研究目的
To develop an improved method for synthesizing heparin-coated Eu3+ doped hydroxyapatite luminescent nanoparticles with enhanced luminescence, stability, and biocompatibility for use as bioimaging agents.
研究成果
The ultrasound-assisted coprecipitation method with steam sterilization successfully produces stable, luminescent SH-Eu:nHAP suspensions with good biocompatibility and potential for bioimaging applications, offering a rapid and efficient synthesis approach.
研究不足
The method may not achieve the highest luminescence intensity compared to high-temperature calcination methods; higher Eu doping content (>2.0%) reduces crystallinity and limits luminescence enhancement; interaction with biological media increases particle size due to protein adsorption, requiring further surface modification for improved resistance.
1:Experimental Design and Method Selection:
Ultrasound-assisted coprecipitation method followed by steam sterilization was used to synthesize SH-Eu:nHAP nanoparticles, leveraging ultrasonic sonochemistry and heparin stabilization.
2:Sample Selection and Data Sources:
Analytically pure raw materials including Ca(NO3)2·4H2O, Eu(NO3)3·6H2O, (NH4)2HPO4, and sodium heparin were used. Samples were characterized at different synthesis stages.
3:List of Experimental Equipment and Materials:
High intensity ultrasound probe, autoclave for steam sterilization, XRD (D/Max-IIIA, Rigaku Co.), FT-IR (Nexus, Thermo Nicolet), ICP-AES (Optima 4300DV, PE Co. Ltd.), HRTEM (JEM-2100F, JEOL), particle size and zeta potential analyzer (Zetasizer 3000HS, Malvern), fluorescence spectrophotometer (970CRT, Shanghai Sanco), microplate reader (Thermo Labsystems), CLSM (AOBS SP2, Leica).
4:Experimental Procedures and Operational Workflow:
Solutions of Ca2+/Eu3+ and PO4^3- were mixed, pH adjusted to 10, precipitated, centrifuged, washed, redispersed with SH, ultrasonicated for 6 min, and steam sterilized at 121°C for 1 h. Biological evaluations included hemolysis tests with rabbit RBCs, cytotoxicity with L-02 cells using MTT assay, and cell labeling with HepG2 cells observed via CLSM.
5:Data Analysis Methods:
XRD for phase composition and crystallinity, FT-IR for functional groups, ICP-AES for elemental content, TEM/HRTEM for morphology, particle size analyzer for size distribution, fluorescence spectrophotometer for luminescence spectra, statistical analysis for biological assays.
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X-ray diffractometer
D/Max-IIIA
Rigaku Co.
Analyze phase composition of samples
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Fourier Transform Infrared Spectrometer
Nexus
Thermo Nicolet
Determine functional groups in samples
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Inductively Coupled Plasma Atomic Emission Spectrometer
Optima 4300DV
PE Co. Ltd.
Detect Ca, Eu, and P contents in samples
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High Resolution Transmission Electron Microscope
JEM-2100F
JEOL
Observe morphology and lattice fringes of samples
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Particle size and zeta potential analyzer
Zetasizer 3000HS
Malvern
Determine particle size distribution and zeta potential
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Microplate reader
Thermo Labsystems
Thermo
Detect absorbance for hemolysis and cytotoxicity assays
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Confocal Laser Scanning Microscope
AOBS SP2
Leica
Observe cell labeling and luminescence
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Fluorescence spectrophotometer
970CRT
Shanghai Sanco
Record photoluminescence spectra
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Ultrasound probe
Apply high intensity ultrasound for dispersion and crystallization
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Autoclave
Perform steam sterilization at 121°C
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