Migration of silver from nanosilver–polyethylene composite packaging into food simulants

An analytical method for the determination of silver in food simulants (3% (w/v) aqueous acetic acid or 95% (v/v) aqueous ethanol) was developed based on inductively coupled plasma mass spectrometry (ICP-MS). Recoveries ranged from 87% to 109% and RSDs ranged from 0.7% to 7.8%. The procedure was applied to determine the migration of silver from nanosilver–polyethylene food packaging film into food simulants at different temperatures and migration times. Results indicated that the maximum migration ratios were 1.70%, 3.00% and 5.60% for 3% (w/v) aqueous acetic acid at 20, 40 and 70°C, respectively, while for 95% (v/v) aqueous ethanol the maximum migration ratios were 0.24%, 0.23% and 0.22% at 20, 40 and 70°C.     

Study of the retention and release of n-hexanal incorporated into soy protein isolate–lipid composite films

This work deals with the study of the kinetic of aroma release, which had been previously incorporated into soy protein isolate (SPI)–lipid composite films. The aim was to determine the influence of type and amount of lipidic material on aroma (n-hexanal) release and retention, as well as the apparent diffusion coefficients. To carry out this study it have been employed SPI-based films containing two SPI:LIPID ratios (1:0.25 and 1:0.5), and two types of lipids, oleic acid (OA) and beeswax (BW), in OA:BW ratios 100:0, 70:30, 50:50, 30:70 and 0:100. The measurements were performed by a gas chromatography technique. The films that showed more retention were SPI:LIPID 1:0.5 100% BW and control film. Concerning release rate, films containing BW as unique lipid material gave the lowest aroma release rate. Apparent diffusion coefficients (D_app) of all films are in the same order of magnitude (10⁻¹⁵ m² s⁻¹). D_app decreases when BW increases in the film matrix and when oleic acid amount decreases. In conclusion, for encapsulating n-hexanal, SPI-BW films demonstrated the best performances, followed by control film (without lipids).     

Role of sepiolite in the release of active compounds from gelatin–egg white films

Nanosized material fillers are widely used to enhance certain properties of polymers. Moreover, the use of nanoclays as a delivery host in pharmaceutical fields has gained a great interest. Sepiolite was incorporated to gelatin–egg white films containing clove essential oil. The effect of the incorporation of both sepiolite and clove essential oil on the physical properties of the resultant films was evaluated. Special attention was given to the role of this nanoclay in the release of antioxidant and antimicrobial compounds from the film matrix. Sepiolite showed a reinforcement effect of Young’s modulus and tensile strength, meanwhile the clove essential oil had a certain plasticizing effect by increasing the elongation at break and water vapour permeability (WVP). When both compounds were added together, a noticeable loss of mechanical properties was observed, related to the loss of gelling capacity (G′), protein self-aggregation and α-helix structure decrease (FTIR). However, the WPV increased, probably due to the presence of cavities in the matrix observed by SEM. The incorporation of sepiolite in these films containing clove essential oil increased the release of both protein components and eugenol from the film matrix, leading to a controlled release of the antioxidant activity measured by ferric reducing ability and radical scavenging capacity, as well as a higher antimicrobial effect.     

Use of Tenax® films to demonstrate the migration of chemical contaminants from cardboard into dry food

ABSTRACT

Contaminants in food packaging are a challenge of our time since the packaging material itself has been found to represent a source of food contamination through the migration of substances from it. Before first use, packaging materials destined for the packaging of dry foods can be evaluated by performing migration experiments with the simulant for dry foods, Tenax®. This simulant is commercially available as a powder that is more difficult to handle during the migration experiments. This paper reports the development of a Tenax film. The film can be applied to the cardboard surface to conduct the migration test. After the migration is completed, the film can be easily extracted to determine the concentration of the contaminants in the film. Finally, the performance of the Tenax film was compared with the conventional Tenax powder for the evaluation of 15 model migrants.     

