In this study, a random sample of chickpeas, lentils, and quinoa was characterized physically, chemically, and nutritionally. The results showed that lentils had a higher level of protein (21%), while chickpeas had higher moisture content (16.1%). Lentils and quinoa contained the same amount of fiber (14%). Mineral content was evaluated in all samples, with quinoa showing the highest amounts of copper (79.63 mg/kg), zinc (24.3 mg/kg), phosphorus (4064 mg/kg), and magnesium (3625 mg/kg). Chickpeas, on the other hand, had higher amounts of sodium (2133 mg/100g) and calcium (1304 mg/100g). Chickpeas also contained higher amounts of ascorbic acid (67 mg/100g), thiamine (1.83 mg/100g), riboflavin (2.03 mg/100g), niacin (23.3 mg/100g), and α-tocopherol (29 mg/100g) compared to quinoa and lentils. Lentils had a higher amount of folate (477.5 µg/100g). Chickpeas also contained higher levels of leucine (7.13 g/100g) and phenylalanine (5.7 g/100g). The total amino acid content in lentils was 37.89 g/100g, with the highest amounts of leucine (7.2 g/100g) and lysine (7.26 g/100g). Quinoa contained the richest amount of leucine (7.03 g/100g), and the total amino acid content in quinoa was 34.93 g/100g. In conclusion, all the samples showed different nutrient values across the grains. Quinoa exhibited higher values in bioactive compounds. Due to their higher nutritional content, these grains are recommended for daily intake.
Key words: antioxidants, cereals, chickpeas, lentils, protein, pulses, quinoa
*Corresponding Authors: Muhammad Umair Arshad, Department of Food Sciences, Government College University, Faisalabad, Pakistan. Email: [email protected]; Tawfiq Alsulami, Department of Food Science & Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia. Email: [email protected]
Academic Editor: Prof. Valeria Sileoni – University of Mercatorum, Italy
Received: 11 October 2024; Accepted: 6 March 2025; Published: 1 July 2025
© 2025 Codon Publications
This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/)
Silva et al. (2009) explained that cereal bars were first developed approximately ten years ago and offer a replacement food that is both functional and easy to ingest. A pulse known as chickpea (Cicer arietinum L.) is very popular and consumed globally. According to Grasso et al. (2022), like all other cereals and carbohydrates, chickpeas are a beneficial source of fats, protein, and fiber . Shevkani et al. (2019) evaluated that chickpeas contain minerals, carbohydrates, lipids, and bioactive substances. In addition to protein, chickpea protein components contain antinutrients, all of which influence the productivity of recovery and critical quality characteristics. Chickpea seeds, and pulses in general, have different nutritional profiles depending on soil nourishment, biology, environment, agronomic techniques, and stress factors, all of which are important to consider. According to Kaur and Parasad (2021), the main component of the carbohydrate fraction is starch (47.4%–66.9%), which accounts for 41.0%–50.8% of the total carbohydrate content in chickpeas, along with crude fiber, digestible sugars, and dietary fiber, which account for the remaining portion of the carbohydrate content. Summo et al. (2019) found that minerals and vitamins are other significant components of chickpeas. Chickpeas contain more nutrients, such as vitamins C, A, E, and K, as well as B-complex vitamins, zinc, and phosphorus, compared to other legumes. Chickpeas also include phenolic compounds (such as formononetin and isoflavones like biochanin A) and carotenoids, which are found in larger amounts in brown and black chickpea cultivars. Brummer et al. (2015) verified this. Lentil (Lens culinaris) is a high-fiber, low-fat leguminous plant. The amount of total soluble fiber is lower in peas and chickpeas than in lentils. Lentils also have a higher nutritional fiber content than beans and chickpeas. Just like most other legumes, lentils have a high protein content, ranging from 20.6% to 31.4%. Lentil proteins are made up of roughly 16% albumins, 11% glutelins, 70% globulins, and 3% prolamins. The lentil crop is generally grown in areas without adequate irrigation, depending on the water contained in the soil after heavy rains in the fall and winter. Lentil crops help fix nitrogen from the air into the soil, reducing the need for nitrogen fertilizers and the soil’s inorganic nitrogen levels. When combined with sulfur-containing amino acids found in wheat, rice, or other cereal grains, lentil protein meets daily critical amino acid requirements without the use of animal proteins. It’s a low-cost source of plant protein that can be used to feed people in impoverished countries. To increase the usage of lentil proteins in foods, supplements, and functional food formulas, two important challenges must be addressed: processing costs and intrinsic tastes. Quinoa’s protein composition ranges from 13.8% to 16.5%, with an average of 15%. Quinoa’s (Chenopodium quinoa Wild.) oil content ranges from 2% to 9.5%, and it is high in essential fatty acids like linoleic and linolenic acid, as well as natural antioxidants like α- and γ-tocopherol. Kaur et al. (2018) established a gluten-free cereal bar made from quinoa with 10.50% protein content, according to the manufacturer. The bar’s crude protein content was 14.43%. Leucine (892.10 mg/100g), isoleucine (688.80 mg/100g), lysine (561.01 mg/100g), and valine (530.40 mg/100g) were all present in high concentrations in the Choco Quinoa Nutri Bar. The threonine concentration was 388.90 mg/100g, with other essential amino acids ranging from 110 to 181 mg/100g. Among the non-essential amino acids detected in the bar, L-Aspartic acid was found in the highest concentration (596.26 mg/100g), followed by L-Proline (308.40 mg/100g) and L-Alanine (301.50 mg/100g). L-Cysteine was detected in the bar in a very small proportion, 30.01 mg/100g (Garg and Brar, 2017). The primary reason for conducting this study is that chickpeas, lentils, and quinoa are rich in nutritional compounds. Chickpeas and quinoa are not commonly used in our daily lives. The purpose of this study is to examine their nutritional and bioactive constituents to explain their health-promoting perspectives. Free radicals cause oxidative stress, high levels of free radical species are known to cause pathological conditions (Akpinar et al., 2023; Al-Saeed et al., 2023; Rakha et al., 2023; Khan et al., 2024; Yiğit et al., 2024; Al-Gheffari et al., 2024; Amrozi et al., 2024; Balgoon et al., 2024; Elzaiat et al., 2024; Rashid et al., 2024; Saadullah et al., 2024). Quinoa, lentils, and chickpeas are high in protein, flavonoids, polyphenols, and tocopherols which exhibit strong antioxidant potential. Quinoa and quinoa products are rich in micronutrients, including polyphenols, vitamins, and minerals, as well as macronutrients like protein, polysaccharides, and lipids. All of these food bars play a vital role in our society because they help prevent diseases and promote good health.
For chemical analysis, the chemical composition of chickpea, lentil, and quinoa samples was analyzed, including moisture content, ash content, crude fat, crude protein, and crude fiber, which were quantified according to their relevant procedures.
Using an oven with a forced draught (Memmet, Germany) set to a temperature of 105±5°C, samples were collected from chickpea, lentil, and quinoa and analyzed for their moisture content, according to method No. 44-I5A AOAC 2000.
