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The work describes the synthesis and in vivo application of Au@GdL (L
=
DTPA-bis(amide) conjugate of cysteine) as a highly efficient MRI/CT multimodal contrast agent.
The synthesis and characterization of gold nanoparticles coated with Gd-chelate (Au@GdL), where L is a conjugate of DTPA and cysteine, is described. These particles are obtained by the replacement of citrate from the gold nanoparticle surfaces with gadolinium chelate (GdL). The average size of Au@GdL is 14
nm with a loading of GdL reaching up to 2.9
×
10
3 per particles, and they demonstrate very high R1 relaxivity (∼10
5
mM
−1
s
−1) as well as X-ray attenuation. The R1 relaxivity per [Gd] is 17.9
mM
−1
s
−1. The present system also exhibits macrophage-specific property, as demonstrated by histological and TEM images as well as CT and MR, rendering itself as a new class of T1 multimodal CT/MR contrast agent.