Department of Energy, Environment and Health, Institute of Material Science of Madrid (ICMM-CSIC), Madrid, Spain.
Phys Chem Chem Phys. 2018 Jul 14;20(26):17829-17838. doi: 10.1039/c8cp03016b. Epub 2018 Jun 20.
The aggregation processes of magnetic nanoparticles in biosystems are analysed by comparing the magnetic properties of three systems with different spatial distributions of the nanoparticles. The first one is iron oxide nanoparticles (NPs) of 14 nm synthesized by coprecipitation with two coatings, (3-aminopropyl)trimethoxysilane (APS) and dimercaptosuccinic acid (DMSA). The second one is liposomes with encapsulated nanoparticles, which have different configurations depending on the NP coating (NPs attached to the liposome surface or encapsulated in its aqueous volume). The last system consists of two cell lines (Pan02 and Jurkat) incubated with the NPs. Dynamic magnetic behaviour (AC) was analysed in liquid samples, maintaining their colloidal properties, while quasi-static (DC) magnetic measurements were performed on lyophilised samples. AC measurements provide a direct method for determining the effect of the environment on the magnetization relaxation of nanoparticles. Thus, the imaginary (χ'') component shifts to lower frequencies as the aggregation state increases from free nanoparticles to those attached or embedded into liposomes in cell culture media and more pronounced when internalized by the cells. DC magnetization curves show no degradation of the NPs after interaction with biosystems in the analysed timescale. However, the blocking temperature is shifted to higher temperatures for the nanoparticles in contact with the cells, regardless of the location, the incubation time, the cell line and the nanoparticle coating, supporting AC susceptibility data. These results indicate that the simple fact of being in contact with the cells makes the nanoparticles aggregate in a non-controlled way, which is not the same kind of aggregation caused by the contact with the cell medium nor inside liposomes.
通过比较三种具有不同纳米粒子空间分布的系统的磁性能,分析了生物体系中磁性纳米粒子的聚集过程。第一个系统是通过共沉淀合成的具有两种涂层(3-氨丙基)三甲氧基硅烷(APS)和二巯基丁二酸(DMSA)的 14nm 氧化铁纳米粒子(NPs)。第二个系统是包裹纳米粒子的脂质体,其具有不同的配置,这取决于 NP 涂层(附着在脂质体表面的 NPs 或包裹在其水相中)。最后一个系统由用 NPs 孵育的两种细胞系(Pan02 和 Jurkat)组成。在保持胶体性质的液体样品中分析动态磁行为(AC),同时对冻干样品进行准静态(DC)磁测量。AC 测量提供了一种直接的方法来确定环境对纳米粒子磁化弛豫的影响。因此,随着从游离纳米粒子到附着在脂质体上或嵌入细胞培养介质中的脂质体中的聚集状态的增加,虚部(χ'‘)分量向更低的频率移动,并且当被细胞内化时更为明显。在分析的时间尺度内,与生物体系相互作用后,DC 磁化曲线未显示 NPs 的降解。然而,对于与细胞接触的纳米粒子,无论位置、孵育时间、细胞系和纳米粒子涂层如何,阻塞温度都转移到更高的温度,这支持了交流磁化率数据。这些结果表明,与细胞接触的简单事实使得纳米粒子以不受控制的方式聚集,这与与细胞介质接触或在脂质体内部引起的聚集不同。