As designated in method No. 46-30 2000, samples of chickpea, lentil, and quinoa were taken, and their protein content was analyzed using Kjeldahl’s method.
The fat content percentage was observed, and samples were taken for the determination of fat content. The Soxhlet apparatus was used for the determination, according to method No. 30-25, AOAC 2000.
For the analysis of crude fiber, samples of chickpea, lentil, and quinoa were taken, following the instructions outlined in Method No. 32-10, AOAC 2000.
A muffle furnace, set to a temperature of 550°C, was used to evaluate the ash content of chickpea, lentil, and quinoa samples by burning them. After burning, a desiccator was used to cool the remaining sample, which was then weighed. The ash content was determined by calculating the variance between the sample’s initial weight and the weight after burning in the muffle furnace. The calculated ash content is expressed as a percentage, according to method No. 08-01, AOAC 2000.
According to method AACC, 2000, iron, sodium, copper, zinc, magnesium, potassium, and calcium are typically determined using two methods: flame photometry and atomic absorption spectrophotometry.
Vitamins were calorimetrically determined using the method of Lebiedzinska et al. (2007), where thiamine is quantified and separated by the HPLC technique. Riboflavin, niacin, and vitamin B-12 were also determined using a chromatographic method (reverse-phase).
A high-speed amino acid analyzer (LA8080 amino SAAYA, High Tec Solution, Japan) was used to determine the amino acids in chickpeas, lentils, and quinoa, according to the technique presented by Biel et al. (2009). After the amino acids were isolated using the cation exchange column, the ninhydrin method was applied to evaluate the amino acids with a UV/VIS spectrophotometer.
Miliauskas et al. (2003) described the Folin-Ciocalteu method for determining the total phenolic levels in chickpeas, lentils, and quinoa.
The total flavonoid content (TFC) of chickpeas, lentils, and quinoa was analyzed using the method of Nongalleima et al. (2017).
Dmitrienko et al. (2012) explained that spectroscopic, chromatographic, and electrophoretic methods are the most common techniques for determining quercetin. Spectrophotometry and luminescence are commonly used to analyze quercetin samples with a relatively simple formulation, particularly dietary supplements and pharmaceutical treatments. In contrast, GC–mass spectrometry, HPLC, and capillary electrophoresis are employed to determine this compound in natural sources and biological fluids. Recently, new electrochemical approaches for identifying quercetin have gained popularity.
Lagarda et al. (2006) explained that HPLC has been the method of choice for the examination of sterols and related substances. As a result, it appears to be ideal for investigating thermally unstable substances like sterols.
The moisture content of chickpeas, lentils, and quinoa was analyzed through physicochemical characterization. The data showed that the mean moisture content of chickpeas was 16.1%, lentils was 17%, and quinoa was 8.75%. The moisture content of lentils was higher than that of the other samples.
The results indicated that the moisture content of chickpeas was 16.1%, which was quite similar to the research conducted by Eissa AH et al. (2010), who found that moisture content ranged from 11.6% to 25.4%. Another researcher, Chelladurai et al. (2020), reported that the moisture content of lentils was 16%, consistent with the results of our study. Jan et al. (2019) investigated the moisture content of quinoa and found it to be 10%. To determine how fermentation affects the structure, quality, digestibility, and non-nutritive components of lentil proteins (Lens culinaris), red in digestibility, secondary protein structural components, sugars, and phenolic compounds were examined. Water kefir seeds were used for the fermentation process. At the end of the fermentation on day 5, the original pH of the unfermented lentil proteins dropped from 6.8 to pH 3.4. Over the 5 days of fermentation, protein digestibility improved from 76.4% to 84.1%. After two days of fermentation, the total phenolic content increased from 443.4 to 792.6 mg GAE/100g, with the sum of detected phenolic compounds from HPLC analysis reaching about 500 mg/100g, as reported by Alrosan et al. (2021). Therefore, all the results from previous investigations are in accordance with our study.
The protein content was evaluated, and the mean ratios of all three samples were analyzed carefully. The mean protein content in chickpeas, lentils, and quinoa was 20%, 21%, and 12.9%, respectively. Therefore, the protein content was higher in lentils compared to quinoa and chickpeas.
The mean results align with some previous findings. Boukid et al. (2021) investigated protein content and found it to be between 17% and 22%, which is comparable to our findings. Another researcher, Lake et al. (2021), reported that the protein content of lentils was 22%. A study by Bawachkar et al. (2021) reported a protein content of 14.43%, which is similar to the findings of this research.
Rachwa-Rosiak et al. (2015) explained that triglycerides make up the majority of neutral lipids, while lecithin makes up the majority of polar lipids. Chickpea grains contain a significant amount of important unsaturated fatty acids in their fat. Lentils, on the other hand, have a relatively low fat content. Fat content was analyzed through physicochemical characterization. The mean values for fat content in chickpeas, lentils, and quinoa were 7.7%, 1.2%, and 4.06%, respectively. The fat content in chickpeas is higher than in the other samples, while lentils have a lower fat content. A study by Ando et al. (2002) reported a fat content of 6.5% in quinoa, which is comparable to the fat content found in chickpeas in our study. Other researchers, Madurapperumage et al. (2021), found that the fat content in chickpeas ranged from 3.8% to 10.2%. Faris et al. (2013) reported that the fat content in lentils was 1.1%, which aligns with the findings of the current study.
The mean values of the results indicated that the crude fiber content in the chickpea sample was 12.36%, in lentils was 14%, and in quinoa was 14.1%. The fiber content in lentils and quinoa was higher compared to chickpeas. Overall, the results showed that all three samples have a rich amount of fiber. Singh et al. (2016) suggested that the fiber content in lentils was 15%, which is comparable to our results. An investigation by Wallace et al. (2016) reported the fiber content in chickpeas as 12%, and the fiber content in quinoa was 13.9%.
The results analyzed the ash content of all three samples. The mean ash content in chickpeas, lentils, and quinoa was 3.57%, 3.14%, and 3.13%, respectively. Ando et al. (2002) evaluated the ash content in quinoa as 3.0%. Researchers, including Ramdath et al. (2020), observed the ash content in lentils to be 3.13%. Another study conducted on chickpeas showed the ash content to be 3.54%, as reported by Khattak et al. (2021), as shown in Table 1.
Table 1. Proximate composition of chickpeas, lentils, and quinoa.
Proximate Testing | Chickpeas % | Lentils % | Quinoa % |
---|---|---|---|
Moisture | 16.1 ± 6.5A | 17 ± 0.81A | 8.75 ± 3.07B |
Protein | 20 ± 2.6A | 21 ± 1.05A | 12.9 ± 1.0B |
Fat | 7.7 ± 1.6A | 1.2 ± 1.7C | 4.6 ± 0.1B |
Ash | 3.57 ± 0.03A | 3.14 ± 0.01AB | 3.13 ± 0.23B |
Crude fiber | 12.3 ± 0.15B | 14.0 ± 1.12A | 14.1 ± 0.30A |
NFE | 40.33B | 43.66B | 56.7A |
Values are mean ± SD. Values within the same column for each parameter that have different letters are significantly different from each other (p ≤ 0. 05).
