The concentration of mobile Hydrogen atoms within a sample of tissue.

See also Hydrogen Density.

(N) The SI units is moles/m³.
Definition: The concentration of nuclei in tissue processing at the Larmor frequency in a given region; one of the principal determinants of the strength of the NMR signal from the region.
For water, there are about 1.1 x 105 moles of hydrogen per m³, or 0.11 moles of hydrogen/cm³.
The signal intensity measured is related to the square of the xy-magnetization, which in a SE pulse sequence is given by
Mxy = Mxy0(1-exp(-TR/T1)) exp(-TE/T2)
where Mxy0 = Mz0 is proportional to the proton or spin density, and corresponds to the z-magnetization present at zero time of the experiment when it is tilted into the xy-plane.
True spin density is not imaged directly, but must be calculated from signals received with different interpulse times. The spin density contrast can be generated by using a long TR and sampling the data immediately after the RF pulse (with a TE as short as possible).

Chemical shift depends on the nucleus and its environment and is defined as nuclear shielding / applied magnetic field. Nuclei are shielded by a small magnetic field caused by circulating electrons, termed nuclear shielding. The strength of the shield depends on the different molecular environment in that the nucleus is embedded. Nuclear shielding is the difference between the magnetic field at the nucleus and the applied magnetic field.
Chemical shift is measured in parts per million (ppm) of the resonance frequency relative to another or a standard resonance frequency.
The major part of the MR signal comes from hydrogen protons; lipid protons contribute a minor part. The chemical shift between water and fat nuclei is about 3.5 ppm (~220 Hz; 1.5T). Through this difference in resonance frequency between water and fat protons at the same location, a misregistration (dislocation) by the Fourier Transformation take place, when converting MR signals from frequency to spatial domain. This effect is called chemical shift artifact or chemical shift misregistration artifact.

Contrast agents are chemical substances introduced to the anatomical or functional region being imaged, to increase the differences between different tissues or between normal and abnormal tissue, by altering the relaxation times. MRI contrast agents are classified by the different changes in relaxation times after their injection.
The design objectives for the next generation of MR contrast agents will likely focus on prolonging intravascular retention, improving tissue targeting, and accessing new contrast mechanisms. Macromolecular paramagnetic contrast agents are being tested worldwide. Preclinical data shows that these agents demonstrate great promise for improving the quality of MR angiography, and in quantificating capillary permeability and myocardial perfusion.
Ultrasmall superparamagnetic iron oxide (USPIO) particles have been evaluated in multicenter clinical trials for lymph node MR imaging and MR angiography, with the clinical impact under discussion. In addition, a wide variety of vector and carrier molecules, including antibodies, peptides, proteins, polysaccharides, liposomes, and cells have been developed to deliver magnetic labels to specific sites. Technical advances in MR imaging will further increase the efficacy and necessity of tissue-specific MRI contrast agents.

See also Adverse Reaction and Nephrogenic Systemic Fibrosis.

See also the related poll result: 'The development of contrast agents in MRI is'

A large vacuum jacketed double walled container generally made out of stainless steel that is used to transport cryogens. Cryogenic liquids are shipped and used non-pressurized in this thermally insulated containers. Dewar flasks are specifically designed to withstand rapid temperature changes and extreme differences in temperature. Flasks containing helium (used in MRI for cooling of superconducting magnets), hydrogen and other low-boiling liquid cryogens have an outer vessel of liquid nitrogen for insulation.
Dewars are also called cryostats.