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A Mini Review on the Recent High-Impact Nanozymatic Sensors Constructed over 2016–2023

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02 September 2023

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05 September 2023

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Abstract
As formally is known, nanozymes are the nanomaterials or nanoscale materials which reveal enzyme-like properties. These nanomaterilas can be utilzied instead of the natural enzymes for simulation of enzymatic reactions in harsh environmental conditions. Among different nanoscale enzyme-like materials, the majority of them reveal peroxidase-like activity, due to the high catalytic efficiency and stability of peroxidase-like nanozymes, they had been widely utilized for sensing and detection via constructing the colorimetric and fluorescence-based analytical and bioanalytical sensors. There are several high impact nanozymatic sensors which reported in the literature. Although the review articles published in this field, however, the current reviews focus on the introducing nanozyme field not description on the best articles published in this filed. Hence, this article aimed to present a brief introduction on the nanozyme-based chemistry with emphasizing on the historical overview of recent nanozymatic sensors. In this regard the best nanozymatic sensors which published over 2016-2023 were briefly described and overviewed.
Keywords: 
Subject: Chemistry and Materials Science  -   Analytical Chemistry

1. Nanozymes: Introduction

Nanozyme chemistry is consisted of design, synthesis, modification, biochemical characterization, structural characterization, and application of nanoscale artificial enzymes as well as evaluation of mechanism of nanozyme-based systems [1,2,3,4,5,6,7,8,9,10,11]. In fact, the fast development of nanoscience and material chemistry has increased interest in researching new and innovative synthesis methods to produce new nanomaterials with unique catalytic activity [12,13], unique optical properties [14,15,16], high active area [17], antibacterial properties [18], and high biocompatibility [19]. The new field of nanozyme-based catalysis, which has been introduced as an alternative to enzyme-based catalysis, is called nanozyme chemistry. On the other hand, nanozymes are known as nanomaterials with high enzyme-like activity and can be used to simulate enzymatic reactions in harsh environmental conditions (for example, higher temperature or wider pH range) [20,21,22,23,24,25,26,27]. As previously reported in the literature [27], native enzymes, for instance, native peroxidases or ureases suffer from several disadvantages and drawbacks such as low pH stability, low thermal stability, low recoverability, and no reusability. Commonly, to solve these difficulties and drawbacks of native enzymes, the development of enzyme immobilization protocols has been widely considered in the literature [27,28,29,30]. Hence to solve these difficulties, the design and development of low-cost nanozymes were considered as an interesting way for performing enzyme-catalyzed reactions in harsh conditions [21,31]. Nanozymes have been used for several applications in catalysis [32], biomedical imaging [33], diagnosis of infection diseases (e.g., COVID-19), treatment of diseases, tumor therapy [34,35], and sensing and detection [36,37,38] (Figure 1). For instance, up to date, different types of nanozyme-based sensors such as single nanozymatic sensors, enzyme-nanozyme hybrid sensors, etc. have been developed [39]. Recently a new generation of nanozyme-based systems called “multinanozyme system’ was introduced by Hormozi Jangi et al. (2020) [40,41]. During the last years, a wide variety of nanozyme-based colorimetric sensors have been developed for the detection and quantification of a variety of analytes for instance, tryptophan [42], glutathione (GSH) [43], dopamine [44], tetracycline [45], metal cations [46], glucose [47], H2O2 [48], explosives [49], and cysteine [50]. Besides, some of the nanozyme-based sensors with fluorescence-based response had been developed and utilized for detecting several analytes [51,52]. It is notable that after the first report of COVID-19 on 2019 [53,54], the nanozymes had been utilized for detection of SARS-CoV-2 [55].

