Antioxidant activity of Litsea petiolata Hk. f

Litsea petiolata Hk. f was included Lauraceae family, and the previous study had been isolated 5 compounds from the Litsea petiolata Hk. f stem bark dichloromethane extract namely harman or aribine, norharman, reticuline, isoboldine, and thalifoline. Antioxidants can prevent tissue damage by free ra...

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Main Authors: Ambarwati, Neneng Siti Silfi, Elya, Berna, Mahayasih, Putu Gita Maya Widyaswari, Awang, Muhammad Shahrul Nizam, Omar, H.
Format: Conference or Workshop Item
Published: 2021
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Online Access:http://eprints.um.edu.my/35469/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85104702393&doi=10.1088%2f1742-6596%2f1869%2f1%2f012055&partnerID=40&md5=d59143fab7f7d2525c0d4e1eaf3f7799
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spelling my.um.eprints.354692023-10-10T02:30:45Z http://eprints.um.edu.my/35469/ Antioxidant activity of Litsea petiolata Hk. f Ambarwati, Neneng Siti Silfi Elya, Berna Mahayasih, Putu Gita Maya Widyaswari Awang, Muhammad Shahrul Nizam Omar, H. QD Chemistry Litsea petiolata Hk. f was included Lauraceae family, and the previous study had been isolated 5 compounds from the Litsea petiolata Hk. f stem bark dichloromethane extract namely harman or aribine, norharman, reticuline, isoboldine, and thalifoline. Antioxidants can prevent tissue damage by free radical. Free radical production continuously in all cells as cellular function usually, but excess production can cause many diseases. The research aimed to assay the activity of antioxidant from the extract and fractions of the Litsea petiolata Hk. f stem bark with DPPH assay and FRAP assay. The extract was obtained by soxhletation used dichloromethane as solvent. The fractions fractionated with column chromatography. The antioxidant test used DPPH assay and FRAP assay. The IC50 values for the 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging test of the dichloromethane extract was 27.36 µg/mL, the fraction A was 113.74 µg/mL, fraction B was 60.17 µg/mL, and the control positive (quercetin) was 3.96 µg/ml. The EC50 values for ferric ion reducing antioxidant potential (FRAP) test of the dichloromethane extract was obtained 13.47 µg/mL, the fraction A was 76.49 µg/mL, fraction B was 55.73 µg/mL, and the control positive (quercetin) was 14.01 µg/ml. The extract had higher antioxidant activity than the fractions, and by FRAP test the extract showed better antioxidant activity than the positive control (quercetin). © Published under licence by IOP Publishing Ltd. 2021-04 Conference or Workshop Item PeerReviewed Ambarwati, Neneng Siti Silfi and Elya, Berna and Mahayasih, Putu Gita Maya Widyaswari and Awang, Muhammad Shahrul Nizam and Omar, H. (2021) Antioxidant activity of Litsea petiolata Hk. f. In: 2nd Annual Conference of Science and Technology, ANCOSET 2020, 28 November 2020, Malang, Virtual. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85104702393&doi=10.1088%2f1742-6596%2f1869%2f1%2f012055&partnerID=40&md5=d59143fab7f7d2525c0d4e1eaf3f7799
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic QD Chemistry
spellingShingle QD Chemistry
Ambarwati, Neneng Siti Silfi
Elya, Berna
Mahayasih, Putu Gita Maya Widyaswari
Awang, Muhammad Shahrul Nizam
Omar, H.
Antioxidant activity of Litsea petiolata Hk. f
description Litsea petiolata Hk. f was included Lauraceae family, and the previous study had been isolated 5 compounds from the Litsea petiolata Hk. f stem bark dichloromethane extract namely harman or aribine, norharman, reticuline, isoboldine, and thalifoline. Antioxidants can prevent tissue damage by free radical. Free radical production continuously in all cells as cellular function usually, but excess production can cause many diseases. The research aimed to assay the activity of antioxidant from the extract and fractions of the Litsea petiolata Hk. f stem bark with DPPH assay and FRAP assay. The extract was obtained by soxhletation used dichloromethane as solvent. The fractions fractionated with column chromatography. The antioxidant test used DPPH assay and FRAP assay. The IC50 values for the 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging test of the dichloromethane extract was 27.36 µg/mL, the fraction A was 113.74 µg/mL, fraction B was 60.17 µg/mL, and the control positive (quercetin) was 3.96 µg/ml. The EC50 values for ferric ion reducing antioxidant potential (FRAP) test of the dichloromethane extract was obtained 13.47 µg/mL, the fraction A was 76.49 µg/mL, fraction B was 55.73 µg/mL, and the control positive (quercetin) was 14.01 µg/ml. The extract had higher antioxidant activity than the fractions, and by FRAP test the extract showed better antioxidant activity than the positive control (quercetin). © Published under licence by IOP Publishing Ltd.
format Conference or Workshop Item
author Ambarwati, Neneng Siti Silfi
Elya, Berna
Mahayasih, Putu Gita Maya Widyaswari
Awang, Muhammad Shahrul Nizam
Omar, H.
author_facet Ambarwati, Neneng Siti Silfi
Elya, Berna
Mahayasih, Putu Gita Maya Widyaswari
Awang, Muhammad Shahrul Nizam
Omar, H.
author_sort Ambarwati, Neneng Siti Silfi
title Antioxidant activity of Litsea petiolata Hk. f
title_short Antioxidant activity of Litsea petiolata Hk. f
title_full Antioxidant activity of Litsea petiolata Hk. f
title_fullStr Antioxidant activity of Litsea petiolata Hk. f
title_full_unstemmed Antioxidant activity of Litsea petiolata Hk. f
title_sort antioxidant activity of litsea petiolata hk. f
publishDate 2021
url http://eprints.um.edu.my/35469/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85104702393&doi=10.1088%2f1742-6596%2f1869%2f1%2f012055&partnerID=40&md5=d59143fab7f7d2525c0d4e1eaf3f7799
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