Magnetic resonance (MR) imaging is based upon the Nuclear Magnetic Res
onance (NMR) experiment. The patient or sample is placed in a strong m
agnetic field which polarizes the populations of hydrogen nuclei so th
at a bulk magnetization appears. This magnetization, flipped by a radi
ofrequency (RF) pulse returns to equilibrium along the direction of th
e main magnetic field, inducing in the detection probe a signal whose
frequency is proportional to the magnetic field intensity. In order to
form an image, the spatial origin of the signal must be precisely loc
alized. Such a localization is achieved by means of magnetic field gra
dients, which establish linear relations between resonance frequency a
nd distance. The spatial resolution is proportional to the product of
the gradient strength by the latter's application duration. So that, i
n theory, there should not be any limit in spatial resolution. In fact
, the latter is limited by the signal to noise ratio, resonance freque
ncy line width and diffusion of the hydrogen nuclei. The spatial resol
ution actually achieved within these constraints is limited to only a
few microns. However, magnetic resonance enables non-destructive measu
rements of physical and chemical characteristics in living samples.