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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Skiba, Elżbieta
Lodz University of Technology
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article
Carbosilane ruthenium metallodendrimer as alternative anti-cancer drug carrier in triple negative breast cancer mouse model: A preliminary study
Abstract
The carbosilane metallodendrimer G1-[[NCPh(o-N)Ru(η6- p-cymene)Cl]Cl]4 (CRD13), based on an arene Ru(II)complex coordinated to imino-pyridine surface groups, has been conjugated with anti-cancer drugs. Rutheniumin the positively-charged dendrimer structure allows this nanoparticle to be considered as an anticancer drugcarrier, made more efficient because ruthenium has anticancer properties. The ability of CRD13 to form complexes with Doxorubicin (DOX), 5-Fluorouracil (5-Fu), and Methotrexate (MTX) has been evaluated using zetapotential measurement, transmission electron microscopy (TEM) and computer simulation. The results show thatit forms stable nanocomplexes with all those drugs, enhancing their effectiveness against MDA-MB-231 cancercells. In vivo tests indicate that the CRD13/DOX system caused a decrease of tumor weight in mice with triplenegative breast cancer. However, the tumors were most visibly reduced when naked dendrimers were injected.