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Self-Oxygenating Biomimetic Nanoplatform for Synergistic Photodynamic and Photothermal Therapy of Triple-Negative Breast Cancer

光热治疗 光动力疗法 光敏剂 肿瘤缺氧 癌症研究 材料科学 肿瘤微环境 癌细胞 纳米颗粒 联合疗法 细胞 荧光 乳腺癌 癌症 转移 热疗 纳米技术 缺氧(环境) 荧光寿命成像显微镜 细胞生长
作者
Xinyi Hou,Fang Wang,Yan Wang,Yan Wang,Pengcheng Pan,Yuanyuan Wang,Yuanyuan Wang,Y Gao,Xiangkun Miao,Junfeng Zhang,Chenchen Li,Yanli Wang,Yanli Wang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
标识
DOI:10.1021/acsami.6c07229
摘要

Triple-negative breast cancer (TNBC) remains a formidable clinical challenge characterized by its aggressive metastasis and a scarcity of effective treatment strategies. However, photodynamic therapy (PDT) is severely limited by the hypoxic tumor microenvironment, and photothermal therapy (PTT) is restricted by the low photothermal conversion efficiency of the photothermal agents. The photosensitizer IR780 has received widespread attention due to its dual potential in both PDT and PTT, but it suffers from insufficient photostability and is prone to fluorescence quenching. To overcome these challenges, this study constructed a multifunctional self-oxygen-supplying biomimetic nanoparticle platform, named CaO2@PDA-IR780@CM (CPIC). In this system, calcium peroxide (CaO2) decomposes in an acidic tumor microenvironment and releases oxygen in situ, effectively alleviating tumor hypoxia and enhancing the PDT efficacy mediated by IR780. Loading IR780 onto polydopamine significantly improved its stability and photothermal performance, achieving a photothermal conversion efficiency of 54.5%, which represents a significant enhancement compared with free IR780. The nanoparticle surface was coated with homologous tumor cell membranes, endowing it with tumor-specific targeting ability. In an orthotopic 4T1 tumor-bearing mouse model, CPIC showed significantly stronger intratumoral fluorescence signals compared with free IR780 and the control nanoparticles without cell membrane coating, thereby confirming its superior tumor targeting efficiency. Furthermore, the combination of PDT/PTT mediated by CPIC significantly suppressed primary tumor growth and effectively inhibited the formation of pulmonary metastatic nodules, highlighting its remarkable translational potential for TNBC treatment.
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