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Adamopoulou, E., Leloudi, M. C., Hatzidimitriou, E.
Xinomavro Naousa red wines typicality; linking sensory and physicochemical data

Typicality rating of 10 red wine samples, using a non-structured scale, at left “very bad example”, at right “very good example” of what a panel of wine experts, professionals, initiated assessors and consumers, considered to be a typical Xinomavro Naoussa wine, was combined to physicochemical analysis (color characteristics, phenolic content) and GC analysis of volatile profile. Assessors were able to successfully identify the Xinomavro Naoussa samples and rate them as the most typical. Based on both physicochemical and sensory data, wines were successfully grouped according to composition and origin (monovarietal or blended, Naoussa or other PDO’s).

Zachia M., Multescu M., Iorga E.
Optimisation of assay conditions for the determination of antioxidant capacity in plant food matrices by using plant food matrices by using photochemiluminescence

In this study, we optimized the extraction conditions (solvents, time of extraction, solvent-to- solid ratio, and sample storage) in order to measure the antioxidant capacity of fruits and vegetables extracts by using photochemiluminescence PCL assay.
Photochem apparatus (Analytic Jena, Germany) employing the built-in protocols for water-soluble (ACW) and lipid-soluble (ACL) bioactive compounds was used for determination. We performed experiments on kiwi, lemon, lemon peel, and broccoli.

Ritzoulis, C., Margelou, I., Rousi, R., Karayannakidis, P., Papageorgiou, M.
Development of in vitro digestion models for food colloids

This is a discussion on the staged development of an in vitro model as constructed during the course of five years at the Department of Food Technology, ATEI Thessaloniki. In its initial form, a direct probe of the interactions between mucin (the principal gastrointestinal mucus component) and sodium caseinate (a model food protein) studied the pH-dependence of the two components' interactions, which can be key to the protein's digestion and eventually its bioavailability. A further refinement includes linking up in vitro mouth and stomach components, aimed in studying the stability and flocculation of protein-stabilized oil- in-water emulsions moving from the model mouth to the stomach. A more recent development includes a set-up including a model mouth, followed by in vitro stomach and duodenum. This model has been used in order to study the kinetics of starch and gluten release from bread during a simulated digestion process.

Kyriakoudi A., Tsimidou, M. Z.
Standardization of sample preparation conditions for crocetin isolation from saffron aided by response surface methodology

The present study aimed at the standardization of sample preparation conditions for the quantitative isolation of crocetin (CRT) from saffron. Response surface methodology (RSM) was employed for the optimization of the first step of the process, i.e. the preparation of a polar saffron extract rich in crocetin sugar esters that represents the most expensive step of the process due to the high price of the starting material.

Sotiroglou, M., Nenadis, N., Xatzidimitriou, E., Blekas, G.
Influence of sulfur dioxide and/or ascorbic acid on the antioxidant activity of resinated wine models and their oxidative stability under accelerated conditions

The impact of sulphur dioxide and/or ascorbic acid on the antioxidant activity of resinated wine models containing (+)-catechin and chlorogenic acid was examined using models containing different levels of the above constituents as well as constituents extracted from the Pinus Halepensis resin. The composition was selected in terms of an experimental design approach (Taguchi method). The antioxidant activity of the prepared models was examined employing the Folin-Ciocalteu assay and the scavenging of the DPPH radical. Selected models were stored under accelerated oxidation conditions (11 days, dark, 55 °C, 33 % headspace) and evaluated for the changes in antioxidant activity and the possible formation of brown pigments (A420). The results indicated that the resin’s constituents did not contribute to the antioxidant activity of the models. Antagonistic phenomena among the constituents were observed which were more pronounced in the case of the DPPH assay. Models using a single typical sulfur dioxide concentration (35 mg/L) with (100, 150 and 200 mg/L) or without ascorbic acid were stored under accelerated oxidation conditions. On the basis of Folin-Ciocalteu assay after the end of the storage the activity was always higher than that of the control (1.08-1.4 fold). Examination with the DPPH assay showed that the activity after storage was higher than that of the control only when ascorbic acid was added at 200 mg/L. Under the experimental conditions employed formation of brown pigments remained low.

