Phytoantioxidant Functionalized Nanoparticles: A Green Approach to Combat Nanoparticle-Induced Oxidative Stress

Nanotechnology is gaining significant attention, with numerous biomedical applications. Silver in wound dressings, copper oxide and silver in antibacterial preparations, and zinc oxide nanoparticles as a food and cosmetic ingredient are common examples. However, adverse effects of nanoparticles in humans and the environment from extended exposure at varied concentrations have yet to be established. One of the drawbacks of employing nanoparticles is their tendency to cause oxidative stress, a significant public health concern with life-threatening consequences. Cardiovascular, renal, and respiratory problems and diabetes are among the oxidative stress-related disorders. In this context, phytoantioxidant functionalized nanoparticles could be a novel and effective alternative. In addition to performing their intended function, they can protect against oxidative damage. This review was designed by searching through various websites, books, and articles found in PubMed, Science Direct, and Google Scholar. To begin with, oxidative stress, its related diseases, and the mechanistic basis of oxidative damage caused by nanoparticles are discussed. One of the main mechanisms of action of nanoparticles was unearthed to be oxidative stress, which limits their use in humans. Secondly, the role of phytoantioxidant functionalized nanoparticles in oxidative damage prevention is critically discussed. The parameters for the characterization of nanoparticles were also discussed. The majority of silver, gold, iron, zinc oxide, and copper nanoparticles produced utilizing various plant extracts were active free radical scavengers. This potential is linked to several surface fabricated phytoconstituents, such as flavonoids and phenols. These phytoantioxidant functionalized nanoparticles could be a better alternative to nanoparticles prepared by other existing approaches.

Despite significant advances in nanomedicine, the longterm implications of NP exposure on human health and the environment are unknown [35]. When NPs enter the environment, they affect water, soil, and the air, where they might persist for a longer duration or be gobbled up by living organisms. They may biodegrade or bioaccumulate in the food chain, posing a hazardous risk [36][37][38]. The membrane injury, inflammatory response, DNA damage, and apoptosis have all been harmful consequences of ZnO NPs in mammalian cells [39][40][41]. Although Ag NPs are highly toxic to cancer cells, their use is limited since they are also hazardous to normal cells [35]. In continuation, when the toxicity of Ag NPs (10 μg/mL) was investigated in human mesenchymal stem cells, DNA damage, impaired functioning, and cell death were observed [42]. Subsequently, ZnO NPs (300 mg/kg) caused oxidative stress in mice, which resulted in DNA damage [43]. Furthermore, intratracheal instillation of TiO 2 NPs in mice resulted in accumulation of ROS, lipid peroxidation, and decreased antioxidant capacity [44]. Metal-derived NPs (copper, iron, cadmium, and silver) produce reactive oxygen species (ROS), which causes oxidative stress, restricting their wide-ranging application [45][46][47][48][49][50].
Keeping in view the problem of nanoparticle-induced oxidative stress, in this review, we attempted to put some light on the antioxidant potential of phytoantioxidant functionalized NPs. Firstly, we have compiled a brief overview of oxidative stress-associated disorders and oxidative stressmediated toxicity of nanoparticles. Secondly, a brief overview of green synthesis using plant extracts and the protective role of phytoantioxidant functionalized NPs as a therapeutic for oxidative stress is highlighted along with its mechanistic approaches.

Search and Inclusion Criteria
Science Direct, PubMed, and Google Scholar databases have been searched in this review with various keywords like oxidative stress, its related disorders, reactive oxygen and nitrogen species, mechanism of action, the toxicity of nanoparticles, oxidative stress-induced toxicity of nanoparticles, green synthesis, and antioxidant activity of nanoparticles. The literature review took place between May 1, 2021, and July 2, 2021. This review only considered full-length, original, and Englishlanguage papers from Web of Science, Scopus-indexed, and peer-reviewed journals.
The protein phosphorylation, transcription factor activation, immunity, apoptosis, and differentiation are all reliant on adequate ROS production within cells, which must be maintained at a minimum level [84]. The ROS generation occurs mainly in the mitochondria, cell membranes, and cytoplasm. Even though these organelles have an inherent potential to scavenge ROS [85], it is noteworthy that this is insufficient to fulfill the cellular demand to eliminate the quantity of ROS generated by mitochondria [86].
