Nanozymes in the Treatment of Diseases Caused by Excessive Reactive Oxygen Specie

References

• Turrens JF. Mitochondrial formation of reactive oxygen species. J Physiol. 2003;552(2):335–344. doi:10.1113/jphysiol.2003.049478
   PubMed Web of Science ®Google Scholar
• Held P. An introduction to reactive oxygen species. Tech Resources-App Guides. 2012;802:5–9.
   Google Scholar
• Bayir H. Reactive oxygen species. Crit Care Med. 2005;33(12 Suppl):S498–501. doi:10.1097/01.ccm.0000186787.64500.12
   PubMed Web of Science ®Google Scholar
• Ray PD, Huang BW, Tsuji Y. Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling. Cell Signal. 2012;24(5):981–990. doi:10.1016/j.cellsig.2012.01.008
   PubMed Web of Science ®Google Scholar
• Dhiman A, Handa M, Ruwali M, Singh DP, Kesharwani P, Shukla R. Recent trends of natural based therapeutics for mitochondria targeting in Alzheimer’s disease. Mitochondrion. 2022;64:112–124. doi:10.1016/j.mito.2022.03.006
   PubMed Web of Science ®Google Scholar
• Mittler R. ROS are good. Trends in Plant Sci. 2017;22(1):11–19. doi:10.1016/j.tplants.2016.08.002
   PubMed Web of Science ®Google Scholar
• Checa J, Aran JM. Reactive oxygen species: drivers of physiological and pathological processes. J Inflamm Res. 2020;13:1057. doi:10.2147/JIR.S275595
   PubMed Web of Science ®Google Scholar
• Kang DH. Oxidative stress, DNA damage, and breast cancer. AACN Adv Crit Care. 2002;13(4):540–549. doi:10.1097/00044067-200211000-00007
   Google Scholar
• Monaghan P, Metcalfe NB, Torres R. Oxidative stress as a mediator of life history trade-offs: mechanisms, measurements and interpretation. Ecol Lett. 2009;12(1):75–92. doi:10.1111/j.1461-0248.2008.01258.x
   PubMed Web of Science ®Google Scholar
• Andersen JK. Oxidative stress in neurodegeneration: cause or consequence? Nat Med. 2004;10(S7):S18–25. doi:10.1038/nrn1434
   PubMed Web of Science ®Google Scholar
• Melo A, Monteiro L, Lima RM, de Oliveira DM, de Cerqueira MD, El-Bachá RS. Oxidative stress in neurodegenerative diseases: mechanisms and therapeutic perspectives. Oxid Med Cell Longev. 2011;2011:1–14. doi:10.1155/2011/467180
   Web of Science ®Google Scholar
• Mittal M, Siddiqui MR, Tran K, Reddy SP, Malik AB. Reactive oxygen species in inflammation and tissue injury. Antioxid Redox Signal. 2014;20(7):1126–1167. doi:10.1089/ars.2012.5149
   PubMed Web of Science ®Google Scholar
• Amani H, Habibey R, Hajmiresmail SJ, Latifi S, Pazoki-Toroudi H, Akhavan O. Antioxidant nanomaterials in advanced diagnoses and treatments of ischemia reperfusion injuries. J Mater Chem B. 2017;5(48):9452–9476. doi:10.1039/c7tb01689a
   PubMed Web of Science ®Google Scholar
• Droge W. Free radicals in the physiological control of cell function. Physiol Rev. 2002;82(1):47–95. doi:10.1152/physrev.00018.2001
   PubMed Web of Science ®Google Scholar
• Wei H, Wang E. Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes. Chem Soc Rev. 2013;42(14):6060–6093. doi:10.1039/c3cs35486e
   PubMed Web of Science ®Google Scholar
• Gao L, Zhuang J, Nie L, et al. Intrinsic peroxidase-like activity of ferromagnetic nanoparticles. Nat Nanotechnol. 2007;2(9):577–583. doi:10.1038/nnano.2007.260
   PubMed Web of Science ®Google Scholar
• Yu X, Xu Z, Wang X, Xu Q, Chen J. Bactrian camel serum albumins-based nanocomposite as versatile biocargo for drug delivery, biocatalysis and detection of hydrogen peroxide. Mater Sci Eng C. 2020;109:110627. doi:10.1016/j.msec.2020.110627
   PubMed Web of Science ®Google Scholar
• Wang D, Jana D, Zhao Y. Metal–organic framework derived nanozymes in biomedicine. Acc Chem Res. 2020;53(7):1389–1400. doi:10.1021/acs.accounts.0c00268
   PubMed Web of Science ®Google Scholar
• Yan X, Gao L. Nanozymology: an Overview. In: Yan X, editor. Nanozymology. Nanostructure Science and Technology. Singapore: Springer; 2020:3–16. doi:10.1007/978-981-15-1490-6_1
   Google Scholar
• Liu T, Xiao B, Xiang F, et al. Ultrasmall copper-based nanoparticles for reactive oxygen species scavenging and alleviation of inflammation related diseases. Nat Commun. 2020;11(1):2788. doi:10.1038/s41467-020-16544-7
   PubMed Web of Science ®Google Scholar
• Wu J, Wang X, Wang Q, et al. Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes (II). Chem Soc Rev. 2019;48(4):1004–1076. doi:10.1039/c8cs00457a
   PubMed Web of Science ®Google Scholar
• Gaur M, Misra C, Yadav AB, et al. Biomedical applications of carbon nanomaterials: fullerenes, quantum dots, nanotubes, nanofibers, and graphene. Materials. 2021;14(20):5978. doi:10.3390/ma14205978
   PubMed Web of Science ®Google Scholar
• Karimi-Maleh H, Beitollahi H, Kumar PS, et al. Recent advances in carbon nanomaterials-based electrochemical sensors for food azo dyes detection. Food Chem Toxicol. 2022;164:112961. doi:10.1016/j.fct.2022.112961
   PubMed Web of Science ®Google Scholar
• Dellinger A, Zhou Z, Connor J, et al. Application of fullerenes in nanomedicine: an update. Nanomedicine. 2013;8(7):1191–1208. doi:10.2217/nnm.13.99
   PubMed Web of Science ®Google Scholar
• Speranza G. Carbon nanomaterials: synthesis, functionalization and sensing applications. Nanomaterials. 2021;11(4):967. doi:10.3390/nano11040967
   Web of Science ®Google Scholar
• Bakry R, Vallant RM, Najam-ul-Haq M, et al. Medicinal applications of fullerenes. Int J Nanomedicine. 2007;2(4):639–649.
