Antioxidant Effect and Characterization of Metabolites in Citrullus lanatus Seed Extract
DOI:
https://doi.org/10.54987/jobimb.v13i2.1158Keywords:
Watermelon, Antioxidant activity, Bioactive profiling, GC-MS, PhenolicsAbstract
Watermelon (Citrullus lanatus) seeds contain a complex matrix of phenolic and lipid derived metabolites capable of modulating oxidative processes at the molecular level. In this study, the antioxidant effect of C. lanatus seed extract was evaluated via in vitro and in vivo assays, and the bioactive were characterized using FTIR and GC–MS. The seeds exhibited a higher total phenolic content (584 ± 26.1 mg/g) than flavonoid content (14.04 ± 0.20 mg/g), indicating a phenolic rich antioxidant system. DPPH assays showed strong radical scavenging activity, with the aqueous fraction displaying the lowest IC₅₀ (1.65 ± 0.13 µg/mL) compared to other fractions, while total antioxidant capacity was highest in the ethyl acetate (355.50 ± 5.20 µg/mL) and n hexane (316.30 ± 0.76 µg/mL) fractions. FTIR analysis revealed characteristic O–H stretching (3286 cm⁻¹), C–H bending (1400–1346 cm⁻¹), and C–O/C–N stretching (1033 cm⁻¹), confirming the presence of alcohols, water, and complex organic functional groups associated with redox activity. GC–MS profiling of the aqueous fraction identified several antioxidant associated metabolites, including dodecanoic acid ethyl ester, decanoic acid ethyl ester, tetradecanoic acid ethyl ester, trilaurin, oleic acid (two peaks), and dodecanoic acid hydroxy ethyl ester. Evaluating the antioxidant activity in vivo demonstrated modulation of oxidative stress biomarkers, with extract treated groups showing reductions in malondialdehyde (e.g., 0.47 ± 0.085 nmol/mg at 250 mg/kg) relative to diabetic controls (0.79 ± 0.038 nmol/mg), alongside dose dependent alterations in catalase and superoxide dismutase activities. These biochemical shifts indicate attenuation of lipid peroxidation and partial restoration of endogenous antioxidant defenses. These findings demonstrate that C. lanatus seeds possess a distinct antioxidant signature driven by phenolic–lipid interactions and enzymatic modulation, supporting their relevance as a natural source of redox active compounds.
References
Shah AA, Rehman AU, Kapoor S, Kaur H, Rohilla B, Bajpai AB, et al. GC-MS analysis of phytoactive compounds, antioxidant and antibacterial activity of citrullus lanatus seeds. Biomed Pharmacol J. 2023;16(1):16. https://dx.doi.org/10.13005/bpj/2589
Pathania R, Chawla P, Sharma A, Kaushik R, Khan MA. GC-MS Characterization, In Vitro Antioxidant, Anti-inflammatory and Potential Antidermatophytic Activity of Citrullus lanatus Seed Oil. Anti-Infective Agents. 2022;20(1):65–73. http://dx.doi.org/10.2174/2211352519666210906151310
Abu OD, Imafidon KE, Obayuwana HO, Onodje S. Quantitative phytochemical evaluation and phenolic contents of extracts of Citrullus lanatus seed. Int J Bioorg Chem Mol Biol. 2020;7(1):31–5. https://doi.org/10.19070/2332-2756-200005
Uwabujo AE. Screening of some Nigerian herbs for potency against selected disease-causing microorganisms. 2005.
Wolfe K, Wu X, Liu RH. Antioxidant Activity of Apple Peels. J Agric Food Chem. 2003;51(3):609–614. https://doi.org/10.1021/jf020782a
Blois MS. Antioxidant determinations by the use of a stable free radical. Nature. 1958;181(4617):1199–200. https://doi.org/10.1038/1811199a0
Stevens-Barrón JC, de la Rosa LA, Wall-Medrano A, Álvarez-Parrilla E, Rodríguez-Ramirez R, Robles-Zepeda RE, et al. Chemical composition and in vitro bioaccessibility of antioxidant phytochemicals from selected edible nuts. Nutrients. 2019;11(10):2303. https://doi.org/10.3390/nu11102303
Guthrie RD. Introduction to Spectroscopy (Pavia, Donald; Lampman, Gary M.; Kriz, George S., Jr.). Journal of Chemical Education [Internet]. 1979 Oct;56(10):A323. https://doi.org/10.1021/ed056pa323.2
Dawood Shah M, Seelan Sathiya Seelan J, Iqbal M. Phytochemical investigation and antioxidant activities of methanol extract, methanol fractions and essential oil of Dillenia suffruticosa leaves. Arab J Chem. 2020;13(9):7170–82. https://doi.org/10.1016/j.arabjc.2020.07.022
Shangari N, O’Brien PJ. Catalase activity assays. Curr Protoc Toxicol. 2006;27(1):7. https://doi.org/10.1002/0471140856.tx0707s27
Flohe L. Superoxide dismutase assays. In: Methods in enzymology. Elsevier; 1984. p. 93–104. https://doi.org/10.1016/s0076-6879(84)05013-8
Tsikas D. Assessment of lipid peroxidation by measuring malondialdehyde (MDA) and relatives in biological samples: Analytical and biological challenges. Anal Biochem. 2017;524:13–30. https://doi.org/10.1016/j.ab.2016.10.021
