首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Chemotherapeutic drug-photothermal agent co-self-assembling nanoparticles for near-infrared fluorescence and photoacoustic dual-modal imaging-guided chemo-photothermal synergistic therapy
【24h】

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

机译:用于近红外荧光和光声双型成像引导的化学光热协同疗法的化学治疗药物 - 光热试剂共同自组装纳米粒子

获取原文
获取原文并翻译 | 示例
           

摘要

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, pi-pi stacking, and hydrophobic interactions). The exceptionally high dual-drug loading (similar to 92 wt%) 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-selfassembly 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.
机译:多式化成像引导的协同组合疗法表现出巨大的癌症治疗潜力。然而,基于纳米载体的治疗系统患有分批的变异,多组分,药物载荷不良和载体相关毒性问题的复杂性。为了解决这些问题,本文我们开发了一种新的载体免疫系统,具有纳米级特征,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疗法(PTT)。吲哚菁绿(ICG)和EPIRUBICIN(EPI)可以通过协作相互作用(静电,PI-PI堆叠和疏水相互作用)将其在水溶液中的小分子纳米颗粒(NPS)中的小分子纳米颗粒(NPS)中。特异性高的双药物负载(类似于92wt%)ICG-EPI NPS显示出良好的生理稳定性,优选的光热响应,优异的NIRF / PA成像性能,pH- /光响应药物释放行为,以及促进细胞内吞作用免费ICG或EPI。重要的是,ICG-EPI NPS显示出优异的肿瘤靶向能力,具有高空间分辨率和通过体内NI​​RF / PA双模态成像的深度渗透。此外,与个体化疗或PTT相比,ICG-EPI NPS的组合化学COMO-PTT治疗ICG-EPI NPS在体外协同诱导癌细胞的细胞凋亡和死亡,并且在高效的情况下证明了体内协同化学-PTT效率肿瘤消融。此外,ICG-EPI NPS表现出不必要的毒性。 FDA批准的代理商的这种共产性在多官能纳米治疗系统的合理设计中提供了一种安全和“分子经济”策略,用于实时自我监测细胞内药物递送和靶向多峰影像引导协同组合治疗。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号