Effects of glycerol,sorbitol, xylitol and fructose plasticisers on mechanical and moisture barrier properties of pullulan–alginate–carboxymethylcellulose blend films

The effects of glycerol, sorbitol, xylitol and fructose plasticisers on water sorption, mechanical properties, water vapour permeability (WVP) and microstructure of pullulan–alginate–carboxymethycellulose (PAC) blend films were investigated. At low plasticiser concentrations (below 7% w/w dry basis), antiplasticisation effect was observed, causing an increase in tensile strength (TS) but a decrease in the equilibrium moisture content. As glycerol concentration increased from 0% to 7%, TS increased from 68.1 to 69.6 MPa, whereas equilibrium moisture contents at 0.84 a_w decreased from 0.37 to 0.3 g H₂O g^?1 dry basis. At higher plasticiser concentrations (14–25% w/w), an opposite trend was observed on the PAC films, resulting in the reduction of TS and elevation of moisture content. Among the four plasticisers tested, the fructose‐plasticised films were the most brittle, showing the highest TS, but had the lowest elongation at break (EAB), WVP and equilibrium moisture content values than films plasticised with other polyols. On the other hand, glycerol resulted in the most flexible film structure, exhibiting opposite materials' properties as compared with the fructose‐plasticised films. For instance, at 25% (w/w) plasticiser concentration, EAB and WVP values of fructose‐plasticised films were 33.5% and 3.48 × 10^?6 g m Pa^?1 h^?1 m^?2, which were significantly lower than that of glycerol‐plasticised films (58.6% and 4.86 × 10^?6 g m Pa^?1 h^?1 m^?2, respectively). Scanning electron microscopy showed that the plasticised PCA films were less homogeneous and more porous than the unplasticised counterparts, indicating that plasticisers had an effect on the microstructural morphology of the film matrix.     

Physico-chemical and film-forming properties of bovine-hide and tuna-skin gelatin: A comparative study

A bovine-hide gelatin and a tuna-skin gelatin, both characterized on the basis of their amino acid composition and molecular weight distribution, were used to prepare edible films by casting with glycerol and sorbitol added as plasticizers. The molecular weight distribution of the tuna-skin gelatin exhibited appreciably higher quantities of β-components (covalently linked α-chain dimers), whereas bovine-hide gelatin showed a certain degradation of α₁-chains being indicative of a greater proteolysis. Intrinsic differences in the gelatin attributes affected in diverse manner some of the physical properties of the films. Thus, water vapour permeability was higher in the bovine-hide gelatin film, whereas deformability was considerably higher (10 times higher) in the tuna-skin gelatin film. In contrast, breaking force and water solubility were basically unaffected by gelatin origin. Analysis of the thermal properties revealed both films to be wholly amorphous with similar glass transition temperature values thanks to the plasticizing effects of the glycerol and sorbitol and the low moisture contents.     

Evaluation of mechanical and water barrier properties of transglutaminase cross‐linked zein films incorporated with oleic acid

In this study, four concentrations of transglutaminase were used in zein films incorporated with four oleic acid concentrations, and subsequently, the mechanical and water barrier properties were evaluated. Enzyme concentration significantly affected mechanical and barrier properties of the films. Transglutaminase concentration at 1% improved tensile strength of control sample from 17.5 to 26.9 MPa while solubility decreased from 6.4% to 4.4%. Incorporation of oleic acid into transglutaminase‐treated zein films irrespective of enzyme concentration decreased water vapour permeability and solubility with the 1% transglutaminase‐treated zein films incorporated with 3% oleic acid registering the lowest permeability (0.37 g mm m^?2 h^?1 kPa^?1) and solubility (2.8%) values while elongation at break was not significantly improved. The use of transglutaminase at 1% concentration in cross‐linking zein films coupled with incorporation of controlled concentrations of oleic acid can be an effective approach in improving mechanical and water barrier properties of zein‐based films.     

