Effect of the solute on the development of compositional profiles in osmotic dehydrated apple slices

Apple (cv. Granny Smith) slices, 30-mm thick, were osmotically dehydrated for 9 h at 30 °C using glucose, sucrose and trehalose solutions with the same water activity (a_w = 0.96). After OD treatment, water and solute content were analysed in 1.5-mm thick serial disks of the apple slices to determine the effect of osmotic dehydration on the compositional profiles. Diffusional and “Advancing Disturbance Front” (ADF) models were applied to the experimental data, both showing a good fit. Changes in the compositional profiles of osmotically dehydrated slices were also analysed throughout storage time. For this purpose, the 30-mm thick dehydrated slices were kept at 10 °C for 7 days in hermetic plastic bags and compositional profiles were analysed after 1, 2, 3 and 7 days and modelled using Fermi's equation. Throughout storage, the profiles became flatter due to the counter-current migration of water and solutes associated to the concentration gradients. Mass transfer rate during dehydration was faster when sucrose or glucose was used, but trehalose implied an increase in the mass transfer resistance of the tissue. This behaviour was also observed in the mass transfer processes during storage. This effect was attributed to the changes induced by trehalose in the permeability of cell membranes through component interactions.     

A headspace solid-phase microextraction gas-chromatographic mass-spectrometric method (HS-SPME–GC/MS) to quantify hexanal in butter during storage as marker of lipid oxidation

A method using headspace solid-phase microextraction (HS-SPME) combined with gas chromatography–mass spectrometry (GC/MS) was developed and validated for the extraction and quantification of hexanal content in butter (at ng g⁻¹ level) during storage at 4 °C. The variability of hexanal content among seasons of production and the influence of high extraction temperature on ex-novo formation of hexanal were also evaluated. The HS-SPME conditions were optimised and analytical parameters of the method (linearity, accuracy, and precision) demonstrate its usefulness. The reproducibility and accuracy of the quantitative analysis was assured by the use of D₁₂-hexanal as internal standard. For the applications, the headspace was extracted using CAR/PDMS fiber for 180 min at 4 °C. Hexanal contents in samples during all storage period (shelf-life) and from butters produced in different seasons were analysed. Butter samples at the end of shelf-life and samples produced in August showed highest values of hexanal, confirming that the temperature both in storage and distribution phases represents a critical factor to maintain the quality of butter.     

Effect of storage conditions on furosine formation in milk–cereal based baby foods

The effect of storage during 9 months at 25, 30 and 37 °C on furosine formation in three milk–cereal based baby foods was studied to evaluate development of the Maillard reaction. Furosine was measured by HPLC-UV. Immediately after the manufacturing process, furosine contents were 310–340 mg/100 g protein and at the 9th storage month were 426–603 mg/100 g protein. Storage time and temperature have a significant increase (p < 0.05) of furosine content during storage. Furosine contents were higher in sample containing honey than in those without honey. Interactions (p < 0.05) between storage time and temperature or type of sample were found. A predictive model equation of the evolution of furosine during storage explaining 80% of the variability in furosine content was obtained. The blockage of lysine through storage calculated using the furosine and total lysine provided values ranged from 9.5% to 18.1% for analysed baby foods.     

Effects of temperature,solid content and pH on the stability of black carrot anthocyanins

