Melola Discovery

← Melola Discovery

Open access Journal SINTA 1

Anticancer Activities and Metabolite Profiling of UHPLC-HRMS Method from Chrysanthemum x morifolium (Ramat.) Hemsl Leaves

HAYATI Journal of Biosciences · Vol. 33 No. 1 (2025) · pp. 167–180

DOI
10.4308/hjb.33.1.167-180
ISSN
2086-4094, 1978-3019
Published
2025-10-16
Publisher
Bogor Agricultural University, Indonesia
Language
eng
License
creativecommons.org/licenses/by-nc/4.0

Abstract

The Chrysanthemum morifolium Ramat, traditionally used for cancer treatment, including breast cancer, possesses anticancer properties. The aim of this study is metabolite profiling using ultra-high-performance liquid chromatography in conjunction with the high-resolution mass spectrometry (UHPLC-HRMS) technique and its correlation with the cytotoxic activity of the extract and ethyl acetate fraction of Chrysanthemum x morifolium (Ramat.) Hemsl leaves on cancer cells. The ethyl acetate fraction from the hydrolyzed ethanol extract of (Chrysanthemum x morifolium (Ramat.) Hemsl) leaves has anticancer activity against the MCF-7 breast cancer cells. Metabolite profiling was used to understand the presence of metabolites that have anticancer activity. UHPLC-HRMS was used to profile their metabolites. Compound Discoverer 3.3 software finished data processing and metabolite annotation. Anticancer activity was performed using the 2-[2-methoxy-4-nitrophenyl]-3[4-nitrophenyl]-5[2,4-disulfophenyl]-2H-tetrazolium (WST-8) assay. As many as 57 secondary metabolites were identified by UHPLC-HRMS analysis. Secondary metabolites that have the potential as anti-breast cancer are glycitein, diosmetin, kaempferol, esculetin, scopoletin, dihydroartemisinin, and Chrysin, with successive percentages of 31.39%, 19.91%, 5.61%, 2.63%, 0.82%, 0.14%, and 0.05%. Ethyl acetate fraction showed stronger cytotoxic activity than ethanol extract against MCF-7 cells with IC50 values of 66.31 ppm at 24 hours incubation and 40.35 ppm at 48 hours. Further research can be conducted on the isolation of flavonoids from the ethyl acetate fraction, as well as the analysis of cell cycle apoptosis stimulation and gene expression mechanisms.

Collaboration network of the authors

40 authors · 91 co-authorship links · 12 across different organisations · showing the 40 most connected

Hover or tap a name to highlight its co-authors. Double-click to open the author's page.