Antioxidant activity and physicochemical properties of chitosan films incorporated with Lycium barbarum fruit extract for active food packaging

Active packaging film was developed by incorporating Lycium barbarum fruit extract (LFE) into chitosan. The effects of LFE on physicochemical properties of the chitosan/LFE films were evaluated. When the weight ratio of LFE to chitosan was increased from 0:1 to 1:1, DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) free radical scavenging activity of the chitosan/LFE films increased near ten‐folds and reached up to 35.8%; water vapour permeability of the chitosan/LFE films decreased 43.0% from 5.67 g m mm^?2 day^?1 kPa^?1_, and water solubility decreased from 100% to 24.52% because of interactions between LFE and hydrophilic groups of chitosan confirmed by FTIR. However, the chitosan/LFE films became darker after LFE was incorporated. The pure chitosan film showed better tensile strength (23.19 MPa) and elongation at break (22.29%) than the chitosan/LFE films (15.52 MPa and 9.58% for the one with weight ratio of LFE to chitosan of 0.6:1).     

Effects of plasticizers, pH and heating of film-forming solution on the properties of pea protein isolate films

Effects of glycerol (3-7% w/w) and sorbitol (4-8% w/w) concentration, pH (7.0, 9.0, 11.0) and heating (90 °C, 20 min) of film-forming solution (FFS) on the water vapor permeability (WVP), moisture content (MC), solubility, light transmission and transparency of pea protein isolate (PPI) films were investigated. Films plasticized with sorbitol exhibited significantly lower WVP, lower MC and higher solubility, in comparison with glycerol-plasticized films. Increasing glycerol content of the films led to increases in WVP and MC but did not affect film solubility. In contrast, increase in sorbitol content had no effect on permeability and MC but resulted in increased film solubility. Moisture sorption isotherms of PPI films suggested that the difference in WVP observed among films plasticized with glycerol and sorbitol might be due to the different hygroscopicity of these plasticizers. The pH of FFS did not have a significant effect on WVP and MC. Solubility of PPI films formed from non-heated FFS was not affected by pH, whereas solubility of films formed from heat-treated FFS generally increased when pH was increased from 7.0 to 11.0. Heating of FFS resulted in improved film transparency. All tested films were characterized by excellent ability to absorb UV radiation. Microstructural observation by scanning electron microscopy did not show differences between sorbitol- and glycerol-plasticized films.     

Physical properties of cassava starch–carnauba wax emulsion films as affected by component proportions

Properties of glycerol‐plasticised cassava starch–carnauba wax emulsion films were studied as functions of carnauba wax/starch (CW/S) ratios. Increases in CW concentrations improved elongation, but impaired tensile strength and elastic modulus, suggesting a plasticising effect by CW and/or the emulsifier. CW reduced water solubility of the films and decreased their water vapour permeability (WVP) up to CW/S ratios of 0.15–0.20, probably because of the decreased water solubility. Higher CW concentrations resulted in increased WVP, possibly due to starch matrix loosening. The opacity imparted by high CW concentrations in films could compromise some applications. The T_g of starch and the expected CW effects on it were not evidenced by DSC thermograms, but CW seems to have affected starch crystallisation, maybe by forming complexes with amylose and/or amylopectin.     

Water barrier and physical properties of starch/decolorized hsian-tsao leaf gum films: Impact of surfactant lamination

The moisture barrier and physical properties of bilayer films prepared by lamination of starch/decolorized hsian-tsao leaf gum (dHG) and surfactant layers were investigated. It was found that the water vapor permeability (WVP) of tapioca starch/dHG film (1.31 × 10^?10 g/m s Pa) pronouncedly decreased by the aid of a surfactant layer lamination (1.36–5.25 × 10^?12 g/m s Pa). The WVP of bilayer film increased with increasing the concentration of starch/dHG in the surfactant layer, but was not significantly influenced when it was thickened. The sorption isotherms of both monolayer and bilayer films made from starch/dHG showed typical behavior of water-vapor-sensitive hydrophilic biopolymers. However, the equilibrium moisture content of the monolayer film was significantly higher than that of bilayer films when water activity (a_w) reaches 0.33. Both the tensile and puncture force of starch/dHG films did not vary significantly by laminating a surfactant layer, indicating the mechanical strength of surfactant layer is relatively weak, and this surfactant layer mainly served as a barrier for moisture. When compared to emulsion-based starch/dHG films with surfactant, the surfactant laminated starch/dHG films showed higher water barrier property, mechanical strength, and transparency.     

