4.8 Article

Gadolinium-functionalised multi-walled carbon nanotubes as a T1 contrast agent for MRI cell labelling and tracking

Journal

CARBON
Volume 97, Issue -, Pages 126-133

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2015.08.051

Keywords

MWNTs; Gadolinium; HUVEC; Cell labelling; T-1-weighted MRI; Endosomal entrapment

Funding

  1. United Kingdom Engineering and Physical Sciences Research Council (EPSRC) [EP/G061882/1]
  2. European Commission FP-7 Marie Sklodowska Curie Actions-Career Development Research Fellowship (NANONEUROHOP) [PIEF-GA-2010-276051]
  3. EPSRC [EP/K005014/1, EP/G061882/1] Funding Source: UKRI
  4. Engineering and Physical Sciences Research Council [EP/G061882/1, EP/K005014/1] Funding Source: researchfish

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The development of efficient contrast agents for cell labelling coupled with powerful medical imaging techniques is of great interest for monitoring cell trafficking with potential clinical applications such as organ repair and regenerative medicine. In this paper, functionalised multi-walled carbon nanotubes (MWNTs) were engineered for cell labelling in T-1-weighted MRI applications. These sophisticated constructs were covalently functionalised with the gadolinium (Gd) chelating agent, diethylene triamine pentaacetic acid (DTPA), enabling tight attachment of Gd atoms onto the nanotube surface. The resulting Gd-labelled MWNTs were found to be stable over 2 weeks in water and mouse serum and high payload of Gd atoms could be loaded onto the nanotubes. The r(1) relaxivity of the Gd-MWNTs was a 3-fold higher than of the clinically approved T-1 contrast agent Magnevist at a magnetic field strength of 7T. The contrast efficiency, expressed as the r(1) relaxivity, of the Gd-MWNTs in Human Umbilical Vein Endothelial cells (HUVEC) was investigated at 7T and was found to be around 6.6 mM(-1) s(-1). There was no reduction of the contrast efficiency after internalisation in HUVECs, which was imparted to the ability of carbon nanotubes to translocate the cell membrane. (C) 2015 The Authors. Published by Elsevier Ltd.

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