Time‐ and temperature‐dependent migration studies of Irganox 1076 from plastics into foods and food simulants

The study provides an exhaustive set of migration data for octadecyl 3‐(3,5‐di‐tert‐butyl‐4‐hydroxyphenyl)propionate (Irganox 1076) from low‐density polyethylene (LDPE) in several food matrices. Irganox 1076 was used as a model migrant because it represents one of the typical substances used as an antioxidant in food packaging polymers. Kinetic (time‐dependent) migration studies of Irganox 1076 were performed for selected foodstuffs chosen with different physical–chemical properties and in relation to the actual European food consumption market. The effect of fat content and of the temperature of storage on the migration from plastic packaging was evaluated. The results show that migration increased with fat content and storage temperature. All data obtained from real foods were also compared with data obtained from simulants tested in the same conditions. In all studied cases, the kinetics in simulants were higher than those in foodstuffs. The work provides data valuable for the extension of the validation of migration model developed on simulants to foodstuffs themselves.     

Comparison of the migration of melamine from melamine–formaldehyde plastics (‘melaware’) into various food simulants and foods themselves

A variety of melaware articles were tested for the migration of melamine into the food simulant 3% w/v acetic acid as a benchmark, and into other food simulants, beverages and foods for comparison. The results indicate that the acidity of the food simulant plays a role in promoting migration, but not by as much as might have been anticipated, since 3% acetic acid gave migration values about double those obtained using water under the same time and temperature test conditions. In contrast, migration into the fatty food simulant olive oil was not detectable and at least 20-fold lower than with the aqueous food simulants. This was expected given the solubility properties of melamine and the characteristics of the melaware plastic. Migration levels into hot acidic beverages (apple juice, tomato juice, red-fruit tea and black coffee) were rather similar to the acetic acid simulant when the same time and temperature test conditions are used, e.g. 2?h at 70°C. However, migration levels into foods that were placed hot into melaware articles and then allowed to cool on standing were much lower (6–14 times lower) than if pre-heated food was placed into the articles and then maintained (artificially) at that high temperature in the same way that a controlled time–temperature test using simulants would be conducted. This very strong influence of time and especially temperature was manifest in the effects seen of microwave heating of food or beverage in the melaware articles. Here, despite the short duration of hot contact, migration levels were similar to simulants used for longer periods, e.g. 70°C for 2?h. This is rationalized in terms of the peak temperature achieved on microwave heating, which may exceed 70°C, counterbalancing the shorter time period held hot. There was also evidence that when using melaware utensils in boiling liquids, as for stovetop use of spatulas, the boiling action of circulating food/simulant can have an additional effect in promoting surface erosion, increasing the plastic decomposition and so elevating the melamine release.     

Levels and temporal trend of bisphenol A in composite food samples from Canadian Total Diet Study 2008–2012

Food composite samples from the Canadian Total Diet Study which was conducted each year from 2008 to 2012 rotating between different cities were analysed for bisphenol A (BPA). The overall levels of BPA in the composite food samples from each of the five years from 2008 to 2012 were similar in general with averages (range) of 7.7 ng/g (0.20–106 ng/g), 7.8 ng/g (0.26–110 ng/g), 6.9 ng/g (0.20–84 ng/g), 7.7 ng/g (0.20–105 ng/g) and 9.0 ng/g (0.15–90 ng/g) for 2008, 2009, 2010, 2011 and 2012, respectively. Levels of BPA in most of the non-canned food composite samples were low and no particular trends were observed. In contrast, the trend of BPA levels in canned food composite samples over the five years (2008–2012) varies. BPA levels in most of the canned food composite samples from 2008 to 2012 were consistent in general (e.g. canned luncheon meat: 10–18 ng/g, canned baked beans: 18–25 ng/g). While BPA levels over the five years were found to decrease for some canned food composite samples (e.g., canned fish: 109 ng/g in 2009 vs. 51 ng/g in 2012), they were also found to increase for some other canned food composite samples (e.g. canned meat soups: 90–104 ng/g in 2011–2012 vs. 29 ng/g in 2008). Thus, recent changes in can coating for food packaging to BPA-free alternatives may have not been fully reflected in all canned food products over the period from 2008 to 2012. Continued monitoring is necessary to more fully assess the potential impact on dietary exposure by the use of BPA alternatives in food contact materials.     

