研究目的
To develop a facile and general method for fabricating fluorescent inorganic nanoparticles with diverse shapes for cell imaging applications, specifically to study the effect of nanoparticle shapes on cellular uptake behaviors.
研究成果
The method successfully fabricates fluorescent inorganic nanoparticles with diverse shapes, showing intense fluorescence, low cytotoxicity, and good photostability. Cell imaging experiments indicate that nanoparticle shape significantly influences cellular uptake, with ellipsoidal shapes having the highest rate. This approach provides a novel way to create morphology-specific fluorescent probes for biological applications.
研究不足
The fluorescence quantum yields are relatively low compared to some silica hybrid nanoparticles, possibly due to thin silica shells not fully restricting AIEgen motions. The study is preliminary, focusing on HeLa cells, and may not generalize to other cell types or in vivo conditions.
1:Experimental Design and Method Selection:
The study uses a sol-gel method to coat hematite nanoparticles (HNPs) with a silica shell containing aggregation-induced emission luminogens (AIEgens) to create fluorescent probes. The rationale is to enable visualization of nanoparticle-cell interactions.
2:Sample Selection and Data Sources:
Hematite nanoparticles (α-Fe2O3) with spindle, ellipsoidal, and quasi-spherical shapes are synthesized via hydrothermal methods. HeLa cells are used for cytotoxicity and imaging studies.
3:List of Experimental Equipment and Materials:
Materials include ferric nitrate nonahydrate, sodium dihydrogen phosphate, polyvinyl pyrrolidone (PVP), AIEgen-Si(OCH3)3, tetraethyl orthosilicate (TEOS), and various solvents. Equipment includes TEM (HITACHI-HT7700), DLS (Zetasizer Nano ZS90), spectrofluorometer (F4600 FL), confocal microscope (Olympus FV1000-IX81), and others for characterization.
4:Experimental Procedures and Operational Workflow:
Synthesis of HNPs with different shapes, adsorption of PVP for stabilization, fabrication of fluorescent HNPs via sol-gel reaction with AIEgen-Si(OCH3)3 and TEOS, cytotoxicity assessment using MTT assay, and cell imaging with confocal microscopy.
5:Data Analysis Methods:
Fluorescence spectra analysis, TEM for morphology, DLS for size and zeta potential, and image analysis using software like Image-J for cellular uptake quantification.
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TEM
HITACHI-HT7700
Hitachi
Transmission electron microscopy for imaging nanoparticle morphology
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DLS
Zetasizer Nano ZS90
Malvern Panalytical
Dynamic light scattering for measuring hydrodynamic diameter and zeta potential
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Spectrofluorometer
F4600 FL
Hitachi
Fluorescence spectra measurement
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Confocal Microscope
Olympus FV1000-IX81
Olympus
Confocal laser scanning microscopy for cell imaging
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NMR Spectrometer
Bruker AV400
Bruker
Nuclear magnetic resonance spectroscopy for chemical analysis
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FTIR Spectrometer
Frontier Mid-IR FTIR
Perkin Elmer
Fourier transform infrared spectroscopy for chemical characterization
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XPS Spectrometer
ESCALAB250Xi
Thermo Scientific
X-ray photoelectron spectroscopy for surface analysis
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Plate Reader
Spectra MAX 340PC
Molecular Devices
Absorbance measurement for MTT assay
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