2. Historical Review of Nanozyme-Based Sensors

Up to now, several reports on nanozymes application in the field of sensing and detection were published as we mentioned above. In this section, the recent published works were reviewed. In 2016, Lu et al. [56] fabricated a new nanozyme based sensor for colorimetric quantification of hydrogen peroxide utilizing a new 3D porous dendrites of PtCu three-dimensional (3D) hierarchical porous. The peroxidase mimic properties of the dendrites were checked by the standard method of 3,3′,5,5′-tetramethyl-benzidine oxidation by hydrogen peroxide. The sensor provided a linear range of over 0.3–325 μM along with a LOD of 0.1 μM for hydrogen peroxide determination which is lower than the accepted level of hydrogen peroxide reported by US FDA (i.e., 15 μM). The method showed good selectivity and was applied for the determination of the hydrogen peroxide content of milk samples.
In 2017, Singh et al. [57] reported a selective nanozyme-based method for the quantification of malathion utilizing the peroxidase-mimicking properties of palladium-gold nanorods. The O- phenylenediamine was used as the chromogenic compound for the detection purpose upon its oxidation by hydrogen peroxide catalyzed by palladium-gold nanozyme. A LOD as low as 60 ng mL-1 was obtained for the detection of malathion along with a recovery percentage of 80–106%. The reproducibility of the sensor was found to be 2.7-6.1% and 3.2-5.9% intra and inter-assay, in turn. In 2017, Zhang et al. [58] immobilized modified the Cu(II)-based MOF-74 and employed them for the sensitive electrochemical detection of 2,4,6-trichlorophenol. XRD, FT-IR, SEM, UV-Vis., and CV measurements were performed for investigation of composite properties. A wide linear range over 0.01-9 μM and LOD of about 0.005 μM was achieved for the determination of 2,4,6-trichlorophenol. The repeatability studies showed an RSD% of 4.6% for determination of 0.5 5 μM 2,4,6-trichlorophenol. In 2018, Chen et al. [59] synthesized honeycomb-like zinc-doped Ni(II)-based MOF with spherical particles using HCl as the modulator upon a microwave-assisted method. The resulting MOFs were used as electrode materials, showed a specific capacity of 237.4 mA h g-1 for 1 A g-1 which can be used as supercapacitor material. In 2018, Yu et al. [60] designed a new sensor for the Pb(II) detection using a Fe(II)-MOFs/Pd-Pt alloys composites via a target-triggered nuclear acid cleavage of Pb2+-specific DNAzyme. Moreover, the DNAzyme was immobilized on streptavidin-modified reduced graphene oxide-tetraethylene pentamine-gold nanoparticles for use as the sensor platform. By introducing the Pb(II), the DNA was cleaved by the DNAzyme and a new single strand of DNA was produced. In the presence of Pb2+, the substrate DNA strand can be specifically cleaved at the ribonucleotide site by DNAzyme to produce a new single-DNA on the interface. Then, the single-strand DNA was used for modification of Fe-MOFs/PdPt NPs for signal amplification. The sensor showed a linear range over 0.005-1000 nM and a LOD of 2 pM (S/N =3) for Pb(II) determination in drinking water. In 2018, Li et al. [61] synthesized and characterized a new iron-base MOF@palladium nanoparticles composite via assembly palladium nanoparticles on the surface of NH2-Fe-MIL-88. The composite was used for the determination of microRNA-122 by the electrocatalytic oxidation of 3,3′,5,5′-tetramethylbenzidine in the presence of H2O2 catalyzed by the developed nanocomposite with intrinsic peroxidase-like activity. A working range over 0.01 fM-10 pM along with a LOD of 0.003 fM (S/N =3) was obtained. In 2018, Lopa et al. [62] used a microwave-assisted solvothermal route for the synthesis of a novel base-stable Cr(III)-MOF and utilized it for the non-enzymatic quantification of hydrogen peroxide via its electro-reduction in 0.1 M NaOH through the redox process of Cr(III)/Cr(II) in the Cr (III)-MOF. A working range of 25-500 mM and a LOD of 3.52 mM was provided for hydrogen peroxide determination. In 2018, Wang et al. [63] used the Ru, Ir, and Pt-based nanozymes for developing a nanozyme sensor array toward biothiols and proteins determination as well as cancer cells discrimination. The sensor array can accurately identify 42 of 45 proteins and 28 of 30 biothiols which makes it applicable for biothiols detection in blood and protein discrimination in urine samples. In 2019, Xue et al. [64] reported a new nanocomposite of silver nanoparticles with amino-functionalized multi-walled carbon nanotubes with high water-processibility, environmental stability, and electrocatalytic capacity via the ultrasonic-assisted liquid-phase exfoliation method. The nanocomposite was then dispersed in carboxymethyl cellulose sodium and applied for the development of electrochemical sensors for single/simultaneous determination of xanthine, uric acid, and hypoxanthine, showing a working range of 0.5–680 μM (LOD=0.021 μM), 0.1–800 μM (LOD= 0.052 μM), and 0.7–320 μM (LOD=0.025 μM), in order. In 2020, Zhu et al. [65] fabricated a nanozymatic sensor array for the