Effect of ascorbyl palmitate on the preservation of α-tocopherol in sunflower oil,alone and with herbs and spices

Ascorbyl palmitate (AP) (200 ppm) preserved α-tocopherol in sunflower oil at 95°C and delayed the onset of rancidity. Both effects increased with AP concentration (r² = 0.96 and 0.97 respectively) but levelled off near ∼700 ppm. The improved anti-rancidity effect was due to the increased preservation (P<0.01). Synergism was observed for both effects for AP combined with sage, turmeric, oregano and marjoram. Clove and thyme gave a smaller synergistic effect whereas basil inhibited. Neither bay nor cumin had any effect. Both the preservative (PF_p) and anti-rancidity effects (PF_r) were directly related to the thyme concentration (0–2000 ppm). Again, the decreased rancidity was due to the increased preservation (P<0.01). The optimum AP concentration (0–1000 ppm) was around 250 ppm (P<0.01) with thyme present (at 500 ppm) (r²=0.99). The increased delay in rancidity was due to the improved preservation of α-tocopherol (r=1, r² = 0.99, P<0.01). Both the logarithm of the induction time and the preservative effect for the mixture of thyme and AP was directly related to the temperature (80–105°C). The mode of action of AP is also discussed.     

Effect of tocopherols,tocotrienols, β-carotene,and chlorophyll on the photo-oxidative stability of red palm oil

Effect of tocols, β-carotene, and chlorophyll on photo-oxidative stability of red palm oil (RPO) were studied. Model systems of triacylglycerols+tocols, triacylglycerols+β-carotene, triacylglycerols +tocols+β-carotene, and triacylglycerols+tocols+β-carotene+chlorophyll were exposed to fluorescent light at intensities of 5,000, 10,000, and 15,000 lux for 7 h at 30±2°C. Changes in concentrations of tocopherols, tocotrienols, β-carotene, chlorophyll, and peroxide values were evaluated every hour. Light intensity accelerated degradation of tocols in the triacylglycerols+tocols system and β-carotene in the triacylglycerols+β-carotene system. Gamma-tocotrienol showed the highest degradation rate and β-carotene was the most sensitive compound to changes in light intensity, indicated by the lowest light intensity coefficient (z_i) value. The presence of tocols and β-carotene together showed protective effects for the photo-oxidative stability of RPO. The presence of chlorophyll increased the rate of photo-oxidation at high light intensities. Interactions between tocols and β-carotene contributed to the photo-oxidative stability of RPO.     

The role of processing and matrix design in development and control of microstructures in dairy food production—a survey

New options to process dairy products by means of new single unit operations or combinations thereof are presented. The innovative possibilities discussed in this paper mainly refer to novel ways of influencing product microstructures or textures as perceived during consumption, by means of contributions of single molecule fractions of complex systems derived from membrane fractionation techniques. In addition, options to integrate physiologically active components which also have a structure forming effect in fermented or other dairy products are highlighted. Alternatives derived from thermal, mechanical and enzymatic processing and from fractionation techniques by means of membranes are presented which can be exploited for fractionation and compositional matrix design of dairy products.     

Method development and validation for analysis of microencapsulated cyanidin-3-O-rutinoside in dairy samples containing juçara palm fruit by high-performance liquid chromatography

Euterpe edulis is a plant native of Brazil and popularly known as juçara. The aim of this study was to develop and validate an analytical method using high-performance liquid chromatography (HPLC) of juçara crude extracts (JCEs) and to evaluate dairy products containing free and microencapsulated extracts. The validated analytical method for JCE was performed using cyanidin-3-O-rutinoside (C3R – isolated and identified as major component from JCE) as a reference: linearity was obtained using ten concentrations between 25 and 250 μg mL⁻¹ (R² = 0.994); limits of detection and quantification were 19.04 μg mL⁻¹ and 57.7 μg mL⁻¹ respectively; accuracy (relative standard deviation) was <5%; recovery was 104.85 μg mL⁻¹; and the method is robust. Physicochemical analyses of the dairy products were evaluated using colour, pH, and concentration of anthocyanins using HPLC calculated as C3R over 21 days of storage. The pH remained stable until the end of the test. The colour and the concentration of anthocyanins remained stable for 9 days. C3R was isolated, the HPLC method was developed and validated, and the colour stability was not altered until 9 days. © 2023 Society of Chemical Industry.     

