4.6 Article

Fabrication of the water-soluble functionalized silicon nanoparticles for biomedical applications

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JOURNAL OF MATERIALS SCIENCE
卷 57, 期 7, 页码 4738-4753

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SPRINGER
DOI: 10.1007/s10853-022-06883-9

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  1. National Natural Science Foundation of China [22074069, 21775077]

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Functionalized water-soluble silicon nanoparticles were successfully synthesized and applied in biomedical imaging. The properties of the functionalized SiNPs, including improved fluorescence intensity, photoluminescence quantum yield, fluorescence lifetimes, photo-stability, and biocompatibility, were significantly enhanced. The longitudinal relaxation of Gd-SiNPs was found to be higher than that of the commercial contrast agent Gd-DTPA. The charming Gd-SiNPs were successfully used as a biologic probe in fluorescence and magnetic resonance dual-mode imaging in vivo and in vitro.
Functionalized water-soluble silicon nanoparticles were fabricated and applied in biomedical imaging. Firstly, hydrophobic hydride-capped silicon nanoparticles (H-SiNPs) were synthesized by hydrogen silsesquioxane, subsequently modified by allylthiourea and further chelated with gadopentetate dimeglumine (Gd-DTPA) to fabricate water-soluble functionalized SiNPs. Fourier transform infrared technology and X-ray photoelectron spectroscopy evidenced the successful function. The properties of functionalized SiNPs were significantly improved including fluorescence intensity, photoluminescence quantum yield (from 0.87 to 14.04%), fluorescence lifetimes (from 29.9 to 63.8 mu s), photo-stability, biocompatibility, etc. Hematoxylin and eosin (H&E) staining assay further demonstrated the low toxicity and the satisfactory biocompatibility of Gd-SiNPs. The longitudinal relaxation (r(1)) of Gd-SiNPs was measured to be 11.59 mM(-1) s(-1) and much higher than that of the commercial contrast agent Gd-DTPA (4.29 mM(-1) s(-1)). Finally, the charming Gd-SiNPs were successfully applied as a biologic probe in fluorescence and magnetic resonance dual-mode imaging in vivo and in vitro. [GRAPHICS] .

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