Anthocyanin stability of black carrots was studied at various solid contents (11, 30, 45 and 64° Brix) and pHs (4.3 and 6.0) during both heating, at 70–90 °C, and storage at 4–37 °C. Monomeric anthocyanin degradation fitted a first-order reaction model. Degradation of monomeric anthocyanins increased with increasing solid content during heating, while it decreased during storage. For example, at pH 4.3, half-life periods for anthocyanins at 30, 45 and 64° Brix were, respectively, 8.4, 6.9 and 5.2 h during heating at 80 °C and 18.7, 30.8 and 35.9 weeks during storage at 20 °C. At 30–64° Brix, increasing pH from 4.3 to 6.0 enhanced the degradation of anthocyanins during heating. The effect of pH on thermal stability of anthocyanins was also studied at six different pHs (2.5–7.0) in citrate-phosphate buffer solutions and significant decrease in anthocyanin stability was observed at pHs above 5.0. Higher activation energies (E_a) were obtained during heating than during storage with increasing solid contents. At 30–64° Brix, E_a values ranged from 68.8 to 95.1 kJ mol⁻¹ during heating and from 62.1 to 86.2 kJ mol⁻¹ during storage. Q₁₀ values at 20–37 °C were as high as 3.1 at 45° Brix and 3.6 at 64° Brix.     

Effects of aqueous chlorine dioxide treatment on browning of fresh-cut lotus root

Effect of aqueous chlorine dioxide (ClO₂) treatment on browning of fresh-cut lotus root (FLR) was investigated to explore the feasibility to apply ClO₂ for browning inhibition of fresh-cut products. Cut lotus roots were treated in ClO₂ solutions at different concentrations (10, 50 and 100 mg/l) for different time (5, 10 and 15 min), followed by chilled storage for 8-10 days at 4 °C. Color parameters (L^∗, a^∗ and b^∗), polyphenol oxidase (PPO) activity and overall visual quality (OVQ) were measured at one-day interval during storage. Results showed that higher ClO₂ concentration and longer treatment time can provide better inhibitory effects on the browning of FLR. ClO₂ concentration, treatment time and storage time were three significant factors (P < 0.05) and some significant interactions were observed. PPO activities were largely inhibited by 100 mg/l ClO₂ treatment for 10 min. The 100 mg/l ClO₂ treatment maintained high OVQ scores during 10-day storage; while 50 mg/l ClO₂ treatment was acceptable for maintaining OVQ during 4-day storage. ClO₂ treatment was demonstrated to be a promising alternative approach to control browning and improve OVQ of FLR.     

Effects of tea polyphenol coating combined with ozone water washing on the storage quality of black sea bream (Sparus macrocephalus)

The present research evaluated the effects of tea polyphenol (TP) combined with ozone water (O₃) on the quality of black sea bream (Sparus macrocephalus) over a period of 15 days storage at 4 °C. A solution of TP (0.2%, w/v) was used to coat the fish after washing with ozone water (1 mg/L). Fish physicochemical (pH, K value, peroxide value, thiobarbituric acid, total volatile basic nitrogen, trimethylamine, texture, and colour), sensory, and bacteriological characteristics were all analysed. TP + O₃ treatment effectively reduced nucleotide breakdown, lipid oxidation, protein decomposition, and microbial growth, and maintained better characteristics of texture, colour, and sensory compared with the control. The efficiency of TP + O₃ treatment was also better than that of TP treatment or O₃ treatment alone. Therefore, tea polyphenol coating combined with ozone water prewashing may be a promising method of maintaining the storage quality of black sea bream and of extending fish post-mortem shelf-life during 4 °C storage.     

Changes in biogenic amine levels during storage of Mexican-style soft and Spanish-style dry-ripened sausages with different aw values under modified atmosphere

Two raw sausages were prepared: a soft and a dry-ripened one, both by local traditional and industrial manufacturing practices. Sausages were packaged under a CO₂/N₂ atmosphere at different targeted activity water (a_w) values: 0.96 and 0.92 (soft sausages) and 0.88 and 0.82 (dry-ripened sausages). Sausages were then stored at 5 °C for 42 days or at 12 °C for 240 days (soft and a dry-ripened sausages, respectively). The time-related changes in dominant microbiota, pH and biogenic amine contents during storage were determined. Tyramine was the most abundant biogenic amine in all the sausages. Biogenic amine levels were higher in dry-ripened sausages than in soft sausages at packaging. However, during refrigerated storage soft sausages were fermented and the levels of biogenic amines increased (P < 0.05). At the end of storage, traditional soft sausages with 0.96 a_w presented comparable levels of biogenic amines to traditional dry-ripened sausages.     

