Sharif Digital Repository

Superparamagnetic iron oxide (SPIO) nanomaterials are widely used as magnetic resonance imaging (MRI) contrast agents (CAs). These CAs significantly shorten transverse relaxation time (T2) and so decrease the intensity of the T2-weighted MRI (negative contrast imaging). However, the partial-volume effect is known to be one of the problems in negative contrast MRI. In this work, SPIO nanoparticles were modified by dextran and graphene oxide (GO) nanosheets to achieve a positive contrast MRI with high intensity. This modification resulted in shortening the longitudinal relaxation time (T1) of the SPIO nanoparticles (in addition to the T2 shortening).... 

Graphene oxide (GO) has never been considered as a Magnetic Resonance Imaging (MRI) contrast agent since it was conceived as a diamagnetic material. There is a possibility that introduction of structural defects or manipulation of oxygen functionalities in GO change its magnetic response and provided a chance for GO to be a contrast agent for MRI. For this purpose, reduced graphene oxide (RGO) was treated by irradiation and annealing procedures. The study on the magnetic properties of the samples confirmed that the competition between the structural defects and oxygen functionalities to magnetic moments determines the magnetism in RGO. © 2018  

Recently, graphene oxide and its unconventional magnetism have attracted much interest due to their novel applications in spintronics, memory chips and theranostics. Owing to the excellent biocompatibility, cellular uptake, bio-conjugation possibilities, flexible chemical modification and characteristic broad-wavelength absorbance, graphene oxide and its derivatives have been utilized as contrast agents for various imaging modalities such as photoluminescence, photoacoustic or ultrasound. Despite their suitable applications in bioimaging and due to lack of magnetic moment, graphene oxide cannot confer magnetic resonance imaging contrast without incorporating the magnetic component. Such... 

Molecular imaging (MI) can provide not only structural images utilizing temporal imaging techniques, but also functional and molecular data using a variety of newly developed imaging techniques. Nanotechnology’s application in MI has commanded a lot of attention in recent decades, and it has provided tremendous potential for imaging living subjects. In this study, D-glucosamine conjugated functionalized magnetic iron oxide nanoparticles (Fe3O4-PEG-DG NPs) were prepared and studied as magnetic resonance imaging (MRI) contrast agents. To evaluate their distribution, single-photon emission computed tomography (SPECT) is performed. Fe3O4 NPs are made using a well-known co-precipitation process... 

In this research, a facile, two-step synthesis of Fe3O4–LCysteine–graphene quantum dots (GQDs) nanocomposite is reported. This synthesis method comprises the preparation of GQDs via hydrothermal route, which should be conjugated to the LCysteine functionalized core–shell magnetic structure with the core of about 7.5-nm iron oxide nanoparticle and 3.5-nm LCysteine shell. LCysteine, as a biocompatible natural amino acid, was used to link magnetite nanoparticles (MNPs) with GQDs. X-ray powder diffraction, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, energy dispersive X-ray were used to investigate the presence and formation of MNPs, L Cysteine functionalized MNPs,... 

In this research, a facile, two-step synthesis of Fe3O4–LCysteine–graphene quantum dots (GQDs) nanocomposite is reported. This synthesis method comprises the preparation of GQDs via hydrothermal route, which should be conjugated to the LCysteine functionalized core–shell magnetic structure with the core of about 7.5-nm iron oxide nanoparticle and 3.5-nm LCysteine shell. LCysteine, as a biocompatible natural amino acid, was used to link magnetite nanoparticles (MNPs) with GQDs. X-ray powder diffraction, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, energy dispersive X-ray were used to investigate the presence and formation of MNPs, L Cysteine functionalized MNPs,...