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Research Articles

Vol. 13 No. sp4 (2026): National Symposium on Recent Advances in Life Sciences

Evaluation of antioxidant potential and quantification of caffeic acid in root bark of Tecomella undulata (Sm.) Seem.

DOI
https://doi.org/10.14719/pst.12885
Submitted
23 November 2025
Published
19-06-2026

Abstract

Tecomella undulata (Sm.) Seem.  an endangered species of the family Bignoniaceae is native to India, Pakistan and Oman. Traditionally, it is used in the treatment of leucorrhea, fever, cough, digestive disorders, skin infections, sexual disorders and pain. The plant is also known for its diverse pharmacological properties, including antioxidant, antidiabetic, anticancer, hepatoprotective, antiobesity and antimicrobial properties.  In the current study total phenolic content (TPC) and total flavonoid content (TFC) along with antioxidant potential of methanolic extract of root bark of T. undulata was evaluated, an important metabolite, caffeic acid, was identified and quantified using high performance thin layer chromatography (HPTLC). The extract exhibited comparatively higher TFC (3.20 mg QE g-1 dry weight of extract) as compared to TPC (2.02 mg GAE g-1 dry weight of extract). A significant antioxidant activity was also observed viz., 2,2-diphenyl-1-picrylhydrazyl (IC50 -151.53 µg mL-1), nitric oxide scavenging assay (IC50- 771.2 µg/mL), deoxyribose degradation assay (IC50- 120.1 µg mL-1) and ferric reducing antioxidant power assay (109.22µmol Fe2+ g-1dry weight of extract). The presence of caffeic acid was confirmed by HPTLC profiling, with linear regression R2 = 0.99848 and Rf = 0.62. The limit of detection (LOD) and limit of quantification (LOQ) were found to be 41.92 and 75.79 ng mL-1, respectively, marking the first report of this compound in the root bark of T. undulata. These data highlight the importance of the tree as a medicinal and antioxidant agent, which makes it an important candidate to be further explored for its bioactive and therapeutic activities.

