Composition of oregano essential oil (Origanum vulgare) as affected by drying method

The influence of the drying method on volatile compounds of Origanum vulgare was evaluated. The drying methods tested were convective (CD) at 60 °C and vacuum-microwave (VMD), as well as a combination of convective pre-drying and VM finish-drying (CPD–VMFD). The volatile compounds of fresh and dried oregano were extracted by steam-hydrodistillation and analyzed by GC–MS. Oregano drying kinetics was described by a simple exponential model for CD and CPD–VMFD, while VMD kinetics consisted of two periods: linear until a critical point and exponential beyond that point. Thirty-four compounds were tentatively identified, with carvacrol, thymol, and γ-terpinene, being the major components. The total volatiles concentration of fresh oregano (33.0 g kg⁻¹) decreased significantly during drying, independently of the method used (CD: 10.2 g kg⁻¹, CPD–VMFD: 13.1 g kg⁻¹, and VMD: 27.9 g kg⁻¹). The final conclusion was that VM dehydrated Polish oregano was of better aromatic quality than that dried using hot air.     

Effects of skin and grilling method on formation of heterocyclic amines in chicken pectoralis superficialis muscle

Mutagenic heterocyclic amines (HAs) originate in processed proteinaceous foods. The effects of the presence of skin (with vs. without) and of grilling method (two plate vs. infrared) on the content of HAs in grilled chicken pectoralis superficialis muscle (temperature, 220 °C) were investigated. HA precursors (creatine, creatinine, free amino acids and carbohydrates) and HAs of these raw and grilled breast muscles were determined. The muscles originated from 24 birds of either sex (provenance Ross; aged 40-45 days). The HA content was determined in homogenates of the upper and lower surface slices of the grilled muscles (T_i = 82 °C). A higher content of total free amino acids was seen for the muscle (27.1 mmol kg⁻¹ raw meat) than for the skin (21.7 mmol kg⁻¹ raw meat). The creatine, creatinine and carbohydrate levels in the skin were below the limits of detection. The contents of creatine (31.8-38.7 mmol kg⁻¹) and creatinine (0.24-0.33 mmol kg⁻¹) in the breast muscle were determined. Relatively high levels were seen for glucose (23 mmol kg⁻¹ raw meat) and fructose (10 mmol kg⁻¹ raw meat) in the muscle, with other sugars present at low levels (<2 mmol kg⁻¹ raw meat). For the chicken muscle grilled on a two-plate grill, the contents of total HAs (PhIP, MeIQx, DiMeIQx, Harman and Norharman) were lower with the skin in place than in the muscle grilled without the skin (3.5 μg kg⁻¹vs. 4.8 μg kg⁻¹). Also, during infrared grilling with the skin, lower amounts of HAs were formed than with grilling on the two-plate grill (2.4 μg kg⁻¹vs. 3.5 μg kg⁻¹). On average, the infrared-grilled samples with skin contained 3-fold more total HAs than similar samples without the skin (2.4 μg kg⁻¹vs. 0.8 μg kg⁻¹), with the highest levels seen for PhIP and MeIQx.     

Ion chromatographic determination of perchlorate in foods consumed in Hatay region

Recently, the exposure to perchlorate was emphasised as an important risk factor for human and especially newborn health. A number of studies were focused on this matter. In this study, samples of soil, vegetable (cabbage, spinach, lettuce, carrot, tomato, red cabbage), fruit (orange, mandarin, lemon, grapefruit), water, milk and fish were taken from 8 different regions of Hatay (Samanda?, K?r?khan, Reyhanl?, Amik Plain, Dörtyol, Yaylada??, Alt?nözü, Erzin). An ion chromatography system (Shimadzu C196-E039A model) was used to determine the concentrations of perchlorate in the samples. 2.5 mM Phthalic acid and 2.4 mM tris (hydroxymethyl)aminomethane solutions (pH = 4) were used as the mobile phase. A flow rate of 1.5 ml min⁻¹ and oven temperature of 40 °C were used during the analysis. The foods had perchlorate concentrations in the range of 0.236–1.218 μg kg⁻¹. The perchlorate concentration varied from 0.30 ± 0.01 to 0.94 ± 0.02 μg l⁻¹ in milk samples. Perchlorate concentrations were determined to be lower in the drinking waters (0.44 ± 0.03 μg l⁻¹) compared to irrigation waters (0.59 ± 0.03 μg l⁻¹). Perchlorate concentrations of the fish samples were ranged from 0.38 ± 0.01 to 0.61 ± 0.01 μg kg⁻¹.     