Physicochemical properties and application of pullulan edible films and coatings in fruit preservation

The effects of water, sorbitol and a sucrose fatty acid ester (SE) on the water sorption behaviour and thermal and mechanical properties of pullulan‐based edible films as well as the physiological responses of fruit coated with pullulan have been studied. Incorporation of sorbitol or SE in pullulan films resulted in lower equilibrium moisture contents at low to intermediate water activities (a_w), but much higher moisture contents at a_w > 0.75; estimates of monolayer values (within 4.1–5.9 gH₂O kg^?1 solids) were given by application of the Brunauer–Emmett–Teller (BET) and Guggenheim–Anderson–DeBoer (GAB) models. A single glass–rubber transition (T_g), attributed to the polysaccharide component, was detected by calorimetry and dynamic mechanical thermal analysis (DMTA) at a sorbitol level of 15–30% DM. With both tests the strong plasticising action of water and polyol was evident in the thermal curves, and the T_g vs moisture content data were successfully fitted to the Gordon–Taylor empirical model. Multifrequency DMTA measurements provided estimates for the apparent activation energy of the glass transition in the range of ? 300–488 kJ mol^?1. With large‐deformation mechanical testing, large decreases in Young's moduli (tensile and three‐point bend tests) were observed as a result of water‐ and/or polyol‐mediated glass‐to‐rubber transition of the polymeric films. In the moisture content range of 2–8%, increases in flexural modulus (E) and maximum stress (σ_max) with small increases in moisture content were found for films made of pullulan or pullulan mixed with 15% DM sorbitol; a strong softening effect was observed when the water content exceeded this range. Addition of sorbitol increased the water vapour transmission rate of the films, whereas addition of SE had the opposite effect. Application of a pullulan/sorbitol/SE coating on strawberries resulted in large changes in internal fruit atmosphere composition which were beneficial for extending the shelf‐life of this fruit; the coated fruit showed much higher levels of CO₂, a large reduction in internal O₂, better firmness and colour retention and a reduced rate of weight loss. In contrast, similar studies on whole kiwifruits showed increased levels of internal ethylene, which caused acceleration of fruit ripening during storage. © 2001 Society of Chemical Industry     

Characterisation of jellyfish protein films with added transglutaminase and wasabi extract

The physical, optical, antimicrobial and antioxidant properties of jellyfish protein (JFP) films with added transglutaminase (TGase) and wasabi extract (WE) were studied. Among the plasticisers, 30% sorbitol was the most desirable. The optimal physical properties of the JFP films were obtained when 15 U transglutaminase g^?1 JFP was added. The incorporation of WE affected the physical properties of the JFP films. The tensile strength (21.68–35.25 MPa), elongation at break (10.85–13.25%) and Young's modulus (920.18–1278.9 MPa) of the films increased as WE concentration increased from 0.5% to 1.5%. The thermal gravimetric analysis results revealed that the thermal stability of the JFP films increased with increasing concentrations of WE. The inhibition zones against Escherichia coli O157:H7 and Listeria monocytogenes and antioxidant activity also increased as the concentration of WE increased. Thus, antimicrobial and antioxidant JFP films could be prepared by the addition of WE.     

Preparation of biopolymer film from chitosan modified with lipid fraction

Films formed from polysaccharides, as chitosan, present a high permeability in water vapour. In order to increase resistance to water vapour for chitosan‐based films, different lipid fractions were incorporated into a filmogenic matrix: fish and vegetable oils, stearic and oleic acids. The chitosan showed a molecular weight of 150 kDa and a deacetylation degree of 86 ± 1%. Results showed that incorporation of different lipid fractions decreased the water vapour permeability (WVP) (1.3–1.8 g mm m^?2 day^?1 kPa^?1) as compared with pure chitosan film (3.8 g mm m^?2 day^?1 kPa^?1). A higher reduction in WVP (65%) was found with the addition of refined fish oil to the continuous matrix of the films than with the addition of refined rice oil, oleic or stearic acid (50–60%). However, pure chitosan films showed better tensile strength (TS = 33 MPa) and elongation percentage (E = 18%) than lipids fraction–chitosan films (7–19 MPa and 7–13%, respectively).     

