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- W3004630128 endingPage "298" @default.
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- W3004630128 abstract "Drug-loaded, PEGylated, organic-modified silica (ORMOSIL) nanoparticles prepared by microemulsion condensation of vinyltriethoxysilane (VTES) were investigated as potential nanovectors for cancer therapy. To target cancer stem cells, anti-CD44v6 antibody and hyaluronic acid (HA) were conjugated to amine-functionalized PEGylated ORMOSIL nanoparticles through thiol-maleimide and amide coupling chemistries, respectively. Specific binding and uptake of conjugated nanoparticles were studied on cells overexpressing the CD44v6 receptor. Cytotoxicity was subsequently evaluated in the same cells after the uptake of the nanoparticles. Internalization of nanocarriers loaded with the anticancer drug 3N-cyclopropylmethyl-7-phenyl-pyrrolo- quinolinone (MG2477) into cells resulted in a substantial increase of the cytotoxicity with respect to the free formulation. Targeting with anti-CD44v6 antibodies or HA yielded nanoparticles with similar effectiveness, in their optimized formulation." @default.
- W3004630128 created "2020-02-14" @default.
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- W3004630128 date "2020-02-10" @default.
- W3004630128 modified "2023-10-16" @default.
- W3004630128 title "Multifunctional, CD44v6-Targeted ORMOSIL Nanoparticles Enhance Drugs Toxicity in Cancer Cells" @default.
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- W3004630128 doi "https://doi.org/10.3390/nano10020298" @default.
- W3004630128 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7075197" @default.
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- W3004630128 hasPublicationYear "2020" @default.
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