Skip to main content

ORIGINAL RESEARCH article

Front. Nutr., 03 September 2020
Sec. Nutrition and Food Science Technology

Development of Electrospun Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) Monolayers Containing Eugenol and Their Application in Multilayer Antimicrobial Food Packaging

  • 1Novel Materials and Nanotechnology Group, Institute of Agrochemistry and Food Technology (IATA), Spanish National Research Council (CSIC), Paterna, Spain
  • 2Polymers and Advanced Materials Group (PIMA), Universitat Jaume I (UJI), Castellón de la Plana, Spain

In this research, different contents of eugenol in the 2.5–25 wt.% range were first incorporated into ultrathin fibers of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) by electrospinning and then subjected to annealing to obtain antimicrobial monolayers. The most optimal concentration of eugenol in the PHBV monolayer was 15 wt.% since it showed high electrospinnability and thermal stability and also yielded the highest bacterial reduction against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). This eugenol-containing monolayer was then selected to be applied as an interlayer between a structural layer made of a cast-extruded poly(3-hydroxybutyrate) (PHB) sheet and a commercial PHBV film as the food contact layer. The whole system was, thereafter, annealed at 160°C for 10 s to develop a novel multilayer active packaging material. The resultant multilayer showed high hydrophobicity, strong adhesion and mechanical resistance, and improved barrier properties against water vapor and limonene vapors. The antimicrobial activity of the multilayer structure was also evaluated in both open and closed systems for up to 15 days, showing significant reductions (R ≥ 1 and < 3) for the two strains of food-borne bacteria. Higher inhibition values were particularly attained against S. aureus due to the higher activity of eugenol against the cell membrane of Gram positive (G+) bacteria. The multilayer also provided the highest antimicrobial activity for the closed system, which better resembles the actual packaging and it was related to the headspace accumulation of the volatile compounds. Hence, the here-developed multilayer fully based on polyhydroxyalkanoates (PHAs) shows a great deal of potential for antimicrobial packaging applications using biodegradable materials to increase both quality and safety of food products.

Introduction

Active antimicrobial packaging is one of the most relevant emerging technologies in the food industry. It aims to control enzymatic, chemical, physical, and microbiological reactions that deteriorate food through the inclusion of active substances and their controlled release to the surface in contact with food (1, 2). Biodegradable polymers have recently emerged as an alternative to gradually replace the use of petrochemical polymers in packaging applications, which are known to generate irreversible environmental damage (3, 4). Furthermore, polymers used in packaging can also be obtained from the valorization of food-processing by-products and agricultural or industrial wastes, being more sustainable and cost-effective (5).

