研究目的
To develop multi-shelled hollow nanospheres as multifunctional therapeutic agents for targeted Zn2+/Cu2+ therapy, induced drug delivery under low pH/red-light conditions, and enhanced phototherapy under single red-light for cancer treatment.
研究成果
The developed RGD@am-ZnO@CuO@Au@DOX HNSs demonstrated effective cancer cell targeting, efficient ROS generation, high photothermal conversion efficiency, and pH-triggered drug release, enabling simultaneous imaging-guided Zn2+/Cu2+ therapy, chemotherapy, and phototherapy. This nanoplatform stands out as a cost-effective theranostic reagent in the field of nanomedicine.
研究不足
The study's limitations include the need for further exploration of the in vivo behavior of RGD@am-ZnO@CuO@Au@DOX HNSs, such as their quantitative pharmacokinetics, biodistribution, and long-term toxicity.
1:Experimental Design and Method Selection:
The study involved the synthesis of multi-shelled hollow nanospheres (RGD@am-ZnO@CuO@Au@DOX HNSs) for targeted cancer therapy. The methodology included the use of resonance energy transfer and broad red-light absorption to enhance photothermal and photodynamic performance.
2:Sample Selection and Data Sources:
Human pulmonary adenocarcinoma (A549) cells were used as the cancer model. Data were collected through in vitro and in vivo experiments, including MR/fluorescence imaging and therapeutic efficacy assessments.
3:List of Experimental Equipment and Materials:
The study utilized transmission electron microscopy (TEM), high-resolution TEM (HRTEM), UV-vis-NIR spectroscopy, and electron paramagnetic resonance (ESR) for characterization. Materials included am-ZnO@CuO@Au HNSs and doxorubicin (DOX).
4:Experimental Procedures and Operational Workflow:
The workflow involved the synthesis of HNSs, their characterization, in vitro and in vivo testing for therapeutic efficacy, and imaging-guided therapy.
5:Data Analysis Methods:
Data were analyzed using statistical techniques and software tools for imaging and therapeutic outcome assessment.
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