The disparities between ROS and RNS generation and antioxidant defenses cause oxidative stress. Furthermore, when the formation of ROS rises, they begin to have adverse effects on essential cellular components (lipids, proteins, and nucleic acids) [77,78,[87][88][89]. A substantial body of evidence suggests that oxidative stress has a role in the genesis and overall progress of various diseases, including diabetes; metabolic disorders; atherosclerosis; neurological, cardiovascular, and respiratory disorders; and cancer [90][91][92]. In Figure 1, several disorders linked to oxidative stress are presented.
On the other hand, oxidative stress disrupts neuronal and cellular processes and has been related to several neurological illnesses, including amyotrophic lateral sclerosis, depression, amnesia, and Parkinson's and Alzheimer's disease [56,111,112]. The lipid membrane is one of the most impacted structures in the brain due to redox imbalance [113]. Moreover, due to higher glucose, insulin blood levels, fatty acids, and impaired glutathione synthesis, diabetes individuals have substantial ROS levels [114]. Increased production of ROS causes a mutation in an oncogene, leading to cancer [115]. ROS disrupt the Akt/PI3K/ERK cell signaling pathway, diminishing proapoptotic proteins while boosting antiapoptotic genes [116,117]. Subsequently, ROS has been linked to acute liver injury pathogenesis for a long time [118]. Similarly, multiple reports have shown that oxidative stress has a role in the etiology of inflammatory disorders like rheumatoid arthritis [119][120][121].

Oxidative Stress-Mediated
Toxicity of Nanoparticles Nanotechnology has found applications in a range of fields, including the environment, energy, food, and medicine. Nanoparticles are employed in biomedical applications because they have several advantages over bulk materials, including a higher surface-to-volume ratio, improved magnetic characteristics, thermal stability, and improved optical and mechanical properties. Despite the widespread use of NPs stated in Introduction, there is still a lack of ample knowledge about NP-mediated toxicity. However, there are reports that NPs induce toxicity via increasing intracellular ROS levels. Nanoparticle toxicity due to oxidative stress is well documented, restricting their usage in human patients. In this context, using carboxy-2 ′ ,7 ′ -dichlorofluorescein diacetate (H 2 DCFDDA) assay, the function of oxidative stress in the toxicity of iron oxide NPs against murine macrophage (J774) cells was examined. It was shown that exposing cells to a higher concentration of NPs (500 μg/mL) enhanced the generation of ROS, resulting in cellular damage and death [122]. Subsequently, when human microvascular endothelial cells were exposed to iron NPs, they showed an increase in permeability, ascribed to ROS generation. Furthermore, when cells are exposed to iron NPs, ROS is proven to be a significant factor in modulating Akt/GSK-3-mediated cell permeability [123].
Ahamed et al. [51] investigated the CuO NP-induced genotoxic reaction in human pulmonary epithelial cells (A549) via the p53 pathway. CuO NPs increased the cell cycle checkpoint protein p53 and the DNA damage repair proteins Rad51 and MSH2. In a dose-dependent manner, CuO NPs also triggered oxidative stress (10, 25, and 50 μg/mL), as evidenced by glutathione, CAT, and SOD depletion and the stimulation of lipid peroxidation. These findings show that CuO NPs exerted genotoxicity in A549 cells, which could be due to oxidative stress. Likewise, using the Alamar blue assay, the cytotoxicity of CuO, silicon oxide, and ferric oxide NPs against human laryngeal epithelial cells (HEp-2) was examined. CuO exhibited cytotoxicity; however, HEp-2 cells were unaffected by silicon oxide or ferric oxide even at high doses (400 μg/cm 2 ). CuO-induced oxidative stress was suggested by a considerable rise in amount of 8-isoprostanes and the ratio of oxidized glutathione to total glutathione [124]. In human liver cells (HepG2), the apoptotic and genotoxic capacity of ZnO NPs was investigated. Their cellular toxicity was also examined at the molecular level. HepG2 viability was reduced on exposure to ZnO NPs (14-20 μg/mL) for 12 h, and the cell death that occurred was apoptosis. They also triggered DNA damage, as demonstrated by an upsurge in formamidopyrimidine DNA glycosylase-(Fpg-) sensitive regions mediated by oxidative stress. ROS led to a decline in mitochondria membrane capacity and a rise in the Bax/Bcl2 ratio, resulting in a mitochondria-mediated apoptosis pathway [2].
