Electronic Posters: Molecular



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Contrast Agents

Hall B Monday 14:00-16:00 Computer 70

14:00 4214. Validation of Optical Tomography in Vivo

Yuting Lin1, Mehmet B. Unlu1, Brian Grimmond2, Anup Sood2, Egidijus E. Uzgiris3, David Thayer1, Han Yan1, Orhan Nalcioglu1, Gultekin Gulsen1

1Center for Functional Onco-Imaging, University of California, Irvine, CA, United States; 2GE Gobal Research, Niskayuna, NY, United States; 3Rensselaer Polytechnic Institute,, Troy, NY, United States

Multi-modality imaging is becoming a trend in developing new generation in vivo imaging techniques for diagnosis. Recently, our group has developed a high temporal resolution dynamic MRI/DOT multi-modality imaging system. In such a multi-modality system, each modality measures a different parameter set, which make it difficult to cross-validate the parameters measured by different modalities. An alternative solution is using a bi-functional contrast agent that provides contrast for both optical and MRI simultaneously. Here, our in vivo small animal study is the first to validate a true multi-modality system with a true multi-modality contrast agent.



14:30 4215. Novel Cross-Linked Liposomal Chemical Saturation Transfer or CEST Agents

Aristarchos Papagiannaros1, Valeria Righi1,2, George Dai2, A Aria Tzika1,2

1NMR Surgical Laboratory, Department of Surgery, Massachusetts General Hospital and Shriners Burns Institute, Harvard Medical School, Boston, MA, United States; 2Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Athinoula A. Martinos Center of Biomedical Imaging, Boston, MA, United States

Liposomal CEST agents are a novel class of contrast agents that demonstrate excellent imaging capacity in phantoms and ex vivo, but their instability is preventing their use in imaging inflammation or cancer. We present cross-linked liposomal CEST agents that efficiently separated the bulk water from the intra-liposomal water signal, while offer increased stability for in vivo applications.



15:00 4216. Novel Metalloporphyrins as Molecular MR Contrast Agents

Talaignair Venkatraman1, Ines Batinic-Haberle2, Vladimir Mouraviev2, Haichen Wang2, Chris lascola2

1Radiology, Duke University Medical Center, Durham, NC, United States; 2Duke University Medical cener

We have investigated a new class of therapeutic metalloporphyrins for their potential as molecular MR imaging probes for prostate cancer detection. Mn(III)TE-2-Pyp5+ (meso-tetrakis(N-ethyl-2-prydil)porphyrin) and Mn(III)TnHex-2-PYP5+ (meso-terakis(N-n-hexyl-2-pyridyl)porphyrin are powerful superoxide dismutase mimics with low toxicity and antineoplastic activity. In phantom experiments, we observe unusually high T1 relaxivity. In vivo, we observe selective accumulation of these probes in prostate tumor xenografts following a single dose of either compound. Relaxation changes in prostate tumors is 10-11 fold greater than in normal prostate gland, suggesting these compounds may be particularly effective at detecting multifocal disease in situ.



15:30 4217. Controlled-Release and Magnetic Resonance Imaging of Doxorubicin-Conjugated Magnetic Nanoparticles from 3D Poly(Propylene Fumarate) Scaffolds

Jonghoon Choi1,2, Kyobum Kim3, Taeho Kim4, Taeghwan Hyeon4, Mike T. McMahon1, Jeff WM Bulte1, John P. Fisher3,5, Assaf A. Gilad1

1Radiology, Johns Hopkins University School of Medicine, Baltimore, MD, United States; 2Biochemical Science, National Institute of Standard and Technology, Gaithersburg, MD, United States; 3Chemical and Biomolecular Engineering, University of Maryland, College Park, MD, United States; 4Chemical Engineering, Seoul National University, Seoul, Korea, Republic of; 5Fischell Department of Bioengineering, University of Maryland, College Park, MD, United States

Three-dimensional PPF (poly(propylene fumarate)) scaffolds carrying cancer drug-coated nanoparticles showed controlled release of drug nanoparticles and bimodal imaging (fluorescence and magnetic resonance) capabilities. This novel biopolymer matrix could be used for many biomedical applications, including MR-guided implantation, as a drug-carrying vehicle, and as a tumor treatment because of the persistent release of drugs in the vicinity of a malignancy.




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