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以血小板为载体的激光触发智能药物递送与抗癌光动力疗法

Laser-triggered intelligent drug delivery and anti-cancer photodynamic therapy using platelets as the vehicle.

作者信息

Li Qi-Rui, Xu Hua-Zhen, Xiao Rong-Cheng, Liu Bin, Ma Tian-Qi, Yu Ting-Ting, Li Liu-Gen, Wang Mei-Fang, Zhao Li, Chen Xiao, Li Tong-Fei

机构信息

Hubei Key Laboratory of Embryonic Stem Cell Research, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan, Hubei, China.

Department of Respiratory, Taihe Hospital of Shiyan, Hubei University of Medicine, Shiyan, Hubei, China.

出版信息

Platelets. 2023 Dec;34(1):2166677. doi: 10.1080/09537104.2023.2166677.

Abstract

In our previous study, target drug delivery and treatment of malignant tumors have been achieved by using platelets as carriers loading nano-chemotherapeutic agents (ND-DOX). However, drug release from ND-DOX-loaded platelets is dependent on negative platelet activation by tumor cells, whose activation is not significant enough for the resulting drug release to take an effective anti-tumor effect. Exploring strategies to proactively manipulate the controlled release of drug-laden platelets is imperative. The present study innovatively revealed that photodynamic action can activate platelets in a spatiotemporally controlled manner. Consequently, based on the previous study, platelets were used to load iron oxide-polyglycerol-doxorubicin-chlorin e6 composites (IO-PG-DOX-Ce6), wherein the laser-triggered drug release ability and anti-tumor capability were demonstrated. The findings suggested that IO-PG-DOX-Ce6 could be stably loaded by platelets in high volume without any decrease in viability. Importantly and interestingly, drug-loaded platelets were significantly activated by laser irradiation, characterized by intracellular ROS accumulation and up-regulation of CD62p. Additionally, scanning electron microscopy (SEM) and hydrated particle size results also showed a significant aggregation response of laser irradiated-drug-loaded platelets. Further transmission electron microscopy (TEM) measurements indicated that the activated platelets released extracellularly their cargo drug after laser exposure, which could be taken up by co-cultured tumor cells. Finally, the co-culture model of drug-loaded platelets and tumor cells proved that laser-triggered delivery system of platelets could effectively damage the DNA and promote apoptosis of tumor cells. Overall, the present study discovers a drug-loaded platelets delivery using photodynamic effect, enabling laser-controlled intelligent drug delivery and anti-tumor therapy, which provides a novel and feasible approach for clinical application of cytopharmaceuticals.

摘要

在我们之前的研究中,通过使用血小板作为载体负载纳米化疗药物(ND-DOX)实现了恶性肿瘤的靶向药物递送和治疗。然而,载有ND-DOX的血小板的药物释放依赖于肿瘤细胞对血小板的负向激活,而肿瘤细胞的这种激活程度不足以使释放的药物产生有效的抗肿瘤作用。探索主动调控载药血小板控释的策略势在必行。本研究创新性地揭示了光动力作用能够以时空可控的方式激活血小板。因此,基于之前的研究,利用血小板负载氧化铁-聚甘油-阿霉素-二氢卟吩e6复合材料(IO-PG-DOX-Ce6),并证明了其激光触发的药物释放能力和抗肿瘤能力。研究结果表明,IO-PG-DOX-Ce6能够被血小板大量稳定负载,且血小板活力无任何下降。重要且有趣的是,载药血小板经激光照射后被显著激活,表现为细胞内活性氧积累和CD62p上调。此外,扫描电子显微镜(SEM)和水合粒径结果也显示激光照射的载药血小板有明显的聚集反应。进一步的透射电子显微镜(TEM)测量表明,激活后的血小板在激光照射后将其负载的药物释放到细胞外,这些药物可被共培养的肿瘤细胞摄取。最后,载药血小板与肿瘤细胞的共培养模型证明,血小板的激光触发递送系统能够有效损伤肿瘤细胞的DNA并促进其凋亡。总体而言,本研究发现了一种利用光动力效应的载药血小板递送方法,实现了激光控制的智能药物递送和抗肿瘤治疗,为细胞药物的临床应用提供了一种新颖且可行的方法。

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