Current Trends in Sample Treatment Techniques for Environmental and Food Analysis

Nowadays, there is a growing need for applications in food and environmental areas able to cope with the analysis of a large number of analytes in very complex matrices [1]. The new analytical procedures demand sensitivity, robustness, effectiveness and high resolution with reduced analysis time. Many of these requirements may be met to a certain extent by the total or partial automation of the conventional analytical methods, including sample preparation or sample pre-treatment coupled on-line to the analytical system. Furthermore, the recent use of ultra-high-performance liquid chromatography (UHPLC) for environmental and food chemical analysis has increased the overall sample throughput and laboratory efficiency without loss (and even with an improvement) of resolution obtained by conventional HPLC systems..

INFLUENCE OF DEEP-FAT FRYING PROCESS ON PHOSPHOLlPID MOLECULAR SPECIES COMPOSITION OF SARDINA PILCHARDUS FILLET

Introduction. Fish is an excellent source of essential nutrients such as essential amino acids, bioactive latty acids, minerals, vitamins, chitin and antioxidants. The nutritional benefit of fish lies, predominantly, in its lipid Iraction which is mainly composed of phospholipids (PL) and triacylglycerols (TAG) exceptionally rich of n-3 polyunsaturated latty acids (n-3 PUFA). Recently, fish PLs have attracted a great deal of attention as they are considered more efficient carriers of n-3 PUFA than fish TAG in terms of n-3 PUFA absorption in different tissues. In addition, fish PLs have also exhibited antitumoral and anti-inllammatory effects. Unfortunately, lish PLs are highly susceptible to lipid oxidation and to thermal damage due to excessive heating. The n-3 PUFA chains in PLs are the primary targets of oxidation which can take piace during cooking processes. Since most fish are consumed cooked, the nutritional value of the final cooked product is of major importance lor human health. Especially, the determination of the effects of frying (a very popular method utilized lor fish cooking) on the n-3 PUFA rich lipid fraction of fish will provide uselul inlormation to consumers and to lood industry to establish the fish quality. Purpose. This study was, therelore, conducted to determine the inlluence of deep fat frying process on PL composition of edible muscle (fillet) of Sardina pilchardus, a fish species commonly consumed in Mediterranean countries. Design/methodology. The effects of deep-fat frying performed using different culinary lats (extra virgin olive oil, conventional sunflower oil and high-oleic sunfiower oil) and different frying temperatures (160 and 180°C) on the phosphatidylethanolamine (PE) and phosphatidylcholine (PC) molecular species composition (the preponderant fish phospholipid classes) were investigated. For each frying test, ten fish fillets were introduced into a deep fryer (capacity 2 L), in a closed environment, lor 5 min. The oil temperature prior to start frying has been set to established value (160 or 180'C) and it was controlled by a specific digital thermometer. Each cooking procedure was done in triplicate. The PL molecular species composition was determined by high pressure liquid chromatography (HPLC) coupled with a second order mass spectrometer (MS-MS) with electronebulization interface (ESI). Findings. The deep-fat frying process caused significative changes on PE and PC molecular species composition of the fish fillet. However, these changes were not related to the nature of the culinary fat and to the frying temperature. In all cases, the deep fat frying process caused a significative increase of the proportion of the PE and PC species formed by the combination of palmitic and docohexanoic acids and a significative decrease of the percentage of the PE and PC species formed by two docohexanoic acid residues. Keywords: Deep fat frying, European pilchard, phosphatidylcholine, phosphatidylethanolamin

Molecularly Imprinted Polymer as Selective Sorbent for the Extraction of Zearalenone in Edible Vegetable Oils