Polyhydroxyalkanoates (PHAs) are among the most commonly used thermoplastic biopolyesters in food packaging applications because they have similar properties to some conventional non-degradable plastics (6, 7). PHAs can be obtained from over 155 monomer subunits through fermentation by some bacteria from different renewable carbon sources that are accumulated as intracellular storage granules (8). For instance, Bhatia et al. (9) obtained high biomass (Yx/s, 0.31 g/g) and PHA (Yp/s, 0.14 g/g) yields using Ralstonia eutropha 5,119 bacteria and Miscanthus biomass hydrolysate (MBH) as carbon source. In another research work, Bhatia et al. (10) obtained a high PHB production (1.24 g/L) with 2% (w/v) starch as carbon source, using a Escherichia coli (E. coli) strain produced using different plasmids containing the amylase gene of Panibacillus sp. and PHB synthesis genes from Ralstonia eutropha. Park et al. (11) studied different PHA-producing strains, concluding that Halomonas sp. YLGW01 produced the highest amount of PHB [94.6 ± 1.8% (w/w)] using fructose as carbon source. Hong et al. (12) determined the optimal growth and production conditions, environments with different salinity, carbon sources, and nitrogen sources of the Vibrio proteolyticus strain in the PHA production. It was concluded that the use of a medium containing 2% (w/v) fructose, 0.3% (w/v) yeast extract, and 5% (w/v) sodium chloride (NaCl) in M9 minimal medium resulted in high PHA (54.7%) and biomass (4.94 g/L) contents. The structure and physical properties of PHAs vary depending on the bacteria specie, substrate (carbon source), and cultivation conditions (13). PHAs are a typically linear aliphatic polyesters consisting of repetitive hydroxy acids (HAs) connected together by an ester bond (14). According to the number of carbon atoms in the monomers, PHAs are classified in groups of short chain length (scl-PHAs), which consists of 3–5 carbon atoms (C3–C5), and medium chain length (mcl-PHAs) with 6–14 carbon atoms (C6–C14) (15, 16). Microbial synthesis of PHAs have the capacity to produce copolymers from mixed substrates by different methods, such as metabolic engineering, co-culture of microbes, and feeding of the various precursors during fermentation (1719). Typical examples of scl-PHAs are poly(3-hydroxybutyrate) (PHB), poly(3-hydroxybutyrate-co-3-hydroxyvalerate (PHBV), and poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3HB-co-4HB)]. The most representative mcl-PHAs are poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) [P(3HB-co-3HHx)] and poly(3-hydroxyhexanoate-co-3-hydroxyoctanoate) [P(3HHx-co-3HO)] (20, 21). PHB is the most abundant type of PHA but it is brittle and shows low thermal stability, which limits their industrial applications. For this reason, PHB is currently being replaced by PHBV due to the better processability and physical properties of the copolyester, such as higher flexibility improved toughness, and lower melting point and level of crystallinity (22, 23). PHAs can be processed by different melt-processing techniques such as injection molding (24), extrusion (25), and compression molding (26). Electrospinning is one of the latest technologies to process PHAs in the form of monolayer and multilayer films by the application of high electric voltages and annealing treatments, having the main advantage to operate at room temperatures (27, 28). The latter process, therefore, opens up the incorporation thermolabile substances into electrospun biopolymer films including natural extracts (29).

Essential oils are natural substances obtained by secondary metabolite of plants such as flowers, stems, leaves, seeds, etc. (30). Different studies have reported multiple active and bioactive properties for essential oils, including antibacterial, antimitotic, antisepticise, and antiviral properties, due to the presence of aldehydes and phenols, for instance carvacrol, eugenol, and thymol (31). Among them, eugenol (C10H12O2) is the main active phenolic compound present in the clove essential oil (32), which shows strong antibacterial activity against a wide range of Gram negative (G-) bacteria, including E. coli, Salmonella typhimurium, Pseudomonas aeruginosa, and also Gram positive (G+) bacteria, including Staphylococcus aureus (S. aureus) and Listeria monocytogenes (L. monocytogenes) (33, 34). The action of essential oils against bacteria is based on interfering chemically with the synthesis or function of principal components of bacteria as well as blocking their antimicrobial resistance mechanisms. In this way, these natural antimicrobial substances are known to affect the bacterial protein biosynthesis, deoxyribonucleic acid (DNA) replication and repair, destroy cell membrane and wall or inhibit metabolism and structural integrity (3538). However, due to its high volatility, water insolubility, poor oxidation, and high thermal sensitivity, essential oils habitually need to be protected to preserve their activity (39). In this way, the electrospinning technology offers multiples advantages for the nanoencapsulation of essential oils such as the use of mild temperatures (40) and materials with high surface-to-volume ratios and controlled porosity (41, 42).

Multilayer films are combinations of different layers typically based on materials with dissimilar properties glued together to fulfill functions that monomaterials do not offer (43, 44). Multilayers are often composed of “structural” and “barrier” layers, usually on the outside and the inside, respectively. An “active” layer can additionally be added either on the outside or inside, depending on the application needs. Layers of adhesive polymers, also named “tie layers”, are used as glue between the different layers where necessary. The purpose of using multilayer systems is to improve the properties of the food packaging due to the majority of polymers, particularly biopolymers, and paper present poor water resistance, low oxygen barrier, and reduced mechanical performance (4547). As a result, the multilayer present higher advantages than monolayer systems in terms of industrial process and applications in food packaging (48, 49). In this context, the electrospinning technology can result very effective to prepare active and bioactive multilayer structures with sustained released capacity by means of coatings or interlayers containing entrapped substances with functionality (50). For instance, electrospun zein fibers in the form of coatings (51) or interlayers (52) have significantly improved the gas barrier properties and provided active performance to polylactide (PLA) films. Similarly, Fabra et al. (53, 54) followed the same strategy to develop multilayer structures based on PHAs biopolyesters and electrospun zein nanofibers. Cherpinski et al. improved the water resistance of paper (55) and nanopaper (56) by coatings of electrospun films of PHB and other biopolymers. Quiles-Carrillo et al. (57) produced bioactive films with sustained antioxidant release capacity by means of multilayer structures of PLA containing electrospun fibers with gallic acid (GA). More recently, Akinalan Balik et al. (58) developed high-barrier multilayer films using an electrospun pectin-based film applied as an interlayer between two external layers of PHBV.

