RESUMO
To treat tumours efficiently and spare normal tissues, targeted drug delivery is a promising alternative to conventional, systemic administered chemotherapy. Drug-carrying magnetic nanoparticles can be concentrated in tumours by external magnetic fields, preventing the nanomaterial from being cleared by metabolic burden before reaching the tumour. Therefore in Magnetic Drug Targeting (MDT) the favoured mode of application is believed to be intra-arterial. Here, we show that a simple yet versatile magnetic carrier-system (hydrodynamic particles diameter <200nm) accumulates the chemotherapeutic drug mitoxantrone efficiently in tumours. With MDT we observed the following drug accumulations relative to the recovery from all investigated tissues: tumour region: 57.2%, liver: 14.4%, kidneys: 15.2%. Systemic intra-venous application revealed different results: tumour region: 0.7%, liver: 14.4 % and kidneys: 77.8%. The therapeutic outcome was demonstrated by complete tumour remissions and a survival probability of 26.7% (P=0.0075). These results are confirming former pilot experiments and implying a milestone towards clinical studies. FROM THE CLINICAL EDITOR: This team of investigators studied drug carrying nanoparticles for magnetic drug targeting (MDT), demonstrating the importance of intra-arterial administration resulting in improved clinical outcomes in the studied animal model compared with intra-venous.
Assuntos
Sistemas de Liberação de Medicamentos , Nanopartículas de Magnetita/química , Mitoxantrona/uso terapêutico , Neoplasias/tratamento farmacológico , Animais , Feminino , Nanopartículas de Magnetita/ultraestrutura , Mitoxantrona/química , Mitoxantrona/farmacologia , Neoplasias/diagnóstico por imagem , Neoplasias/metabolismo , Neoplasias/patologia , Tamanho da Partícula , Coelhos , Radiografia , Espectrofotometria Infravermelho , Distribuição TecidualRESUMO
Here we demonstrate, for the first time, the heterogeneous nucleation and growth of silver patches on submicrometer silica spheres. While patches can be grown directly onto native silica particles, it is shown that a higher patch yield can be obtained by first treating the silica with a mixture of an alkanolamine and silver nitrate. Variation of the pretreatment and subsequent coating reactions allowed the patch yield, number, size, thickness, and shape to be adjusted. The patchy particles were shown to possess plasmon modes extending from the visible into the near-IR region, making these structures highly interesting for both their asymmetric morphological and functional properties.