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Chitosan Xylotrupes gideon encapsulated lemongrass leaf ethanol extract reduce H2O2‐induced oxidative stress in human dermal fibroblast

Indonesian Journal of Biotechnology · Vol. 28 No. 4 (2023) · hlm. 191–199

DOI
10.22146/ijbiotech.81544
ISSN
2089-2241, 0853-8654
Terbit
2023-12-30
Penerbit
Universitas Gadjah Mada
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-sa/4.0

Abstrak

During phagocytosis, phagocyte cells discharge reactive oxygen species referred to as respiratory bursts, inducing a rise in pro‐oxidants and subjecting the cell to oxidative stress. Such stress is a biological mechanism related to an imbalance in pro‐oxidant/antioxidant homeostasis, which generates toxic reactive oxygen. Encapsulation is a coating process to improve the stability of bioactive compounds from lemongrass extract. Therefore, this study aims to determine the encapsulation activity of lemongrass leaf extract with chitosan X. gideon (LEChXg) to reduce the oxidative stress of fibroblasts. The research used the human dermal fibroblast (HDF) cell line, comprising negative and positive controls and use of LEChXg 100, 200, 300, 400, and 500 µg/mL. HDF cell migration was evaluated by employing the scratch wound healing method and the wound closure was oberseved at 0, 2, 4, 6, and 24 h intervals. The cell proliferation was observed at 24, 48, and 72 h using CCK‐8 at a 450 nm wavelength. The results showed that the observations at 0, 2, and 4 h did not demonstrate any significant difference on the cell migration (p > 0.05) among the groups. However, the wound closure at 4 and 6 h showed a significant difference (p < 0.05) with LEChXg 300 µg/mL. Despite the lack of any significant variation observed up to 24 h, fibroblast subjected to the stressor did not achieve complete closure. The groups treated with LEChXg were more stable in maintaining fibroblast proliferation up to the end of the observation than those with stressors at 24, 48, and 72 h. Fibroblast induced with a stressor was also more stable in maintaining migration and proliferation in groups receiving LEChXg 300 µg/mL.

