| Literature DB >> 33406699 |
Candace M Day1, Martin J Sweetman1,2, Shane M Hickey1, Yunmei Song1, Yongjun Liu3, Na Zhang3, Sally E Plush1,2, Sanjay Garg1,2.
Abstract
Conventional chemotherapies used for breast cancer (BC) treatment are non-selective, attacking both healthy and cancerous cells. Therefore, new technologies that enhance drug efficacy and ameliorate the off-target toxic effects exhibited by currently used anticancer drugs are urgently needed. Here we report the design and synthesis of novel mesoporous silica nanoparticles (MSNs) equipped with the hormonal drug tamoxifen (TAM) to facilitate guidance towards estrogen receptors (ERs) which are upregulated in breast tumours. TAM is linked to the MSNs using a poly-ʟ-histidine (PLH) polymer as a pH-sensitive gatekeeper, to ensure efficient delivery of encapsulated materials within the pores. XRD, HR-TEM, DLS, SEM, FT-IR and BET techniques were used to confirm the successful fabrication of MSNs. The MSNs have a high surface area (>1000 m2/g); and a mean particle size of 150 nm, which is an appropriate size to allow the penetration of premature blood vessels surrounding breast tumours. Successful surface functionalization was supported by FT-IR, XPS and TGA techniques, with a grafting ratio of approximately 29%. The outcomes of this preliminary work could be used as practical building blocks towards future formulations.Entities:
Keywords: breast cancer; functionalized nanostructures; mesoporous silica nanoparticles; poly-ʟ-histidine; surface reactivity; tamoxifen; targeting vector
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Year: 2021 PMID: 33406699 PMCID: PMC7795496 DOI: 10.3390/molecules26010219
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411