Estimation of Total Quercetin and Rutin Content in <i>Malus domestica</i> of Nepalese Origin by HPLC Method and Determination of Their Antioxidative Activity

Pandey, Jitendra; Bastola, Tonking; Tripathi, Julu; Tripathi, Milu; Rokaya, Rabindra Kumar; Dhakal, Bhawana; D. C., Rabin; Bhandari, Ravin; Poudel, Amrit

doi:https://doi.org/10.1155/2020/8853426

Journal of Food Quality

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Abstract Introduction Materials and Methods Results Discussion Conclusion Data Availability Disclosure Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 8853426 | https://doi.org/10.1155/2020/8853426

Estimation of Total Quercetin and Rutin Content in Malus domestica of Nepalese Origin by HPLC Method and Determination of Their Antioxidative Activity

Jitendra Pandey,^1,2Tonking Bastola,²Julu Tripathi,²Milu Tripathi,^2,3Rabindra Kumar Rokaya,^2,4Bhawana Dhakal,⁵Rabin D. C.,⁶Ravin Bhandari,¹and Amrit Poudel^2,7

Academic Editor: Alessandro Di Cerbo

Received04 Jul 2020

Revised03 Sept 2020

Accepted05 Sept 2020

Published03 Nov 2020

Abstract

Malus domestica (Apple) is one of the most widely cultivated cash crops of Nepal. Jumla and Mustang are two major pocket areas for the production of apple. Flavonoids including quercetin and rutin are potent antioxidants present in apples. This study was designed to quantify and compare the presence of quercetin and rutin in different plant parts (peel, leaf, and bark) among various cultivars of Malus domestica from two pocket zones of Nepal. A new HPLC-UV method was developed and validated for the quantification of quercetin and rutin. Polyphenols, flavonoids, and carbohydrate contents were determined by colorimetric methods. 2,2′-Diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay was carried out to measure in vitro antioxidative activity. Acid hydrolysis of each extract was carried out by the standard method to measure aglycone quercetin content after hydrolysis of its glycosides. The total rutin content ranged from 3.69 ± 1.34 to 374.50 ± 2.35 mg/100g dry extract weight. Before the acidic hydrolysis, the total quercetin content ranged from 2.96 ± 0.13 to 171.05 ± 0.95 mg/100g dry extract weight whereas its amount increased highly after the hydrolysis and it ranged from 80.84 ± 19.65 to 7445.32 ± 29.25 mg/100g dry extract weight. Total polyphenol content ranged from 19.48 ± 0.23 to 123.48 ± 1.84 µg gallic acid equivalent/mg of dry extract weight. Similarly, flavonoid content ranged from 2.21 ± 0.72 µg to 755.54 ± 1.91 µg quercetin equivalent/mg of dry extract weight. Total carbohydrate content ranged from 144.15 ± 3.73 to 484.65 ± 2.63 µg glucose equivalent per 0.5 mg dry extract weight. All the extracts showed the various degrees of antioxidant activity in a dose-dependent manner. Among them, stem bark of the Jonathan Jumla showed potent antioxidant activity with IC₅₀ value of 13.003 µg/mL. The present study provides the information about variation of the phytochemical content among the different cultivars, parts, and geographic locations. Furthermore, it revealed that bark of Malus domestica cultivars had high quercetin and rutin content with high antioxidant activity.

1. Introduction

From the prehistoric time, Malus domestica has been used as a delicious fruit [1]. Despite the great advances in modern pharmaceuticals in recent decades, nutritive plants still make an important contribution to health care. Uncontrolled production of the reactive oxygen species (ROS) leads to oxidative damage of biomolecules and results in degenerative disorders including cancer, diabetes, neuronal disorders, and aging [2]. Larger numbers of medicinal plants have been investigated for the antioxidant properties. Natural antioxidants are very effective to prevent oxidative stress and are believed to protect against degenerative diseases [3].

