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化疗药物-光热剂共自组装纳米粒子用于近红外荧光和光声双模成像引导的化疗-光热协同治疗。

Chemotherapeutic drug-photothermal agent co-self-assembling nanoparticles for near-infrared fluorescence and photoacoustic dual-modal imaging-guided chemo-photothermal synergistic therapy.

机构信息

College of Materials & School of Pharmaceutical Science, Xiamen University, Fujian Provincial Key Laboratory of Innovative Drug Target Research & Fujian Provincial Key Laboratory for Soft Functional Materials Research, Xiamen 361005, PR China; State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry & Chemical Engineering, Xiamen University, Xiamen 361005, PR China.

College of Materials & School of Pharmaceutical Science, Xiamen University, Fujian Provincial Key Laboratory of Innovative Drug Target Research & Fujian Provincial Key Laboratory for Soft Functional Materials Research, Xiamen 361005, PR China.

出版信息

J Control Release. 2017 Jul 28;258:95-107. doi: 10.1016/j.jconrel.2017.05.011. Epub 2017 May 10.

Abstract

Multimodal imaging-guided synergistic combination therapy has shown great potential for cancer treatment. However, the nanocarrier-based theranostic systems suffer from batch-to-batch variation, complexity of multicomponent, poor drug loading, and carrier-related toxicity issues. To address these issues, herein we developed a novel carrier-free theranostic system with nanoscale characteristics for near-infrared fluorescence (NIRF) and photoacoustic (PA) dual-modal imaging-guided synergistic chemo-photothermal therapy (PTT). Indocyanine green (ICG) and epirubicin (EPI) could co-self-assemble into small molecular nanoparticles (NPs) in aqueous solution without any molecular precursor or excipient via collaborative interactions (electrostatic, π-π stacking, and hydrophobic interactions). The exceptionally high dual-drug loading (∼92wt%) ICG-EPI NPs showed good physiological stability, preferable photothermal response, excellent NIRF/PA imaging properties, pH-/photo-responsive drug release behavior, and promoted cellular endocytosis compared with free ICG or EPI. Importantly, the ICG-EPI NPs showed excellent tumor targeting ability with high spatial resolution and deep penetration via in vivo NIRF/PA dual-modal imaging. Moreover, in comparison with individual chemotherapy or PTT, the combinational chemo-PTT therapy of ICG-EPI NPs with NIR laser irradiation synergistically induced apoptosis and death of cancer cells in vitro, and showed synergistic chemo-PTT efficiency in vivo as evidenced by highly efficient tumor ablation. Furthermore, the ICG-EPI NPs exhibited inappreciable toxicity. This co-self-assembly of both FDA-approved agents provides a safe and "Molecular economical" strategy in the rational design of multifunctional nano-theranostic systems for real-time self-monitoring intracellular drug delivery and targeting multimodal imaging-guided synergistic combination therapy.

摘要

多模态影像引导协同组合治疗在癌症治疗方面显示出巨大的潜力。然而,基于纳米载体的治疗诊断系统存在批次间差异、多组分复杂性、药物载量差和载体相关毒性等问题。为了解决这些问题,本文开发了一种具有纳米级特性的新型无载体治疗诊断系统,用于近红外荧光(NIRF)和光声(PA)双模态成像引导协同化学-光热治疗(PTT)。吲哚菁绿(ICG)和表阿霉素(EPI)可以通过协同相互作用(静电、π-π堆积和疏水相互作用)在水溶液中共同自组装成小分子纳米颗粒(NPs),而无需任何分子前体或赋形剂。高载药量(约 92wt%)的ICG-EPI NPs 具有良好的生理稳定性、优异的光热响应、良好的 NIRF/PA 成像性能、pH/光响应药物释放行为以及与游离 ICG 或 EPI 相比促进细胞内吞作用。重要的是,与游离 ICG 或 EPI 相比,ICG-EPI NPs 通过体内 NIRF/PA 双模态成像具有优异的肿瘤靶向能力,具有高空间分辨率和深穿透性。此外,与单独的化疗或 PTT 相比,ICG-EPI NPs 联合 NIR 激光照射的化疗-PTT 协同诱导体外癌细胞凋亡和死亡,并通过高效的肿瘤消融在体内显示出协同的化疗-PTT 效率。此外,ICG-EPI NPs 表现出可忽略不计的毒性。两种 FDA 批准药物的共自组装为合理设计多功能纳米治疗诊断系统提供了一种安全且“分子经济”的策略,用于实时自我监测细胞内药物输送和靶向多模态成像引导协同组合治疗。

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