研究目的
To develop a personalized local therapeutic platform combining photothermal therapy (PTT) with long-acting chemotherapy for the treatment of multidrug-resistant colorectal cancer (MDR CRC).
研究成果
The GNRs-TPGS-PTX NC-gel platform effectively combines photothermal therapy and chemotherapy, showing significant reduction in tumor growth and recurrence in MDR CRC models with minimal systemic toxicity. It offers a personalized approach with adjustable doses, making it a promising candidate for localized cancer treatment.
研究不足
The study is limited to in vitro and animal models (mice), specifically for colorectal cancer with multidrug resistance. Potential long-term toxicity of gold nanoparticles and applicability to other cancer types or human use require further investigation. The localized delivery system depends on intratumoral injection, which may not be feasible for all tumor types.
1:Experimental Design and Method Selection:
The study involved synthesizing PEG-coated gold nanorods (PEG-GNRs) and TPGS-coated paclitaxel nanocrystals (TPGS-PTX NC), incorporating them into a thermosensitive in situ hydrogel system (Pluronic P407/P188), and evaluating their combined effects through in vitro and in vivo experiments. Methods included seed-mediated growth for GNRs, film hydration for NCs, and dialysis for drug release studies.
2:Sample Selection and Data Sources:
Drug-resistant SW620 AD300 cells and parental SW620 cells were used, sourced from Dr. Susan E Bates. Male Nu/Nu nude mice were used for in vivo studies.
3:List of Experimental Equipment and Materials:
Equipment included Zetasizer (Nano ZS90), TEM (Hitachi HT7700), rheometer (AR1500ex), infrared thermal imager (VarioCAM HD), HPLC-UV (Agilent 1260), and Microplate reader (Thermo Scientific Multiskan GO). Materials included F127, F68, mPEG-SH, CTAB, TPGS, HAuCl4, PTX, and others from specified suppliers.
4:Experimental Procedures and Operational Workflow:
Synthesis of GNRs and PEG-GNRs, preparation of TPGS-PTX NC, formulation of gel systems, characterization (zeta potential, morphology, stability, rheology), photothermal conversion tests, in vitro drug release and erosion studies, cytotoxicity assays (MTT), in vivo photothermal imaging, and antitumor efficacy and toxicity assessments in mice.
5:Data Analysis Methods:
Data were analyzed using Prism 4.0 for IC50 calculations, Student's t-test for statistical significance, with P<0.05 considered significant.
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