Malus domestica is a small deciduous tree (3 to 12 meters) belonging to the Rosaceae family [4]. It is widely distributed in the temperate zone throughout the world [5]. Traditionally, the infusion of the dried flower and leaves is used to control the blood pressure, fruit vinegar is given to the hearing impaired patient, and the fruit is used as diuretics, antidiarrheal, and soft laxative. Diverse class of flavonoids and polyphenols such as quercetin, rutin, quercetin-3-galactoside, catechin, epicatechin, procyanidin, cyanidin-3-galactoside, coumaric acid, chlorogenic acid, gallic acid, and phloridzin are present in apple fruit along with its leaves and bark [4]. Moreover, various biological activities such as antioxidant [6], anti-inflammatory [7], antiulcer [8], and neuroprotective effect [9] have been reported from this plant. Apple fruit is a major source of rutin, quercetin, and other flavonoids [10]. Quercetin glycosides and flavonols are present mainly in the peels whereas phenolic acids are present mainly in the fruit cortex [11]. Quercetin is mostly bounded with sugar moiety. Thus, the amount of free quercetin gets increased after acid hydrolysis [12]. The presence of quercetin and rutin in Malus domestica can be quantitatively determined by High Performance Liquid Chromatography (HPLC) [13].

The present study was designed to estimate total quercetin and rutin content in different Malus domestica of Nepalese origin by new HPLC method and evaluate their antioxidant activity along with total flavonoid, polyphenol, and carbohydrate content. The developed method is also used to compare quercetin and rutin content within different parts (peel, leaves, and stem bark) from six different cultivars.

2. Materials and Methods

2.1. Collection and Extraction of Plants

Fresh and healthy parts (fruit, leaves, and stem bark) of Malus domestica were collected from Marpha, Mustang (temperate region, 2650 m above the sea level), and Khalanga, Jumla (temperate region, 2518 m above the sea level), in August and September 2019. Six different cultivars were collected for the study (Table 1). The fruits were collected after maturation. The identification of plants was done by senior taxonomist Dr. Radhyashyam Kayastha and the voucher specimens were labelled and preserved at the herbarium unit of Pokhara University, Kaski, Nepal. The voucher numbers are as shown in Table 1. The fruit peels were separated by using a steel peeler. Seeds were removed from the pulp manually. All the plant materials were cut into 1 × 1 cm slices. All the sliced plant materials were spread over the clean filter paper and placed in the laboratory having a well-ventilated room at 25°C for 15 days. Plant materials were constantly turned to prevent the possible fungal growth. After the plant parts were dried, they were ground to a fine powder using a portable grinding machine. The reduced powder mass was then passed through the sieve of mesh size 40. The dried slice of the pulp was extracted without grinding due to its sticky nature. Triple cold maceration technique was adopted for the extraction process in which 100 g of each sample was soaked with 1000 mL methanol using conical flasks with occasional shaking for 24 hours; then liquids were strained and the marcs were pressed. The strained liquids were then subjected to filtration. The operation was repeated up to three times and filtrate was mixed. The filtrate obtained was dried by using a rotary vacuum evaporator at 40°C to get viscous concentrate which was further dried by using a vacuum desiccator and so obtained extract was stored at 4°C until use.

2.2. Phytochemical Screening

All the plant extracts were screened for the presence of alkaloid, saponin, terpenoid, anthraquinone, tannin, cardiac glycosides, flavonoid, carbohydrate, polyphenols, protein, amino acid, resin, and phytosterol according to previously established method [14–16].

2.3. Estimation of Total Phenolic Content

Total phenolic content (TPC) was determined by Folin–Ciocalteu (FC) method with slight modification [17]. In this analysis, 1 mL of the sample (1 mg/mL) was mixed with 1 mL of the 2N FC reagent followed by the addition of 5 mL distilled water and mixed thoroughly. After 5 min, 1 mL of the 10% Na₂CO₃ was added to the mixture and incubated at room temperature for 1 hour. Finally, the absorbance of the reaction mixture was measured at 725 nm against a blank. The estimation of the phenolic compound was carried out in triplicate. The TPC was expressed as μg gallic acid equivalent (GAE)/mg of dry extracts using the calibration curve of gallic acid.

2.4. Estimation of Total Flavonoid Content

Total flavonoid content (TFC) was determined by adopting an established method with slight modification [18]. 1 mL of the sample (1 mg/mL) was mixed with 4 mL of the distilled water and 0.3 mL of the 5% NaNO_2. After 5 min, 0.3 mL of the 10% AlCl₃ was added and then incubated for 5 min. Then 2 mL of the 1M NaOH was added and the solution was mixed well. After 30 min, the absorbance was measured against the blank solution at 510 nm. The estimation of the flavonoid compound was carried out in triplicate. TFC was expressed as μg of quercetin equivalents (QE/mg) of dry extracts, using calibration curve of quercetin.