   PubMed Web of Science ®Google Scholar
• Xiao L, Takada H, Gan X, Miwa N. The water-soluble fullerene derivative “Radical Sponge” exerts cytoprotective action against UVA irradiation but not visible-light-catalyzed cytotoxicity in human skin keratinocytes. Bioorg Med Chem Lett. 2006;16(6):1590–1595. doi:10.1016/j.bmcl.2005.12.011
   PubMed Web of Science ®Google Scholar
• Castro E, Garcia AH, Zavala G, Echegoyen L. Fullerenes in Biology and Medicine. J Mater Chem B. 2017;5(32):6523–6535. doi:10.1039/C7TB00855D
   PubMed Web of Science ®Google Scholar
• Cheng X, Ni X, Wu R, et al. Evaluation of the structure–activity relationship of carbon nanomaterials as antioxidants. Nanomedicine. 2018;13(7):733–747. doi:10.2217/nnm-2017-0314
   PubMed Web of Science ®Google Scholar
• Yudoh K, Karasawa R, Masuko K, Kato T. Water-soluble fullerene (C60) inhibits the development of arthritis in the rat model of arthritis. Int J Nanomedicine. 2009;4:217–225. doi:10.2147/ijn.s7653
   PubMed Web of Science ®Google Scholar
• Hao T, Li J, Yao F, et al. Injectable fullerenol/alginate hydrogel for suppression of oxidative stress damage in brown adipose-derived stem cells and cardiac repair. ACS Nano. 2017;11(6):5474–5488. doi:10.1021/acsnano.7b00221
   PubMed Web of Science ®Google Scholar
• Aqel A, Abou El-Nour KM, Ammar RA, Al-Warthan A. Carbon nanotubes, science and technology part (I) structure, synthesis and characterisation. Arab J Chem. 2012;5(1):1–23. doi:10.1016/j.arabjc.2010.08.022
   Web of Science ®Google Scholar
• Fenoglio I, Tomatis M, Lison D, et al. Reactivity of carbon nanotubes: free radical generation or scavenging activity? Free Radic Biol Med. 2006;40(7):1227–1233. doi:10.1016/j.freeradbiomed.2005.11.010
   PubMed Web of Science ®Google Scholar
• Qiu Y, Wang Z, Owens AC, et al. Antioxidant chemistry of graphene-based materials and its role in oxidation protection technology. Nanoscale. 2014;6(20):11744–11755. doi:10.1039/c4nr03275f
   PubMed Web of Science ®Google Scholar
• Ren C, Hu X, Zhou Q. Graphene oxide quantum dots reduce oxidative stress and inhibit neurotoxicity in vitro and in vivo through catalase-like activity and metabolic regulation. Adv Sci. 2018;5(5):1700595. doi:10.1002/advs.201700595
   Web of Science ®Google Scholar
• Han J, Kim YS, Lim MY, et al. Dual roles of graphene oxide to attenuate inflammation and elicit timely polarization of macrophage phenotypes for cardiac repair. ACS Nano. 2018;12(2):1959–1977. doi:10.1021/acsnano.7b09107
   PubMed Web of Science ®Google Scholar
• Chen Z, Yin JJ, Zhou YT, et al. Dual enzyme-like activities of iron oxide nanoparticles and their implication for diminishing cytotoxicity. ACS Nano. 2012;6(5):4001–4012. doi:10.1021/nn300291r
   PubMed Web of Science ®Google Scholar
• Gao L, Fan K, Yan X. Iron oxide nanozyme: a multifunctional enzyme mimetic for biomedical applications. Theranostics. 2017;7(13):3207–3227. doi:10.7150/thno.19738
   PubMed Web of Science ®Google Scholar
• Zhang Y, Wang Z, Li X, et al. Dietary iron oxide nanoparticles delay aging and ameliorate neurodegeneration in Drosophila. Adv Mater. 2016;28(7):1387–1393. doi:10.1002/adma.201503893
   PubMed Web of Science ®Google Scholar
• Wei Z, Wang L, Tang C, et al. Metal-phenolic networks nanoplatform to mimic antioxidant defense system for broad-spectrum radical eliminating and endotoxemia treatment. Adv Funct Mater. 2020;30(49):2002234. doi:10.1002/adfm.202002234
   Web of Science ®Google Scholar
• Zhang W, Ma D, Du J. Prussian blue nanoparticles as peroxidase mimetics for sensitive colorimetric detection of hydrogen peroxide and glucose. Talanta. 2014;120:362–367. doi:10.1016/j.talanta.2013.12.028
   PubMed Web of Science ®Google Scholar
• Zhang W, Hu S, Yin JJ, et al. Prussian blue nanoparticles as multienzyme mimetics and reactive oxygen species scavengers. J Am Chem Soc. 2016;138(18):5860–5865. doi:10.1021/jacs.5b12070
   PubMed Web of Science ®Google Scholar
• Zhao J, Cai X, Gao W, et al. Prussian blue nanozyme with multienzyme activity reduces colitis in mice. ACS Appl Mater Interfaces. 2018;10(31):26108–26117. doi:10.1021/acsami.8b10345
   PubMed Web of Science ®Google Scholar
• Estelrich J, Busquets MA. Prussian blue: a nanozyme with versatile catalytic properties. Int J Mol Sci. 2021;22(11):5993. doi:10.3390/ijms22115993
   PubMed Web of Science ®Google Scholar
• Chen J, Wang Q, Huang L, et al. Prussian blue with intrinsic heme-like structure as peroxidase mimic. Nano Res. 2018;11(9):4905–4913. doi:10.1007/s12274-018-2079-8
   Web of Science ®Google Scholar
• Bai H, Kong F, Feng K, et al. Prussian blue nanozymes prevent anthracycline-induced liver injury by attenuating oxidative stress and regulating inflammation. ACS Appl Mater Interfaces. 2021;13(36):42382–42395. doi:10.1021/acsami.1c09838
   PubMed Web of Science ®Google Scholar
• Xie X, Zhao J, Gao W, et al. Prussian blue nanozyme-mediated nanoscavenger ameliorates acute pancreatitis via inhibiting TLRs/NF-κB signaling pathway. Theranostics. 2021;11(7):3213–3228. doi:10.7150/thno.52010
   PubMed Web of Science ®Google Scholar
