Issue 7, 2004

Characterization of a gadolinium-tagged modular contrast agent by element and molecular mass spectrometry

Abstract

A modular gadolinium-tagged contrast agent for magnetic resonance imaging has been characterized by mass spectrometry. The synthetic construct exhibits a molecular weight of about 8 kDa and is composed of three modules, (i) a diethylene triamine pentaacetic acid (DTPA) module for complexation of Gd3+, (ii) a peptide nucleic acid (PNA) sequence for hybridisation with a complementary nucleic acid sequence, and (iii) a peptide transmembrane transport module. Electrospray mass spectrometry (nanoESI-MS) was used for determination of the molecular weight of the intact functional peptide and of a synthetic intermediate. In general, signals were observed for both the Gd-complexed and uncomplexed forms. For measurement of the Gd saturation size-exclusion chromatography (SEC) was coupled on-line to high-resolution inductively coupled plasma mass spectrometry (ICP-MS) and 32S, 34S and 157Gd were simultaneously monitored. The monitoring of sulfur as a marker element for the organic part of the molecule is possible due to the presence of a disulfide bridge and a methionine residue. The molar Gd/S ratio provides a measure of the Gd saturation, which was found to be in the range of 55% to 85% in the samples investigated. Moreover, a small amount of iron tightly complexed to the contrast agent constructs was detected and was probably taken up during synthesis or purification. Thus, the combined application of SEC-ICP-MS and nanoESI-MS delivers the complementary element and molecular information required for a reliable characterization of metal-tagged contrast agents of complex, modular design.

Article information

Article type
Paper
Submitted
02 Dec 2003
Accepted
04 Feb 2004
First published
17 Mar 2004

J. Anal. At. Spectrom., 2004,19, 852-857

Characterization of a gadolinium-tagged modular contrast agent by element and molecular mass spectrometry

R. Krüger, K. Braun, R. Pipkorn and W. D. Lehmann, J. Anal. At. Spectrom., 2004, 19, 852 DOI: 10.1039/B315649D

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