An important trend in MR in recent years has been the move towards higher magnetic field (B0) strengths, which promises to advance disease understanding and diagnosis with enhancements in detection sensitivity, metabolite resolution, imaging speed, and tissue contrast. However there are technical challenges that severely hamper the practice of human high field MR, including a major one that accompanies the creation of MR signal using radio frequency EM fields - B1 and concomitant E fields. As B0 strength increases, the degradation in B1 homogeneity due to increased wave behavior often causes severe image quality issues. Meanwhile E-induced RF heating of the subject body (SAR) poses increasingly inhibiting constraints on the application of high-performance MR sequences. With a great capacity for alleviating the limitations imposed by B1 inhomogeneity and SAR exacerbation, parallel RF transmit is emerging as a key enabling technology for high field MR. This project aims at significantly improving human high field MR capability and safety by creating innovative solutions to spin excitation, RF apparatus, and RF energy deposition in subjects. This will be accomplished with specific efforts on a) developing a much needed non-invasive method for measuring, predicting, and proactively managing SAR, b) leveraging the method in optimizing parallel excitation pulses and in breaking new ground of 7T MR applications, and c) transforming RF hardware and pulse designs to considerably boost high field MR system performance. The successful completion of this project will lead to quantitative / predictive methods that enable the fulfillment of the full potential of in vivo imaging at high field, high impact body imaging applications, and innovative RF methods that promise to bring signal creation and detection performance to a new level.

Public Health Relevance

This project will create a vital RF solution to human high field MR, and will enable the fulfillment of the full potential of high field MR in the detection and diagnosis of diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB011551-03
Application #
8433352
Study Section
Biomedical Imaging Technology Study Section (BMIT)
Program Officer
Liu, Guoying
Project Start
2011-02-01
Project End
2015-07-31
Budget Start
2013-02-01
Budget End
2014-07-31
Support Year
3
Fiscal Year
2013
Total Cost
$622,040
Indirect Cost
$210,052
Name
New York University
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
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