Original ArticleFree Radicals and AntioxidantsVol. 4 | Issue 1 | pp. 24–31Open access
Assessment of the antioxidant and antiradicalic capacities in vitro of different phenolic derivatives
- 1*,
- 2
- 1 Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, 25240 Erzurum-Turkey.
- 2 Department of Food Technology, Erzurum Vocational Training School, Ataturk University, 25240 Erzurum-Turkey.
Published in Free Radicals and Antioxidants
Correspondence: Kaan Kucukoglu
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, 25240 Erzurum-Turkey.
Email: kucukogluk@yahoo.com.tr
- Received:
- Nov 18, 2013
- DOI:
- 10.5530/fra.2014.1.5
How to cite
Kucukoglu, K., & Nadaroglu, H. Assessment of the antioxidant and antiradicalic capacities in vitro of different phenolic derivatives. Free Radicals and Antioxidants, 4(1), 24–31. https://doi.org/10.5530/fra.2014.1.5
Abstract
Introduction: The antioxidant and radical scavenging properties of some of the hydroxy phenyl derivatives such as 4-Hydroxybenzoic acid (1), 3-Hydroxy-4-methoxycinnamic acid (2), 3-(4-Hydroxy-3,5-dimethoxyphenyl)prop-2- enoic acid (Sinapic acid) (3), 4-Hydroxy-3,5-dimethoxybenzoic acid (4), 3,4-Dihydroxycinnamic acid (Caffeic acid) (5) and 5-Isopropyl-2-methylphenol (6), which are naturally present in fruits and vegetables, were investigated. Methods: The following analysis were conducted: The total antioxidant activity via the ferric thiocyanate method; 2,2’-azinobis-(3-ethylbenzothiazole-6-sulphonate) (ABTS) radical scavenging activity; superoxide anion radical (O2 •- ) scavenging activity; the total reduction power through potassium ferricyanide reduction method; Cupric ions (Cu2+) reduction capacity through Cuprac method; hydrogen peroxide scavenging activity and chelating activity of ferrous ions (Fe2+). Furthermore, α-tocopherol, butylatedhydroxyanisole (BHA) and quercetin were used as the reference antioxidant compounds. Results: In the comparison of initial states and the products, it’s observed that at the 50th hour the linoleic acid emulsion at 30 μg/mL concentration inhibited the lipid peroxidation by 85%, 60.7%, 69%, 45.4%, 80.4% and 31%, respectively. On the other hand, it’s observed that the linoleic acid emulsion of α-tocopherol, (BHA) and quercetin inhibited the lipid peroxidation by 62.65%, 35.84% and 34.82% respectively, at the same concentration. Conclusions: It’s found as a result of our studies that some of the phenolic compounds such as 4-Hydroxybenzoic acid (1), 3-Hydroxy-4-methoxycinnamic acid (2), 3-(4-Hydroxy-3,5-dimethoxyphenyl)prop-2-enoic acid (3), 4-Hydroxy-3,5- dimethoxybenzoic acid (4), 3,4-Dihydroxycinnamic acid (5) and 5-Isopropyl-2-methylphenol (6) which are naturally present in foods. They have higher total antioxidant activity, radical scavenging and metal chelating activities than the widely used powerful antioxidant compounds such as BHA, Quercetin and α-tocopherol.
Keywords
Subject
Article metadata
| Title | Assessment of the antioxidant and antiradicalic capacities in vitro of different phenolic derivatives |
|---|---|
| Authors | Kaan Kucukoglu; Hayrunnisa Nadaroglu |
| Affiliations | Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, 25240 Erzurum-Turkey.; Department of Food Technology, Erzurum Vocational Training School, Ataturk University, 25240 Erzurum-Turkey. |
| Corresponding author | kucukogluk@yahoo.com.tr |
| Journal | Free Radicals and Antioxidants |
| Volume / Issue | Vol. 4, Issue 1 |
Also in this issue
- Antioxidant and drug metabolismpp. 1–2
- Protective effect of Ficus bengalensis L. extract against H2 O2 induced DNA damage and repair in neuroblastoma cellspp. 3–7
- Antioxidant activity and free radical scavenging potential of alpha lipoic acid and quercetin against Al2 O3 nanoparticle-induced toxicity in micepp. 8–14
- Antioxidant Activity and Phenolics Analysis by HPLC-DAD of Solanum thomasiifolium Sendtner (Solanaceae)pp. 15–23
- Candesartan modulates the antioxidant effect of silymarin against CCl4 -induced liver injury in ratspp. 32–38