• Sahu A, Jeon J, Lee MS, Yang HS, Tae G. Antioxidant and anti-inflammatory activities of Prussian blue nanozyme promotes full-thickness skin wound healing. Mater Sci Eng C Mater Biol Appl. 2021;119:111596. doi:10.1016/j.msec.2020.111596
   PubMed Web of Science ®Google Scholar
• Zhang K, Tu M, Gao W, et al. Hollow Prussian blue nanozymes drive neuroprotection against ischemic stroke via attenuating oxidative stress, counteracting inflammation, and suppressing cell apoptosis. Nano Lett. 2019;19(5):2812–2823. doi:10.1021/acs.nanolett.8b04729
   PubMed Web of Science ®Google Scholar
• Feng L, Dou C, Xia Y, et al. Neutrophil-like cell-membrane-coated nanozyme therapy for ischemic brain damage and long-term neurological functional recovery. ACS Nano. 2021;15(2):2263–2280. doi:10.1021/acsnano.0c07973
   PubMed Web of Science ®Google Scholar
• He W, Zhou YT, Wamer WG, et al. Intrinsic catalytic activity of Au nanoparticles with respect to hydrogen peroxide decomposition and superoxide scavenging. Biomaterials. 2013;34(3):765–773. doi:10.1016/j.biomaterials.2012.10.010
   PubMed Web of Science ®Google Scholar
• Liu Z, Shen Y, Wu Y, et al. An intrinsic therapy of gold nanoparticles in focal cerebral ischemia-reperfusion injury in rats. J Biomed Nanotechnol. 2013;9(6):1017–1028. doi:10.1166/jbn.2013.1597
   PubMed Web of Science ®Google Scholar
• Liu CP, Wu TH, Lin YL, Liu CY, Wang S, Lin SY. Tailoring enzyme-like activities of gold nanoclusters by polymeric tertiary amines for protecting neurons against oxidative stress. Small. 2016;12(30):4127–4135. doi:10.1002/smll.201503919
   PubMed Web of Science ®Google Scholar
• Schubert D, Dargusch R, Raitano J, Chan SW. Cerium and yttrium oxide nanoparticles are neuroprotective. Biochem Biophys Res Commun. 2006;342(1):86–91. doi:10.1016/j.bbrc.2006.01.129
   PubMed Web of Science ®Google Scholar
• Pirmohamed T, Dowding JM, Singh S, et al. Nanoceria exhibit redox state-dependent catalase mimetic activity. Chem Commun (Camb). 2010;46(16):2736–2738. doi:10.1039/b922024k
   PubMed Web of Science ®Google Scholar
• Li Y, He X, Yin JJ, et al. Acquired superoxide-scavenging ability of ceria nanoparticles. Angew Chem Int Ed Engl. 2015;54(6):1832–1835. doi:10.1002/anie.201410398
   PubMed Web of Science ®Google Scholar
• Akhtar MJ, Ahamed M, Alhadlaq HA, Khan MAM, Alrokayan SA. Glutathione replenishing potential of CeO2 nanoparticles in human breast and fibrosarcoma cells. J Colloid Interface Sci. 2015;453:21–27. doi:10.1016/j.jcis.2015.04.049
   PubMed Web of Science ®Google Scholar
• Hirst SM, Karakoti AS, Tyler RD, Sriranganathan N, Seal S, Reilly CM. Anti-inflammatory properties of cerium oxide nanoparticles. Small. 2009;5(24):2848–2856. doi:10.1002/smll.200901048
   PubMed Web of Science ®Google Scholar
• Pagliari F, Mandoli C, Forte G, et al. Cerium oxide nanoparticles protect cardiac progenitor cells from oxidative stress. ACS Nano. 2012;6(5):3767–3775. doi:10.1021/nn2048069
   PubMed Web of Science ®Google Scholar
• Dowding JM, Song W, Bossy K, et al. Cerium oxide nanoparticles protect against Abeta-induced mitochondrial fragmentation and neuronal cell death. Cell Death Differ. 2014;21(10):1622–1632. doi:10.1038/cdd.2014.72
   PubMed Web of Science ®Google Scholar
• Singh R, Singh S. Redox-dependent catalase mimetic cerium oxide-based nanozyme protect human hepatic cells from 3-AT induced acatalasemia. Colloids Surf B Biointerfaces. 2019;175:625–635. doi:10.1016/j.colsurfb.2018.12.042
   PubMed Web of Science ®Google Scholar
• Bao Q, Hu P, Xu Y, et al. Simultaneous blood-brain barrier crossing and protection for stroke treatment based on edaravone-loaded ceria nanoparticles. ACS Nano. 2018;12(7):6794–6805. doi:10.1021/acsnano.8b01994
   PubMed Web of Science ®Google Scholar
• Kim CK, Kim T, Choi IY, et al. Ceria nanoparticles that can protect against ischemic stroke. Angew Chem Int Ed Engl. 2012;51(44):11039–11043. doi:10.1002/anie.201203780
   PubMed Web of Science ®Google Scholar
• Kwon HJ, Cha MY, Kim D, et al. Mitochondria-targeting ceria nanoparticles as antioxidants for Alzheimer’s disease. ACS Nano. 2016;10(2):2860–2870. doi:10.1021/acsnano.5b08045
   PubMed Web of Science ®Google Scholar
• Kim D, Kwon HJ, Hyeon T. Magnetite/ceria nanoparticle assemblies for extracorporeal cleansing of amyloid-beta in Alzheimer’s disease. Adv Mater. 2019;31(19):e1807965. doi:10.1002/adma.201807965
   PubMed Web of Science ®Google Scholar
• Chen Q, Du Y, Zhang K, et al. Tau-targeted multifunctional nanocomposite for combinational therapy of Alzheimer’s disease. ACS Nano. 2018;12(2):1321–1338. doi:10.1021/acsnano.7b07625
   PubMed Web of Science ®Google Scholar
• Fu S, Chen H, Yang W, et al. ROS-targeted depression therapy via BSA-incubated ceria nanoclusters. Nano Lett. 2022;22(11):4519–4527. doi:10.1021/acs.nanolett.2c01334
   PubMed Web of Science ®Google Scholar
• Kim J, Hong G, Mazaleuskaya L, et al. Ultrasmall antioxidant cerium oxide nanoparticles for regulation of acute inflammation. ACS Appl Mater Interfaces. 2021;13(51):60852–60864. doi:10.1021/acsami.1c16126
   PubMed Web of Science ®Google Scholar