Culetu, A., Eglantina Duta, D., Mohan, G., Iorga, E.
Evaluation of antioxidant capacity and total polyphenol content of bread

The aim of this study was to determine the total polyphenol content and antioxidant capacity of bread prepared with a tea fraction enriched in polyphenols. The best performance regarding bread extraction procedure was achieved with 80% aqueous methanol. The total polyphenol content and DPPH radical scavenging activity in the enriched bread were 4.8 mg GAE/g and 6.7 mg Trolox/g, respectively (results expressed on the sample dry matter basis). During bread shelf-life a reduction in TPC by 5% was obtained, whereas no change was observed in the antioxidant capacity.

Leyva-Jiménez, F. J., Lozano-Sánchez, J., Arráez-Román, D., Segura-Carretero, A.
Encapsulation and controlled release of bioactive phenolic compounds: phenolic acids, flavonoids and phenylpropanoids

In this work the effectiveness of spray drying encapsulation as a new strategy to increase bioavailability of bioactive compounds has been evaluated. Thus, an experimental design based on a central composite 22 model was carried out to encapsulate different phenolic compounds from vegetable sources. Inlet air temperature and ratio sample/encapsulation agent (inuline) were selected as independent variable. The results pointed out a great yield was obtained under all experimental conditions. Encapsulation efficiency presented variability depending on the chemical group studied.

de la Luz Cádiz-Gurrea, M., Fernández-Arroyo, S., Joven, J., Segura-Carretero, A.
Different behavior of food polyphenols from Theobroma cacao in energy metabolism of lipopolysaccharide-stimulated cells

Theobroma cacao is worldwide consumed and common ingredient of many food products. Cocoa, containing high-degree of polymerization proanthocyanidins, is a valuable source of bioactive compounds. Mouse embryonic fibroblast (MEF) cell lines, PON-1 KO and MCP-1 KI, were used as potential oxidant and inflammatory scenarios, respectively. Energy metabolism changes drastically when MEF are incubated with LPS. Cacao has an important effect on PON-1 KO incubated with LPS, leading metabolite values to these found in WT (particularly those related to the glycolysis).

de la Luz Cádiz-Gurrea, M., Fernández-Arroyo, S., Segura-Carretero, A.
Extensive characterization of phenolic composition from Pine Bark concentrated extract as a food supplement by HPLC-ESI/DAD-QTOF-MS

Pine bark is used as a dietary supplement and phytochemical remedy for several diseases. A comprehensive characterization of the bioactive compounds using advanced and powerful techniques as HPLC-ESI-QTOF-MS and their antioxidant capacity are crucial in food supplement studies. A total of 37 compounds were identified belonging to various structural classes being the most representative ones flavan-3-ols (oligomeric forms). Moreover, the extract showed antioxidant activity decreasing the generation of ROS and high values were obtained by TPC and flavan-3-ol content assays.

Kissoudi, M., Samanidou, V.
Extraction, purification and evaluation of food-grade phycocyanin from Spirulina Platensis

Phycocyanin (C-PC) is the major phycobiliprotein in Spirulina (Arthrospira) platensis (Sp.), which is a cyanobacterium with a massive commercial value representing a nutrient-dense food source. This study describes a simple protocol for purifying C-phycocyanin from Spirulina Sp.. The cell lysis of blue-green algae has been carried out by sonication and repeated cycles of freezing and thawing. Among the various buffers used for phycocyanin yield efficiency, phosphate buffer (pH 7, 0.1 M) was found to be the most suitable for highest yield. The purification process involves a multistep treatment of the crude extract, of purity 1.41, by fractional precipitation with ammonium sulfate followed by dialysis and ion-exchange chromatography on DEAE-Sepharose Fast Flow column obtaining food-grade phycocyanin. The purity of phycocyanobilin chromophore has been tested by UV-Vis spectrophotometry by monitoring the absorption after each stage of purification. Also, separation and identification of the purified protein has been achieved by High Performance Liquid Chromatography with Photodiode-array Detection.

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