Center for Rehabilitation Medicine, Rehabilitation & Sports Medicine Research Institute of Zhejiang Province, Department of Rehabilitation Medicine, Cancer Center, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China.
Clinical Research Institute, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 310014, China.
Small. 2024 Sep;20(37):e2309891. doi: 10.1002/smll.202309891. Epub 2024 May 9.
Although the current cancer photothermal therapy (PTT) can produce a powerful therapeutic effect, tumor cells have been proved a protective mechanism through autophagy. In this study, a novel hybrid theranostic nanoparticle (CaCO@CQ@pDB NPs, CCD NPs) is designed and prepared by integrating a second near-infrared (NIR-II) absorbed conjugated polymer DTP-BBT (pDB), CaCO and autophagy inhibitor (chloroquine, CQ) into one nanosystem. The conjugated polymer pDB with asymmetric donor-acceptor structure shows strong NIR-II absorbing capacity, of which the optical properties and photothermal generation mechanism of pDB are systematically analyzed via molecular theoretical calculation. Under NIR-II laser irradiation, pDB-mediated PTT can produce powerful killing ability to tumor cells. At the same time, heat stimulates a large amount of Ca inflow, causing calcium overload induced mitochondrial damage and enhancing the apoptosis of tumor cells. Besides, the released CQ blocks the self-protection mechanism of tumor cells and greatly enhances the attack of PTT and calcium overload therapy. Both in vitro and in vivo experiments confirm that CCD NPs possess excellent NIR-II theranostic capacity, which provides a new nanoplatform for anti-tumor therapy and builds great potential for future clinical research.
虽然目前的癌症光热治疗(PTT)可以产生强大的治疗效果,但肿瘤细胞已经被证明通过自噬产生了一种保护机制。在这项研究中,通过将第二个近红外(NIR-II)吸收共轭聚合物 DTP-BBT(pDB)、CaCO 和自噬抑制剂(氯喹,CQ)整合到一个纳米系统中,设计并制备了一种新型的杂化治疗诊断纳米粒子(CaCO@CQ@pDB NPs,CCDNPs)。具有非对称供体-受体结构的共轭聚合物 pDB 具有很强的 NIR-II 吸收能力,通过分子理论计算系统地分析了 pDB 的光学性质和光热产生机制。在 NIR-II 激光照射下,pDB 介导的 PTT 可以对肿瘤细胞产生强大的杀伤能力。同时,热量刺激大量 Ca 流入,导致钙超载诱导的线粒体损伤,并增强肿瘤细胞的凋亡。此外,释放的 CQ 阻断了肿瘤细胞的自我保护机制,极大地增强了 PTT 和钙超载治疗的攻击。体外和体内实验均证实 CCDNPs 具有优异的 NIR-II 治疗诊断能力,为抗肿瘤治疗提供了新的纳米平台,并为未来的临床研究奠定了巨大潜力。