• Zhao S, Li Y, Liu Q, et al. An orally administered CeO2 montmorillonite nanozyme targets inflammation for inflammatory bowel disease therapy. Adv Funct Mater. 2020;30(45). doi:10.1002/adfm.202004692
   Web of Science ®Google Scholar
• Lin A, Sun Z, Xu X, et al. Self-cascade uricase/catalase mimics alleviate acute gout. Nano Lett. 2022;22(1):508–516. doi:10.1021/acs.nanolett.1c04454
   PubMed Web of Science ®Google Scholar
• Wu L, Liu G, Wang W, et al. Cyclodextrin-modified CeO2 nanoparticles as a multifunctional nanozyme for combinational therapy of psoriasis. Int J Nanomedicine. 2020;15:2515–2527. doi:10.2147/IJN.S246783
   PubMed Web of Science ®Google Scholar
• Soh M, Kang DW, Jeong HG, et al. Ceria-zirconia nanoparticles as an enhanced multi-antioxidant for sepsis treatment. Angew Chem Int Ed Engl. 2017;56(38):11399–11403. doi:10.1002/anie.201704904
   PubMed Web of Science ®Google Scholar
• Li F, Qiu Y, Xia F, et al. Dual detoxification and inflammatory regulation by ceria nanozymes for drug-induced liver injury therapy. Nano Today. 2020;35:100925. doi:10.1016/j.nantod.2020.100925
   Web of Science ®Google Scholar
• Adebayo OA, Akinloye O, Adaramoye OA. Cerium oxide nanoparticles attenuate oxidative stress and inflammation in the liver of diethylnitrosamine-treated mice. Biol Trace Elem Res. 2020;193(1):214–225. doi:10.1007/s12011-019-01696-5
   PubMed Web of Science ®Google Scholar
• Kwon HJ, Kim D, Seo K, et al. Ceria nanoparticle systems for selective scavenging of mitochondrial, intracellular, and extracellular reactive oxygen species in Parkinson’s disease. Angew Chem Int Ed Engl. 2018;57(30):9408–9412. doi:10.1002/anie.201805052
   PubMed Web of Science ®Google Scholar
• Heckman KL, DeCoteau W, Estevez A, et al. Custom cerium oxide nanoparticles protect against a free radical mediated autoimmune degenerative disease in the brain. ACS Nano. 2013;7(12):10582–10596. doi:10.1021/nn403743b
   PubMed Web of Science ®Google Scholar
• Yu Y, Zhao S, Gu D, et al. Cerium oxide nanozyme attenuates periodontal bone destruction by inhibiting the ROS-NFκB pathway. Nanoscale. 2022;14(7):2628–2637. doi:10.1039/d1nr06043k
   PubMed Web of Science ®Google Scholar
• Korschelt K, Ragg R, Metzger CS, et al. Glycine-functionalized copper(ii) hydroxide nanoparticles with high intrinsic superoxide dismutase activity. Nanoscale. 2017;9(11):3952–3960. doi:10.1039/c6nr09810j
   PubMed Web of Science ®Google Scholar
• Hao C, Qu A, Xu L, et al. Chiral molecule-mediated porous CuxO nanoparticle clusters with antioxidation activity for ameliorating Parkinson’s disease. J Am Chem Soc. 2019;141(2):1091–1099. doi:10.1021/jacs.8b11856
   PubMed Web of Science ®Google Scholar
• Liu X, Wang Q, Zhao H, Zhang L, Su Y, Lv Y. BSA-templated MnO2 nanoparticles as both peroxidase and oxidase mimics. Analyst. 2012;137(19):4552–4558. doi:10.1039/c2an35700c
   PubMed Web of Science ®Google Scholar
• Li W, Liu Z, Liu C, Guan Y, Ren J, Qu X. Manganese dioxide nanozymes as responsive cytoprotective shells for individual living cell encapsulation. Angew Chem Int Ed Engl. 2017;56(44):13661–13665. doi:10.1002/anie.201706910
   PubMed Web of Science ®Google Scholar
• Yao J, Cheng Y, Zhou M, et al. ROS scavenging Mn3O4 nanozymes for in vivo anti-inflammation. Chem Sci. 2018;9(11):2927–2933. doi:10.1039/c7sc05476a
   PubMed Web of Science ®Google Scholar
• Singh N, Savanur MA, Srivastava S, D’Silva P, Mugesh G. A manganese oxide nanozyme prevents the oxidative damage of biomolecules without affecting the endogenous antioxidant system. Nanoscale. 2019;11(9):3855–3863. doi:10.1039/c8nr09397k
   PubMed Web of Science ®Google Scholar
• Singh N, Savanur MA, Srivastava S, D’Silva P, Mugesh G. A redox modulatory Mn3O4 nanozyme with multi-enzyme activity provides efficient cytoprotection to human cells in a Parkinson’s disease model. Angew Chem Int Ed Engl. 2017;56(45):14267–14271. doi:10.1002/anie.201708573
   PubMed Web of Science ®Google Scholar
• Huang Y, Liu C, Pu F, Liu Z, Ren J, Qu X. A GO-Se nanocomposite as an antioxidant nanozyme for cytoprotection. Chem Commun (Camb). 2017;53(21):3082–3085. doi:10.1039/c7cc00045f
   PubMed Web of Science ®Google Scholar
• Huang Y, Liu Z, Liu C, Zhang Y, Ren J, Qu X. Selenium-based nanozyme as biomimetic antioxidant machinery. Chemistry. 2018;24(40):10224–10230. doi:10.1002/chem.201801725
   PubMed Web of Science ®Google Scholar
• Chen X, Zhu X, Gong Y, et al. Porous selenium nanozymes targeted scavenging ROS synchronize therapy local inflammation and sepsis injury. Appl Mater Today. 2021;22. doi:10.1016/j.apmt.2020.100929
   Web of Science ®Google Scholar
• Chen B, Xiang S, Qian G. Metal-organic frameworks with functional pores for recognition of small molecules. Acc Chem Res. 2010;43(8):1115–1124. doi:10.1021/ar100023y
   PubMed Web of Science ®Google Scholar
• Kreno LE, Leong K, Farha OK, Allendorf M, Van Duyne RP, Hupp JT. Metal-organic framework materials as chemical sensors. Chem Rev. 2012;112(2):1105–1125. doi:10.1021/cr200324t
   PubMed Web of Science ®Google Scholar
