A water-soluble triiodo amino acid and its dendrimer conjugate for computerized tomography (CT) imaging

Author:

Yordanov Alexander1,Mollov Nikolay1,Lodder Adriana2,Woller Eric3,Cloninger Mary3,Walbridge Stuart4,Milenic Diane1,Brechbiel Martin1

Affiliation:

1. Radiommune & Inorganic Chemistry Section, Radiation Oncology Branch, Center for Cancer Research, Bethesda, Maryland

2. Wyatt Technology Corporation, Santa Barbara, California

3. Montana State University - Department of Chemistry and Biochemistry, Bozeman, Montana, USA

4. Surgical Neurology Branch, National Institute of Neurological Disorder and Stroke, National Institutes of Health, Bethesda, Maryland

Abstract

Prolonging the circulation of an imaging agent is vital for making it suitable for blood pool (vascular) imaging. Medical applications of vascular imaging include cardiovascular disease, abnormal capillary permeability, and tumor neovascularity. As low molecular weight computerized tomography (CT) enhancement agents are characterized by inconveniently fast clearance, macromolecular compounds (both natural and synthetic) have gained a wide recognition 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-dimethylaminoacetyl) amino]-?-ethyl-2,4,6-triiodobenzenepropanoic acid (DMAA-IPA) and its Starburst PAMAM generation 4.0 dendrimer conjugate, G-4-(DMAA-IPA)37 are described. The applicability of G-4-(DMAA-IPA)37 as a potential macromolecular angiographic CT contrast agent is discussed. The linear relationship between organically bound iodine concentration and CT Hounsfield units has been established thus allowing for quantification uses of CT imaging as well.

Publisher

National Library of Serbia

Subject

General Chemistry

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