研究目的
To construct and evaluate MnO2-mSiO2@Au-HA nanoparticles for multimodal imaging-guided and hypoxia-maneuvered radiotherapy in cancer treatment.
研究成果
The MAHNPs demonstrated effective multimodal imaging capabilities (MSOT, CT, MR) and synergistic therapeutic effects (PTT and RT) in vitro and in vivo, leading to significant tumor suppression with good biocompatibility. This nanoplatform holds promise for future clinical applications in cancer theranostics.
研究不足
Potential limitations include the complexity of nanoparticle synthesis, possible toxicity at higher doses, and the need for further optimization for clinical translation. The study is limited to specific cancer cell lines and animal models, and long-term effects were not fully explored.
1:Experimental Design and Method Selection:
The study involved synthesizing MnO2-mSiO2 nanohybrids via a one-pot method, growing gold nanoshells via seed-mediated growth, and modifying with hyaluronic acid-dopamine complex. Methods included characterization using TEM, SEM, DLS, UV-vis, FT-IR, NMR, ICP-AES, and various imaging and therapeutic assessments.
2:Sample Selection and Data Sources:
Murine breast cancer 4T1 cells were used for in vitro studies, and female nude and Kunming mice with 4T1 xenograft tumors for in vivo studies. Data were sourced from experimental measurements and imaging systems.
3:List of Experimental Equipment and Materials:
Equipment included TEM (JEM-100CX), SEM (SU8020), DLS (Zetasizer Nano ZS), UV-vis spectrophotometer (Cary 60), FT-IR spectrophotometer (TESOR-27), NMR spectrometer (AVANCE III TM HD 400 MHz), ICP-AES (7700x), laser (LASERGLOW Technologies), digital thermometer (TASI-8620), infrared camera (TI400), MSOT imaging system, CT scanner (Gamma Medical-Ideas), MR scanner (Magnetom Trio with Tim), and flow cytometer (MerckMillipore). Materials included chemicals like KMnO4, CTAB, TEOS, HAuCl4, APTES, EDC, HA, MTT, and cell culture reagents.
4:Experimental Procedures and Operational Workflow:
Synthesis steps involved preparing MNHs, Au nanoshells, HA-DN complex, and MAHNPs. In vitro tests included cytotoxicity, hemolysis, hypoxia evaluation, and imaging. In vivo tests involved tumor modeling, imaging (MSOT, CT, MR), blood circulation, biodistribution, and therapeutic efficacy assessments with PTT and RT.
5:Data Analysis Methods:
Data were analyzed using statistical methods (ANOVA, t-test), ImageJ for image analysis, and software for imaging systems. Photothermal conversion efficiency was calculated using a specific formula.
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Transmission Electron Microscope
JEM-100CX
JEOL
Obtaining TEM images for nanoparticle characterization
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Scanning Electron Microscope
SU8020
Hitachi
Obtaining SEM images for surface morphology analysis
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Dynamic Light Scattering Instrument
Zetasizer Nano ZS
Malvern
Measuring particle size and zeta potential
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UV-vis Spectrophotometer
Cary 60
Agilent
Recording UV-vis spectra
Cary 60 UV-Vis Spectrophotometer
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FT-IR Spectrophotometer
TESOR-27
Bruker
Measuring FT-IR spectra
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NMR Spectrometer
AVANCE III TM HD 400 MHz NanoBAY
Bruker
Examining 1H-NMR spectroscopy
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ICP-AES
7700x
Agilent
Measuring concentrations of Au and Mn
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Infrared Camera
TI400
Fluke
Recording thermal images
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MR Scanner
Magnetom Trio with Tim
Siemens
Performing magnetic resonance imaging
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Confocal Fluorescence Microscope
Leica SP5
Leica
Imaging cells for hypoxia evaluation and immunofluorescence analysis
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X-ray Micro CT Scanner
Quantum FX
PerkinElmer
Conducting in vivo CT imaging
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Clinical Linear Accelerator
Siemens Primus
Siemens
Administering X-ray radiation for radiotherapy
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Laser
Not specified
LASERGLOW Technologies
Conducting laser irradiation for photothermal therapy
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Digital Thermometer
TASI-8620
TASI
Gauging solution temperature
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MSOT Imaging System
Not specified
Not specified
Performing multispectral optoacoustic tomography imaging
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CT Scanner
Gamma Medical-Ideas
Not specified
Conducting computed tomography imaging
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Flow Cytometer
Not specified
MerckMillipore
Analyzing cell apoptosis and necrosis
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