2.5. Estimation of Total Carbohydrate Content

The total carbohydrate was determined by the phenol-sulphuric acid method [19]. In a 10 mL of test tube, 1mL of the sample (1 mg/mL), 1 mL of the 5% phenol solution and 5 mL of the concentrated sulphuric acid were mixed properly. After 10 min, the contents of the tube were mixed and placed in a water bath set at 25–30°C for 20 min and the absorbance was measured against the blank at 490 nm. The standard curve for total carbohydrate content was made using a glucose standard solution. Total carbohydrate content was expressed as μg of glucose equivalents per 0.5 mg of dry extracts.

2.6. DPPH Radical Scavenging Activity

The antioxidant capacity of peel, leaves, and stem bark samples from all the cultivars was confirmed by 2,2′-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity assay according to established method with slight modification [20,21]. DPPH solution was prepared in methanol at a concentration of 0.1 mM. Five different concentrations of plant extracts were prepared by serial dilution (250–15.625 µg/mL). 2 mL of each test sample and 2 mL of prepared DPPH solution were mixed with vigorous shaking and kept in dark at room temperature. After 15 min, absorbance was measured at 517 nm by using a UV spectrophotometer. Methanol and ascorbic acid were used as negative and positive controls, respectively. The entire test was performed in triplicate. The percentage of radical scavenging was calculated using the following formula.where was the absorbance of DPPH solution and was the absorbance of the sample.

2.7. Optimization of the HPLC Method for Analysis

Quantitative analysis of quercetin and rutin in different samples was done using an HPLC system of LC2010CHT (Shimadzu, Japan), lab-solution software, UV-Visible detector set at 374 nm, and autosampler set at 10 μL injection. All chromatographic analysis was performed at 40°C on the C18 column (J Sphere ODS-L80, 5-4 μm, 4.6 150) and a flow rate of 1 mL/min. The mobile phase consisted of methanol (A) and 100 mM sodium dihydrogen phosphate buffer with P^H 2.1 (B) with gradient elution for better separation. The gradient solvent system was optimized as 5% A (0–5 min), 5–10% A (5–10 min), 10% A (10–15 min), 10–15% A (15–20 min), 15% A (20–25 min), 15–20% A (25–30 min), 20% A (30–35 min), 20–22% A (35–40 min), 22% A (40–45 min), 22–25% A (45–50 min), 25% A (50–55 min), 25–30% A (55–60 min), 30–35% A (60–65 min), and 35–50% A (65–70 min).

2.7.1. Preparation of Standard and Sample Solution

The stock solutions of quercetin and rutin were prepared in methanol at the concentration of 2 mg/mL. Both stock solutions were diluted serially as necessary to plot the calibration curve. The sample solutions of peel (200 mg/mL), leaf, and stem bark extracts (50 mg/mL) of M. domestica were prepared in HPLC grade methanol using an ultrasonic water bath at a temperature of 40°C. All the sample solutions were filtered with the help of 0.20 µm filters (PTFE filters, Thermo Scientific, Waltham, MA, USA) before injection.

2.7.2. Acid Hydrolysis of Extract

Hydrolysis of peel, leaves, and stem bark extract was carried out by using 1.5 M HCl [12, 22]. Five mL of methanolic peel (400 mg/mL), leaf, and stem bark (100 mg/mL) extract solution was placed in airtight tube followed by the addition of 3 M HCl (5 mL). The tubes were then heated at 60°C in a water bath with continuous shaking. The acid hydrolysis was carried out for different time intervals (30 min, 45 min, and 1 hour). After hydrolysis, samples were centrifuged. The filtrate so obtained was injected in HPLC for analysis of peak area.

2.7.3. Method Validation

The method was validated for linearity, limit of detection and quantification (LOD and LOQ), precision (intraday and interday variation and repeatability), and accuracy (recovery) following ICH guideline [23] and some report in literature [24].

2.7.4. Quantification of Quercetin and Rutin from M. domestica Extracts

The validated analytical method was used to determine total quercetin and rutin content simultaneously in different samples. The quantification of quercetin and rutin before and after the acid hydrolysis of all the extract was done by linear regression of the standards. All the samples were analyzed in triplicate to determine the average content. The content of quercetin and rutin in sample extract was expressed as mg/100 g of dry extract.

2.8. Statistical Analysis

All the tests were done in triplicate and the data were expressed as mean ± SD. Statistical significance of differences was determined using a one-way analysis of variance (One-way ANOVA), with Tukey post hoc test using GraphPad Prism 6.0 software. A -value < 0.05 was considered significant.