Quinoa is higher in quality protein and contains more nutrients than most other cereals. It is rich in several minerals, including manganese, phosphorus, copper, folate, iron, magnesium, and zinc, among others. Lentils are high in fiber and minerals, making them a healthy choice for managing heart health, blood pressure, and cholesterol levels. The calcium, magnesium, fiber, and other nutrients found in chickpeas and other legumes contribute to strong bones.
Table 2 shows the results of the different mineral content in the quinoa, lentils, and chickpeas samples. The mean values of mineral content evaluated in quinoa were 880 mg/kg for Ca, 98.4 mg/kg for Fe, 3625 mg/kg for Mg, 4064 mg/kg for P, 201 mg/kg for Na, 24.3 mg/kg for Zn, and 79.63 mg/kg for Cu. The mean mineral content in chickpeas was 1304 mg/100g for Ca, 4.61 mg/100g for Fe, 403 mg/100g for Mg, 253 mg/100g for P, 2133 mg/100g for Na, 16 mg/100g for Zn, and 3.33 mg/100g for Cu. The mean mineral content of lentils was evaluated as 58 mg/100g for Ca, 7.8 mg/100g for Fe, 125 mg/100g for Mg, 457 mg/100g for P, 8 mg/100g for Na, 5.3 mg/100g for Zn, and 1.16 mg/100g for Cu.
Table 2. Mineral composition of chickpeas, lentils, and quinoa (mg /100g ash a sample; on dry weight basis).
Minerals | Chickpeas mg/100g | Lentils mg/100g | Quinoa mg/kg |
---|---|---|---|
Calcium | 1304 ± 0.67A | 58 ± 0.45C | 880 ± 3.21B |
Iron | 4.61 ± 2.12C | 7.8 ± 1.15B | 98.4 ± 4.1A |
Magnesium | 403 ± 5.0B | 125 ± 4.3C | 3625 ± 4.0A |
Phosphorous | 253 ± 4.04C | 457 ± 4.58B | 4064 ± 7.02A |
Sodium | 2133 ± 2.34A | 8.12 ± 2.2C | 201 ± 3.6B |
Zinc | 16 ± 1.12B | 5.3 ± 0.45C | 24.3 ± 3.5A |
Copper | 3.33 ± 1.5B | 1.16 ± 0.70C | 79.63 ± 1.12A |
Values are presented as mean ± SD. Values within the same column for each parameter that have different letters are significantly different from each other (p ≤ 0. 05).
Similar outcomes have been reported by various studies. Nowak et al. (2015) conducted a study with results similar to those found for quinoa. Additionally, Wallace et al. (2016) had comparable outcomes for chickpeas. Faris et al. (2013) conducted a study in which the results for lentils were in accordance with our findings.
Vitamins are water-soluble compounds that are essential for human and animal health. They are categorized into two classes based on their solubility: lipophilic (fat-soluble) and hydrophilic (water-soluble). Vitamins have traditionally been among the most extensively used chemical agents to enhance the nutritional value of food products. Chickpeas contain a moderate amount of calories along with several vitamins and minerals. Vitamin E is a crucial component of quinoa because, at the cell membrane level, it acts as an antioxidant, preventing free radical damage to the fatty acids in cell membranes (Repo-Carrasco et al., 2003). Table 3 shows the main vitamins found in quinoa, chickpeas, and lentils. Higher amounts of ascorbic acid (67 mg/100g), thiamine (1.83 mg/100g), riboflavin (2.03 mg/100g), niacin (23.3 mg/100g), and α-tocopherol (29 mg/100g) are present in chickpeas compared to quinoa and lentils. Lentils are particularly high in folate (477.5 µg/100g).
Table 3. Vitamin E and B-complex of chickpeas, lentils, and quinoa (mg /100g).
Vitamins | Chickpeas mg/100g | Lentils mg/100g | Quinoa mg/100g |
---|---|---|---|
Ascorbic Acid (Vitamin C) | 67 ± 2.82A | 4.6 ± 0.70C | 8.5 ± 2.12B |
Thiamine (B1) | 1.83 ± 0.30A | 1.5 ± 0.36A | 0.38 ± 0.04B |
Riboflavin (B2) | 2.03 ± 0.41A | 0.36 ± 0.37B | 0.41 ± 0.03B |
Niacin (B3) | 23.3 ± 3.51A | 2.2 ± 2.51B | 1.05 ± 0.03C |
Folate | 405.5 µg/100g ± 6.36AB | 477.5 µg/100g± 9.19A | 395.5 µg/100g ± 7.77B |
α-tocopherol (Vit E) | 29 ± 3.6A | 0.53 ± 0.35C | 5.42 ± 0.05B |
Values are presented as mean ± SD. Values within the same column for each parameter that have different letters are significantly different from each other (p ≤ 0. 05).
Vega-Gálvez et al. (2010) evaluated the vitamin content in quinoa, which aligns with our results. They reported the following vitamin contents in quinoa: ascorbic acid (C) 4.0 mg/100g, α-tocopherol (E) 5.37 mg/100g, thiamine (B1) 0.38 mg/100g, riboflavin (B2) 0.39 mg/100g, and niacin (B3) 1.06 mg/100g. Wallace et al. (2016) observed the vitamin content in chickpeas, with the following results: ascorbic acid (C) 60 mg/100g, α-tocopherol (E) 30 mg/100g, thiamine (B1) 1.5 mg/100g, riboflavin (B2) 1.7 mg/100g, niacin (B3) 20 mg/100g, and folate 400 µg/100g. Takruri et al. (2013) also concluded similar results for lentils.
Lentils, chickpeas, and quinoa are significant sources of essential amino acids. Like most other plant-based protein sources, chickpeas do not provide a complete protein, as they lack all nine essential amino acids. Chickpeas are particularly high in arginine and lysine but low in methionine and cysteine, which are sulfur-containing amino acids. Lentils contain essential amino acids such as isoleucine and lysine, but are generally low in methionine and cysteine. Despite being a small seed, quinoa is rich in protein. Unlike some other plant proteins, quinoa is considered a complete protein, meaning it contains all nine essential amino acids that the human body cannot produce on its own.
Table 4 shows the results of all amino acids in the three grains. The total amount of amino acids in chickpeas is 38.6g/100g. The mean values are presented, with chickpeas having the highest amounts of leucine (7.13g/100g) and phenylalanine (5.7g/100g). The total amino acid content in lentils is 37.89g/100g, with the highest amounts of leucine (7.2g/100g) and lysine (7.26g/100g). Quinoa contains the richest amount of amino acid leucine (7.03g/100g), and the total amino acids in quinoa amount to 34.93g/100g.
Table 4. Amino acid content of chickpeas, lentils, and quinoa (mg /100g).