A study of the ice crystals in vacuum-packed salmon fillets (Salmon salar) during superchilling process and following storage

The aim of this work was to study the microstructure of vacuum-packed salmon fillets superchilled in an impingement freezer at −30 °C (air temperature) and 227 W/m² K (surface heat transfer coefficient, SHTC) for 2.1 min prior to storage at a superchilling storage temperature of −1.7 ± 0.3 °C for 28 days. The microstructure of vacuum-packed salmon fillets were analysed at the surface, mid-centre and centre layers. Significant differences were observed between the ice crystals formed at the surface, mid-centre and centre layers. The size of ice crystals at the centre of the superchilled fillets was 3 times larger than those at the surface layer. Significant differences were observed between the size of ice crystals formed during the superchilling process and following storage. The results further indicated that, after temperature equalisation (1 day of storage) the growth of the intracellular ice crystal was not significant at (P < 0.05) at any storage time.     

The kinetics of Maillard reaction in lactose-hydrolysed milk powder and related systems containing carbohydrate mixtures

The kinetics of Maillard reaction in lactose-hydrolysed skim milk powder and related systems containing carbohydrate mixtures were analysed. The effect of the increase of water activity and temperature during storage of the commercial product was also evaluated. In systems with two and three carbohydrates, a marked decrease of the reaction rate was observed when monosaccharides were partially replaced by lactose, notwithstanding the fact that the former still remained in a higher proportion than lysine. The rate of available lysine loss in lactose-hydrolysed milk was mostly affected by the presence of galactose. The reaction rate constants at a_w 0.52 and at 37 and 50 °C were higher than at a_w 0.33. However, no significant differences were observed at 60 °C. Temperature is the most important factor to be controlled in order to minimise nutritional deterioration during storage.     

Effect of storage temperature on phenolics stability in hawthorn (Crataegus pinnatifida var. major) fruits and a hawthorn drink

The stability of five major phenolics, namely (−)-epicatechin (EC), procyanidin B₂ (PC-B₂), chlorogenic acid (ChA), hyperoside (HP) and isoquercitrin (IQ), in hawthorn fruits and a canned hawthorn drink were evaluated during 6 months of storage in the dark at three different temperatures (4, 23 and 40 °C). HPLC with a diode-array detector was used to determine the contents of the individual compounds. The results showed that the studied phenolics in the hawthorn fruits and the drink were both stable at 4 °C and relatively unstable at 23 and 40 °C with varied extents of degradation. At room temperature (23 °C), marked degradations of EC and PC-B₂ were observed in both the fruits and the drink with around 50% and 30% decrease after a 6-month storage, respectively. A more significant decrease of the phenolics was observed at 40 °C, especially for EC and PC-B₂, which were almost completely degraded after a 6-month storage. HP, IQ and ChA were relatively stable at 23 °C, but unstable at 40 °C. Therefore, low-temperature storage is recommended for maintaining the quality and efficacy of hawthorn fruits and its preparations.     

The effect of delactosed whey permeate on phytochemical content of canned tomatoes

The effect of delactosed whey permeate (DWP) treatment on antioxidant and phyto-chemical components of canned Irish plum tomatoes were investigated. Tomatoes were sterilised for 5 min (F₀) at 120 °C and stored for 6 months. The DWP treatment retained significantly (p < 0.05) higher levels of ascorbic acid and lycopene of tomatoes. The antioxidant activity of DWP treated tomatoes was higher (7%) than the control at the end of storage. The firmness in DWP-treated fruits was around 40% higher than that in control. All the parameters decreased significantly (p < 0.05) during storage except lycopene and total phenols. Lycopene content showed no significant change and total phenols increased during storage. The changes in ascorbic acid, antioxidant activity and texture were fitted well to Weibull kinetic models with high coefficients of determination (R²) and low RMSE (root mean sum of squared error). The results clearly indicate that DWP enhanced the retention of antioxidant compounds in tomatoes during storage.     

