Cebadero-Domínguez Óscar, Diez-Quijada Leticia, López Sergio, Sánchez-Ballester Soraya, Puerto María, Cameán Ana M, Jos Angeles
Area of Toxicology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.
Department of Cell Biology, Faculty of Biology, Universidad de Sevilla, 41012 Seville, Spain.
Nanomaterials (Basel). 2023 Aug 9;13(16):2285. doi: 10.3390/nano13162285.
The growing interest in graphene derivatives is a result of their variety of applications in many fields. Due to their use, the oral route could be a potential way of entrance for the general population. This work assesses the biotransformation of reduced graphene oxide (rGO) after an in vitro digestion procedure (mouth, gastric, intestinal, and colon digestion), and its toxic effects in different cell models (HepG2, Caco-2, and 3D intestinal model). The characterization of rGO digestas evidenced the agglomeration of samples during the in vitro gastrointestinal (g.i.) digestion. Internalization of rGO was only evident in Caco-2 cells exposed to the colonic phase and no cellular defects were observed. Digestas of rGO did not produce remarkable cytotoxicity in any of the experimental models employed at the tested concentrations (up to 200 µg/mL), neither an inflammatory response. Undigested rGO has shown cytotoxic effects in Caco-2 cells, therefore these results suggest that the digestion process could prevent the systemic toxic effects of rGO. However, additional studies are necessary to clarify the interaction of rGO with the g.i. tract and its biocompatibility profile.
对石墨烯衍生物兴趣日增是因其在许多领域的多种应用。由于其应用,口服途径可能成为普通人群的潜在接触途径。本研究评估了还原氧化石墨烯(rGO)在体外消化过程(口腔、胃、小肠和结肠消化)后的生物转化及其在不同细胞模型(HepG2、Caco-2和3D肠道模型)中的毒性作用。rGO消化物的表征证明了样品在体外胃肠道消化过程中的团聚。rGO的内化仅在暴露于结肠阶段的Caco-2细胞中明显,且未观察到细胞缺陷。在测试浓度(高达200μg/mL)下,rGO消化物在任何所采用的实验模型中均未产生显著的细胞毒性,也未引发炎症反应。未消化的rGO在Caco-2细胞中显示出细胞毒性作用,因此这些结果表明消化过程可能会预防rGO的全身毒性作用。然而,需要进一步的研究来阐明rGO与胃肠道的相互作用及其生物相容性特征。