Amino acids | Chickpeas g/100g | Lentils g/100g | Quinoag/100g |
---|---|---|---|
Phenylalanine | 5.7 ± 0.26A | 4.5 ± 0.40B | 4.2 ± 0.288B |
Leucine | 7.1 ± 0.65 | 7.2 ± 0.65 | 7.03 ± 0.68 |
Isoleucine | 4.6 ± 0.30A | 4.4 ± 0.41AB | 3.9 ± 0.90B |
Lysine | 6.4 ± 0.30B | 7.2 ± 0.25A | 4.3 ± 0.55C |
Methionine | 1.3 ± 0.20B | 0.39 ± 0.44C | 1.6 ± 0.2A |
Valine | 4.23 ± 0.25C | 5.3 ± 0.32A | 4.40 ± 0.40B |
Tyrosine | 2.8 ± 0.30B | 3.10 ± 0.26A | 2.20 ± 0.35B |
Histidine | 3.1 ± 0.31A | 2.8 ± 0.55B | 2.9 ± 0.20B |
Threonine | 3.2 ± 0.41AB | 3.1 ± 0.45B | 3.8 ± 0.30A |
Values are presented as mean ± SD. Values within the same column for each parameter that have different letters are significantly different from each other (p ≤ 0. 05).
Miranda et al. (2012) reported similar findings regarding the amino acids in quinoa grains, with the highest quantity of leucine being 6.8g/100g. Samaranayaka et al. (2017) also found results that align with our study. The findings for chickpeas and lentils in the current study are consistent with previous research.
Ganesan et al. (2017) explained that lentils have the highest total phenolic concentration. Lentils, rich in polyphenols, offer potential health benefits as alternative and complementary treatments, including antioxidant, antiviral, cardioprotective, antibacterial, nephroprotective, antifungal, anti-inflammatory, and antidiabetic properties. Chickpeas were also investigated for their phenolic profiles, though they contain fewer phenolic acids compared to other grains. Quinoa, on the other hand, had the highest concentration of bound phenolics. A higher phenolic content in quinoa was associated with stronger antioxidant properties, as well as the inhibition of pancreatic lipase and beta-glucosidase activities.
The mean values of all phenolic acids are presented in Table 5. The highest concentration of phenolic acids is found in quinoa grains, while the lowest is found in chickpeas, as shown in the table. Liu et al. (2020) reported similar results for lentils in line with our study. Similar findings for quinoa were observed in a study by Repo-Carrasco-Valencia et al. (2010). Quintero-Soto et al. (2018) also reported similar results for chickpeas.
Table 5. Phenolic acids in chickpeas, lentils, and quinoa (µg/100g).
Phenolic acids | Chickpeas µg/100g | Lentils µg/100g | Quinoa µg/100g |
---|---|---|---|
Ferulic acid | 8.52 ± 0.40C | 12.48 ± 0.03B | 15.36 ± 0.15A |
p-Coumaric acid | 2.5 ± 0.4C | 13.7 ± 0.19A | 6.45 ± 0.05B |
p-OH-benzoic acid | 4.86 ± 0.20A | 1.55 ± 0.05C | 3.73 ± 0.19B |
Vanillic acid | 0.48 ± 0.03C | 6.17 ± 0.01B | 8.95 ± 0.03A |
Protocatechuic | 1.8 ± 0.025B | 5.89 ± 0.061A | 1.92 ± 0.03B |
Values are presented as mean ± SD. Values within the same column for each parameter that have different letters are significantly different from each other (p ≤ 0. 05).
Antioxidants and phenolic compounds are helpful in improving human health (Abd-El Ghany et al., 2023; Tahir et al., 2024; Rueangsri et al., 2025). These antioxidants have a positive effect on nutrient digestibility (Hegazy et al., 2023). Wang et al. (2021) explained that chickpeas contain various beneficial and abundant compounds. The bioactivities of the chickpea plant have been observed in several areas of the plant. Lentil (Lens culinaris; Fabaceae) is high in polyphenol compounds that possess a variety of health-promoting characteristics. Lentils, being high in polyphenols, may have a positive effect on human well-being. Polyphenols, which include flavonoids, phenolic acids, and tannins, are secondary plant metabolites with bioactive properties that contribute to a wide range of physiological benefits, including anti-carcinogenic, antimicrobial, anti-inflammatory, antioxidant, and antitumor effects, according to Benavente-Garca et al. (2008).
Phenolic compounds have antioxidant effect (Ramaiyulis et al., 2023). The total phenolic content of chickpeas was 124.33 mg/100g, lentils 28 mg/100g, and quinoa 54.66 mg/100g. The highest phenolic content is present in chickpeas among all. The mean result for the total phenolic content (TPC) of chickpeas was 124.33 mg/100g. León-López et al. (2020) obtained similar results in their study, evaluating the total phenolic content at 128.3 mg/100g. Kalogeropoulos et al. (2010) discussed the total phenolic content of lentils in their research and found similar results, with a content of 26 mg/100g. On the other hand, a study by Repo-Carrasco-Valencia et al. (2010) investigated the total phenolic content in quinoa, reporting values ranging from 16.8 to 59.7 mg/100g.
Flavonoids are group of antioxidant compounds found in many different plants, and they have diverse biological activities (Tuyen et al., 2025). Flavonoids have antioxidant, anti-inflammatory, anti-tumor, and blood clot-inhibiting properties. Each of these traits supports overall health (Anwar et al., 2023). On the other hand, the results showed that the mean flavonoid content in chickpeas was 27.36 mg/100g, in lentils 151.66 mg/100g, and in quinoa 126.66 mg/100g. The highest flavonoid content was observed in lentils. Similar to the total phenolic content, total flavonoids have been studied in many researches. The mean flavonoid content in chickpeas was 27.36 mg/100g. León-López et al. (2020) reported similar findings, evaluating the flavonoid content in chickpeas at 27.6 mg/100g. Xu et al. (2011) also found a high amount of flavonoids in their research, estimating the flavonoid content in lentils at 221 mg/100g, which aligns with our study.
Quercetin being a notable polyphenol exhibit strong antioxidant and antibacterial potential (Ahmad et al., 2024). As shown in Table 7, the amount of quercetin was highest in quinoa at 19.83 mg/100g, followed by lentils at 1.77 mg/100g, and the lowest amount was found in chickpeas at 0.89 mg/100g. Hirose et al. (2010) reported the total quercetin content in quinoa as 22.5 mg/100g, which aligns with our findings. Han et al. (2008) evaluated the quercetin content in lentils as 1.78 mg/100g and in chickpeas as 0.84 mg/100g.
Kaempferol is a flavonoid found naturally in a variety of plants and plant-derived foods. It is known to reduce the risk of chronic diseases, particularly cancer. As shown in Table 6, the kaempferol content in chickpeas was 48.9 mg/100g, in lentils was 50.5 mg/100g, and in quinoa was 43.23 mg/100g. Díaz-Batalla et al. (2006) investigated that the kaempferol content in lentils was 52.3 mg/100g, which aligns with our study. Another researcher, Lee et al. (2018), conducted a study in which he reported that the kaempferol content in quinoa was 45.12 mg/100g.
