Phosphonate-titanium dioxide assemblies: platform for multimodal diagnostic-therapeutic nanoprobes
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
21662977
DOI
10.1021/jm200449y
Knihovny.cz E-resources
- MeSH
- Affinity Labels chemical synthesis chemistry pharmacology MeSH
- Fluorescent Dyes chemical synthesis chemistry pharmacology MeSH
- Microscopy, Fluorescence MeSH
- Gadolinium MeSH
- HeLa Cells MeSH
- Coordination Complexes chemical synthesis chemistry pharmacology MeSH
- Humans MeSH
- Magnetic Resonance Imaging MeSH
- Mesenchymal Stem Cells metabolism MeSH
- Mice MeSH
- Nanoparticles * MeSH
- Organophosphonates chemical synthesis chemistry pharmacology MeSH
- Antineoplastic Agents chemical synthesis chemistry pharmacology MeSH
- Drug Screening Assays, Antitumor MeSH
- T-Lymphocytes metabolism MeSH
- Titanium chemistry pharmacology MeSH
- Ultraviolet Rays MeSH
- Cell Survival drug effects MeSH
- Structure-Activity Relationship MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Affinity Labels MeSH
- Fluorescent Dyes MeSH
- Gadolinium MeSH
- Coordination Complexes MeSH
- Organophosphonates MeSH
- Antineoplastic Agents MeSH
- Titanium MeSH
- titanium dioxide MeSH Browser
Multimodal imaging-therapeutic nanoprobe TiO(2)@RhdGd was prepared and successfully used for in vitro and in vivo cell tracking as well as for killing of cancer cells in vitro. TiO(2) nanoparticles were used as a core for phosphonic acid modified functionalities, responsible for contrast in MRI and optical imaging. The probe shows high (1)H relaxivity and relaxivity density values. Presence of fluorescent dye allows for visualization by means of fluorescence microscopy. The applicability of the probe was studied, using mesenchymal stem cells, cancer HeLa cells, and T-lymphocytes. The probe did not exhibit toxicity in any of these systems. Labeled cells were successfully visualized in vitro by means of fluorescence microscopy and MRI. Furthermore, it was shown that the probe TiO(2)@RhdGd can be changed into a cancer cell killer upon UV light irradiation. The above stated results represent a valuable proof of a principle showing applicability of the probe design for diagnosis and therapy.
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