Cyclen-based Gd3+ complexes as MRI contrast agents: Relaxivity enhancement and ligand design. Issue 22 (15th November 2016)
- Record Type:
- Journal Article
- Title:
- Cyclen-based Gd3+ complexes as MRI contrast agents: Relaxivity enhancement and ligand design. Issue 22 (15th November 2016)
- Main Title:
- Cyclen-based Gd3+ complexes as MRI contrast agents: Relaxivity enhancement and ligand design
- Authors:
- Rashid, Haroon Ur
Martines, Marco Antonio Utrera
Jorge, Juliana
de Moraes, Paula Martin
Umar, Muhammad Naveed
Khan, Kamin
Rehman, Hanif Ur - Abstract:
- Graphical abstract: Abstract: Magnetic Resonance Imaging (MRI) is a noninvasive radiology technique used to examine the internal organs of human body. It is useful for the diagnosis of structural abnormalities in the body. Contrast agents are used to increase the sensitivity of this technique. 1, 4, 7, 10-Tetraazacyclododecane (cyclen) is a macrocyclic tetraamine. Its derivatives act as useful ligands to produce stable complexes with Gd 3+ ion. Such chelates are investigated as MRI contrast agents. Free Gd 3+ ion is extremely toxic for in vivo use. Upon complexation with a cyclen-based ligand, it is trapped in the preformed central cavity of the ligand resulting in the formation of a highly stable Gd 3+ -chelate. Better kinetic and thermodynamic stability of cyclen-based MRI contrast agents decrease their potential toxicity for in vivo use. Consequently, such agents have proved to be safest for clinical applications. Relaxivity is the most important parameter used to measure the effectiveness of a contrast agent. A number of factors influence this parameter. This article elucidates detailed strategies to increase relaxivity of cyclen-based MRI contrast agents. 1, 4, 7, 10-Tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid (DOTA) and 1, 4, 7, 10-tetraazacyclododecane-1, 4, 7-triacetic acid (DO3A) are two key ligands derived from cyclen. They also act as building blocks for the synthesis of novel ligands. A few important methodologies for the synthesis of DOTA and DO3AGraphical abstract: Abstract: Magnetic Resonance Imaging (MRI) is a noninvasive radiology technique used to examine the internal organs of human body. It is useful for the diagnosis of structural abnormalities in the body. Contrast agents are used to increase the sensitivity of this technique. 1, 4, 7, 10-Tetraazacyclododecane (cyclen) is a macrocyclic tetraamine. Its derivatives act as useful ligands to produce stable complexes with Gd 3+ ion. Such chelates are investigated as MRI contrast agents. Free Gd 3+ ion is extremely toxic for in vivo use. Upon complexation with a cyclen-based ligand, it is trapped in the preformed central cavity of the ligand resulting in the formation of a highly stable Gd 3+ -chelate. Better kinetic and thermodynamic stability of cyclen-based MRI contrast agents decrease their potential toxicity for in vivo use. Consequently, such agents have proved to be safest for clinical applications. Relaxivity is the most important parameter used to measure the effectiveness of a contrast agent. A number of factors influence this parameter. This article elucidates detailed strategies to increase relaxivity of cyclen-based MRI contrast agents. 1, 4, 7, 10-Tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid (DOTA) and 1, 4, 7, 10-tetraazacyclododecane-1, 4, 7-triacetic acid (DO3A) are two key ligands derived from cyclen. They also act as building blocks for the synthesis of novel ligands. A few important methodologies for the synthesis of DOTA and DO3A derivatives are described. Moreover, the coordination geometry of chelates formed by these ligands and their derivatives is discussed as well. Novel ligands can be developed by the appropriate derivatization of DOTA and DO3A. Gd 3+ -chelates of such ligands prove to be useful MRI contrast agents of enhanced relaxivity, greater stability, better clearance, lesser toxicity and higher water solubility. … (more)
- Is Part Of:
- Bioorganic & medicinal chemistry. Volume 24:Issue 22(2016)
- Journal:
- Bioorganic & medicinal chemistry
- Issue:
- Volume 24:Issue 22(2016)
- Issue Display:
- Volume 24, Issue 22 (2016)
- Year:
- 2016
- Volume:
- 24
- Issue:
- 22
- Issue Sort Value:
- 2016-0024-0022-0000
- Page Start:
- 5663
- Page End:
- 5684
- Publication Date:
- 2016-11-15
- Subjects:
- QBPPRVHXOZRESW-UHFFFAOYSA-N -- GSKFRYPMANPIFA-UHFFFAOYSA-N -- IQUHNCOJRJBMSU-UHFFFAOYSA-N -- GMECCVFSBLSIKE-UHFFFAOYSA-N -- GJLCFYNSBAWKRC-UHFFFAOYSA-L -- PGOBIYLZGKUZRI-UHFFFAOYSA-M -- DKPDCUHILIVCHH-UHFFFAOYSA-N -- PTHWUBKVGQPQBJ-UHFFFAOYSA-I -- QGOCMKXJEQGYCN-UHFFFAOYSA-N -- QBKSRNQDZWPQAM-UHFFFAOYSA-N -- GOPRNAXREFXRPT-IVLVDKQOSA-N
Cyclen -- Chelate -- Contrast agent -- Relaxivity -- Octadentate -- Gadolinium
Bioorganic chemistry -- Periodicals
Pharmaceutical chemistry -- Periodicals
Biochemistry -- Periodicals
Chemistry, Clinical -- Periodicals
Chemistry, Organic -- Periodicals
Chimie bio-organique -- Périodiques
Chimie pharmaceutique -- Périodiques
615.19 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09680896 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.bmc.2016.09.069 ↗
- Languages:
- English
- ISSNs:
- 0968-0896
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.325000
British Library DSC - BLDSS-3PM
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- 1315.xml