| Literature DB >> 30035345 |
Viktor Reshetnikov1, Steffen Daum1, Christina Janko2, Weronika Karawacka1,2, Rainer Tietze2, Christoph Alexiou2, Solomiya Paryzhak3, Tetiana Dumych3, Rostyslav Bilyy3, Philipp Tripal4, Benjamin Schmid4, Ralf Palmisano4, Andriy Mokhir1.
Abstract
Mitochondrial membrane potential is more negative in cancer cells than in normal cells, allowing cancer targeting by delocalized lipophilic cations (DLCs). However, as the difference is rather small, these drugs affect also normal cells. Now a concept of pro-DLCs is proposed based on an N-alkylaminoferrocene structure. These prodrugs are activated by the reaction with reactive oxygen species (ROS) forming ferrocenium-based DLCs. Since ROS are overproduced in cancer, the high-efficiency cancer-cell-specific targeting of mitochondria could be achieved as demonstrated by fluorescence microscopy in combination with two fluorogenic pro-DLCs in vitro and in vivo. We prepared a conjugate of another pro-DLC with a clinically approved drug carboplatin and confirmed that its accumulation in mitochondria was higher than that of the free drug. This was reflected in the substantially higher anticancer effect of the conjugate.Entities:
Keywords: aminoferrocene; anticancer prodrugs; cancer; mitochondria targeting; reactive oxygen species
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Year: 2018 PMID: 30035345 DOI: 10.1002/anie.201805955
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336