Tianjin Key Laboratory of Drug Delivery & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, 300072, Tianjin, PR, China.
Nanoscale. 2017 May 4;9(17):5551-5564. doi: 10.1039/c6nr09219e.
In this study, we report a strategy for integrating hyaluronic acid (HA), polyaniline (PANI), WS nanodots (WS), and chlorin e6 (Ce6) into a single nanoplatform (HA-WS@PANI/Ce6) for fluorescence, photoacoustic, and computed tomography multi-modality imaging-guided trimodal photothermal/radiation/photodynamic combination therapy of tumors. The WS nanodot core is used as the radiosensitizer with the PANI shell as the hyperthermal agent and the photosensitizer reservoir. HA and Ce6 were adsorbed on the outer shell for tumor targeting and photodynamic therapy, respectively. The in vivo trimodal imaging uncovered that HA-WS@PANI/Ce6 nanoparticles showed enhanced tumor uptake and diagnosis effects after intravenous injection. More importantly, in the in vitro and in vivo experiments, the nanoparticles exhibited an evident near-infrared induced photothermal effect, which remarkably improved the radiation and photodynamic therapy efficiency by accelerating the blood flow and subsequently increasing oxygen supply in the tumor. The nanohybrids were found to be safe to cells in vitro and organs in vivo. Taken together, our current work demonstrates a nanoplatform for multimodal imaging guided targeted triple-therapy, which reveals a potential strategy for tumor treatment.
在这项研究中,我们报告了一种将透明质酸(HA)、聚苯胺(PANI)、WS 纳米点(WS)和氯乙锭(Ce6)整合到单个纳米平台(HA-WS@PANI/Ce6)中的策略,用于荧光、光声和计算机断层扫描多模态成像引导的肿瘤三模态光热/辐射/光动力联合治疗。WS 纳米点核用作放射增敏剂,PANI 壳用作高热剂和光敏剂储库。HA 和 Ce6 分别吸附在外壳上用于肿瘤靶向和光动力治疗。体内三模态成像揭示,静脉注射后,HA-WS@PANI/Ce6 纳米粒子表现出增强的肿瘤摄取和诊断效果。更重要的是,在体外和体内实验中,纳米粒子表现出明显的近红外诱导光热效应,通过加速血流,随后增加肿瘤中的氧气供应,显著提高了辐射和光动力治疗的效率。该纳米杂化物在体外细胞和体内器官中均表现出安全性。总之,我们目前的工作展示了一种用于多模态成像引导靶向三联治疗的纳米平台,为肿瘤治疗提供了一种潜在的策略。