PHYTOCHEMICAL STUDY AND ANTIMICROBIAL PROPERTIES OF FILMY FERN (HYMENOPHYLLUM IMBRICATUM BLUME)

Authors

  • NOVA SYAFNI Department of Pharmacy, Faculty of Pharmacy, Universitas Andalas, Padang, Indonesia. Sumatran Biota Laboratory, Universitas Andalas, Padang, Indonesia
  • YOGIE PRATAMA SANDI Department of Pharmacy, Faculty of Pharmacy, Universitas Andalas, Padang, Indonesia. Kota Baru Health Center, Indragiri Hilir, Indonesia
  • HERNAWATI Department of Forestry, Faculty of Forestry, Muhammadiyah University of West Sumatra, Padang, Indonesia
  • DAYAR ARBAIN Department of Pharmacy, Faculty of Pharmacy, Universitas Andalas, Padang, Indonesia. Sumatran Biota Laboratory, Universitas Andalas, Padang, Indonesia. Faculty of Pharmacy, University 17 Agustus 1945, North Jakarta, Indonesia

DOI:

https://doi.org/10.22159/ijap.2025.v17s1.16

Keywords:

Filmy fern, Hymenophyllum imbricatum blume, Antimicrobial, Human pathogen bacterial

Abstract

Objective: The research aimed for phytochemical study and screening antimicrobial activities of filmy fern Hymenophyllum imbricatum Blume.

Methods: Antimicrobial assay used agar diffusion method against several pathogenic bacteria: Staphylococcus aureus ATCC 25923, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Salmonella typhimurium ATCC 14028, Salmonella typhosa NCTC 786, Bacillus subtillis ATCC 6633, Enterococcus faecalis ATCC 29212, Micrococcus luteus ATCC 10240, Salmonella typhi, Staphylococcus epidermidis ATCC 12228, Streptococcus mutans ATCC 25175, Vibrio cholera Inaba and Methicillin-Resistant Staphylococcus aureus (MRSA), the isolation used silica column chromatography, purification by recrystallization, and identification by spectroscopic techniques (NMR, MS, UV-Vis, IR).

Results: Two compounds have been isolated from the aerial part of Hymenophyllum imbricatum Blume as 4-acetylphenyl ether (1) and genkwanin-4”-O-β-glucopyranose (2). The activity inhibition of isolated compounds against some human pathogenic bacteria S. aureus ATCC 25923, E. coli ATCC 25922, P. aeruginosa ATCC 27853, S. typhimurium ATCC 14028, S. typhosa NCTC 786, B. subtillis ATCC 6633, E. faecalis ATCC 29212, M. luteus ATCC 10240, S. typhi, S. epidermidis ATCC 12228, S. mutans ATCC 25175, V. cholera Inaba, and Methicillin-Resistant S. aureus (MRSA) was inhibited at concentrations ranging from 0.6-10 µg/disc.

Conclusion: Flavonoid glycoside and dimer compounds were isolated from Himenophyllum imbricatum; both isolated compounds showed lower inhibition in some bacteria compared to the ethyl acetate fraction, which obtained moderate inhibition against all the testing bacteria.

References

Syafni N, Putra DP, Arbain D. 3,4-dihydroxybenzoic acid and 3,4-dihydroxybenzaldehyde from the fern Trichomanes Chinense L.; isolation, antimicrobial and antioxidant properties. Indones J Chem. 2012 Sep 5;12(3):273-8. doi: 10.22146/ijc.21342.

Anggia V, Bakhtiar A, Arbain D. Chemical constituents and antibacterial activities of leaves of sumatran king fern (Angiopteris evecta G. Forst. HOFFM.). J Farmasi Indones. 2015;7(4):195-202.

Nofrizal PDP, Arbain D. Antioxidant and antibacterial constituents from two sumatran ferns, Trichomanes javanicum and Oleandra pistillaris. J Nat Prod. 2017;12(8):1263-4.

Syafni N, Bakhtiar A. Ethnobotanical study of ferns as traditional medicine in Central Siberut, Mentawai Island. JBioUA. 2022 Mar 16;10(1):10-4. doi: 10.25077/jbioua.10.1.10-14.2022.

Oiso Y, Toyota M, Asakawa Y. Hymenosides A-F, Six new hemiterpene glucosides from the Japanese fern Hymenophyllum barbatum. Chem Pharm Bull (Tokyo). 2001;49(1):126-8. doi: 10.1248/cpb.49.126, PMID 11201218.

Toyota M, Oiso Y, Asakawa Y. New bitter-tasting hemiterpene glycosides from the Japanese fern Hymenophyllum barbatum. Chem Pharm Bull (Tokyo). 2001;49(12):1567-72. doi: 10.1248/cpb.49.1567, PMID 11767076.

