4.5 Article

Cytotoxic and DNA-binding Capacity of Titanocene Functionalized Mesoporous Nanoparticles in Breast Cancer Cell Lines MCF-7 and MDA-MB-231

Journal

CURRENT PHARMACEUTICAL DESIGN
Volume 29, Issue 22, Pages 1791-1799

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1381612829666230727115356

Keywords

Titanocene; anticancer; mesoporous silica; DNA-binding; breast cancer; nanoparticles

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This study aimed to prepare and structurally characterize titanocene functionalized mesoporous silica nanoparticles and evaluate their cytotoxic activity against cancer cells. The titanocene-functionalized mesoporous silica nanoparticles showed promising antitumoral activity against breast cancer cells.
Aims The fight against cancer is an active research topic that combines several disciplines to find suitable agents to treat various tumours.Background Following cisplatin, organometallic compounds, including titanocene derivatives, have been tested as antitumoral agents. However, key issues still need to be addressed in metallodrug chemotherapy relating to solubility, stability, and dosage. Mesoporous silica nanoparticles, being low toxic biocompatible materials with high loading capacity, are ideal candidates to overcome these problems.Objective This study aimed to prepare and structurally characterize titanocene functionalized mesoporous silica nanoparticles and evaluate their cytotoxic activity against cancer cells.Methods The preparation of titanocene functionalized mesoporous silica nanoparticles was achieved by synthetic protocols, involving either grafting or tethering. Characterization was carried out using standard techniques, FT-IR, XRD, XRF, TEM, and BET. The titanocene functionalized materials were studied as antitumoral agents in the breast cancer lines MCF-7 and MDA-MB-231.Results The functionalized MSN showed promising antitumoral activity against cells lines MCF-7 and MDA-MB-231 up to 9 times more than titanocene alone.Conclusion This study reported the potential of titanocene-functionalized mesoporous silica nanoparticles in future chemotherapeutic actions.

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