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仿生高密度脂蛋白纳米颗粒介导吲哚菁绿的肿瘤靶向递送以增强光动力治疗

Biomimetic HDL nanoparticle mediated tumor targeted delivery of indocyanine green for enhanced photodynamic therapy.

作者信息

Wang Yazhe, Wang Cheng, Ding Yang, Li Jing, Li Min, Liang Xiao, Zhou Jianping, Wang Wei

机构信息

State Key Laboratory of Natural Medicines, Department of Pharmaceutics, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, China.

Center for Drug Delivery and Nanomedicine, Department of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE, USA.

出版信息

Colloids Surf B Biointerfaces. 2016 Dec 1;148:533-540. doi: 10.1016/j.colsurfb.2016.09.037. Epub 2016 Sep 26.

Abstract

Photodynamic therapy has emerged as a promising strategy for cancer treatment. To ensure the efficient delivery of a photosensitizer to tumor for anticancer effect, a safe and tumor-specific delivery system is highly desirable. Herein, we introduce a novel biomimetic nanoparticle named rHDL/ICG (rHDL/I), by loading amphiphilic near-infrared (NIR) fluorescent dye indocyanine green (ICG) into reconstituted high density lipoproteins (rHDL). In this system, rHDL can mediate photoprotection effect and receptor-guided tumor-targeting transportation of cargos into cells. Upon NIR irradiation, ICG can generate fluorescent imaging signals for diagnosis and monitoring therapeutic activity, and produce singlet oxygen to trigger photodynamic therapy (PDT). Our studies demonstrated that rHDL/I exhibited excellent size and fluorescence stability, light-triggered controlled release feature, and neglectable hemolytic activity. It also showed equivalent NIR response compared to free ICG under laser irradiation. Importantly, the fluorescent signal of ICG loaded in rHDL/I could be visualized subcellularly in vitro and exhibited metabolic distribution in vivo, presenting superior tumor targeting and internalization. This NIR-triggered image-guided nanoparticle produced outstanding therapeutic outcomes against cancer cells, demonstrating great potential of biomimetic delivery vehicles in future clinical practice.

摘要

光动力疗法已成为一种很有前景的癌症治疗策略。为确保将光敏剂有效递送至肿瘤以发挥抗癌作用,非常需要一种安全且肿瘤特异性的递送系统。在此,我们通过将两亲性近红外(NIR)荧光染料吲哚菁绿(ICG)载入重组高密度脂蛋白(rHDL)中,引入了一种名为rHDL/ICG(rHDL/I)的新型仿生纳米颗粒。在该系统中,rHDL可介导光保护作用以及将货物受体引导的肿瘤靶向转运至细胞内。在近红外照射下,ICG可产生用于诊断和监测治疗活性的荧光成像信号,并产生单线态氧以触发光动力疗法(PDT)。我们的研究表明,rHDL/I表现出优异的尺寸和荧光稳定性、光触发控释特性以及可忽略不计的溶血活性。在激光照射下,它与游离ICG相比还表现出相当的近红外响应。重要的是,载入rHDL/I中的ICG的荧光信号在体外可在亚细胞水平可视化,并在体内表现出代谢分布,呈现出优异的肿瘤靶向性和内化作用。这种近红外触发的图像引导纳米颗粒对癌细胞产生了出色的治疗效果,证明了仿生递送载体在未来临床实践中的巨大潜力。

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