Author/Authors :
Bales, Brian C GE Research - Niskayuna, USA , Grimmond, Brian GE Research - Niskayuna, USA , Johnson, Bruce F GE Research - Niskayuna, USA , Todd Luttrell, M GE Research - Niskayuna, USA , Meyer, Dan E GE Research - Niskayuna, USA , Polyanskaya, Tatyana GE Research - Niskayuna, USA , Rishel, Michael J GE Research - Niskayuna, USA , Roberts, Jeannette GE Research - Niskayuna, USA
Abstract :
Contrast-enhanced magnetic resonance imaging is an essential tool for disease diagnosis and management; all marketed clinical
magnetic resonance imaging (MRI) contrast agents (CAs) are gadolinium (Gd) chelates and most are extracellular fluid (ECF)
agents. After intravenous injection, these agents rapidly distribute to the extracellular space and are also characterized by low
serum protein binding and predominant renal clearance. Gd is an abiotic element with no biological recycling processes; low levels
of Gd have been detected in the central nervous system and bone long after administration. These observations have prompted
interest in the development of new MRI contrast agents based on biotic elements such as iron (Fe); Fe-HBED (HBED = N,N′-
bis(2-hydroxyphenyl)ethylenediamine-N,N′-diacetic acid), a coordinatively saturated iron chelate, is an attractive MRI CA
platform suitable for modication to adjust relaxivity and biodistribution. Compared to the parent Fe-HBED, the Fe-HBED
analogs reported here have lower serum protein binding and higher relaxivity as well as lower relative liver enhancement in mice,
comparable to that of a representative gadolinium-based contrast agent (GBCA). Fe-HBED analogs are therefore a promising class
of non-Gd ECF MRI CA.
Keywords :
Fe-HBED , Magnetic , GBCA , MRI