Elinge CM, Muhammad A, Atiku FA, Itodo AU, Peni IJ, Sanni OM, et al. Proximate, mineral and anti-nutrient composition of pumpkin (Cucurbita pepo L) seeds extract. Int J plant Res. 2012;2(5):146–50. https://doi.org/10.5923/j.plant.20120205.02
Tabiri B, Agbenorhevi JK, Wireko-Manu FD, Ompouma EI. Watermelon seeds as food: Nutrient composition, phytochemicals and antioxidant activity. 2016;’IJNSF 5(2): 139-144. https://doi.org/10.11648/j.ijnfs.20160502.18
Eke R, Ejiofor E, Oyedemi S, Onoja S, Omeh N. Evaluation of nutritional composition of Citrullus lanatus Linn.(watermelon) seed and biochemical assessment of the seed oil in rats. J Food Biochem. 2021;45(6):e13763. https://doi.org/10.1111/jfbc.13763
Pisoschi AM, Pop A. The role of antioxidants in the chemistry of oxidative stress: A review. Eur. J. Med. Chem. 97 (2015) 55-74 https://doi.org/10.1002/chin.201531310
Arawande JO, Orimoloye OR, Adeleke AR, Adewole MA, Aladejimokun AO. Phytochemical Screening and Quantitative Determination of Antioxidant Properties of Watermelon Rinds and Seeds. J Nutr Food Process. 2024;7(1). https://doi.org/10.31579/2637-8914/187
Rao YK, Geethangili M, Fang SH, Tzeng YM. Antioxidant and cytotoxic activities of naturally occurring phenolic and related compounds: a comparative study. Food Chem Toxicol. 2007;45(9):1770–6. https://doi.org/10.1016/j.fct.2007.03.012
Gabriel AF, Igwemmar NC, Sadam AA, Babalola SA. Characterization of seed oil from Citrullus lanatus (Watermelon). Direct Res J Public Heal Environ Technol. 2018;3(2):34–40. https://doi.org/10.26765/DRJPHET.2018.7842
Ghaffar N, Perveen A. Solvent polarity effects on extraction yield, phenolic content, and antioxidant properties of Malvaceae family seeds: a comparative study. New Zeal J Bot. 2025;63(4):627–37. https://doi.org/10.1080/0028825x.2024.2392705
El-Adawy TA, Taha KM. Characteristics and composition of watermelon, pumpkin, and paprika seed oils and flours. J Agric Food Chem. 2001;49(3):1253–9. https://doi.org/10.1021/jf001117+
Kazlauskienė D, Kasparavičienė G, Nenortienė P, Marksa M, Jukilaitytė J, Velžienė S, et al. Determination of fatty acid composition and antioxidant activity in vegetable oils. Chemija. 2021;32(1). https://doi.org/10.6001/chemija.v32i1.4397
Poljšak Nina, Kočevar Glavač Nina. Analytical Evaluation and Antioxidant Activity of Selected Vegetable Oils to Support Evidence-Based use in Dermal Products. Nat Prod Commun [Internet]. 2024 Sep 1;19(9):1-10. https://doi.org/10.1177/1934578x241281245
Ourradi H, Ennahli S, Martos MV, Hernadez F, Dilorenzo C, Hssaini L, et al. Proximate composition of polyphenolic, phytochemical, antioxidant activity content and lipid profiles of date palm seeds oils (Phoenix dactylifera L.). J Agric Food Res. 2021; 6: 100217. https://doi.org/10.1016/j.jafr.2021.100217
Aluyor EO, Ori-Jesu M. The use of antioxidants in vegetable oils–A review. African J Biotechnol. 2008;7(25). https://doi.org/10.4314/ajb.v7i25.59677
Maritim A, Dene BA, Sanders RA, Watkins III JB. Effects of pycnogenol treatment on oxidative stress in streptozotocin‐induced diabetic rats. J Biochem Mol Toxicol. 2003;17(3):193–9. https://doi.org/10.1002/jbt.10078
Olatunji BP, Fasola TR, Onasanwo SA, Akinyemi AJ, Adeniyi PA, Ishola AO. Neuronal alterations and antioxidant status of lipopolysaccharide induced neuronal damage in mice: Efficacy of three medicinal plants. J Appl Pharm Sci. 2017;7(12):156–62. https://doi.org/10.7324/japs.2017.71222
Galati G, O’brien PJ. Potential toxicity of flavonoids and other dietary phenolics: significance for their chemopreventive and anticancer properties. Free Radic Biol Med. 2004;37(3):287–303. https://doi.org/10.1016/j.freeradbiomed.2004.04.034
El-Missiry MA, El Gindy AM. Amelioration of alloxan induced diabetes mellitus and oxidative stress in rats by oil of Eruca sativa seeds. Ann Nutr Metab. 2000;44(3):97–100. https://doi.org/10.1159/000012829
Messaoudi S, Tebibel S, Beladjila AK, Touhami FK, Kabouche Z. Anti-hyperlipidemic, Anti-inflammatory and Antioxidant Activities of Citrullus lanatus. World J Environ Biosci. 2019;8(1–2019):100–6.
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Copyright (c) 2025 Husna Usman Turadu, Fatima AbdulGaffar Nasir, Aminu Jibril Sufyan, Nafisa Isiyaka Rabiu, Amina Abdulmalik Juda, Zainab Bello Musa, Aisha Abubakar Jinjiri, Amina Lawal Garba, Haruna Bala ts, Abba Babandi, Innocent Ojeba Musa, Miracle Uwa Livinus, Hafeez Muhammad Yakasai

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