detection of aromatic pesticides using heteroatom-doped graphene. The enzyme-like activity of nanozyme was inhibited in the presence of the different pesticides with a characteristic distinguish between them. This sensor array can determine the lactofen, bensulfuron-methyl, fluoroxypyr-meptyl, diafenthiuron, and fomesafen over 5-500 μM. The array was practically applied for the analysis of soil samples. In 2020, Hormozi Jangi et al. [49] developed a novel naked-eye method for field detection of notorious explosive triacetone triperoxide via the oxidation of 3, 3′-diaminobenzidine in the presence of hydrogen peroxide produced from the acidic decomposition of triacetone triperoxide catalyzed by MnO2 nanozymes. A linear range of 1.57-10.50 mg L−1, a LOD of 0.34 mg L−1, and a fast spot test analyzing time of 5 s were provided. Since the DAB oxidation was selectively proceeded by hydrogen peroxide not, by molecular oxygen, hence, this method can be eliminated the common false-positive results from laundry detergents. In 2020, Lin et al. [66] synthesized the gold alloy-based nanozymes which showed better catalytic performances than the common gold nanoparticles. The developed nanozymes were used for the discrimination of cysteine, glutathione, mercaptoacetic acid, dithiothreitol, mercaptosuccinic acid, and mercaptoethanol in the human serum samples. In 2021, Soltani et al. [67] synthesized and characterized a carboxylic acid-functionalized layered double hydroxide/MOF nanocomposite via growing the UiO-66-(Zr)-(COOH)2 MOF on the surface of COOH-functionalized Ni50Co50- layered double hydroxide nanosheets at 100 °C. The product was used for Cd(II) and Pb(II) removal from the water via surface adsorption mechanism, showing an adsorption capacity of 415.3 and 301.4 mg g−1 for Cd(II) and Pb(II), in turn. The method showed a Langmuir adsorption isotherm and a pseudo-first-order kinetic model. In 2021, Butova et al. [68] reported a scalable route for the synthesis of MOF-801. They evaluated the effect of the concentration of mono-carboxylic acids on the water and hydrogen uptake, porosity, crystallinity, size, and shape of particles. They revealed that heating and small grains in powders are suitable for the fast release of water. The properties of the MOF-801 can enhance by both formic and acetic acid. The resulted MOF-801 showed 1.1 wt% hydrogen uptake at 750 mmHg and 20% water uptake at ambient temperature. In 2021, He et al. [69] prepared stable MOF based on porphyrinic for the encapsulation of metal nanoparticles via stirring at ambient temperature. In this regard, Pt NPs encapsulated into the MOF can be produced by stirring the Pt NPs solution in the presence of the MOFs. In 2021, Kang et al. [70] reported a nanozyme based sensor for the determination of dopamine using hemin-doped-HKUST-1. The hemin-doped-HKUST-1 was prepared using a one-pot hydrothermal method and combined with reduced graphene oxide modified on a glassy carbon electrode. The composite exhibited high electrocatalytic activity toward electro-oxidation of dopamine. Using this sensor, a linear range of 0.03–10 μM and a LOD of 3.27 × 10−8 M (S/N = 3) was obtained for the quantification of dopamine. In 2021, Hermosilla et al. [71] proposed a new colorimetric method for assaying the oxidase-mimicking properties of MnFe2O4 NPs (size, 3.19 nm). The protocol was based on the oxidation of 3-methyl-2-benzothiazolinone-hydrazone to 3-(dimethylamino) benzoic acid. The pH and temperature effect on the assay response was evaluated, revealing an optimum pH of 3.9 at 30 °C. The Michaelis Menten model supported the kinetic behavior of the nanozyme catalyzed reaction, obtaining a Km of 13.59 µM and a kcat of 5.25 × 107 s−1 along with a kcat/Km ratio of 3.86 × 1012 M−1 s−1. In 2022, Wu et al. [72] developed a MnO2 nanozyme-mediated CRISPR-Cas12a system for naked-eye diagnosis of COVID-19. In this system, the MnO2 nanorods were initially linked to magnetic beads using a single-stranded DNA (ssDNA). The as-prepared nanozymes show high oxidase-like activity and can catalyze the oxidation of TMB to a blue-colored product. However, the detection color will change by activation of Cas12a by SARS-CoV-2 and cleaving the ssDNA which was used as a basis for the detection of SARS-3CoV-2. In 2023, He et al. [73] performed a nanozyme-based colorimetric method for naked-eye diagnosis of COVID-19 by iron manganese silicate nanozymes as peroxidase-like nanozymes. The nanozymes activity can be inhibited by introducing the pyrophosphate ions which are generated by amplification processes and can be used for optical diagnosis of COVID-19. Besides, Chu et al. (2023) [74] developed a robust colorimetric immunosensing method using liposome-encapsulated MnO2 nanozymes for diagnosis of COVID-19 via detection of SARS-CoV-2 antigen using TMB as the chromogenic substrate. Moreover, Vafabakhsh et al. (2023) [75] reported a paper-based colorimetric nanozyme-based sensor for diagnosis of COVID-19 using aptamer-modified ChF/ZnO/CNT nanohybrids as peroxidase mimics and TMB as the chromogenic substrate.