The main objective of this study was to develop a novel multilayer system based on PHBV with antimicrobial properties by electrospinning. To achieve this end, electrospun mats of PHBV fibers containing different amounts of eugenol were characterized and the most efficient was selected to coat PHB sheets. Thereafter, a food contact layer of PHBV was put on the eugenol-containing electrospun layer and the whole structure was subjected to annealing at mild temperature to form a multilayer without the need to use a tie layer. The morphological, thermal, mechanical adhesion, and barrier properties to water and limonene vapors were determined. Finally, the antimicrobial activity of the multilayers against S. aureus and E. coli in both an open and closed system was tested for 15 days in order to ascertain their potential in active food packaging.

Materials and Methods

Materials

Bacterial aliphatic copolyester PHBV was ENMATTM Y1000P, produced by Tianan Biologic Materials (Ningbo, China) and supplied by Ocenic Resins SL (Valencia, Spain). The biopolymer resin was delivered in pellets with a true density of 1.23 g/cm3. The molar fraction of HV in the copolymer is 2–3%, while the molecular weight (MW) is ~2.8 × 105 g/mol. Bacterial aliphatic homopolyester PHB was provided in pellets by Biomer (Krailling, Germany) as P226F. It has a density of 1.25 g/cm3, a melt flow rate (MFR) of 10 g/10 min at 180°C and 5 kg, a MW of 500 kDa, and a polydispersity index (PI) of 2. A 25-μm film of PHBV with a molar fraction of HV of 8 mol.% was purchased at GoodFellow Cambridge Limited (Huntindgon, UK) with the commercial reference BV301025. All the PHA grades are certified by the manufacturers both as compostable and food contact. 2,2,2-trifluorethanol (TFE), with 99% purity, and eugenol, ReagentPlus®, with 99% purity, were both purchased from Sigma-Aldrich S.A. (Madrid, Spain). Glycerol, phosphate buffered saline (PBS), and tryptic soy broth (TSB) were provided by Conda Laboratories (Madrid, Spain).

Preparation of the Structural Layer by Cast Extrusion

The PHB pellets were cast-extruded into sheets using a cast-roll machine MINI CAST 25 from EUR.EX.MA (Venegono, Italy). The extrusion speed was set at 25 rpm and the temperature profile, from the feeding zone to die head, was adjusted to 180–175–170–170–165–165–160°C. PHBV sheets with an average thickness of ~500 μm were obtained by adjusting the speed of the calendar and the drag.

Preparation of the Multilayers by Electrospinning and Annealing

Solutions for Electrospinning

Different solutions for electrospinning were prepared by dissolving 10% in weight (wt.%) of PHBV in TFE at room temperature. Eugenol was incorporated into the solutions at 2.5, 5, 10, 15, 20, and 25 wt.% in relation to the PHBV content.

Electrospinning

The PHBV solutions containing eugenol were processed in a Fluidnatek® LE10 electrospinning benchtop equipment from Bioinicia S.L. (Valencia, Spain) with a variable high-voltage 0–30 kV power supply and a motorized scanning injector. The PHBV solutions were transferred to a 30-mL plastic syringe and coupled by a Teflon tube to a stainless-steel needle (Ø = 0.9 mm) that was connected to the power supply. Thus, each PHBV solution was electrospun at room temperature, that is, 25°C, for 2 h under a steady flow-rate of 6 mL/h, scanning horizontally toward the cast-extruded PHB sheet attached to the metallic collector. The applied voltage was 15 kV while the distance between the injector and collector was optimal at 15 cm. An electrospun mat of PHBV without eugenol was also deposited on the PHB sheets in the same conditions to produce the control multilayer. The same process was also carried out to collect individual interlayers on the collector without using the PHB sheets. In all cases, the resultant electrospun materials were stored in a desiccator at 25°C and 0% relative humidity (RH) for, at least, 48 h.

