ELECTRONIC POSTER - ismrm
ELECTRONIC POSTER - ismrm
ELECTRONIC POSTER - ismrm
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14:30 3755. The Use of Cellular MRI and Magnetic Particles to Study Cancer Stem Cells<br />
Emeline Julie Ribot 1 , Carmen Simedrea 2 , Patricia McGowan 2 , Ann Chambers 2 , Paula J.<br />
Foster 1<br />
1 Imaging Laboratories, Robarts Research Institute, London, Ontario, Canada; 2 Medical Biophysics, University<br />
of Western Ontario, London, Ontario, Canada<br />
In this abstract, we describe technology developed in our labs for tracking stem-like cancer cells (CSC), in a mouse model of breast<br />
cancer metastasis to the brain, using MRI and magnetic particles. A human breast cancer cell line was sorted by flow cytometry into<br />
two distinct populations: CD44high/CD24low and CD44low/CD24high, representing the CSC-like and non-CSC cells, respectively.<br />
The sorted cell populations can be labeled efficiently and without toxicity with the iron agent MoldayION Rhodamine B. Labeled<br />
CSC can be detected in vivo in images of the mouse brain after injection into the left ventricle of the heart in nude mice.<br />
15:00 3756. Development of Cationic Gd(III) Chelate as Potential Tumor-Selective MRI<br />
Contrast Agent<br />
Chang-Tong Yang 1 , Cai-Xian Yong 1 , Chew-Yuan Tuang 2 , Young-Tae Chang 2 , Kai-<br />
Hsiang Chuang 1<br />
1 Laboratory of Molecular Imaging, Singapore Bioimaging Consortium, Agency for Science,Technology and<br />
Research, Singapore, Singapore; 2 Laboratory of Bioimaging Probe Development, Singapore Bioimaging<br />
Consortium, Agency for Science,Technology and Research, Singapore, Singapore<br />
We developed a new Gd(III) chelate by conjugating GdDO3A with 2-(diphenylphosphoryl)ethyldiphenylphosphonium cation --<br />
Gd(DO3A-xy-TPEP)+ to form a cationic MRI contrast agent. This contrast agent has been synthesized and characterized in vitro and<br />
in vivo. In vitro cell viability showed insignificant cytotoxicity at low [Gd] concentrations up to 0.2 mM. The in vitro T1 relaxivity<br />
measured at 7.0 T is about 50% higher than that of clinically used Gd-DTPA and Gd-DOTA. In vivo imaging study in mice<br />
demonstrated longer tissue retention especially in the liver. It indicated that Gd(DO3A-xy-TPEP)+ could potentially be used to detect<br />
tumor which generally has larger negative mitochondrial transmembrane potential.<br />
Human MRA<br />
Hall B Monday 14:00-16:00 Computer 41<br />
14:00 3757. Clinical Evaluation of Peripheral Vascular Disease Using a Hybrid Approach:<br />
Unenhanced Quiescent Interval Single Shot and Low-Dose TWIST MR Angiography<br />
Philip Anthony Hodnett 1,2 , Ioannis Kokztzoglou 3 , Timothy Scanlon, Jeremy Collins 4 , John<br />
Sheehan, Eugene Dunkle, James C. Carr, Robert Edelman<br />
1 Northwestern University, Chicago, IL, United States; 2 Northshore University Healthcare System, Chicago, IL,<br />
United States; 3 Northshore University Healthcare System, United States; 4 Northwestern University, United<br />
States<br />
Imtroduction:The purpose of this study was to test the hypothesis that a hybrid technique employing a new unenhanced MRA<br />
technique, quiescent interval single shot (QISS) in combination with a low-dose time resolved (TWIST)of the calf provides<br />
comparable diagnostic accuracy to the standard hybrid approach using low-dose TWIST of the calf and high-dose stepping table CE-<br />
MRA. Materials and Methods:20 prospective patients referred for evaluation of peripheral arterial disease underwent unenhanced and<br />
combined low-dose time-resolved (TWIST)evaluation followed by standard hybrid stepping table bolus chase MRA. Results:The<br />
combined unenhanced QISS technique and low-dose time resolved (TWIST ) calf study resulted in an overall sensitivity of 97.4%,<br />
specificity of 98.3%, a negative predictive value of 98.7% and a positive predictive value of 96.7% using CE-MRA as the reference<br />
standard. Cohen kappa analysis for inter-rater indicates almost perfect agreement (©§= 0.86) between the hybrid approach of<br />
unenhanced QISS and TWIST and standard hybrid CE-MRA. Conclusion: This hybrid strategy permits a dramatic reduction in<br />
contrast agent dosage with no loss of diagnostic accuracy.<br />
14:30 3758. "Does Higher R1 Relaxivity Transfer in Improved Vessel Enhancement of the Run-<br />
Off Vasculature?" - Evaluation of Macrocylic Gadolinium Chelates for Peripheral MR-<br />
Angiography at 3 T by an Inter-Individual Comparison of Gadobutrol Vs Gadoterate<br />
Meglumine, Bo<br />
Ulrike I. Attenberger 1 , Matthias Voth 2 , Andre Luckscheiter 3 , Stefan Haneder 1 , Stefan O.<br />
Schoenberg 4 , Henrik J. Michaely 1<br />
1 Department of Clinical Radiology and Nuclear Medicine, University Medical Center Manheim, Mannheim,<br />
Germany; 2 Bayer Schering AG, Berlin, Germany; 3 University of Heidelberg, Heidelberg, Germany;<br />
4 Department of Clinical Radiology and Nuclear Medicine, University Medical Center Manheim , Mannheim,<br />
Germany<br />
Since nephrogenic systemic fibrosis (NSF) has been linked to gadolinium-chelate administration in patients with impaired renal<br />
function, contrast agent dose and chelate stability have attracted broad attention. Numerous studies have demonstrated linear<br />
compounds to be the least stable, whereas the macrocyclic compounds are the most stable. With the approval of gadobutrol, a double<br />
concentrated macrocyclic gadolinium chelate became available, characterized by the highest R1-relaxivity among the macrocyclic<br />
gadolinium chelates. The aim of this study was to evaluate the enhancement characteristics of gadobutrol and gadoterate meglumine,<br />
both injected at a dose level of 0.07 mmol/kg BW, for peripheral MR-angiography.