Engineering lanthanide complexes with controlled water exchange rates for magnetic resonance imaging

Mark Woods, A. Dean Sherry

Research output: Chapter in Book/Report/Conference proceedingConference contribution

4 Citations (Scopus)

Abstract

The control of the rate of water exchange in lanthanide complexes is critical to their future development as contrast agents in magnetic resonance imaging. In traditional T 1 shortening agents an optimal water residence lifetime (τ M) of around 25 ns is required if the highest relaxivities are to be achieved. In contrast the newer PARACEST agents require that water exchange is much slower with τ M on the order of microseconds. It is now possible to rationally design complexes that exhibit water exchange rates that are ideal for their intended use. The selection of appropriate ligating groups allow a broad control mechanism. Anionic ligating groups such as carboxylates favour faster exchange whereas neutral ligands such as amides favour slower exchange. By altering the steric hindrance around the water coordination site water exchange rates can be fine tuned. The steric hindrance can be altered by controlling the coordination environment of the lanthanide ion and optimal water exchanges rates so achieved.

Original languageEnglish (US)
Title of host publicationAnnual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings
Pages5254-5257
Number of pages4
Volume26 VII
StatePublished - 2004
EventConference Proceedings - 26th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2004 - San Francisco, CA, United States
Duration: Sep 1 2004Sep 5 2004

Other

OtherConference Proceedings - 26th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2004
CountryUnited States
CitySan Francisco, CA
Period9/1/049/5/04

Fingerprint

Lanthanoid Series Elements
Magnetic resonance
Rare earth elements
Imaging techniques
Water
Amides
Contrast Media
Ion exchange
Ligands
Ions

Keywords

  • Lanthanides
  • MRI contrast agents
  • Water exchange rates

ASJC Scopus subject areas

  • Bioengineering

Cite this

Woods, M., & Sherry, A. D. (2004). Engineering lanthanide complexes with controlled water exchange rates for magnetic resonance imaging. In Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings (Vol. 26 VII, pp. 5254-5257)

Engineering lanthanide complexes with controlled water exchange rates for magnetic resonance imaging. / Woods, Mark; Sherry, A. Dean.

Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings. Vol. 26 VII 2004. p. 5254-5257.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Woods, M & Sherry, AD 2004, Engineering lanthanide complexes with controlled water exchange rates for magnetic resonance imaging. in Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings. vol. 26 VII, pp. 5254-5257, Conference Proceedings - 26th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2004, San Francisco, CA, United States, 9/1/04.
Woods M, Sherry AD. Engineering lanthanide complexes with controlled water exchange rates for magnetic resonance imaging. In Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings. Vol. 26 VII. 2004. p. 5254-5257
Woods, Mark ; Sherry, A. Dean. / Engineering lanthanide complexes with controlled water exchange rates for magnetic resonance imaging. Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings. Vol. 26 VII 2004. pp. 5254-5257
@inproceedings{326f4c97b1cc457385023ac0ce9cbfae,
title = "Engineering lanthanide complexes with controlled water exchange rates for magnetic resonance imaging",
abstract = "The control of the rate of water exchange in lanthanide complexes is critical to their future development as contrast agents in magnetic resonance imaging. In traditional T 1 shortening agents an optimal water residence lifetime (τ M) of around 25 ns is required if the highest relaxivities are to be achieved. In contrast the newer PARACEST agents require that water exchange is much slower with τ M on the order of microseconds. It is now possible to rationally design complexes that exhibit water exchange rates that are ideal for their intended use. The selection of appropriate ligating groups allow a broad control mechanism. Anionic ligating groups such as carboxylates favour faster exchange whereas neutral ligands such as amides favour slower exchange. By altering the steric hindrance around the water coordination site water exchange rates can be fine tuned. The steric hindrance can be altered by controlling the coordination environment of the lanthanide ion and optimal water exchanges rates so achieved.",
keywords = "Lanthanides, MRI contrast agents, Water exchange rates",
author = "Mark Woods and Sherry, {A. Dean}",
year = "2004",
language = "English (US)",
volume = "26 VII",
pages = "5254--5257",
booktitle = "Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings",

}

TY - GEN

T1 - Engineering lanthanide complexes with controlled water exchange rates for magnetic resonance imaging

AU - Woods, Mark

AU - Sherry, A. Dean

PY - 2004

Y1 - 2004

N2 - The control of the rate of water exchange in lanthanide complexes is critical to their future development as contrast agents in magnetic resonance imaging. In traditional T 1 shortening agents an optimal water residence lifetime (τ M) of around 25 ns is required if the highest relaxivities are to be achieved. In contrast the newer PARACEST agents require that water exchange is much slower with τ M on the order of microseconds. It is now possible to rationally design complexes that exhibit water exchange rates that are ideal for their intended use. The selection of appropriate ligating groups allow a broad control mechanism. Anionic ligating groups such as carboxylates favour faster exchange whereas neutral ligands such as amides favour slower exchange. By altering the steric hindrance around the water coordination site water exchange rates can be fine tuned. The steric hindrance can be altered by controlling the coordination environment of the lanthanide ion and optimal water exchanges rates so achieved.

AB - The control of the rate of water exchange in lanthanide complexes is critical to their future development as contrast agents in magnetic resonance imaging. In traditional T 1 shortening agents an optimal water residence lifetime (τ M) of around 25 ns is required if the highest relaxivities are to be achieved. In contrast the newer PARACEST agents require that water exchange is much slower with τ M on the order of microseconds. It is now possible to rationally design complexes that exhibit water exchange rates that are ideal for their intended use. The selection of appropriate ligating groups allow a broad control mechanism. Anionic ligating groups such as carboxylates favour faster exchange whereas neutral ligands such as amides favour slower exchange. By altering the steric hindrance around the water coordination site water exchange rates can be fine tuned. The steric hindrance can be altered by controlling the coordination environment of the lanthanide ion and optimal water exchanges rates so achieved.

KW - Lanthanides

KW - MRI contrast agents

KW - Water exchange rates

UR - http://www.scopus.com/inward/record.url?scp=11144304106&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=11144304106&partnerID=8YFLogxK

M3 - Conference contribution

AN - SCOPUS:11144304106

VL - 26 VII

SP - 5254

EP - 5257

BT - Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings

ER -