Similarly, the impact of oxidative stress in the toxicity of ZnO NPs against human skin melanoma (A375) cells was studied. ZnO NPs were reported to cause oxidative stress, as evidenced by lipid peroxidation and the depletion of antioxidant enzymes. In cells exposed to the ZnO NPs, DNA damage was seen, which could be mediated by oxidative stress [125]. The occurrence of oxidative damage in lipids and proteins of MRC-5 human lung fibroblasts after exposure to Au NPs was investigated in vitro by Li et al. [126]. In addition, Au NP-treated cells produced considerably higher lipid hydroperoxides, indicating lipid peroxidation. Furthermore, oxidative damage was confirmed by verifying malondialdehyde (MDA) protein adducts using western blot study.
The impact of oxidative stress on the cytotoxic and genotoxic potential of Ag NPs was investigated against human lung fibroblasts (IMR-90) and the human glioma (U251) cell lines. The findings revealed mitochondrial malfunction and ROS generation by Ag NPs, which resulted in DNA damage and chromosomal abnormalities. The mitochondrial respiratory chain disruption by Ag NPs is thought to cause the generation of ROS and the cessation of ATP synthesis, which leads to DNA damage [35]. Chairuangkitti et al. [127] evaluated the in vitro mechanisms of Ag NP (<100 nm) toxicity in connection to the ROS generation in A549 cells. Surprisingly, both ROS-dependent (cytotoxicity) and ROS-independent (cell cycle arrest) mechanisms are involved in Ag NP toxicity in A549 cells. The oxidative stress-dependent activity of NPs is depicted in Figure 2.
Several investigations using various human cells have added to our understanding of the underlying mechanism of NPs concerning ROS production. To a large extent, ROS formation causes cytotoxicity, genotoxicity, and signaling and inflammatory response activation, revealing the mutagenic and carcinogenic properties of NPs [51,128,129]. Increased ROS production is highly linked to the size and shape of NPs [130,131]. However, because research reports vary, it is difficult to draw broad conclusions about shape and size.
In the event of NP exposure to cells, ROS generation is enhanced and leads to hyperoxidation of cell organelles, disruption of mitochondrial activity, endoplasmic reticulum (ER) stress, and unfolded protein response [129,[132][133][134][135][136][137]. Mitochondrial and ER stresses have cumulative effects on cell ROS production and apoptotic cell death, referred to as cytotoxicity [35,132]. Furthermore, NPs in the nucleus cause oxidative base damages (8-oxoguanine), strand breakage, and mutations in DNA, resulting in genotoxicity [138][139][140][141]. Furthermore, NPs can mediate oxidativesensitive activation of signaling cascades such as mitogenactivated protein kinase (MAPK), epidermal growth factor receptor, transcription factor activator protein-1, and nuclear factor-kappa B (NF-κB), as well as activate the inflammatory response, which plays a role in mammalian growth and proliferative and developmental processes [97,129,142]. Subsequently, when phagocytes, such as neutrophils and macrophages, fail to phagocytose NPs completely, the NADPH-oxidase enzyme system produces ROS. The stimulation of cell signaling pathways such as MAPK, NF-κB, Akt, and RTK by NP-induced ROS promotes an inflammatory cascade of chemokine and cytokine expression. The majority of the subsequent adverse effects elicited by NPs are due to ROS [129]. 4 Oxidative Medicine and Cellular Longevity For instance, Chen and Schluesener [143] demonstrated that, to the human primary organ system, silver is relatively nontoxic and nonmutagenic. In contrast to antimicrobial metallic NPs (Au, Pt, Cu, Zn, Ti, and so on), silver is recognized to have the most potent antibacterial activity. Ag NPs' powerful antibacterial, antifungal, and antiviral properties are related to their potential to produce H 2 O 2 , O 2 ⋅− , ⋅ OH, and hypochlorous acid (HOCl) singlet oxygen [20,[144][145][146][147]. Furthermore, free radicals induced by Ag NPs reduce glutathione to glutathione disulfide that leads to oxidative stress, apoptosis, and stimulation of oxidative signaling pathways [51,90,128,129,148].
