Abstract

1 H Fast Field Cycling NMR (FFC-NMR) relaxometry is proposed as a powerful method to investigate tumour stroma in vivo upon the administration of a Gd-based contrast agent. To perform this study, an FFC-NMR equipment endowed with a wide bore magnet was used for the acquisition of Nuclear Magnetic Resonance Dispersion profiles on healthy muscle and tumour tissue in living mice. At magnetic field strengths < of ca. 1MHz, the differences in the relaxation rates of the intra and extracellular compartment become of the same order of magnitude of the exchange rate across the cellular membranes. Under this condition, the water exchange rate between the two compartments yields to a biexponential magnetization recovery that can be analysed by fitting the experimental data with the two-Site eXchange (2SX) model. Using this model, it was possible to obtain, for the two compartments, both relaxation properties and water kinetic constants for water exchange across cell membranes. The method allowed us to determine the effect of the "matrix" on the water proton relaxation times and, in turn, to get some insights of the composition of this compartment, till now, largely unknown.

Highlights

  • R1ex is influenced by the contrast agent (CA) extravasation from blood capillaries to the extracellular space,[19] yielding R1ex = R1ex0 + r1[Gd]ex, where R1ex0 is the contribution in the absence of exchange and CA and r1 and [Gd]ex are the extracellular CA relaxivity and millimolar concentration, respectively

  • In the range 0.01–1 MHz, that represents the proton Larmor frequencies at which the Nuclear Magnetic Relaxation Dispersion (NMRD) profiles were acquired, the predominant contribution arises from R1in, and the condition │R1in − R1ex│ ~ kin + kex is expected to be met, even in the presence of ProHance

  • Upon the analysis of the experimental data obtained in the 0.01–1 MHz range by means of the 2SX procedure before the CA injection, it has been possible to extract the relaxation rate values for the extracellular and intracellular compartment (R1ex0 and R1in), the intracellular water residence time and the intracellular water fraction (Vin = 1‐Vex)

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Summary

| INTRODUCTION

Benign and malignant lesions (in breast cancer for example), relies on the use of Dynamic Contrast Enhancement. Water proton 1/T1 NMRD measured in vivo on implanted mammary tumours showed a marked T1 elongation at low magnetic fields (

| MATERIALS AND METHODS
| RESULTS AND DISCUSSION
| CONCLUSION
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