Nutritional composition and sensory attributes of Alaskan flatfishes compared to plaice (Pleuronectes platessa)

Proximate composition, fatty acids profiles and other nutritional values were evaluated for fillets of Limanda aspera (yellowfin sole), Lepidopsetta bilineata (southern rock sole) and Lepidopsetta polyxystra (northern rock sole) and compared to North Sea plaice (Pleuronectes platessa). Additional information is given on the composition of fillets from arrowtooth flounder (Atheresthes stomias). Plaice (0.8% lipid) and Alaska soles (1.0–1.2% lipid) can be classified as lean species, resulting in low 0.3–0.5 g ∑EPA+DHA/100 g muscle, although the fatty acid profiles of the extracted lipids were characterised by high amount of n‐3 fatty acids (33.2–47.3%). Arrowtooth flounder belong to the medium‐fat species (4.3%). Taurine was the most prevalent free amino acid; mean values ranging between 221 mg100 g^?1 and 247 mg100 g^?1 wet weight. The selenium content varied between 130 and 310 μg kg^?1 ww. Sensory attributes of Southern and Northern rock sole were comparable to plaice.     

Development and characterization of cassava starch and soy protein concentrate based edible films

The sensory attributes, mechanical, water vapour permeability (WVP) and solubility properties of cassava starch and soy protein concentrate (SPC)‐based edible films of varying levels of glycerol were studied. Addition of SPC and glycerol up to 30% and 20%, respectively, reduced stickiness and improved colour and appearance of the films. Tensile strength (TS), elastic modulus (EM) and elongation at break (EAB) of films increased, while film solubility (FS) and WVP decreased with SPC and glycerol up to 50% and 20% level, respectively, ranging from 20.33 to 26.94 MPa (TS), 41.33 to 72.76 MPa (EM), 7.90 to 12.28 MPa (EAB), 15.07 to 31.90% (FS) and 2.62 to 4.13 g H₂O mm m^?2 day kPa (WVP). The TS, EAB and WVP were higher for the biofilms than for low‐density polyethylene and cellophane films.     

Antimicrobial, water vapour permeability, mechanical and thermal properties of casein based Zataraia multiflora Boiss. Extract containing film

Hydrophobic sodium caseinate based edible films were prepared by incorporating stearic and oleic acids. Films were produced with a protein/lipid ratio of 1.05. Antimicrobial films were produced based on the hydrophobic films by adding the essential oil of Zataraia multiflora Boiss. Water vapour permeability, microstructure, antimicrobial, mechanical and thermal properties of these films were studied. Water vapour permeability decreased from 2.18 × 10⁻⁹ to 7.81 × 10⁻¹¹ gPa⁻¹s⁻¹ m⁻¹ on the addition of lipid compounds to film. Scanning electron microscopy showed a partial phase separation of lipid compounds and protein. This fact was confirmed by obtaining two endothermic peaks for lipid containing films during Differential scanning calorimeter. The incorporation of fatty acids into the film structure increased the total specific thermal capacity. The presence of lipids and essential oil decreased tensile strength but increased the elongation at break. Films containing essential oil exhibited a large inhibitory effect on Staphylococcus aureus, as compared to Salmonella typhimurium and Escherichia coli O157:H7.     