• Tan H, Ma C, Gao L, et al. Metal–organic framework‐derived copper nanoparticle@ carbon nanocomposites as peroxidase mimics for colorimetric sensing of ascorbic acid. Chem Eur J. 2014;20(49):16377–16383. doi:10.1002/chem.201404960
   PubMed Web of Science ®Google Scholar
• Zhang JW, Zhang HT, Du ZY, Wang X, Yu SH, Jiang HL. Water-stable metal-organic frameworks with intrinsic peroxidase-like catalytic activity as a colorimetric biosensing platform. Chem Commun (Camb). 2014;50(9):1092–1094. doi:10.1039/c3cc48398c
   PubMed Web of Science ®Google Scholar
• Qi Z, Wang L, You Q, Chen Y. PA-Tb-Cu MOF as luminescent nanoenzyme for catalytic assay of hydrogen peroxide. Biosens Bioelectron. 2017;96:227–232. doi:10.1016/j.bios.2017.05.013
   PubMed Web of Science ®Google Scholar
• Chen WH, Vazquez-Gonzalez M, Kozell A, Cecconello A, Willner I. Cu2+-modified metal-organic framework nanoparticles: a peroxidase-mimicking nanoenzyme. Small. 2018;14(5). doi:10.1002/smll.201703149
   Web of Science ®Google Scholar
• Zheng HQ, Liu CY, Zeng XY, et al. MOF-808: a metal-organic framework with intrinsic peroxidase-like catalytic activity at neutral pH for colorimetric biosensing. Inorg Chem. 2018;57(15):9096–9104. doi:10.1021/acs.inorgchem.8b01097
   PubMed Web of Science ®Google Scholar
• Zhang K, Meng X, Cao Y, et al. Metal-organic framework nanoshuttle for synergistic photodynamic and low-temperature photothermal therapy. Adv Funct Mater. 2018;28(42):1804634. doi:10.1002/adfm.201804634
   Web of Science ®Google Scholar
• Li H, Cao X, Fei X, Zhang S, Xian Y. Nanoscaled luminescent terbium metal–organic frameworks for measuring and scavenging reactive oxygen species in living cells. J Mater Chem B. 2019;7(18):3027–3033. doi:10.1039/c9tb00361d
   Web of Science ®Google Scholar
• Zhang L, Zhang Y, Wang Z, et al. Constructing metal–organic framework nanodots as bio-inspired artificial superoxide dismutase for alleviating endotoxemia. Mater Horiz. 2019;6(8):1682–1687. doi:10.1039/c9mh00339h
   Web of Science ®Google Scholar
• Liu H, Yang Y, Liu Y, et al. Melanin-like nanomaterials for advanced biomedical applications: a versatile platform with extraordinary promise. Adv Sci. 2020;7(7):1903129. doi:10.1002/advs.201903129
   Web of Science ®Google Scholar
• Yue Y, Zhao X. Melanin-like nanomedicine in photothermal therapy applications. Int J Mol Sci. 2021;22(1):399. doi:10.3390/ijms22010399
   PubMed Web of Science ®Google Scholar
• Tada M, Kohno M, Niwano Y. Scavenging or quenching effect of melanin on superoxide anion and singlet oxygen. JClinbiochem nutr. 2010;46:224–228. doi:10.3164/jcbn.09-84
   PubMed Web of Science ®Google Scholar
• Liu Y, Ai K, Lu L. Polydopamine and its derivative materials: synthesis and promising applications in energy, environmental, and biomedical fields. Chem Rev. 2014;114(9):5057–5115. doi:10.1021/cr400407a
   PubMed Web of Science ®Google Scholar
• Hu J, Yang L, Yang P, Jiang S, Liu X, Li Y. Polydopamine free radical scavengers. Biomater Sci. 2020;8(18):4940–4950. doi:10.1039/d0bm01070g
   PubMed Web of Science ®Google Scholar
• Sun T, Jiang D, Rosenkrans ZT, et al. A melanin-based natural antioxidant defense nanosystem for theranostic application in acute kidney injury. Adv Funct Mater. 2019;29(48):1904833. doi:10.1002/adfm.201904833
   Web of Science ®Google Scholar
• Yang XF, Wang A, Qiao B, Li J, Liu J, Zhang T. Single-atom catalysts: a new frontier in heterogeneous catalysis. Acc Chem Res. 2013;46(8):1740–1748. doi:10.1021/ar300361m
   PubMed Web of Science ®Google Scholar
• Jiao L, Yan H, Wu Y, et al. When nanozymes meet single-atom catalysis. Angew Chem Int Ed Engl. 2020;59(7):2565–2576. doi:10.1002/anie.201905645
   PubMed Web of Science ®Google Scholar
• Pei J, Zhao R, Mu X, Wang J, Liu C, Zhang XD. Single-atom nanozymes for biological applications. Biomater Sci. 2020;8(23):6428–6441. doi:10.1039/d0bm01447h
   PubMed Web of Science ®Google Scholar
• Cao F, Zhang L, You Y, Zheng L, Ren J, Qu X. An enzyme‐mimicking single‐atom catalyst as an efficient multiple reactive oxygen and nitrogen species scavenger for sepsis management. Angewandte Chemie. 2020;132(13):5146–5153. doi:10.1002/ange.201912182
   Google Scholar
• Yan R, Sun S, Yang J, et al. Nanozyme-based bandage with single-atom catalysis for brain trauma. ACS nano. 2019;13(10):11552–11560. doi:10.1021/acsnano.9b05075
   PubMed Web of Science ®Google Scholar
• Korsvik C, Patil S, Seal S, Self WT. Superoxide dismutase mimetic properties exhibited by vacancy engineered ceria nanoparticles. Chem Commun (Camb). 2007;(10):1056–1058. doi:10.1039/b615134e
   PubMed Web of Science ®Google Scholar
• Xi Z, Gao W, Xia X. Size effect in Pd-Ir core-shell nanoparticles as nanozymes. Chembiochem. 2020;21(17):2440–2444. doi:10.1002/cbic.202000147
   PubMed Web of Science ®Google Scholar
• Xu R, Wang D, Zhang J, Li Y. Shape-dependent catalytic activity of silver nanoparticles for the oxidation of styrene. Chem Asian J. 2006;1(6):888–893. doi:10.1002/asia.200600260
   PubMed Web of Science ®Google Scholar
