研究目的
To develop and evaluate hyaluronic acid functionalized nanoparticles loaded with IR780 and DOX for enhanced cancer chemo-photothermal therapy, addressing the limitations of IR780 such as poor water solubility and cytotoxicity.
研究成果
The HA-based nanoparticles successfully encapsulated IR780 and DOX, improving IR780's photothermal properties and cytocompatibility. They showed higher uptake in cancer cells than normal cells, penetrated 3D spheroids, and demonstrated effective chemo-photothermal therapy, with IR/DOX-HPN combined with NIR light reducing spheroid viability to 34%. These nanoformulations are promising for cancer treatment, but further in vivo studies are needed.
研究不足
The study is limited to in vitro models (2D and 3D cell cultures), and in vivo evaluation is suggested for future work to fully disclose therapeutic potentials. The photothermal effect may be limited by IR780 degradation under NIR light.
1:Experimental Design and Method Selection:
The study used a nanoprecipitation method to formulate nanoparticles (IR-HPN and IR/DOX-HPN) from a novel HA-based amphiphilic polymer (HA-g-PMAO). Theoretical models included characterization of physicochemical properties, photothermal effects, and biological assays.
2:Sample Selection and Data Sources:
Cell lines used were MCF-7 (breast cancer cells) and NHDF (normal human dermal fibroblasts) obtained from ATCC and Promocell, respectively. Materials included IR780 iodide, DOX, HA sodium salt, and various chemicals from suppliers like Sigma-Aldrich and Thermo Fisher Scientific.
3:List of Experimental Equipment and Materials:
Equipment included Zetasizer Nano ZS for DLS, Hitachi-HT7700 TEM, Evolution 201 UV-Vis spectrophotometer, Spectramax Gemini EM spectrofluorometer, Zeiss LSM 710 confocal microscope, and others. Materials included culture media, reagents for synthesis, and dialysis membranes.
4:Experimental Procedures and Operational Workflow:
Steps included synthesis of HA-g-PMAO, formulation of nanoparticles via nanoprecipitation, characterization (size, zeta potential, encapsulation efficiency), photothermal studies with NIR laser irradiation, cytocompatibility assays using resazurin method, cellular uptake studies via CLSM, and therapeutic efficacy tests in 2D and 3D cell models.
5:Data Analysis Methods:
Statistical analysis used one-way ANOVA with Student-Newman-Keuls test; data presented as mean ± standard deviation. ImageJ software was used for image analysis.
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Zetasizer Nano ZS
Nano ZS
Malvern Instruments Ltd.
Evaluating size distribution and zeta potential of nanoparticles using dynamic light scattering.
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Transmission Electron Microscope
HT7700
Hitachi Ltd.
Analyzing morphology of nanoparticles with staining and imaging at 100 kV accelerating voltage.
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UV-Visible Spectrophotometer
Evolution 201
Thermo Fisher Scientific Inc.
Measuring absorbance for encapsulation efficiency and loading content determination.
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Confocal Microscope
LSM 710
Carl Zeiss AG
Imaging cellular uptake and therapeutic effects using fluorescence channels.
ZEISS LSM 990 Spectral Multiplex
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Spectrofluorometer
Spectramax Gemini EM
Molecular Devices LLC
Measuring fluorescence for drug content and cell viability assays.
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NIR Laser
Irradiating samples for photothermal therapy studies at 808 nm wavelength.
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Freeze Dryer
CoolSafe
LaboGene ApS
Freeze-drying nanoparticle samples for further analysis.
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Cell Culture Plates
Thermo Fisher Scientific
Culturing cells for in vitro assays.
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Imaging Plates
μ-slide 8-well
Ibidi GmbH
Seeding cells for confocal microscopy studies.
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Dialysis Membrane
500-1000 Da cut-off
Dialysis for nanoparticle purification and release studies.
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