Annealing

The multilayer systems were produced according to the process schemed in Figure 1. Briefly, once the electrospun PHBV mats containing eugenol were coated on the cast-extruded PHB sheets, the food contact film of PHBV was deposited on the electrospun layer and the whole system was subjected to annealing. This thermal post-treatment was performed at 160°C, below the biopolymer's melting point, for 10 ± 1 s, without pressure, using a hydraulic press 4122-model from Carver, Inc. (Wabash, IN, USA). The resultant multilayers were finally air cooled at room temperature. These conditions were selected based on our previous studies for thermally post-processing PHAs (59). The same process was applied to single electrospun monolayers of PHBV for comparison purposes.

FIGURE 1
www.frontiersin.org

Figure 1. Process to obtain the multilayer system of poly(3-hydroxybutyrate) (PHB) sheet/electrospun poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) interlayer containing eugenol/PHBV film.

Characterization of the Electrospun Monolayers and Multilayer

Thickness

Before testing, the thicknesses of all the monolayer and multilayer structures were measured using a digital micrometer (S00014, Mitutoyo, Corp., Kawasaki, Japan) with ±0.001 mm accuracy. Measurements were performed and averaged in five different points with two in each end and one in the middle.

Morphology

The morphology of the electrospun fibers and the cross-sections of the films were examined by scanning electron microscopy (SEM). Cryofracture of the films was previously carried out by immersing the samples in liquid nitrogen. The SEM micrographs were obtained using a Hitachi S-4800 electron microscope (Tokyo, Japan) at an accelerating voltage of 10 kV and a working distance of 8–10 mm. Prior to examination, all the samples were fixed to beveled holders using a conductive double-sided adhesive tape and sputtered for 3 min with a mixture of gold–palladium mixture under vacuum. Fiber sizes and film thickness were determined by means of the ImageJ 1.50i software using the SEM micrographs in their original magnification. At least 25 micrographs of each sample were used for the measurements.

Thermal Analysis

Thermogravimetric analysis (TGA) of the neat eugenol oil and PHBV films was performed under nitrogen atmosphere in a Thermobalance TG-STDA Mettler Toledo model TGA/STDA851e/LF/1600 analyzer (Greifensee, Switzerland). TGA curves were obtained after conditioning the samples in the sensor for 5 min at 30°C. The samples were then heated from 25 to 700°C at a heating rate of 10°C/min. All the thermal tests were carried out in triplicate.

Water Contact Angle

The wettability of the interlayers and multilayers surface was evaluated by the measurement of the dynamic water contact angle (WCA) in an Optical Tensiometer (Theta Lite, Staffordshire, UK). Five droplets were seeded at 5 μL/s on the surfaces of each studied sample sizing 2 × 5 cm2 and the WCA values were averaged. Measurements were performed at 25°C.

Mechanical Adhesion

The adhesion capacity of the electrospun PHBV layer was assessed by a T-peel test according to ISO 11339:2010. To this end, the multilayer structure was assembled by sandwiching an electrospun PHBV interlayer in between two cast-extruded PHB films (200 mm × 150 mm) according to the sample geometry shown in Figure 2. Prior to the annealing step, a 150 mm × 50 mm Teflon film was inserted along the edge of the PHB sheets in order to prevent adhesion in the grip zone of the specimens (see zone 1 in Figure 2). Adhesion tests consisted on measuring the force required to peel the two PHB sheets adhered by the electrospun PHBV interlayer by means of a uniaxial tensile test in a universal testing machine (Shimadzu AGS-X 500 N, Shimadzu Corporation, Kyoto, Japan) at room temperature with a cross-head speed of 10 mm/min.

FIGURE 2
www.frontiersin.org

Figure 2. Sample geometry for the T-peel adhesion test.