Fish and food safety: Determination of formaldehyde in 12 fish species by SPME extraction and GC–MS analysis

The formaldehyde (FA) content in different fish products was evaluated using a solid phase microextraction (SPME)-GC–MS method based on fiber derivatisation with pentafluorobenzyl-hydroxyl-amine hydrochloride. LOD and LOQ values of 17 and 28 μg kg⁻¹, respectively were calculated. Fish quality was assessed by the analysis of 12 species (sea-fish, freshwater-fish and crustaceans), revealing variable FA levels. Fresh, deep frozen, canned, boiled and roasted fish were analysed; cooking always produced a decrease in the analyte content. Fish belonging to the Gadidae family were the samples with the highest FA concentration (from 6.4 ± 1.2 mg kg⁻¹ to 293 ± 26 mg kg⁻¹), in four cases out of 14 exceeding the value of 60 mg kg⁻¹ proposed by the Italian Ministry of Health. Storage on ice was also investigated, showing moderate FA production also at temperature around 0 °C. FA contents lower than 22 mg kg⁻¹ were finally found in all the other samples.     

Improving the rheological and thermal properties of wheat dough by the addition of γ-polyglutamic acid

The rheological and thermal properties of wheat dough with the addition of γ-polyglutamic acid (PGA) (0.5, 1.0, 5.0 g kg⁻¹, w/w) was evaluated by the measurements of farinography, rapid visco analysis and differential scanning calorimetry. Adding 5.0 g kg⁻¹ PGA in wheat dough increased the mixing stability and raised the pasting temperature from 75.8 to 84.4 °C, but decreased the peak viscosity and breakdown. The water holding capacity of wheat dough increased with the addition of 5.0 g kg⁻¹ of PGA. At 5.0 g kg⁻¹ level, PGA caused significant declines in the enthalpy, onset and peak temperatures of ice-melting transition of wheat dough. Scanning electron microscopy showed that wheat bread with the addition of 1.0 and 5.0 g kg⁻¹ PGA exhibited microstructures with smoother surfaces. During storage, PGA retarded the staling process of wheat bread.     

Daily selenium intake in a moderate selenium deficiency area of Suzhou,China

In this study the daily dietary Selenium (Se) intake in Suzhou was investigated to determine whether residents in such a developed region were susceptible to moderate Se deficiency. Concentrations of Se in typically consumed foods in Suzhou were determined. Based on food Se content and the daily per capita consumption, the estimated Se intake in Suzhou was 43.9 ± 3.8 μg day⁻¹. The results revealed that pork and cereals were the major sources of Se daily intake and contributed 24.7% and 22.6% to the daily Se intake, respectively. The Se content in hair of local residents was 389.9 ± 103.6 μg kg⁻¹ for male and 322.9 ± 101.8 μg kg⁻¹ for female. A significant linear correlation between the daily Se intake and the hair Se concentration was established. The hair Se concentration could be used to bioindicate the level of Se intake for longer period.     

