Villuendas Helena, Vilches Clara, Quidant Romain
Nanophotonic Systems Laboratory, Department of Mechanical and Process Engineering, ETH Zürich, 8092 Zürich, Switzerland.
ICFO - Institut de Ciències Fotòniques, the Barcelona Institute of Science and Technology, 08860 Castelldefels (Barcelona), Spain.
ACS Nanosci Au. 2022 Jul 27;2(6):494-502. doi: 10.1021/acsnanoscienceau.2c00023. eCollection 2022 Dec 21.
In plasmonic photothermal therapy (PPTT), illuminated gold nanoparticles are locally heated to produce selective damage in cells. While PPTT is expected to strongly depend on the cell line, available data are sparse and critical parameters remain unclear. To elucidate this pivotal aspect, we present a systematic study of diseased and nondiseased cells from different tissues to evaluate cytotoxicity, uptake of gold nanorods (AuNRs), and viability after PPTT. We identified differences in uptake and toxicity between cell types, linking AuNR concentrations to toxicity. Furthermore, the cell death mechanism is shown to depend on the intensity of the irradiated light and hence the temperature increase. Importantly, the data also underline the need to monitor cell death at different time points. Our work contributes to the definition of systematic protocols with appropriate controls to fully comprehend the effects of PPTT and build meaningful and reproducible data sets, key to translate PPTT to clinical settings.
在等离子体光热疗法(PPTT)中,受光照的金纳米颗粒会局部受热,从而对细胞产生选择性损伤。虽然预计PPTT在很大程度上取决于细胞系,但现有的数据稀少,关键参数仍不明确。为了阐明这一关键方面,我们对来自不同组织的病变细胞和非病变细胞进行了系统研究,以评估细胞毒性、金纳米棒(AuNRs)的摄取情况以及PPTT后的细胞活力。我们确定了不同细胞类型在摄取和毒性方面的差异,将AuNRs浓度与毒性联系起来。此外,细胞死亡机制显示取决于照射光的强度,进而取决于温度升高。重要的是,这些数据还强调了在不同时间点监测细胞死亡的必要性。我们的工作有助于定义具有适当对照的系统方案,以全面理解PPTT的效果,并建立有意义且可重复的数据集,这是将PPTT转化为临床应用的关键。