3. Results

3.1. Phytochemical Screening

Phytochemical screening of different samples of M. domestica showed the presence of varied degree of alkaloid, saponin, terpenoid, anthraquinones, tannin, cardiac glycoside, flavonoid, carbohydrate, polyphenol, protein and amino acid, resin, and phytosterol. The results are summarized in Table 2.

3.2. Total Phenolic Content (TPC)

The quantitative determination of total phenol was carried out using Folin–Ciocalteu reagent with the help of gallic acid calibration curve and was expressed as μg of gallic acid equivalent per milligram dry extract weight, which revealed that the highest TPC was shown by Jonathan stem bark Jumla (123.48 ± 1.84 μg) whereas peel extract of Golden Jumla revealed the lowest value (19.48 ± 0.23 μg). Figure 1 shows the comparison of TPC of different extract of Malus domestica. Analysis of variance (ANOVA) indicated that the total phenol content of apple bark extracts was significantly higher than peel and leaf extracts. Between peel and leaf, leaf contained significantly higher amount of polyphenol. Among the varieties, bark extract of Jonathan cultivar contained significantly higher amount of polyphenol than other varieties.

3.3. Total Flavonoid Content (TFC)

The TFC of plant extracts was expressed as μg of quercetin equivalent per milligram dry extract weight (Figure 2). The value ranged from 2.21 to 755.54 µg QE/mg of dry extract. The stem bark of the Chocolate Jumla was found to contain the highest flavonoid whereas the lowest TFC was reported in Golden peel Jumla. Analysis of variance (ANOVA) indicated that the total flavonoid content of apple bark extracts was significantly higher than peel and leaf extracts. Between peel and leaf, leaf contained significantly higher amount of flavonoids. Among the varieties, bark extract of Chocolate cultivar contained significantly higher amount of flavonoid than other varieties.

3.4. Total Carbohydrate Content (TCC)

To investigate the variation in nutritional value among the apple fruits of different cultivars at two different regions, the total carbohydrate content was calculated using phenol-sulphuric method in terms of glucose equivalent. As shown in Figure 3, the highest carbohydrate content was detected in Royal pulp Mustang (484.649 ± 2.631 µg glucose/0.5 mg dry extract) and Golden pulp Jumla had shown lowest carbohydrate content (393.97 ± 0.68 µg glucose/0.5 mg dry extract). Analysis of variance (ANOVA) indicated that the total carbohydrate content of apple pulp extracts was significantly higher than peel, leaf, and bark extracts. Between bark and leaf; bark contained significantly higher amount of carbohydrate within the same cultivar.

3.5. Antioxidant Activity

Among 27 different extracts of M. domestica, stem bark extracts of Jonathan Jumla showed strong antioxidant activity (IC₅₀ : 13.01 μg/mL) as determined by DPPH radical scavenging assay method whereas lowest antioxidant activity (IC₅₀ : 242.34 μg/mL) was shown by fruit peel extract of the same plant. IC₅₀ value of all the extract is depicted in Table 3. Similarly, Figures 4 and 5 represent the DPPH radical scavenging potency of different parts of M. domestica from Jumla and Mustang, respectively.

3.6. Optimization of Chromatographic Conditions

The HPLC conditions were investigated for the mobile phase and detection wavelength for better chromatographic resolution. To obtain accurate valid and optimal chromatographic conditions, various mobile phases (methanol-water and acetonitrile-water with different modifiers including glacial acetic acid and phosphoric acid) with different analysis time were examined. The optimized gradient solvent system consists of methanol/sodium dihydrogen phosphate buffer with P^H 2.1 in the water at column temperature 40°C with a flow rate of 1 mL/min. The analysis time was optimized with 70 min. The choice of 374 nm as wavelength enabled a high absorbance of both standards. Figure 6 represents the chromatogram of a standard mixture of quercetin and rutin. Similarly, chromatogram of peel, leaf, and stem bark extract is shown in Figure 7.

(a)

(b)

(c)

3.7. Method Validation

Chromatographic investigation for linearity, precision, and accuracy was conducted to ensure the selectivity, preciseness, and reproducibility of the optimized technique. For the linearity, seven different concentrations (7.8125–500 µg/mL) for rutin and quercetin were injected separately. Calibration curve equations were obtained by plotting peak area versus concentration. Since the correlation coefficient (R²) of both standards was 0.9999 and 0.9996, linearity was verified. Detail information regarding the calibration curve, linear range, LOD, and LOQ is listed in Table 4.

