​One of the main challenges in the treatment of genetic disorders, such as cancer, is of drug delivery systems and their inability to monitor and track delivered drug to the targeted site. Therefore, the design of novel with dual capabilities of nuclear drug delivery and tracking into a research priority for this field’s The aim of this study is to design based on both non-cytotoxic quantum dots and chimeric peptides, with dual tracking and delivering small genetic agents into the nucleus. The GQDs with green emission color were synthesized by Hummer’s and methods and characterized by UV-Vis, photoluminescence (PL), Raman spectroscopies, and scanning electron microscopy (SEM). conjugated with MPG-2H1 chimeric peptides through noncovalent interactions. Following conjugation step, the ζ-potential of the complex increased (From -38.6 to -11.1 in complex1, -9.6 in complex2 and -5.74 in complex3). The conjugation was confirmed by native acrylamide gel retardation assay. The of the GQDs was investigated by MTT assay and finally, was carried out. The results showed that MPG-2H1/ GQD complexes can enter cells; however, free-GQDs didn’t enter the cells significantly.

Graphene quantum dots (GQDs) have attracted increasing attention due to their unique properties such as high water solubility, photoluminescence activity, good biocompatibility, physical, chemical and electrical properties which makes them appropriate candidates for use in a variety of bio-applications, sensors and photocatalysts. The objective of this study is synthesis of GQDs and improving their surface properties via chemical modification.
Here, urea and citric acid as carbon precursor were used.  Citric acid was self-assembled into graphene framework via hydrothermal method at 160 °C for 4 h.  Then, the synthesized GQDs were carbonized and chemically activated by KOH treatment. The surface area and pore structures of GQDs were analyzed by nitrogen adsorption/desorption isotherms. The results showed that the specific surface area of carbonized-activated graphene quantum dots (CA-GQDs) have been increased from 0.06 to 1204.0 m²/g and pore structures have been enhanced significantly. The XRD pattern of GQDs confirmed the basic structure of graphite layer. The TEM images indicated the unique morphology of GQDs and the sizes of GQDs  were less than 5 nm. Thus, our applied method is an effective approach in the formation of GQDs with large BET surface area and narrow pore structures which reveals their potential applicability in biomedical field.