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用于光动力疗法-化疗协同联合诱导胃癌细胞焦亡的仿生金属有机框架纳米颗粒

Biomimetic Metal-Organic Framework Nanoparticles for Synergistic Combining of SDT-Chemotherapy Induce Pyroptosis in Gastric Cancer.

作者信息

Yu Zhu, Cao Wenlong, Han Chuangye, Wang Zhen, Qiu Yue, Wang Jiancheng, Wei Mengda, Wang Junfu, Zhang Siwen, Liu Senfeng, Mo Shutian, Chen Junqiang

机构信息

Department of Gastrointestinal Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Guangxi Key Laboratory of Enhanced Recovery After Surgery for Gastrointestinal Cancer, Nanning, China.

出版信息

Front Bioeng Biotechnol. 2022 Feb 21;10:796820. doi: 10.3389/fbioe.2022.796820. eCollection 2022.

Abstract

In recent years, sonodynamic therapy (SDT) has been widely developed for cancer research as a promising non-invasive therapeutic strategy. Here, we synthesized zeolitic imidazole frameworks-8 (ZIF-8) and utilized its properties to encapsulate hydrophobic Chlorin e6 (Ce6) and hydrophilic tirapazamine (TPZ) for a synergistic sonodynamic chemotherapy, which was also accompanied by the modification of cytomembrane of gastric cancer (GC) cells. Thus, we enabled the biomimetic property to achieve targeted delivery. Ce6-mediated SDT, in combination with ultrasound irradiation, could target the release of reactive oxygen species (ROS) to aggravate further hypoxia and activate TPZ. Combining these effects could induce the pyroptosis of GC cells and play the anti-tumor function, which could provide a potential therapeutic method for cancer therapy.

摘要

近年来,作为一种有前景的非侵入性治疗策略,声动力疗法(SDT)在癌症研究中得到了广泛发展。在此,我们合成了沸石咪唑框架-8(ZIF-8),并利用其特性封装疏水性的氯e6(Ce6)和亲水性的替拉扎明(TPZ)以进行协同声动力化疗,同时还对胃癌(GC)细胞的细胞膜进行了修饰。因此,我们赋予了其仿生特性以实现靶向递送。Ce6介导的声动力疗法与超声照射相结合,可靶向释放活性氧(ROS)以进一步加重缺氧并激活TPZ。综合这些效应可诱导GC细胞发生焦亡并发挥抗肿瘤作用,这可为癌症治疗提供一种潜在的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed79/8899015/1b6da2ab98f1/fbioe-10-796820-g001.jpg

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