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金属有机框架介导的抗氧化酶递送在疾病治疗中的应用

Metal-organic framework-mediated antioxidant enzyme delivery in disease treatment.

作者信息

Yayun Jiang, Qianqian Ge, Xihang Sun, Yang Hong, Zhenping Hou, Yuying Li, Xiancheng Ma, Qian Jiang, Pengjun Shi

机构信息

College of Animal Science and Technology, Hunan Agricultural University, Changsha, 410000, China; Institute of Bast Fiber Crops Chinese Academy of Agricultural Sciences, Changsha, 410205, China.

Institute of Bast Fiber Crops Chinese Academy of Agricultural Sciences, Changsha, 410205, China.

出版信息

Redox Biol. 2025 Jul 18;85:103778. doi: 10.1016/j.redox.2025.103778.

Abstract

Excessive reactive oxygen species (ROS) induce oxidative stress (OS), resulting in biomolecular damage. ROS are closely linked to diseases such as inflammatory bowel disease (IBD), diabetes, and cancer. Antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), and glucose oxidase (GOX) play crucial roles in alleviating OS by effectively reducing ROS levels through synergistic action. However, these antioxidant enzymes exhibit poor stability in complex biological environments and lack adequate targeting capability, thereby limiting their applications in disease treatment. Metal-organic frameworks (MOFs) serve as carriers that significantly enhance enzyme stability and targeting ability, thereby boosting catalytic efficiency and therapeutic outcomes. This review discusses the classification of antioxidant enzymes and their role in ROS regulation, the types and physicochemical properties of MOFs, and the assembly methods of enzyme@MOF systems. Furthermore, it examines the potential of integrating MOFs with antioxidant enzymes for the treatment of diseases associated with OS. Although the strategy of enzyme immobilization with MOFs shows great application prospects, further optimization is required in terms of biocompatibility, long-term stability, and delivery efficiency to promote the clinical translation of these results.

摘要

过量的活性氧(ROS)会引发氧化应激(OS),导致生物分子损伤。ROS与炎症性肠病(IBD)、糖尿病和癌症等疾病密切相关。超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPX)和葡萄糖氧化酶(GOX)等抗氧化酶通过协同作用有效降低ROS水平,在减轻氧化应激方面发挥着关键作用。然而,这些抗氧化酶在复杂的生物环境中稳定性较差,且缺乏足够的靶向能力,从而限制了它们在疾病治疗中的应用。金属有机框架(MOF)作为载体,可显著提高酶的稳定性和靶向能力,从而提高催化效率和治疗效果。本文综述了抗氧化酶的分类及其在ROS调节中的作用、MOF的类型和理化性质,以及酶@MOF系统的组装方法。此外,还探讨了将MOF与抗氧化酶整合用于治疗与氧化应激相关疾病的潜力。尽管用MOF固定酶的策略显示出巨大的应用前景,但在生物相容性、长期稳定性和递送效率方面仍需进一步优化,以促进这些成果的临床转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abbf/12312119/8c935933dc95/gr1.jpg

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