Antioxidant activity

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The Phytochemical Analysis and Antioxidant Activity Assessment of Orange Peels (Citrus Sinensis) Cultivated in Greece-Crete Indicates a New Commercial Source of Hesperidin

Journal Title, Volume, Page: 
Biomedical Chromatography Volume 23, Issue 3, pages 239–249
Year of Publication: 
2009
Authors: 
Firas I. Kanaze
Laboratory of Pharmacognosy, Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece
Current Affiliation: 
Department of Pharmacy,Faculty of Medicine & Health Sciences, An-Najah National University, Nablus, Palestine
Aikaterini Termentzi
Laboratory of Pharmacognosy, Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece
Chrysi Gabrieli
Laboratory of Pharmacognosy, Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece
Ioannis Niopas
Laboratory of Pharmacology, Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece
Manolis Georgarakis
Department of Pharmaceutical Technology, School of Pharmacy, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece
Eugene Kokkalou
Laboratory of Pharmacognosy, Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece
Preferred Abstract (Original): 

The flavonoid content of several methanolic extract fractions of Navel orange peel (flavedo and albedo of Citrus sinensis) cultivated in Crete (Greece) was first analysed phytochemically and then assessed for its antioxidant activity in vitro. The chemical structures of the constituents fractionated were originally determined by comparing their retention times and the obtained UV spectral data with the available bibliographic data and further verified by detailed LC-DAD-MS (ESI+) analysis. The main flavonoid groups found within the fractions examined were polymethoxylated flavones, O-glycosylated flavones, C-glycosylated flavones, O-glycosylated flavonols, O-glycosylated flavanones and phenolic acids along with their ester derivatives. In addition, the quantitative HPLC analysis confirmed that hesperidin is the major flavonoid glycoside found in the orange peel. Interestingly enough, its quantity at 48 mg/g of dry peel permits the commercial use of orange peel as a source for the production of hesperidin. The antioxidant activity of the orange peel methanolic extract fractions was evaluated by applying two complementary methodologies, DPPH assay and the Co(II)/EDTA-induced luminol chemiluminescence approach. Overall, the results have shown that orange peel methanolic extracts possess moderate antioxidant activity as compared with the activity seen in tests where the corresponding aglycones, diosmetin and hesperetin were assessed in different ratios. Copyright © 2008 John Wiley & Sons, Ltd.

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Syntheses, Physico-Chemical Studies and Antioxidant Activities of Transition Metal Complexes with a Perimidine Ligand

Journal Title, Volume, Page: 
Zeitschrift für anorganische und allgemeine Chemie, Volume 638, Issue 5, pages 881–886, April 2012
Year of Publication: 
2012
Authors: 
Dr. Mohammad Azam
Department of Chemistry, King Saud University, P. O. Box 2455, Riyadh 11451, KSA
Ismail Warad
Department of Chemistry, King Saud University, P. O. Box 2455, Riyadh 11451, KSA
Current Affiliation: 
Department of Chemistry, Faculty of Science, An-Najah National University, Nablus, Palestine
Saud Al-Resayes
Department of Chemistry, King Saud University, P. O. Box 2455, Riyadh 11451, KSA
Maryam Zahin
Department of Agricultural Microbiology, Faculty of Agricultural Sciences, Aligarh Muslim University, Aligarh 202 002, India
Iqbal Ahmad
Department of Agricultural Microbiology, Faculty of Agricultural Sciences, Aligarh Muslim University, Aligarh 202 002, India
Mohammad Shakir
Department of Chemistry, Aligarh Muslim University, Aligarh 202002, India
Preferred Abstract (Original): 
A series of mononuclear complexes of the type, [MLCl2] [M = CoII, NiII, CuII, and ZnII] with a pyrimidene-type ligand, which was synthesized by the reaction of 2-furaldehyde and 1, 8-diaminonaphthalene, was obtained. The ligand and its complexes were characterized by elemental analysis, IR, NMR, EPR, and UV/Vis spectroscopy, ESI-mass spectrometry, magnetic susceptibility, molar conductivity, and thermogravimetric analyses. On the basis of UV/Vis spectroscopic and magnetic susceptibility data, an octahedral arrangement was assigned around all metal ions. The low molar conductivity data for all the complexes show their non-electrolytic nature. The thermal behavior of the complexes was studied by TGA analyses. The electrochemical study carried out on the CuII complex exhibits a quasi reversible redox process. The ligand and its complexes showed potential antioxidant and antimicrobial activities.
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