Citation:
LIU Kai-Min, ZHANG Jun, XING Geng-Mei, ZHAO Yu-Liang. Synthesis and Usage of Gd@C82(OH)16 as MRI Contrast Agent[J]. Chinese Journal of Applied Chemistry,
;2007, 24(1): 90-94.
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Metallofullerene Gd@C82 was synthesized via electric arc method and separated by two-step HPLC with 95% purity, and its derivative Gd@C82(OH)x was synthesized by the reaction of Gd@C82 with NaOH catalyzed by tetrabutylammonium hydroxide(TBAH).The hydroxyl number of Gd@C82(OH)x was determined by XPS on its C1s spectrum and the compound was assigned as Gd@C82(OH)16.The proton relaxivity and MRI photographs of Gd@C82(OH)16 were evaluated in vitro and in vivo on a Bruker 4.7T/30 cm Biospec magnetic resonance imaging scanner.Results show that Gd@C82(OH)16 has a high proton relaxivity in vitro, even higher than that of (NMG)2-Gd-DTPA, which is the most popularly used MRI contrast agent clinically.Compared to that of (NMG)2-Gd-DTPA, relaxitivity R1 of Gd@C82(OH)16 increased 3 times, relaxitivity R2 increased 7 times.In vivo experiments found Gd@C82(OH)16 helped to generate high quality MRI photographs.The bio-distribution results indicate that Gd@C82(OH)16 tends to be entrapped in the liver and kidney and remained in these organs for about 2 hours.These results indicate that the metallofullerene derivative Gd@C82(OH)16 might be the potential candidate as a new MRI contrast agent.
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Keywords:
- metallofullerene,
- Gd@C82(OH)16,
- relaxivity,
- MRI contrast agent
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