Water-Soluble Gadofullerenes: Toward High-Relaxivity, pH-Responsive MRI Contrast Agents

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Abstract
The water-soluble endohedral gadofullerene derivatives, [email protected]60(OH)x and [email protected]60[C(COOH)2]10, have been characterized with regard to their MRI contrast agent properties. Water-proton relaxivities have been measured in aqueous solution at variable temperature (278−335 K), and for the first time for gadofullerenes, relaxivities as a function of magnetic field (5 × 10-4 to 9.4 T; NMRD profiles) are also reported. Both compounds show relaxivity maxima at high magnetic fields (30−60 MHz) with a maximum relaxivity of 10.4 mM-1 s-1 for [email protected]60[C(COOH)2]10 and 38.5 mM-1 s-1 for [email protected]60(OH)x at 299 K. Variable-temperature, transverse and longitudinal 17O relaxation rates, and chemical shifts have been measured at three magnetic fields (B = 1.41, 4.7, and 9.4 T), and the results point exclusively to an outer sphere relaxation mechanism. The NMRD profiles have been analyzed in terms of slow rotational motion with a long rotational correlation time calculated to be τR298 = 2.6 ns. The proton exchange rate obtained for [email protected]60[C(COOH)2]10 is kex298 = 1.4 × 107 s-1 which is consistent with the exchange rate previously determined for malonic acid. The proton relaxivities for both gadofullerene derivatives increase strongly with decreasing pH (pH: 3−12). This behavior results from a pH-dependent aggregation of [email protected]60(OH)x and [email protected]60[C(COOH)2]10, which has been characterized by dynamic light scattering measurements. The pH dependency of the proton relaxivities makes these gadofullerene derivatives prime candidates for pH-responsive MRI contrast agent applications.

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