Gadolinium‐containing carbon nanomaterials are a new class of contrast agent for magnetic resonance imaging. They are characterized by a superior proton relaxivity to any current commercial gadolinium contrast agent and offer the possibility to design multifunctional contrasts. Intense efforts have been made to develop these nanomaterials because of their potential for better results than the available gadolinium contrast agents. The aim of the present work is to provide a review of the advances in research on gadolinium‐containing carbon nanomaterials and their advantages over conventional gadolinium contrast agents. Due to their enhanced proton relaxivity, they can provide a reliable imaging contrast for cells, tissues or organs with much smaller doses than currently used in clinical practice, thus leading to reduced toxicity (as shown by cytotoxicity and biodistribution studies). Their active targeting capability allows for improved MRI of molecular or cellular targets, overcoming the limited labelling capability of available contrast agents (restricted to physiological irregularities during pathological conditions). Their potential of multifunctionality encompasses multimodal imaging and the combination of imaging and therapy.

Gold nanoparticles (AuNPs) are considered valuable nanomaterials for the design of radiolabeled nanoprobes for single-photon emission computed tomography (SPECT) imaging. Radiolabeled and functionalized AuNPs could improve lymphatic mapping by enhancing the radioactive signaling of individual particles in the sentinel node. In this study, an alternative method for functionalizing commercial AuNps with mannose is described. The chemical derivatization and biofunctionalization of AuNPs were performed with lipoic acid and mannose, respectively. Several levels of mannose were tested; the thiolate hydrazinonicotinamide-glycine-glycine-cysteine (HYNIC) molecule was also used for ^99mTc radiolabeling. Physicochemical characterization of this system includes U-V spectroscopy, dynamic light scattering, Fourier-transform infrared spectroscopy, and transmission electron microscopy. The most stable nanoprobe, in terms of the aggregation, radiolabeling efficiency, and purity, was tested in a sentinel lymph node model in a rat by microSPECT/computed tomography (CT) imaging. The SPECT images revealed that ^99mTc-radiolabeled AuNPs functionalized with mannose can track and accumulate in lymph nodes in a similar way to the commercial ^99mTc-Sulfur colloid, commonly used in clinical practice for sentinel lymph node detection. These promising results support the idea that ^99mTc-AuNPs-mannose could be used as a SPECT contrast agent for lymphatic mapping.

Coralline red algae assimilate HCO3– to precipitate CaCO3 in their tissues in the form of calcite or aragonite. A characterization of the biomolecular content and the crystalline structure of the biomineral of coralline red algae from the Pacific coast of Mexico was performed by powder X-ray diffraction (XRD), scanning electron (SEM) and tunneling microscopy (STM), and Fourier transform infrared spectroscopy (FTIR). The preliminary conclusion drawn from the results is that this type of calcite-aragonite biomineral has a very low organic content occluded within the crystals. FTIR bands at 2945 and 2889 cm–1 indicate that the most likely organic molecules are carbohydrates; moreover, peptide bond bands (amide I ~1640 and amide II ~1540 cm–1) were not detected, suggesting that proteins are not related to mineral synthesis or their stabilization. This could be explained if the biomineral is synthesized by a biologically controlled extracellular mineralization process. The XRD study showed two main mineral phases, calcite and aragonite, with very similar structural parameters to the inorganic mineral counterparts. The crystallite shapes, seen by STM, were found as plates and needles with different sizes, between 20 and 100 nm.