Issue 10, 2010

A novel solid phase extraction method for pre-concentration of gadolinium and gadolinium based MRI contrast agents from the environment

Abstract

An efficient solid phase extraction (SPE) method using bis-(2-ethylhexyl)-phosphate (HDEHP) coated reverse phase C18 support has been developed for the pre-concentration of Gadolinium (Gd) and Gd contrast agents widely used in magnetic resonance imaging (MRI). Enrichment of Gd in the ionic form has been compared with strong cation exchange material Chromabond SA (SCX), weak ion exchange material Chelex-100 and also with lanthanide specific HDEHP modified reverse phase C18. The determination of Gd and its complexes after enrichment were performed using inductively coupled plasma mass spectrometry (ICP-MS) and on the basis of 158Gd. Among the three SPE materials, HDEHP coated reverse phase C18 SPE has been found to be most efficient, yielding a hundredfold Gd enrichment with > 95% recovery for linear and cyclic contrast agents like Gd-DTPA (Magnevist), Gd-DOTA (Dotarem), Gd-BOPTA (Multihance), and Gd-BT-DO3A (Gadovist). The developed SPE method has been successfully applied to the surface water and waste water samples originated from different places in Berlin, Germany. The results were in good agreement with the results obtained with direct measurement with ICP-MS. The developed pre-concentration method can be efficiently used for the determination of trace levels of gadolinium in the environment even with less sensitive analytical techniques.

Graphical abstract: A novel solid phase extraction method for pre-concentration of gadolinium and gadolinium based MRI contrast agents from the environment

Article information

Article type
Paper
Submitted
16 Feb 2010
Accepted
26 May 2010
First published
05 Jul 2010

J. Anal. At. Spectrom., 2010,25, 1573-1580

A novel solid phase extraction method for pre-concentration of gadolinium and gadolinium based MRI contrast agents from the environment

Chinthalapati Siva Kesava Raju, D. Lück, H. Scharf, N. Jakubowski and U. Panne, J. Anal. At. Spectrom., 2010, 25, 1573 DOI: 10.1039/C003251D

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