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Issue 3, 2003
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New routes to bioconjugates of rhenium using the oxobis(dithiolato)rhenate(V) core

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Abstract

The development of the rhenium-188 generator has provided a convenient and economic source of radionuclide for targeted radionuclide therapy of cancer. To exploit this more widely, mild, convenient and efficient methods for stable incorporation of the radionuclide into biomolecules are required. The aim of this work is to exploit the tumour targeting therapeutic radiopharmaceutical [ReO(dmsa)2] (H2dmsa = meso-dimercaptosuccinic acid), which is easily synthesised in radioactive form and highly stable in vivo, for this purpose. A new efficient synthesis of [ReO(dmsa)2], as a single isomer (syn-endo), from perrhenate using acetylhydrazine as reductant, is reported. Dehydration of the two dicarboxylic acid groups of [ReO(dmsa)2] with dicyclohexylcarbodiimide gives the yellow cyclic dianhydride [ReO(dmsaa)2] (H2dmsaa = meso-dimercaptosuccinic anhydride) without disrupting the ReOS4 core. As its tetraethylammonium salt, [ReO(dmsaa)2] was characterised crystallographically as a distorted square pyramidal complex with an axial oxo-group and a syn-endo orientation of the two anhydride rings with respect to this oxo-group. [ReO(dmsaa)2] reacts with primary and secondary amines including lysine residues of peptides, to form amide-linked conjugates, which were identified by ES-MS. The syntheses are fast, efficient and employ mild conditions, making them readily adaptable for a kit-based approach to rhenium and technetium radiopharmaceuticals.

Graphical abstract: New routes to bioconjugates of rhenium using the oxobis(dithiolato)rhenate(v) core

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Publication details

The article was received on 07 Oct 2002, accepted on 29 Nov 2002 and first published on 23 Dec 2002


Article type: Paper
DOI: 10.1039/B209820B
Citation: Dalton Trans., 2003,0, 311-317
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    New routes to bioconjugates of rhenium using the oxobis(dithiolato)rhenate(V) core

    U. Choudhry, W. E. P. Greenland, W. A. Goddard, T. A. J. Maclennan, S. J. Teat and P. J. Blower, Dalton Trans., 2003, 0, 311
    DOI: 10.1039/B209820B

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