The cytotoxicity, genotoxicity, and inflammatory response of Ag NPs in cells have raised concerns about their unintended human exposure [149]. Ag NPs' cytotoxic, genotoxic, apoptotic, and antiproliferative effects, on the other hand, can be employed to treat glioblastoma [150,151]. Dakal et al. [152] reported that Ag NP-induced ROS production and increased oxidative stress are linked to antimicrobial effects, with cytotoxic and genotoxic consequences. The most devastating and undeniable issue with using silver or any other nanoparticles in humans is their biosafety and biocompatibility.

Green Synthesis of NPs: A Brief Overview
Several methods for the synthesis of NPs have been developed, but their use in biomedical applications is limited due to the use of toxic compounds, the high energy requirements, and the formation of toxic by-products. The choice of a solvent medium, an environmentally friendly reducing agent, and a nontoxic substance for NP stabilization are all important components to consider during the NP preparation process [153]. In this context, green synthesis, which encompasses synthesis through plants, bacteria, fungi, algae, and others, is an effective way for generating NPs [64,154] as shown in Figure 3(a). The ability of numerous biological entities, such as those indicated above, to generate metal nanoparticles for diverse pharmacological applications has been extensively researched. In general, plant extracts and microorganisms are used in the green, environmentally acceptable synthesis of NPs [65,66].
Plant-derived NPs overwhelm microorganism-derived NPs, owing to the former's single-step, nonhazardous fabricating process [72]. Furthermore, phyto-mediated synthesis is preferable to microbial synthesis, which requires timeconsuming and expensive downstream processing [71]. The plant extract is combined with a metal salt solution in the green synthesis of metal nanoparticles. The electrochemical potential of a metal ion and the pH of the reaction mixture, temperature, concentration, and reaction time are all critical aspects to consider. The phytoconstituents promote metal ion reduction to zero-valent state, followed by nucleation and growth to generate metal NPs [72,154,155] as depicted in Figure 3(b).
The plant-mediated synthesis is attributed to protein, phenols, terpenoids, ascorbic acid, and flavonoids that are capable of reducing the ions to nanosize and capping of nanoparticles [156,157]. This method has several advantages, including energy savings due to the lack of high energy and pressure, use of biological entities that work as both reducing and stabilizing agents, environmental friendliness, lower costs, and the capacity to be employed on a large scale [64,68,69,154]. Several NPs such as TiO 2 using Azadirachta indica [9],

Antioxidant Potential of Phytoantioxidant Functionalized Nanoparticles
Green synthesis is an innovative method of synthesizing phytoantioxidant functionalized NPs using plant extracts. It is gaining popularity as a result of its cost-effective, environmentally friendly, and large-scale production capabilities.
As the importance of green synthesis using plant extracts is already highlighted in Section 5, in ), respectively; this demonstrated its role in the prevention of oxidative stress, which is a significant factor in the progression of a variety of diseases. The action of DBTE is believed to be due to its substantial ascorbic acid content [162].
The aqueous fruit extract of Couroupita guianensis (CG), a promising bioreductant for reducing Au 3+ ions into their nanoscale analogs, was used to produce gold nanoparticles (Au NPs) in a smaller duration of time. Au NPs have exceptional antioxidant characteristics; DPPH radical scavenging at 100 μg/mL was 70.6%, compared to 96.28% for ascorbic acid. Further, they showed dose-dependent ferric ion  Oxidative Medicine and Cellular Longevity    9 Oxidative Medicine and Cellular Longevity reduction activity and hydroxyl ( ⋅ OH) radical scavenging ability, which is primarily due to the presence of antioxidant residues, such as phenolics from the CG on its surface, which have been recognized, using various analytical techniques [67]. Subsequently, Au NPs were synthesized using Rhus coriaria, which is used as a reducing and capping agent. The plant polyphenols may play a role in reducing gold ions, as evident from FT-IR analysis. In vitro, antioxidant activity studies showed that DPPH (85.73% at 800 μM) and ABTS activities (96.83% at 800 μM) increased in a dose-dependent manner (25-800 μM) which is related to the adsorption of phytocompounds on the surface of the Au NPs [163].
