Amphiphilic EuDOTA-tetraamide complexes form micelles with enhanced CEST sensitivity

Osasere M. Evbuomwan, Garry Kiefer, A. Dean Sherry

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

The synthesis and characterization of four new DOTA-tetraamide ligands having variable alkyl chain lengths (C 1, C 12, C 14, and C 16) and their respective europium(III) complexes are reported. The three EuL complexes having long alkyl chains spontaneously form micelles of variable size. The critical micelle concentration differed for each complex (lower for the C 16 complex than the C 12 complex) while micelle size increased with increasing alkyl chain length. Chemical exchange saturation transfer (CEST) experiments showed that all four Eu III complexes displayed slow-to-intermediate water exchange kinetics. As expected, the CEST signals in these complexes decreased with increasing temperatures due to faster water exchange but, interestingly, the CEST signals for the C 14 and C 16 complexes approached a maximum near 25 °C consistent with exchange limited CEST at or near room temperature. The water residence lifetimes obtained by fitting the CEST spectra to the Bloch equations increased in parallel with an increase in alkyl carbon chain-length. By comparisons with the monomethylamide complex, which served as control, the data illustrate that micelle formation serves to slow the rate of water exchange in these systems. The complex having the largest CEST effect per unit Eu III concentration (the C 16 analog) had a detection limit of 5.3 μM. This represents an approximate 250-fold increase in sensitivity relative to the monomethylamide control (detection limit â 1.3 mM). These features highlight the potential of using micelle-based systems such as these as paramagnetic chemical exchange saturation transfer (PARACEST) agents for molecular imaging by MRI. Four new EuDOTA-tetraamides with variable alkyl chains lengths were synthesized and their CEST properties were extensively studied. Three of these complexes werefound to spontaneously form micelles due to their long alkyl chains which resulted in a dramatic increase in their CEST sensitivities.

Original languageEnglish (US)
Pages (from-to)2126-2134
Number of pages9
JournalEuropean Journal of Inorganic Chemistry
Issue number12
DOIs
StatePublished - Apr 2012

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Micelles
Chain length
Water
Europium
Molecular imaging
Critical micelle concentration
Magnetic resonance imaging
Carbon
Ligands
Temperature
Kinetics
Experiments

Keywords

  • Europium
  • Imaging agents
  • Micelles

ASJC Scopus subject areas

  • Inorganic Chemistry

Cite this

Amphiphilic EuDOTA-tetraamide complexes form micelles with enhanced CEST sensitivity. / Evbuomwan, Osasere M.; Kiefer, Garry; Sherry, A. Dean.

In: European Journal of Inorganic Chemistry, No. 12, 04.2012, p. 2126-2134.

Research output: Contribution to journalArticle

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abstract = "The synthesis and characterization of four new DOTA-tetraamide ligands having variable alkyl chain lengths (C 1, C 12, C 14, and C 16) and their respective europium(III) complexes are reported. The three EuL complexes having long alkyl chains spontaneously form micelles of variable size. The critical micelle concentration differed for each complex (lower for the C 16 complex than the C 12 complex) while micelle size increased with increasing alkyl chain length. Chemical exchange saturation transfer (CEST) experiments showed that all four Eu III complexes displayed slow-to-intermediate water exchange kinetics. As expected, the CEST signals in these complexes decreased with increasing temperatures due to faster water exchange but, interestingly, the CEST signals for the C 14 and C 16 complexes approached a maximum near 25 °C consistent with exchange limited CEST at or near room temperature. The water residence lifetimes obtained by fitting the CEST spectra to the Bloch equations increased in parallel with an increase in alkyl carbon chain-length. By comparisons with the monomethylamide complex, which served as control, the data illustrate that micelle formation serves to slow the rate of water exchange in these systems. The complex having the largest CEST effect per unit Eu III concentration (the C 16 analog) had a detection limit of 5.3 μM. This represents an approximate 250-fold increase in sensitivity relative to the monomethylamide control (detection limit {\^a} 1.3 mM). These features highlight the potential of using micelle-based systems such as these as paramagnetic chemical exchange saturation transfer (PARACEST) agents for molecular imaging by MRI. Four new EuDOTA-tetraamides with variable alkyl chains lengths were synthesized and their CEST properties were extensively studied. Three of these complexes werefound to spontaneously form micelles due to their long alkyl chains which resulted in a dramatic increase in their CEST sensitivities.",
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AB - The synthesis and characterization of four new DOTA-tetraamide ligands having variable alkyl chain lengths (C 1, C 12, C 14, and C 16) and their respective europium(III) complexes are reported. The three EuL complexes having long alkyl chains spontaneously form micelles of variable size. The critical micelle concentration differed for each complex (lower for the C 16 complex than the C 12 complex) while micelle size increased with increasing alkyl chain length. Chemical exchange saturation transfer (CEST) experiments showed that all four Eu III complexes displayed slow-to-intermediate water exchange kinetics. As expected, the CEST signals in these complexes decreased with increasing temperatures due to faster water exchange but, interestingly, the CEST signals for the C 14 and C 16 complexes approached a maximum near 25 °C consistent with exchange limited CEST at or near room temperature. The water residence lifetimes obtained by fitting the CEST spectra to the Bloch equations increased in parallel with an increase in alkyl carbon chain-length. By comparisons with the monomethylamide complex, which served as control, the data illustrate that micelle formation serves to slow the rate of water exchange in these systems. The complex having the largest CEST effect per unit Eu III concentration (the C 16 analog) had a detection limit of 5.3 μM. This represents an approximate 250-fold increase in sensitivity relative to the monomethylamide control (detection limit â 1.3 mM). These features highlight the potential of using micelle-based systems such as these as paramagnetic chemical exchange saturation transfer (PARACEST) agents for molecular imaging by MRI. Four new EuDOTA-tetraamides with variable alkyl chains lengths were synthesized and their CEST properties were extensively studied. Three of these complexes werefound to spontaneously form micelles due to their long alkyl chains which resulted in a dramatic increase in their CEST sensitivities.

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