A Comparative Study of the Ionization Modes in GC–MS Multi-residue Method for the Determination of Organochlorine Pesticides and Polychlorinated Biphenyls in Crayfish

A gas chromatography–mass spectrometry (GC–MS) multi-residue method with different ionization modes has been developed for the determination of 23 organochlorine pesticides and ten polychlorinated biphenyls (PCBs) in crayfish. The approach was based on an extraction with acetonitrile saturated by hexane (containing 0.1 % acetic acid), followed by a dispersed solid-phase extraction cleanup with primary secondary amine and octadecylsilane, and finally analyzed by GC–MS/MS operated in electron impact (EI) and positive chemical ionization (PCI), and GC–MS in negative chemical ionization (NCI), respectively. An isotope internal standard, DDT-D₈, was used for quantification. These three GC–MS procedures were validated and compared using crayfish samples fortified at three levels (5, 10 and 20 ng/g). Good linearity, accuracy, precision and sensitivity were achieved by all three ionization modes with recoveries in the range of 70 to 112 %, relative standard deviations (RSDs) below 10 % and limits of detection (LODs) in the range of 0.002 to 8 ng/g. Extremely high selectivity was obtained by both EI- and PCI-MS/MS, while PCI was more sensitive to compounds containing nitro and carbonyl groups, and EI was a better choice for dieldrin, endosulfan, and its metabolites. NCI-MS had the highest sensitivity but lower anti-interference ability and was not suitable for the determination of DDTs and PCBs. These three ionization modes can be used as complementary and alternative in routine GC–MS analysis of organochlorine pesticides and polychlorinated biphenyls in food.     

Application of Fast Gas Chromatography–Mass Spectrometry in Combination with the QuEChERS Method for the Determination of Pesticide Residues in Fruits and Vegetables

A fast gas chromatography–mass spectrometry method has been developed for multiresidue determination of up to 56 pesticides in fruits and vegetables in a chromatographic run time of <10 min, using a single quadrupole mass spectrometer operating in selected ion monitoring mode. The well-known acetate-buffering version of the QuEChERS method has been used for sample preparation. Programmable temperature vaporizer injection of 3 μL allowed reaching limits of detection between 0.15 and 15 μg/kg for most compounds in the sample matrices tested. The applicability of the method has been evaluated in apple, orange, carrot, and tomato. Recoveries at three fortification levels (0.01, 0.1 and 0.5 mg/kg) ranged from 70 to 120 % for most compounds, with relative standard deviations below 20 % in all cases. The developed method has been applied to fruit and vegetable samples from different Spanish provinces.     

Effects of abomasal infusion of conjugated linoleic acids, Sterculia foetida oil,and fish oil on production performance and the extent of fatty acid Δ-desaturation in dairy cows

The purpose of this study was to determine the effects of conjugated linoleic acid (CLA), Sterculia foetida oil (STO), and fish oil (FO) on milk yield and composition, milk FA profile, Δ⁹-desaturation activity, and mammary expression of 2 isoforms of stearoyl-coenzyme A desaturase (SCD-1 and SCD-5) in lactating dairy cows. Eight multiparous Holstein cows (69 ± 13 d postpartum) were used in a double 4 × 4 Latin square design with 28-d periods. For the first 14 d of each period, cows received an abomasal infusion of (1) 406 g of a saturated fatty acid (SFA) supplement (112 g of 16:0 + 230 g of 18:0) used as a control (CTL), (2) 36 g of a CLA supplement (13.9 g of trans-10,cis-12 18:2) + 370 g of SFA, (3) 7 g of STO (3.1 g of 19:1 cyclo) + 399 g of SFA, or (4) 406 g of FO (55.2 g of cis-5,-8,-11,-14,-17 20:5 + 59.3 g of cis-4,-7,-10,-13,-16,-19 22:6). Infusions were followed by a 14-d washout interval. Compared with CTL, STO decreased milk yield from 38.0 to 33.0 kg/d, and increased milk fat concentration from 3.79 to 4.45%. Milk fat concentration was also decreased by CLA (2.23%) and FO (3.34%). Milk fat yield was not affected by STO (1,475 g/d) compared with CTL (1,431 g/d), but was decreased by CLA (774 g/d) and FO (1,186 g/d). Desaturase indices for 10:0, 12:0, and 20:0 were decreased, whereas the extent of desaturation of 14:0, 16:0, 17:0, and 18:0 was not affected by CLA treatment compared with CTL. Infusion of STO significantly decreased all calculated desaturase indices compared with CTL; the 14:0 index was reduced by 80.7%. Infusion of FO decreased the desaturase indices for 10:0, 14:0, 20:0, trans-11 18:1, and 18:0. The effect of FO on the 14:0 index indicates a decrease in apparent Δ⁹-desaturase activity of 30.2%. Compared with CTL, mammary mRNA abundance of SCD-1 was increased by STO (+30%) and decreased by CLA (−24%), whereas FO had no effect. No effect was observed on mRNA abundance of SCD-5. In conclusion, abomasal infusion of CLA, STO, and FO were shown to exhibit varying and distinct effects on desaturase indices, an indicator of apparent SCD activity, and mammary mRNA abundance of SCD-1.     

