Melola Discovery

← Melola Discovery

Akses terbuka Jurnal SINTA 1

Extraction, Purification, and Bioactivity of Fucoxanthin from Brown Seaweed Sargassum hystrix

Jurnal Ilmiah Perikanan dan Kelautan · Vol. 18 No. 2 (2026) · hlm. 670–679

DOI
10.20473/jipk.v18i2.84197
ISSN
2528-0759, 2085-5842
Terbit
2026-02-03
Penerbit
Faculty of Fisheries and Marine Universitas Airlangga
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-nc-sa/4.0

Abstrak

Graphical Abstract Highlight Research 1. UAE at 45°C for 30 min produced the highest crude extract yield (19.90%). 2. Ethyl acetate:n-butanol (8:2) yielded the highest fucoxanthin fraction (1.31 mg/g). 3. Fucoxanthin fractions showed strong antioxidant activity (DPPH IC₅₀ 86.18±5.06 µg/mL). 4. Purified fractions exhibited strong tyrosinase inhibition (IC₅₀ 76.04±3.24 µg/mL). Abstract Fucoxanthin is the major carotenoid present in brown seaweeds and exhibits strong biological activities, particularly as an antioxidant and anti-aging agent. However, efficient extraction and purification conditions for fucoxanthin from Sargassum hystrix, along with its functional evaluation, remain limited. This research aimed to establish the most effective extraction conditions for obtaining fucoxanthin from S. hystrix using Ultrasound Assisted Extraction (UAE), determine the optimal solvent system for purification, and evaluate the antiox- idant and anti-aging activities of both the extracted and purified fucoxanthin. Extraction was carried out using UAE with 96% ethanol at temperatures of 35- 45°C and durations of 20-30 min. Purification was conducted through column chromatography using three solvent systems: n-hexane:acetone (6:4 v/v), methanol:chloroform (7:3 v/v), and ethyl acetate:n-butanol (8:2 v/v). Fucoxanthin was identified by thin-layer chromatography and fucoxanthin was quantified using reversed-phase high-performance liquid chromatography (HPLC) equipped with a C18 column, while antioxidant activity was measured using the DPPH method and anti-aging activity was assessed via tyrosinase inhibition. The results showed that optimal extraction occurred at 40-45°C for 25-30 min, yielding 18.33-19.9% crude extract, and the ethyl acetate:nbutanol (8:2 v/v) system produced the highest fucoxanthin fraction yield (8.26-9.54%), with fraction F22 containing the highest fucoxanthin level at 1.31 mg/g. The fucoxanthin fraction displayed markedly enhanced activity, with strong antioxidant capacity (IC₅₀ = 86.18±5.06 μg/mL, an 83.8% improvement over the crude extract) and strong tyrosinase inhibition (IC₅₀ = 76.04±3.24 μg/mL). Overall, fucoxanthin derived from S. hystrix demonstrates substantial promise as an active antioxidant and anti-aging compound for nutraceutical and cosmetic applications, suggesting that future studies should focus on scaling up the extraction and purification pro- cess and further elucidating its mechanisms of action and stability in formulated products. The fraction is a promising candidate for further in vitro candidate and formulation-based cosmeceutical evaluation.

Kata kunci

Jaringan kolaborasi para penulis

40 penulis · 95 tautan kepenulisan bersama · 14 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 Gadjah Mada
  • Universitas Teuku Umar
  • Ministry of Marine Affairs and Fisheries
  • Indonesian Institute of Sciences
  • Hasanuddin University
  • Universitas Halu Oleo
  • IPB University
  • 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
Amir HusniAfiliasi tidak diketahui7
Indun Dewi PuspitaUniversitas Gadjah Mada4
Siti Ari BudhiyantiUniversitas Gadjah Mada3
U. UstadiUniversitas Gadjah Mada2
Nurfitri EkantariUniversitas Gadjah Mada2
Venny AgustinUniversitas Gadjah Mada2
Yohanes HarvindaUniversitas Gadjah Mada1
Ustadi UstadiUniversitas Gadjah Mada1
Anandita Perwita KurniawanUniversitas Gadjah Mada1
Muwantoko MurwantokoAfiliasi tidak diketahui1
Alim IsnansetyoUniversitas Gadjah Mada1
Indah IstiqomahUniversitas Gadjah Mada1
Toni KuswoyoMinistry of Marine Affairs and Fisheries1
Prihati Sih NugraheniUniversitas Gadjah Mada1
Khofifah Fajar FitrianiUniversitas Gadjah Mada1
Antarif Kusuma BrataUniversitas Gadjah Mada1
Maria MadalenaUniversitas Gadjah Mada1
Ervika Rahayu Novita HerawatiIndonesian Institute of Sciences1
Yusuf Kalingga MurdaUniversitas Gadjah Mada1
Almira Islamei PratiwiUniversitas Gadjah Mada1
Bambang Retno AjiUniversitas Gadjah Mada1
Rani LaksanawatiUniversitas Gadjah Mada1
A A S E MaharaniUniversitas Gadjah Mada1
Ivana M. DiharningrumUniversitas Gadjah Mada1
Rizqi Wahyu HerdiantoUniversitas Gadjah Mada1
Amir MugozinAfiliasi tidak diketahui1
Amir MugozinUniversitas Gadjah Mada1
KasmiatiHasanuddin University1
SuadiAfiliasi tidak diketahui1
AsnaniUniversitas Halu Oleo1
Komala Putu Tara HradayaUniversitas Gadjah Mada1
Pris LarasatiUniversitas Gadjah Mada1
Zuriat ZuriatAfiliasi tidak diketahui1
Rina SyafitriUniversitas Teuku Umar1
Mohamad GazaliAfiliasi tidak diketahui1
Mila Novalita SuhardaniAfiliasi tidak diketahui1
Nurjanah - NurjanahIPB University1