Mechanical properties and water vapour permeability of hydrolysed collagen–cocoa butter edible films plasticised with sucrose

The aim of this study was to develop and characterise edible films produced from hydrolysed collagen and cocoa butter and plasticised with sucrose. The mechanical properties, water vapour permeability, opacity and morphology of the films were characterised. The film composition that yielded the best results was used to produce a coating for application in chocolate panned products. A water-based coating with desirable barrier properties that could replace shellac is important for the environment as well as health, and also because chocolate products have great appeal among children. The films obtained were easily manageable and flexible. Sucrose reduced tensile strength (TS), while hydrolysed collagen at concentrations above 15% increased it. Cocoa butter resulted in less-resistant films. The elongation at break values (EAB%) were higher for films containing higher sucrose concentrations. The water vapour permeability (WVP) ranged from 0.32 to 0.63 g mm m⁻² h⁻¹ kPa⁻¹. For the same concentration of cocoa butter, the WVP was directly affected by the thickness of the film, i.e., the greater the thickness, the higher the WVP. Cocoa butter increased film opacity, while sucrose decreased it, particularly at concentrations above 17.5%. High concentrations of hydrolysed collagen produced films with more homogeneous surfaces. The brightness of the product with the coating developed in this study was attractive; however the brightness of the product with shellac was considered more intense. The properties of these films indicate that they are promising systems for coating chocolate panned products.     

Properties and release kinetics of pine bark incorporated agar and carrageenan film

Effects of plasticisers (glycerol, sorbitol and polypropylene glycol) and blend ratios on release behaviour, molecular vibration, mechanical and water barrier properties in agar and carrageenan films incorporating pine bark extract were investigated. Infrared spectra indicated hydrogen bonding of sorbitol and polypropylene glycol with film polymers which improved water diffusion and agar solubility but showed no effect in carrageenan films due to high water affinity. Hydrophilicity of the plasticisers modified dissolution of films and strongly affected the release behaviours of polyphenols and antioxidant capacity (DPPH• and FRAP). Film solubility showed high correlation to release behaviours. Fick’s diffusion kinetics fitted well to release behaviour of pine bark to aqueous media (water, 3% acetic acid and 10% ethanol). Agar gave a higher diffusion coefficient that was improved by the addition of sorbitol and polypropylene glycol. Increased diffusion coefficients enhanced degree of release, with some diversions suggesting that solvent modified matrices and, hence, release properties.     

Role of lignosulphonate in properties of fish gelatin films

A commercial low-gelling fish skin gelatin was used to prepare edible films by casting with glycerol and sorbitol added as plasticizers. In order to improve the extremely low water resistance of gelatin films, composite films were prepared with increasing concentrations (wt/wt) of lignosulphonate (LS) from eucalyptus wood (100:0, 85:15, 80:20, 75:25, 70:30 and 65:35, gelatin:LS). How gelatin film properties were affected by the different types of gelatin and LS was determined by comparing bovine gelatin and three different LS (Ca²⁺, Mg²⁺ and Na⁺) in a mixture ratio of 80:20. Physical properties of films were characterized in terms of tensile strength, elongation at break, water solubility, water vapour permeability and opacity. Dynamic oscillatory tests of film-forming solutions revealed strong LS interference with the cold-renaturation ability of gelatin. LS ratios equal to or higher than the 80:20 blend interfered with intermolecular aggregation of gelatin helices. Supposedly, LS acted as a filler, inducing mostly nonbonding interactions with gelatin, as deduced from Attenuated Total Reflectance Fourier Transform Infrared spectroscopy (ATR-FTIR) and Differential Scanning Calorimetry (DSC) studies. Lignosulphonate significantly reduced the elongation at break of fish gelatin films, water solubility being drastically reduced with a mixture ratio of 80:20 or higher. The water solubility of bovine gelatin-LS composite films was significantly lower than that for fish gelatin, regardless of the type of LS employed. For potential food packaging applications, the three LS were characterized in terms of cytotoxicity, radical scavenging capacity (DPPH assay) and antimicrobial capacity. The effective antioxidant levels (IC₅₀: 83.4-97.5 μg/mL) were noticeably lower than the cytotoxic ones (IC₅₀: 1480-1745 μg/mL), indicating that these compounds could be used as antioxidants at non-cytotoxic concentrations. No relationship between antioxidant and antimicrobial properties could be observed, the only notable antimicrobial finding being some activity against yeasts.     

