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Research Articles

Vol. 12 No. 3 (2025)

Phytochemical characterization by GC-MS and in vitro evaluation of antioxidant potential of Walsura piscidia Roxb. leaves extract

DOI
https://doi.org/10.14719/pst.8653
Submitted
3 April 2025
Published
25-06-2025 — Updated on 01-07-2025
Versions

Abstract

Walsura piscidia Roxb. (Family: Meliaceae) is currently known for rich sources of bioactive compounds with growing multiple therapeutic and medicinal importance. The main objectives of this study were to characterize the phytochemical profile of the leaves of W. piscidia by Gas Chromatography-Mass Spectrometry (GC-MS), followed by the evaluation of its antioxidant potential by quantifying the amounts of phenols and flavonoids present within the extracts, through the existing methods of detection. The extractive yield calculated after Soxhlet extraction was seen to be higher for the ethanolic extract with a value of 21.9 %, followed by the methanolic extracts (21.06 %) and the qualitative phytochemical tests gave similar classes of phytochemicals like triterpenoids, phenolic compounds and tannins in the methanolic and ethanolic extracts. The total phenolic content was seen to be higher in the ethanolic extract with a value of 26.192 ± 0.401 mg GAE/g and the total flavonoid content was seen to be higher in the methanolic extract with a value of 42.972 ± 0.214 mg QE/g. The methanolic extract showed promising results in the antioxidant assays with a significantly low IC50 value in DPPH assay and high ferric reducing power in ferric reducing antioxidant power (FRAP) assay. The GC-MS chromatograms showed almost similar compounds for both the methanolic and ethanolic leaf extracts, some important ones being n-Hexadecanoic acid, stigmasterol, campesterol, 5-hydroxymethyl furfural, etc, displaying properties of interest like antioxidant, anti-inflammatory, anti-microbial, etc. This work contributes to our better understanding of the medicinal properties of the leaves of W. piscidia and has also provided a strong scientific basis to the traditional usage claims of this tree.