Water Vapor Permeance

The water vapor permeability (WVP) of the different multilayers was determined according to the ASTM 2011 gravimetric method using Payne permeability cups (Elcometer SPRL, Hermelle/s, Liege, Belgium) of 3.5 cm diameter. One side of the films was exposed to 100% RH by avoiding direct contact with liquid water. Then, the cups containing the films were secured with silicon rings and stored in a desiccator at 25°C and 0% RH. The cups were weighed periodically after the steady state was reached. Water vapor permeation rate corresponded to the slope value of the steady state line of time vs. weight loss per unit area and the weight loss was calculated as the total loss minus the loss through the sealing. Water vapor permeance was obtained by correcting the water vapor permeation rate for the permeant partial pressure. Measurements were done in triplicate for each type of samples.

Limonene Vapor Permeance

Limonene permeability (LP) was measured as described above for WVP. For this, 5 mL of D-limonene was placed inside the Payne permeability cups and the cups containing the films were placed at controlled room conditions of 25°C and 40% RH. The limonene vapor permeation rates were estimated from the steady-state permeation slopes and the weight loss was calculated as the total cell loss minus the loss through the sealing. Limonene permeance was obtained by correcting the limonene vapor permeation rate for the permeant partial pressure. Tests were conducted in triplicate.

Antimicrobial Tests

The antimicrobial performance of the monolayers and multilayer was evaluated according to the Japanese Industrial Standard (JIS) Z 2801:2010. S. aureus CECT240 (ATCC 6538P) and E. coli CECT434 (ATCC 25922) strains were obtained from the Spanish Type Culture Collection (CECT) (Valencia, Spain) and stored in phosphate buffered saline (PBS) with 10 wt.% tryptic soy broth (TSB) and 10 wt.% glycerol at −80°C. Previous to each study, a loopful of bacteria was transferred to 10 ml of TSB and incubated at 37°C for 24 h. A 100-μL aliquot from the culture was again transferred to TSB and grown at 37°C to the mid-exponential phase of growth. An approximate count of 5 × 105 colony forming units (CFU)/mL of a culture having an absorbance value of 0.20 as determined by optical density at 600 nm using an UV–Vis spectrophotometer VIS3000 (Dinko, Instruments, Barcelona, Spain) was used. A microorganism suspension of S. aureus and E. coli was applied onto the test monolayer and multilayer films sizing 1.5 cm × 1.5 cm containing eugenol that were placed in hermetically closed and open bottles, the here so-called closed and open systems, respectively. The electrospun PHBV monolayer without eugenol was used as the control film since it shows no antimicrobial activity (60, 61). After incubation at 24°C and, at least, 95% RH, for 24 h, bacteria were recovered with PBS, 10-fold serially diluted, and incubated at 37°C for 24 h in order to quantify the number of viable bacteria by conventional plate count. The antimicrobial activity was evaluated at 1 (right after the film production), 8, and 15 days in both the closed and open systems. The value of the antimicrobial reduction (R) was calculated using the expression:

R=[log(BA)-log(CA)]=log(BC)    (1)

Where A is the mean of bacterial counts of the control sample immediately after inoculation, B is the mean of bacterial counts of the control sample after 24 h, and C is the mean of bacterial counts of the test sample after 24 h. Antimicrobial activity was evaluated with the following assessment: Non-significant (R < 0.5), slight (R ≥ 0.5 and < 1), significant (R ≥ 1 and < 3), and strong (R ≥ 3) (62).

Statistical Analysis

The thermal and mechanical properties, contact angle measurements, and water and limonene vapor permeance were evaluated by analysis of variance (ANOVA) and a multiple comparison test (Tukey) with 95% significance level (p ≤ 0.05). For this purpose, the software OriginPro8 (OriginLab Corporation, Northampton, MA, USA) was used.

