研究目的
Investigating the therapeutic effects of a hydrogen peroxide responsive iron oxide nanoplatform on cancer through multimodal imaging–guided photodynamic therapy and photothermal therapy.
研究成果
The IONPs-ICG-HA nanoplatform demonstrates significant potential for cancer treatment through synergistic photodynamic and photothermal therapy, guided by multimodal imaging. The study provides a foundation for further research into TME-responsive nanoplatforms for enhanced cancer therapy.
研究不足
The study focuses on the synergistic effects of PDT and PTT but may not address all potential side effects or the applicability to all cancer types. The in vivo model uses a specific tumor type, which may limit the generalizability of the findings.
1:Experimental Design and Method Selection:
The study employed a solvothermal method to synthesize iron oxide nanoparticles (IONPs) and decorated them with indocyanine green (ICG) and hyaluronic acid (HA) through electrostatic interaction to form the IONPs-ICG-HA nanoplatform.
2:Sample Selection and Data Sources:
Human colon carcinoma cell line (HCT-116 cells) and human ovarian cell line (A2780 cells) were used for in vitro experiments, and female nude mice were used for in vivo experiments.
3:List of Experimental Equipment and Materials:
Instruments included TEM (JEOL JEM-2010), XRD (Bruker diffractometer D8 advance), and a thermal camera (FLIR E50). Materials included Fe(acac)3, ICG, mPEG-NH2, and HA.
4:0). Materials included Fe(acac)3, ICG, mPEG-NH2, and HA. Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: The nanoplatform was characterized for its photothermal and photodynamic properties, and its therapeutic efficacy was evaluated in vitro and in vivo.
5:Data Analysis Methods:
Data were analyzed using SPSS software for statistical significance, and flow cytometry was used to study the mechanism of apoptosis.
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