Institute of Biodesign and Modeling of Complex Systems, Center of Bioelementology and Human Ecology, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.
Department of Hospital Surgery, Pirogov Russian National Research Medical University, 117997 Moscow, Russia.
Int J Mol Sci. 2023 Sep 24;24(19):14501. doi: 10.3390/ijms241914501.
In the ongoing search for practical uses of rare-earth metal nanoparticles, cerium dioxide nanoparticles (nanoceria) have received special attention. The purpose of this research was to study the biomedical effects of nanocrystalline forms of cerium oxide obtained by different synthesis schemes and to evaluate the effect of different concentrations of nanoceria (from 10 to 10 M) on cells involved in the regeneration of skin cell structures such as fibroblasts, mesenchymal stem cells, and keratinocytes. Two different methods of nanoceria preparation were investigated: (1) CeO-NPs-1 by precipitation from aqueous solutions of cerium (III) nitrate hexahydrate and citric acid and (2) CeO-NPs-2 by hydrolysis of ammonium hexanitratocerate (IV) under conditions of thermal autoclaving. According to the X-ray diffraction, transmission electron microscopy, and dynamic light scattering data, CeO-1 consists of individual particles of cerium dioxide (3-5 nm) and their aggregates with diameters of 60-130 nm. CeO-2 comprises small aggregates of 8-20 nm in diameter, which consist of particles of 2-3 nm in size. Cell cultures of human fibroblasts, human mesenchymal stem cells, and human keratinocytes were cocultured with different concentrations of nanoceria sols (10, 10, 10, 10, and 10 mol/L). The metabolic activity of all cell types was investigated by MTT test after 48 and 72 h, whereas proliferative activity and cytotoxicity were determined by quantitative cell culture counting and live/dead test. A dependence of biological effects on the method of nanoceria preparation and concentration was revealed. Data were obtained with respect to the optimal concentration of sol to achieve the highest metabolic effect in the used cell cultures. Hypotheses about the mechanisms of the obtained effects and the structure of a fundamentally new medical device for accelerated healing of skin wounds were formulated. The method of nanoceria synthesis and concentration fundamentally and significantly change the biological activity of cell cultures of different types-from suppression to pronounced stimulation. The best biological activity of cell cultures was determined through cocultivation with sols of citrate nanoceria (CeO-NPs-1) at a concentration of 10-10 M.
在寻找稀土金属纳米粒子实际用途的过程中,二氧化铈纳米粒子(纳米氧化铈)受到了特别关注。本研究的目的是研究通过不同合成方案获得的纳米晶氧化铈的生物医学效应,并评估不同浓度的纳米氧化铈(从 10 到 10 M)对参与皮肤细胞结构再生的细胞的影响,如成纤维细胞、间充质干细胞和角质细胞。研究了两种不同的纳米氧化铈制备方法:(1)通过硝酸铈(III)六水合物和柠檬酸的水溶液沉淀制备的 CeO-NPs-1,(2)通过在热高压釜条件下水解六硝酸高铈铵(IV)制备的 CeO-NPs-2。根据 X 射线衍射、透射电子显微镜和动态光散射数据,CeO-1 由二氧化铈(3-5nm)的单个颗粒及其直径为 60-130nm 的聚集体组成。CeO-2 由直径为 8-20nm 的小聚集体组成,这些小聚集体由 2-3nm 大小的颗粒组成。将人成纤维细胞、人间充质干细胞和人角质细胞的细胞培养物与不同浓度的纳米氧化铈溶胶(10、10、10、10 和 10 mol/L)共培养。在 48 和 72 小时后通过 MTT 试验研究所有细胞类型的代谢活性,而通过定量细胞培养计数和死活试验确定增殖活性和细胞毒性。揭示了生物效应与纳米氧化铈制备方法和浓度的依赖性。获得了在所用细胞培养物中实现最高代谢效应的溶胶最佳浓度的数据。提出了关于获得的效应的机制和用于加速皮肤伤口愈合的新型医疗设备的结构的假设。纳米氧化铈的合成方法和浓度从根本上显著改变了不同类型细胞培养物的生物活性-从抑制到明显的刺激。通过与浓度为 10-10 M 的柠檬酸纳米氧化铈(CeO-NPs-1)的溶胶共培养确定了细胞培养物的最佳生物活性。