Effect of κ-carrageenan on rheological properties, microstructure, texture and oxidative stability of water-in-oil spreads

The effect of κ-carrageenan concentration (0-7.5 g kg⁻¹) on the rheology, microstructure, texture and oxidative stability of water-in-oil (W/O) spreads (600 g fat kg⁻¹ emulsion) was examined over 60 days storage time. Results showed that increasing the κ-carrageenan concentration to 7.5 g kg⁻¹ significantly increased the viscosity of the aqueous phase (to 42.7 mPa s at 60 °C) resulting in gelation of the aqueous phase on cooling. The microstructure of the spreads was disrupted by higher levels of κ-carrageenan, resulting in a less homogeneous distribution of the aqueous phase. Melt temperature (where tan δ > 1) decreased significantly from 62 to 56.2 °C with increasing κ-carrageenan concentration from 0 to 7.5 g kg⁻¹. The firmness and the G′ at 6 °C for all samples were significantly increased after 60 days storage with only small effects due to κ-carrageenan levels. Oxidation of the fat phase was evident by the significant increases in peroxide values of all spreads on storage, with κ-carrageenan exhibiting no antioxidant behaviour. While increased κ-carrageenan levels modified the microstructure of W/O spreads in terms of the droplet size of the aqueous phase and its distribution few changes were evident in the continuous fat phase.     

A rapid and simple fluorometric method for quantifying isoeugenol in seawater and in plasma and white muscle from Australasian snapper (Pagrus auratus)

Isoeugenol residues in Australasian snapper (Pagrus auratus) white muscle, blood plasma and seawater were accurately and precisely quantified after extraction with acetonitrile using fluorometric detection (ex. 260 nm, em. 340 nm) without chromatographic separation. Isoeugenol residues in Australasian snapper (P. auratus) muscle tissue following 30 min exposure to 58.2 μmol L⁻¹ isoeugenol (ca. 20 ppm of the aquatic anaesthetic AQUI-S™) reached a maximum of 134.37 ± 8.13 μmol kg⁻¹ (±SEM; n = 6). Blood plasma isoeugenol concentrations following this harvesting regime were 253.2 ± 25.1 μmol L⁻¹. After 7 h recovery, fillet isoeugenol residues reduced to 7.89 ± 1.67 μmol kg⁻¹. Storage of fillets from fish harvested with AQUI-S™ at 3.87 ± 0.54 °C for 5 days resulted in a rate of isoeugenol decay in the fillets of 6.51 ± 1.19 μmol kg⁻¹ day⁻¹. The method reported can be used for measuring isoeugenol residues in food products or to further study the physiological and biological effects of isoeugenol in fish.     

Analysis of potential adulteration in herbal medicines and dietary supplements for the weight control by capillary electrophoresis

Four different phytopharmaceutical dosage forms for use in weight control programs were analyzed. Two different ground herbal blends and their correspondent infusions, a capsule and a tincture were investigated for the presence of compounds used as adulterants in these products. A capillary electrophoresis (CE) method was developed and validated. The optimized experimental conditions were: BGE, sodium tetraborate buffer 20 mM, pH 9.2, voltage applied 30 kV, capillary temperature 25 °C, injection sample at 0.5 Psi during 5 s. Ephedrine, norephedrine, caffeine and furosemide were baseline separated in less than 7 min; the migration times were found to be 2.65, 2.90, 3.75 and 6.58 min, respectively. The analysis showed in sample 3 concentrations of 0.45 ± 0.03 mg g⁻¹ (ephedrine), 0.33 ± 0.02 mg g⁻¹ (norephedrine), 1.09 ± 0.41 mg g⁻¹ (caffeine) and 0.80 ± 0.17 mg g⁻¹ (furosemide). Caffeine content in samples 1, 2 and 4 was 0.61 ± 0.06 mg g⁻¹, 15.66 ± 1.05 mg g⁻¹ and 2.27 ± 0.13 mg ml⁻¹, respectively. Linearity was obtained in the concentration range of 1–1000 μg ml⁻¹. Limits of detection (LOD) and quantification (LOQ) were determined as 0.42 μg ml⁻¹ and 1.40 μg ml⁻¹ (ephedrine), 0.47 μg ml⁻¹ and 1.40 μg ml⁻¹ (norephedrine), 0.12 μg ml⁻¹ and 0.48 μg ml⁻¹ (caffeine), 0.22 μg ml⁻¹ and 0.73 μg ml⁻¹ (furosemide).     

