Dr. Timothy J. Hoffman, Ph.D.,
VA-BIC Director
Said Daibes Figueroa, MS, CNMT, Sr. Research Specialist
Lixin Ma, PhD., Research Assistant Professor
The VA Biomolecular Imaging Center (BIC) located at the Harry S Truman Memorial VA Hospital offers VA, and affiliated MU researchers, state of the art molecular and anatomic in vivo imaging capabilities. The imaging center houses a Philips Medical Systems MOSAIC Small Animal PET system, an ImTEK, Inc. combined Micro-SPECT/CT system, and in 2005 will acquire a Varian Inc., actively shielded 7 Tesla 210-mm Small Horizontal Bore MRI system. This research center is designed to make high resolution anatomic and molecular imaging studies available to radiopharmaceutical, oncology, and general biomedical researchers who utilize conventional and immunocompromised animal models as a component of their respective research programs. All research conducted at the VA-BIC requires prior approval by the VA Subcommittee for Animal Studies and the VA Radiation Safety Committee.
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John Lever , PhD, Core Leader Radiopharmacology
Wynn A. Volkert, PhD, Co-Investigator
Bennett S. Greenspan, MD, MS, Collaborator
The overall purpose of the Radiopharmacology / Imaging Core Resource facility is to provide NIH funded
researchers with the resources and expertise necessary to perform in vivo pharmacokinetic studies on normal and
human tumor xenografted rodents, as well as provide scintigraphic imaging equipment and expertise to
complement the pharmacokinetic data. Each of the projects outlined in this proposal will utilize the resources that
this core provides in order to evaluate a variety of new potential radiopharmaceuticals.
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George P. Smith , PhD, Core Leader
Susan Deutscher, Ph.D., Associate Core Director
Fabio Gallazzi, PhD, Co-Investigator
Robert Davis, Sr. Tech
Dr. Deutscher
The main purpose of this Biotechnology Core Resource (BC) facility is to provide researchers, primarily those
involved in the P50 Research and Development Programs with key technical and intellectual resources to exploit
biotechnology and combinatorial chemistry to rapidly evolve and improve peptide based molecules as cancer
imaging agents (Figure 1). The majority of the proposed projects utilize biotechnologies centered around
combinatorial chemistry that include genetic approaches such as phage peptide display and chemical approaches
such as peptide synthesis.
A central core that houses
the genetic combinatorial
biotechnology resources
including bacterial strains
and phage libraries was
generated in the P20
phase of the ICMIC. A
central core that houses
the strains and phage
libraries has greatly
facilitated projects and
investigators employing
this methodology. The
highly infectious nature of
phage has made it
imperative to have
equipment and facility
dedicated for these
purposes.
Kattesh V. Katti, Ph D, Director
Silvia S. Jurisson, Ph D, Co-Director
Susan Lever, Ph D, Collaborator
Wynn A. Volkert, Ph D, Collaborator
Alan R. Ketring, Ph D, Collaborator
The Radiochemistry/Bioconjugation Core (RBCC) resource provides service in all aspects of
ligands/bifunctional chelating agents (BFCAs) design and development, radiochemistry optimization in labeling
with 99mTc and 111In, bioconjugation chemistry for
linking BFCAs (or 99mTc/111In labeled BFCs) to
tumor avid target specific peptides. The RBCC
facility also provides a complete range of
services toward the development and full
characterization of metal complexes at
macroscopic levels via the synthesis of Tc-99/Re
complexes or In conjugates from appropriate
BFCAs or peptide conjugates.A major goal of the Radiochemistry and Bioconjugation Chemistry Core Facility (RBCC) is to provide
service in bifunctional chelating agent (BFCAs) design, develop radiolabeling protocols (using 99mTc or 111In)
and provide bioconjugation strategies for linking BFCAs or radiometal labeled BFCs to target specific
biomolecules used within the P50 program. The RBCC resource will have state of the art infrastructure and
expertise all aimed at providing radiolabeling and bioconjugation strategies to accomplish specific goals of the
P-50 program toward conducting pilot imaging studies using the optimal 99mTc or 111In labeled peptide
conjugates.
We have an IRB approved bank of human tissue to provide both malignant and benign samples, which have been snap
frozen and histopathologically reviewed. Whenever possible, we will obtain matched malignant and benign
specimens from the same subject. A tube of blood will also be obtained, when possible. Clinical information will
also be available as needed by the investigators.
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