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Nanoporous Silica Nanoparticles Coated with Peptide P14 and Decorated with 5-Fluorouracil and Indocyanine Green for NIR-Triggered Photothermal/Photodynamic Therapy

光热治疗 吲哚青绿 光动力疗法 纳米颗粒 细胞凋亡 药物输送 纳米技术 细胞毒性 体内 生物物理学 癌细胞 癌症研究 化学 材料科学 癌症 体外 病理 医学 生物化学 生物 有机化学 内科学 生物技术
作者
Ping Song,Guanglin Xu,Guanglan Peng,Lin Gui,Wanzhen Li,Wenlong Li,Liping Zhu,Yugui Tao,Weiwei Zhang,Fei Ge
出处
期刊:ACS applied nano materials [American Chemical Society]
卷期号:6 (24): 23264-23278
标识
DOI:10.1021/acsanm.3c04631
摘要

Nowadays, many cancer treatment paradigms are being rewritten due to advances in materials science, nanotechnology, and biomedicine. With the aid of nanomaterials and nanotechnology, many positive and meaningful attempts and breakthroughs in drug delivery and multistrategy collaborative chemotherapy have been made during traditional cancer chemotherapy treatment. In this work, a nanoparticle 5-FU/ICG@NP has been synthesized, with 5-Fluorouracil (5-FU) and indocyanine green (ICG) co-loaded within the nanoporous silica nanoparticles (NSN) decorated with amphiphilic targeting polypeptide P14 (NSN-P14, NP). The nanoparticles 5-FU/ICG@NP have been proven to have outstanding dimensional stability, photothermal effect, reactive oxygen species (ROS) generation, and tumor cell targeting capacity. The in vitro anticancer activity of the nanoparticles was evaluated by cytotoxicity, apoptosis, live and dead staining, cell cycle, and cell ultrathin section analysis. The results showed that the nanoparticles could effectively exert the combined effects of 5-FU chemotherapy and ICG photothermal and photodynamic therapy and effectively inhibit the activity of MCF-7 cells. Finally, the therapeutic effects of nanoparticles on tumor-bearing mouse models were evaluated systematically through small animal imaging and HE and TUNEL staining. The results showed that fluorescence-labeled nanoparticles exhibited initial accumulation at the tumor site approximately 1 h after intravenous injection. The fluorescence intensity peaked at the tumor site within 6 h and remained relatively stable during continuous monitoring for 48 h. The nanoparticles effectively induced apoptosis of tumor cells in vivo through the combination of 5-FU chemotherapy with near-infrared-triggered ICG photothermal and photodynamic therapy. Therefore, the nanoparticles synthesized in this work are an efficient nanodrug delivery platform, which has potential clinical applications in combination with tumor chemotherapy/photothermal/photodynamic therapy in future.
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