| Literature DB >> 28585348 |
Katja Seidel1, Asha Balakrishnan2, Christoph Alexiou3, Christina Janko3, Ronja-Melinda Komoll2, Liang-Liang Wang1, Andreas Kirschning1, Michael Ott2.
Abstract
Conjugates based on nanostructured, superparamagnetic particles, a thermolabile linker and a cytotoxic maytansinoid were developed to serve as a model for tumour-selective drug delivery and release. It combines chemo- with thermal therapy. The linker-modified toxin was prepared by a combination of biotechnology and semisynthesis. Drug release was achieved by hyperthermia through an external oscillating electromagnetic field that induces heat inside the particles. Efficacy of this release concept was demonstrated both for cancer cell proliferation in vitro, and for tumour growth in vivo, in a xenograft mouse model. Biocompatibility studies for these magnetic-nanoparticle/ansamitocin conjugates complement this work.Entities:
Keywords: antitumour agents; biotransformations; in vivo studies; iron; maytansin; nanoparticles
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Year: 2017 PMID: 28585348 DOI: 10.1002/chem.201701491
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236