• Ge C, Fang G, Shen X, et al. Facet energy versus enzyme-like activities: the unexpected protection of palladium nanocrystals against oxidative damage. ACS Nano. 2016;10(11):10436–10445. doi:10.1021/acsnano.6b06297
   PubMed Web of Science ®Google Scholar
• He W, Wu X, Liu J, et al. Design of AgM bimetallic alloy nanostructures (M = Au, Pd, Pt) with tunable morphology and peroxidase-like activity. Chem Mater. 2010;22(9):2988–2994. doi:10.1021/cm100393v
   Web of Science ®Google Scholar
• Wu J, Qin K, Yuan D, et al. Rational design of Au@Pt multibranched nanostructures as bifunctional nanozymes. ACS Appl Mater Interfaces. 2018;10(15):12954–12959. doi:10.1021/acsami.7b17945
   PubMed Web of Science ®Google Scholar
• Xia X, Zhang J, Lu N, et al. Pd–Ir core–shell nanocubes: a type of highly efficient and versatile peroxidase mimic. Acs Nano. 2015;9(10):9994–10004. doi:10.1021/acsnano.5b03525
   PubMed Web of Science ®Google Scholar
• Gao Z, Ye H, Tang D, et al. Platinum-decorated gold nanoparticles with dual functionalities for ultrasensitive colorimetric in vitro diagnostics. Nano Lett. 2017;17(9):5572–5579. doi:10.1021/acs.nanolett.7b02385
   PubMed Web of Science ®Google Scholar
• Lv F, Gong Y, Cao Y, et al. A convenient detection system consisting of efficient Au@PtRu nanozymes and alcohol oxidase for highly sensitive alcohol biosensing. Nanoscale Adv. 2020;2(4):1583–1589. doi:10.1039/d0na00002g
   PubMed Web of Science ®Google Scholar
• Mu X, Wang J, Li Y, et al. Redox trimetallic nanozyme with neutral environment preference for brain injury. ACS Nano. 2019;13(2):1870–1884. doi:10.1021/acsnano.8b08045
   PubMed Web of Science ®Google Scholar
• Wang Q, Cheng C, Zhao S, et al. A valence‐engineered self‐cascading antioxidant nanozyme for the therapy of inflammatory bowel disease. Angew Chem Int Ed Engl. 2022. doi:10.1002/anie.202201101
   Web of Science ®Google Scholar
• Wang C, Ren G, Yuan B, et al. Enhancing enzyme-like activities of Prussian blue analog nanocages by molybdenum doping: toward cytoprotecting and online optical hydrogen sulfide monitoring. Anal Chem. 2020;92(11):7822–7830. doi:10.1021/acs.analchem.0c01028
   PubMed Web of Science ®Google Scholar
• Liu Y-Q, Mao Y, Xu E, et al. Nanozyme scavenging ROS for prevention of pathologic α-synuclein transmission in Parkinson’s disease. Nano Today. 2021;36:101027. doi:10.1016/j.nantod.2020.101027
   Web of Science ®Google Scholar
• Liu B, Liu J. Surface modification of nanozymes. Nano Res. 2017;10(4):1125–1148. doi:10.1007/s12274-017-1426-5
   Web of Science ®Google Scholar
• Liu B, Huang Z, Liu J. Boosting the oxidase mimicking activity of nanoceria by fluoride capping: rivaling protein enzymes and ultrasensitive F− detection. Nanoscale. 2016;8(28):13562–13567. doi:10.1039/c6nr02730j
   PubMed Web of Science ®Google Scholar
• Wang S, Chen W, Liu AL, Hong L, Deng HH, Lin XH. Comparison of the peroxidase-like activity of unmodified, amino-modified, and citrate-capped gold nanoparticles. Chemphyschem. 2012;13(5):1199–1204. doi:10.1002/cphc.201100906
   PubMed Web of Science ®Google Scholar
• Zhang XQ, Gong SW, Zhang Y, Yang T, Wang CY, Gu N. Prussian blue modified iron oxide magnetic nanoparticles and their high peroxidase-like activity. J Mater Chem. 2010;20(24). doi:10.1039/c0jm00174k
   Web of Science ®Google Scholar
• Liu X, Wei W, Yuan Q, et al. Apoferritin-CeO2 nano-truffle that has excellent artificial redox enzyme activity. Chem Commun (Camb). 2012;48(26):3155–3157. doi:10.1039/c1cc15815e
   PubMed Web of Science ®Google Scholar
• Asati A, Santra S, Kaittanis C, Nath S, Perez JM. Oxidase-like activity of polymer-coated cerium oxide nanoparticles. Angew Chem Int Ed Engl. 2009;48(13):2308–2312. doi:10.1002/anie.200805279
   PubMed Web of Science ®Google Scholar
• Pautler R, Kelly EY, Huang PJ, Cao J, Liu B, Liu J. Attaching DNA to nanoceria: regulating oxidase activity and fluorescence quenching. ACS Appl Mater Interfaces. 2013;5(15):6820–6825. doi:10.1021/am4018863
   PubMed Web of Science ®Google Scholar
• Fan K, Wang H, Xi J, et al. Optimization of Fe3O4 nanozyme activity via single amino acid modification mimicking an enzyme active site. Chem Commun (Camb). 2017;53(2):424–427. doi:10.1039/C6CC08542C
   Web of Science ®Google Scholar
• Sun Y, Zhao C, Gao N, Ren J, Qu X. Stereoselective nanozyme based on ceria nanoparticles engineered with amino acids. Chem Eur J. 2017;23(72):18146–18150. doi:10.1002/chem.201704579
   PubMed Web of Science ®Google Scholar
• Zhang R, Zhou Y, Yan X, Fan K. Advances in chiral nanozymes: a review. Mikrochim Acta. 2019;186(12):782. doi:10.1007/s00604-019-3922-7
   PubMed Web of Science ®Google Scholar
• Chen JLY, Pezzato C, Scrimin P, Prins LJ. Chiral nanozymes–gold nanoparticle‐based transphosphorylation catalysts capable of enantiomeric discrimination. Chem Eur J. 2016;22(21):7028–7032. doi:10.1002/chem.201600853
   PubMed Web of Science ®Google Scholar
• Zhan P, Wang ZG, Li N, Ding B. Engineering gold nanoparticles with DNA ligands for selective catalytic oxidation of chiral substrates. ACS Catal. 2015;5(3):1489–1498. doi:10.1021/cs5015805
   Web of Science ®Google Scholar