Hippophae rhamnoides leaves were utilized by Kalaiyarasan et al. [164] for the biosynthesis of silver NPs (Ag NPs). As the sample concentrations (5-25 μg/mL) began to rise, the DPPH radical scavenging abilities increased, indicating that the antioxidant capabilities of the samples are dosage-dependent. The activity of Ag NPs has enhanced by more than tenfold when compared to that of the plant extract alone, which can be attributable to the presence of plant phytochemicals, including flavonoids. Due to these flavonoids and silver ions, antioxidant activity may occur via a single electron transfer mode [186,187]. Similarly, Ag NPs developed using Costus after leaves were more effective DPPH scavengers than the leaf extract alone, and their antioxidant activity was comparable to those of ascorbic acid with IC 50 value < 50 μg/mL [165]. Ag NPs fabricated using Taraxacum officinale leaves demonstrated substantial antioxidant capability against ABTS (IC 50 45.6 μg/mL), DPPH (IC 50 56.1 μg/mL), and NO (IC 50 55.2 μg/mL). Catechol and ascorbic acid were utilized as controls, with IC 50 40 to 60 μg/mL [166]. Ag NPs synthesized using Erythrina suberosa leaves demonstrated significant antioxidant activity in a DPPH radical scavenging experiment, with IC 50 30.04 μg/mL. The BHT was used as a standard. The findings significantly support the use of Ag NPs as natural antioxidants against oxidative stress-linked degenerative disorders [167].
Ag NPs synthesized using Cestrum nocturnum leaves, when evaluated for antioxidant activity, were found more active scavengers of DPPH (29.55% at 100 μg/mL) as compared to ascorbic acid at a similar concentration (24.28%). Further, Ag NPs showed 45.41 and 20% scavenging of H 2 O 2 and ⋅ OH as compared to ascorbic acid (65.63 and 9.47% at 250 μg/mL, respectively). However, negligible activity was reported in the O 2 ⋅− scavenging assay [168]. Subsequently, DPPH, H 2 O 2 , and FRAP assays were used to estimate the antioxidant activity of Ag NPs prepared using Cassia angustifolia flowers. Ag NPs were found to have FRAP and DPPH IC 50 values of 63:21 ± 0:75 and 47:24 ± 0:5 μg/mL, respectively. On the other hand, in the H 2 O 2 assay, the IC 50 value was 78:10 ± 1:2 μg/mL [169]. The H 2 O 2 scavenging is well related to the presence of phenolic components in the samples [188]. A compound mixture containing Camellia sinensis leaves, Allium sativum bulbs, and Curcuma longa rhizome mediated Ag NPs which were found highly active scavengers of ABTS, DPPH, ⋅ OH, O 2 ⋅− , and H 2 O 2 radicals with IC 50 ranging between 5:02 ± 1:11 and 22:93 ± 0:34 μg/mL in comparison to rutoside and ascorbic acid (IC 50 between 7:14 ± 1:02 and 14:17 ± 0:24 μg/mL) [170]. Interestingly, Ag NPs synthesized using a spice blend exhibited IC 50 < 31:25 and 68.75 μg/mL against DPPH and ABTS, respectively, and the findings are comparable to standard rutoside. The different functional groups of spice blends present on the surface of Ag NPs could be responsible for the activity [171]. Psidium guajava leaves were utilized by Wang et al. [172] for the successful synthesis of Ag NPs, which were found to be highly active in scavenging free radicals with IC 50 52:53 ± 0:31 μg/mL (DPPH) and 55:10 ± 0:29 μg/mL (ABTS). In contrast, standard ascorbic acid showed IC 50 < 40 μg/mL against both DPPH and ABTS radicals. On the other hand, Berberis aristata leaf-mediated ZnO NPs, when evaluated for antioxidant activity using DPPH, showed 61.63% scavenging at 5 μg/mL, lower than ascorbic acid (87.76%) at the same concentration [173]. On the other hand, Ag NPs synthesized using Ananas comosus fruit peel exhibited a moderate ABTS and DPPH and reduced power and nitric oxide (NO) scavenging activity as compared to standard BHT [174]. The action is due to the involvement of numerous plant functional groups attached to the surface of Ag NPs [189].
