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Journal : Sinteza

Bioactive Compound Profiling of Ethyl Acetate Fraction from Oil Palm (Elaeis guineensis Jacq.) Leaves using Liquid Chromatography High Resolution Mass Spectrometry (LC-HRMS) Deni Setiawan; Samsul Hadi; Nur Mahdi; Nurul Mardiati; Normaidah; Nabila Hadiah Akbar; Muhammad Rasyid Ridha; Fitri Apriliany
Sinteza Vol. 5 No. 2 (2025): August
Publisher : Universitas Hamzanwadi

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.29408/sinteza.v5i2.30147

Abstract

Oil palm leaves could yield various health benefits, potentially leading to innovative applications in natural remedies, supplements, and dietary products. Targeted extraction and sophisticated analytical methods have become necessary for investigating bioactive compounds in plant materials. The combination of liquid chromatography and high-resolution mass spectrometry (LC–HRMS) makes for a potent technique for analyzing a wide range of metabolites, allowing for the precise and sensitive identification of various plant compounds. This investigation aimed to examine the active compounds in the ethyl acetate fraction of Elaeis guineensis leaves using LC–HRMS to identify potential new avenues for drug research. The simplicia was extracted by completely immersing 500 g of granules in acetone for three days. The crude extract was fractionated with n-hexane, ethyl acetate, and n-butanol solvents to separate components according to their polarity. The ethyl acetate part was analyzed using LC–HRMS with specific settings, including a temperature of 30°C and a gas flow rate of 11.01 L/min. The extract yield from dense oil palm leaves was 32.5 g, equivalent to 6.5%. Subsequently, the components were separated by fractionating the complete yield. The n-hexane fraction yield was 7.085 g or 21.83%, the ethyl acetate fraction yield was 3.38 g or 10.4%, the n-butanol fraction yield was 8.84 g or 27.2%, and the remaining fraction yield was 3.93 g or 12.1%. In conclusion, oil palm leaves are a prospective source of zingerol compounds, suggesting potential to be used as an alternative to rhizomes.
Co-Authors Achyadi, Ryan Ahmad Nazar Winarto Akbar, Nabila Hadiah Andi Sultang AS Apriyanti, Anna Aulia Rahmah Aulia, Hilma Azhara, Desiya Ramayanti Buih, Putri Helena Junjung Chatarina Umbul Wahyuni Dewi Kartika Dian Kusuma Putra Dindin Hiayatul Mursyidin Dinna Fitria Kumala Elita Fitriah Endah Puwarastuti Fajar Firdaus, Fajar Fathul Jannah, Fathul Faturakhim, Faturakhim Febriani, Noor Rahmi Fery Ramadhan Fitri Apriliany Fitria Handayani Gunawan Gunawan Gunawan Gunawan Hakim, Ade Syarif Hayatun Izma Herningtyas Nautika Lingga Ika Nuriama Septiana Sari Indriani, Erika Khadijah, Nor Khoirunnisa Muslimawati Kunti Nastiti Kunti Nastiti Kunti Nastiti Liling tryasmono Liling Tryasmono Maharani, Ni Ayu Mahdi, Lukman Mahfuzatul Ajmi Maryani, Henny Melindawati, Vina Muhammad Firman Akbar Muhammad Rasyid Ridha Muhammad Syihab Setia Budi Mulia, Radha Eka Muliani, Putri Sari Nabila Hadiah Akbar Nadya Novani Nadya Rahmi Naila Azizah Nashrul Wathan Nastiti, Kunti Nazrin Wahidi Nisa Handayani Noor Rizkiyah Normaidah Noval Noval Noval Noval Nur Indriyani Syarifuddin, Nur Indriyani Nur Mahdi Nur Mahdi Nur Meina Anjeli Nurul Mardiati Nurul Mardiati Nurul Mardiati Nurul Savira Fahira Okta Muthia Sari Okta Sari, Okta Pratiwi, Desy Putra, Aditya Maulana Perdana Putri, Indah Pebriani Raden Mohamad Herdian Bhakti Rafiah Anggianingrum Rahmadina, Nazwa Rahmatullah, Satrio Wibowo Rahmawati, Nanda Hesti Ramadani, Rizka aulia Rezka Fajar Ramadhan Ridho Hairil Herdin Prasetyo Rinda, Ririn Purnama Risye Hendry Rizka Aulia Norsafitri Salsabila, Risma Zahra Salwa, Helmina Samsul Hadi Samsul Hadi Samsul Hadi Samsul Hadi Sandi, Dita Ayulia Dwi Sari, Okta Mutia Sari, Risa Purnama Savitri, Riswandayani Shindi, Muhammad Riki Siti Bahzah Sofa, Maida Solly Aryza Sukmana, M. Laily Qadry Ulfah Ulfah, Nahdiati Viogenta, Pratika Wijaya, Eka Setya Wilda Maulida Nur Fatimatuzzahra Yudhi Ahmad Nazari Yusri Yusri Yusri Yusri