A method based on the selective extraction of zearalenone (ZON) from edible vegetable oils using molecularly imprinted polymer (MIP) has been developed and validated. Ultra-high-pressure liquid chromatography coupled with a fluorescence detection system was employed for the detection of zearalenone. The method was applied to the analysis of zearalenone in maize oil samples spiked at four concentration levels within the maximum permitted amount specified by the European Commission Regulation (EC) No. 1126/2007. As a result, the proposed methodology provided high recoveries (>72%) with good linearity (R2 > 0.999) in the range of 10-2000 μg/kg and a repeatability relative standard deviation below 1.8%. These findings meet the analytical performance criteria specified by the European Commission Regulation No. 401/2006 and reveal that the proposed methodology can be successfully applied for monitoring zearalenone at trace levels in different edible vegetable oils. A comparison of MIP behavior with the ones of QuEChERS and liquid-liquid extraction was also performed, showing higher extraction rates and precision of MIP. Finally, the evolution of ZON contamination during the maize oil refining process was also investigated, demonstrating how the process is unable to completely remove (60%) ZON from oil samples

A Rapid Procedure for the Simultaneous Determination of Eugenol, Linalool and Fatty Acid Composition in Basil Leaves

Eugenol and linalool are often the most abundant volatile compounds found in basil (Ocimum basilicum L., Lamiaceae) leaves, and they are interesting for the aroma they provide and for their numerous beneficial bioactivities. Their determination is thus needed for several purposes. In the present study, to avoid the previous isolation of essential oil, the direct solvent extraction is proposed coupled with a transmethylation to convert acyl lipids into fatty acids methyl esters (FAMEs), thus assessing the possible simultaneous analysis of eugenol and linalool with FAMEs by gas chromatography coupled to flame ionization detector (GC-FID). The method has been validated and applied to ten basil leaves samples in which eugenol and linalool were found in mean concentrations of 2.80 +/- 0.15 and 1.01 +/- 0.04 g kg(-1) (dry weight), respectively. FAMEs composition was dominated by linolenic acid (52.1-56.1%) followed by palmitic acid (19.3-22.4%) and linoleic acid (9.6-11.3%). The ratio of n6-polyunsaturated fatty acids (PUFAs)/n3-PUFAs was in the range of 0.17-0.20 in the investigated samples. The proposed method exploits a rapid procedure requiring 40 min, making use of a small amount of solvent and allowing the simultaneous determination of molecules contributing to assess the quality of this worldwide appreciated herb

Influence of Dietary Supplementation with Prebiotic, Oregano Extract, and Vitamin E on Fatty Acid Profile and Oxidative Status of Rabbit Meat

The effect of dietary supplementation with vitamin E, oregano, and prebiotic on fatty acids and oxidative profiles of rabbit meat (loin and hind leg) was evaluated. New Zealand white rabbits weaned at 30 days of age were fed with one of six diets until 80 days of age: standard diet includingω3 polyunsaturated fatty and conjugated linolenic acids sources (S) and five diets adding vitamin E (150 ppm, E), oregano water extract (2 g/kg feed diet, O), prebiotic (THEPAX® 1.5 g/kg feed diet, T), vitamin E plus prebiotic (TE), and oregano water extract plus prebiotic (TO), respectively. The lipid oxidative status (TBARS) showed lower values with respect to S, mainly when vitamin E was administered. In particular, all the experimental diets decreased TBARS values with respect to the control group in the loin, but no effect was found in the hind leg. In all feed samples, the amounts of fatty acid classes increased in the following order: polyunsaturated fatty acids > monounsaturated fatty acid > saturated fatty acid. The dietary supplementations did not affect the fatty acid composition of meat. The experimented diets compared to the control were not able to provide a selective increase of bioactive fatty acid in meat samples; however, the six nutritional strategies led to highly nutritional rabbit meat with an interesting value of theω6/ω3 ratio

Prunus persica var. platycarpa (Tabacchiera Peach): bioactive compounds and antioxidant activity of pulp, peel and seed ethanolic extracts

