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• W1805178021 startingPage "262" @default.
• W1805178021 abstract "In this study, a new structure of methotrexate/hydroxyapatite (MTX/HAp) nanorods via a facile hydrothermal route was reported. The as-synthesized samples were then characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), thermogravimetric (TG) and differential scanning calorimetry (DSC) analysis. In order to explore the formation mechanism, the effects of reaction time, MTX concentrations and addition of ethylene glycol (PEG) were emphatically examined. The results indicated that, with the increase in reaction time, the fibrous nanoparticles turned to needle-like and then to rod-like. Our study also proved that reaction time of 12 h was enough for the full-growth of the nanostructure. Drug-loading capacities (AIn) rose dramatically in the first 12 h and reached a plateau afterwards. Importantly, MTX played a critical role in the longitudinal growth of MTX/HAp nanostructure and polyethylene glyco (PEG) was a good dispersing agent to improve the monodispersity. As expected, the functional agent of MTX was served as both the target anticancer drug loaded in HAp and effective complex agents to modify and control the morphologies of MTX/HAp. Lastly, in vitro bioassay tests gave us evidence that obvious tumor inhibition can be achieved when MTX was hybridized with HAp." @default.
• W1805178021 created "2016-06-24" @default.
• W1805178021 creator A5008050294 @default.
• W1805178021 creator A5066556669 @default.
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• W1805178021 date "2015-12-01" @default.
• W1805178021 modified "2023-09-26" @default.
• W1805178021 title "Synthesis of nanostructured methotrexate/hydroxyapatite: Morphology control, growth mechanism, and bioassay explore" @default.
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• W1805178021 doi "https://doi.org/10.1016/j.colsurfb.2015.09.015" @default.
• W1805178021 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26409253" @default.
• W1805178021 hasPublicationYear "2015" @default.
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