Radiation-Activated Cobalt-Based Zeolite Imidazolate Frameworks for Tumor Multitherapy.

IF 8.1 Q1 ENGINEERING, BIOMEDICAL
Biomaterials research Pub Date : 2025-04-15 eCollection Date: 2025-01-01 DOI:10.34133/bmr.0164
Qijun Du, Hongwei Jiang, Di Wu, Changlong Song, Wenqi Hu, Qinrui Lu, Chenwei Sun, Jie Liu, Guohua Wu, Shuqi Wang
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Abstract

Radiation dynamic therapy (RDT) is known to induce cancer apoptosis and death with minimal side effects and high accuracy. However, low efficiency of radiation sensitization and persistent hypoxic environment in tumors pose marked challenges for successful RDT. To address these challenges, a novel biodegradable drug delivery system was developed, using quercetin and sorafenib-loaded ZIF67 nanoparticles (QSZP NPs) coated with polydopamine. This system effectively controlled the tumor microenvironment (TME), overcame hypoxia, and was thus utilized for collaborative RDT and radiotherapy (RT). The QSZP NPs demonstrated great potential in x-ray sensitization and reactive oxygen species (ROS)-mediated effects in vitro. Furthermore, they continuously generated oxygen and increased ROS levels in the TME with x-ray irradiation to achieve RDT. In vivo studies showed that QSZP NPs had no apparent systemic toxicity and showed good therapeutic effect in a HepG2 tumor-bearing model. Due to its unique and outstanding combinational effect of RDT/RT/antiangiogenic cancer therapy, these synthesized NPs offer a promising method for radiation-based cancer treatment.

辐射激活钴基咪唑酸沸石框架用于肿瘤的综合治疗。
放射动态治疗(RDT)是已知的诱导肿瘤细胞凋亡和死亡,副作用小,准确度高。然而,肿瘤的低致敏效率和持续的缺氧环境是RDT成功的一大挑战。为了解决这些挑战,研究人员开发了一种新的可生物降解的药物递送系统,该系统使用槲皮素和索拉非尼负载的ZIF67纳米颗粒(QSZP NPs)包被聚多巴胺。该系统有效控制肿瘤微环境(TME),克服缺氧,可用于协同RDT和放疗(RT)。QSZP NPs在x射线致敏和活性氧(ROS)介导的体外效应方面显示出巨大的潜力。此外,它们在x射线照射下不断产生氧气并增加TME中的ROS水平,以实现RDT。体内研究表明,QSZP NPs在HepG2荷瘤模型中无明显的全身毒性,并表现出良好的治疗效果。由于其独特而突出的RDT/RT/抗血管生成癌症治疗联合效应,这些合成的NPs为基于放射的癌症治疗提供了一种很有前景的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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