Determination of Antioxidant, Anti-Alzheimer, Antidiabetic, Antiglaucoma and Antimicrobial Effects of Zivzik Pomegranate (Punica granatum)—A Chemical Profiling by LC-MS/MS

Zivzik pomegranate (Punica granatum) has recently sparked considerable interest due to its nutritional and antioxidant properties. To evaluate the antioxidant capacities of P. granatum juice, ethanol (EEZP), and water (WEZP) extracts from peel and seed, the antioxidant methods of 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid radical (ABTS•+) scavenging, 1,1-diphenyl-2-picrylhydrazyl free radical (DPPH•) scavenging, Fe3+-2,4,6-tris(2-pyridyl)-S-triazine (TPTZ) reducing, Fe3+ reducing, and Cu2+ reducing methods were used. The antioxidant capacities of samples were compared with the most commonly used synthetic antioxidants, i.e., BHA, BHT, α-tocopherol, and Trolox. In terms of setting an example, the IC50 values of EEZP for ABTS•+ and DPPH• scavenging activities were found to be lower than standards, at 5.9 and 16.1 μg/mL, respectively. The phenolic and flavonoid contents in EEZP peel were 59.7 mg GAE/g and 88.0 mg QE/g, respectively. Inhibition of α-glycosidase, α-amylase, acetylcholinesterase, and human carbonic anhydrase II (hCA II) enzymes was also investigated. EEZP demonstrated IC50 values of 7.3 μg/mL against α-glycosidase, 317.7 μg/mL against α-amylase, 19.7 μg/mL against acetylcholinesterase (AChE), and 106.3 μg/mL against CA II enzymes. A total of 53 phenolic compounds were scanned, and 30 compounds were determined using LC-MS/MS. E. coli and S. aureus bacteria were resistant to all four antibiotics used as standards in hospitals.


Introduction
Pomegranate (Punica granatum L.) is an antiquity fruit that is primarily grown in western Asia, although it is also grown in other parts of the world, including the Mediterranean region. Its utilization has been linked to a variety of health advantages since ancient times [1,2]. Pomegranates are members of the Punicaceae family and have distinctive characteristics. Unsaturated-polyunsaturated fatty acids, vitamins, sugar, polysaccharides, polyphenols, and minerals can all be found in pomegranate seeds. Pomegranate seed oil in particular contains significant amounts of phenolic compounds, fatty acids, linoleic acid, gallic acid, and ellagic acid [3]. Pomegranate is one of the fruits that contain significant amounts of bioactive phenolic compounds, which are frequently used as botanical components in dietary supplements and herbal medicines [4]. Anthocyanins, anthocynidins, proanthocyanidins, flavonoids, vitamins, sterols, lignans, saccharides, fatty acids, organic acids, terpenes, and terpenoids are just a few of the bioactive components of pomegranates P. granatum peel and seeds that had been ground in a mill. This mixture was boiled for 20 min in a magnetic stirrer. The filtrates of the extracts were frozen and lyophilized in a lyophilizator at −50 • C under a pressure of 5 mmHg (Labconco, Freezone).
For ethanol extracts of P. granatum (WEZP), 25 g of dried P. granatum peel and seeds were milled before being combined with 100 mL of ethanol and stirred in a magnetic stirrer for 1 h. Filtrates were collected after the extracts had been filtered. A rotary evaporator (RE 100 Bibby, Stone Staffordshire, England) operating at 50 • C was used to remove the ethanol. Before being used in experimental studies, all of the extracts were kept in a dark plastic bottle at a temperature of 20 • C [37]. The yield of P. granatum extraction was calculated using the following equation: Yield = Weight of P. granatum extract (g)/weight of raw extract (g) ×100% The yield of P. granatum extracts were calculated as follows: WEZP peel = 9.4/15 × 100 = 62.7%; WEZP seed = 8.6/15 × 100 = 57.3%; EEZP peel = 4/15 × 100 = 26.7%; EEZP seed = 2.92/15 × 100 = 19.5%. In order to obtain P. granatum juice, first, P. granatum were peeled, and pomegranate seeds were obtained. Then, P. granatum juice was obtained by pressing the P. granatum arils through a cheesecloth.

Total Phenolic Contents
The method described by Singleton and Rossi [38] was used to quantify the phenolics in the WEZP and EEZP peel and seed and P. granatum juice with a few minor modifications [39,40]. First 0.5 mL of each extracted sample was transferred to Folin-Ciocalteu reagent (FCR, 1.0 mL). The solution was then thoroughly blended and neutralized with carbonate (0.5 mL, 1%). After two hours of incubation in the dark at room temperature, the absorbances were measured at 760 nm in comparison to a blank sample, which included water. The phenolic content was expressed as milligrams of gallic acid equivalents (GAE) per gram of WEZP, EEZP, and P. granatum juice. The standard curve of gallic acid for total phenolic contents (r 2 : 0.9408) is presented in Figure 1.

