Gnerucci Alessio, Romano Giovanni, Ratto Fulvio, Centi Sonia, Baccini Michela, Santosuosso Ugo, Pini Roberto, Fusi Franco
Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, viale Pieraccini 6, I-50139 Florence, Italy.
Institute of Applied Physics "Nello Carrara", National Research Council, via Madonna del Piano 10, I-50019 Sesto Fiorentino, Italy.
Phys Med. 2016 Jul;32(7):938-43. doi: 10.1016/j.ejmp.2016.06.007. Epub 2016 Jul 2.
In the fields of nanomedicine, biophotonics and radiation therapy, nanoparticle (NP) detection in cell models often represents a fundamental step for many in vivo studies. One common question is whether NPs have or have not interacted with cells. In this context, we propose an imaging based technique to detect the presence of NPs in eukaryotic cells. Darkfield images of cell cultures at low magnification (10×) are acquired in different spectral ranges and recombined so as to enhance the contrast due to the presence of NPs. Image analysis is applied to extract cell-based parameters (i.e. mean intensity), which are further analyzed by statistical tests (Student's t-test, permutation test) in order to obtain a robust detection method. By means of a statistical sample size analysis, the sensitivity of the whole methodology is quantified in terms of the minimum cell number that is needed to identify the presence of NPs. The method is presented in the case of HeLa cells incubated with gold nanorods labeled with anti-CA125 antibodies, which exploits the overexpression of CA125 in ovarian cancers. Control cases are considered as well, including PEG-coated NPs and HeLa cells without NPs.
在纳米医学、生物光子学和放射治疗领域,在细胞模型中检测纳米颗粒(NP)通常是许多体内研究的基本步骤。一个常见的问题是纳米颗粒是否与细胞发生了相互作用。在此背景下,我们提出一种基于成像的技术来检测真核细胞中纳米颗粒的存在。在不同光谱范围内获取低倍(10×)细胞培养物的暗场图像,并进行重组,以增强由于纳米颗粒的存在而产生的对比度。应用图像分析来提取基于细胞的参数(即平均强度),然后通过统计检验(学生t检验、排列检验)进行进一步分析,以获得一种可靠的检测方法。通过统计样本量分析,根据识别纳米颗粒存在所需的最小细胞数来量化整个方法的灵敏度。该方法以用抗CA125抗体标记的金纳米棒孵育的HeLa细胞为例进行了介绍,该方法利用了卵巢癌中CA125的过表达。同时也考虑了对照情况,包括聚乙二醇包被的纳米颗粒和没有纳米颗粒的HeLa细胞。