A comparative analysis of ethanol extracts from peel, pulp and seed of Prunus persica var. platycarpa (Tabacchiera peach) was done. The total phenols, flavonoids and carotenoids content as well as the antioxidant properties were evaluated. Peach pulp extract was characterized by the highest total phytonutrients content and exhibited the highest antioxidant activity in all in vitro assays. Interestingly, pulp extract showed IC50 values of 2.7 and 2.2 g/mL at 30 and 60 minutes of incubation, respectively using -carotene bleaching test. A remarkable result was also obtained by using Fe-chelating assay (IC50 of 2.9 g/mL vs 1.3 g/mL for positive control BHT). Pulp extract was subjected to liquid chromatography-electrospray-tandem mass spectrometry (HPLC-ESI-MS/MS). Six main compounds, namely gallic acid, protocatechuic acid, protocatechualdehyde, chlorogenic acid, p-coumaric acid, and ferulic acid, were identified. Overall, the results suggest that Prunus persica var. platycarpa displays a good antioxidant activity and its consumption could be promote

[The role of eggs in the diet: nutraceutical and epigenetic aspects].

The use of eggs in human diet has been object of many prejudices which are not yet completely disappeared The evolution of knowledge in the field of nutrition has, partially, countered these prejudices by highlighting the biological importance of several compounds present in the eggs. The nutritional and commercial revaluation of the eggs are passed through the enrichment of the lipid fraction in omega3 polyunsaturated fatty acids (PUFA omega3) which, have shown positive effects against cardiovascular diseases and development of the central nervous system and retina. The enrichment of eggs lipid with omega3 fatty acids is carried out by the integration of feeding hens with oils rich in omega3 fatty acids such as plant or marine oils. The results showed that the accumulation of omega3 in the egg yolk lipids is strongly affected by the type of oil used as supplement and by the amounts of oils administrated to the hens

Spent espresso coffee grounds as a source of anti-proliferative and antioxidant compounds

Disposal of spent espresso coffee grounds (SCG) is costly and leads to the loss of bioactive compounds that could be fractionated, in several applications. This work aimed to investigate phenolic profile, tocopherols, and antioxidant and anti-proliferative activities of SCGs ethanolic extracts from coffee powders differing in coffee provenience and composition (arabica/robusta). Tyrosol, detected for the first time in SCGs, was the most abundant phenolic measured (121-1,084 mg/kg in the extract), along with 4-hydroxybenzoic acid and vanillin (885-1813 and 340-1103 mg/kg, respectively). Extract derived from 100% robusta from Guatemala (S7-R) showed the highest α- to ß-tocopherol ratio of 1.2 and the highest antioxidant potential as evidenced by RACI and GAS values of -0.43 and 0.20, respectively. Moreover, S7-R showed a promising anti-proliferative activity toward human lung carcinoma cells (A549), with IC50 value of 61.2 ug/mL comparable to that given by the positive control vinblastine (IC50 value of 67.3 ug/mL)

Glucosinolates and polyphenols of colored Cauliflower as chemical discriminants based on cooking procedures

The impact of mild oven treatments (steaming or sous vide) and boiling at 10 min, 25 min, or 40 min on health-promoting phytochemicals of orange and violet cauliflower (Brassica oleracea L. var. botrytis) was investigated. For this purpose, targeted ultra-high performance liquid chro-matography-high resolution mass spectrometry analysis of phenolics and glycosylates com-bined with chemometrics was employed. Regardless of cooking time, clear differentiation of cooked samples obtained using different procedures was achieved, thus demonstrating the dis-tinct impact of cooking approaches on sample phytochemical profile (both, compound distribu-tion and content). The main responsible components for the observed discrimination were de-rivatives of hydroxycinnamic acid and kaempferol, organic acids, indolic and aromatic glucos-inolates, with glucosativin that was found, for the first time, as discriminant chemical descriptor in colored cauliflower submitted to steaming and sous-vide. The obtained findings also high-lighted a strict relationship between the impact of the cooking technique used and the type of cauliflower. The boiling process significantly affected phytochemicals in violet cauliflowers whereas orange cauliflower boiled samples were grouped between raw and either steamed or sous-vide cooked samples. Finally, the results confirm that the proposed methodology is capa-ble of discriminating cauliflower samples based on their phytochemical profiles and of identi-fying the cooking procedure able to preserve bioactive constituents