays of NP cytotoxicity were performed on breast cancerous cells (4T1) by MTT and ROS assays. It was found that the MN and MHN have a diameter around 24 and 33 nm, respectively. Also, the hydrodynamic radius of MN and MHN coated with Lf were 30 and 38 nm, and their zeta potential values at pH = 7.5 were -5.3 and -4.2 mV, respectively. Besides, the results of TGA, magnetism saturation and FTIR showed that Lf was successfully loaded onto NPs. Molecular modelling investigation depicted that dimethylamine moiety of the linker provides an intense reactive region for non-bonding linkages with Lf molecules. Cellular studies exhibited that Lf increased the toxicity of NPs and synthesized Lf-MNs provide the highest potency both on mortality and ROS level. This research may provide promising data for development of potential anticancer agents.Communicated by Ramaswamy H. Sarma.
关于纳米材料抗癌效果的研究,是癌症组织临床实践和治疗中非常重要的一步。由于 IONPs 具有很高的癌症治疗潜力,因此其抗癌特性可以帮助我们解决一些治疗问题。为此,除了合成两种类型的 IONPs(MN 和 MHN)之外,还使用乳铁蛋白(Lf)涂层来提高它们的抗癌活性。MN 和 MHN 分别通过水热法和热解法合成,并通过 SEM、zeta 电位、DLS、FTIR、TGA 和磁化率饱和来检查其物理化学性质。还进行了分子建模,以模拟 IONPs 表面的两个功能化步骤。为了证明所制备的 NPs 的生物活性,通过 MTT 和 ROS 测定法在乳腺癌细胞(4T1)上进行了 NP 细胞毒性的实验研究。结果发现,MN 和 MHN 的直径分别约为 24nm 和 33nm。此外,Lf 涂层的 MN 和 MHN 的水动力半径分别为 30nm 和 38nm,其在 pH = 7.5 时的 zeta 电位值分别为-5.3mV 和-4.2mV。此外,TGA、磁化率饱和和 FTIR 的结果表明 Lf 已成功负载到 NPs 上。分子建模研究表明,连接体的二甲胺部分为与 Lf 分子形成非键合键提供了强烈的反应区域。细胞研究表明,Lf 增加了 NPs 的毒性,并且合成的 Lf-MNs 在死亡率和 ROS 水平上均具有最高的效力。这项研究可能为开发潜在的抗癌药物提供有希望的数据。