Université de Lorraine, Centre de Recherche en Automatique de Nancy (CRAN), UMR 7039, Vandœuvre-lès-Nancy, France.
PLoS One. 2012;7(11):e48617. doi: 10.1371/journal.pone.0048617. Epub 2012 Nov 7.
Nanoparticles are widely suggested as targeted drug-delivery systems. In photodynamic therapy (PDT), the use of multifunctional nanoparticles as photoactivatable drug carriers is a promising approach for improving treatment efficiency and selectivity. However, the conventional cytotoxicity assays are not well adapted to characterize nanoparticles cytotoxic effects and to discriminate early and late cell responses. In this work, we evaluated a real-time label-free cell analysis system as a tool to investigate in vitro cyto- and photocyto-toxicity of nanoparticles-based photosensitizers compared with classical metabolic assays. To do so, we introduced a dynamic approach based on real-time cell impedance monitoring and a mathematical model-based analysis to characterize the measured dynamic cell response. Analysis of real-time cell responses requires indeed new modeling approaches able to describe suited use of dynamic models. In a first step, a multivariate analysis of variance associated with a canonical analysis of the obtained normalized cell index (NCI) values allowed us to identify different relevant time periods following nanoparticles exposure. After light irradiation, we evidenced discriminant profiles of cell index (CI) kinetics in a concentration- and light dose-dependent manner. In a second step, we proposed a full factorial design of experiments associated with a mixed effect kinetic model of the CI time responses. The estimated model parameters led to a new characterization of the dynamic cell responses such as the magnitude and the time constant of the transient phase in response to the photo-induced dynamic effects. These parameters allowed us to characterize totally the in vitro photodynamic response according to nanoparticle-grafted photosensitizer concentration and light dose. They also let us estimate the strength of the synergic photodynamic effect. This dynamic approach based on statistical modeling furnishes new insights for in vitro characterization of nanoparticles-mediated effects on cell proliferation with or without light irradiation.
纳米粒子被广泛认为是靶向药物输送系统。在光动力疗法(PDT)中,使用多功能纳米粒子作为光激活药物载体是提高治疗效率和选择性的一种有前途的方法。然而,传统的细胞毒性测定方法并不适合于表征纳米粒子的细胞毒性作用,也不能区分早期和晚期的细胞反应。在这项工作中,我们评估了一种实时无标记细胞分析系统,作为一种工具,用于研究基于纳米粒子的光敏剂的体外细胞毒性和光细胞毒性,与经典的代谢测定方法相比。为此,我们引入了一种基于实时细胞阻抗监测和基于数学模型分析的动态方法,以表征测量的动态细胞反应。实时细胞反应的分析确实需要新的建模方法,这些方法能够描述动态模型的合适使用。在第一步中,我们对获得的归一化细胞指数(NCI)值进行了多元方差分析和典型分析,这使我们能够识别出纳米粒子暴露后不同的相关时间段。在光照后,我们以浓度和光剂量依赖的方式,证明了细胞指数(CI)动力学的判别谱。在第二步中,我们提出了一个与 CI 时间响应的混合效应动力学模型相关的完全析因实验设计。所估计的模型参数导致了对动态细胞反应的新的特征描述,例如对光诱导的动态效应的瞬态相的幅度和时间常数。这些参数使我们能够根据纳米粒子接枝光敏剂的浓度和光剂量来完全表征体外光动力反应。它们还让我们估计协同光动力效应的强度。这种基于统计建模的动态方法为研究有无光照的情况下,纳米粒子对细胞增殖的介导作用的体外特性提供了新的见解。
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