研究目的
Investigating the therapeutic effects of functionalized polypyrrole nanoparticles (PPI NPs) on tumor treatment through enhanced photoacoustic imaging and photothermal therapy.
研究成果
The designed PPI NPs demonstrated enhanced NIR responsive property, excellent biocompatibility, and effective tumor accumulation, leading to successful photoacoustic imaging-guided photothermal therapy. The study highlights the potential of PPI NPs as a promising platform for cancer theranostic applications.
研究不足
The study focuses on the enhanced NIR responsive property of PPI NPs for tumor theranostic applications, but the long-term biocompatibility and potential side effects in humans are not fully explored. Additionally, the study is limited to HeLa cells and tumors, and the applicability to other cancer types requires further investigation.
1:Experimental Design and Method Selection:
The study involved the design and synthesis of PEGylated indocyanine green (ICG)-loaded polypyrrole nanoparticles (PPI NPs) using polydopamine as a linkage. The methodology included polymerization of pyrrole monomers, polydopamine coating, PEG linkage, and ICG loading.
2:Sample Selection and Data Sources:
HeLa cells and nude mice bearing HeLa tumors were used as models for in vitro and in vivo studies, respectively.
3:List of Experimental Equipment and Materials:
Materials included pyrrole, dopamine hydrochloride, poly(vinyl alcohol), iron(III) chloride hexahydrate, and indocyanine green. Equipment included field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), dynamic light scattering (DLS), UV-vis-NIR spectrophotometer, and photoacoustic imaging appliance.
4:Experimental Procedures and Operational Workflow:
The synthesis of PPI NPs, characterization, NIR performance evaluation, cellular uptake and intracellular localization assay, cell viability assay, in vitro PTT, in vivo biochemical assay and hematology analysis, in vivo PA imaging, and in vivo PTT were conducted.
5:Data Analysis Methods:
Data were analyzed using flow cytometry, confocal laser scanning microscopy, CCK-8 assay, and statistical techniques for photothermal conversion efficiencies calculation.
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