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载药胶束,高效近红外光敏剂,用于耐药性癌症的联合影像引导光动力治疗和化学治疗。

Drug delivery micelles with efficient near-infrared photosensitizer for combined image-guided photodynamic therapy and chemotherapy of drug-resistant cancer.

机构信息

State Key Laboratory of Luminescent Materials and Devices, Center for Aggregation-Induced Emission, South China University of Technology, Guangzhou, 510640, China.

Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences, 388 Lumo Road, Wuhan, 430074, China; College of Pharmacy, Gannan Medical University, Ganzhou, 341000, China.

出版信息

Biomaterials. 2019 Oct;218:119330. doi: 10.1016/j.biomaterials.2019.119330. Epub 2019 Jul 2.

DOI:10.1016/j.biomaterials.2019.119330
PMID:31301577
Abstract

The combination of photodynamic therapy (PDT) and chemotherapy (CT) offers a promising approach for the tumor eradication for overcoming multidrug resistance (MDR), which is a major obstacle to effective cancer treatment. However, for PDT, simultaneously achieving near-infrared (NIR) emission and efficient reactive oxygen species (ROS) generation with low dark toxicity is urgently needed but remains challenging. Herein, a series of novel fluorophores with strong NIR emission, hybridized local and charge transfer characteristics, good two-photon absorption, high photostability, low dark cytotoxicity and excellent ROS generation ability are developed. By encapsulating the NIR fluorophore (DEB-BDTO) as a photosensitizer along with a drug resistance inhibitor tariquidar (TQR) within a polymeric prodrug (PMP), a reduction-sensitive drug co-delivery system (DEB/TQR@PMP micelles) is constructed. The DEB/TQR@PMP micelles exhibit a prominent synergistic lethal effect of PDT and CT on SKOV-3 cells and SKOV-3/MDR cells, and can apparently enhance the inhibition of tumor growth compared with sole PDT or CT in the tumor-bearing mouse model. Both in vitro and in vivo experiments prove that the new NIR fluorophores are excellent photosensitizers and can furnish an efficient combination therapy of image-guided PDT and CT within drug delivery micelles, which is particularly useful for eradicating multidrug resistance cancer.

摘要

光动力疗法 (PDT) 和化学疗法 (CT) 的联合为克服多药耐药性 (MDR) 提供了一种有前途的肿瘤消除方法,因为 MDR 是癌症治疗的主要障碍。然而,对于 PDT 而言,同时实现近红外 (NIR) 发射和高效的活性氧 (ROS) 生成,同时又具有低暗毒性,这是迫切需要的,但仍然具有挑战性。在此,开发了一系列具有强近红外发射、混合局部和电荷转移特性、良好的双光子吸收、高光稳定性、低暗细胞毒性和出色的 ROS 生成能力的新型荧光团。通过将 NIR 荧光团 (DEB-BDTO) 封装为一种光敏剂,并将耐药抑制剂他利喹达 (TQR) 封装在聚合物前药 (PMP) 内,构建了一种还原敏感的药物共递送系统 (DEB/TQR@PMP 胶束)。DEB/TQR@PMP 胶束对 SKOV-3 细胞和 SKOV-3/MDR 细胞表现出 PDT 和 CT 的协同致死作用,并且在荷瘤小鼠模型中与单独的 PDT 或 CT 相比,能够明显增强对肿瘤生长的抑制作用。体外和体内实验均证明,新型 NIR 荧光团是出色的光敏剂,并能够在药物递送胶束内提供高效的图像引导 PDT 和 CT 联合治疗,这对于消除多药耐药性癌症特别有用。

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