Total Flavonoid Contents
A class of polyphenolic substances known as flavonoids is widely distributed in plants and frequently found in the human diet. Based on a previously described method [41], a colorimetric assay was used to estimate the total flavonoid contents in WEZP,

Total Flavonoid Contents
A class of polyphenolic substances known as flavonoids is widely distributed in plants and frequently found in the human diet. Based on a previously described method [41], a colorimetric assay was used to estimate the total flavonoid contents in WEZP, EEZP, and P. granatum juice. To this end, 0.5 mL of sample was combined with 1.5 mL of 95% methanol. Then, 0.5 mL CH 3 COOK (1.0 M) and 2.3 mL of deionized water were combined with 1.5 mL of 10% Al(NO 3 ), and the samples were vortexed. Then, the vortexed samples were kept at 25 • C for 40 min in the dark. Absorbance measurements were taken at a wavelength of 415 nm. Quercetin equivalents (QE) are reported as mg per gram of extract in this study. The standard curve of total flavonoid contents is obtained from Figure 2.

Sample preparation
First, 100 mg of each WEZP and EEZP was dissolved in 5 mL of water-ethanol (50:50 v/v) in a volumetric flask, and 1 mL of this solution was added to another volumetric flask with a capacity of 5 mL. Then, 100 μL of P. granatum extracts were added and diluted to the volume with water-ethanol (50:50 v/v). An aliquot of 1.5 mL from the final solution was transferred into a vial with a cap, and 10 μL of the sample was injected into the LC-MS/MS. Throughout the experiment, the samples in the autosampler were kept at 15 °C [42].

Method Validation Parameters and LC-MS/MS Analysis
The analytical approach utilized in this investigation was in accordance with the latest studies. The LC-MS/MS study was carried out by the Dicle University Central Research Laboratory. This chromatographic method was successfully carried out by Yılmaz [43] and adapted for P. granatum ethanol extracts. A total of 53 phytochemical standards were obtained as reference from Sigma-Aldrich (Steinheim, Germany). They were used to ana- First, 100 mg of each WEZP and EEZP was dissolved in 5 mL of water-ethanol (50:50 v/v) in a volumetric flask, and 1 mL of this solution was added to another volumetric flask with a capacity of 5 mL. Then, 100 µL of P. granatum extracts were added and diluted to the volume with water-ethanol (50:50 v/v). An aliquot of 1.5 mL from the final solution was transferred into a vial with a cap, and 10 µL of the sample was injected into the LC-MS/MS. Throughout the experiment, the samples in the autosampler were kept at 15 • C [42].

Method Validation Parameters and LC-MS/MS Analysis
The analytical approach utilized in this investigation was in accordance with the latest studies. The LC-MS/MS study was carried out by the Dicle University Central Research Laboratory. This chromatographic method was successfully carried out by Yılmaz [43] and adapted for P. granatum ethanol extracts. A total of 53 phytochemical standards were Life 2023, 13, 735 6 of 27 obtained as reference from Sigma-Aldrich (Steinheim, Germany). They were used to analyze phytochemicals in EEZP and WEZP.

Fe 3+ Reducing Capacity
The Fe 3+ reducing capacities of P. granatum, EEZP, WEZP, and P. granatum juice were assessed on the basis of the method proposed by Oyaizu [44], as also previously described in [45]. In a summary, various concentrations of samples in 0.75 mL of distilled water (10-30 µg/mL) were added into the same volume of buffer solution (1.25 mL, pH 6.6; 0.2 M) and 1.25 mL of K 3 Fe(CN) 6 (1%, w/w). Trichloroacetic acid (TCA) (1.25 mL, 10%) was used to acidify the mixture after it has been incubated at 50 • C for 30 min. The absorbances of the fruit extracts were recorded at 700 nm after an aliquot of 0.1%, 0.25 mL, and FeCl 3 solution had been added to the mixture. Phosphate buffer solution was used as a blank sample. Activity measurements for the Fe 3+ reducing ability at each concentration were conducted in triplicate.

