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Book of Abstracts - Ruhr-Universität Bochum

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P-16<br />

ISBOMC `10 5.7 – 9.7. 2010 <strong>Ruhr</strong>-<strong>Universität</strong> <strong>Bochum</strong><br />

Conjugation <strong>of</strong> Rheniumtricarbonyl Bisimine Complexes to Polylactides -<br />

Fluorescent Polymers for in vivo Tumour Diagnostics<br />

Nadine E. Brückmann a and Peter C. Kunz* a<br />

a Heinrich-Heine-University <strong>of</strong> Düsseldorf, Department <strong>of</strong> Inorganic Chemistry I,<br />

<strong>Universität</strong>sstr. 1, 40225, Düsseldorf, Germany. E-mail: peter.kunz@uni-duesseldorf.de<br />

In order to improve current cancer pharmaceuticals, new polymer-based transport systems are being<br />

developed that deliver the drug directly to the tumour, where it can subsequently be released.<br />

Macromolecules can accumulate in tumours due to the EPR-effect. 1 Although polymers are now<br />

widely used in therapeutic approaches, only a few examples <strong>of</strong> diagnostically applied polymerconjugates<br />

exist. 2 Rheniumtricarbonyl bisimines e.g. are useful as dyes for fluorescence microscopy.<br />

Their fluorescence emission lies in the visible light spectrum, resulting from a metal-to-ligand-chargetransfer<br />

(MLCT). These transitions typically have large Stokes shifts, which makes the fluorescence<br />

easily destinguishable from tissue aut<strong>of</strong>luorescence. 3 Attachment <strong>of</strong> these rhenium cores to ligandfunctionalised<br />

polylactides leads to biodegradable fluorescent polymers.<br />

In particular, rheniumtricarbonyl complexes <strong>of</strong> 2,2’bipyridine (bipy), 1,10-phenanthroline (phen) as<br />

well as dipyrido[3,2-a:2’,3’-c]phenazine (dppz) were prepared. Absorption and emission data were<br />

ascertained, cytotoxicity was determined on A2780 ovarian cancer cell lines and the in vivo<br />

localisation was examined by confocal microscopy. Investigations into their degradation kinetics are<br />

currently ongoing.<br />

References<br />

1. H. Maeda, J. Wu, T. Sawa, Y. Matsamura, K. Hori, J. Cont. Rel. 2000, 65, 271-284.<br />

2. A. Mitra, A. Nan, H. Ghandehari et al., Pharm. Res. 2004, 21(7), 1153-1159.<br />

3. A. Amoroso, M. Coogan, J.E. Dunne et al., Chem. Commun. 2007, 29, 3066-3068.<br />

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