Results and Discussion

Characterization and Selection of the Electrospun Active PHBV Monolayer

Morphology

Figure 3 shows the morphology and the fiber diameters histogram of the electrospun PHBV fiber mats containing eugenol prior to annealing. In Figure 3A one can observe that the neat PHBV fibers presented a mean diameter of ~0.95 μm. Figure 3B corresponds to electrospun PHBV fibers with 2.5 wt.% of eugenol, which had a mean diameter of ~0.90 μm. In Figure 3C it can be seen that the fibers containing 5 wt.% of eugenol showed a mean diameter of ~0.7 μm, whereas the diameters in the fibers containing 10 wt.% of eugenol was ~0.6 μm (Figure 3D) and in the fibers with 15 wt.% eugenol was ~0.5 μm (Figure 3E). As it can be seen in the histograms, the fiber size decreased as the eugenol concentration increased. This effect can be ascribed to the plasticizing effect and reduction in the solution viscosity due to the presence of the oily substance (63, 64). Indeed, solution viscosity plays a major role in the fiber diameter during electrospinning and solutions with lower viscosities tend to result in fibers with lower diameters (65, 66). One can also observe in the SEM micrographs that higher concentrations of eugenol impaired the formation of PHBV fibers during electrospinning due to the potential agglomeration of the essential oil. In particular, Figure 3F shows that 20 wt.% of eugenol resulted in a partial breakage of the PHBV fibers, while 25 wt% yielded fibers with beaded regions (see Figure 3G). Similar results were obtained during the electrospinning of PHBV with various essential oils, in which high contents of oil molecules prevented the formation of homogeneous fibers since the surface tension in the charged jet changed into droplets (59, 67). Therefore, eugenol contents of up to 15 wt.% led to electrospun PHBV fibers with smooth surfaces and free of defects or beaded regions so that higher contents of the essential oil were ruled out of the study.

FIGURE 3
www.frontiersin.org

Figure 3. Scanning electron microscopy (SEM) micrographs of electrospun fiber mats of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing eugenol and their histograms: (A) Neat PHBV; (B) 2.5 wt.%; (C) 5 wt.%; (D) 10 wt.%; (E) 15 wt.%; (F) 20 wt.%; (G) 25 wt.%.

The electrospun fibers mats were turned into actual films by the application of annealing at 160°C for 10 s. The morphologies of the top views and cross-sections of the PHBV films containing eugenol were analyzed by SEM and they are gathered in Figure 4. It can be observed that the films of neat PHBV (Figures 4A,B) and PHBV containing 2.5 wt.% (Figures 4C,D), 5 wt.% (Figures 4E,F), 10 wt.% (Figures 4G,H), and 15 wt.% (Figures 4I,J) of eugenol were very similar. In all cases, the individual electrospun PHBV fibers successfully coalesced and merged without melting. All the films presented uniform and homogeneous surfaces, which is an indication of the good cohesion of the materials. The cross-sections of the films presented nearly the same thicknesses (~70 μm), demonstrating that the addition of eugenol did not affect the morphology of the films. Similar observations were reported by Shen and Kamdem (68) who developed active biodegradable films of chitosan containing 10–30% wt/wt of citronella essential oil and cedarwood oil by casting and solvent-evaporation methods, showing a uniform film thicknesses. On the other hand, however, Haghighi et al. (69) observed a changed in the microstructure of films based on chitosan and gelatin after the incorporation of the essential oils eugenol and ginger. The authors observed the presence of pores in the films that indicated the occurrence of collapsed oil droplets due to the separation of aqueous phase during the drying step as result of their hydrophobic nature. In this way, the annealed electrospun mats present the advantage to develop more homogenous and continuous films containing essential oils over the casting method due to the drying steps are not necessary.

FIGURE 4
www.frontiersin.org

Figure 4. Scanning electron microscopy (SEM) micrographs of the electrospun monolayers of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing eugenol: (A,B) neat PHBV; (C,D) 2.5 wt.%, eugenol; (E,F) 5 wt.%; (G,H) 10 wt.%; (I,J) 15 wt.% eugenol. Scale markers of 30 μm for top views and of 50 μm for cross-sections.