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) https://e-journal.unair.ac.id/index.php/JIPK/oai, pertama di-harvest 9 Nov 2026, terakhir terlihat 9 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-US">Extraction, Purification, and Bioactivity of Fucoxanthin from Brown Seaweed Sargassum hystrix</dc:title>
	<dc:creator>Mufarocha, Nungky</dc:creator>
	<dc:creator>Husni, Amir</dc:creator>
	<dc:creator>Putra, Masagus Muhammad Prima</dc:creator>
	<dc:subject xml:lang="en-US">Ultrasonication</dc:subject>
	<dc:subject xml:lang="en-US">Tyrosinase</dc:subject>
	<dc:subject xml:lang="en-US">Antioxidant</dc:subject>
	<dc:subject xml:lang="en-US">Fucoxanthin</dc:subject>
	<dc:description xml:lang="en-US">Graphical Abstract

Highlight Research
1. UAE at 45°C for 30 min produced the highest crude extract yield (19.90%).
2. Ethyl acetate:n-butanol (8:2) yielded the highest fucoxanthin fraction (1.31 mg/g).
3. Fucoxanthin fractions showed strong antioxidant activity (DPPH IC₅₀ 86.18±5.06 µg/mL).
4. Purified fractions exhibited strong tyrosinase inhibition (IC₅₀ 76.04±3.24 µg/mL).
 
Abstract
Fucoxanthin is the major carotenoid present in brown seaweeds and exhibits strong biological activities, particularly as an antioxidant and anti-aging agent. However, efficient extraction and purification conditions for fucoxanthin from Sargassum hystrix, along with its functional evaluation, remain limited. This research aimed to establish the most effective extraction conditions for obtaining fucoxanthin from S. hystrix using Ultrasound Assisted Extraction (UAE), determine the optimal solvent system for purification, and evaluate the antiox- idant and anti-aging activities of both the extracted and purified fucoxanthin. Extraction was carried out using UAE with 96% ethanol at temperatures of 35- 45°C and durations of 20-30 min. Purification was conducted through column chromatography using three solvent systems: n-hexane:acetone (6:4 v/v), methanol:chloroform (7:3 v/v), and ethyl acetate:n-butanol (8:2 v/v). Fucoxanthin was identified by thin-layer chromatography and fucoxanthin was quantified using reversed-phase high-performance liquid chromatography (HPLC) equipped with a C18 column, while antioxidant activity was measured using the DPPH method and anti-aging activity was assessed via tyrosinase inhibition. The results showed that optimal extraction occurred at 40-45°C for 25-30 min, yielding 18.33-19.9% crude extract, and the ethyl acetate:nbutanol (8:2 v/v) system produced the highest fucoxanthin fraction yield (8.26-9.54%), with fraction F22 containing the highest fucoxanthin level at 1.31 mg/g. The fucoxanthin fraction displayed markedly enhanced activity, with strong antioxidant capacity (IC₅₀ = 86.18±5.06 μg/mL, an 83.8% improvement over the crude extract) and strong tyrosinase inhibition (IC₅₀ = 76.04±3.24 μg/mL). Overall, fucoxanthin derived from S. hystrix demonstrates substantial promise as an active antioxidant and anti-aging compound for nutraceutical and cosmetic applications, suggesting that future studies should focus on scaling up the extraction and purification pro- cess and further elucidating its mechanisms of action and stability in formulated products. The fraction is a promising candidate for further in vitro candidate and formulation-based cosmeceutical evaluation.
 </dc:description>
	<dc:publisher xml:lang="en-US">Faculty of Fisheries and Marine Universitas Airlangga</dc:publisher>
	<dc:date>2026-02-03</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>text/xml</dc:format>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://e-journal.unair.ac.id/JIPK/article/view/84197</dc:identifier>
	<dc:identifier>10.20473/jipk.v18i2.84197</dc:identifier>
	<dc:source xml:lang="en-US">Jurnal Ilmiah Perikanan dan Kelautan; Vol. 18 No. 2 (2026): JURNAL ILMIAH PERIKANAN DAN KELAUTAN; 670-679</dc:source>
	<dc:source>2528-0759</dc:source>
	<dc:source>2085-5842</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://e-journal.unair.ac.id/JIPK/article/view/84197/40587</dc:relation>
	<dc:relation>https://e-journal.unair.ac.id/JIPK/article/view/84197/38865</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2026 Jurnal Ilmiah Perikanan dan Kelautan</dc:rights>
	<dc:rights xml:lang="en-US">http://creativecommons.org/licenses/by-nc-sa/4.0</dc:rights>
</oai_dc:dc>