3. Perspectives

The nanozyme chemistry is new filed and on its initial steps. As a perspective to future of this filed, it can be pointed to the following items;
✓
Developing nanozymes with higher catalytic efficiency and higher substrate affinity in their native form.
✓
Developing nanozymes with intrinsic activity of commercial enzymes such as lipase and urease for application in industrial process in real world.
✓
Extending the multinanozyme systems for improving sensitivity and selectivity of nanozymatic sensors
✓
Design of biocompatible nanozymes with drug-like properties for treatment of diseases with minimal side effects.
✓
Developing simple surface modification of nanozymes for enhancing their specificity.
✓
Evaluating biochemical behavior of nanozymes for better understanding their best performances
✓
Developing reusable nanozymes with high cycling stability and simple recovery suitable for real practical applications
✓
Design of specific nanozyme-based sensors compared of current selective sensors
✓
etc.

4. Conclusions

As formally is known, nanozymes are the nanomaterials or nanoscale materials which reveal enzyme-like properties. These nanomaterilas can be utilzied instead of the natural enzymes for simulation of enzymatic reactions in harsh environmental conditions. Among different nanoscale enzyme-like materials, the majority of them reveal peroxidase-like activity, due to the high catalytic efficiency and stability of peroxidase-like nanozymes, they had been widely utilized for sensing and detection via constructing the colorimetric and fluorescence-based analytical and bioanalytical sensors. There are several high impact nanozymatic sensors which reported in the literature. Although the review articles published in this field, however, the current reviews focus on the introducing nanozyme field not description on the best articles published in this filed. Hence, this article aimed to present a brief introduction on the nanozyme-based chemistry with emphasizing on the historical overview of recent nanozymatic sensors. In this regard the best nanozymatic sensors which published over 2016-2023 were briefly described and overviewed.

Acknowledgments

The authors gratefully thank the Hormozi Laboratory of Chemistry and Biochemistry (Zabol, Iran) for the support of this work.

Conflicts of Interest

None.

