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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.

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