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Research Articles

Vol. 12 No. 4 (2025)

Isolation, characterization of lignan compound Pinoresinol in Iraqi Mesembryanthemum Cordifolium

DOI
https://doi.org/10.14719/pst.10382
Submitted
30 June 2025
Published
23-09-2025 — Updated on 10-10-2025
Versions

Abstract

Among the Aizoaceae family, Mesembryanthemum cordifolium remains significantly understudied regarding its therapeutic properties despite its abundance. This large family is mostly native to Southern Africa and counts at least 120 genera. M. cordifolium's traditional anti-inflammatory and antidepressant uses are scientifically supported. Its antioxidant, analgesic and cytotoxic properties and promising antidepressant activity, highlight its significant pharmacological potential, warranting further research. This study addresses this research gap by conducting the first investigation into the phytochemical components of Iraqi M. cordifolium and the isolation of a key compound. For 24 h, the entire plant powder, 100 g, was immersed in 100 mL n-hexane to remove any fat. After that, the defatted plant material was extracted with eighty-five percent methanol using the Soxhlet apparatus until it was entirely exhausted. The extract undergoes sequential liquid-liquid fractionation using solvents of increasing polarity: petroleum ether, chloroform and ethyl acetate, using a separatory funnel. This process allows for the separation of compounds based on their differential solubility in immiscible solvents. The results of the phytochemical analysis show that the methanolic crude extract contains steroids, tannins, alkaloids, flavonoids, phenols and saponins. Pinoresinol compound was identified using the technique of high-performance liquid chromatography (HPLC). Pinoresinol was isolated using preparative layer chromatography (PLC) and its identification was confirmed using Fourier transform infrared (FTIR) and proton nuclear magnetic resonance (1H NMR) and Liquid chromatography-mass spectrometry (LC-MS). Analyses revealed that the plant contains lignan compounds with useful medicinal properties, so additional research into the M. cordifolium plant is necessary because it contains a wealth of components with promising health benefits for humans.

