研究目的
To develop a facile and robust method for synthesizing highly asymmetric Au nanobottles with controllable sizes and uniform shapes for applications in plasmonics, drug delivery, and combined chemo-photothermal therapy.
研究成果
A facile method for synthesizing Au nanobottles with tunable sizes and plasmonic properties is developed. These nanobottles show high potential for drug delivery and combined chemo-photothermal therapy, with optimized opening size (44 nm) providing high drug encapsulation and low burst release. The study paves the way for biomedical applications leveraging magnetic plasmon resonance.
研究不足
The method relies on PbS nanooctahedra as templates, which may introduce complexity. The photothermal conversion efficiency from simulations does not fully match experimental values due to re-absorption effects. The drug encapsulation efficiency is moderate (up to 23.6%), and the approach is limited to in vitro studies; in vivo applications are not explored.
1:Experimental Design and Method Selection:
The synthesis involves using PbS nanooctahedra as sacrificial templates for asymmetric Au overgrowth, followed by HCl etching to remove PbS and produce Au nanobottles. Anisotropic oxidation with H2O2 and HCl is used for further size control. Drug encapsulation and release studies are conducted with doxorubicin, camptothecin, and actinomycin D. Photothermal therapy and combined therapy are evaluated using cell cultures and laser irradiation.
2:Sample Selection and Data Sources:
PbS nanooctahedra are synthesized with varying edge lengths (20-200 nm) by controlling reaction temperature and duration. Human glioblastoma U-87 MG cells are used for in vitro studies.
3:List of Experimental Equipment and Materials:
Equipment includes FEI Quanta 400 FEG SEM, FEI Tecnai Spirit TEM, Lambda 950 spectrophotometer, Agilent 7500a ICP-AES system, Olympus IX71 microscope. Materials include HAuCl4, ascorbic acid, CTAB, HCl, H2O2, mPEG-SH, tetraethylorthosilicate, doxorubicin, camptothecin, actinomycin D, Cell Counting Kit-8, calcein-AM.
4:Experimental Procedures and Operational Workflow:
Synthesis of PbS nanooctahedra at 60-90°C for 2-8 h. Au overgrowth by adding HAuCl4 and ascorbic acid to CTAB solution with PbS seeds, stirring, and HCl etching. Oxidation with H2O2 and HCl. Surface modification with mPEG-SH and silica coating. Drug loading by incubating nanobottles with drug solutions. Cell viability assays and photothermal therapy with 808 nm laser.
5:Data Analysis Methods:
SEM and TEM for size measurement, extinction spectra for plasmon properties, ICP-AES for concentration, CCK-8 assay and calcein-AM staining for cell viability, FDTD simulations for photothermal conversion efficiency.
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SEM microscope
Quanta 400 FEG
FEI
Imaging and energy-dispersive X-ray analysis of samples
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TEM microscope
Tecnai Spirit
FEI
Transmission electron microscopy imaging
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Spectrophotometer
Lambda 950
Perkin Elmer
Acquiring extinction spectra in ultraviolet/visible/NIR range
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ICP-AES system
7500a
Agilent
Inductively coupled plasma atomic emission spectrometry for elemental analysis
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Microscope
IX71
Olympus
Detecting fluorescence from live cells
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FDTD software
FDTD Solutions v8.7
Lumerical Solutions
Simulating plasmonic properties using finite-difference time-domain method
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Cell Counting Kit
CCK-8
Assaying cell viability
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mPEG-SH
MW 5000
RAPP Polymere
Surface modification for biocompatibility
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