Abstract

Nanomaterial-based delivery platforms have indeed revolutionized drug delivery systems in recent years. These platforms, which are based on various types of nanoparticles, offer several advantages over traditional drug delivery systems. Therefore, during this work, we synthesized gold nanoparticles (GNPs) and graphene oxide (GO) as representative nanomaterials and assessed their biocompatibility and cytoplasmic localization in vitro. Structural characterization of the prepared nanoparticles was performed by using different techniques. For instance, laser diffraction spectrometry using a Nano-ZS Zetasizer was used to determine the particles size, and Zeta potential. High-resolution transmission electron microscopy (HR-TEM) were utilized to evaluate Particle sizes and morphologies of the prepared nanoparticles. Additionally, the chemical structure of the prepared nanoparticles was assessed by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The effects of the different concentrations of GNPs and GO nanosheets on cell viability and proliferation were evaluated by WST-1 cell proliferation assays. Ultimately, in vitro studies were performed by confocal microscopy to characterize the cellular uptake of the prepared nanoparticles. The net results of this study suggest that both nanomaterials showed a cytoplasmic entry without penetrating the nucleus. They may be useful for slow drug release as well as photothermal and photodynamic therapy using a low-powered laser or IR radiation.

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