Hyperbranched polyglycerol-grafted WOx nanowires: Synthesis, characterization, functionalization and as effective drug targeted delivery vehicle
Autor: | Wenlong Wang, Xiulan Cai, Jie Wang, Xiaoyun Mo, Xiaoxin Yang, Binglong Yu |
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Rok vydání: | 2020 |
Předmět: |
Biocompatibility
Nanowire chemistry.chemical_element 02 engineering and technology Tungsten 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences 0104 chemical sciences Nanomaterials Colloid and Surface Chemistry Targeted drug delivery Chemical engineering chemistry Photocatalysis Surface modification 0210 nano-technology Drug carrier |
Zdroj: | Colloids and Surfaces A: Physicochemical and Engineering Aspects. 596:124734 |
ISSN: | 0927-7757 |
DOI: | 10.1016/j.colsurfa.2020.124734 |
Popis: | Tungsten oxide (WOx) is an important n-type semiconductor, which has attracted wide attention in the fields of gas sensing materials, photocatalysis, photoluminescence and electrochemistry due to its excellent electro-optical properties. However, the application potential of WOx-based nanomaterials in biomedicine has been neglected. In this paper, we firstly synthesized tungsten oxide nanowires (WOx NWs) by one-step method using tungsten chloride and triethylene glycol as raw materials, and reported an effective surface engineering strategy for polyglycerol-functionalized tungsten oxide nanowires (WOx-PG) to enhance their colloidal stability, biocompatibility, and selective toxicity to specific cancer cells in dispersion media. The WOx-PG was further derivatized and covalently combined with FA (WOx-PG-FA) as a drug targeting vector to deliver doxorubicin (DOX) to cancer cells. Compared with WOx NWs, WOx-PG exhibits smaller size (30−90 nm), more uniform distribution, better solubility and biocompatibility. The hemolysis rate of PG-modified WOx NWs was significantly reduced, being only 1.35 % at 200 μg/ml. The in vitro drug release percentage of WOx-PG-FA/DOX reached 80.78 % within 48 h at pH 5.2. In vitro toxicity assays and confocal laser scanning microscope (CLSM) results indicated that PG-functionalized WOx NWs were not cytotoxic, and WOx-PG-FA/DOX had highly selective cytotoxicity on HeLa cells. These results indicate that WOx-PG-FA is a potential drug carrier for effective targeting of cancer therapy. |
Databáze: | OpenAIRE |
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