Assessment of T1 and T effects in vivo and ex vivo using iron oxide nanoparticles in steady state—dependence on blood volume and water exchange

Abstract

Accurate knowledge of the relationship between contrast agent concentration and tissue relaxation is a critical requirement for quantitative assessment of tissue perfusion using contrast‐enhanced MRI. In the present study, using a pig model, the relationship between steady‐state blood concentration levels of an iron oxide nanoparticle with a hydrated diameter of 12 nm (NC100150 Injection) and changes in the transverse and longitudinal relaxation rates (1/T and 1/T₁, respectively) in blood, muscle, and renal cortex was investigated at 1.5 T. Ex vivo measurements of 1/T and 1/T₁ were additionally performed in whole pig blood spiked with different concentrations of the iron oxide nanoparticle. In renal cortex and muscle, 1/T increased linearly with contrast agent concentration with slopes of 101 ± 22 s⁻¹mM⁻¹ and 6.5 ± 0.9 s⁻¹mM⁻¹ (mean ± SD), respectively. In blood, 1/T increased as a quadratic function of contrast agent concentration, with different quadratic terms in the ex vivo vs. the in vivo experiments. In vivo, 1/T₁ in blood increased linearly with contrast agent concentration, with a slope (T₁‐relaxivity) of 13.9 ± 0.9 s⁻¹mM⁻¹. The achievable increase in 1/T₁ in renal cortex and muscle was limited by the rate of water exchange between the intra‐ and extravascular compartments and the 1/T₁‐curves were well described by a two‐compartment water exchange limited relaxation model. Magn Reson Med 47:461–471, 2002.