• Wang H, Yu D, Fang J, et al. Phenol-like group functionalized graphene quantum dots structurally mimicking natural antioxidants for highly efficient acute kidney injury treatment. Chem Sci. 2020;11(47):12721–12730. doi:10.1039/d0sc03246h
   PubMed Web of Science ®Google Scholar
• Sun X, Guo S, Chung CS, Zhu W, Sun S. A sensitive H2O2 assay based on dumbbell-like PtPd-Fe3O4 nanoparticles. Adv Mater. 2013;25(1):132–136. doi:10.1002/adma.201203218
   PubMed Web of Science ®Google Scholar
• Liu M, Li Z, Li Y, Chen J, Yuan Q. Self-assembled nanozyme complexes with enhanced cascade activity and high stability for colorimetric detection of glucose. Chin Chem Lett. 2019;30(5):1009–1012. doi:10.1016/j.cclet.2018.12.021
   Web of Science ®Google Scholar
• Wang Z, Dong K, Liu Z, et al. Activation of biologically relevant levels of reactive oxygen species by Au/g-C3N4 hybrid nanozyme for bacteria killing and wound disinfection. Biomaterials. 2017;113:145–157. doi:10.1016/j.biomaterials.2016.10.041
   PubMed Web of Science ®Google Scholar
• Zhang L, Pan J, Long Y, et al. CeO2-encapsulated hollow Ag-Au nanocage hybrid nanostructures as high-performance catalysts for cascade reactions. Small. 2019;15(43):e1903182. doi:10.1002/smll.201903182
   PubMed Web of Science ®Google Scholar
• Zhang S, Li H, Wang Z, et al. A strongly coupled Au/Fe3O4/GO hybrid material with enhanced nanozyme activity for highly sensitive colorimetric detection, and rapid and efficient removal of Hg2+ in aqueous solutions. Nanoscale. 2015;7(18):8495–8502. doi:10.1039/c5nr00527b
   PubMed Web of Science ®Google Scholar
• Huang Y, Liu Z, Liu C, et al. Self‐assembly of multi‐nanozymes to mimic an intracellular antioxidant defense system. Angew Chem Int Ed Engl. 2016;128(23):6758–6762. doi:10.1002/ange.201600868
   Google Scholar
• He L, Huang G, Liu H, Sang C, Liu X, Chen T. Highly bioactive zeolitic imidazolate framework-8–capped nanotherapeutics for efficient reversal of reperfusion-induced injury in ischemic stroke. Sci Adv. 2020;6(12):eaay9751. doi:10.1126/sciadv.aay9751
   PubMed Web of Science ®Google Scholar
• Zhang K, Kaufman RJ. From endoplasmic-reticulum stress to the inflammatory response. Nature. 2008;454(7203):455–462. doi:10.1038/nature07203
   PubMed Web of Science ®Google Scholar
• Guo H, Callaway JB, Ting JP. Inflammasomes: mechanism of action, role in disease, and therapeutics. Nat Med. 2015;21(7):677–687. doi:10.1038/nm.3893
   PubMed Web of Science ®Google Scholar
• Ferrucci L, Fabbri E. Inflammageing: chronic inflammation in ageing, cardiovascular disease, and frailty. Nat Rev Cardiol. 2018;15(9):505–522. doi:10.1038/s41569-018-0064-2
   PubMed Web of Science ®Google Scholar
• Simmonds N, Rampton D. Inflammatory bowel disease--a radical view. Gut. 1993;34(7):865. doi:10.1136/gut.34.7.865
   PubMed Web of Science ®Google Scholar
• Qin Z, Li Y, Gu N. Progress in applications of Prussian blue nanoparticles in biomedicine. Adv Healthc Mater. 2018;7(20):1800347. doi:10.1002/adhm.201800347
   Web of Science ®Google Scholar
• Qiu H, Gong H, Bao Y, Jiang H, Tong W. Reactive oxygen species-scavenging hollow MnO2 nanozymes as carriers to deliver budesonide for synergistic inflammatory bowel disease therapy. Biomater Sci. 2022;10(2):457–466. doi:10.1039/d1bm01525g
   PubMed Web of Science ®Google Scholar
• Zhong G, Yang X, Jiang X, et al. Dopamine-melanin nanoparticles scavenge reactive oxygen and nitrogen species and activate autophagy for osteoarthritis therapy. Nanoscale. 2019;11(24):11605–11616. doi:10.1039/c9nr03060c
   PubMed Web of Science ®Google Scholar
• Kumar S, Adjei IM, Brown SB, Liseth O, Sharma B. Manganese dioxide nanoparticles protect cartilage from inflammation-induced oxidative stress. Biomaterials. 2019;224:119467. doi:10.1016/j.biomaterials.2019.119467
   PubMed Web of Science ®Google Scholar
• Bao X, Zhao J, Sun J, Hu M, Yang X. Polydopamine nanoparticles as efficient scavengers for reactive oxygen species in periodontal disease. ACS Nano. 2018;12(9):8882–8892. doi:10.1021/acsnano.8b04022
   PubMed Web of Science ®Google Scholar
• Zerna C, Thomalla G, Campbell BC, Rha J-H, Hill MD. Current practice and future directions in the diagnosis and acute treatment of ischaemic stroke. The Lancet. 2018;392(10154):1247–1256. doi:10.1016/S0140-6736(18)31874-9
   PubMed Web of Science ®Google Scholar
• Rzigalinski BA, Meehan K, Davis RM, Xu Y, Miles WC, Cohen CA. Radical nanomedicine. Nanomedcine. 2006;1(4):399–412. doi:10.2217/17435889.1.4.399
   PubMed Web of Science ®Google Scholar
• Liu Y, Ai K, Ji X, et al. Comprehensive insights into the multi-antioxidative mechanisms of melanin nanoparticles and their application to protect brain from injury in ischemic stroke. J Am Chem Soc. 2017;139(2):856–862. doi:10.1021/jacs.6b11013
   PubMed Web of Science ®Google Scholar
• Huang G, Zang J, He L, et al. Bioactive nanoenzyme reverses oxidative damage and endoplasmic reticulum stress in neurons under ischemic stroke. ACS Nano. 2021. doi:10.1021/acsnano.1c07205
   Web of Science ®Google Scholar