Changes in strawberry phenolics, anthocyanins, and antioxidant capacity in response to high oxygen treatments

Changes in fruit quality, decay, phenolic and anthocyanin content, and antioxidant capacity of strawberries (Fragaria × ananassa Duch. cv. Allstar) stored under air and high oxygen atmospheres at 5 °C were investigated. Freshly harvested strawberries were placed in jars and ventilated continuously with air or with 40, 60, 80, or 100 kPa O₂ at 5 °C for up to 14 days. Samples were taken initially, and after 3, 7, 10 and 14 days of storage. While fruit quality parameters such as titratable acidity, total soluble solids and surface color were only slightly affected by differing levels of O₂, the higher oxygen concentration treatments significantly reduced decay. Oxygen concentrations higher than 60 kPa also promoted increases in ORAC values, total phenolics and total anthocyanins as well as individual phenolic compounds analysed by HPLC during the initial 7 days of storage. However, this effect diminished with prolonged storage. No significant differences in ORAC values, total phenolics, total anthocyanins, or the individual phenolic compounds were observed among the high O₂ and air-stored fruits after 14 days of storage. These results indicate that high oxygen treatments exert the most effects on fruit quality and antioxidant capacity of strawberry fruit in the first 7 days of storage.     

Modified atmosphere packaging and vacuum packaging for long period chilled storage of dry-cured Iberian ham

Dry-cured Iberian ham slices were stored under vacuum and under four different modified atmospheres (60/40 = 60%N₂ + 40%CO₂; 70/30 = 70%N₂ + 30%CO₂; 80/20 = 80%N₂ + 20%CO₂; argon = 70%argon + 30%CO₂) at 4 ± 1 °C during 120 days. Gas composition, moisture content, pH, colour, pigment content, and lipid stability were measured, as well as sensory and microbial analysis were carried out throughout storage. A loss of intensity of red colour (a^*-values) was observed during storage in ham slices (P < 0.05). Consistently, MbFe(II)NO content also decreased throughout storage (P > 0.05). Slices of ham packed in 40%CO₂ (60/40) and 30%CO₂ (70/30) showed lower a^*-values than the rest of the batches after 60 days (P < 0.05), though differences were not evident after 120 days (P > 0.05). TBARs values showed an upward trend during the storage of packaged slices (P < 0.05). Vacuum-packed slices showed the lowest TBARs values and those packed with 40%CO_2, the highest. Sensory attributes did not vary significantly (P > 0.05) throughout storage under refrigeration and packed either in vacuum or in modified atmospheres. No safety problems were detected in relation to the microbial quality in any case.     

Antioxidant phytochemical and fruit quality changes in mango (Mangifera indica L.) following hot water immersion and controlled atmosphere storage

Tropical fruits such as mangoes destined for import into the United States are commonly required to have a thermal treatment against invasive pests, which could be combined with controlled atmosphere (CA) storage to prolong shelf life and preserve fruit quality. Changes in antioxidant phytochemicals and resultant quality during storage and ripening were investigated in fresh mangoes, as influenced by application of CA in combination with a hot water immersion quarantine treatment (46 °C for 75 min). Mature-green mangoes with or without a hot water treatment, were held in air, 3% O₂ + 97% N₂, or 3% O₂ + 10% CO₂ + 87% N₂ and evaluated for external quality and phytochemical differences after storage for 2 weeks at 10 °C and after subsequent ripening in air at 25 °C. Visible appearance of anthracnose during ripening was effectively inhibited by the hot water treatments combined with CA. Concentrations of gallic acid and numerous hydrolysable tannins and their resultant antioxidant capacity were unaffected by the hot water treatment, while total polyphenolics naturally decreased throughout fruit ripening, regardless of hot water treatment or storage atmosphere. However, the overall decline in polyphenolic concentration was inhibited by the CA treatments, as a result of delayed ripening. Quality parameters such as flesh colour and titratable acidity provided supporting evidence that the CA conditions helped to delay fruit ripening.     