Cu 2+ Reducing Capacity
The Cu 2+ reducing abilities of EEZP, WEZP, and P. granatum juice were measured according to the method used by Apak et al. [46], which was thoroughly described in [47], To this end, the same volumes of 0.25 mL of CuCl 2 solution (10 mM), 0.25 mL of neocuproine solution (7.5 mM), and 0.25 mL of acetate buffer (1.0 M) were added to the EEZP and WEZP solutions (10-30 µg/mL) in a test tube. The total volumes of mixtures were adjusted to 2 mL with distilled water and vigorously mixed. Then, the glass tubes were closed and retained at 25 • C until use in experiments. Finally, after 30 min, the absorbances were spectrophotometrically recorded at 450 nm. Acetate buffer solution was used as a blank sample. Increased reaction mixture absorbance suggests increased reduction capacity. Activity measurements for Cu 2+ reducing ability at each concentration conducted in triplicate [48].

DPPH • Scavenging Activity
The bleaching of a purple DPPH solution in methanol allows for the presence of certain pure antioxidant compounds with hydrogen-atom-or electron-donating properties to be determined. Stable DPPH • is the reagent used in this spectrophotometric assay [51]. The method described by Blois [52], as previously applied by Gulcin [53], was used with minor modification to estimate the DPPH • free radical scavenging capacity of EEZP, WEZP, and P. granatum juice; a stable free radical called DPPH was monitored for bleaching at a specific wavelength while the sample was present. The DPPH • solution was prepared daily. Aluminum foil was used to cover the solution flask, which was stirred for 16 h at 4 • C while being kept in the dark. Shortly after preparing a 0.1 mM DPPH • solution in ethanol, 0.5 mL of this solution was combined with 2 mL of EEZP, WEZP, and P. granatum juice at various concentrations (10-30 g/mL). After being vortexed, the samples were incubated at 30 • C in the dark for 30 min. Absorbance was measured at 517 nm in comparison to blank samples. The scavenging of DPPH free radicals is indicated by a decrease in absorbance [54]. When DPPH is reduced by an antioxidant or another radical species, its absorption falls below that of the radical form, which absorbs at 517 nm. The absorbance at 517 nm decreased proportionately to an increase in DPPH's non-radical forms when a hydrogen atom or electron was transferred to the odd electron [55]. Absorbance decreases indicate that DPPH is actively scavenging free radicals. Activity measurements for DPPH radical scavenging activity at each concentration were conducted in triplicate [56].

ABTS •+ Scavenging Activity
A relatively stable free radical, ABTS, also decolorizes in its non-radical state. The method of Re et al. [57] was used to determine ABTS •+ scavenging activity. This technique involves adding an antioxidant to a prepared ABTS radical solution, and after a set amount of time, the remaining ABTS •+ is measured spectrophotometrically at 734 nm [58]. Then, 2 mM ABTS in water was combined with 2.45 mM potassium persulfate (K 2 S 2 O 8 ) to create ABTS •+ , which was then left to sit for 6 h at room temperature in the dark. The ABTS started to oxidize right away, but it took over 6 h for the absorbance to reach its peak and stabilize. Under storage conditions at room temperature in the dark, the radical cation is stable in this form for longer than two days. In order to perform the assay, the solution was diluted in phosphate buffer (pH 7.4), providing an absorbance of 0.700 ± 0.025 at 734 nm and equilibrated to 30 • C, the temperature at which all assays were carried out. Then, 3 mL of EEZP, WEZP, and P. granatum juice in ethanol at 10-30 µg/mL were combined with 1 mL of the ABTS •+ solution. After mixing for 30 min, the absorbance was measured, and the radical scavenging percentage was computed for each concentration in comparison to a blank containing no scavenger. The percentage reduction in absorbance was used to determine the degree of decolorization. Activity measurements for ABTS radical scavenging activity at each concentration were conducted in triplicate [59].

α-Glycosidase Inhibition Study
The inhibitory abilities of the WEZP, EEZP, and P. granatum juice on α-glycosidase were determined based on the method of Tao et al. [63], as described in detail in [64]. Various amounts of WEZP, EEZP, and P. granatum juice were transferred to phosphate buffer (75 µL, pH 7.4) for this purpose. Then, 20 µL of α-glycosidase solution was transferred to the same buffer and incubated for 10 min. The final mixture was mixed with 50 µL of p-nitrophenyl-D-glycopyranoside (p-NPG) dissolved in the same buffer. The mixture was then incubated again at room temperature (37 • C), and the absorbances were measured at 405 nm against a blank sample made up of phosphate buffer.

