Zou Zheng, Bi Xiaojun, Ma Huan, Chen Ligang, Jin Hai, Gong Shun, Li Xinning, Liu Xiyu
Department of Neurosurgery, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.
Department of Urology, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.
Int J Nanomedicine. 2025 Jul 29;20:9447-9472. doi: 10.2147/IJN.S540010. eCollection 2025.
Atherosclerosis (AS) is a complex, multifactorial cardiovascular disease characterized by lipid accumulation, chronic inflammation, oxidative stress, and endothelial dysfunction. Conventional therapies, including lipid-lowering and anti-inflammatory agents, offer limited efficacy due to inadequate lesion targeting, low bioavailability, and systemic side effects. Nanozymes, which engineered nanomaterials with intrinsic enzyme-mimetic catalytic activities have recently emerged as a transformative therapeutic strategy capable of simultaneously modulating oxidative stress, inflammation, and lipid metabolism. This review comprehensively summarizes recent advances in nanozyme-based interventions for AS, focusing on representative systems such as Prussian blue, cerium oxide, selenium-based, and multifunctional composite nanozymes. We critically discuss their design principles, catalytic mechanisms, lesion-targeting strategies, and therapeutic outcomes in preclinical models. Additionally, we highlight key translational challenges, including biosafety concerns, pharmacokinetic limitations, and manufacturing standardization, which currently impede clinical application. By integrating catalytic activity with targeted delivery and microenvironment-responsive functionalities, nanozymes offer a promising paradigm for precision therapy in AS. Future research should prioritize enhancing biocompatibility, optimizing therapeutic specificity, and establishing scalable, reproducible fabrication methods to facilitate clinical translation. This review aims to provide a systematic framework and insightful guidance for advancing nanozyme-based therapeutics toward clinical application in cardiovascular disease management.
动脉粥样硬化(AS)是一种复杂的多因素心血管疾病,其特征为脂质蓄积、慢性炎症、氧化应激和内皮功能障碍。包括降脂药和抗炎药在内的传统疗法,由于病变靶向性不足、生物利用度低和全身副作用,疗效有限。纳米酶是一类具有内在类酶催化活性的工程纳米材料,最近已成为一种变革性的治疗策略,能够同时调节氧化应激、炎症和脂质代谢。本文综述全面总结了基于纳米酶的AS干预措施的最新进展,重点关注普鲁士蓝、氧化铈、硒基和多功能复合纳米酶等代表性体系。我们批判性地讨论了它们的设计原理、催化机制、病变靶向策略以及在临床前模型中的治疗效果。此外,我们强调了关键的转化挑战,包括生物安全性问题、药代动力学限制和制造标准化,这些目前阻碍了临床应用。通过将催化活性与靶向递送和微环境响应功能相结合,纳米酶为AS的精准治疗提供了一个有前景的范例。未来的研究应优先提高生物相容性、优化治疗特异性,并建立可扩展、可重复的制造方法,以促进临床转化。本文综述旨在为推进基于纳米酶的治疗方法在心血管疾病管理中的临床应用提供一个系统的框架和有见地的指导。