In Vitro Toxicology Group, Institute of Life Science, Swansea Univeristy Medical School, Swansea University, Singleton Park, Swansea, SA2 8PP, Wales, UK.
School of Chemical and Process Engineering, University of Leeds, Leeds LS2 9JT, UK.
Toxicol In Vitro. 2022 Sep;83:105415. doi: 10.1016/j.tiv.2022.105415. Epub 2022 Jun 13.
Due to the expansive application of TiO and its variance in physico-chemical characteristics, the toxicological profile of TiO, in all its various forms, requires evaluation. This study aimed to assess the hazard of five TiO particle-types in relation to their cytotoxic profile correlated to their cellular interaction, specifically in human lymphoblast (TK6) and type-II alveolar epithelial (A549) cells. Treatment with the test materials was undertaken at a concentration range of 1-100 μg/cm over 24 and 72 h exposure. TiO interaction with both cell types was visualised by transmission electron microscopy, supported by energy-dispersive X-ray. None of the TiO materials tested promoted cytotoxicity in either cell type over the concentration and time range studied. All materials were observed to interact with the A549 cells and were further noted to be internalised following 24 h exposure. In contrast, only the pigmentary rutile was internalised by TK6 lymphoblasts after 24 h exposure. Where uptake was observed there was no evidence, as determined by 2D microscopy techniques, of particle localisation within the nucleus of either cell type. This study indicates that industrially relevant TiO particles demonstrate cell interactions that are cell-type dependent and do not induce cytotoxicity at the applied dose range.
由于 TiO 的广泛应用及其物理化学特性的差异,需要对其所有形式的毒性特征进行评估。本研究旨在评估五种 TiO 颗粒类型的危害,以及它们与细胞相互作用相关的细胞毒性特征,特别是在人淋巴母细胞(TK6)和 II 型肺泡上皮(A549)细胞中。在 24 和 72 h 暴露的浓度范围内,将测试材料处理至 1-100 μg/cm。通过透射电子显微镜观察 TiO 与两种细胞类型的相互作用,并辅以能谱 X 射线。在所研究的浓度和时间范围内,没有一种 TiO 材料在两种细胞类型中促进细胞毒性。所有材料均被观察到与 A549 细胞相互作用,并在 24 h 暴露后进一步被观察到内化。相比之下,只有颜料金红石在 24 h 暴露后被 TK6 淋巴母细胞内化。在观察到摄取的情况下,通过 2D 显微镜技术,没有证据表明在任何一种细胞类型的核内存在颗粒定位。本研究表明,工业相关的 TiO 颗粒表现出细胞相互作用,这种相互作用依赖于细胞类型,并且在应用的剂量范围内不会诱导细胞毒性。