The precision of the optimized analytical method was verified by interday and intraday variation together with the repeatability of sixtuplets. The RSD of intraday and interday analysis were reported to be in the range of 0.16–0.71% and 0.14–0.97%, respectively (Table 5).

The repeatability of quercetin and rutin was evaluated by injecting standard mixture six times in the same day. The RSD was found to be 0.72 and 1.48% for quercetin and rutin, respectively (Table 6).

The accuracy was measured by determining the recovery of the spiked standard to the extract. The three different concentrations (low, medium, and high) of the standard were added to the known sample. The percentage of recovery and RSD were calculated, which showed a recovery of 96.67–102.89% and RSD of 0.03–0.53% (Table 7).

3.8. Quantitative Determination of Quercetin and Rutin in M. domestica Sample

Peel, leaf, and stem bark extracts of six different M. domestica cultivars from two different regions of Nepal were quantitatively examined for the amount of quercetin and rutin with the help of the newly optimized validated method (Table 8). Total quercetin and rutin contents were expressed as mg per 100 g dry extract. The stem bark extract of Chocolate Jumla was reported to contain 171.05 mg/100 g of quercetin while peel extract of Richard Mustang was reported to contain 2.66 mg/100 g of quercetin. Similarly, the stem bark extract of Jonathan Jumla exhibited the highest amount (374.5 mg/100 g) of rutin whereas lowest rutin content was detected in the peel extract of Richard Mustang (3.59 mg/100 g). As shown in Table 8, there was some variation among the extracts of same cultivar (Red Delicious, Royal Delicious, and Golden) collected from the different locations. In case of fruits, the content of quercetin and rutin was comparatively higher from Mustang. Oppositely, the content of both compounds from the Mustang sample was relatively low as compared to Jumla in case of leaf and bark extract. Furthermore, leaf and bark extract of M. domestica showed comparatively higher quercetin and rutin content than peel. Analysis of variance (ANOVA) indicated that the total rutin and quercetin content of apple bark extracts was significantly higher than peel and leaf extracts within the same cultivar. Between peel and leaf, leaf contained significantly higher amount of rutin and quercetin. Among the varieties, bark extract of Jonathan cultivar contained significantly higher amount of rutin and bark of Royal Jumla cultivar contained significantly higher amount of quercetin than other varieties.

Acid hydrolysis was optimized for 45 min which increased the total amount of quercetin in peel, leaf, and steam bark extracts. Hydrolysis of the sample also led to the conversion of rutin into free quercetin form. As shown in Table 9, the total content of quercetin was found to be highest in Royal bark Jumla (7445.32 mg/100 g dry extract) and the lowest quercetin was reported in the peel extract of Richard Jumla (80.84 mg/100 g dry extract). Analysis of variance (ANOVA) indicated that after acid hydrolysis also the quercetin content of apple bark extracts was significantly higher than peel and leaf extracts within the same cultivar. Between peel and leaf, leaf contained significantly higher amount of quercetin. Among the varieties, bark of Royal Jumla cultivar contained significantly higher amount of quercetin than other varieties.

4. Discussion

Preliminary investigation of phytochemicals is a crucial step for identifying various pharmacologically effective secondary metabolites of plants exhibiting a vital role towards the advantageous medicinal and physiological properties such as antioxidant, antidiabetic, anticarcinogenic, and antimicrobial activities [25]. The phytochemical screening proclaimed the presence of polyphenol, saponins, terpenoid, flavonoid, and phytosterol in the methanolic extract of all samples. In this study, alkaloids were present only in leaf and stem bark extract. Protein, amino acid, and cardiac glycosides were present only in pulp and peel extract. Resins were not present in the pulp, anthraquinones were not present in leaf, and tannins were not present in the bark.

Phenolic compounds are the major phytochemical constituents of plants to exhibit the antioxidant action and various therapeutic activities such as cardiovascular protective, antiatheroscleretic, anti-inflammatory, anticarcinogenesis, and antiaging, due to the scavenging capacity of their hydroxyl group [26]. The phenolic compounds such as flavonoids and phenolic acid are attributed to the antioxidant activity of M. domestica [27, 28]. Among the analyzed twenty-seven extract samples, the highest phenolic content was found in Jonathan stem bark extract whereas the lowest content was reported in Golden peel Jumla. Our study revealed almost a similar amount of phenolic content in fruit extract in comparison to the previous study [29–31]. Flavonoids are the most diverse and widespread group of natural phenolic compounds. Hydroxyl position in the flavonoid molecule determines antioxidant properties and it depends on the ability to donate hydrogen or electron to a free radical [32]. Among the investigated plant extracts, the highest flavonoid content was found in Chocolate stem bark extract of the Jumla whereas the lowest content was detected in Golden peel Jumla. In this study, the total flavonoid content of fruit peel extract was comparable to the previous study [33]. The presence of major chemicals such as procyanidin, anthocyanins, quercetin glycosides, and cyaniding glycosides in the peels is responsible for higher flavonoid content [34]. Among all the analyzed sample extracts, the stem bark contains higher flavonoid and polyphenol content than other plant parts and the result was reported for the first time.

