Antioxidant Activity and Lipoxygenase Enzyme Inhibitory Assay with Total Flavonoids Content from Garcinia hombroniana Pierre Stem Bark Extract

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Submitted by sys1 on Wed, 02/15/2017 - 15:00
Pharmacognosy Journal,2017,9,2,276-279.
Published:February 2017
Type:Original Article

Antioxidant Activity and Lipoxygenase Enzyme Inhibitory Assay with Total Flavonoids Content from Garcinia hombroniana Pierre Stem Bark Extract

Amanda Listiyani, Berna Elya*, Nuraini Puspitasari

Department of Pharmacognosy- Phytochemistry, Faculty of Pharmacy, Universitas Indonesia, Kampus Baru UI Depok, 16424, Depok, INDONESIA.

Abstract:

Introduction: Garcinia has been known as a rich source of xanthones, flavonoids, and phenols. The aim of this research is to obtain data of antioxidant activity and to observe potential inhibition of lipoxygenase activity that most active from methanolic, ethyl acetate and n-hexane extracts with total flavonoids content from most active extracts from the bark of Garcinia hombroniana Pierre. Methods: The antioxidant activity was measured using the ferric reducing antioxidant power (FRAP), the anti-inflammatory assay was measured using inhibition of lipoxygenase activity test, qualitative analysis of flavonoids using thin layer chromatography, and total flavonoids content was measured using AlCl3 colorimetric method. Results: The results showed that the ethyl acetate extract from G. hombroniana Pierre stem bark as the most active extract for antioxidant and lipoxygenase inhibition activity with EC50 and IC50 value consecutively 15.34 μg /ml; 0.26 μg /ml. Total flavonoids content of ethyl acetate is 7.430 mg QE/g extract. The results of this study showed bark extract Garcinia hombroniana Pierre has antioxidant activity and potent to inhibit lipoxygenase activity. Conclusion: Based on the research for methanolic, ethyl acetate and n-hexane extract, it can be concluded that the ethyl acetate extract of G. hombroniana Pierre as the most active extract for antioxidant and lipoxygenase inhibition activity.

Spot of ethyl acetate extract AND n-hexane extract