Table 6. Bioactive components of chickpeas, lentils, and quinoa.
Bioactive contents | Flavonoids mg/100g | TPC mg/100g | Quercetin mg/100g | Kaempferol mg/100g |
---|---|---|---|---|
Chickpeas | 27.36 ± 1.66C | 124.33 ± 3.53A | 0.89 ± 2.753D | 48.9 ± 1.67B |
Lentils | 151.66 ± 2.14A | 28 ± 1.15C | 1.77 ± 0.049D | 50.5 ± 2.23B |
Quinoa | 126.66 ± 3.51A | 54.66 ± 2.41B | 19.83 ± 0.045D | 43.23 ± 3.34C |
Values are presented as mean ± SD. Values within the same column for each parameter that have different letters are significantly different from each other (p ≤ 0. 05).
Phytosterols are lipophilic molecules that resemble cholesterol in structure. According to intervention trials, epidemiological evidence, and meta-analyses, phytosterols have a significant impact on lowering cholesterol levels in individuals (Graf et al., 2010). Phytosterols reduce blood cholesterol by competing with cholesterol for absorption in the intestine and inhibiting the formation of atherogenic lipoproteins in both the liver and intestines (Ho and Pal, 2005). As shown in Table 8, the phytosterol content in chickpeas (204.6 mg/100g) is higher than in the other grains. Lentils (154 mg/100g) and quinoa (116.3 mg/100g) have lower amounts of phytosterols and their constituents.
The phytosterol content in chickpeas and lentils was found to be 204.6 mg/100g and 154 mg/100g, respectively. These results were similar to those evaluated by Singh et al. (2017), who reported phytosterol content in chickpeas (205 mg/100g) and lentils (158 mg/100g). Navruz-Varli et al. (2016) suggested that quinoa contained 118 mg/100g of phytosterol content. These researchers also analyzed other phytosterol constituents. Ryan et al. (2007) reported that the β-sitosterol content in chickpeas and lentils was 159.8 mg/100g and 123.4 mg/100g, respectively, as shown in Table 7.
Table 7. Phytosterol components of chickpeas, lentils, and quinoa.
Phytosterols | Chickpeas mg/100g | Lentils mg/100g | Quinoa mg/100g |
---|---|---|---|
Phytosterol | 204.6 ± 3.51A | 154.0 ± 4.58B | 116.3 ± 3.78C |
β-sitosterol | 154.2 ± 4.81A | 126.8 ± 2.98B | 66.9 ± 2.81C |
Campesterol | 19.46 ± 2.24A | 16.66 ± 1.52B | 17.53 ± 1.74AB |
Stigmasterol | 21.3 ± 2.2A | 18.26 ± 2.1B | 4.50 ± 1.2C |
Δ5-avenasterol | 3.46 ± 0.13A | 2.28 ± 0.064AB | 2.16 ± 0.04B |
Values are presented as mean ± SD. Values within the same column for each parameter that have different letters are significantly different from each other (p ≤ 0. 05).
The findings of this scientific study indicate that all three grains—chickpeas, lentils, and quinoa—are rich in nutrients that offer significant health benefits. These grains serve as excellent substitutes for animal proteins and are also high in other valuable functional properties, such as total flavonoid and total phenolic content. Moreover, lentils, quinoa, and chickpeas can be used as food fusion ingredients and are promising options for designing functional foods, thanks to their bioactive compounds and nutraceutical potential. This type of research is currently unexplored in Pakistan, as no previous study of this magnitude has been conducted. This work represents a significant step forward for the processing sector, as it aims to isolate and extract bioactive substances with nutritional relevance that can contribute to reducing the prevalence of chronic diseases. Ultimately, this study could open the door for further research into the phytochemicals with nutraceutical value present in these grains.
The authors would like to express their gratitude to Government College University for providing the literature collection facilities. The authors thank Researchers Supporting Project number (RSPD2025R641), King Saud University, Riyadh, Saudi Arabia for funding this research.
The datasets generated used and/or analyzed during the current study available from the corresponding author on reasonable request.
All the co-authors are willing to participate in this manuscript.
All authors are willing for publication of this manuscript
Sharafat Ali Anjum: original draft, methodology equal; Muhammad Umair Arshad: supervision, draft writing and reviewing equal; Ali Imran: formal analysis and reviewing equal; Hamad Rafique and Tawfiq Alsulami: reviewing, editing and submission.
The authors declare that they have no conflict of interest.
The authors thank Researchers Supporting Project number (RSPD2025R641), King Saud University, Riyadh, Saudi Arabia for funding this research.
AACC. (2000). Approved methods of the American Association of Cereal Chemists (10th ed.). The American Association of Cereal Chemists, Inc.
Abd-El Ghany, F. T., Morsy, S. H., Hassan, H. M. A., & Samy, A. (2023). Evaluation of olive leaves and pomace extracts in growing rabbit diets on productive performance, nutrient digestibility, carcass characteristics, antioxidant status and economic efficiency. International Journal of Veterinary Science, 12(1), 37–44.
Ahmad, H. M., Jabeen, H., Ahmad, S., & Syed, A. (2024). Nutritional and sensory evaluation of gluten-free muffins prepared by using maize, sorghum, and chickpea. Agrobiological Records, 17, 58–68. 10.47278/journal.abr/2024.023
Ahmad, S., Aqib, A. I., Ghafoor, M., Shoaib, M., ul Haq, S., Ataya, F. S., & Jianxi, L. (2024). Drug resistance modulation of dairy MRSA through Berberine. Artesunate and Quercetin in Combination with β-Lactams, Pakistan Veterinary Journal, 44(2), 510–516. 10.29261/pakvetj/2024.171
Akpinar, D., Mercan, T., Demir, H., Ozdemir, S., Demir, C., & Kavak, S. (2023). Protective Effects of Thymoquinone on Doxorubicin-induced Lipid Peroxidation and Antioxidant Enzyme Levels in Rat Peripheral Tissues. Pakistan Veterinary Journal, 43(4), 651–658. 10.29261/pakvetj/2023.070
Al-Gheffari, H. K., Aljahdali, S. M., Albalawi, M., Obidan, A., Binothman, N., Aljadani, M.,... & Bouqellah, N. A. (2024). Mycogenic Zinc Nanoparticles with Antimicrobial, Antioxidant, Antiviral, Anticancer and anti-Alzheimer Activities Mitigate the Aluminium Toxicity in Mice: Effects on Liver, Kidney, and Brain Health and Growth Performance. Pakistan Veterinary Journal, 44(3), 763–775. 10.29261/pakvetj/2024.252
Al-Saeed, F. A., Naz, S., Saeed, M. H., Hussain, R., Iqbal, S., Mustafa Chatha, A. M., ... & Akram, R. (2023). Oxidative Stress, Antioxidant Enzymes, Genotoxicity and Histopathological Profile in Oreochromis niloticus exposed to Lufenuron. Pakistan Veterinary Journal, 43(1), 160–166. 10.29261/pakvetj/2023.012
Alrosan, M., Tan, T. C., Mat Easa, A., Gammoh, S., & Alu’datt, M. H. (2021). Effects of fermentation on the quality, structure, and nonnutritive contents of lentil (Lens culinaris) proteins. Journal of Food Quality, 2021, 1–7. 10.1155/2021/5556450
American Association of Cereal Chemists. (2000). Approved methods of the American Association of Cereal Chemists. American Association of Cereal Chemists.
