ANTIOXIDANT ACTIVITIES AND MARKER COMPOUND OF KALANGKALA (LITSEA GARCIAE VIDAL) EXTRACT

Background and purpose: Free radicals are highly reactive molecules because they have unpaired electrons. Antioxidants are compounds that can capture free radicals. One source of natural antioxidants is Litsea garciae or kalangkala which known as a typical Kalimantan plant. This research was cond...

Full description

Saved in:
Bibliographic Details
Main Author: Kamalia, Noor
Format: Theses
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/72170
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:72170
spelling id-itb.:721702023-03-06T11:32:55ZANTIOXIDANT ACTIVITIES AND MARKER COMPOUND OF KALANGKALA (LITSEA GARCIAE VIDAL) EXTRACT Kamalia, Noor Indonesia Theses antioxidant, kalangkala, Litsea garciae, DPPH, CUPRAC, FRAP INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/72170 Background and purpose: Free radicals are highly reactive molecules because they have unpaired electrons. Antioxidants are compounds that can capture free radicals. One source of natural antioxidants is Litsea garciae or kalangkala which known as a typical Kalimantan plant. This research was conducted to determine the antioxidant activity of extracts from several parts of kalangkala (included nonedible parts), to analyze the relationship between total phenolic content (TPC) and total flavonoid content (TFC) on antioxidant activity, as well as to identify and quantify marker compound. Method: Extraction was carried out by reflux method using n-hexane, ethyl acetate, and 96% ethanol. Antioxidant activity was determined using 2,2-diphenyl-1picrylhydrazil (DPPH), cupric ion reducing antioxidant capacity (CUPRAC), and ferric reducing antioxidant power (FRAP). The correlation between TPC and TFC with antioxidant activity and the correlation between the three methods were analyzed using the Pearson method. High performance liquid chromatography (HPLC) was performed to identify and quantify the marker compounds. Results: Antioxidant activity with the DPPH method ranged from 0.062-174.377, CUPRAC method 2.827-120.026, and FRAP method 5.291-1233.940 mg ascorbic acid equivalent antioxidant capacity (AEAC)/g extract. The highest TPC was shown by ethanol leaves extract (27.863 ± 2.140 g GAE/100 g extract) and the highest TFC was exposed by ethyl acetate leaves extract (10.644 ± 1.569 g QE/100 g extract). Conclusion: Phenolic compounds were the main contributor in antioxidant activity of kalangkala extract using the DPPH, CUPRAC, and FRAP methods. The DPPH, CUPRAC, and FRAP methods gave linear results for the antioxidant activity of the extract. Rutin was a marker of the ethanol kalangkala leaves extract with a value of 0.2996 ± 0.022%. Non-edible parts of kalangkala (leaves, twigs and seeds) can be developed for further sources of natural antioxidants. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Background and purpose: Free radicals are highly reactive molecules because they have unpaired electrons. Antioxidants are compounds that can capture free radicals. One source of natural antioxidants is Litsea garciae or kalangkala which known as a typical Kalimantan plant. This research was conducted to determine the antioxidant activity of extracts from several parts of kalangkala (included nonedible parts), to analyze the relationship between total phenolic content (TPC) and total flavonoid content (TFC) on antioxidant activity, as well as to identify and quantify marker compound. Method: Extraction was carried out by reflux method using n-hexane, ethyl acetate, and 96% ethanol. Antioxidant activity was determined using 2,2-diphenyl-1picrylhydrazil (DPPH), cupric ion reducing antioxidant capacity (CUPRAC), and ferric reducing antioxidant power (FRAP). The correlation between TPC and TFC with antioxidant activity and the correlation between the three methods were analyzed using the Pearson method. High performance liquid chromatography (HPLC) was performed to identify and quantify the marker compounds. Results: Antioxidant activity with the DPPH method ranged from 0.062-174.377, CUPRAC method 2.827-120.026, and FRAP method 5.291-1233.940 mg ascorbic acid equivalent antioxidant capacity (AEAC)/g extract. The highest TPC was shown by ethanol leaves extract (27.863 ± 2.140 g GAE/100 g extract) and the highest TFC was exposed by ethyl acetate leaves extract (10.644 ± 1.569 g QE/100 g extract). Conclusion: Phenolic compounds were the main contributor in antioxidant activity of kalangkala extract using the DPPH, CUPRAC, and FRAP methods. The DPPH, CUPRAC, and FRAP methods gave linear results for the antioxidant activity of the extract. Rutin was a marker of the ethanol kalangkala leaves extract with a value of 0.2996 ± 0.022%. Non-edible parts of kalangkala (leaves, twigs and seeds) can be developed for further sources of natural antioxidants.
format Theses
author Kamalia, Noor
spellingShingle Kamalia, Noor
ANTIOXIDANT ACTIVITIES AND MARKER COMPOUND OF KALANGKALA (LITSEA GARCIAE VIDAL) EXTRACT
author_facet Kamalia, Noor
author_sort Kamalia, Noor
title ANTIOXIDANT ACTIVITIES AND MARKER COMPOUND OF KALANGKALA (LITSEA GARCIAE VIDAL) EXTRACT
title_short ANTIOXIDANT ACTIVITIES AND MARKER COMPOUND OF KALANGKALA (LITSEA GARCIAE VIDAL) EXTRACT
title_full ANTIOXIDANT ACTIVITIES AND MARKER COMPOUND OF KALANGKALA (LITSEA GARCIAE VIDAL) EXTRACT
title_fullStr ANTIOXIDANT ACTIVITIES AND MARKER COMPOUND OF KALANGKALA (LITSEA GARCIAE VIDAL) EXTRACT
title_full_unstemmed ANTIOXIDANT ACTIVITIES AND MARKER COMPOUND OF KALANGKALA (LITSEA GARCIAE VIDAL) EXTRACT
title_sort antioxidant activities and marker compound of kalangkala (litsea garciae vidal) extract
url https://digilib.itb.ac.id/gdl/view/72170
_version_ 1822992462662074368