References

  1. Huang, Y.; Ren, J.; Qu, X. Nanozymes: Classification, Catalytic Mechanisms, Activity Regulation, and Applications. Chem. Rev. 2019, 119, 4357–4412. [Google Scholar] [CrossRef]
  2. Wu, J.; Wang, X.; Wang, Q.; Lou, Z.; Li, S.; Zhu, Y.; Qin, L.; Wei, H. Nanomaterials with enzyme-like characteristics (nanozymes): Next-generation artificial enzymes (II). Chem. Soc. Rev. 2018, 48, 1004–1076. [Google Scholar] [CrossRef]
  3. Liang, M.; Yan, X. Nanozymes: From new concepts, mechanisms, and standards to applications. Acc. Chem. Res. 2019, 52, 2190–2200. [Google Scholar] [CrossRef]
  4. Wei, H.; Wang, E. Nanomaterials with Enzyme-like Characteristics (Nanozymes): Next-Generation Artificial Enzymes. Chem. Soc. Rev. 2013, 42, 6060–6093. [Google Scholar] [CrossRef]
  5. Wang, Z.; Zhang, R.; Yan, X.; Fan, K. Structure and activity of nanozymes: Inspirations for de novo design of nanozymes. Mater. Today 2020, 41, 81–119. [Google Scholar] [CrossRef]
  6. Zhang, R.; Yan, X.; Fan, K. Nanozymes Inspired by Natural Enzymes. Accounts Mater. Res. 2021, 2, 534–547. [Google Scholar] [CrossRef]
  7. Wang, X.; Hu, Y.; Wei, H. Nanozymes in bionanotechnology: From sensing to therapeutics and beyond. Inorg. Chem. Front. 2015, 3, 41–60. [Google Scholar] [CrossRef]
  8. Jiao, L.; Yan, H.; Wu, Y.; Gu, W.; Zhu, C.; Du, D.; Lin, Y. When nanozymes meet single-atom catalysis. Angew. Chem. 2020, 132, 2585–2596. [Google Scholar]
  9. Liu, B.; Liu, J. Surface modification of nanozymes. Nano Res. 2017, 10, 1125–1148. [Google Scholar] [CrossRef]
  10. Wang, D.; Jana, D.; Zhao, Y. Metal–Organic Framework Derived Nanozymes in Biomedicine. Accounts Chem. Res. 2020, 53, 1389–1400. [Google Scholar] [CrossRef]
  11. Dong, S.; Dong, Y.; Jia, T.; Liu, S.; Liu, J.; Yang, D.; Lin, J. GSH-depleted nanozymes with hyperthermia-enhanced dual enzyme-mimic activities for tumor nanocatalytic therapy. Adv. Mater. 2020, 32, 2002439. [Google Scholar] [CrossRef] [PubMed]
  12. Jangi, S.R.H. Low-temperature destructive hydrodechlorination of long-chain chlorinated paraffins to diesel and gasoline range hydrocarbons over a novel low-cost reusable ZSM-5@Al-MCM nanocatalyst: A new approach toward reuse instead of common mineralization. Chem. Pap. 2023, 77, 4963–4977. [Google Scholar] [CrossRef]
  13. Hormozijangi, S.R.; Akhond, M. High throughput green reduction of tris (p-nitrophenyl) amine at ambient temperature over homogenous AgNPs as H-transfer catalyst. J. Chem. Sci. 2020, 132, 1–8. [Google Scholar]
  14. Dehghani, Z.; Akhond, M.; Jangi, S.R.H.; Absalan, G. Highly sensitive enantioselective spectrofluorimetric determination of R-/S-mandelic acid using l-tryptophan-modified amino-functional silica-coated N-doped carbon dots as novel high-throughput chiral nanoprobes. Talanta 2024, 266, 124977. [Google Scholar]
  15. Jangi, S.R.H.; Gholamhosseinzadeh, E. Developing an ultra-reproducible and ultrasensitive label-free nanoassay for L-methionine quantification in biological samples toward application in homocystinuria diagnosis. Chem. Pap. 2023, 1–13. [Google Scholar] [CrossRef]
  16. Jangi, S.R.H.; Akhond, M. Ultrasensitive label-free enantioselective quantification of d-/l-leucine enantiomers with a novel detection mechanism using an ultra-small high-quantum yield N-doped CDs prepared by a novel highly fast solvent-free method. Sens. Actuators B Chem. 2021, 339, 129901. [Google Scholar]
  17. Thakkar, K.N.; Mhatre, S.S.; Parikh, R.Y. Biological synthesis of metallic nanoparticles. Nanomed. Nanotechnol. Biol. Med. 2010, 6, 257–262. [Google Scholar] [CrossRef]
  18. Hajipour, M.J.; Fromm, K.M.; Ashkarran, A.A.; de Aberasturi, D.J.; de Larramendi, I.R.; Rojo, T.; Serpooshan, V.; Parak, W.J.; Mahmoudi, M. Antibacterial properties of nanoparticles. Trends Biotechnol. 2012, 30, 499–511. [Google Scholar] [CrossRef]
  19. Jangi, S.R.H. Synthesis and characterization of magnesium-based metal-organic frameworks and investigating the effect of coordination solvent on their biocompatibility. 2023.
  20. Hormozi Jangi, S.R. Biochemical characterization of enzyme-like silver nanoparticles toward nanozyme-catalysed oxidation reactions. Micromater. Interfaces 2023, 1, 2170. [Google Scholar]
  21. Hormozi Jangi, S.R. Evaluation of Biochemical Behavior and Stability of Gold Nanoparticles with High Intrinsic Peroxidase-Like Activity. Petro. Chem. Indus. Intern. 2023, 6, 234–239. [Google Scholar]
