Melola Discovery

← Melola Discovery

Akses terbuka Jurnal 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) · hlm. 167–180

DOI
10.4308/hjb.33.1.167-180
ISSN
2086-4094, 1978-3019
Terbit
2025-10-16
Penerbit
Bogor Agricultural University, Indonesia
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-nc/4.0

Abstrak

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.

Jaringan kolaborasi para penulis

40 penulis · 91 tautan kepenulisan bersama · 12 lintas organisasi · menampilkan 40 yang paling banyak terhubung

Arahkan kursor atau ketuk sebuah nama untuk menyorot rekan penulisnya. Klik dua kali untuk membuka halaman penulis.

  • Universitas Jambi
  • Universitas Islam Negeri Antasari Banjarmasin
  • Universitas Halu Oleo
  • Sekolah Tinggi Agama Buddha Negeri Raden Wijaya Wonogiri
  • Afiliasi tidak diketahui
  • Organisasi berbeda
  • Organisasi sama
  • Afiliasi tidak diketahui
  • Garis lebih tebal = lebih banyak artikel bersama · lingkaran lebih besar = lebih banyak artikel
Tampilkan sebagai tabel
Rekan penulisOrganisasiArtikel bersama
Wilda SyahriAfiliasi tidak diketahui11
Yusnaidar YusnaidarUniversitas Jambi4
Anis Yohana ChaerunisaaAfiliasi tidak diketahui3
Damris MuhammadUniversitas Jambi2
Aghnia HazrinaAfiliasi tidak diketahui2
Rifanza HirzanAfiliasi tidak diketahui2
Epinur EpinurAfiliasi tidak diketahui2
Abu BakarAfiliasi tidak diketahui2
Madyawati LatiefAfiliasi tidak diketahui2
Andita Fitri Mutiara RizkiAfiliasi tidak diketahui2
Wihda Aisarul AzmiAfiliasi tidak diketahui2
Melva LouisaAfiliasi tidak diketahui2
I Made ArtikaAfiliasi tidak diketahui2
Josephine Elizabeth SiregarAfiliasi tidak diketahui2
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 PradiptaAfiliasi tidak diketahui1
Dedi SuyatnoAfiliasi tidak diketahui1
Widya Naftalia WijasaAfiliasi tidak diketahui1
Ahmad Hamdani HasanuddinAfiliasi tidak diketahui1
Rahma AuliaAfiliasi tidak diketahui1
Hamdan YeewaeAfiliasi tidak diketahui1
Melinda BerlianaAfiliasi tidak diketahui1
Hutwan SyarifuddinAfiliasi tidak diketahui1
Edisar YantoAfiliasi tidak diketahui1
Restina BemisUniversitas Jambi1
Heriyanti HeriyantiAfiliasi tidak diketahui1
Sutrisno SutrisnoSekolah Tinggi Agama Buddha Negeri Raden Wijaya Wonogiri1
Ratih Dyah PuspitasariAfiliasi tidak diketahui1
Syaiful SyaifulAfiliasi tidak diketahui1
Emi AndriyaniAfiliasi tidak diketahui1
Devi Trianauli SiraitAfiliasi tidak diketahui1

Afiliasi berasal dari OpenAlex; metadata OAI-PMH jurnal tidak memuatnya. Penulis tanpa ID OpenAlex dicocokkan berdasarkan nama, sehingga dua orang bisa tergabung atau satu orang bisa terpisah.

Sumber metadata: OAI-PMH (metadata jurnal) http://journal.ipb.ac.id/index.php/hayati/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (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>