PHYTOCHEMICAL INVESTIGATION, ANTIMICROBIAL ACTIVITY, AND CYTOTOXIC POTENTIAL OF EUPATORIUM FORTUNEI TURCZ. CULTIVATED IN TAM DAO, VIETNAM

Các tác giả

  • TA VAN DIEP
  • TRAN HOANG KHANH HUYEN
  • PHAM MANH HA
  • CAI THI LAN HUONG
  • NGUYEN THI TUYET
  • TRAN ANH NGOC
  • TRAN DUC DAI

DOI:

https://doi.org/10.51453/3093-3706/2026/1488

Tóm tắt

Eupatorium fortunei Turcz. (Asteraceae) is a medicinal plant widely used in traditional medicine and reported to possess various biological activities. However, information regarding the phytochemical composition and biological properties of E. fortunei cultivated at the Tam Dao Medicinal Plant Research Center remains limited. This study aimed to investigate the phytochemical constituents, antimicrobial activity, and cytotoxic potential of solvent fractions obtained from the aerial parts of E. fortunei. Preliminary phytochemical screening and thin-layer chromatography (TLC) analyses were performed to characterize major secondary metabolites. Antimicrobial activity was evaluated against eight standard microbial strains using the broth microdilution method, while cytotoxic activity against human cancer cell lines (HepG2, MCF-7, and A549) was assessed using the MTT assay.

Phytochemical screening revealed the presence of alkaloids, coumarins, flavonoids, terpenoids, and proanthocyanidins. TLC analysis demonstrated a diverse chemical profile, with at least 10 constituents detected in the n-hexane fraction (EFH) and 16 constituents in the ethyl acetate fraction (EFE). Among the tested extracts, EFH exhibited the strongest antimicrobial activity against Candida albicans with a minimum inhibitory concentration (MIC) of 100 μg/mL, whereas the remaining antimicrobial effects were weak (MIC ≥ 200 μg/mL). Cytotoxicity assays showed selective activity of EFH against MCF-7 breast cancer cells (IC₅₀ = 31.45 ± 1.18 μg/mL), while EFE displayed the most potent activity against A549 lung cancer cells (IC₅₀ = 27.36 ± 1.05 μg/mL) and moderate activity against HepG2 cells (IC₅₀ = 87.39 ± 2.51 μg/mL).

These findings demonstrate that E. fortunei cultivated in Tam Dao is a rich source of bioactive secondary metabolites and possesses promising antifungal and selective anticancer activities. The ethyl acetate fraction, in particular, warrants further bioassay-guided fractionation to identify compounds responsible for its cytotoxic effects against lung cancer cells.

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Tài liệu tham khảo

[1] Do Tat Loi, Medicinal Plants and Medicinal Substances of Vietnam, Hanoi, VietNam: Medical Publishing House, 2004.

[2] Vo Van Chi, "Dictionary of Vietnamese Medicinal Plants," Hanoi, Vietnam: Medical Publishing House, vol. 2, 2012.

[3] Do Huy Bich, B. X, "Medicinal Plants and Medicinal Animals of Vietnam," Hanoi, Vietnam: Science and Technology Publishing House, vol. 2, 2006.

[4] Jian Qiang Ma, Y. P, "Eupatorium fortunei Turcz.: An updated review on the botany, phytochemistry, pharmacology, and toxicology," Molecules, vol. 31, no. 7, p. 1137, 2026.

[5] Rui Dong, S. L, "Diverse thymol analogs from Eupatorium fortunei: Their anti-inflammatory activity and mechanism," Fitoterapia, vol. 191, p. 107249, 2016.

[6] Lei Miao, Q. W, "Chemical constituents from Eupatorium fortunei and their anti-inflammatory evaluation by in silico and experimental approaches," Fitoterapia, vol. 171, p. 105700, 2023.

[7] Yanqun Li, D. K, "The effect of developmental and environmental factors on secondary metabolites in medicinal plants," Plant Physiology and Biochemistry, vol. 148, pp. 80-89, 2020.

[8] Poonam Pant, S. P, "The influence of environmental conditions on secondary metabolites in medicinal plants: A literature review," Chemistry & Biodiversity, vol. 18, no. 11, p. e2100345, 2024.

[9] Li Yang, K. S.-X, "Response of plant secondary metabolites to environmental factors," Molecules, vol. 23, no. 4, p. 762, 2018.

[10] Ministry of Health of Vietnam, "Vietnamese Pharmacopoeia V," Hanoi, Vietnam: Medical Publishing House, 2018.

[11] T. T. An, "Analytical Chemistry," Hanoi, Vietnam: Medical Publishing House, vol. 2, pp. 168-212, 2012.

