Synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. In vitro relaxivity studies at 0.2 T

In this study a novel ligand with three carboxylic groups (H3L1) was synthesized. Its non-ion complex with GdL1 holding promise of magnetic resonance imaging (MRI) was synthesized, and the relaxivity of the complex determined. The relaxivity of GdL1 (R1 = 4.5 Mmol- 1•s-1) was larger than that of Gd(...

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Publicado: 2015
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13877003_v51_n_p110_Martinez
http://hdl.handle.net/20.500.12110/paper_13877003_v51_n_p110_Martinez
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spelling paper:paper_13877003_v51_n_p110_Martinez2023-06-08T16:13:00Z Synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. In vitro relaxivity studies at 0.2 T Contrast agent Gadolinium Macrocycle Magnetic resonance imaging Relaxivity In this study a novel ligand with three carboxylic groups (H3L1) was synthesized. Its non-ion complex with GdL1 holding promise of magnetic resonance imaging (MRI) was synthesized, and the relaxivity of the complex determined. The relaxivity of GdL1 (R1 = 4.5 Mmol- 1•s-1) was larger than that of Gd(DTPA)2-(R1 = 3.9 Mmol- 1•s-1). The results showed that the non-ion complex is a prospective MRI contrast agent. © 2014 Elsevier B.V. All rights reserved. 2015 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13877003_v51_n_p110_Martinez http://hdl.handle.net/20.500.12110/paper_13877003_v51_n_p110_Martinez
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Contrast agent
Gadolinium
Macrocycle
Magnetic resonance imaging
Relaxivity
spellingShingle Contrast agent
Gadolinium
Macrocycle
Magnetic resonance imaging
Relaxivity
Synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. In vitro relaxivity studies at 0.2 T
topic_facet Contrast agent
Gadolinium
Macrocycle
Magnetic resonance imaging
Relaxivity
description In this study a novel ligand with three carboxylic groups (H3L1) was synthesized. Its non-ion complex with GdL1 holding promise of magnetic resonance imaging (MRI) was synthesized, and the relaxivity of the complex determined. The relaxivity of GdL1 (R1 = 4.5 Mmol- 1•s-1) was larger than that of Gd(DTPA)2-(R1 = 3.9 Mmol- 1•s-1). The results showed that the non-ion complex is a prospective MRI contrast agent. © 2014 Elsevier B.V. All rights reserved.
title Synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. In vitro relaxivity studies at 0.2 T
title_short Synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. In vitro relaxivity studies at 0.2 T
title_full Synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. In vitro relaxivity studies at 0.2 T
title_fullStr Synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. In vitro relaxivity studies at 0.2 T
title_full_unstemmed Synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. In vitro relaxivity studies at 0.2 T
title_sort synthesis and characterization of a new polyaminocarboxylic macrocyclic ligand and its non-ion gadolinium complex. in vitro relaxivity studies at 0.2 t
publishDate 2015
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13877003_v51_n_p110_Martinez
http://hdl.handle.net/20.500.12110/paper_13877003_v51_n_p110_Martinez
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