Janus Mesoporous Silica Nanoparticles for Dual Targeting of Tumor Cells and Mitochondria.
Victoria LópezMaria Rocío VillegasVerónica RodríguezGonzalo VillaverdeDaniel LozanoAlejandro BaezaMaría Vallet-RegíPublished in: ACS applied materials & interfaces (2017)
The development of targeted nanocarriers able to be selectively internalized within tumor cells, and therefore to deliver anti-tumor drugs specifically to diseased cells, constitutes one of the most important goals in nano-oncology. Herein, the development of Janus mesoporous silica particles asymmetrically decorated with two targeting moieties, one of them selective for folate membrane cell receptors (folic acid) and the other one able to bind to mitochondria membrane (triphenylphosphine, TPP), is described in order to achieve sequential cell to organelle vectorization. The asymmetric decoration of each side of the particle allows fine control in the targeting attachment process in comparison with the use of symmetric nanocarriers. The presence of folic acid induces a higher increase in particle accumulation inside tumor cells, and once there, these nanocarriers are guided close to mitochondria by the action of the TPP moiety. This strategy can be applied for improving the therapeutic efficacy of current nanomedicines.
Keyphrases
- cancer therapy
- drug delivery
- cell death
- single cell
- cell therapy
- drug release
- reactive oxygen species
- induced apoptosis
- cell cycle arrest
- endoplasmic reticulum
- palliative care
- public health
- quantum dots
- air pollution
- stem cells
- mesenchymal stem cells
- oxidative stress
- global health
- signaling pathway
- walled carbon nanotubes
- drug induced
- solid state