α-Amylase Inhibition Study
The inhibitory effects of WEZP, EEZP, and P. granatum juice on α-amylase were measured according to Xiao et al [65]. Briefly, 40 mL of 0.4 M alkaline solution was used to dissolve 1 g of starch, which was then heated for 30 min at 80 • C. The pH of the mixture was adjusted to 6.9, and the total volume was adjusted to 100 mL with deionized water. Then, different amounts of WEZP, EEZP, and P. granatum juice and 35 µL of starch prepared in buffer solution (pH 6.9) were mixed. Then, 20 µL of enzyme was added to the mixture and incubated at 40 • C for 60 min. Finally, 50 µL of HCl (0.1 M) was added to the mixture, and the reaction was stopped. The absorbance of samples was measured at 580 nm. The blank sample contained buffer solution (pH 6.9). The sepharose-4B-L-tyrosine sulfanilamide affinity technique was used to separate and purify CA II isoenzymes using human blood samples, as previously reported [66]. The protein levels were determined at 595 nm using the Bradford method after the enzymes had been purified [67]. The spectrophotometric Verpoorte's method (Shimadzu, UVmini-1240 UV-VIS) was used to perform CA activity [68]. Acetazolamide (AZA) was utilized as a reference standard [69]. Microorganisms that can be potentially harmful to humans were used in this study. Gram-positive bacteria (S. aureus ATCC 25923) and Gram-negative bacteria (E. coli clinical isolate) were used for the assessment of antibacterial activity [70]. Bacterial strains were derived from stock cultures (clinical isolates and standard strains) of Kahramanmaras Sutcuİmam University Faculty of Medicine, Department of Medical Microbiology, Microbiology Laboratory.

Identification of E. coli Clinical Isolates
The identification of E. coli clinical isolates was realized according to the method of Deniz et al. [71]. Pathogen bacterial isolations from various clinical samples collected from patients and delivered to the laboratory under sterile conditions were inoculated on blood agar and EMB agar, and the media were incubated at 37 • C for 48 h. Colonies of E. coli bacteria grown in culture media were identified as species by Gram staining, biochemical tests, and the BD Phoenix 100 identification system.

Antimicrobial Activity Determination
The antimicrobial activity of the WEZP, EEZP, and P. granatum juice was determined by a disk diffusion method [72]. The test microorganism agar cultures were prepared in accordance with the procedure described by Gulcin et al. [73]. Bacterial strains were grown on blood agar medium (Oxoid CM55, Basingstoke, Hampshire, UK). In the study, pathogens to be evaluated were inoculated into Tryptone soy broth (Oxoid CM129, Basingstoke, Hampshire, UK). Facultative anaerobes and aerobes, including some fungi, were cultivated using tryptone soy broth, a highly nutritive and versatile medium that is recommended for general laboratory use. Prepared cultures were incubated for 24 h at 37 • C. For the antimicrobial test, 50 µL of WEZP, EEZP, and P. granatum juice was added to sterile 6 mm diameter filter paper discs, and susceptibility measurements were conducted on Mueller Hinton agar (Oxoid CM337, Basingstoke, Hampshire, UK) medium with the diffusion technique prescribed in Clinical and Laboratory Standards (CLSI 2018).
The growth inhibition zones around the discs containing antibiotics and WEZP, EEZP, and P. granatum juice were measured and recorded. The presence of antimicrobial activity was shown by clear zones of inhibition surrounding the discs [74]. Plant extracts, amoxicillin-clavulanic acid (20/10 µg/disc), gentamicin (10 µg/disc), ampicillin-sulbactam (10/10 µg/disc), and ciprofloxacin (5 µg/disc, BD BBL™ Sensi-Disc™) were compared with standard antimicrobial discs. Antimicrobial test results were analyzed according to the references suggested by the Clinical and Laboratory Standards [75].

Statistical Analysis
All experiments are repeated three times for each sample. The results are reported as the mean ± SD. (n = 3) and were evaluated using one-way ANOVA followed by Tukey's post hoc test; p < 0.05 was considered statistically significant.

