Physicochemical characterization of a novel graphene-based magnetic resonance imaging contrast agent

79Citations
Citations of this article
66Readers
Mendeley users who have this article in their library.

Abstract

We report the synthesis and characterization of a novel carbon nanostructure-based magnetic resonance imaging contrast agent (MRI CA); graphene nanoplatelets intercalated with manganese (Mn2+) ions, functionalized with dextran (GNP-Dex); and the in vitro assessment of its essential preclinical physicochemical properties: osmolality, viscosity, partition coefficient, protein binding, thermostability, histamine release, and relaxivity. The results indicate that, at concentrations between 0.1 and 100.0 mg/mL, the GNP-Dex formulations are hydrophilic, highly soluble, and stable in deionized water, as well as iso-osmolar (upon addition of mannitol) and isoviscous to blood. At potential steady-state equilibrium concentrations in blood (0.1-10.0 mg/mL), the thermostability, protein-binding, and histamine-release studies indicate that the GNP-Dex formulations are thermally stable (with no Mn2+ ion dissociation), do not allow non-specific protein adsorption, and elicit negligible allergic response. The r1 relaxivity of GNP-Dex was 92 mM-1s-1 (per-Mn2+ ion, 22 MHz proton Larmor frequency); ~20- to 30-fold greater than that of clinical gadolinium (Gd3+)- and Mn2+-based MRI CAs. The results open avenues for preclinical in vivo safety and efficacy studies with GNP-Dex toward its development as a clinical MRI CA. © 2013 Kanakia et al, publisher and licensee Dove Medical Press Ltd.

Cite

CITATION STYLE

APA

Kanakia, S., Toussaint, J. D., Mullick Chowdhury, S., Lalwani, G., Tembulkar, T., Button, T., … Sitharaman, B. (2013). Physicochemical characterization of a novel graphene-based magnetic resonance imaging contrast agent. International Journal of Nanomedicine, 8, 2821–2833. https://doi.org/10.2147/IJN.S47062

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free