References

  1. 1. Sundara Raj T, Dinesh A. Healthcare-seeking behaviour of elderly indigenous Malayali tribal women in South India. Contemporary Voice of Dalit. 2025. https://doi.org/10.1177/2455328X241308396
  2. 2. Amir Rawa MS, Mazlan MK, Ahmad R, Nogawa T, Wahab HA. Roles of Syzygium in anti-cholinesterase, anti-diabetic, anti-inflammatory, and antioxidant: from Alzheimer’s perspective. Plants. 2022;11(11):1476. https://doi.org/10.3390/plants11111476
  3. 3. Nong Y, Xu CG, Wei GY, Yan KJ, Qu XC, Zhang ZJ, et al. Walsura guangxiensis (Meliaceae), a new species from Guangxi, China. PhytoKeys. 2023;234:219. https://doi.org/10.3897/phytokeys.234.106205
  4. 4. Pham TV, Le AT, Nguyen NH, Nguyen HH, Tran GB, Do BH. Phytochemical analysis and investigation of the anti-inflammatory and anticancerous activity of Walsura robusta leaf volatile compounds. Journal of Essential Oil Bearing Plants. 2025:28(1):83-94. https://doi.org/10.1080/0972060X.2025.2451383
  5. 5. Govindachari TR, Kumari GK, Suresh G. Triterpenoids from Walsura piscidia. Phytochemistry. 1995;39(1):167-70. https://doi.org/10.1016/0031-9422(94)00851-J
  6. 6. Purushothaman KK, Duraiswamy K, Connolly JD, Rycroft DS. Triterpenoids from Walsura piscidia. Phytochemistry. 1985;24(10):2349-54. https://doi.org/10.1016/S0031-9422(00)83040-X
  7. 7. Dalawai D, Murthy HN, Dewir YH, Sebastian JK, Nag A. Phytochemical composition, bioactive compounds, and antioxidant properties of different parts of Andrographis macrobotrys nees. Life. 2023;13(5):1166. https://doi.org/10.3390/life13051166
  8. 8. Shaikh JR, Patil M. Qualitative tests for preliminary phytochemical screening: An overview. International Journal of Chemical Studies. 2020;8(2):603-8. https://doi.org/10.22271/chemi.2020.v8.i2i.8834
  9. 9. Tambe BR, Vikhe SR, Pathade PM. Detection of phytochemicals in the methanol extract of Urginea indica (R.) BULB. WJBPHS. 2025;21(01):768-73. https://doi.org/10.30574/wjbphs.2025.21.1.0025
  10. 10. Iqbal E, Salim KA, Lim LB. Phytochemical screening, total phenolics and antioxidant activities of bark and leaf extracts of Goniothalamus velutinus (Airy Shaw) from Brunei Darussalam. Journal of King Saud University-Science. 2015;27(3):224-32. https://doi.org/10.1016/j.jksus.2015.02.003
  11. 11. Thamer NA, Hammadi AH, Yaseen MM. Evaluation of antioxidant activity and cytotoxic potential of Thymus vulgaris leaf extracts. TJNPR. 2021;5(8):1389-96. https://doi.org/10.26538/tjnpr/v5i8.11
  12. 12. Kanimozhi M, Rose C. Screening and evaluation of potential antifungal plant extracts against skin infecting fungus Trichophyton rubrum. Pharmacognosy Research. 2023;15(2):328-37. https://doi.org/10.5530/pres.15.2.035
  13. 13. Nurcholis W, Putri DN, Husnawati H, Aisyah SI, Priosoeryanto BP. Total flavonoid content and antioxidant activity of ethanol and ethyl acetate extracts from accessions of Amomum compactum fruits. Annals of Agricultural Sciences. 2021;66(1):58-62. https://doi.org/10.1016/j.aoas.2021.04.001
  14. 14. Farishta P, Sharma R. Phytochemical profiling and GC-MS analysis of methanolic leaf extract of Persicaria hydropiper (L.) H. Gross: An important ethnomedicinal plant. Plant Science Today. 2024;11(sp1). https://doi.org/10.14719/pst.3306
  15. 15. Ghosh S. Triterpenoids: structural diversity, biosynthetic pathway, and bioactivity. Studies in Natural Products Chemistry. 2020;67:411-61. https://doi.org/10.1016/B978-0-12-819483-6.00012-6
  16. 16. Do QD, Angkawijaya AE, Tran-Nguyen PL, Huynh LH, Soetaredjo FE, Ismadji S, et al. Effect of extraction solvent on total phenol content, total flavonoid content, and antioxidant activity of Limnophila aromatica. Journal of Food and Drug Analysis. 2014;22(3):296-302. https://doi.org/10.1016/j.jfda.2013.11.001
  17. 17. Truong DH, Nguyen DH, Ta NT, Bui AV, Do TH, Nguyen HC. Evaluation of the use of different solvents for phytochemical constituents, antioxidants, and in vitro anti‐inflammatory activities of Severinia buxifolia. Journal of Food Quality. 2019;(1):8178294. https://doi.org/10.1155/2019/8178294
  18. 18. Sokmen BB, Hasdemir B, Yusufoglu A, Yanardag R. Some monohydroxy tetradecanoic acid isomers as novel urease and elastase inhibitors and as new antioxidants. Applied Biochemistry and Biotechnology. 2014;172:1358-64. https://doi.org/10.1007/s12010-013-0595-2