Amrozi, A., Hayanti, S. Y., Sholikin, M. M., Pardede, B. P., Herdis, H., Lase, J. A., ... & Jayanegara, A. (2024). Antioxidant Glutathione Supplementation in Semen Extenders and its Effect on the Quality of Cryopreserved Bull Sperm: A Meta-Analysis. Pakistan Veterinary Journal, 44(4), 988–997. 10.29261/pakvetj/2024.266
Ando, H., Chen, Y. C., Tang, H., Shimizu, M., Watanabe, K., & Mitsunaga, T. (2002). Food components in fractions of quinoa seed. Food Science and Technology Research, 8(1), 80–84. 10.3136/fstr.8.80
Anwar, A., Ali, E., Nisar, W., Ashraf, S., Javed, N., Anwar, L., Zulfiqar, A., Nazir, M.A. & Tahir, F. (2024). Development and quality evaluation of functional carbonated pomegranate orange nectar. Agrobiological Records, 15, 52–58. 10.47278/journal.abr/2023.048
AOAC. (2000). Official methods of analysis (15th ed.). Association of Analytical Chemists.
Balgoon, M. J., & Alghamdi, A. M. (2024). Biochemical Assessment of Boswellic Acid Enrich Frankincense Extract and its Antioxidant, Antibacterial, Anticancer and Anti-inflammatoryPotential in Ameliorating the Glycerol-Toxicity in Rats. Pakistan Veterinary Journal, 44(4), 1023–1032. 10.29261/pakvetj/2024.290
Bawachkar, R. R., More, D. R., & Praveen, B. R. (2021). Quinoa bar a novel food: A review. SP-10(6), 82–86.
Benavente-García, O., & Castillo, J. (2008). Update on uses and properties of citrus flavonoids: New findings in anticancer, cardiovascular, and anti-inflammatory activity. Journal of Agricultural and Food Chemistry, 56(18), 6185–6205. 10.1021/jf8006568
Biel, W., Bobko, K., & Maciorowski, R. (2009). Chemical composition and nutritive value of husked and naked oats grain. Journal of Cereal Science, 49(3), 413–418. 10.1016/j.jcs.2009.01.009
Boukid, F. (2021). Chickpea (Cicer arietinum L.) protein as a prospective plant-based ingredient: A review. International Journal of Food Science & Technology, 56(11), 5435–44. 10.1111/ijfs.15046
Boye, J., Zare, F., & Pletch, A. (2010). Pulse proteins: Processing, characterization, functional properties, and applications in food and feed. Food Research International, 43(2), 414–431. 10.1016/j.foodres.2009.09.003
Brummer, Y., Kaviani, M., & Tosh, S. M. (2015). Structural and functional characteristics of dietary fibre in beans, lentils, peas and chickpeas. Food Research International, 67, 117–125. 10.1016/j.foodres.2014.11.009
Chelladurai, V., & Erkinbaev, C. (2020). Lentils. In Pulses 2020 (pp. 129–143). Springer, Cham. 10.1007/978-3-030-41376-7_8
Díaz-Batalla L., Widholm J. M., Fahey G. C., Castaño-Tostado E., Paredes-López O. (2006). Chemical components with health implications in wild and cultivated Mexican common bean seeds (Phaseolus vulgaris L.). Journal of Agricultural and Food Chemistry. 2006 Mar 22;54(6), 2045–52. 10.1021/jf051706l
Dmitrienko, S. G., Kudrinskaya, V. A., & Apyari, V. V. (2012). Methods of extraction, preconcentration, and determination of quercetin. Journal of Analytical Chemistry, 67(4), 299–311. 10.1134/S106193481204003X
Elzaiat, M. A., Mandour, A. S., Youssef, M. A., Wafa, H. A., Aljahdali, S. M., Shakak, A. O., ... & Heakel, R. M. (2024). Biochemical and Molecular Characterization of Five Basil Cultivars Extract for Enhancing the Antioxidant, Antiviral, Anticancer, Antibacterial and Antifungal Activities. Pakistan Veterinary Journal, 44(4), 1105–1119. 10.29261/pakvetj/2024.279
Faris, M. E., Takruri, H. R., & Issa, A. Y. (2013). Role of lentils (Lens culinaris L.) in human health and nutrition: A review. Mediterranean Journal of Nutrition and Metabolism, 6(1), 3–16. 10.3233/s12349-012-0109-8
Garg, P., & Brar, J. K. (2017). Development and organoleptic evaluation of nutritious bars by using defatted peanut flour, roasted soybean seeds for gym trainees. Chemical Science and Review Letters, 6(23), 2051–2057.
