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治疗性纳米酶的安全格局及未来研究方向

Safety Landscape of Therapeutic Nanozymes and Future Research Directions.

作者信息

Tagaras Nikolaos, Song Haihan, Sahar Shafaq, Tong Weijun, Mao Zhengwei, Buerki-Thurnherr Tina

机构信息

Laboratory for Particles-Biology Interactions, Swiss Federal Laboratories for Materials Science and Technology (Empa), St. Gallen, 9014, Switzerland.

Department of Health Sciences and Technology, ETH Zurich, Zurich, 8093, Switzerland.

出版信息

Adv Sci (Weinh). 2024 Dec;11(46):e2407816. doi: 10.1002/advs.202407816. Epub 2024 Oct 24.


DOI:10.1002/advs.202407816
PMID:39445544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11633477/
Abstract

Oxidative stress and inflammation are at the root of a multitude of diseases. Treatment of these conditions is often necessary but current standard therapies to fight excessive reactive oxygen species (ROS) and inflammation are often ineffective or complicated by substantial safety concerns. Nanozymes are emerging nanomaterials with intrinsic enzyme-like properties that hold great promise for effective cancer treatment, bacterial elimination, and anti-inflammatory/anti-oxidant therapy. While there is rapid progress in tailoring their catalytic activities as evidenced by the recent integration of single-atom catalysts (SACs) to create next-generation nanozymes with superior activity, selectivity, and stability, a better understanding and tuning of their safety profile is imperative for successful clinical translation. This review outlines the current applied safety assessment approaches and provides a comprehensive summary of the safety knowledge of therapeutic nanozymes. Overall, nanozymes so far show good in vitro and in vivo biocompatibility despite considerable differences in their composition and enzymatic activities. However, current safety investigations mostly cover a limited set of basic toxicological endpoints, which do not allow for a thorough and deep assessment. Ultimately, remaining research gaps that should be carefully addressed in future studies are highlighted, to optimize the safety profile of therapeutic nanozymes early in their pre-clinical development.

摘要

氧化应激和炎症是多种疾病的根源。治疗这些病症往往是必要的,但目前对抗过量活性氧(ROS)和炎症的标准疗法往往无效,或因重大安全问题而变得复杂。纳米酶是新兴的具有类酶特性的纳米材料,在有效的癌症治疗、细菌清除以及抗炎/抗氧化治疗方面具有巨大潜力。虽然在调整其催化活性方面取得了快速进展,如最近通过整合单原子催化剂(SACs)来创建具有卓越活性、选择性和稳定性的下一代纳米酶所证明的那样,但为了成功实现临床转化,更好地理解和调整其安全性至关重要。本综述概述了当前应用的安全评估方法,并全面总结了治疗性纳米酶的安全知识。总体而言,尽管纳米酶在组成和酶活性方面存在很大差异,但迄今为止它们在体外和体内均表现出良好的生物相容性。然而,目前的安全性研究大多只涵盖了有限的一组基本毒理学终点,无法进行全面深入的评估。最终,强调了未来研究中应仔细解决的剩余研究空白,以便在临床前开发早期优化治疗性纳米酶的安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/a34155d14ea0/ADVS-11-2407816-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/dd2435e9ce7b/ADVS-11-2407816-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/cf88ca82ed7a/ADVS-11-2407816-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/0accd04ebadd/ADVS-11-2407816-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/4bdc1d0d91c9/ADVS-11-2407816-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/a34155d14ea0/ADVS-11-2407816-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/dd2435e9ce7b/ADVS-11-2407816-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/cf88ca82ed7a/ADVS-11-2407816-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/0accd04ebadd/ADVS-11-2407816-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/4bdc1d0d91c9/ADVS-11-2407816-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72cb/11633477/a34155d14ea0/ADVS-11-2407816-g002.jpg

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本文引用的文献

[1]
Protein Corona-Mediated Inhibition of Nanozyme Activity: Impact of Protein Shape.

J Am Chem Soc. 2024-4-17

[2]
Single Atom Catalysts Remodel Tumor Microenvironment for Augmented Sonodynamic Immunotherapy.

Adv Mater. 2024-6

[3]
Bioinspired Nanozymes as Nanodecoys for Urinary Tract Infection Treatment.

ACS Nano. 2024-3-26

[4]
Spatial engineering of single-atom Fe adjacent to Cu-assisted nanozymes for biomimetic O activation.

Nat Commun. 2024-3-12

[5]
PBA-Derived Heteroatom-Doped Mesoporous Graphitic Spheroids as Peroxidase Nanozyme for In Vitro Tumor Cells Detection.

ACS Appl Bio Mater. 2024-3-18

[6]
An ATPase-Mimicking MXene nanozyme pharmacologically breaks the ironclad defense system for ferroptosis cancer therapy.

Biomaterials. 2024-6

[7]
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ACS Omega. 2024-2-8

[8]
Glutathione Induced In situ Synthesis of Cu Single-Atom Nanozymes with Anaerobic Glycolysis Metabolism Interference for Boosting Cuproptosis.

Angew Chem Int Ed Engl. 2024-4-24

[9]
Ultrasmall metal alloy nanozymes mimicking neutrophil enzymatic cascades for tumor catalytic therapy.

Nat Commun. 2024-2-22

[10]
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RSC Adv. 2024-1-29

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