Total Phenolics, Total Flavonoids, and LC-MS/MS Analysis Results
The phenolic and flavonoid contents in EEZP peel were measured as 59.7 mg GAE/g and 88.0 mg QE/g, respectively, in this study. Between 6.36 and 1.78 mg GAE/100 mL of total phenolics were present in five different pomegranate cultivars. The total flavonoid content varied from 4.93 to 2.24 mg GAE/100 mL [2]. "Wonderful" pomegranate fruit mineral concentration, bioactivity, and internal quality were improved using foliar nutrient applications. Total phenolic content in P. granatum juice ranged from 2091 to 3735 mg/L GAE [76]. The polyphenol and flavonoid contents of pomegranate peel acetone extract (338 ± 20 mg/g GAE and 60.8 ± 9.3 mg/g QE, respectively) were significantly (p < 0.05) higher than those of water and ethanol extracts. Additionally, it was discovered that the polyphenol and flavonoid levels of acetone extract were higher than those found in methanol, ethanol, and ethyl acetate extracts of the fruit peels of various Pakistani pomegranate varieties, including "Desi", "Kandhari", and "Badana" [77]. In this study, P. granatum extracts were shown to have comparable effective amounts of polyphenolics.
In inhibition studies conducted using similar methods, P. granatum extracts and juice were assayed for α-amylase inhibition ability, the results of which are presented in Table 4.  Table 4). In addition, dominant cytosolic CA II isoform is frequently linked to a number of illnesses, including osteoporosis, glaucoma, and renal tubular acidosis. The CA inhibitory effects of P. granatum extracts and juice were decreased in the following order (Table 4) AZA was employed as a control for the inhibition of CA isoenzymes [78].
AChE was the first FDA-approved therapeutic target for the AD treatment, and many drugs are currently produced and marketed for this purpose. The AChE-inhibitory capacity of P. granatum extracts and juice was enhanced in the following order (Table 4) [79].
Urinary tract infections, respiratory pneumonia, surgical site infections, bacteremia, gastrointestinal disorders, and skin infections are among the most common nosocomial infections. Staphylococcus aureus, as a Gram-positive microorganism, and E. coli, as a Gramnegative microorganism, are the most prevalent pathogens that cause these infections according to the Center for Disease Control and Prevention (Atlanta, USA) [80]. We chose to test the effectiveness of P. granatum extracts and juice against these microorganisms since they are notoriously difficult to eradicate due to their resistance to most antimicrobial agents. Antimicrobial results are shown in Table 5. Table 5. Antimicrobial activities of P. granatum extracts (50 µg/disk). Amc 30: amoxycillin/clavulanic acid antimicrobial susceptibility disks (30 µg/disk); Sxt 25: trimethoprim/sulfamethoxazole (25 µg/disk); Cip 5: ciprofloxacin (5 µg/disk); Gnt 10: gentamicin (10 µg/disk).

Sample
Antimicrobial Zone (mm)