  • Universitas Jambi
  • Universitas Islam Negeri Antasari Banjarmasin
  • Universitas Halu Oleo
  • Sekolah Tinggi Agama Buddha Negeri Raden Wijaya Wonogiri
  • Affiliation unknown
  • Different organisations
  • Same organisation
  • Affiliation unknown
  • Thicker line = more joint articles · bigger circle = more articles
Show as table
Co-authorOrganisationJoint articles
Wilda SyahriAffiliation unknown11
Yusnaidar YusnaidarUniversitas Jambi4
Anis Yohana ChaerunisaaAffiliation unknown3
Damris MuhammadUniversitas Jambi2
Aghnia HazrinaAffiliation unknown2
Rifanza HirzanAffiliation unknown2
Epinur EpinurAffiliation unknown2
Abu BakarAffiliation unknown2
Madyawati LatiefAffiliation unknown2
Andita Fitri Mutiara RizkiAffiliation unknown2
Wihda Aisarul AzmiAffiliation unknown2
Melva LouisaAffiliation unknown2
I Made ArtikaAffiliation unknown2
Josephine Elizabeth SiregarAffiliation unknown2
Ainul Hayatin NisaUniversitas Islam Negeri Antasari Banjarmasin1
Fithriana SyarqawieUniversitas Islam Negeri Antasari Banjarmasin1
Ilham AkbarUniversitas Halu Oleo1
Rimayanti RimayantiUniversitas Islam Negeri Antasari Banjarmasin1
Sabri AminUniversitas Jambi1
Kamid KamidUniversitas Jambi1
Ivan PradiptaAffiliation unknown1
Dedi SuyatnoAffiliation unknown1
Widya Naftalia WijasaAffiliation unknown1
Ahmad Hamdani HasanuddinAffiliation unknown1
Rahma AuliaAffiliation unknown1
Hamdan YeewaeAffiliation unknown1
Melinda BerlianaAffiliation unknown1
Hutwan SyarifuddinAffiliation unknown1
Edisar YantoAffiliation unknown1
Restina BemisUniversitas Jambi1
Heriyanti HeriyantiAffiliation unknown1
Sutrisno SutrisnoSekolah Tinggi Agama Buddha Negeri Raden Wijaya Wonogiri1
Ratih Dyah PuspitasariAffiliation unknown1
Syaiful SyaifulAffiliation unknown1
Emi AndriyaniAffiliation unknown1
Devi Trianauli SiraitAffiliation unknown1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) http://journal.ipb.ac.id/index.php/hayati/oai, first harvested 8 Nov 2026, last seen 8 Nov 2026.
Original metadata (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/  http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en">Anticancer Activities and Metabolite Profiling of UHPLC-HRMS Method from Chrysanthemum x morifolium (Ramat.) Hemsl Leaves</dc:title>
	<dc:creator xml:lang="en">Maesaroh, Imas</dc:creator>
	<dc:creator xml:lang="en">Barliana, Melisa Intan</dc:creator>
	<dc:creator xml:lang="en">Abdulah, Rizky</dc:creator>
	<dc:creator xml:lang="en">Muhaimin, Muhaimin</dc:creator>
	<dc:description xml:lang="en">The Chrysanthemum morifolium Ramat, traditionally used for cancer treatment, including breast cancer, possesses anticancer properties. The aim of this study is metabolite profiling using ultra-high-performance liquid chromatography in conjunction with the high-resolution mass spectrometry (UHPLC-HRMS) technique and its correlation with the cytotoxic activity of the extract and ethyl acetate fraction of Chrysanthemum x morifolium (Ramat.) Hemsl leaves on cancer cells. The ethyl acetate fraction from the hydrolyzed ethanol extract of (Chrysanthemum x morifolium (Ramat.) Hemsl) leaves has anticancer activity against the MCF-7 breast cancer cells. Metabolite profiling was used to understand the presence of metabolites that have anticancer activity. UHPLC-HRMS was used to profile their metabolites. Compound Discoverer 3.3 software finished data processing and metabolite annotation. Anticancer activity was performed using the 2-[2-methoxy-4-nitrophenyl]-3[4-nitrophenyl]-5[2,4-disulfophenyl]-2H-tetrazolium (WST-8) assay. As many as 57 secondary metabolites were identified by UHPLC-HRMS analysis. Secondary metabolites that have the potential as anti-breast cancer are glycitein, diosmetin, kaempferol, esculetin, scopoletin, dihydroartemisinin, and Chrysin, with successive percentages of 31.39%, 19.91%, 5.61%, 2.63%, 0.82%, 0.14%, and 0.05%. Ethyl acetate fraction showed stronger cytotoxic activity than ethanol extract against MCF-7 cells with IC50 values of 66.31 ppm at 24 hours incubation and 40.35 ppm at 48 hours. Further research can be conducted on the isolation of flavonoids from the ethyl acetate fraction, as well as the analysis of cell cycle apoptosis stimulation and gene expression mechanisms.</dc:description>
	<dc:publisher xml:lang="en">Bogor Agricultural University, Indonesia</dc:publisher>
	<dc:date>2025-10-16</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>http://journal.ipb.ac.id/hayati/article/view/62069</dc:identifier>
	<dc:identifier>10.4308/hjb.33.1.167-180</dc:identifier>
	<dc:source xml:lang="en">HAYATI Journal of Biosciences; Vol. 33 No. 1 (2026): January 2026; 167-180</dc:source>
	<dc:source>2086-4094</dc:source>
	<dc:source>1978-3019</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>http://journal.ipb.ac.id/hayati/article/view/62069/31817</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2025 Imas Maesaroh, Melisa Intan Barliana, Rizky Abdulah, Muhaimin Muhaimin</dc:rights>
	<dc:rights xml:lang="en">https://creativecommons.org/licenses/by-nc/4.0</dc:rights>
</oai_dc:dc>