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Hank F. Kung, Ph.D.


Professor of Radiology and Pharmacology
Department of Radiology
Radiopharmaceutical Chemistry Section
3700 Market Street, Room 305
(215) 662-3096 Fax: (215) 349-5035
email: kunghf@sunmac.spect.upenn.edu


For more information,visit theRadiopharmaceutical Chemistry Section


Click here for selected publications since Dr. Kung's arrival at Penn



RESEARCH INTERESTS

Current research interests include 1).developing imaging agents for CNS receptors (dopamine and serotonin neurotransmitter systems), 2). agents for imaging Alzheimer's disease, and 3) neuronal functional imaging of the heart.

RESEARCH TECHNIQUES

drug design, organic synthesis, radiochemistry, receptor pharmacology, pharmacokinetics, and physics and instrumentation of gamma imaging tomography devices.

RESEARCH SUMMARY

The focus of my research group is on the development of new radiopharmaceuticals that provide diagnostic information on various organs in normal and disease states, such as Parkinson's, depression and Alzheimer's diseases.

Dr. Kung's research group is interested in development of selective radiotracers for in vitro and in vivo studies of CNS receptors. The development of new tracers involve multi disciplinary efforts including: synthesis of new ligands, evaluation of structure-activity relationship, radiochemistry of Tc-99m and I-123, and in vitro and in vivo studies of binding affinity and selectivity in cloned cell membrane and brain tissue preparations. When the tracers are tested in human in conjunction with Single Photon Emission Computed Tomography (SPECT) they may provide diagnostic information not attainable by other imaging techniques. In the past few years, many novel iodinated ligands selective for CNS dopamine and serotonin receptors have been developed. Specifically, I-123 IBZM (iodo-benzamide) and Tc-99m TRODAT-1 are currently used worldwide as a D2/D3 dopamine receptor and dopamine transporter imaging agents with SPECT for differential diagnosis of Parkinson's disease and other mental disorders related to changes on postsynaptic dopamine receptor function.

KEY WORDS:
Receptor imaging, Dopamine and Serotonins systems, beta amyloid


 
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