Discussion
A vital and important component of the human diet is phenolic chemicals, which are present in all plants. Their biological activity, which includes antioxidant properties, has attracted considerable attention [81]. Ellagic acid, a phenolic compound found in large amounts in dicotyledonous plants, has been shown in numerous studies to possess potent anti-inflammation and antioxidant properties. Furthermore, research shows that ellagic acid can lessen damage in neurodegenerative conditions such as AD, Parkinson's disease, and cerebral ischemia by enhancing neuronal viability, reducing neuronal defects, and preventing neuronal damage [82]. A brand-new diabetes medication was made with plant flavonoids including epicatechin, catechin, and rutin, which have strong antiinflammatory and antioxidant properties. Their combination can be improved through a mixture design experiment to produce a novel, safe, multitarget antidiabetic formulation, making it an effective combination for the management of diabetes and the associated complications. Rutin, catechin, and epicatechin all have strong antihyperglycemic properties; their synergistic combination assures a novel formulation that might actually be a viable alternative to current medications [83]. Accounting for roughly 59% of the total catechins, epigallocatechin gallate (EGCG) is the most prevalent flavanol. The beneficial effects of EGCG include its impact on metabolism, which lowers the risk of type 2 diabetes; its ability to block antimicrobial activity; and its antioxidant properties against neurodegenerative diseases such as AD [84]. In multi-infarct dementia model rats, nicotiflorin has protective effects such as energy metabolism failure, lowering memory dysfunction, and oxidative stress [85]. Astragalin has a wide spectrum of medicinal effects, including anti-inflammatory, antioxidant, neurological, cardioprotective, antidiabetic, and anticancer effects [86]. Resveratrol, quercetin, catechin, and gallic acid are examples of polyphenols that have antioxidant properties that prevent oxidative damage to DNA and inhibit LDL oxidation in vitro [87]. Antioxidant quinic acid has demonstrated anticancer activity by inducing apoptosis-mediated cytotoxicity in breast cancer cells. Additionally, it has shown a potent affinity for selectins, angiogenesis factors that are elevated in breast cancer tissue [88]. Tannic acid has antimutagenic and anticancer properties. Microorganisms can be killed by tannic acid (bacteria and viruses). Additionally, it functions as a homeostatic agent and an antioxidant. Tannic acid also has the ability to reduce the development of free radicals, which are responsible for a number of diseases, including those that affect the cardiovascular system, Parkinson's disease, diabetes, and AD. Tannic acid also has demonstrated anticancer properties. Tannic acid is currently being researched as an organic polymer additive owing to its bioactive characteristics and its ability to improve the capabilities of materials for biomedical applications [89]. By restoring the normal expression levels of the genes related to insulin signaling and glucose metabolism that were disturbed in the liver of high-fat-diet-induced obese mice, hesperidin has the potential to have an antidiabetic effect [90].
An important indication of a compound's potential antioxidant activity may be found in the reduction capacity of that substance. ROS and free radicals are capable of receiving electron donations from antioxidant compounds, which converts them into more stable and unreactive species [91]. The diversity, high amount of ingredients, and rich phenolic contents might contribute to the antioxidant potential of P. granatum. The reduction potentials of phenolic compounds in P. granatum were determined with reduction systems, including Cu 2+ , Fe 3+ , and Fe 3+ -TPTZ reducing abilities. The radical scavenging properties of P. granatum ethanol extracts was examined by DPPH and ABTS radical scavenging assays. P. granatum possesses reducing properties, which may neutralize oxidants and ROS.
The reduction of Fe 3+ (CN − ) 6 to Fe 2+ (CN − ) 6 and the absorbance resulting formation of Perl's Prussian Blue complex after the addition of excess ferric ions (Fe 3+ ) were used to measure the ability of P. granatum extracts to reduce Fe 3+ . The reducing power assay described by Oyaizu [44], with a minor modification, was applied to assess the reducing ability of P. granatum extracts [92]. In this assay, Fe 3+ was converted to Fe 2+ in the pres-ence of reductants or plant extracts [93]. The addition of Fe 3+ to compounds caused an Fe 4 [Fe(CN − ) 6 ] 3 complex, with maximum absorption at 700 nm [94].
The chromogenic oxidant of neocuproine (Nc) was used in the CUPRAC method. Antioxidants reduce the cupric neocuproine complex [Cu(II)-Nc] to the cuprous neocuproine complex [Cu(I)-Nc], which exhibits maximum absorbance at 450 nm [95]. The CUPRAC method is a convenient, inexpensive, selective, stable of antioxidants [96,97]. The reducing capacity of pure compounds or plant extracts can be determined using the FRAP test. A ferric salt is utilized as an oxidant in the electron transfer process, which is the basis of the FRAP test. Due to its colored combination with TPTZ, which exhibits maximum absorbance at 593 nm, Fe 2+ may be recorded spectrophotometrically [98]. The reducing capacity can be effectively ascertained using this method. First, in a redox-linked colorimetric reaction, the FRAP assay uses the sample's antioxidants as reductants. Second, the FRAP assay procedure is fairly straightforward and is simple to standardize. The FRAP assay was created to assess the ability of biological fluids and aqueous solutions of pure compounds to reduce ferric ions. It has also been used to assess the antioxidant capacity of polyphenols [99]. In this study, we determined the Fe 3+ , Cu 2+ , and Fe 3+ -TPTZ reducing abilities of aqueous extract of P. granatum peel as concentration-dependent (10-30 µg/mL). In this test, the test solution's color changed from yellow to various shades of green and blue depending on the antioxidant samples' reducing power. A compound's reducing capacity might be a good predictor of its potential antioxidant action.
In terms of the harm caused to living organisms by free radicals and ROS, radical scavenging is very important [100]. Due to its quick analysis time compared to other techniques, DPPH's scavenging ability for free radicals has been commonly used to assess antioxidant activity [101]. For example, the DPPH • test, which is based on scavenging of DPPH radicals to the non-radical form of DPPH-H, is commonly used to determine antioxidant activity [102,103]. A freshly made DPPH solution displays a deep purple hue with an absorption peak at 517 nm. When an antioxidant is present in the medium, this purple color typically vanishes. An indicator of the amount of free DPPH that has been reduced by the antioxidant is a decrease in absorbance [104]. As observed in this and previous studies, P. granatum has a comparable or better antioxidant potential relative to standard antioxidants. In another study, the IC 50 values of acetone and ethanol extracts of P. granatum peel for DPPH scavenging activity were found to be 1.56 and 7.09 µg/mL, respectively [77]. The IC 50 of methanolic extract of P. granatum for DPPH radical scavenging was reported to be 0.16 ± 0.07 mg/mL [105]. The IC 50 values of aqueous and ethanolic extracts from P. granatum fruit peel for DPPH radical scavenging were found to be 471.7 and 509.16 g/mL, respectively, [106]. All analyses were performed in triplicate.
The ABTS radicals were produced in an ABTS/K 2 S 2 O 8 system. The test is a decolorization approach in which the ABTS radical is created directly in a stable state prior to treatment with suspected antioxidants. The improved approach for producing ABTS •+ reported here involves the direct creation of a blue/green ABTS •+ chromophore via a reaction between ABTS and K 2 S 2 O 8 [107]. One spectrophotometric technique used to assess the overall antioxidant ability of pure materials, mixtures, and beverages is based on the generation of an ABTS radical cation [108]. When compared to positive controls, the data clearly reveal that P. granatum approximated an effective ABTS •+ scavenging ability. P. granatum samples showed a radical scavenging effect higher than that of reference standard antioxidants. A lower IC 50 value, as in DPPH free radical scavenging activity, suggests more ABTS •+ scavenging ability.