References

  1. 1. Hasan T, Kadhim EJ. Phytochemical investigation of Corchorus olitorius L. leaves cultivated in iraq and it’s in vitro antiviral activity. Iraqi J Pharm Sci. 2018;27(2):115–22. https://doi.org/10.31351/vol27iss2pp115-122
  2. 2. Notaraj R, Shoja HM, Kazemi EM. The Effect of UV-B radiation on morphological, anatomical and biochemical traits of Aptenia cordifolia. Spec J Agric Sci. 2019;5(1):34–49.
  3. 3. Al-Baaj AS, Abdul-Jalil TZ. Phytochemical screening of petroleum ether fractions by gc/ms and isolation of lupeol from two different parts of Iraqi Leucaena leucocephala. Iraqi J Pharm Sci. 2022;31:62–74. https://doi.org/10.31351/vol31isssuppl.pp62-74
  4. 4. Elhawary S, Hassan MHA, Mostafa D, AbouZid S, Sleem AA, Mohammed R. Comparative phytochemical and biological study for mesembryanthemum nodiflorum and Aptenia Cordifolia plants growing in Egypt. Egypt J Chem. 2020;63:2511–24. https://doi.org/10.21608/ejchem.2020.20877.2248
  5. 5. Arroyo-Leuenberger S, Bayer MB, Bogner J, Eggli U, Forster PI, Hunt DR, et al . Illustrated handbook of succulent plants: Monocotyledons. Springer Science & Business Media; 2001. https://doi.org/10.1007/978-3-642-56715-5
  6. 6. Klak C, Hanáček P, Bruyns PV. Out of Southern Africa: origin, biogeography and age of the aizooideae (Aizoaceae). Mol Phylogenet Evol. 2017;109:203–16. https://doi.org/10.1016/j.ympev.2016.12.016
  7. 7. Ferren WR Jr, Bleck J, Vivrette N. Malephora crocea (Aizoaceae) naturalized in California. Madroño. 1981;28(2):80–5.
  8. 8. Kalicharan B, Naidoo Y, van Staden J. Ethnopharmacology and biological activities of the Aizoaceae. J Ethnopharmacol. 2023;303:115988. https://doi.org/10.1016/J.JEP.2022.115988
  9. 9. Van Der Watt E, Pretorius JC. Purification and identification of active antibacterial components in Carpobrotus edulis L. J Ethnopharmacol. 2001;76:87–91. https://doi.org/10.1016/S0378-8741(01)00197-0
  10. 10. Khadim EJ, Abdulrasool AA, Awad ZJ. Phytochemical investigation of alkaloids in the Iraqi Echinops heterophyllus (Compositae). Iraqi J Pharm Sci. 2014;23:26–34. https://doi.org/10.31351/vol23iss1pp26-34
  11. 11. Said AAE, Attia EZ, Abdelmohsen UR, Fouad MA. Natural products potential of the genus aptenia. J Adv Biomed Pharm Sci. 2019;2:59–62. https://doi.org/10.21608/jabps.2019.6908.1032
  12. 12. Abdlkareem SKM, Kadhim EJ. Isolation, identification and quantification of two compounds from Cassia glauca cultivated in Iraq. Iraqi J Pharm Sci. 2023;32:95–104. https://doi.org/10.31351/vol32iss3pp95-104
  13. 13. Fradi AJ. The effective concentration of the crude extract of Mentha picata and Eucalyptus against the growth of Fusarium oxysporum. Ibn Al-Haitham J Pure Appl Sci. 2022;35:1–4. https://doi.org/10.30526/35.4.2848
  14. 14. Mall RAS, Kathier SA. Effect of alcoholic phenol and nanocapsules extract from grape seed (Vitis vinifera) on egg hatching and adult death of southern cowpea beetles. Ibn Al-Haitham J Pure Appl Sci. 2024;37:66–74. https://doi.org/10.30526/37.1.3283
  15. 15. Mahesh SK, Fathima J, Veena VG. Cosmetic potential of natural products: industrial applications. In: Swamy M, Akhtar M, editors. Natural Bio-active Compounds. Singapore: Springer; 2019. p. 215-50. https://doi.org/10.1007/978-981-13-7205-6_10
  16. 16. Ong ES. Extraction methods and chemical standardization of botanicals and herbal preparations. J Chromatogr B Analyt Technol Biomed Life Sci. 2004;812:23–33. https://doi.org/10.1016/j.jchromb.2004.07.041
  17. 17. Khamees AH, Kadhim EJ. Isolation, characterization and quantification of a pentacyclic triterpinoid compound ursolic acid in Scabiosa palaestina L. Distributed in the North of Iraq. Plant Sci Today. 2022;9:178–82. https://doi.org/10.14719/pst.1398
  18. 18. Jewely HM, Abdul-Jalil TZ. Extraction, isolation and identification of caffeic acid and p-coumaric acid from n-butanol fraction of Iraqi Osteospermum ecklonis (F. Asteraceae). Int J Drug Deliv Technol. 2022;12:648–53. https://doi.org/10.25258/ijddt.12.2.31
  19. 19. Abubakar AR, Haque M. Preparation of medicinal plants: basic extraction and fractionation procedures for experimental purposes. J Pharm Bioallied Sci. 2020;12:1–10. https://doi.org/10.4103/jpbs.jpbs_175_199
  20. 20. Sasidharan S, Chen Y, Saravanan D, Sundram KM, Latha Y. Extraction, isolation and characterization of bioactive compounds from plants’ extracts. African J Tradit Complement Altern Med. 2010;8:1–10. https://doi.org/10.4314/ajtcam.v8i1.60483
  21. 21. Youssef FS, Ashour ML, El-Beshbishy HA, Hamza AA, Singab ANB, Wink M. Pinoresinol-4-o-β-d-glucopyranoside: a lignan from prunes (Prunus domestica) attenuates oxidative stress, hyperglycaemia and hepatic toxicity in vitro and in vivo. J Pharm Pharmacol. 2020;72:1830–9. https://doi.org/10.1111/jphp.13358
  22. 22. Pitt JJ. Principles and applications of liquid chromatography-mass spectrometry in clinical biochemistry. Clin Biochem Rev. 2009;30:19
  23. 23. Nørskov NP, Knudsen KEB. Validated LC-MS/MS method for the quantification of free and bound lignans in cereal-based diets and feces. J Agric Food Chem. 2016;64:8343–51. https://doi.org/10.1021/ACS.JAFC.6B03451
  24. 24. Schroeder FC, Del Campo ML, Grant JB, Weibel DB, Smedley SR, Bolton KL, et al. Pinoresinol: A lignol of plant origin serving for defense in a caterpillar. Proc Natl Acad Sci U S A. 2006;103:15497. https://doi.org/10.1073/PNAS.0605921103
  25. 25. Sepporta MV, Mazza T, Morozzi G, Fabiani R. Pinoresinol inhibits proliferation and induces differentiation on human HL60 leukaemia cells. Nutr Cancer. 2013;65:1208–18. https://doi.org/10.1080/01635581.2013.828089
  26. 26. Crouch NR, Smith GF, Smith MT. Aptenia cordifolia (L. f.) Schwantes (Mesembryanthemaceae) in Zulu traditional medicine overview. Haseltonia. 2000;(7):30–6.

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