Effects of nano‐clay type and content on the physical properties of sesame seed meal protein composite films

Sesame seed meal protein (SSMP)/nano‐clay composite films were prepared, and the physical properties of the films were determined. The SSMP film was prepared with 5 g of SSMP and 2 g of glycerol in 100 mL of film‐forming solution, and the tensile strength (TS), elongation (E) and water vapour permeability (WVP) of the SSMP film were 2.51 MP, 21.84% and 3.23 × 10^?9 g m m^?2s^?1 Pa^?1, respectively. Two types of nano‐clays were incorporated to enhance the physical properties of the SSMP film. The TSs of the SSMP film with 5% Cloisite Na⁺ and 7% Cloisite 10A were 6.32 and 5.76 MPa, respectively, and the WVPs of the SSMP nanocomposite films were 2.04 × 10^?9 g m m^?2s^?1 Pa^?1 compared with the SSMP film without nano‐clay, which was 3.23 × 10^?9 g m m^?2s^?1 Pa^?1. Therefore, these results indicate that the SSMP nanocomposite film can be applied in food packaging.     

Optimization of amaranth flour films plasticized with glycerol and sorbitol by multi-response analysis

The optimal formulation for the preparation of amaranth flour films plasticized with glycerol and sorbitol was obtained by a multi-response analysis. The optimization aimed to achieve films with higher resistance to break, moderate elongation and lower solubility in water. The influence of plasticizer concentration (Cg, glycerol or Cs, sorbitol) and process temperature (Tp) on the mechanical properties and solubility of the amaranth flour films was initially studied by response surface methodology (RSM). The optimized conditions obtained were Cg 20.02 g glycerol/100 g flour and Tp 75 °C, and Cs 29.6 g sorbitol/100 g flour and Tp 75 °C. Characterization of the films prepared with these formulations revealed that the optimization methodology employed in this work was satisfactory. Sorbitol was the most suitable plasticizer. It furnished amaranth flour films that were more resistant to break and less permeable to oxygen, due to its greater miscibility with the biopolymers present in the flour and its lower affinity for water.     

Mechanical and water vapor barrier properties of extruded and heat-pressed gelatin films

Gelatin-based edible films were produced by extruding hot melt of gelatin-based resins through a die with slot orifice and followed by heat-pressed method. The resins were plasticized with glycerol, sorbitol and the mixture of glycerol and sorbitol (MGS). The effect of type of plasticizer on extruded and heat-pressed (EHP) film-forming capacity was studied, and the mechanical and water barrier properties of resulting EHP gelatin films were compared with those of gelatin films prepared by solution casting method. Stretchable films were formed when glycerol or MGS were used as plasticizer, whereas resins plasticized with sorbitol were extruded in non-stretchable sheets. Glycerol plasticized gelatin film showed the highest flexibility and transparency among the EHP films tested. Tensile strength (TS), elongation (E) and water vapor permeability (WVP) of glycerol plasticized EHP gelatin films were 17.3 MPa, 215.9% and 2.46 ng m/m² s Pa, respectively, and EHP gelatin films had higher E values, lower TS values and higher WVP values compared to the glycerol plasticized cast gelatin films.     

Optimisation of spray drying process parameters for low‐fat honey‐based milk powder with antioxidant activity

The purpose of this study was to optimise process parameters to prepare spray‐dried honey‐based milk powder containing functional properties of honey. Experimental design with temperature (180 to 200 °C), honey concentration (5–15%) and feed flow rate (8–10 rpm) as independent variables was studied to investigate the effect on product responses. Results showed that increasing the temperature resulted in powder with lower moisture, bulk density, antioxidant activity, total phenolic contents, total flavonoid contents and higher water solubility index. Increasing feed flow rate resulted in higher moisture, bulk density, antioxidant activity, reduced water solubility index, total phenolic content and total flavonoid content, whereas increasing honey concentration resulted in increase in antioxidant activity, total phenolic content and total flavonoid content. The moisture content, bulk density, water solubility index, DPPH scavenging activity, total phenolic content and total flavonoid content were 3.27%, 0.44 g cc^?1, 96.67 g g^?1, 17.45%, 2.54 GAE g^?1 powder and 1.40 RE g^?1 powder, respectively.