Magnetic Resonance Specimen Evaluation Using Multiple Pulse Field Gradient Sequences

Description:

Abstract:

Researchers at the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) developed an MRI-method that is based on the acquisition of multiple pulsed field gradient (m-PFG) rather than single-pulsed field gradient (s-PFG) MRI sequences. In particular, double PFG (dPFG) MRI sequences offer higher sensitivity and greater robustness, as they are more sensitive to the effects of “restriction;” i.e., to water trapped within the axon’s intracellular space, and thus to the diameter of the axons. Thus, it renders the MRI data more sensitive to “pore size” and “pore shape,” making the measurement of the average axon diameter (AAD), and the axon diameter distribution (ADD) more sensitive and accurate. Moreover, measurements using the multiple-PFG sequence can be performed readily at ‘low b” or “low q” – making it biologically relevant and clinically feasible. 

Competitive Advantages:

  • Non-invasive, painless, in vivo measurement of tissue microstructure and the microenvironment;
  • Contrast agents not required;
  • Modest data requirements allow for scans to be performed in a clinically feasible time-frame.

Commercial Applications:

  • In vivo MRI of humans and animals;
  • Drug development;
  • Material Science;
  • Food processing.
Patent Information:
For Information, Contact:
Richard Girards
Senior Technology Transfer Manager
NIH Technology Transfer
240-276-6825
richard.girards@nih.gov
Inventors:
Peter Basser
Evren Ozarslan
Keywords:
Axon diameter distribution
double PFG
d-PFG
MRI diagnostic
Multiple Pulsed Field Gradient
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