Characterisation of the glycerophospholipid fraction in flaxseed oil using liquid chromatography–mass spectrometry

A high-performance liquid chromatographic method coupled with mass spectrometry was used to characterise the natural phospholipid (PL) classes and molecular species in flaxseed oils. The PL fraction included phosphatidylethanolamine (PE) (27–40%), phosphatidylinositol (PI) (29–32%), phosphatidylcholine (PC) (7–18%), lysophosphatidylcholine (LPC) (8–21%), phosphatidylglycerol (PG) (1–4%) and phosphatidic acid (PA) (1–9%). The distribution of fatty acids was found to differ between phospholipids. Stearic acid was mainly present in the form of PC and LPC. Palmitic acid was present in the most abundant molecular species in PI, PG and PA whereas linoleic acid formed the most abundant molecular species in PE.     

HPLC–ESI-MS investigation of tyrosol and hydroxytyrosol oxidation products in virgin olive oil

The aim of this research is the characterisation of the oxidation products of several hydrophilic phenols of virgin olive oil (VOO), such as hydroxytyrosol (3,4-DHPEA) and tyrosol (p-HPEA) and, their identification in the product during storage. This work is aimed at finding analytical indicators that can be used both as molecular markers of VOO “freshness” and for the evaluation of the shelf life of the product itself. Two oxidation systems were examined for the oxidation of p-HPEA and 3,4-DHPEA: enzymatic oxidation and Fenton oxidation. Reaction products were different for the two systems and were identified as quinones, dimers, and acids. During the autoxidation process, Fenton reaction oxidation products, but not enzymatic oxidation products, were found in VOO.     

An Italian survey of undeclared allergens in food over the years 2014–2018

ABSTRACT

Large population studies estimated that the frequency of food allergies is increasing worldwide. In the last two decades, a ‘second wave’ of the allergy epidemic has emerged as a growing public health problem. EU regulation strengthened information to consumers about allergens in pre-packed food, since December 2014 it has been extended to non-prepacked foods by the Regulation (EU) No 1169/2011 of the European Commission. The present work aims to present a five-year survey on the presence of nine types of allergen in several foods, including food of animal origin and baby food. The concentration found for each irregular allergen is generally low, but some samples with no gluten indication contained a concentration above 10 mg kg^?1 with the highest value of 138.5 mg kg^?1 in a dietetic food, during the screening in 2017. These data underline the importance and the necessity of a complete food labelling to protect the majority of allergic individuals.     

Natural occurrence of fumonisins and ochratoxin A in some herbs and spices commercialized in Poland analyzed by UPLC–MS/MS method

Unsanitary conditions during harvesting, drying, packing and storage stages in production and processing of spices and herbs could introduce mycotoxin contamination. The occurrence of ochratoxin A and fumonisins in popular spices and herbs was studied, using liquid chromatography-electrospray-mass spectrometry. Apart from mycotoxins, ergosterol as a factor indicating fungal development was also analysed. A total of 79 different samples commercialized in Poland were randomly purchased from popular markets were tested for mycotoxins. The frequency of samples with fumonisins was lower (31%) than ochratoxin A (49%). Free from mycotoxins were samples of bay leaf and white mustard. ERG content – in spice samples with high concentration level of mycotoxins – was also significantly higher than in samples with little to no mycotoxins.     

Influence of α-, γ-, and δ-tocopherol on the radiation induced formation of peroxides in rapeseed oil triacylglycerols

The effect of α-, γ-, and δ-tocopherols (enrichment: 1000 ppm) on the peroxide formation in rapeseed oil triacylglycerols (RSOTG) was evaluated. The oxidation process was initiated by gamma-irradiation with doses of 4 and 10 kGy. Whereas a pronounced antioxidant effect was observed for γ- and δ-tocopherol (sequence: δ- > γ-tocopherol), the inhibition extent of α-tocopherol was insignificant.     