  22. Jangi, S.R.H. Introducing a High Throughput Nanozymatic Method for Eco-Friendly Nanozyme-Mediated Degradation of Methylene Blue in Real Water Media. Sustain. Chem. Eng. 2023, 90–99. [Google Scholar] [CrossRef]
  23. Hormozi Jangi, S.R.; Dehghani, Z. Kinetics and biochemical characterization of silver nanozymes and investigating impact of storage conditions on their activity and shelf-life. Chem. Res. Nanomater. 2023, 1, 25–33. [Google Scholar]
  24. Jangi, S.R.H. Determining kinetics parameters of bovine serum albumin-protected gold nanozymes toward different substrates. Qeios 2023. [Google Scholar] [CrossRef]
  25. Jangi, S.R.H. Effect of daylight and air oxygen on nanozymatic activity of unmodified silver nanoparticles: Shelf-stability. Qeios 2023. [Google Scholar] [CrossRef]
  26. Ahmadi-Leilakouhi, B.; Jangi, S.R.H.; Khorshidi, A. Introducing a novel photo-induced nanozymatic method for high throughput reusable biodegradation of organic dyes. Chem. Pap. 2022, 77, 1033–1046. [Google Scholar] [CrossRef]
  27. Hormozi Jangi, S.R. A Comparative Study on Kinetics Performances of BSA-gold Nanozymes for Nanozyme-mediated Oxidation of 3,3',5,5'-Tetramethylbenzidine and 3,3'-Diaminobenzidine. Biochem. Mol. Biol. J. 2023, 9, 21. [Google Scholar]
  28. Jangi, S.R.H.; Akhond, M. High throughput urease immobilization onto a new metal-organic framework called nanosized electroactive quasi-coral-340 (NEQC-340) for water treatment and safe blood cleaning. Process. Biochem. 2021, 105, 79–90. [Google Scholar] [CrossRef]
  29. Jangi, S.R.H.; Akhond, M. Introducing a covalent thiol-based protected immobilized acetylcholinesterase with enhanced enzymatic performances for biosynthesis of esters. Process. Biochem. 2022, 120, 138–155. [Google Scholar] [CrossRef]
  30. Jangi, S.R.H.; Akhond, M.; Dehghani, Z. High throughput covalent immobilization process for improvement of shelf-life, operational cycles, relative activity in organic media and enzymatic kinetics of urease and its application for urea removal from water samples. Process. Biochem. 2019, 90, 102–112. [Google Scholar] [CrossRef]
  31. Wang, Q.; Wei, H.; Zhang, Z.; Wang, E.; Dong, S. Nanozyme: An emerging alternative to natural enzyme for biosensing and immunoassay. TrAC Trends Anal. Chem. 2018, 105, 218–224. [Google Scholar] [CrossRef]
  32. Lu, W.; Guo, Y.; Zhang, J.; Yue, Y.; Fan, L.; Li, F.; Dong, C.; Shuang, S. A High Catalytic Activity Nanozyme Based on Cobalt-Doped Carbon Dots for Biosensor and Anticancer Cell Effect. ACS Appl. Mater. Interfaces 2022, 14, 57206–57214. [Google Scholar] [CrossRef] [PubMed]
  33. Ren, X.; Chen, D.; Wang, Y.; Li, H.; Zhang, Y.; Chen, H.; Li, X.; Huo, M. Nanozymes-recent development and biomedical applications. J. Nanobiotechnol. 2022, 20, 1–18. [Google Scholar] [CrossRef]
  34. Tang, G.; He, J.; Liu, J.; Yan, X.; Fan, K. Nanozyme for tumor therapy: Surface modification matters. Exploration 2021, 1, 75–89. [Google Scholar] [CrossRef] [PubMed]
  35. Li, M.; Zhang, H.; Hou, Y.; Wang, X.; Xue, C.; Li, W.; Cai, K.; Zhao, Y.; Luo, Z. State-of-the-art iron-based nanozymes for biocatalytic tumor therapy. Nanoscale Horizons 2019, 5, 202–217. [Google Scholar] [CrossRef]
  36. Yu, R.; Wang, R.; Wang, Z.; Zhu, Q.; Dai, Z. Applications of DNA-nanozyme-based sensors. Anal. 2021, 146, 1127–1141. [Google Scholar] [CrossRef]
  37. Chang, Y.; Gao, S.; Liu, M.; Liu, J. Designing signal-on sensors by regulating nanozyme activity. Anal. Methods 2020, 12, 4708–4723. [Google Scholar] [CrossRef]
  38. Arshad, F.; Mohd-Naim, N.F.; Chandrawati, R.; Cozzolino, D.; Ahmed, M.U. Nanozyme-based sensors for detection of food biomarkers: A review. RSC Adv. 2022, 12, 26160–26175. [Google Scholar] [CrossRef]
  39. Jangi, A.R.H.; Jangi, M.R.H.; Jangi, S.R.H. Detection mechanism and classification of design principles of peroxidase mimic based colorimetric sensors: A brief overview. Chin. J. Chem. Eng. 2020, 28, 1492–1503. [Google Scholar] [CrossRef]
  40. Jangi, S.R.H.; Akhond, M.; Absalan, G. A novel selective and sensitive multinanozyme colorimetric method for glutathione detection by using an indamine polymer. Anal. Chim. Acta 2020, 1127, 1–8. [Google Scholar] [CrossRef]
  41. Jangi, S.R.H.; Davoudli, H.K.; Delshad, Y.; Jangi, M.R.H.; Jangi, A.R.H. A novel and reusable multinanozyme system for sensitive and selective quantification of hydrogen peroxide and highly efficient degradation of organic dye. Surf. Interfaces 2020, 21, 100771. [Google Scholar] [CrossRef]
