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1.
J Food Sci ; 81(8): C1914-20, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27387389

ABSTRACT

Eight phenolic compounds including: p-coumaric acid, vanillic acid, caffeic acid, chlorogenic acid, trolox, quercetin, curcumin, and resveratrol were treated with riboflavin (RF) photosensitization and in vitro antioxidant capacities of the mixtures were determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2' azino bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS), and ferric reducing antioxidant power (FRAP) assays. Mixtures containing p-coumaric acid and vanillic acid under RF photosensitization showed increases in ferric ion reducing ability and radical scavenging activity of DPPH, whereas mixtures of other compounds had decreases in both radical scavenging ability and ferric reducing antioxidant power. Hydroxycoumaric acid and conjugated hydroxycoumaric and coumaric acids were tentatively identified from RF photosensitized p-coumaric acid, whereas dimmers of vanillic acid were tentatively identified from RF photosensitized vanillic acid. RF photosensitization may be a useful method to enhance antioxidant properties like ferric ion reducing abilities of some selected phenolic compounds.


Subject(s)
Antioxidants/pharmacology , Light , Phenols/pharmacology , Plant Extracts/pharmacology , Riboflavin/chemistry , Antioxidants/chemistry , Benzothiazoles/metabolism , Biphenyl Compounds/metabolism , Caffeic Acids/chemistry , Caffeic Acids/pharmacology , Chlorogenic Acid/chemistry , Chlorogenic Acid/pharmacology , Chromans/chemistry , Chromans/pharmacology , Coumaric Acids/chemistry , Coumaric Acids/pharmacology , Curcumin/chemistry , Curcumin/pharmacology , Molecular Structure , Oxidation-Reduction , Phenols/chemistry , Picrates/metabolism , Plant Extracts/chemistry , Propionates , Quercetin/chemistry , Quercetin/pharmacology , Resveratrol , Stilbenes/chemistry , Stilbenes/pharmacology , Sulfonic Acids/metabolism , Vanillic Acid/chemistry , Vanillic Acid/pharmacology
2.
J Food Sci ; 77(12): C1263-8, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23170822

ABSTRACT

Differentiating blended sesame oils from authentic sesame oil (SO) is a critical step in protecting consumer rights. Stable carbon isotope ratios (δ(13) C), color, fluorescence intensity, and fatty acid profiles were analyzed in SO prepared from sesame seeds with different roasting conditions and in corn oil blended with SO. Sesame seeds were roasted at 175, 200, 225, or 250 °C for 15 or 30 min at each temperature. SO was mixed with corn oil at varying ratios. Roasting conditions ranging from175 to 250 °C at the 30 min time point did not result in significant changes in δ(13) C (P > 0.05). Values of δ(13) C in corn oil and SO from sesame seeds roasted at 250 °C for 15 min were -17.55 and -32.13 ‰, respectively. Fatty acid ratios, including (O + L)/(P × Ln) and (L × L)/O, where O, L, P, and Ln were oleic, linoleic, palmitic, and linolenic acids, respectively, showed good discriminating abilities among the SO blended with corn oil. Therefore, using different combinations of stable carbon isotope ratios and some fatty acid ratios can allow successful differentiation of authentic SO from SO blended with corn oil.


Subject(s)
Food Handling/methods , Sesame Oil/analysis , Sesamum/chemistry , Carbon Isotopes/analysis , Color , Corn Oil/analysis , Corn Oil/chemistry , Fatty Acids/analysis , Seeds/chemistry , Sesame Oil/chemistry
3.
J Food Sci ; 76(6): C808-16, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21623788

ABSTRACT

UNLABELLED: Perilla seeds have more than 60% of α-linolenic acid, one of omega-3 essential fatty acids. Headspace volatiles and physicochemical properties including color, fluorescence intensity, and the oxidation products in perilla oil (PO) from perilla seeds roasted at different conditions were analyzed. Roasting temperature was 150, 170, 190, and 210°C, and roasting time was 15 and 30 min at each roasting temperature. PO from higher roasting temperature and longer roasting time had lower L* values, higher a*, b*, and chroma values, more brown pigments and fluorescence intensity, and more conjugated dienoic acids. Pyrazines were major volatiles in PO, and furans, sulfur-containing compounds, and hydrocarbons were also detected by a solid phase microextraction gas chromatography/mass spectrometry. In PO, 2,5-Dimethylpyrazine and 2-furancarboxaldehyde were 2 major volatiles. The principal component analysis of volatiles showed the 1st principal component (PC1) and the 2nd principal component (PC2) express 56.64% and 22.72% of the volatile variability in PO, respectively, which can differentiate PO prepared from roasting conditions clearly. Some physicochemical properties especially brown pigment and volatiles were positively correlated with each other in PO. PRACTICAL APPLICATION: Perilla oil (PO) from perilla seeds possesses more than 60% of α-linolenic acid, one of omega-3 fatty acids. Roasting process has been used to extract oil from perilla seeds. Understanding physicochemical properties of PO from diverse roasting conditions are important steps to produce PO in food industry. Roasting process induces darkening of color, increase of fluorescence intensity, and brown pigments in PO. Pyrazines and furans are major headspace volatiles in PO roasted above 170°C. The results of this study can help to produce PO in industrial scales with desired headspace volatiles, colors, and oxidative state.


Subject(s)
Food Handling/methods , Perilla/chemistry , Seeds/chemistry , Volatile Organic Compounds/analysis , alpha-Linolenic Acid/chemistry , Aldehydes/analysis , Aldehydes/chemistry , Chemical Phenomena , Fatty Acids, Volatile/analysis , Fatty Acids, Volatile/chemistry , Furans/analysis , Furans/chemistry , Gas Chromatography-Mass Spectrometry , Hot Temperature , Maillard Reaction , Pigmentation , Plant Oils/chemistry , Principal Component Analysis , Pyrazines/analysis , Pyrazines/chemistry , Solid Phase Microextraction , Sulfur Compounds/analysis , Sulfur Compounds/chemistry , Time Factors , Volatile Organic Compounds/chemistry , alpha-Linolenic Acid/analysis
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