The antioxidant activity of Ag NPs fabricated using Prosopis farcta (PF) fruits was evaluated using DPPH and FRAP assay. Ag NPs had a scavenging activity of 43 to 63% at doses of 0.2-1 mg/mL; however, the effect was lower (74% at 1 mg/mL) than that of standard ascorbic acid. Ag NPs were also found active with FRAP activity > 25 mmol Fe(II)/mg extract at 1 mg/mL [175]. The primary phytochemicals responsible for the antioxidant capacity are phenolics and flavonoids, abundant in PF [190]. Subsequently, Vitex negundo leaf-mediated Au NPs exhibited IC 50 values of 62.18 and 70.45 μg/mL in DPPH and nitric oxide assays, respectively [176]. Moreover, Morus alba leaves were utilized by Das et al. [177] for synthesizing Ag NPs. When compared to ascorbic acid (10-50 μg/mL), antioxidant activity of produced NPs against DPPH, ABTS, superoxide, and nitric oxide was dose-dependent with IC 50 ranging between 25.9 and 97.2 μg/mL. The lowest IC 50 (25.9 μg/mL) of Ag NPs was observed in the ABTS assay.
The DPPH radical scavenging activity of Lavandula stoechas aerial part-mediated Ag NPs (75% scavenging at 25 mg/mL) is attributed to phytochemical compounds such as phenol and terpenoid flavonoids that are involved in the reduction of Ag + to Ag 0 [178]. Nothapodytes foetida leafmediated Ag NPs (100 μg/mL) exhibited strong antioxidant potential with 93.80% inhibition of DPPH and comparatively lower ABTS radical scavenging activity (84.59% at the same conc.); however, results are comparable to standard BHT [179].
Likewise, Ansar et al. [180] utilized Brassica oleracea leaves for Ag NP synthesis. Ag NPs revealed a strong antioxidant potential against DPPH, NO, superoxide (O 2 ⋅− ), and hydroxyl radical ( ⋅ OH) with percent scavenging ranged between 60 and 80% at 200 μg/mL as compared to standard ascorbic acid (>80% at 200 μg/mL). The antioxidant capacity of these nanoparticles could be attributed to the abundance of surface fabricated flavonoids and phenolics as capping agents [180]. In another study, Akintola et al. [181] 10 Oxidative  The frequency of methodologies utilized for characterization of NPs, their significance, methods used for assessing antioxidant activity, plant parts used in green synthesis, and choice of NPs were all examined critically. The most commonly used strategy for antioxidant investigations was observed to be DPPH, followed by ABTS, superoxide, nitric oxide, and others. Surprisingly, all of the free radicals were successfully scavenged by the tested NPs. On the other hand, almost all plant parts have been used, but leaves are primarily harvested to synthesize NPs ( Figure 4 and Table 1). Ag NPs are frequently employed in practice due to their inclusion in various formulations; the majority of researchers are currently focusing on these NPs, with silver topping the list of studies, followed by gold, copper, iron, and zinc oxide NPs.
The most common approach for measuring surface plasmon resonance and investigating the optical characteristics of produced NPs is UV-visible absorption spectroscopy, followed by FT-IR analysis to identify functional groups corresponding to surface-attached bioactive compounds responsible for reduction and stabilization. In 14, 21, and 18 investigations included in this study (N = 26), the shape and size of produced NPs were analyzed using scanning electron microscopy, transmission electron microscopy, and X-ray diffraction analysis. Dynamic light scattering analysis was also used to determine hydrodynamic size and surface charge. Zeta potential measurements were carried out to assess NP stability; a relatively high zeta potential value shows that the surface has a substantial electric charge, demonstrating its stability. The thermal stability of NPs was evaluated using thermal gravimetric analysis (TGA) in a single study (Figure 4 and Table 1). Furthermore, elemental analysis was carried out using energy-dispersive X-ray analysis (EDX), which is used to detect impurities [67,163,166,169,177,182,183].

