Guan Wang1,
2, Yingli Fu1, Steven M. Shea3, Judy Cook1,
Dara L. Kraitchman1, 4
1Radiology
and Radiological Science, Johns Hopkins University, Baltimore, MD, United
States; 2Electrical and Computer Engineering, Johns Hopkins
University, Baltimore, MD, United States; 3Center for Applied
Medical Imaging, Siemens Corporation, Corporate Research and Technology,
Baltimore, MD, United States; 4Molecular and Comparative
Pathobiology, Johns Hopkins University, Baltimore, MD, United States
Microencapsulated stem cell (SC) offers a novel means to transplant mismatched SCs to avoid immunorejection for the treatement of peripheral arterial disease (PAD) that is too extensive for the conventional therapy. We produced dual X-ray/MR-visible microcapsules (XMRCaps) by impregnated the perfluorooctyl bromine (PFOB) to enable cell tracking with non-invasive imaging modalities. Here we first explore quantitative serial cell tracking using c-arm CT and 19F-MRI of XMRCaps in a rabbit PAD model using conventional clinical imaging systems. Results indicate that in vivo XMRCaps volume tracking could be achieved by both CT and MRI, while only MRI demonstrates the XMRCaps degradation.
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