Interaction of phosphatidylcholine and α-tocopherol on the oxidation of sunflower oil and content changes of phosphatidylcholine and tocopherol in the emulsion under singlet oxygen

Abstract: Interaction of phosphatidylcholine (PC) and α‐tocopherol (α‐Toc) on the oxidation of oil in the emulsion consisting of sunflower oil and water under singlet oxygen at 25 °C was studied by determining peroxide value (PV) and conjugated dienoic acid (CDA) contents. Singlet oxygen was produced by chlorophyll b under 1700 lux. Single addition of PC or α‐Toc decreased the values of peroxides and CDAs of oil in the emulsion via singlet oxygen quenching. PC and α‐Toc showed simply additive interaction in decreasing the singlet oxygen oxidation of oil in the emulsion. α‐Toc was a physical quencher of singlet oxygen in the emulsion, but PC involved chemical quenching in the antioxidant action. Chlorophyll and PC contents were decreased in the emulsion under singlet oxygen, while α‐Toc was not. α‐Toc protected chlorophyll and PC from degradation, and was a more important component than PC in the oil oxidation under singlet oxygen in the emulsion.     

Comparison of headspace-SPME-GC–MS and LC–MS for the detection and quantification of coumarin,vanillin, and ethyl vanillin in vanilla extract products

A headspace-solid phase micro-extraction (HS-SPME) GC–MS method has been developed for the determination of coumarin, vanillin and ethyl vanillin in vanilla products. Limits of detection ranged from 1.33 to 13.2 ng mL⁻¹. Accuracy and precision data for the method were measured and compared to those obtained using LC-ESI-MS. A survey of 24 commercially available vanilla products was completed using both techniques. No coumarin was detected in any of the samples. Examination of the GC–MS chromatograms revealed the presence of 18 other flavor related compounds in the samples. The method validation and sample analysis data using HS-SPME-GC–MS were comparable to those obtained using the LC–MS method. Because the two methods are conceptually different from one another, both methods would not be subject to the same interferences. This would allow them to be used as confirmatory methods for each other.     

Validation of a LC–MS Method for the Determination of Urea Contamination in Market Teas

Tea is one of the most widely consumed beverages in the world preceded only by water. In some culture style of tea plant, urea fertilizer is sprayed on tea leaf in order to increase crop output; besides, in some processing method of green tea, urea is illegally added to maintain tea’s vivid color. The above-mentioned process may unavoidably cause urea residue, and prolonged or repeated exposure of body to urea may cause adverse effects. In this work, an easy and reliable hydrophilic interaction liquid chromatography/mass spectrometry analytical method for determination of urea in tea was firstly validated; the method exhibited a linear response from 4 to 60 μg mL^?1 (R ²?>?0.9996), the limit of quantitation for urea is 4 μg mL^?1, the mean recoveries of urea spiked at levels of 10 and 20 μg mL^?1 were 95–110 %, and the relative standard deviations of intra- and inter-day measurements were less than 7.8 %. The method was later successfully applied to the analysis of urea residue in some market tea samples. The result showed that there is obvious urea contamination in some market teas, and the contamination percentage is especially high in green tea samples. Among the samples investigated, urea was detected at concentration ranges of 24.02–46.02 mg/kg. Some attention should be paid on the health effect resulting from such urea contamination in tea.     

Concentrations of dioxins and dioxin-like PCBs in feed materials in the Netherlands, 2001–11

This study aimed to obtain insights into contamination of feed materials used in the Netherlands with dioxins (polychlorinated dibenzo-p-dioxins and dibenzofurans) and dioxin-like polychlorinated biphenyls (PCBs). Monitoring results from the period 2001–11, covering in total 4938 samples, were statistically analysed and evaluated against the statutory limits set at the beginning or during this period. The percentage of samples exceeding maximum levels set within the European Union for either dioxins or the sum of dioxins and dioxin-like PCBs were below 1% for most feed categories, except for fish meal (4.1%), clay minerals (binders and anti-caking agents) (3.4%), and vegetable oils and byproducts (1.7%). For most feed categories, non-compliance with the action threshold (roughly 33% lower than maximum levels) for either dioxins or dioxin-like PCBs was up to three times higher than non-compliance with the respective maximum levels. Exceedance of action thresholds was just above 1% for animal fat, pre-mixtures and feed materials of plant origin excluding vegetable oils. For the categories fish meal, clay minerals, and vegetable oils and byproducts, the action thresholds were exceeded by 5.0%, 9.8% and 3.0% of the samples, respectively. In general, the percentages of samples that exceeded the action thresholds and maximum levels were lower than those reported for the European Union by the European Food Safety Authority (EFSA). In most of the feed materials, there seems to be a decreasing trend in concentrations of dioxins or dioxin-like PCBs over the years. However, a lowering of the limits of quantification during this period and the low concentrations in most samples precludes drawing strong conclusions.