[12] L. Mckane, "Bacterial growth and laboratory cultivation," Microbiology Essentials and Applications, New York, NY, USA: McGraw-Hill, vol. 97, p. 335, 1996.

[13] D. A. Vanden Berghe, "Screening methods for antibacterial and antiviral agents from higher plants," in Methods in Plant Biochemistry, vol. 6, pp. 47-69, 1991.

[14] T. Mosmann, "Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assay," Journal of Immunological Methods, vol. 65, pp. 55-63, 1983.

[15] Ke Son Phan, P. T, "Dual loading of doxorubicin and magnetic iron oxide into PLA-TPGS nanoparticles: Design, in vitro drug release kinetics, and biological effects on cancer cells," ChemMedChem, vol. 16, no. 23, pp. 3615-3625, 2021.

[16] M. K. H. Dvora, "10 - Microbial production of flavonoids and terpenoids," Woodhead Publishing Series in Food Science, Technology and Nutrition, pp. 234-261, 2013.

[17] J. B. Harborne, "Phytochemical Methods: A Guide to Modern Techniques of Plant Analysis," London, UK: Chapman & Hall, 1972.

[18] G. A. Cordell, "Biodiversity and drug discovery—A symbiotic relationship," Phytochemistry, vol. 55, no. 6, pp. 463-480, 2000.

[19] D. S. Seigler, "Plant Secondary Metabolism," New York, NY, USA: Springer Science & Business Media, pp. 506-513, 1998.

[20] J. M. Robert D. H. Murray, "The Natural Coumarins: Occurrence. Chemistry and Biochemistry," Chichester, UK: Wiley, p. 702, 1982.

[21] H. W. Bladt, "Plant Drug Analysis: A Thin Layer Chromatography Atlas, 2nd ed," Berlin, Germany: Springer-Verlag, pp. 305-334, 1996.

[22] J. Gross, "Pigments in Vegetables: Chlorophylls and Carotenoids," New York, NY, USA: Van Nostrand Reinhold, pp. 3-25, 1991.

[23] A. Marston, "Thin-layer chromatography with biological detection in phytochemistry," Journal of Chromatography A, vol. 1218, no. 19, pp. 2676-2683, 2011.

[24] T. K. Mieczysław, "Thin-Layer Chromatography (TLC) in the Screening of Botanicals–Its Versatile Potential and Selected Applications," Molecules, vol. 27, pp. 1-23, 2022'.

[25] S. I. Behbahani, "Applications of ultraviolet visualization in thin-layer chromatography for screening of secondary plant metabolites," Phytochemical Analysis, vol. 28, no. 4, pp. 211-219, 2017.

[26] J. B. Harborne, "Phytochemical Methods: A Guide to Modern Techniques of Plant Analysis," 3rd ed. London, UK: Chapman & Hall, pp. 40-90, 1998.

[27] R. H. D A Scudiero, "Evaluation of a soluable tetrazolium/formazan assay for cell growth and drug sensitivity in culture using human and other tumor cell lines," Cancer Research, vol. 48, pp. 4827-4833, 1988.

[28] M. Sainsbury, "The anticancer substance ellipticine and its derivatives," Synthesis, vol. 24, no. 7, pp. 437-448, 1977.

[29] I. G. Mohammad Adam Mustapa, "Anti-Breast Cancer Activity of Essential Oil: A Systematic Review," Applied Sciences, vol. 12, no. 24, p. 12738, 2022.

[30] A. M.-N. Shaza H. Aly, "Unveiling the pharmacological potential of plant triterpenoids in breast cancer management: an updated review," Naunyn-Schmiedeberg's Archives of Pharmacology, vol. 397, pp. 5571-5596, 2024.

[31] A. G. Linara Gabitova, "Molecular Pathways: Sterols and Receptor Signaling in Cancer," Clinical Cancer Research, vol. 20, no. 1, pp. 28-34, 2014.

[32] A. J. T P Tim Cushnie, "Recent advances in understanding the antibacterial and anticancer activities of flavonoids," Phytochemistry Reviews, vol. 14, no. 5, pp. 741-759, 2015.

Tải xuống

Đã Xuất bản

2026-07-06

Cách trích dẫn

TA VAN DIEP, TRAN HOANG KHANH HUYEN, PHAM MANH HA, CAI THI LAN HUONG, NGUYEN THI TUYET, TRAN ANH NGOC, & TRAN DUC DAI. (2026). PHYTOCHEMICAL INVESTIGATION, ANTIMICROBIAL ACTIVITY, AND CYTOTOXIC POTENTIAL OF EUPATORIUM FORTUNEI TURCZ. CULTIVATED IN TAM DAO, VIETNAM. SCIENTIFIC JOURNAL OF TAN TRAO UNIVERSITY, 12(2). https://doi.org/10.51453/3093-3706/2026/1488