NMR Transversal relaxivity of aqueous suspensions of particles of Ln(3+)-based zeolite type materials

abstract

A series of zeolite-type silicates containing stoichiometric amounts of Ln(3+) ions in the framework (Ln-AV-9 materials), with composition (Na4K2)(Ln(2)Si(16)O(38)) center dot 10H(2)O (Ln = Nd, Sm, Eu, Tb, Gd, Dy) has recently been synthesized and characterized. They form paramagnetic microparticles, which as aqueous suspensions have negligible water H-1 longitudinal relaxivities (r(1)) for all Ln(3+) ions studied and quite large transverse relaxivities (r(2)). In this work we further analysed the size distribution of the Ln-AV-9 particles and their r(2)* and r(2) relaxivities. The r(2)* relaxivity effects are explained by the static dephasing regime (SDR) theory. The r(2) relaxivities appear to be strongly dependent on the interval between two consecutive refocusing pulses (tau(CP)) in the train of 180 degrees pulses applied. For long tau(CP) values, the r(2) of the systems saturates at a value, which is always an order of magnitude smaller than r(2)*. These features are explained by a crude model, which takes into account the residual diffusion effect in the static dephasing regime. The large microparticles, although not efficient in T-1 relaxation, are quite effective in enhancing T-2 relaxation, particularly at high magnetic fields. The r(2)* values and the saturation values for r(2) were found to increase linearly with B-0 and mu(2)(0). The largest transversal relaxation rate enhancements were observed for Dy-AV-9 with a saturation value of r2 of 60 s(-1) mM(-1) and a r(2)* value of 566 s(-1) mM(-1) at 9.4 T and 298 K.

keywords

MRI CONTRAST AGENTS; MAGNETIC-SUSCEPTIBILITY SHIFTS; OXIDE NANOPARTICLES; RELAXATION; RESONANCE; EXCHANGE; TISSUES; SPHERES; MODEL

subject category

Chemistry

authors

Pereira, GA; Norek, M; Peters, JA; Ananias, D; Rocha, J; Geraldes, CFGC

our authors

Share this project:

Related Publications

We use cookies for marketing activities and to offer you a better experience. By clicking “Accept Cookies” you agree with our cookie policy. Read about how we use cookies by clicking "Privacy and Cookie Policy".