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  • Universitas Muhammadiyah Malang
  • Universitas Halu Oleo
  • Biju Patnaik University of Technology
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  • Organisasi berbeda
  • Organisasi sama
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Rekan penulisOrganisasiArtikel bersama
Dwi Priyo AriyantoAfiliasi tidak diketahui9
Jauhari SyamsiyahAfiliasi tidak diketahui5
Sumani SumaniAfiliasi tidak diketahui5
Mujiyo MujiyoAfiliasi tidak diketahui3
Nur Putri HidayahAfiliasi tidak diketahui2
Sri HartatiAfiliasi tidak diketahui2
Widyatmani Sih DewiAfiliasi tidak diketahui2
Siddhartha BeheraAfiliasi tidak diketahui2
Manoj kumar SahuAfiliasi tidak diketahui2
Aktavia HerawatiAfiliasi tidak diketahui2
Muhamad Khoiru ZakiAfiliasi tidak diketahui2
Keigo NodaAfiliasi tidak diketahui2
Suntoro SuntoroAfiliasi tidak diketahui2
Nur Putri HidayahUniversitas Muhammadiyah Malang1
Ahmad Dzaki AbidinUniversitas Muhammadiyah Malang1
Torri JustiansyahUniversitas Muhammadiyah Malang1
Aldi Malik FarhadUniversitas Muhammadiyah Malang1
Karina Ghea SilvanaUniversitas Muhammadiyah Malang1
Ordelia Julayta SyahidahUniversitas Muhammadiyah Malang1
Tinuk Dwi CahyaniAfiliasi tidak diketahui1
Tinuk Dwi Cahyani CahyaniAfiliasi tidak diketahui1
Taufiq Perak SanjayaAfiliasi tidak diketahui1
RAHAYU RAHAYUUniversitas Halu Oleo1
Irvan Septrian Syah Putra RasadAfiliasi tidak diketahui1
Maylan NimasAfiliasi tidak diketahui1
Nadira SyabillaAfiliasi tidak diketahui1
Twinkle HazraAfiliasi tidak diketahui1
Rabindra BeheraAfiliasi tidak diketahui1
Sunila Kumar SwainAfiliasi tidak diketahui1
Itishree SahuAfiliasi tidak diketahui1
Sritam ParidaAfiliasi tidak diketahui1
Saroja Kumar DashBiju Patnaik University of Technology1
Tatag WidodoAfiliasi 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) https://jurnal.ugm.ac.id/ijbiotech/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-US">Chitosan Xylotrupes gideon encapsulated lemongrass leaf ethanol extract reduce H2O2‐induced oxidative stress in human dermal fibroblast</dc:title>
	<dc:creator>Komariah, Komariah</dc:creator>
	<dc:creator>Trisfilha, Pretty</dc:creator>
	<dc:creator>Wahyudi, Rahman</dc:creator>
	<dc:creator>Erica, Nada</dc:creator>
	<dc:creator>Nugroho, Didi</dc:creator>
	<dc:creator>Ariesanti, Yessy</dc:creator>
	<dc:creator>Swain, Sarat Kumar</dc:creator>
	<dc:subject xml:lang="en-US">Chitosan X. gideon; Lemongrass leaf; Migration; Oxidative stress; Proliferation</dc:subject>
	<dc:description xml:lang="en-US">During phagocytosis, phagocyte cells discharge reactive oxygen species referred to as respiratory bursts, inducing a rise in pro‐oxidants and subjecting the cell to oxidative stress. Such stress is a biological mechanism related to an imbalance in pro‐oxidant/antioxidant homeostasis, which generates toxic reactive oxygen. Encapsulation is a coating process to improve the stability of bioactive compounds from lemongrass extract. Therefore, this study aims to determine the encapsulation activity of lemongrass leaf extract with chitosan X. gideon (LEChXg) to reduce the oxidative stress of fibroblasts. The research used the human dermal fibroblast (HDF) cell line, comprising negative and positive controls and use of LEChXg 100, 200, 300, 400, and 500 µg/mL. HDF cell migration was evaluated by employing the scratch wound healing method and the wound closure was oberseved at 0, 2, 4, 6, and 24 h intervals. The cell proliferation was observed at 24, 48, and 72 h using CCK‐8 at a 450 nm wavelength. The results showed that the observations at 0, 2, and 4 h did not demonstrate any significant difference on the cell migration (p &gt; 0.05) among the groups. However, the wound closure at 4 and 6 h showed a significant difference (p &lt; 0.05) with LEChXg 300 µg/mL. Despite the lack of any significant variation observed up to 24 h, fibroblast subjected to the stressor did not achieve complete closure. The groups treated with LEChXg were more stable in maintaining fibroblast proliferation up to the end of the observation than those with stressors at 24, 48, and 72 h. Fibroblast induced with a stressor was also more stable in maintaining migration and proliferation in groups receiving LEChXg 300 µg/mL.</dc:description>
	<dc:publisher xml:lang="en-US">Universitas Gadjah Mada</dc:publisher>
	<dc:contributor xml:lang="en-US"></dc:contributor>
	<dc:date>2023-12-30</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-US">Original Research Articles</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.ugm.ac.id/ijbiotech/article/view/81544</dc:identifier>
	<dc:identifier>10.22146/ijbiotech.81544</dc:identifier>
	<dc:source xml:lang="en-US">Indonesian Journal of Biotechnology; Vol 28, No 4 (2023); 191-199</dc:source>
	<dc:source>2089-2241</dc:source>
	<dc:source>0853-8654</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.ugm.ac.id/ijbiotech/article/view/81544/38151</dc:relation>
	<dc:relation>https://journal.ugm.ac.id/ijbiotech/article/downloadSuppFile/81544/25072</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2023 The Author(s)</dc:rights>
	<dc:rights xml:lang="en-US">http://creativecommons.org/licenses/by-sa/4.0</dc:rights>
</oai_dc:dc>