  42. Xu, S.; Zhang, S.; Li, Y.; Liu, J. Facile Synthesis of Iron and Nitrogen Co-Doped Carbon Dot Nanozyme as Highly Efficient Peroxidase Mimics for Visualized Detection of Metabolites. Molecules 2023, 28, 6064. [Google Scholar] [CrossRef] [PubMed]
  43. Jangi, S.R.H.; Akhond, M. Synthesis and characterization of a novel metal-organic framework called nanosized electroactive quasi-coral-340 (NEQC-340) and its application for constructing a reusable nanozyme-based sensor for selective and sensitive glutathione quantification. Microchem. J. 2020, 158, 105328. [Google Scholar] [CrossRef]
  44. Ray, S.; Biswas, R.; Banerjee, R.; Biswas, P. A gold nanoparticle-intercalated mesoporous silica-based nanozyme for the selective colorimetric detection of dopamine. Nanoscale Adv. 2019, 2, 734–745. [Google Scholar] [CrossRef] [PubMed]
  45. Shen, Y.; Wei, Y.; Liu, Z.; Nie, C.; Ye, Y. Engineering of 2D artificial nanozyme-based blocking effect-triggered colorimetric sensor for onsite visual assay of residual tetracycline in milk. Microchim. Acta 2022, 189, 1–11. [Google Scholar] [CrossRef] [PubMed]
  46. Akhond, M.; Jangi, S.R.H.; Barzegar, S.; Absalan, G. Introducing a nanozyme-based sensor for selective and sensitive detection of mercury(II) using its inhibiting effect on production of an indamine polymer through a stable n-electron irreversible system. Chem. Pap. 2019, 74, 1321–1330. [Google Scholar] [CrossRef]
  47. Chen, J.; Wu, W.; Huang, L.; Ma, Q.; Dong, S. (2019). Self-indicative gold nanozyme for H2O2 and glucose sensing. Chem.–A Eur. J. 2019, 25, 11940–11944. [Google Scholar] [CrossRef]
  48. Jangi, S.R.H.; Dehghani, Z. Spectrophotometric quantification of hydrogen peroxide utilizing silver nanozyme. 2023.
  49. Jangi, S.R.H.; Akhond, M.; Absalan, G. A field-applicable colorimetric assay for notorious explosive triacetone triperoxide through nanozyme-catalyzed irreversible oxidation of 3, 3′-diaminobenzidine. Microchim. Acta 2020, 187, 1–10. [Google Scholar] [CrossRef]
  50. Singh, M.; Weerathunge, P.; Liyanage, P.D.; Mayes, E.; Ramanathan, R.; Bansal, V. Competitive Inhibition of the Enzyme-Mimic Activity of Gd-Based Nanorods toward Highly Specific Colorimetric Sensing of l-Cysteine. Langmuir 2017, 33, 10006–10015. [Google Scholar] [CrossRef]
  51. Wang, M.; Zhang, J.; Zhou, X.; Sun, H.; Su, X. Fluorescence sensing strategy for xanthine assay based on gold nanoclusters and nanozyme. Sensors Actuators B: Chem. 2022, 358, 131488. [Google Scholar] [CrossRef]
  52. Heo, N.S.; Song, H.P.; Lee, S.M.; Cho, H.-J.; Kim, H.J.; Huh, Y.S.; Kim, M.I. Rosette-shaped graphitic carbon nitride acts as a peroxidase mimic in a wide pH range for fluorescence-based determination of glucose with glucose oxidase. Microchim. Acta 2020, 187, 1–11. [Google Scholar] [CrossRef]
  53. Hormozi Jangi, S.R. A Brief Overview on Clinical and Epidemiological Features, Mechanism of Action, and Diagnosis of Novel Global Pandemic Infectious Disease, Covid-19, And its Comparison with Sars, Mers, And H1n1. World J. Clin. Med. Img. 2023, 2, 45–52. [Google Scholar]
  54. Jangi, S.R.H. Natural Polyphenols of Pomegranate and Black Tea Juices can Combat COVID-19 through their SARS-CoV-2 3C-like Protease-inhibitory Activity. Qeios. 2023. [Google Scholar]
  55. Liang, C.; Liu, B.; Li, J.; Lu, J.; Zhang, E.; Deng, Q.; Li, T. (2021). A nanoenzyme linked immunochromatographic sensor for rapid and quantitative detection of SARS-CoV-2 nucleocapsid protein in human blood. Sens. Actuators B Chem. 2021, 349, 130718. [Google Scholar] [CrossRef] [PubMed]
  56. Lu, Y.; Ye, W.; Yang, Q.; Yu, J.; Wang, Q.; Zhou, P.; Wang, C.; Xue, D.; Zhao, S. Three-dimensional hierarchical porous PtCu dendrites: A highly efficient peroxidase nanozyme for colorimetric detection of H2O2. Sens. Actuators B Chem. 2016, 230, 721–730. [Google Scholar] [CrossRef]
  57. Singh, S.; Tripathi, P.; Kumar, N.; Nara, S. Colorimetric sensing of malathion using palladium-gold bimetallic nanozyme. Biosens. Bioelectron. 2017, 92, 280–286. [Google Scholar] [CrossRef] [PubMed]
  58. Zhang, T.; Wang, L.; Gao, C.; Zhao, C.; Wang, Y.; Wang, J. Hemin immobilized into metal–organic frameworks as an electrochemical biosensor for 2, 4, 6-trichlorophenol. Nanotechnology 2018, 29, 074003. [Google Scholar] [CrossRef]
  59. Chen, Y.; Ni, D.; Yang, X.; Liu, C.; Yin, J.; Cai, K. Microwave-assisted synthesis of honeycomblike hierarchical spherical Zn-doped Ni-MOF as a high-performance battery-type supercapacitor electrode material. Electrochim. Acta 2018, 278, 114–123. [Google Scholar] [CrossRef]