Graf B. L., Rojas-Silva P., Rojo L. E., Delatorre-Herrera J., Baldeón M. E., Raskin I. (2015). Innovations in health value and functional food development of quinoa (Chenopodium quinoa Willd.). Comprehensive Reviews in Food Science and Food Safety., 14(4), 431–45. 10.1111/1541-4337.12135
Grasso, N., Lynch, N. L., Arendt, E. K., & O’Mahony, J. A. (2022). Chickpea protein ingredients: A review of composition, functionality, and applications. Comprehensive Reviews in Food Science and Food Safety, 21(1), 435–452. 10.1111/1541-4337.12878
Han H., Baik B. K. (2008). Antioxidant activity and phenolic content of lentils (Lens culinaris), chickpeas (Cicer arietinum L.), peas (Pisum sativum L.) and soybeans (Glycine max), and their quantitative changes during processing. International Journal of Food Science & Technology., 43(11), 1971–8. 10.1111/j.1365-2621.2008.01800.x
Hegazy, S. A., Abd Elmawla, S. M., Khorshed, M. M., & Salem, F. A. (2023). Productive and immunological performance of small ruminants offered some medicinal plants as feed additives. International Journal of Veterinary Science, 12(1), 120–125. 10.47278/journal.ijvs/2022.163
Hirose Y., Fujita T., Ishii T., & Ueno N. (2010). Antioxidative properties and flavonoid composition of Chenopodium quinoa seeds cultivated in Japan. Food Chemistry., 2010 119(4), 1300–1306. 10.1016/j.foodchem.2009.09.008
Ho S.S., & Pal S. (2005). Margarine phytosterols decrease the secretion of atherogenic lipoproteins from HepG2 liver and Caco2 intestinal cells. Atherosclerosis., 2005 Sep 1;182(1), 29–36. 10.1016/j.atherosclerosis.2005.01.031
Jan, K.N., Panesar, P.S., & Singh, S. (2019). Effect of moisture content on the physical and mechanical properties of quinoa seeds. International Agrophysics, 33(1), 107–115. 10.31545/intagr/104374
Jukanti, A.K., Gaur, P.M., Gowda, C.L., & Chibbar, R. N. (2012). Nutritional quality and health benefits of chickpea (Cicer arietinum L.): A review. British Journal of Nutrition, 108(S1), S11–S26. 10.1017/S0007114512000797
Kalogeropoulos N., Chiou A., Ioannou M., Karathanos V. T., Hassapidou M., & Andrikopoulos N.K. (2010). Nutritional evaluation and bioactive microconstituents (phytosterols, tocopherols, polyphenols, triterpenic acids) in cooked dry legumes usually consumed in the Mediterranean countries. Food Chemistry, 121(3), Food Chem 121:682–690. 10.1016/j.foodchem.2010.01.005
Kaur, R., & Prasad, K. (2021). Technological, processing and nutritional aspects of chickpea (Cicer arietinum)–A review. Trends in Food Science & Technology, 109, 448–463. 10.1016/j.tifs.2021.01.044
Kaur, R., Ahluwalia, P., Sachdev, P.A., & Kaur, A. (2018). A development of gluten-free cereal bar for gluten intolerant population by using quinoa as major ingredient. Journal of Food Science and Technology, 55(9), 3584–3591. 10.1007/s13197-018-3284-x
Khan, S. R., Iqbal, R., Hussain, R., Ali, M., Khalid, M., Nazish, N., & Naqvi, S. S. (2024). Broccoli partially lowers oxidative stress, histopathological lesions and enhances antioxidant profile of mono sex Tilapia exposed to zinc oxide nanoparticles. Pakistan Veterinary Journal, 44(2), 306–313. 10.29261/pakvetj/2024.159
Khattak, A.M., Ullah, S., Anjum, F., Shah, H.U., & Alam, S. (2021). Proximate composition and mineral content of selected chickpea cultivars. Sarhad Journal of Agriculture, 37(2), 683–689. 10.17582/journal.sja/2021/37.2.683.689
Lagarda, M. J., García-Llatas, G., & Farré, R. (2006). Analysis of phytosterols in foods. Journal of Pharmaceutical and Biomedical Analysis, 41(5), 1486–1496. 10.1016/j.jpba.2006.02.052
Lake, L., Kutchartt, D. G., Calderini, D. F., & Sadras, V. O. (2021). Critical developmental period for grain yield and grain protein concentration in lentil. Field Crops Research, 270, 108203. 10.1016/j.fcr.2021.108203
Lebiedzińska, A., Marszałł, M. L., Kuta, J., & Szefer, P. (2007). Reversed-phase high-performance liquid chromatography method with coulometric electrochemical and ultraviolet detection for the quantification of vitamins B1 (thiamine), B6 (pyridoxamine, pyridoxal, and pyridoxine) and B12 in animal and plant foods. Journal of Chromatography A, 1173(1–2), 71–80. 10.1016/j.chroma.2007.09.072
Lee M. J., & Sim K. H. (2018). Nutritional value and the kaempferol and quercetin contents of quinoa (Chenopodium quinoa Willd.) from different regions. Korean Journal of Food Science and Technology, 50(6), 680–687.
León-López, L., Escobar-Zúñiga, Y., Salazar-Salas, N.Y., Mora Rochín, S., Cuevas-Rodríguez, E.O., Reyes-Moreno, C., & Milán-Carrillo, J. (2020). Improving polyphenolic compounds: Antioxidant activity in chickpea sprouts through elicitation with hydrogen peroxide. Foods, 9(12), 1791. 10.3390/foods9121791
Liu, Y., Ragaee, S., Marcone, M.F., & Abdel-Aal, E.S. (2020). Composition of phenolic acids and antioxidant properties of selected pulses cooked with different heating conditions. Foods, 9(7), 908. 10.3390/foods9070908
Madurapperumage, A., Tang, L., Thavarajah, P., Bridges, W., Shipe, E., Vandemark, G., & Thavarajah, D. (2021). Chickpea (Cicer arietinum L.) as a source of essential fatty acids–A biofortification approach. Frontiers in Plant Science, 12, 2204. 10.3389/fpls.2021.734980
Miliauskas, G., Venskutonis, P. R., & Van Beek, T. A. (2004). Screening of radical scavenging activity of some medicinal and aromatic plant extracts. Food Chemistry, 5(2), 231–237. 10.1016/j.foodchem.2003.05.007
Miranda, M., Vega-Gálvez, A., Martinez, E., López, J., Rodríguez, M.J., Henríquez, K., & Fuentes, F. (2012). Genetic diversity and comparison of physicochemical and nutritional characteristics of six quinoa (Chenopodium quinoa Willd.) genotypes cultivated in Chile. Food Science and Technology, 32(4), 835–843. 10.1590/S0101-20612012005000114
Navruz-Varli S., & Sanlier N. (2016). Nutritional and health benefits of quinoa (Chenopodium quinoa Willd.). Journal of Cereal Science. 2016 May 1;69, 371–6. 10.1016/j.jcs.2016.05.004
Nongalleima, K., Ajungla, T., & Singh, C.B. (2017). Photochemical, total phenolic, total flavonoid, and total flavonol content estimation in Citrus macroptera Montruz. Journal of Medicinal Plants, 5(3), 114–118.
