Department of Ultrasound, Zhongshan Hospital, Fudan University, No. 180 Fenglin Road, Shanghai, 200032, China.
State Key Laboratory of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China.
Nanoscale. 2020 Mar 5;12(9):5587-5600. doi: 10.1039/c9nr10735e.
As one of the most promising noninvasive therapeutic modalities, sonodynamic therapy (SDT) can focus the ultrasound energy on tumor sites located in deep tissue and locally activate the preloaded sonosensitizer to kill tumor cells. However, exploring sonosensitizers with high SDT efficacy and desirable biosafety is still a significant challenge. Herein, we utilized the hydrophilic-hydrophobic self-assembly technology to assemble the hydrophobic organic dye Ce6 and broad spectral anti-cancer agent Paclitaxel with hydrophilic organic dye IR783 to generate a nanoscale sonosensitizer, Ce6-PTX@IR783, without the introduction of extra nanomaterials into the fabrication to guarantee high therapeutic biosafety and further potential clinical translation. The constructed nanodrug was endowed with an external ultrasound-activatable chemo-sonodynamic effect and photoacoustic imaging performance via integrating multiple moieties into one nanosystem. Ce6 could enhance the sonodynamic effect, while PTX exerted a chemotherapeutic effect, and IR783 was applied to increase tumor-specific accumulation and assist in fulfilling photoacoustic imaging. In particular, the small particle size (70 nm) of Ce6-PTX@IR783 contributed to the increased tumor accumulation via the enhanced permeability and retention effect. The high synergistically chemo-sonodynamic therapeutic efficacy has been successfully demonstrated in vitro and in vivo, in addition to the demonstrated high biodegradability, biocompatibility and biosafety. This facile self-assembly procedure provides an intriguing strategy for highly efficient utilization of hydrophobic drugs and is liable to realize large-scale production and further clinical translation.
作为最有前途的非侵入性治疗方式之一,声动力学疗法(SDT)可以将超声能量聚焦在位于深部组织的肿瘤部位,并局部激活预先加载的声敏剂来杀死肿瘤细胞。然而,探索具有高 SDT 疗效和理想生物安全性的声敏剂仍然是一个重大挑战。在此,我们利用亲水-亲脂自组装技术将疏水性有机染料 Ce6 和广谱抗癌剂紫杉醇与亲水性有机染料 IR783 组装成纳米级声敏剂 Ce6-PTX@IR783,在制备过程中不引入额外的纳米材料,以保证高治疗生物安全性和进一步的潜在临床转化。通过将多种基团整合到一个纳米系统中,构建的纳米药物具有外部超声激活的化学-声动力学效应和光声成像性能。Ce6 可以增强声动力学效应,而 PTX 发挥化学治疗作用,IR783 用于增加肿瘤特异性积累并协助光声成像。特别是,Ce6-PTX@IR783 的小粒径(70nm)通过增强的通透性和保留效应增加了肿瘤的积累。体外和体内研究均成功证明了高协同化学-声动力学治疗效果,同时还证明了其具有高的生物降解性、生物相容性和生物安全性。这种简便的自组装方法为高效利用疏水性药物提供了一种有趣的策略,有望实现大规模生产和进一步的临床转化。