Mechanistic Basis of Oxidative Stress Management by Phytoantioxidant Functionalized NPs
Antioxidant defenses mitigate the detrimental effects of ROS and RNS, which are generated by a variety of endogenous and external mechanisms [88]. NADPH oxidase, lipoxygenase, angiotensin II, and myeloperoxidase (MPO) are all endogenous producers of ROS and RNS [191]. NADPH oxidase produces superoxide radical (O 2 ⋅− ), which in turn is dissociated into the H 2 O 2 by SOD [192]. Glutathione peroxidase (GPx), SOD, and CAT aid in the breakdown of free radicals into safe and less active molecules (H 2 O 2 /alcohol, and O 2 ) [2,[193][194][195][196][197][198]. The phytoconstituents upregulate the level of antioxidant enzymes, and SOD is a significant force in radical neutralization [198]. As previously stated, SOD converts O 2 ⋅− to H 2 O 2 , which is then degraded by CAT and GPx into water and oxygen, preventing the formation of ⋅ OH [199,200]. Glutathione-S-transferase and

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Oxidative Medicine and Cellular Longevity glucose-6-phosphate dehydrogenase are two other antioxidant enzymes [200]. The inhibition of ⋅ OH generation contributed to lipid radical (LR * ) inhibition, which is generated due to the interplay between ⋅ OH and lipid membrane [198,199]. GPx inhibits the peroxynitrite anion produced by numerous interactions, such as when combined with carbon dioxide to make nitrosoperoxycarbonate, which disintegrates over time to form nitrogen dioxide and carbonate radicals [198,201].
On the other hand, nonenzymatic antioxidants interact with ROS and RNS to stop the free radical chain. In continuation, blood contains α-tocopherol, bilirubin, and β-carotene whereas albumin and uric acid make about 85% of antioxidant defense in plasma [89]. The phytoconstituents on nanoparticle surfaces reduce oxidative stress [72]. In Figure 5, a mechanistic approach to the protective impact of phytoantioxidant functionalized nanoparticles in the regulation of oxidative stress is highlighted.
The abundance of terpenoids, ascorbic acid, flavonoids, phenols, and other bioactive phytoconstituents on the surface of NPs is strongly correlated with their antioxidant activity [178,180]. The phytoantioxidant functionalized nanoparticles would upregulate the antioxidant enzymes, and nonenzymatic components such as ascorbic acid on the surface of these NPs would also neutralize the adverse effects of free radicals.

Conclusion and Perspectives
In conclusion, the evidence of oxidative stress caused by nanoparticle exposure raises concerns about their use in humans. Although the antioxidant potential of phytoantioxidant functionalized NPs is well documented, the majority of the researches have been conducted in vitro. The bioactive substances like flavonoids and phenols are correlated to the antioxidant action of these NPs. The stability of nanoparticles is an important aspect, but only three articles have investigated the storage stability of these NPs. Most studies lack a zeta potential measurement, which is an indicator of stability. The data compiled in this review is expected to serve as a roadmap for researchers to fulfill various gaps. Because of their widespread use in a variety of industries, Ag NPs are the most investigated NPs. It is suggested that the plant utilized for green synthesis should be selected carefully, as antioxidant action is linked to phytoconstituents. As an alternative to NPs, phytoantioxidant functionalized NPs could be employed; however, high-quality toxicity studies are necessary. Nanotechnology is rapidly expanding, but research into the nanoparticles' toxicological impacts on human health and the environment is still in its early stages.

Data Availability
All data are included in the manuscript.

Conflicts of Interest
The authors declare no conflict of interest.

Authors' Contributions
A.B. supervised the first draft. A.K. and V.A. wrote the first draft of the manuscript. A.R. and A.K. contributed in figures and in providing literature. R.V., D.K., N.T., E.N., O.K., and K.K. critically reviewed the first draft. A.K. and V.A. improved the first draft. The final submitted version of the manuscript has been seen and approved by all contributors.