• Hardy J, Selkoe DJ. The amyloid hypothesis of Alzheimer’s disease: progress and problems on the road to therapeutics. Science. 2002;297(5580):353–356. doi:10.1126/science.1072994
   PubMed Web of Science ®Google Scholar
• Polanco JC, Li C, Bodea LG, Martinez-Marmol R, Meunier FA, Götz J. Amyloid-β and tau complexity—towards improved biomarkers and targeted therapies. Nat Rev Neurol. 2018;14(1):22–39. doi:10.1038/nrneurol.2017.162
   PubMed Web of Science ®Google Scholar
• Cheignon C, Tomas M, Bonnefont-Rousselot D, Faller P, Hureau C, Collin F. Oxidative stress and the amyloid beta peptide in Alzheimer’s disease. Redox Biol. 2018;14:450–464. doi:10.1016/j.redox.2017.10.014
   PubMed Web of Science ®Google Scholar
• Savelieff MG, Nam G, Kang J, Lee HJ, Lee M, Lim MH. Development of multifunctional molecules as potential therapeutic candidates for Alzheimer’s disease, Parkinson’s disease, and amyotrophic lateral sclerosis in the last decade. Chem Rev. 2019;119(2):1221–1322. doi:10.1021/acs.chemrev.8b00138
   PubMed Web of Science ®Google Scholar
• Jenner P. Oxidative stress in Parkinson’s disease. Ann Reurol. 2003;53(S3):S26–S38. doi:10.1002/ana.10483
   Web of Science ®Google Scholar
• Spillantini MG, Schmidt ML, Lee VM-Y, Trojanowski JQ, Jakes R, Goedert M. α-Synuclein in Lewy bodies. Nature. 1997;388(6645):839–840. doi:10.1038/42166
   PubMed Web of Science ®Google Scholar
• Ma X, Hao J, Wu J, Li Y, Cai X, Zheng Y. Prussian blue nanozyme as a pyroptosis inhibitor alleviates neurodegeneration. Adv Mater. 2022;34(15):2106723. doi:10.1002/adma.202106723
   Web of Science ®Google Scholar
• Ni D, Jiang D, Kutyreff CJ, et al. Molybdenum-based nanoclusters act as antioxidants and ameliorate acute kidney injury in mice. Nat Commun. 2018;9(1):5421. doi:10.1038/s41467-018-07890-8
   PubMed Web of Science ®Google Scholar
• Zhang J, Pei W, Xu Q, Jiang H, Chen J. Desolvation-induced formation of recombinant camel serum albumin-based nanocomposite for glutathione colorimetric determination. Sens Actuators B Che. 2022;1;357.
   Google Scholar
• Zhang J, Xu Q, Pei W, et al. Self-assembled recombinant camel serum albumin nanoparticles-encapsulated hemin with peroxidase-like activity for colorimetric detection of hydrogen peroxide and glucose. Int J Biol Macromol. 2021;193:2103–2112. doi:10.1016/j.ijbiomac.2021.11.042
   PubMed Web of Science ®Google Scholar
• Ryan JJ, Bateman HR, Stover A, et al. Fullerene nanomaterials inhibit the allergic response. J Immunol. 2007;179(1):665–672. doi:10.4049/jimmunol.179.1.665
   PubMed Web of Science ®Google Scholar
• Jacevic V, Djordjevic A, Srdjenovic B, et al. Fullerenol nanoparticles prevents doxorubicin-induced acute hepatotoxicity in rats. Exp Mol Pathol. 2017;102(2):360–369. doi:10.1016/j.yexmp.2017.03.005
   PubMed Web of Science ®Google Scholar
• Zhao S, Duan H, Yang Y, Yan X, Fan K. Fenozyme protects the integrity of the blood-brain barrier against experimental cerebral malaria. Nano Lett. 2019;19(12):8887–8895. doi:10.1021/acs.nanolett.9b03774
   PubMed Web of Science ®Google Scholar
• Kalashnikova I, Chung SJ, Nafiujjaman M, et al. Ceria-based nanotheranostic agent for rheumatoid arthritis. Theranostics. 2020;10(26):11863–11880. doi:10.7150/thno.49069
   PubMed Web of Science ®Google Scholar
• Bailey ZS, Nilson E, Bates JA, et al. Cerium oxide nanoparticles improve outcome after in vitro and in vivo mild traumatic brain injury. J Neurotrauma. 2020;37(12):1452–1462. doi:10.1089/neu.2016.4644
   PubMed Web of Science ®Google Scholar
• Cheng Y, Cheng C, Yao J, et al. Mn3O4 nanozyme for inflammatory bowel disease therapy. Adv Ther. 2021;4(9). doi:10.1002/adtp.202100081
   Web of Science ®Google Scholar
• Zhang X, Zhang S, Yang Z, Wang Z, Tian X, Zhou R. Self-cascade MoS2 nanozymes for efficient intracellular antioxidation and hepatic fibrosis therapy. Nanoscale. 2021;13(29):12613–12622. doi:10.1039/d1nr02366g
   PubMed Web of Science ®Google Scholar
• Onizawa S, Aoshiba K, Kajita M, Miyamoto Y, Nagai A. Platinum nanoparticle antioxidants inhibit pulmonary inflammation in mice exposed to cigarette smoke. Pulm Pharmacol Ther. 2009;22(4):340–349. doi:10.1016/j.pupt.2008.12.015
   PubMed Web of Science ®Google Scholar
• Katsumi H, Fukui K, Sato K, et al. Pharmacokinetics and preventive effects of platinum nanoparticles as reactive oxygen species scavengers on hepatic ischemia/reperfusion injury in mice. Metallomics. 2014;6(5):1050–1056. doi:10.1039/c4mt00018h
   PubMed Web of Science ®Google Scholar
• Zhao H, Zeng Z, Liu L, et al. Polydopamine nanoparticles for the treatment of acute inflammation-induced injury. Nanoscale. 2018;10(15):6981–6991. doi:10.1039/c8nr00838h
   PubMed Web of Science ®Google Scholar
• Liu Y, Cheng Y, Zhang H, et al. Integrated cascade nanozyme catalyzes in vivo ROS scavenging for anti-inflammatory therapy. Sci Adv. 2020;6(29):eabb2695. doi:10.1126/sciadv.abb2695
   PubMed Web of Science ®Google Scholar
• Huang Y, Ren J, Qu X. Nanozymes: classification, catalytic mechanisms, activity regulation, and applications. Chem Rev. 2019;119(6):4357–4412. doi:10.1021/acs.chemrev.8b00672
   PubMed Web of Science ®Google Scholar