References

  1. 1. Cragg GM, Newman DJ. Natural products: a continuing source of novel drug leads. Biochim Biophys Acta Gen Subj. 2013;1830(6):3670–95. https://doi.org/10.1016/j.bbagen.2013.02.008
  2. 2. Khan SR, Al Rijjal D, Piro A, Wheeler MB. Integration of AI and traditional medicine in drug discovery. Drug Discov Today. 2021;26(4):982–92. https://doi.org/10.1016/j.drudis.2021.01.008
  3. 3. Weidinger A, Kozlov AV. Biological activities of reactive oxygen and nitrogen species: oxidative stress versus signal transduction. Biomolecules. 2015;5(2):472–84. https://doi.org/10.3390/biom5020472
  4. 4. Valko M, Jomova K, Rhodes CJ, Kuča K, Musílek K. Redox- and non-redox-metal-induced formation of free radicals and their role in human disease. Arch Toxicol. 2016;90(1):1–37. https://doi.org/10.1007/s00204-015-1579-5
  5. 5. Nasri H, Shirzad H, Baradaran A, Rafieian-Kopaei M. Antioxidant plants and diabetes mellitus. J Res Med Sci. 2015;20(5):491–502. https://doi.org/10.4103/1735-1995.163977
  6. 6. 6. Rohilla R, Garg M. Phytochemistry and pharmacology of Tecomella undulata. Int J Green Pharm. 2014;8(1). https://doi.org/10.4103/0973-8258.126811
  7. 7. Ravishankar B, Shukla VJ. Indian systems of medicine: a brief profile. Afr J Tradit Complement Altern Med. 2007;4(3):319. https://doi.org/10.4314/ajtcam.v4i3.31226
  8. 8. Khare CP, editor. Indian herbal remedies: rational western therapy, ayurvedic and other traditional usage, botany. Springer Science & Business Media; 2011.
  9. 9. Jain M, Kapadia R, Jadeja RN, Thounaojam MC, Devkar RV, Mishra SH. Hepatoprotective potential of Tecomella undulata stem bark is partially due to the presence of betulinic acid. J Ethnopharmacol. 2012;143(1):194–200. https://doi.org/10.1016/j.jep.2012.06.023
  10. 10. Laghari AQ, Memon S, Nelofar A, Laghari AH. Tecomella undulata G. Don: a rich source of flavonoids. Ind Crops Prod. 2013;43:213–7. https://doi.org/10.1016/j.indcrop.2012.07.025
  11. 11. Ali M, Abra HH, Sultana S, Mir SR. Phytochemical investigation of the stem bark of Tecomella undulata (Sm.) Seem. Mod Org Chem Res. 2017;2:159–71. https://doi.org/10.22606/mocr.2017.24002
  12. 12. Bhardwaj R. GC-MS analysis and antimicrobial activity of alkaloids of Tecomella undulata. J Med Plant Stud. 2018;6(6):68–72.
  13. 13. Vats S, Bhandari N, Ganie SA, Mir MA, Bashir N. Ethnomedicinal, phytochemical, pharmacological and conservation studies of an endangered plant: the desert teak (Tecomella undulata (Sm.) Seem.). Front Pharmacol. 2025;16:1665446. https://doi.org/10.3389/fphar.2025.1665446
  14. 14. Kumadoh D, Adase E, Archer MA, Ankutse P, Kyene MO, Yeboah GN. Optimizing particle size for enhanced aqueous extraction of phytochemicals from medicinal plants. S Afr J Bot. 2026;189:517–29. https://doi.org/10.1016/j.sajb.2025.12.013
  15. 15. Vats S. Effect of initial temperature treatment on phytochemicals and antioxidant activity of Azadirachta indica A. Juss. Appl Biochem Biotechnol. 2016;178(3):504–12. https://doi.org/10.1007/s12010-015-1890-x
  16. 16. Antony A, Farid M. Effect of temperatures on polyphenols during extraction. Appl Sci. 2022;12(4):2107. https://doi.org/10.3390/app12042107
  17. 17. Singleton VL, Rossi JA Jr. Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents. Am J Enol Vitic. 1965;16(3):144–58. https://doi.org/10.5344/ajev.1965.16.3.144
  18. 18. Vats S, Kamal R. Cassia occidentalis L. (a new source of rotenoids): its in vitro regulation by feeding precursors and larvicidal efficacy. Plant Cell Tissue Organ Cult. 2014;116(3):403–9. https://doi.org/10.1007/s11240-013-0409-9
  19. 19. Vats S, Kamal R. In vivo and in vitro evaluation of sterols from Gymnema sylvestre R. Br. Pak J Biol Sci. 2013;16(23):1771–5. https://doi.org/10.3923/pjbs.2013.1771.1775
  20. 20. Halliwell B, Gutteridge JM, Aruoma OI. The deoxyribose method: a simple "test-tube" assay for determination of rate constants for reactions of hydroxyl radicals. Anal Biochem. 1987;165(1):215–9. https://doi.org/10.1016/0003-2697(87)90222-3
  21. 21. Benzie IF, Strain JJ. The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": the FRAP assay. Anal Biochem. 1996;239(1):70–6. https://doi.org/10.1006/abio.1996.0292
  22. 22. Ciumărnean L, Milaciu MV, Runcan O, Vesa ȘC, Răchișan AL, Negrean V, et al. The effects of flavonoids in cardiovascular diseases. Molecules. 2020;25(18):4320. https://doi.org/10.3390/molecules25184320
  23. 23. ICH. Q2 (R1): Validation of analytical procedures: text and methodology. International Conference on Harmonisation, Geneva. 2005.
  24. 24. Ebrahimzadeh MA, Nabavi SF, Nabavi SM, Pourmorad F. Nitric oxide radical scavenging potential of some Elburz medicinal plants. Afr J Biotechnol. 2010;9(32):5212–7.
  25. 25. Gliszczyńska-Świgło A. Antioxidant activity of water-soluble vitamins in the TEAC and FRAP assays. Food Chem. 2006;96(1):131–6. https://doi.org/10.1016/j.foodchem.2005.02.018
  26. 26. Chaudhary P, Janmeda P, Docea AO, Yeskaliyeva B, Abdull Razis AF, Modu B, et al. Oxidative stress, free radicals and antioxidants: potential crosstalk in the pathophysiology of human diseases. Front Chem. 2023;11:1158198. https://doi.org/10.3389/fchem.2023.1158198
  27. 27. Bhardwaj R, Yadav A, Sharma R. Tecomella undulata-phenolic compounds and antioxidant activities. Res J Med Plant. 2014;8(5):223–30. https://doi.org/10.3923/rjmp.2014.223.230
  28. 28. Wink M. Evolution of secondary metabolites from an ecological and molecular phylogenetic perspective. Phytochemistry. 2003;64(1):3–19. https://doi.org/10.1016/S0031-9422(03)00300-5
  29. 29. Akula R, Ravishankar GA. Influence of abiotic stress signals on secondary metabolites in plants. Plant Signal Behav. 2011;6(11):1720–31. https://doi.org/10.4161/psb.6.11.17613
  30. 30. Vats S, Gupta T. Evaluation of bioactive compounds and antioxidant potential of hydroethanolic extract of Moringa oleifera Lam. from Rajasthan, India. Physiol Mol Biol Plants. 2017;23(1):239–48. https://doi.org/10.1007/s12298-016-0407-6
  31. 31. Yang L, Wen KS, Ruan X, Zhao YX, Wei F, Wang Q. Response of plant secondary metabolites to environmental factors. Molecules. 2018;23(4):762. https://doi.org/10.3390/molecules23040762
  32. 32. Sharma BK, Kulshreshtha S, Rahmani AR, editors. Faunal heritage of Rajasthan, India. Springer; 2013. https://doi.org/10.1007/978-3-319-01345-9
  33. 33. Easwari DV, Suresh SN, Sagadevan P. Studies on phytochemical analysis and antioxidant activity of methanolic leaf extract Tecomella undulata. J Pharm Biol Res. 2014;2:143–7.
  34. 34. Pourbagher-Shahri AM, Farkhondeh T, Talebi M, Kopustinskiene DM, Samarghandian S, Bernatoniene J. An overview of NO signaling pathways in aging. Molecules. 2021;26(15):4533. https://doi.org/10.3390/molecules26154533
  35. 35. Piacenza L, Zeida A, Trujillo M, Radi R. The superoxide radical switch in the biology of nitric oxide and peroxynitrite. Physiol Rev. 2022. https://doi.org/10.1152/physrev.00005.2022
  36. 36. Katbamna RV, Rana MG, Manvar M. Phytochemical analysis, in vitro anti-coagulant activity of different solvent fractions of Citrus medica fruit extract. 2023.
  37. 37. Hou L, Ma J, Feng X, Chen J, Dong BH, Xiao L, et al. Caffeic acid and diabetic neuropathy: investigating protective effects and insulin-like growth factor 1 (IGF-1)-related antioxidative and anti-inflammatory mechanisms in mice. Heliyon. 2024;10(12):e32623. https://doi.org/10.1016/j.heliyon.2024.e32623
  38. 38. Balkrishna A, Sharma N, Srivastava D, Kukreti A, Srivastava S, Arya V. Exploring the safety, efficacy and bioactivity of herbal medicines: bridging traditional wisdom and modern science in healthcare. Future Integr Med. 2024;3(1):35–49. https://doi.org/10.14218/FIM.2023.0008

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