研究目的
To develop functional protein-assisted fabrication of Fe-gallic acid (GA) nanonetworks via a mild and facile biomineralization for photothermal therapy, aiming to enhance photothermal therapeutic efficacy with minimal side effects by reducing leakage to surrounding normal tissues and retaining the intrinsic bioactivity of proteins.
研究成果
The study successfully demonstrated the fabrication of functional protein-Fe-GA nanonetworks with excellent photothermal performance and biocompatibility. These nanonetworks showed potential for localized photothermal therapy and immune activation, indicating a promising approach for cancer treatment and the development of multifunctional nanovaccines.
研究不足
The study primarily focuses on the synthesis and preliminary in vitro and in vivo evaluation of protein-Fe-GA nanonetworks. Further optimization and comprehensive toxicity studies are needed to fully assess their clinical applicability.
1:Experimental Design and Method Selection:
The study involved the synthesis of protein-Fe-GA nanonetworks through a mild and facile biomineralization approach under mild alkaline conditions to ensure intense near-infrared absorption and minimal impairment to protein function.
2:Sample Selection and Data Sources:
Bovine serum albumin (BSA), human serum albumin (HSA), and ovalbumin (OVA) were used as protein templates for the fabrication of Fe-GA coordination polymers.
3:List of Experimental Equipment and Materials:
Instruments included transmission electron microscopy (TEM), dynamic light scattering (DLS), Fourier transform-infrared spectroscopy (FT-IR), and inductively coupled plasma-atomic emission spectrometry (ICP-AES). Materials included FeCl3·6H2O, gallic acid (GA), and various proteins.
4:Experimental Procedures and Operational Workflow:
The synthesis involved dissolving protein and FeCl3·6H2O in water, adjusting pH with NaOH, adding GA aqueous solution, and purifying the resulting nanonetworks by dialysis.
5:Data Analysis Methods:
The photothermal performance was evaluated by measuring temperature elevation under 808-nm laser irradiation, and the immune activation effect was assessed by flow cytometry and ELISA.
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