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A water-soluble triiodo amino acid and its dendrimer conjugate for computerized tomography (CT) imaging
Author(s) -
Alexander T. Yordanov,
Nikolay Mollov,
Adriana Lodder,
Eric K. Woller,
Mary J. Cloninger,
Stuart Walbridge,
Diane E. Milenic,
Martin W. Brechbiel
Publication year - 2005
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc0502163y
Subject(s) - hounsfield scale , conjugate , dendrimer , chemistry , amino acid , computed tomography , macromolecule , tomography , molecular imaging , medicine , radiology , biochemistry , in vivo , mathematical analysis , mathematics , microbiology and biotechnology , biology
Prolonging the circulation of an imaging agent is vital for making it suit- able for blood pool (vascular) imaging. Medical applications of vascular imaging in- clude cardiovascular disease, abnormal capillary permeability, and tumor neovascu- larity. As low molecular weight computerized tomography (CT) enhancement agents are characterized by inconveniently fast clearance, macromolecular com- pounds (both natural and synthetic) have gained a wide recongnition for possessing better characteristics for performing blood imaging tasks. Herein, the syntheses and characterization of a new water-soluble triiodo amino acid, 3-(N,N-dimethylami- noacetyl)amino)--ethyl-2,4,6-triiodobenzenepropanoic acid (DMAA-IPA) and its Starburst PAMAM generation 4.0 dendrimer conjugate, G-4-(DMAA-IPA)37 are de- scribed. The applicability of G-4-(DMAA-IPA)37 as a potential macromolecular angiographic CT contrast agent is discussed. The linear relationship between organ- ically bound iodine concentration and CT Hounsfield units has been established thus allowing for quantification uses of CT imaging as well.

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