posted on 2012-07-25, 00:00authored byMingming Zhen, Junpeng Zheng, Lei Ye, Shumu Li, Chan Jin, Kai Li, Dong Qiu, Hongbin Han, Chunying Shu, Yongji Yang, Chunru Wang
Macromolecular magnetic resonance imaging (MRI) contrast
agent
Gd-DTPA-HSA (DTPA, diethylene triamine pentacetate acid; HSA, human
serum albumin) as a model has been successfully conjugated with trimalonic
acid modified C60 for contrast enhancement at clinically
used magnetic field strength. The Gd-DTPA-HSA-C60 conjugate
exhibit maximal relaxivity (r1 = 86 mM–1 s–1 at 0.5 T, 300 K) reported so
far, which is much superior to that of the control Gd-DTPA-HSA (r1 = 38 mM–1 s–1) under the same condition and comparable to the theoretical maximum
(r1 = 80–120 mM–1 s–1, at 20 MHz and 298 K), indicating the synergistic
effect of HSA and carboxylfullerene on the increased contrast enhancement.
TEM characterization reveals that both Gd-DTPA-HSA-C60 and
Gd-DTPA-HSA can penetrate the cells via endocytosis and trans-membrane,
respectively, suggesting the potential to sensitively image the events
at the cellular and subcellular levels. In addition, the fusion of
fullerene with Gd-DTPA-HSA will further endow the resulting complex
with photodynamic therapy (PDT) property and thus combine the modalities
of therapy (PDT) and diagnostic imaging (MRI) into one entity. More
importantly, the payloaded Gd-DTPA may substitute for other more stable
Gd-DOTA and HSA as a theranostic package can further work as a drug
delivery carrier and effectively control drug release through proteolysis.