Residue analyses and exposure assessment of the Irish population to nitrofuran metabolites from different food commodities in 2009–2010

An exposure assessment to nitrofuran residues was performed for three human populations (adults, teenagers and children), based on residue analyses of foods of animal origin (liver, honey, eggs and aquaculture) covering the 2-year period 2009–2010. The occurrence of nitrofuran metabolites in food on the Irish market was determined for the selected period using the data from Ireland’s National Food Residue Database (NFRD) and from results obtained from the analysis of retail samples (aquaculture and honey). Laboratory analyses of residues were performed by methods validated in accordance with Commission Decision 2002/657/EC regarding performance of the analytical method and interpretation of results. Semicarbazide (SEM) was the contaminant most frequently identified and its content ranged from 0.09 to 1.27 μg kg^?1. SEM is currently used as a marker of nitrofuran abuse, but it may also occur from other sources. The presence of nitrofuran metabolite 3-amino-2-oxazolidinone (AOZ) was detected in two aquaculture samples (prawns) at 1.63 and 1.14 μg kg^?1, but such a low number of positive cases did not present sufficient data for a full AOZ exposure assessment. Therefore, the evaluation of exposure was focused on SEM-containing food groups only. Exposure assessments were completed using a probabilistic approach that generated 10 iterations. The results of both the upper- and lower-bound exposure assessments demonstrate that SEM exposure for Irish adults, teenagers and children from selected food commodities are well below EFSA-estimated safe levels.     

Extreme weather,food security and the capacity to adapt – the case of crops in China

Three extreme weather scenarios are examined for agriculture in China in this study. One scenario assumes a year when every province has precipitation corresponding to the lowest level experienced in the province over the last three decades. Another scenario assumes the highest experienced precipitation for every province is happening; and the last one assumes that the most harmful level of precipitation on crops occurs for every province – whether too little or too much. We studied the role of autonomous adaptation by farmers and through markets as embodied in a computable general equilibrium model. The results show that observed extreme impacts of precipitation on crop harvests are not serious for China at national level. The maize harvest is the most negatively affected with a reduction of 4 % without adaptation and less than 1 % reduction with adaptation. However, the impacts within a province may be serious and even become worse with adaptation. Good harvests might not make farmers better off due to lower crop prices even though consumers benefit. Sensitivity analysis shows that the ability to adapt assumed in the analysis may not be present in the short term.     

Water–water and water–macromolecule interactions in food dehydration and the effects of the pore structures of food on the energetics of the interactions

A molecular dynamics (MD) modeling and simulations approach has been rationally built and developed to study porous food systems constructed with amylose and dextran chains. The findings from our MD studies indicate that the presence of food macromolecules decreases the energetics of the water–water interactions for the nearby water molecules in the pore space, but provides additional water–macromolecule interactions that can significantly outweigh the partial loss of water–water interactions to make the adjacent water molecules strongly bound to the food macromolecules so that the water activity and water removal rate are decreased as dehydration proceeds and, thus, the dehydration energy requirement would be increased. The effects of pore structures are greater in systems with higher densities of food macromolecules, smaller in size pores, and stronger water–macromolecule interactions. Dehydration of food materials can thus be reasonably expected to start from the largest pores and from the middle of the pores, and to have non-uniform water removal rates and non-planar water–vapor interfaces inside individual pores as well as across sections of the food materials. The food porous structures are found to have good pore connectivity for water molecules. As dehydration proceeds, water content and the support from water–water and water–macromolecule interactions both decrease, causing the food porous structures to adopt more compact conformations and their main body to decrease in size. Dehydration in general also reduces pore sizes and the number of pore openings, increases the water–macromolecule interactions, and leads to the reduction of the overall thermal conductivity of the system, so that more energy (heat), longer times, and/or greater temperature gradients are needed in order to further dehydrate the porous materials. Our thermodynamic analysis also shows that the average minimum entropy requirement for food dehydration is greater when the water–macromolecule interactions are stronger and the food macromolecular density is higher. The importance of the physicochemical affinity of food molecules for water and of the compatibility of the resultant porous structures with water configurational structures in determining food properties and food processing through the water–macromolecule interactions, is clearly and fundamentally verified by the results and discussion presented in this work.     