α-Glycosidase plays a crucial role in the metabolism of carbohydrates and is associated with diabetes, cancer, and viral infections. Because of its numerous biological functions, α-Glycosidase is regarded as a promising drug target [109]. Several α-glycosidase inhibitors have recently been found and are currently being researched. Acarbose and miglitol, two commonly prescribed diabetes medications, competitively inhibit α-glycosidase in the brush border of the small intestine. This prevents the hydrolysis of carbohydrates and reduces postprandial hyperglycemia [110]. α-Glycosidase inhibitors may play a significant role in the therapeutic approach to type 2 diabetes mellitus. Postprandial hyperglycemia is a notable and early defect in diabetic diseases, and lowering blood glucose levels can slow the progression of secondary complications related to diabetic diseases [111]. The results reveal that ethanol extract of P. granatum has less inhibitory effects than that of acarbose (IC 50 : 22,800 nM) [63]. According to various subsequent studies, IC 50 value of P. granatum peel extract for inhibition of α-glycosidase activity was 5.56 2.23 µg/mL. Punicalagins may be responsible for this activity [112]. The ethanolic extract of P. granatum fruit peel demonstrated concentration-dependent inhibition of α-glucosidase, with activity ranging from 53.34 2.0 to 15.18 1.4 U/L. Aqueous extract, on the other hand, showed activity ranging from 65.48 1.8 to 20.2 1.3 U/L at the different tested concentrations [105]. The results of α-glycosidase inhibition of P. granatum extract are quite significant and indicate potential use of P. granatum for DM disease.
In order to properly digest carbohydrates, digestive enzymes such as α-amylase and αglycosidase are essential glycoside hydrolases. Both of these enzymes are found on the cells that line the intestine, where they hydrolyze polysaccharides into monosaccharide units that can be absorbed. Certain inhibitors can block the actions of both digestive enzymes to reduce body weight and regulate blood glucose levels. A relatively safe source of inhibitors is plant-based food [113]. Because α-amylase plays a significant role in the digestion of dietary starches, its inhibition helps to prevent and control postprandial hyperglycemia. As a result, numerous studies have looked into and discovered the inhibition of α-amylase by natural products, such as plant extracts, in recent years [114]. P. granatum peel extracts in both aqueous and methanolic form were found to have no effect on the enzyme αamylase in earlier research [115]. The acetone extract of P. granatum peel demonstrated excellent α-amylase inhibitory glycemic control potential, as well as dose-dependent but moderate antiglycation activity (IC 50 : 16.2 5.6 µg/mL), with 61% inhibition at 80 g/mL [77]. Measurements of the in vitro inhibition of α-glucosidase and α-amylase by P. granatum bark extracts were performed at two different concentrations (166 and 332 µg/mL) [115].
The most common and primary cause of dementia in the elderly is AD, a common neurodegenerative disease. The most significant biochemical change associated with AD is a decrease in AChE levels in the brain [116]. According to studies, the decline in acetyltransferase activity and choline (Ch) causes acetylcholine (ACh) to decrease as a neurotransmitter. As a result, cholinesterase (ChE) inhibitors have been the focus of research studies on the treatment of this illness as a symptomatic intervention [117]. AChE-inhibitory medicines are utilized in the treatment of AD. However, these medications have several undesired side effects. Therefore, research on use of novel AChE inhibitors with antioxidant ability is greatly needed [118]. It is known that the predominant AChE inhibitory effects are related to aromatic chemicals and, to a lesser extent, aliphatic molecules [119]. Although AChE inhibitors are used to treat AD, they can only bring about short-term relief. Medicinal herbs have long been known to rich in cholinesterase inhibitors. Phenolic chemicals are primarily responsible for medicinal plants' suppression of cholinergic enzymes [120]. The in vitro cholinesterase-inhibitory effect of P. granatum peel extract is noteworthy, and its methanol extract was found to be more effective than its ethanol extract. The higher AChE activity of methanolic (IC 50 : 32 µg/mL) and ethanolic (IC 50 : 42 µg/mL) extract was correlated with the bioactive metabolite content of the extracts [121]. The inhibition level of P. granatum ethanol extract was slightly lower compared to that of tacrine.
Numerous diseases, including glaucoma, epilepsy, edema, and altitude sickness, are caused by the ubiquitous, physiologically dominant cytosolic isoform CA II [122]. CA isoform activation and inhibition are important therapeutic targets to treat a variety of diseases, including glaucoma, cancer, edema, obesity, epilepsy, hypertension, and osteoporosis [123]. CA II suppression reduces HCO 3 − generation and, as a result, aqueous humor secretion, resulting in reduced ocular pressure [124]. Among them, glaucoma is a multifactorial optical disease that is mostly associated with high intraocular pressure (IOP), which can result in blindness. Therefore, hCA inhibitor medications such as acetazolamide, brinzolamide, and dorzolamide can reduce IOP after topical treatment [125].
One of the most prevalent Gram-positive bacteria that causes food poisoning among is Staphylococcus aureus, which is derived people who consumed contaminate food [126]. A Gram-negative bacterium called Escherichia coli is a part of the typical human flora. Preservatives are required to stop its growth because an enterohemorrhagic strain of E. coli has been implicated in severe cases of food poisoning [14]. Bacteria (E. coli and S. aureus) were resistant to all four antibiotics used as standards. Although some of them had a zone diameter of 10 mm, etc., they were considered resistant because they could not reach the standard sensitivity diameter according to the CLSI criteria.
Some of the extracts were resistant (R) because they did not form any zone diameter (N.D.). However, in some extracts, zones with 7-10 mm intervals, that is, areas in which the extract had an antimicrobial effect and the bacteria were destroyed, were observed. Discs with diameters of 7-10 mm formed at 50 µg (concentration-adjusted) ratios on each extraction disc are very good when compared to standard antibiotics, as observed in extracts that were completely zoneless, that is, resistant.
The benefits of P. granatum can be increased by drinking smoothies made from minor Mediterranean crop purées and P. granatum juice as a good way to increase the consumption of these healthy but underutilized fruits. The effects of an ethanol extract of P. granatum seeds on the central nervous system (CNS) in mice were studied. The results showed that P. granatum extract exhibit anxiolytic activity at all doses and induced increased sleeping latency and decreased sleeping time.
The effects of an ethanolic extract of P. granatum seeds on the CNS of mice were studied. The results showed that P. granatum extract exhibited anxiolytic activity at all dose levels and induced increased sleeping latency and decreased sleeping time [127]. The flavonoids in P. granatum vary greatly. For instance, flavonoids in plants can be found either in free form (aglycones) or linked to sugars. Glycosylated flavonoids are the most common, and glycosylated anthocyanidins, for example, are recognized as an essential flavonoid class known as anthocyanins. Anthocyanidins are light-sensitive and have been linked to sugars. O-glycosides are the most common type of flavonoid glycoside, but C-glycosides are also present. The benefits of P. granatum can be increased by drinking smoothies made from minor Mediterranean crop purées and P. granatum juice as a good way to increase consumption of these healthy but underutilized fruits [128,129].

