The Hyperpolarized MRI Technology Resource Center is designed to develop new HP MR instrumentation, techniques, and analysis software through close interactions with funded Collaborative Project investigators and then disseminate these techniques to the Service Project Investigators for extramural feedback and to the general scientific community through the website, symposia, a dedicated Center Workshop, and direct hands- on training. In order to accomplish all these goals and functions requires a well-constructed administrative plan with a defined but dynamic structure that can be modified to meet new challenges and changing collaborative, service, training and dissemination needs. The HMTRC administrative structure and implementation has developed considerably since the original submission, because the interactions and complexity of the whole P41 has increased dramatically over the past 4 years. The HMTRC administrative infrastructure now extends nationally and internationally to provide information, dissemination of MR sequences, and analysis software to Service Projects and other investigators utilizing DNP polarizers for HP 13C MRI research. The operation of the HMTRC will continue to be directed by the Executive Committee with the PI, Dr. Daniel Vigneron PhD as the Chair. Dr. Sarah Nelson PhD, who is the Project Leader for TR&D Project 3, Director of the Surbeck Laboratory for Advanced Imaging and Dr. John Kurhanewicz PhD who is the Project Leader of TR&D Project 2 & Director of the UCSF Biomedical NMR Lab will also serve on the HMTRC Executive Committee. In this current center, these three professors have collaborated closely making this center very successful. With a history of successful collaborations and with offices in close proximity, they will continue to collaborate in this renewal project to ensure the continue productivity and success of the HMTRC. Dr. Robert Bok MD, PhD will also serve on the Executive Committee. He has extensive experience in preclinical and clinical research and oversees the animal facilities in the Surbeck Laboratory for Advanced Imaging and the Biomedical NMR lab and has led the animal model aspects of the current preclinical hyperpolarized MR studies. New member to the Executive Committee is Dr. Peder Larson PhD who will be the PI of CP5 in this renewal project with particular focus on RF pulse design and translational 13C MR acquisition developments and brings the first hand experience of a junior faculty member establishing an independent HP 13C research program.

Public Health Relevance

The ultimate goal of this center is to collaboratively develop methods that advance the emerging field of hyperpolarized carbon-13 MR and benefit other researchers and enable multi-site research studies of this powerful molecular imaging method. The administrative structure has been developed to enable the functioning of the center and its many aspects.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Biotechnology Resource Grants (P41)
Project #
5P41EB013598-07
Application #
9324236
Study Section
Special Emphasis Panel (ZEB1-OSR-B)
Project Start
2011-08-01
Project End
Budget Start
2017-05-01
Budget End
2018-04-30
Support Year
7
Fiscal Year
2017
Total Cost
$140,691
Indirect Cost
$51,927
Name
University of California San Francisco
Department
Type
Domestic Higher Education
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
Chen, Hsin-Yu; Larson, Peder E Z; Gordon, Jeremy W et al. (2018) Technique development of 3D dynamic CS-EPSI for hyperpolarized 13 C pyruvate MR molecular imaging of human prostate cancer. Magn Reson Med 80:2062-2072
Milshteyn, Eugene; von Morze, Cornelius; Reed, Galen D et al. (2018) Using a local low rank plus sparse reconstruction to accelerate dynamic hyperpolarized 13C imaging using the bSSFP sequence. J Magn Reson 290:46-59
Milshteyn, Eugene; von Morze, Cornelius; Gordon, Jeremy W et al. (2018) High spatiotemporal resolution bSSFP imaging of hyperpolarized [1-13 C]pyruvate and [1-13 C]lactate with spectral suppression of alanine and pyruvate-hydrate. Magn Reson Med 80:1048-1060
von Morze, Cornelius; Reed, Galen D; Larson, Peder E et al. (2018) In vivo hyperpolarization transfer in a clinical MRI scanner. Magn Reson Med 80:480-487
Taglang, CĂ©line; Korenchan, David E; von Morze, Cornelius et al. (2018) Late-stage deuteration of 13C-enriched substrates for T1 prolongation in hyperpolarized 13C MRI. Chem Commun (Camb) 54:5233-5236
Gordon, Jeremy W; Hansen, Rie B; Shin, Peter J et al. (2018) 3D hyperpolarized C-13 EPI with calibrationless parallel imaging. J Magn Reson 289:92-99
Maidens, John; Gordon, Jeremy W; Chen, Hsin-Yu et al. (2018) Spatio-Temporally Constrained Reconstruction for Hyperpolarized Carbon-13 MRI Using Kinetic Models. IEEE Trans Med Imaging 37:2603-2612
Qin, Hecong; Carroll, Valerie N; Sriram, Renuka et al. (2018) Imaging glutathione depletion in the rat brain using ascorbate-derived hyperpolarized MR and PET probes. Sci Rep 8:7928
Marco-Rius, Irene; Gordon, Jeremy W; Mattis, Aras N et al. (2018) Diffusion-weighted imaging of hyperpolarized [13 C]urea in mouse liver. J Magn Reson Imaging 47:141-151
von Morze, Cornelius; Tropp, James; Chen, Albert P et al. (2018) Sensitivity enhancement for detection of hyperpolarized 13 C MRI probes with 1 H spin coupling introduced by enzymatic transformation in vivo. Magn Reson Med 80:36-41

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