Migration of α-tocopherol from LDPE films to corn oil and its effect on the oxidative stability

The migration of α-tocopherol (α-T) from low density polyethylene (LDPE) films, added with 20 (film A) and 40 mg g^?1 (film B) to corn oil for 12 weeks at 5, 20 and 30 °C was determined. A LDPE film added with no α-T was used as control (film C). Diffusion coefficient (D) values for the film A system were 1.4 × 10^?11, 7.1 × 10^?11 and 30.3 × 10^?11 cm² s^?1 at 5, 20 and 30 °C, respectively. Meanwhile, D values for the film B system were 1.3 × 10^?11, 9.6 × 10^?11 and 51.1 × 10^?11 cm² s^?1 at the same temperatures. The activation energy (E_a) for the diffusion of α-T was 126.5 (film A) and 105.9 kJ mol^?1 (film B). The effect of the migration of α-T on the oxidative stability of corn oil was evaluated by monitoring hexanal content by solid phase micro-extraction (SPME) and gas chromatography. The hexanal content in the oil showed that both films added with α-T resulted suitable to maintain the oxidative stability of the oil for about 16 weeks at 30 °C, compared to 12 weeks for the oil in contact with the film C.     

Investigation of the composite system of β-lactoglobulin and pectin in aqueous solutions

The compatibility in aqueous systems of β-lactoglobulin (β-lg) with low and high esterified-sodium polypectates (LMP and HMP) was investigated. The mixture did not separate into two co-existing liquid phases in any case studied. At pH above the isoelectric point (IP) of β-lg, the behavior of LMP and HMP was similar when mixing with β-lg. Pectins and β-lg were co-soluble was around a particular ionic strength (μ) (0.07 M for HMP and 0.3 M for LMP). In these circumstances, the flow behavior of pectin was hardly affected by the addition of β-1g . At all other μ, the mixture formed a liquid phase containing both β-lg and pectin and a small amount of β-lg precipitates. Here, the viscosity of the liquid phase was slightly higher than the viscosity of a solution containing the same concentration of pectin. At pH 3.5, i.e. pH⩽IP of β-lg, the behavior of LMP and HMP was different when mixing with β-lg. LMP formed insoluble complexes with β-lg at low μ (⩽0.25 M), but precipitation was suppressed at high μ (0.5 M). The composite system of β-lg/HMP formed a white, homogeneous and stable dispersion at low μ (0.07 M). The viscosity of this dispersion was much higher than the additive viscosity of individual solutions would be. Probably, the oppositely charged β-lg and HMP formed soluble complexes, which further associated into large aggregates. This complexation was also suppressed at high μ (0.5 M).     

Influence of β-carotene-rich vegetables on the bioaccessibility of zinc and iron from food grains

Widespread deficiencies of iron and zinc, commonly found in populations dependent on plant foods, necessitate food-based strategies to maximise their bioavailability from plant foods. In this study, β-carotene-rich vegetables were evaluated for their effects on the bioaccessibility of iron and zinc from cereals and pulses by employing a simulated gastrointestinal digestion procedure involving equilibrium dialysis. Addition of carrot or amaranth (2.5 g and 5 g per 10 g of grain) significantly enhanced the bioaccessibility of iron and zinc from the food grains, the percent increase being 13.8–86.2 in the case of carrot and 11–193% in the case of amaranth. Pure β-carotene added at an equivalent level also enhanced the bioaccessibility of iron (19.6–102% increase) and zinc (16.5–118.0% increase) from the cereals examined. This is the first report on the beneficial influence of β-carotene on iron and zinc bioaccessibilities.     

