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New Calcium‐Selective Smart Contrast Agents for Magnetic Resonance Imaging
Author(s) -
Verma Kirti Dhingra,
Forgács Attila,
Uh Hyounsoo,
Beyerlein Michael,
Maier Martin E.,
Petoud Stéphane,
Botta Mauro,
Logothetis Nikos K.
Publication year - 2013
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201300169
Subject(s) - extracellular , chemistry , calcium , homeostasis , functional magnetic resonance imaging , biophysics , nuclear magnetic resonance , calcium metabolism , magnetic resonance imaging , biochemistry , neuroscience , medicine , physics , organic chemistry , radiology , biology
Calcium plays a vital role in the human body and especially in the central nervous system. Precise maintenance of Ca 2+ levels is very crucial for normal cell physiology and health. The deregulation of calcium homeostasis can lead to neuronal cell death and brain damage. To study this functional role played by Ca 2+ in the brain noninvasively by using magnetic resonance imaging, we have synthesized a new set of Ca 2+ ‐sensitive smart contrast agents (CAs). The agents were found to be highly selective to Ca 2+ in the presence of other competitive anions and cations in buffer and in physiological fluids. The structure of CAs comprises Gd 3+ ‐DO3A (DO3A=1,4,7‐tris(carboxymethyl)‐1,4,7,10‐tetraazacyclododecane) coupled to a Ca 2+ chelator o ‐amino phenol‐ N , N , O ‐triacetate (APTRA). The agents are designed to sense Ca 2+ present in extracellular fluid of the brain where its concentration is relatively high, that is, 1.2–0.8 m M . The determined dissociation constant of the CAs to Ca 2+ falls in the range required to sense and report changes in extracellular Ca 2+ levels followed by an increase in neural activity. In buffer, with the addition of Ca 2+ the increase in relaxivity ranged from 100–157 %, the highest ever known for any T 1 ‐based Ca 2+ ‐sensitive smart CA. The CAs were analyzed extensively by the measurement of luminescence lifetime measurement on Tb 3+ analogues, nuclear magnetic relaxation dispersion (NMRD), and 17 O NMR transverse relaxation and shift experiments. The results obtained confirmed that the large relaxivity enhancement observed upon Ca 2+ addition is due to the increase of the hydration state of the complexes together with the slowing down of the molecular rotation and the retention of a significant contribution of the water molecules of the second sphere of hydration.