Evaluation of intracellular distribution of
folate functionalized silica nanoparticles using fluorescence and hyperspectral enhanced dark field microscopy
Miclea, Luminita Claudia; Mihailescu, Mona; Tarba, Nicolae; Brezoiu, Ana-Maria; Sandu, Ana Maria; Mitran, Raul-Augustin; Berger, Daniela; Matei, Cristian; Moisescu, Mihaela Georgeta; Savopol, Tudor
Folic-Acid, Cell Turnover, Binding-Protein, Cancer, Delivery, Receptor, Expression, Cytotoxicity, Differentiation, Trafficking
Using nanoparticles as carriers for drug delivery systems has become a widely applied strategy in therapeutics and diagnostics. However, the pattern of their intracellular distribution is yet to be clarified. Here we present an in vitro study on the incorporation of mesoporous silica nanoparticles conjugated with folate and loaded with a cytotoxic drug, Irinotecan. The nanoparticles count and distribution within the cell frame were evaluated by means of enhanced dark field microscopy combined with hyperspectral imagery and 3D reconstructions from double-labeled fluorescent samples. An original post-processing procedure was developed to emphasize the nanoparticles’ localization in 3D reconstruction of cellular compartments. By these means, it has been shown that the conjugation of mesoporous silica nanoparticles with folate increases the efficiency of nanoparticles entering the cell and their preferential localization in the close vicinity of the nucleus. As revealed by metabolic viability assays, the nanoparticles functionalized with folate enhance the cytotoxic efficiency of Irinotecan.