The antibacterial activity and antibacterial mechanism of the tea polyphenol liposomes/lysozyme–chitosan gradual sustained release composite coating

To obtain long-lasting preservation materials, the tea polyphenol liposomes (TP-Lips)/lysozyme (LZM)–chitosan (CS) composite coating with the gradual sustained property was prepared by tape casting method. These coatings were characterised, and their physicochemical properties were measured. Meanwhile, the antibacterial mechanisms of coatings were studied using the spoilage bacteria of aquatic products (Shewanella putrefaciens and Pseudomonas fluorescens) as target strains. Compared with CS coating, the incorporation of TP-Lips makes the cracks and granular matter of the coatings increase. Except for the oxygen permeabilities (OP) and carbon dioxide permeabilities (CDP), the rest of the physicochemical properties are decreased, including tensile strength (Ts), elongation at break (EB) and light transmittance (T). Antibacterial mechanisms indicate that TP and LZM have a synergistic antibacterial effect. The slow-release system composed of liposomes and coating prolongs the action time of TP and LZM. Hence, the TP-Lips/LZM-CS coating could be a hopeful material in food preservation field with excellent antibacterial properties.     

Micro/nano emulsion delivery systems: Effects of potato protein/chitosan complex on the stability,oxidizability, digestibility and β - carotene release characteristics of the emulsion

The stability, antioxidant activity, digestibility and β - carotene sustained - release mechanism of Pickering emulsion stabilized by potato protein/chitosan (PP/CS) complex were investigated. The results exhibited that the isoelectric point of PP increased from 4.30 to 6.50 and 7.00 after adding 0.2% and 0.4% CS to improve its surface hydrophilicity, leading to a uniform dispersion of PP. Simultaneously, the average particle size of the emulsion stabilized by the PP showed a decrease from 5102.50 nm to 784.90 and 1268.50 nm and zeta - potential of the emulsion stabilized by the PP exhibited an increase from 40.63 to 48.50 and 53.73 mV after adding 0.2% and 0.4% CS to improve the stability of the emulsion. In addition, the emulsion stabilized by the PP/CS complex was found to have a smaller storage modulus (G′), loss modulus(G″), apparent viscosity and better physical stability, which was less affected by storage time, temperature and salt ion concentration. Moreover, the emulsion stabilized by the PP/CS complex exhibited better oxidation resistance. Furthermore, the emulsion stabilized by the PP/CS complex showed good anti-digestibility and slowed the sustained release rate of β - carotene. These results will provide a theoretical basis for the application of a novel food emulsifier PP/CS complex in nano - colloid delivery system.     

Metal–organic framework for the extraction and detection of pesticides from food commodities

Pesticide residues in food matrices, threatening the survival and development of humanity, is one of the critical challenges worldwide. Metal–organic frameworks (MOFs) possess excellent properties, which include excellent adsorption capacity, tailorable shape and size, hierarchical structure, numerous surface-active sites, high specific surface areas, high chemical stabilities, and ease of modification and functionalization. These promising properties render MOFs as advantageous porous materials for the extraction and detection of pesticides in food samples. This review is based on a brief introduction of MOFs and highlights recent advances in pesticide extraction and detection through MOFs. Furthermore, the challenges and prospects in this field are also described.     

Have changes to meat and poultry food safety regulation in Australia affected the prevalence of Salmonella or of salmonellosis?

During the 1990s, there was radical change in regulation of meat and poultry hygiene in Australia, and Australian Standards were developed for each sector of the meat industry. Systems for industry/government co-regulation and company-employed meat inspection were introduced based on company HACCP programs approved and audited by the Controlling Authority. However, in the 5 years since regulatory changes took full effect, rates of salmonellosis have not decreased (surveillance and reporting systems have remained unchanged). Using statistics gathered by the National Enteric Pathogens Surveillance Scheme, an attempt was made to link Salmonella serovars isolated from meat and poultry with those causing salmonellosis. Two periods were studied, 1993/1994, before regulations were introduced, and 2000/2001, when regulations should be having an effect. For red meat, the same serovars were prominent among the top 10 isolates both before and after regulation, and there was little linkage with salmonelloses. For poultry, frequently isolated serovars differed pre- and post-regulation, however, in both periods there was some linkage between serovars isolated from poultry and those causing salmonelloses. Using published and unpublished survey data, it was concluded that there had been improvements in microbiological quality of red meat and poultry over the same timeframe as regulatory changes. That these improvements apparently have not carried through to reduced case-rates for salmonellosis may be due to numerous causes, including lack of control in the food processing, food service and home sectors. The present paper illustrates difficulties faced by governments in measuring public health outcomes of changes to food hygiene regulation.