Comparison of the cell wall composition for flesh and skin from five different plums

Cell walls were isolated from flesh and skin of five plum varieties corresponding to three species (Prunus domestica L., Prunus salicina Lindl. and Prunus insititia Lindl.) using the alcohol-insoluble solids (AIS) procedure. Yields varied from 83 to 114 g kg⁻¹ dry weight in the flesh and from 192 to 361 g kg⁻¹ dry weight in the skins. Their main sugars were uronic acid (224–322 mg g⁻¹ AIS), cellulosic glucose (139–170 mg g⁻¹ AIS), galactose and arabinose. Galactose and arabinose ratio were variable between the varieties. The degrees of methylation were high (62–84).     

In vitro digestion rate and resistant starch content of tortillas stored at two different temperatures

In vitro indicators of starch bioavailability were evaluated in freshly prepared maize tortillas and compared to those exhibited by 24, 48 or 72 h-stored samples. Storage took place either at room temperature (approx. 25 °C) or under refrigeration (4 °C). Potentially available starch (AS) content decreased from 670 g kg⁻¹ in the control tortilla to 583 g kg⁻¹ in 72 h-stored preparations. Concomitant increases in total resistant starch (RS) and retrograded resistant starch (RRS) were recorded upon storage. RRS content in 72 h-stored samples (35-39 g kg⁻¹) doubled that of freshly prepared tortillas. Changes in AS, RS and RRS were not affected by storage temperature. Both initial rate and final point of starch hydrolysis by pancreatic amylase were reduced in samples kept for 48 and 72 h, without influence of storage temperature. Storage length is suggested as a major determinant of the bioavailability of starch in tortillas.     

Trace element levels in honeys from different regions of Turkey

A survey of 25 honey samples from different botanical origin, collected all over the Turkey was conducted to assess their trace element contents. The aim of this study was to determine the levels of cadmium (Cd), lead (Pb), iron (Fe), manganese (Mn), copper (Cu), nickel (Ni), chromium (Cr), zinc (Zn), aluminium (Al) and selenium (Se) in honey samples from different regions of Turkey. Trace element contents were determined by a flame and graphite furnace atomic absorption spectrometry technique after dry-ashing, microwave digestion and wet-digestion. The accuracy of the method was corrected by the standard reference material, NIST-SRM 1515 Apple leaves. The contents of trace elements in honey samples were in the range of 0.23–2.41 μg g⁻¹, 0.32–4.56 μg g⁻¹, 1.1–12.7 μg g⁻¹, 1.8–10.2 μg g⁻¹, 8.4–105.8 μg kg⁻¹, 2.6–29.9 μg kg⁻¹, 2.4–37.9 μg kg⁻¹, 0.9–17.9 μg kg⁻¹, 83–325 μg kg⁻¹ and 38–113 μg kg⁻¹ for Cu, Mn, Zn, Fe, Pb, Ni, Cr, Cd, Al and Se, respectively. Iron was the most abundant element while cadmium was the lowest element in the Turkish honeys surveyed. The results showed that trace element concentrations in the honeys from different regions were generally correlated with the degree of trace element contamination of the environment.     

Effect of postharvest dehydration on the composition of pinot noir grapes (Vitis vinifera L.) and wine