  19. 19. Aparna V, Dileep KV, Mandal PK, Karthe P, Sadasivan C, Haridas M. Anti‐inflammatory property of n‐hexadecanoic acid: structural evidence and kinetic assessment. Chemical Biology & Drug Design. 2012;80(3):434-9. https://doi.org/10.1111/j.1747-0285.2012.01418.x
  20. 20. Sunarwidhi AL, Rahmaniar W, Prasedya ES, Padmi H, Widyastuti S, Pangestu KWJ, et al. In vitro anti-oxidant, in vivo anti-hyperglycemic, and untargeted metabolomics-aided in silico screening of macroalgae lipophilic extracts for anti-diabetes mellitus and anti-COVID-19 potential metabolites. Metabolites. 2023;13(12):1177. https://doi.org/10.3390/metabo13121177
  21. 21. Tripathi N, Kumar S, Singh R, Singh C, Singh P, Varshney VK. Isolation and identification of γ-sitosterol by GC-MS from roots of Girardinia heterophylla. Oriental Journal of Chemistry. 2013;29(2):705-7. https://doi.org/10.13005/ojc/290245
  22. 22. Bakrim S, Benkhaira N, Bourais I, Benali T, Lee LH, El Omari N, et al. Health benefits and pharmacological properties of stigmasterol. Antioxidants. 2022;11(10):1912. https://doi.org/10.3390/antiox11101912
  23. 23. Nazir S, Chaudhary WA, Mobashar A, Anjum I, Hameed S, Azhar S. Campesterol: a natural phytochemical with anti-inflammatory properties as a potential therapeutic agent for rheumatoid arthritis: a systematic review. Pakistan Journal of Health Sciences. 2023. https://doi.org/10.54393/pjhs.v4i05.792
  24. 24. Chan P, Niu CS, Cheng JT, Tsao CW, Tsai SK, Hong CY. Trilinolein preserves mitochondria ultrastructure in isolated rat heart subjected to global ischemia through antioxidant activity as measured by chemiluminescence. Pharmacology. 1996;52(4):216-25. https://doi.org/10.1159/000139386
  25. 25. Huang ZR, Lin YK, Fang JY. Biological and pharmacological activities of squalene and related compounds: potential uses in cosmetic dermatology. Molecules. 2009;14(1):540-54. https://doi.org/10.3390/molecules14010540
  26. 26. El-Gazzar N, Said L, Al-Otibi FO, AbdelGawwad MR, Rabie G. Antimicrobial and cytotoxic activities of natural (Z)-13-docosenamide derived from Penicillium chrysogenum. Frontiers in Cellular and Infection Microbiology. 2025;15:1529104. https://doi.org/10.3389/fcimb.2025.1529104
  27. 27. Pereira CB, de Sá NP, Borelli BM, Rosa CA, Barbeira PJS, Cota BB, et al. Antifungal activity of eicosanoic acids isolated from the endophytic fungus Mycosphaerella sp. against Cryptococcus neoformans and C. gattii. Microbial Pathogenesis. 2016;100:205-12. https://doi.org/10.1016/j.micpath.2016.09.022
  28. 28. Kumar D, Khan A. Analysis of bioactive compounds from Sapindus marginatus (Willd.) by using gas chromatography-mass spectrometry technique. Applied Biological Research. 2023;25(1);127-31. https://doi.org/10.5958/0974-4517.2023.00014.9
  29. 29. Zhao L, Chen J, Su J, Li L, Hu S, Li B, et al. In vitro antioxidant and antiproliferative activities of 5-hydroxymethylfurfural. Journal of Agricultural and Food Chemistry. 2013;61(44):10604-11. https://doi.org/10.1021/jf403098y
  30. 30. Karthikeyan SC, Velmurugan S, Donio MBS, Michaelbabu M, Citarasu T. Studies on the antimicrobial potential and structural characterization of fatty acids extracted from Sydney rock oyster Saccostrea glomerata. Annals of Clinical Microbiology and Antimicrobials. 2014;13:1-11. https://doi.org/10.1186/s12941-014-0057
  31. 31. López‐Lara IM, Nogales J, Pech‐Canul Á, Calatrava‐Morales N, Bernabéu‐Roda LM, Durán P, et al. 2‐Tridecanone impacts surface‐associated bacterial behaviours and hinders plant–bacteria interactions. Environmental Microbiology. 2018;20(6):2049-65. https://doi.org/10.1111/1462-2920.14083
  32. 32. Meng X, Yang Q, Li Z, Zhou P, Li W, Liang Q, et al. The association between docosanoic acid and the risks of occurrence and mortality of chronic kidney disease. medRxiv. 2025. https://doi.org/10.1101/2025.03.14.25322644
  33. 33. Marchetti DP, Steffens L, Jacques CE, Guerreiro GB, Mescka CP, Deon M, et al. Oxidative imbalance, nitrative stress, and inflammation in C6 glial cells exposed to hexacosanoic acid: protective effect of N-acetyl-L-cysteine, trolox, and rosuvastatin. Cellular and Molecular Neurobiology. 2018;38:1505-16. https://doi.org/10.1007/s10571-018-0626-1
  34. 34. Meulmeester FL, Luo J, Martens LG, Mills K, van Heemst D, Noordam R. Antioxidant supplementation in oxidative stress-related diseases: What have we learned from studies on alpha-tocopherol? Antioxidants (Basel). 2022;11(12):2322. https://doi.org/10.3390/antiox11122322

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