光热治疗
癌症研究
化学
肝细胞癌
体内
声动力疗法
索拉非尼
细胞凋亡
电穿孔
荧光寿命成像显微镜
癌细胞
体内分布
活性氧
药物输送
黑色素瘤
肝癌
细胞
微泡
临床前影像学
癌症
单线态氧
纳米棒
免疫系统
纳米医学
放射治疗
联合疗法
免疫疗法
生物物理学
荧光
光动力疗法
作者
Pengcheng Pan,Xinyi Hou,Yue Wang,Huan Lin,Xiangkun Miao,Yue Wang,Y Gao,Chenyu Hu,Pir Muhammad,L Gao,Junhua Zhang,Chenchen Li,Yanli Wang,Chenchen Li,Yanli Wang,Yanli Wang
摘要
Hepatocellular carcinoma (HCC) remains refractory to systemic therapy due to poor tumor selectivity, rapid drug clearance, and acquired resistance to sorafenib (SF). Here, we report a membrane-engineered biomimetic gold-carbon theranostic nanoplatform (ARG-SF@M) that integrates immune evasion, homologous targeting, dual-modal imaging, and synergistic chemo-photothermal therapy (chemo-PTT) within a single nanosystem. The platform is constructed by co-assembling gold nanorods (AuNRs) and a fluorescent carbon nanomaterial (GTTN) for efficient SF loading, followed by cloaking with HCC cell membranes to confer prolonged circulation and tumor-homotypic recognition. AuNRs enable efficient near-infrared photothermal conversion and thermal imaging (TI), while GTTN provides stable fluorescence imaging (FI) for real-time biodistribution monitoring. The membrane camouflage markedly enhances tumor accumulation and reduces off-target distribution, thereby improving SF delivery efficiency. In vivo studies demonstrate that ARG-SF@M achieves a tumor inhibition rate of 81.92%, significantly higher than that of free SF (42.43%) and non-biomimetic ARG-SF (66.05%). Under NIR irradiation, tumor suppression further increases to 90.77%, substantially outperforming AuNRs + L (55.35%), confirming strong chemo-PTT synergy. Mechanistically, photothermal activation induces intratumoral hyperthermia, mitochondrial dysfunction, excessive reactive oxygen species generation, HSP70 upregulation, and activation of the mitochondrial apoptotic pathway. Collectively, this work presents a rational biomimetic membrane-engineering strategy for imaging-guided precision HCC theranostics.
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