Conclusions
Zivzik pomegranate (Punica granatum) has various qualities and contains quantities of bioactive secondary metabolites, phenolics, and flavonoids. This product, which is rich, nutritious, and contributes to human health, has been used since prehistoric times. In LC-MS/MS analysis, the major components detected in P. granatum extracts were ellagic acid, catechin, epigallocatechin gallate, epicatechin, nicotiflorin, astragalin, gallic acid, epigallocatechin, quinic acid, tannic acid, aconitic acid, hesperidin, isoquercitrin, rutin, fumaric acid, cosmosiin, luteolin, and epicatechin gallate. Furthermore, the P. granatum ethanol extract was found to be rich in phenolic contents, antioxidant ability, reducing power, AChE, α-glycosidase, α-amylase, and hCA II inhibition. P. granatum can also be used as a natural remedy to treat severe T2DM, AD, and glaucoma disease, as well as in food and pharmaceutical applications. From this perspective, inhibition studies on the AChE enzyme are planned to determine the anti-Alzheimer effects of WEZP and EEZP. In addition, the inhibition of CA II enzyme was analyzed to determine the link with glaucoma. Similarly, some studies have been carried out to identify the antidiabetic potential of P. granatum extracts on α-amylase and α-glycosidase. Additionally, Fe 2+ , Cu 2+ , and Fe 3+ -TPTZ reduction, as well as DPPH and ABTS scavenging, tests were performed to understand the antioxidant potential of P. granatum. Furthermore, total phenolic and flavonoid contents in P. granatum were established for both extracts. Finally, an analysis of the phenolic compounds was performed via LC-MS/MS to define the biological activity of the chemical profile of P. granatum. However, the possible cytotoxic or other undesirable effects of P. granatum should be more comprehensively detailed in the future.