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Issue 43, 2006
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Synthesis and characterization of a novel paramagnetic macromolecular complex [Gd(TTDASQ–protamine)]

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Abstract

Adenocarcinomas in rats and humans frequently contain perivascular, degranulating mast cells that release heparin. Protamine is a low-molecular weight, cationic polypeptide that binds to heparin and neutralizes its anticoagulant properties. A novel magnetic resonance imaging (MRI) contrast agent containing protamine was synthesized. TTDASQ, the derivative of TTDA (3,6,10-tri(carboxymethyl)-3,6,10-triazadodecanedioic acid), was also synthesized and the kinetic stability of [Gd(TTDASQ)] chelate containing phosphate buffer and ZnCl2 to measure the relaxation rate (R1) at 20 MHz was studied by transmetallation with Zn(II). The water-exchange rate (kex298) of [Gd(TTDASQ)] is 6.4 × 106 s−1 at 25.0 ± 0.1 °C which was obtained from the reduced 17O relaxation rates (1/T1r and 1/T2r) and chemical shift (ωr) of H217O, and it is compared with that previously reported for the other gadolinium(III) complex, [Gd(DO3ASQ)]. The binding affinity assay showed that the (TTDASQ)3–pro19 has higher activity toward heparin. On the other hand, the effect of heparin on the relaxivity of the [Gd(TTDASQ)3–pro19] conjugate shows the binding strength (KA) is 7669 dm3 mol−1 at pH 7.4 and the relaxivity (rb1) of the [Gd(TTDASQ)3–pro19]–heparin adduct is 30.9 dm3 mmol−1 s−1.

Graphical abstract: Synthesis and characterization of a novel paramagnetic macromolecular complex [Gd(TTDASQ–protamine)]

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Supplementary files

Article information


Submitted
06 Apr 2006
Accepted
08 Sep 2006
First published
18 Sep 2006

Dalton Trans., 2006, 5149-5155
Article type
Paper

Synthesis and characterization of a novel paramagnetic macromolecular complex [Gd(TTDASQ–protamine)]

T. Cheng, W. Lee, J. Jeng, C. Wu, G. Liu, M. Y. N. Chiang and Y. Wang, Dalton Trans., 2006, 5149 DOI: 10.1039/B604783A

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