In this study, we determined the potential of polyethylene glycol-encapsulated iron oxide nanoparticles (IONP) for the intracellular delivery of the chemotherapeutic doxorubicin (IONP) to enhance the cytotoxic effects of ionizing radiation. The biological effects of IONP and X-ray irradiation (50 kV and 6 MV) were determined in HeLa cells using the colony formation assay (CFA) and detection of γH2AX foci. Data are presented as mean ± SEM.
View Article and Find Full Text PDFThe purpose of this study was to construct and characterize iron oxide nanoparticles (IONP) for intracellular delivery of the anthracycline doxorubicin (DOX; IONP) in order to induce tumor cell inactivation. More than 80% of the loaded drug was released from IONP within 24 h (100% at 70 h). Efficient internalization of IONP and IONP in HeLa cells occurred through pino- and endocytosis, with both IONP accumulating in a perinuclear pattern.
View Article and Find Full Text PDFLocalization microscopy has shown to be capable of systematic investigations on the arrangement and counting of cellular uptake of gold nanoparticles (GNP) with nanometer resolution. In this article, we show that the application of specially modified RNA targeting gold nanoparticles ("SmartFlares") can result in ring like shaped GNP arrangements around the cell nucleus. Transmission electron microscopy revealed GNP accumulation in vicinity to the intracellular membrane structures including them of the endoplasmatic reticulum.
View Article and Find Full Text PDFPodocytes are lost by detachment from the GBM as viable cells; details are largely unknown. We studied this process in the rat after growth stimulation with FGF-2. Endothelial and mesangial cells responded by hyperplasia, podocytes underwent hypertrophy, but, in the long run, developed various changes that could either be interpreted showing progressing stages in detachment from the GBM or stages leading to a tighter attachment by foot process effacement (FPE).
View Article and Find Full Text PDFUnlabelled: Gold nanoparticles (GNP) enhance the absorbance of photons thereby increasing emission of Auger-/photoelectrons in the nm-μm range. Yet, a major disadvantage is their diameter-dependent cellular uptake with an optimum of ~50 nm which may not offer optimal radiosensitization. A method was developed to enhance the uptake of small GNP.
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