Different postharvest strategies to preserve broccoli quality during storage and shelf life: Controlled atmosphere and 1-MCP

Broccoli (Brassica oleracea var. italica) is a vegetable that requires the application of postharvest techniques to extend its marketability. Controlled atmosphere and 1-MCP treatments are most used to extend the shelf life of broccoli and reduce post-harvest deterioration. The aim of this study was to evaluate the visual, physicochemical and functional changes of broccoli head samples stored at 1–2 °C and 85–90% relative humidity (RH) in air (Control samples), under controlled atmospheres (10% O₂ and 5% CO₂) (CA samples) and treated with 1-MCP (0.6 μL/L). After storage all samples were maintained at 20 °C for 2 and 4 days, in order to assess their shelf life. The most suitable postharvest treatment to extend broccoli quality during storage and shelf life, in terms of maintaining the visual quality and reducing loss of health-promoting compounds, was achieved by storage under controlled atmosphere conditions. The use of 1-MCP reduced the loss of green colour and chlorophyll pigments, but only during cold storage not during shelf life at 20 °C.     

The in vitro protein digestibility,microbiological quality and gelatinization behaviour of macaroni as affected by cowpea flour addition

Cowpeas were germinated, fermented, cooked, ground to flour and added to standard durum wheat semolina at 20% (w/w) level for macaroni production. Macaroni samples were analysed for in vitro protein digestibility, microbial count (total bacteria, mould and yeast) and gelatinization behaviour over a 6-month storage period at room temperature (<25 °C). Starch gelatinization behaviour of the samples was analysed using differential scanning calorimetry. Supplementing semolina with cowpea flour did not have a significant affect on in vitro protein digestibilities or aerobic plate counts of macaroni samples (p < 0.05). There was a small but significant increase in mold and yeast counts after 6 months of storage in cowpea treated samples. Two endothermic peaks were observed with significant differences in ΔH values of control and cowpea treated macaroni samples. The transition peak (T_p) temperatures were in the range of 66.9–67.9 and 86.9–100.4 °C for the first and second peaks, respectively. The transition enthalpies (ΔH) were in the range 2.41–4.21 and 1.71–3.86 J/g for the first and second peaks, respectively.     

Nucleotide degradation and biogenic amine formation of wild white grouper (Epinephelus aeneus) stored in ice and at chill temperature (4 °C)

Sensory (cooked and uncooked), chemical (proximate composition, TVB-N, nucleotide degradation products and biogenic amines) and microbiological quality (TVC and total coliform) changes were investigated during storage of ungutted white grouper kept in ice and at chill temperature (4 °C). According to the sensory assessment, the shelf life of white grouper was 16 days in ice and 4 days for fish stored at chill temperature. TVB-N values increased with storage time. Amines found in white grouper stored in ice were TMA, putrescine, cadaverine, 2-phenylethylamine, dopamine, agmatine, tryptamine and serotonin. Histamine, spermine, spermidine were never detected with either storage condition. The acceptability limit in terms of microbial count was exceeded at 8 days in ice and at 4 days for fish stored at chill temperature. Total coliform count was 2.8 log₁₀ cfu/ml at 1 day and reached 10⁵ cfu/ml for both storage conditions.     