The present study showed that the Royal Mustang pulp contains highest and Golden Jumla pulp has lowest carbohydrate content. The experiment also showed that higher carbohydrate content was present in peel and pulp compared to leaf and bark extracts. The study on carbohydrate content in M. domestica of Nepalese origin has not been reported before. Free radical scavengers such as polyphenol, flavonoids, and phenolic compounds which are derived from the plants are responsible for antioxidant activity and protect us from different life-threatening diseases [35]. In the present study, the antioxidant activity was performed by DPPH radical scavenging assay. Among twenty-seven different extracts, the stem bark extract of Jonathan Jumla, Chocolate Jumla, and leaf extract of Red Jumla showed the most significant radical scavenging activity with IC₅₀ value of 13.003 µg/mL, 14.605 µg/mL, and 15.49 µg/mL, respectively. Higher value of total phenol and flavonoid content might be responsible for potent antioxidant activity of these extracts. Antioxidant capacities of the peel extracts in this study are comparable to a previous study [30, 31].

For the quantitative analysis of total quercetin and rutin content, the HPLC method was optimized for simultaneous determination of quercetin and rutin in peel, leaf, and steam bark extract of M. domestica. The method was validated for various parameters like linearity, LODs, LOQs, precision, and accuracy. All these parameters were found to be within the range of ICH guidelines. The quercetin and rutin contents in different plants parts were found in increasing order as peel < leaf < stem bark. The total concentrations of quercetin and rutin were found to be varied among the cultivars. The highest amount of quercetin and rutin was quantified in Royal Jumla stem bark extract. The variation in genetic makeup, cultivation condition, phases of growth, soil condition, and fertilization condition may contribute to the difference in the quantitative composition of phytochemical among the cultivars. Moreover, differences in weather condition and meteorological and geographical condition might also be a possible factor [36–38]. Quercetin can be found freely as well in glycosidic form [13]. Acid hydrolysis was carried out in this study for the conversion of the glycosidic form of quercetin into aglycone form. Hydrochloric acid was chosen for this purpose as it is efficient as compared to sulphuric acid [12]. The total amount of quercetin was increased in all the extracts after the acid hydrolysis. Quercetin content in peel extract was reported to increase by about 12 times after acid hydrolysis, which was also supported by literature [12]. Interestingly, while comparing the apple cultivars of two different climates, the experiment showed that fruits of Mustang were better as compared to fruits of Jumla but leaf and stem bark of the Jumla were found to be better than the Mustang.

5. Conclusion

The present study showed that methanolic extract of peel, leaf, and stem bark of M. domestica exhibited potent antioxidant activity due to the presence of polyphenols, flavonoids, and other various phytochemicals. Peel and pulp contain higher carbohydrate content and are responsible for nutritional value along with pleasant taste. The study provides strong evidence about the presence of high quercetin and rutin content in stem bark relative to peel and leaf of M. domestica of Nepalese origin. Moreover, we can conclude that the content of quercetin and rutin may vary among the different cultivars and different plant parts and also influenced by the geographical locations.

Data Availability

All the data used to support the result of this research are available from the authors Tripathi J. and Tripathi M. upon request.

Disclosure

This research was performed as part of the partial fulfillment of academic degree at Pokhara University.

Conflicts of Interest

The authors declare no conflicts of interest.

Authors’ Contributions

Jitendra Pandey, Tonking Bastola, Julu Tripathi, Milu Tripathi, and Rabindra Kumar Rokaya contributed equally to this work.

Acknowledgments

The authors are very much grateful to the Department of Pharmacy, Pokhara University, for providing all the technical support. The authors would like to acknowledge sincerely Mr. Bal Krishna Adhikari, Botanist of Temperate Horticulture Development Center, Marpha, Mustang, and Mr. Kalam Bahadur Khatri, JTA, Jumla, for providing plant samples.

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Copyright © 2020 Jitendra Pandey et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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