  60. Yu, Y.; Yu, C.; Niu, Y.; Chen, J.; Zhao, Y.; Zhang, Y.; Gao, R.; He, J. Target triggered cleavage effect of DNAzyme: Relying on Pd-Pt alloys functionalized Fe-MOFs for amplified detection of Pb2+. Biosens. Bioelectron. 2018, 101, 297–303. [Google Scholar] [CrossRef]
  61. Li, Y.; Yu, C.; Yang, B.; Liu, Z.; Xia, P.; Wang, Q. Target-catalyzed hairpin assembly and metal-organic frameworks mediated nonenzymatic co-reaction for multiple signal amplification detection of miR-122 in human serum. Biosens. Bioelectron. 2018, 102, 307–315. [Google Scholar] [CrossRef]
  62. Lopa, N.S.; Rahman, M.; Ahmed, F.; Sutradhar, S.C.; Ryu, T.; Kim, W. A base-stable metal-organic framework for sensitive and non-enzymatic electrochemical detection of hydrogen peroxide. Electrochimica Acta 2018, 274, 49–56. [Google Scholar] [CrossRef]
  63. Wang, X.; Qin, L.; Zhou, M.; Lou, Z.; Wei, H. Nanozyme Sensor Arrays for Detecting Versatile Analytes from Small Molecules to Proteins and Cells. Anal. Chem. 2018, 90, 11696–11702. [Google Scholar] [CrossRef] [PubMed]
  64. Xue, T.; Sheng, Y.; Xu, J.; Li, Y.; Lu, X.; Zhu, Y.; Duan, X.; Wen, Y. In-situ reduction of Ag+ on black phosphorene and its NH2-MWCNT nanohybrid with high stability and dispersibility as nanozyme sensor for three ATP metabolites. Biosens. Bioelectron. 2019, 145, 111716. [Google Scholar] [CrossRef]
  65. Zhu, Y.; Wu, J.; Han, L.; Wang, X.; Li, W.; Guo, H.; Wei, H. Nanozyme Sensor Arrays Based on Heteroatom-Doped Graphene for Detecting Pesticides. Anal. Chem. 2020, 92, 7444–7452. [Google Scholar] [CrossRef]
  66. Lin, J.; Wang, Q.; Wang, X.; Zhu, Y.; Zhou, X.; Wei, H. Gold alloy-based nanozyme sensor arrays for biothiol detection. Anal. 2020, 145, 3916–3921. [Google Scholar] [CrossRef] [PubMed]
  67. Soltani, R.; Pelalak, R.; Pishnamazi, M.; Marjani, A.; Albadarin, A.B.; Sarkar, S.M.; Shirazian, S. Synthesis of multi-organo-functionalized fibrous silica KCC-1 for highly efficient adsorption of acid fuchsine and acid orange II from aqueous solution. Sci. Rep. 2021, 11, 1–13. [Google Scholar] [CrossRef] [PubMed]
  68. Butova, V.V.; Pankin, I.A.; Burachevskaya, O.A.; Vetlitsyna-Novikova, K.S.; Soldatov, A.V. New fast synthesis of MOF-801 for water and hydrogen storage: Modulator effect and recycling options. Inorganica Chim. Acta 2020, 514, 120025. [Google Scholar] [CrossRef]
  69. He, H.; Li, L.; Liu, Y.; Kassymova, M.; Li, D.; Zhang, L.; Jiang, H.-L. Rapid room-temperature synthesis of a porphyrinic MOF for encapsulating metal nanoparticles. Nano Res. 2020, 14, 444–449. [Google Scholar] [CrossRef]
  70. Kang, K.; Wang, B.; Ji, X.; Liu, Y.; Zhao, W.; Du, Y.; Guo, Z.; Ren, J. Hemin-doped metal–organic frameworks based nanozyme electrochemical sensor with high stability and sensitivity for dopamine detection. RSC Adv. 2021, 11, 2446–2452. [Google Scholar] [CrossRef]
  71. Hermosilla, E.; Seabra, A.B.; Lourenço, I.M.; Ferreira, F.F.; Tortella, G.; Rubilar, O. Highly sensitive oxidation of MBTH/DMAB by MnFe2O4 nanoparticles as a promising method for nanozyme-based sensor development. Colloids Surf. A Physicochem. Eng. Asp. 2021, 621. [Google Scholar] [CrossRef]
  72. Wu, L.; Wang, X.; Wu, X.; Xu, S.; Liu, M.; Cao, X.; Huang, H. MnO2 nanozyme-mediated CRISPR-Cas12a system for the detection of SARS-CoV-2. ACS Appl. Mater. Interfaces 2022, 14, 50534–50542. [Google Scholar] [CrossRef]
  73. He, M.; Xu, X.; Wang, H.; Wu, Q.; Zhang, L.; Zhou, D.; Liu, H. Nanozyme-Based Colorimetric SARS-CoV-2 Nucleic Acid Detection by Naked Eye. Small 2023, 19, 208167. [Google Scholar] [CrossRef] [PubMed]
  74. Chu, C.; Jiang, M.; Hui, Y.; Huang, Y.; Kong, W.; Zhu, W.; Ji, L. Colorimetric immunosensing using liposome encapsulated MnO2 nanozymes for SARS-CoV-2 antigen detection. Biosens. Bioelectron. 2023, 239, 115623. [Google Scholar] [CrossRef] [PubMed]
  75. Vafabakhsh, M.; Dadmehr, M.; Noureini, S.K.; Es' haghi, Z.; Malekkiani, M.; Hosseini, M. Colorimetric detection of COVID-19 using aptasenor based on biomimetic peroxidase like activity of ChF/ZnO/CNT nano-hybrid. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2023, 301, 122980. [Google Scholar] [CrossRef] [PubMed]
Preprints 84045 g001
Figure 1. Different applications of nanozymes in real world.
Figure 1. Different applications of nanozymes in real world.
Preprints 84045 g001
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