Effect of high-pressure processing on reduction of Listeria monocytogenes in packaged Queso Fresco

The effect of high-hydrostatic-pressure processing (HPP) on the survival of a 5-strain rifampicin-resistant cocktail of Listeria monocytogenes in Queso Fresco (QF) was evaluated as a postpackaging intervention. Queso Fresco was made using pasteurized, homogenized milk, and was starter-free and not pressed. In phase 1, QF slices (12.7 × 7.6 × 1 cm), weighing from 52 to 66 g, were surface inoculated with L. monocytogenes (ca. 5.0 log₁₀ cfu/g) and individually double vacuum packaged. The slices were then warmed to either 20 or 40°C and HPP treated at 200, 400, and 600 MPa for hold times of 5, 10, 15, or 20 min. Treatment at 600 MPa was most effective in reducing L. monocytogenes to below the detection level of 0.91 log₁₀ cfu/g at all hold times and temperatures. High-hydrostatic-pressure processing at 40°C, 400 MPa, and hold time ≥15 min was effective but resulted in wheying-off and textural changes. In phase 2, L. monocytogenes was inoculated either on the slices (ca. 5.0 log₁₀ cfu/g; ON) or in the curds (ca. 7.0 log₁₀ cfu/g; IN) before the cheese block was formed and sliced. The slices were treated at 20°C and 600 MPa at hold times of 3, 10, and 20 min, and then stored at 4 and 10°C for 60 d. For both treatments, L. monocytogenes became less resistant to pressure as hold time increased, with greater percentages of injured cells at 3 and 10 min than at 20 min, at which the lethality of the process increased. For the IN treatment, with hold times of 3 and 10 min, growth of L. monocytogenes increased the first week of storage, but was delayed for 1 wk, with a hold time of 20 min. Longer lag times in growth of L. monocytogenes during storage at 4°C were observed for the ON treatment at hold times of 10 and 20 min, indicating that the IN treatment may have provided a more protective environment with less injury to the cells than the ON treatment. Similarly, HPP treatment for 10 min followed by storage at 4°C was the best method for suppressing the growth of the endogenous microflora with bacterial counts remaining below the level of detection for 2 out of the 3 QF samples for up to 84 d. Lag times in growth were not observed during storage of QF at 10°C. Although HPP reduced L. monocytogenes immediately after processing, a second preservation technique is necessary to control growth of L. monocytogenes during cold storage. However, the results also showed that HPP would be effective for slowing the growth of microorganisms that can shorten the shelf life of QF.     

TBARS predictive models of pork sausages stored at different temperatures

2-Thiobarbituric acid reactive substances (TBARS) is an important quality index for pork sausages. To study this in pork sausages during storage, kinetic models were developed to predict TBARS content changes of pork sausages at different temperatures. The predictive models of TBARS content with respect to storage time and temperature were developed based on primary and Arrhenius equations. The regression coefficients (R² > 0.95) indicated the acceptability of the primary reaction and Arrhenius model for predicting TBARS content changes of pork sausages. The activation energy (E_A) of TBARS is 14.12 kJ mol^− 1, and the corresponding rate constant (k₀) is 9.262 × 10¹⁰. Relative errors between predicted and measured values of TBARS content are all within ± 8%. Thus, the established model could effectively predict the TBARS content of pork sausages between 5 and 35 °C during storage.     

Establishment of kinetic models based on electrical conductivity and freshness indictors for the forecasting of crucian carp (Carassius carassius) freshness

To study quality changes in cold chain circulation, kinetic models were developed to predict the freshness of crucian carp at different temperatures during storage. Electrical conductivity (EC) and freshness indictors (Total volatile basic nitrogen, Total aerobic count and K-value) at 270, 273, 277, 282 and 288 K were accessed to investigate the relation between the crucian carp’s freshness and storage condition (storage temperature and storage time). The kinetic models were developed based on Arrhenius equation. Activation energies (E_A) of EC and Total aerobic count (TAC) are 97.75 and 105.93 kJ mol⁻¹, and corresponding rate constants (k₀) are 5.25 × 10¹⁶ and 5.70 × 10¹⁸, respectively. Relative errors between predicted and values of EC are all within ±5%. The kinetic model established through EC can accurately describe the changes of crucian carp’s quality during the storage within 270-288 K. The kinetic model established based on TAC can accurately forecast crucian carp’s early freshness.