Toyota M, Oiso Y, Asakawa Y. New glycosides from the Japanese fern Hymenophyllum barbatum. Chem Pharm Bull (Tokyo). 2002;50(4):508-14. doi: 10.1248/cpb.50.508, PMID 11963999.

Holtum RE. A revised flora of malaya Vol. II. Fern of Malaya. Singapore: Government Prints Office; 1967. p. 1-653.

Roskov Y, Ower G, Orrell T, Nicolson D, Bailly N, Kirk PM. editors. Species 2000 and ITIS catalogue of life, 29th Nov 2018. Digital resource at www. catalogueoflife. org/Col. species 2000. Leiden, the Netherlands: Naturalis; 2018.

Chen IN, Chang CC, Ng CC, Wang CY, Shyu YT, Chang TL. Antioxidant and antimicrobial activity of zingiberaceae plants in taiwan. Plant Foods Hum Nutr. 2008;63(1):15-20. doi: 10.1007/s11130-007-0063-7, PMID 18157743.

Tavares TD, Antunes JC, Padrao J, Ribeiro AI, Zille A, Amorim MT. Activity of specialized biomolecules against gram-positive and gram-negative bacteria. Antibiotics (Basel). 2020;9(6):314. doi: 10.3390/antibiotics9060314, PMID 32526972.

Al-Bogami AS, Mekky AE. Microwave-assisted regioselective synthesis of novel bis(azoles) and bis(azoloazines). J Heterocycl Chem. 2016;53(5):1554-62. doi: 10.1002/jhet.2462.

Lee CK, Lu CK, Kuo YH, Chen JZ, Sun GZ. New prenylated flavones from the roots of Ficus beecheyana. J Chinese Chemical Soc. 2004;51(2):437-41. doi: 10.1002/jccs.200400067.

Veit M, Geiger H, Czygan FC, Markham KR. Malonylated flavone 5-O-glucosides in the barren sprouts of Equisetum arvense. Phytochemistry. 1990;29(8):2555-60. doi: 10.1016/0031-9422(90)85187-K.

http://www.chemspider.com/chemical-[Structure].16520.html. [Last accessed on 10 Sep 2024].

https://www.chemicalbook.com/ChemicalProductProperty_EN_CB0104067.html. [Last accessed on 10 Sep 2024].

https://us.vwr.com/store/product/8979771/4-acetylphenyl-ether-98.Vol.2. [Last accessed on 10 Sep 2020].

Zi Y, Zhu M, Li X, Xu Y, Wei H, Li D. Effects of carboxyl and aldehyde groups on the antibacterial activity of oxidized amylose. Carbohydr Polym. 2018;192:118-25. doi: 10.1016/j.carbpol.2018.03.060, PMID 29691003.

El Menyiy NE, Aboulaghras S, Bakrim S, Moubachir R, Taha D, Khalid A. Genkwanin: an emerging natural compound with multifaceted pharmacological effects. Biomed Pharmacother. 2023;165:115159. doi: 10.1016/j.biopha.2023.115159, PMID 37481929.

Wu T, He M, Zang X, Zhou Y, Qiu T, Pan S. A structure-activity relationship study of flavonoids as inhibitors of E. coli by membrane interaction effect. Biochim Biophys Acta. 2013;1828(11):2751-6. doi: 10.1016/j.bbamem.2013.07.029, PMID 23938956.

Wu T, Zang X, He M, Pan S, Xu X. Structure-activity relationship of flavonoids on their anti-Escherichia coli activity and inhibition of DNA gyrase. J Agric Food Chem. 2013;61(34):8185-90. doi: 10.1021/jf402222v, PMID 23926942.

Vaou N, Stavropoulou E, Voidarou CC, Tsakris Z, Rozos G, Tsigalou C. Interactions between medical plant-derived bioactive compounds: focus on antimicrobial combination effects. Antibiotics (Basel). 2022;11(8):1014. doi: 10.3390/antibiotics11081014, PMID 36009883.

Bucar F, Wube A, Schmid M. Natural product isolation-how to get from biological material to pure compounds. Nat Prod Rep. 2013;30(4):525-45. doi: 10.1039/c3np20106f, PMID 23396532.

Published

24-02-2025

How to Cite

SYAFNI, N., SANDI, Y. P., HERNAWATI, & ARBAIN, D. (2025). PHYTOCHEMICAL STUDY AND ANTIMICROBIAL PROPERTIES OF FILMY FERN (HYMENOPHYLLUM IMBRICATUM BLUME). International Journal of Applied Pharmaceutics, 17(1), 107–111. https://doi.org/10.22159/ijap.2025.v17s1.16

Issue

Section

Original Article(s)

Similar Articles

<< < 5 6 7 8 9 > >> 

You may also start an advanced similarity search for this article.