Nowak, V., Du, J., & Charrondière, U.R. (2015). Assessment of the nutritional composition of quinoa (Chenopodium quinoa Willd.). Food Chemistry, 193, 47–54. 10.1016/j.foodchem.2015.02.111
Quintero-Soto, M.F., Saracho-Peña, A.G., Chavez-Ontiveros, J., Garzon-Tiznado, J.A., Pineda-Hidalgo, K.V., Delgado-Vargas, F., & Lopez-Valenzuela, J.A. (2018). Phenolic profiles and their contribution to the antioxidant activity of selected chickpea genotypes from Mexico and ICRISAT collections. Plant Foods for Human Nutrition, 73(2), 122–129. 10.1007/s11130-018-0661-6
Rachwa-Rosiak, D., Nebesny, E., & Budryn, G. (2015). Chickpeas—Composition, nutritional value, health benefits, application to bread and snacks: A review. Critical Reviews in Food Science and Nutrition, 55(8), 1137–1145. 10.1080/10408398.2012.687418
Rakha, S.I., Elmetwally, M.A., Ali, H.E.S., Balboula, A.Z., Mahmoud, A.M., & Zaabel, S.M. (2023). Lycopene improves maturation rate and antioxidant status of in vitro matured mouse oocytes. International Journal of Veterinary Science, 12(2), 248–254. 10.47278/journal.ijvs/2022.183
Ramaiyulis, R., Mairizal, M., Salvia, S., Fati, N., & Malvin, T. (2023). Effects of dietary catechin uncaria gambir extract on growth performance, carcass characteristics, plasma lipids, antioxidant activity and nutrient digestibility in broiler chickens. International Journal of Veterinary Science, 12(2), 169–174. 10.1016/j.psj.2024.104176
Ramdath, D.D., Lu, Z.H., Maharaj, P.L., Winberg, J., Brummer, Y., & Hawke, A. (2020). Proximate analysis and nutritional evaluation of twenty Canadian lentils by principal component and cluster analyses. Foods, 9(2), 175. 10.3390/foods9020175
Rashid, M.H.U., Mehwish, Wahab, H., Ahmad, S., Ali, L., Ahmad, N., Ali, M., & Fazal, H. (2024). Unraveling the combinational approach for the antibacterial efficacy against infectious pathogens using the herbal extracts of the leaves of Dodonaea viscosa and fruits of Rubus fruticosus. Agrobiological Records, 16, 57–66. 10.47278/journal.abr/2024.012
Repo-Carrasco, R., Espinoza, C., & Jacobsen, S.E. (2003). Nutritional value and use of the Andean crops quinoa (Chenopodium quinoa) and kaniwa (Chenopodium pallidicaule). Food Reviews International, 19(3), 179–189. 10.1081/FRI-1200188843
Repo-Carrasco-Valencia, R., Hellström, J.K., Pihlava, J.M., & Mattila, P.H. (2010). Flavonoids and other phenolic compounds in Andean indigenous grains: Quinoa (Chenopodium quinoa), kañiwa (Chenopodium pallidicaule) and kiwicha (Amaranthus caudatus). Food Chemistry, 120(1), 128–133. 10.1016/j.foodchem.2009.09.087
Rueangsri, K., Lasunon, P., Kwantrairat, S., & Taweejun, N. (2025). Effect of Ultrasound-assisted Aqueous Two-phase Extraction on Phenolic Compounds from Nymphaea Pubescens Willd., and its Antioxidant and Antimicrobial Properties. International Journal of Agriculture and Biosciences, 14(1), 1–10. 10.47278/journal.ijab/2024.187
Ryan E., Galvin K., O’Connor T.P., Maguire A.R., O’Brien N.M. (2007). Phytosterol, squalene, tocopherol content and fatty acid profile of selected seeds, grains, and legumes. Plant Foods for Human Nutrition. 2007 Sep;62(3):85–91. 10.1007/s11130-007-0046-8
Saadullah, M., Ahmed, I., Kashif, M., Rafique, M. K., Yousaf, M. S., Meraj, M. T., ... & Ur Rehman, T. (2024). Antioxidant Status and Biochemical Alterations in Chlamydia abortus and Coxiella burnetii Infected Small Ruminants. Pakistan Veterinary Journal, 44(4), 1153–1160. 10.29261/pakvetj/2024.283
Samaranayaka, A. (2017). Lentil: Revival of poor man’s meat. In sustainable protein sources (pp. 185–196). Academic Press. 10.1016/B978-0-12-802778-3.00011-1
Silva, I.Q., Oliveira, B.C.F., Lopes, A.S., & Pena, R.S. (2009). Obtenção de barra de cereais adicionada do resíduo da indústria de maracujá. Alimentos e Nutrição, 20(2), 321–329.
Singh B., Singh J. P., Shevkani K., Singh N., Kaur A. (2017). Bioactive constituents in pulses and their health benefits. Journal of Food Science and Technology., 54(4), 858–70. 10.1007/s13197-016-2391-9
Singh, J., Srivastava, R.P., Gupta, S., Basu, P.S., & Kumar, J. (2016). Genetic variability for vitamin B9 and total dietary fiber in lentil (Lens culinaris L.) cultivars. International Journal of Food Properties, 19(4), 936–943. 10.1080/10942912.2015.1048353
Summo, C., De Angelis, D., Ricciardi, L., Caponio, F., Lotti, C., Pavan, S., & Pasqualone, A. (2019). Nutritional, physico-chemical and functional characterization of a global chickpea collection. Journal of Food Composition and Analysis, 84, 103306. 10.1016/j.jfca.2019.103306
Tahir, F., Fatima, F., Fatima, R., & Ali, E. (2024). Fruit peel extracted polyphenols through ultrasonic assisted extraction: A review. Agrobiological Records, 15, 1–12. 10.47278/journal.abr/2023.043
Takruri, H.R., & Issa, A.Y. (2013). Role of lentils (Lens culinaris L.) in human health and nutrition: A review. Mediterranean Journal of Nutrition and Metabolism, 6(1), 3–16. 10.3233/s12349-012-0109-8
Tosh, S.M., & Yada, S. (2010). Dietary fibres in pulse seeds and fractions: Characterization, functional attributes, and applications. Food Research International, 43(2), 450–460. 10.1016/j.foodres.2009.09.005
Tuyen, V. T. X., Khai, T. V., Diem, N. T. T., Xuan, L. N. T., & Tan, N. D. (2025). Effect of supplied salt concentrations in the nutrient solution during hydroponic production on phytochemicals and antioxidant activity of ice plants (Mesembryanthemum crystallinum L.). International Journal of Agriculture and Biosciences, 14, 59–67. 10.47278/journal.ijab/2024.190
Vega-Gálvez, A.V., Miranda, M., Vergara, J., Uribe, E., & Puente, L. (2010). Nutrition facts and functional potential of quinoa (Chenopodium quinoa Willd.), an ancient Andean grain: A review. Journal of the Science of Food and Agriculture, 90(15), 2541–2547. 10.1002/jsfa.4158
Vega-Gálvez, A., Miranda, M., Vergara, J., Uribe, E., Puente, L., & Martínez, E. A. (2010). Nutrition facts and functional potential of quinoa (Chenopodium quinoa Willd.), an ancient Andean grain: A review. Journal of the Science of Food and Agriculture, 90(15), 2541–2547. 10.1002/jsfa.4158
Wallace, T.C., Murray, R., & Zelman, K.M. (2016). The nutritional value and health benefits of chickpeas and hummus. Nutrients, 8(12), 766. 10.3390/nu8120766
Wang, J., Li, Y., Li, A., Liu, R.H., Gao, X., Li, D., Kou, X., & Xue, Z. (2021). Nutritional constituent and health benefits of chickpea (Cicer arietinum L.): A review. Food Research International, 150, 110790. 10.1016/j.foodres.2021.110790
Xu, B., Chang S. K. C. (2011) Phenolic substance characterization and chemical and cell-based antioxidant activities of 11 lentils grown in the Northern United States. Journal of Agricultural and Food Chemistry, 58, 1509–1517. 10.1021/jf903532y
Yiğit, F., Esener, O., Unali, M., Aktaş, A., Sari, A., Güngör, Z., ... & Armutak, E. (2024). Evaluation of Antioxidant Potential of Noni (Morinda citrifolia L.) Fruit Juice against 3-Methyl 4-nitrophenol (PNMC)-Induced Acute Nephrotoxicity in Rats. Pakistan Veterinary Journal, 44(2), 526–534. 10.29261/pakvetj/2024.201