This study was conducted in order to improve our understanding of how phenolics and aroma compounds change in wine grapes during postharvest dehydration. Pinot noir grapes grown in the Willamette Valley of Oregon were harvested at 22.0 and 24.0 °Brix. Grapes harvested at 22.0 °Brix were divided into three equal lots with one lot immediately used for wine production, and the remaining two lots placed inside an air tunnel with an air speed of 1.0–1.8 m s⁻¹, 38% relative humidity and a temperature of 22 °C. The soluble solids content and weight loss were measured daily and wines were made from grapes when they reached 24.8 and 26.7 °Brix. The soluble solids of grapes increased about 1 °Brix per day; therefore, on the third and fourth day the berries reached the desired concentration; weight loss was 14 and 16%, respectively. Results from berry phenolic analysis indicated that per berry anthocyanin amount remained unchanged during dehydration. The composition of proanthocyanidins isolated from berries changed during dehydration. Volatile compounds in wines made from dehydrated grapes contained more terpenes and norisoprenoids (β-ionone, β-damascenone) when compared to wine made from the original fruit. Wines made from increasingly dehydrated grapes tended to resemble the composition and flavour profile of wines made from grapes left on the vine (i.e. with extended ripening). The results of this study suggest that postharvest flavour changes consistent with changes during fruit ripening can occur in grapes when harvested early and allowed to dehydrate under controlled conditions prior to fermentation.     

Physical properties and microstructure of pidan yolk as affected by different divalent and monovalent cations

Changes in physical property and microstructure of pidan yolk were monitored during pickling in the presence of different divalent (CaCl₂, MgCl₂) and monovalent (KCl) cations at different levels (2 and 5 g kg⁻¹) up to 3 weeks, followed by ageing for another 3 weeks. Pidan prepared following the commercial process, in which PbO₂ or ZnCl₂ at a level of 2 g kg⁻¹ was incorporated, was also tested. Hardness, hardening ratio, NaCl content and pH of yolk gradually increased, whereas moisture content, cohesiveness and adhesiveness decreased as the pickling/ageing time increased up to 6 weeks, regardless of cations used. During pickling/ageing, L* and b* values of interior yolk and a* of exterior yolk decreased, while L* and b* values of exterior yolk and a* value of interior yolk increased (P < 0.05). Yolk of pidan treated with PbO₂ at a level of 2 g kg⁻¹ was semisolid with lower hardening ratio, hardness, cohesiveness and adhesiveness, compared with those from other treatments. Those treated with ZnCl₂ or CaCl₂ at a level of 2 g kg⁻¹ yielded higher hardening ratio, hardness and cohesiveness but lower adhesiveness than others. Confocal laser scanning microscope indicated that the greater dehydration and release of lipids took place in pidan yolk during pickling/ageing of 6 weeks.     

Determination of trace elements in Croatian floral honey originating from different regions

The concentrations of As, Cd, Cu, Hg and Pb were determined in 54 multi-floral honey samples collected from five regions of Croatia during 2009 and 2010. Element contents decreased in the following order: Cu > Pb > As > Hg > Cd. Significant differences in lead and copper levels were observed between regions. Mean levels of elements (μg kg⁻¹) in all honey samples measured were: 19.7 for As, 1.51 for Cd, 1074 for Cu, 2.72 for Hg and 65.2 for Pb. Copper and lead were the most abundant elements in the Centre region, with range and mean contents of 108–41,271 and 3232 μg kg⁻¹ and 22.0–440 and 131 μg kg⁻¹, respectively. The highest element contents were: As 23.8 μg kg⁻¹ in the South region, Cd 2.11 μg kg⁻¹ in the Southwest region and Hg 2.63 μg kg⁻¹ in the Northeast region. The finding that lead contents in Croatian honey were higher than most reported lead levels in honey from other European countries is of particular concern. These indicate that attention must be focused on setting positions for honey production hives in areas distant from highways and railways.     

Determination of patulin in fruit juices using HPLC-DAD and GC-MSD techniques

A high performance liquid chromatography with a diode-array detector (HPLC-DAD) and a gas chromatography with a mass spectrometer (GC-MSD) are described for the determination of patulin (PAT) in apple juice. The limits of detection (DL) and quantification (QL) for the HPLC-DAD and GC-MSD method were found to be (DL = 0.23 μg kg⁻¹ QL = 1.2 μg kg⁻¹) and (DL = 5.8 μg kg⁻¹ and QL = 13.8 μg kg⁻¹), respectively. The recovery factors for HPLC-DAD and GC-MSD were found to be 99.5% (RSD% = 0.73) and 41% (RSD% = 10.03), respectively. The HPLC-DAD method was used to determine the occurrence of PAT in 90 samples of fruit juices.     

