首页> 美国卫生研究院文献>Theranostics >Theranostic Nanodots with Aggregation-Induced Emission Characteristic for Targeted and Image-Guided Photodynamic Therapy of Hepatocellular Carcinoma
【2h】

Theranostic Nanodots with Aggregation-Induced Emission Characteristic for Targeted and Image-Guided Photodynamic Therapy of Hepatocellular Carcinoma

机译:具有聚集诱导发射特征的治疗性纳米点对肝细胞癌的靶向和影像引导光动力治疗

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Photosensitizer (PS) serves as the central element of photodynamic therapy (PDT). The use of common nanoparticles (NPs) for PDT has typically been rendered less effective by the undesirable aggregation-caused quenching (ACQ) effect, resulting in quenched fluorescence and reduced reactive oxygen species (ROS) generation that diminish the imaging quality and PDT efficacy. To overcome the ACQ effect and to enhance the overall efficacy of PDT, herein, integrin ανβ3-targeted organic nanodots for image-guided PDT were designed and synthesized based on a red emissive aggregation-induced emission (AIE) PS.>Methods: The TPETS nanodots were prepared by nano-precipitation method and further conjugated with thiolated cRGD (cRGD-SH) through a click reaction to yield the targeted TPETS nanodots (T-TPETS nanodots). Nanodots were characterized for encapsulation efficiency, conjugation rate, particle size, absorption and emission spectra and ROS production. The targeted fluorescence imaging and antitumor efficacy of T-TPETS nanodot were evaluated both in vitro and in vivo. The mechanism of cell apoptosis induced by T-TPETS nanodot mediated-PDT was explored. The biocompatibility and toxicity of the nanodots was examined using cytotoxicity test, hemolysis assay, blood biochemistry test and histological staining.>Results: The obtained nanodots show bright red fluorescence and highly effective 1O2 generation in aggregate state. Both in vitro and in vivo experiments demonstrate that the nanodots exhibit excellent tumor-targeted imaging performance, which facilitates image-guided PDT for tumor ablation in a hepatocellular carcinoma model. Detailed analysis reveals that the nanodot-mediated PDT is able to induce time- and concentration-dependent cell death. The use of PDT at a high PDT intensity leads to direct cell necrosis, while cell apoptosis via the mitochondria-mediated pathway is achieved under low PDT intensity.>Conclusion: Our results suggest that well-designed AIE nanodots are promising for image-guided PDT applications.
机译:光敏剂(PS)是光动力疗法(PDT)的核心要素。通过不良的聚集引起的猝灭(ACQ)效应,通常使普通的纳米颗粒(NPs)用于PDT的效果降低,导致猝灭的荧光和减少的活性氧(ROS)生成,从而降低了成像质量和PDT的功效。为了克服ACQ效应并增强PDT的整体功效,本文基于红色发射聚集诱导发射(AIE)PS设计并合成了用于图像引导PDT的整联蛋白ανβ3靶向有机纳米点。>方法: 通过纳米沉淀法制备TPETS纳米点,然后通过点击反应将其与硫醇化cRGD(cRGD-SH)偶联,以生成目标TPETS纳米点(T-TPETS纳米点)。纳米点的包封效率,结合率,粒径,吸收和发射光谱和ROS产生的特点。在体外和体内均评估了T-TPETS纳米点的靶向荧光成像和抗肿瘤功效。探索了T-TPETS纳米点介导的PDT诱导细胞凋亡的机制。通过细胞毒性试验,溶血分析,血液生化试验和组织学染色检查了纳米点的生物相容性和毒性。>结果:获得的纳米点显示亮红色荧光,非常有效 1 聚集状态下产生O2。体外和体内实验均表明,纳米点具有出色的肿瘤靶向成像性能,这有助于在肝细胞癌模型中进行图像引导的PDT消融肿瘤。详细的分析表明,纳米点介导的PDT能够诱导时间和浓度依赖性细胞死亡。在高PDT强度下使用PDT会导致直接细胞坏死,而在低PDT强度下通过线粒体介导的途径实现细胞凋亡。>结论:我们的结果表明,精心设计的AIE纳米点是对于图像引导的PDT应用很有希望。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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