Determination of ultratrace levels of selenium in fruit and vegetable samples grown and consumed in Portugal

The selenium content in fruit and vegetable samples from two regions in Portugal were analysed using hydride generation atomic fluorescence spectrometry (HG-AFS) and radiochemical nuclear activation analysis (RNAA) – two analytical methods with very low limits of detection. The lower detection limits of HG-AFS, 3 μg kg⁻¹ and 8 μg kg⁻¹ (according to conditions used for digestion), and for RNAA, 10 μg kg⁻¹, meant that it was possible to determine selenium in samples previously analysed using the replicate sample instrumental nuclear activation analysis (RSINAA) with a higher detection limit associated.     

Effects of vacuum level and microwave power on rosemary volatile composition during vacuum-microwave drying

The influence of the vacuum level and the microwave power on aroma compounds and sensory quality of Rosmarinus officinalis dehydrated by vacuum-microwave (VM) method was evaluated. VM drying kinetics consisted of two periods: linear until a critical point and exponential beyond that point. The time needed to dry rosemary was shorter for high values of microwave power and vacuum intensity. Volatile compounds of rosemary samples were extracted by steam-hydrodistillation and analyzed by GC-MS. Thirty-one compounds were identified, with α-pinene, verbenone and 1,8-cineole being the major components; monoterpenoids were the predominant chemical family. The total quantity of volatiles of fresh rosemary (27.2 g kg⁻¹) decreased during drying, independently of treatments, to a mean of 14.8 g kg⁻¹. Soft conditions of VM drying (low vacuum level and microwave power) are recommended to get the highest concentrations of volatiles and the best sensory quality (e.g. 72-74 kPa and 360 W).     

Natural levels of ethyl formate in stored grains determined using an improved method of analysis

Ethyl formate was readily determined with a gas chromatograph (GC) equipped with a flame ionisation detector. Natural levels of ethyl formate in Australian wheat, barley, oats, and canola were analysed by GC, after extraction with ammonium nitrate solution. Background levels of ethyl formate were present in newly harvested and stored grain. The levels of ethyl formate (0.1-0.6 mg kg⁻¹) in grains varied with commodity, temperature, moisture and period of storage. The values ranged from 0.1 to 0.2 mg kg⁻¹ for newly harvested wheat, barley and oats, and 0.3-0.4 mg kg⁻¹ for newly harvested canola. Ethyl formate was present in grains at harvest, increased during the first 7 months of storage, and then began to decline, particularly at grain temperatures higher than 25°C and moisture contents higher than 12.5% (for wheat, barley and oats) and 6.5% (for canola). The natural levels of ethyl formate should be considered when establishing maximum residue limits.     

Development of fish gelatin edible films using extrusion and compression molding

Fish gelatin was plasticized with 20% and 25% glycerol (w/w of gelatin) and used to develop edible films by twin-screw extrusion at 110 and 120 °C followed by compression molding at 80 °C. Tensile and moisture barrier properties and glass transition temperature were then measured and compared with solution-cast films. The films extruded at 110 °C and with 25% glycerol had the highest percent elongation at break of 293 ± 27%. The water vapor permeability values of extruded films (the highest value being 2.9 ± 0.2 g mm h⁻¹ cm⁻² Pa⁻¹) were higher than those of solution-cast films while the glass transition temperatures (T_g) of the extruded films were generally lower than those of solution-cast films. Films with 25% glycerol that were extruded at 110 °C had the lowest T_g (2.10 ± 0.31 °C). This investigation showed that extrusion processing followed by compression molding is a feasible method to produce fish gelatin films for commercial applications in a wide range of food products.