Thermal Stability

Figure 5 shows the TGA curves obtained for the neat eugenol and the electrospun PHBV films containing eugenol. Table 1 gathers the most relevant thermal stability parameters obtained from the TGA curves, that is, the onset degradation temperature (Tonset), measured at 5% of weight loss (T5%), the degradation temperature (Tdeg), and the mass loss at Tdeg. One can observe that neat eugenol initiated thermal decomposition at ~110°C, showing a T5% of 121.3°C and presenting a maximum degradation peak, that is, Tdeg, at 203.5°C with a mass loss at Tdeg of 86.68%. This result confirms that this essential oil is thermally unstable and it cannot be processed at high temperatures. In this regard, Shao et al. (70) reported a thermal value for the maximum degradation of eugenol at 195°C, which is characteristic of its low-MW substances. It has been reported that eugenol decomposition is based on a first low-intense mass loss around 44°C associated to the release of volatiles molecules and the second mass loss occurs at 200°C where it takes places the complete degradation of the organic compounds (71). As opposite, one can observe that the electrospun PHBV films were relatively stable, showing values of T5% of 276.6°C and Tdeg of 304.7°C with a mass loss at Tdeg of 61.01%. The films containing 2.5 wt.% and 5 wt.% of eugenol showed very similar thermal decomposition profiles, presenting their onset of degradation at 264.2 and 265°C, respectively, and exhibiting Tdeg values of 291.4 and 293.3°C with respective mass losses of 71.18 and 72.14%. The electrospun PHBV film containing 10 wt.% of eugenol started thermal decomposition from 245.8°C, presenting a Tdeg value of 293.1°C with a mass loss of 74.60%. Finally, in the case of the electrospun PHBV film containing 15 wt.% of eugenol, it showed a significantly lower value of T5%, that is, 160.8°C, while Tdeg was similar to the other films, that is, 293.3°C (76.36%). The reduction observed in the onset of thermal degradation can be attributed to the low thermal stability of eugenol.

FIGURE 5
www.frontiersin.org

Figure 5. Thermogravimetric analysis (TGA) curves of eugenol and electrospun monolayers of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing eugenol.

TABLE 1
www.frontiersin.org

Table 1. Thermal properties of eugenol and electrospun monolayers of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing eugenol in terms of: temperature at 5% weight loss (T5%), degradation temperature (Tdeg), mass loss at Tdeg, and mass loss at 230°C.

In order to better ascertain the thermal protection offered by the electrospun PHBV fibers, the mass loss of the samples was determined at 230°C since, at this temperature, eugenol was completely degraded (mass loss > 98%). This is in agreement with the findings reported by Cao et al. (32), who indicated that neat eugenol completely degrades at 225°C with a weight loss of 96%. Alternatively, it can be observed that PHBV remained highly stable at 230°C (mass loss < 5%) since this temperature is below its Tonset. One can observe that the mass loss at 230°C increased from 2.15%, for the electrospun PHBV film containing 2.5 wt% of eugenol, up to 7.02%, for the film with 15 wt% of eugenol. However, one can also notice that the thermal stability of eugenol was relatively similar in all the PHBV films since the mass loss at 230°C decreased proportionally to the eugenol content. Therefore, the eugenol encapsulated in the PHBV films showed a significantly higher thermal stability than the free essential oil, though certain amount of eugenol was thermally degraded at temperatures above 200°C. Similar results were obtained by da Silva et al. (72), who observed that eugenol entrapped in cellulose nanostructures and then incorporated in the poly(butylene adipate-co-terephthalate) (PBAT) prepared by solvent casting improved the thermal stability of pure eugenol. Likewise, the previous reports of our research group agreed with the thermal properties attain in the present study, showing that the thermal stability of essential oils incorporated into PHAs by electrospinning was improved (59, 67, 73). Therefore, the development of thermally stable systems expands the potential use of electrospinning for the design of active food packaging as an alternative to melt processing technologies such as extrusion or compression molding.

Antimicrobial Activity

Table 2 shows the antimicrobial results of the electrospun PHBV monolayers containing different concentrations of eugenol evaluated after 24 h in the open system. This assessment was performed to determine the optimal concentration of eugenol in the PHBV monolayers to, thereafter, develop the multilayer active system. The antimicrobial results of the electrospun PHBV monolayers containing 2.5 and 5 wt.% eugenol showed both significant reduction values (R ≥ 1 and < 3), whereas eugenol concentrations of 10 and 15 wt.% showed both a strong reduction (R ≥ 3) against S. aureus. Similar results were obtained for E. coli, in which the reduction was slight (R ≥ 0.5 and < 1) for 2.5 wt.% eugenol and significant (R ≥ 1 and < 3) for 5, 10, and 15 wt.% eugenol. A high inhibition was obtained for contents of 15 wt.% of eugenol, reaching a reduction of 3.35 and 2.90 against S. aureus and E. coli, respectively. Differences observed for both bacteria in the antimicrobial performance of eugenol have been ascribed to variances in the action mechanism of essential oils in the bacterial cell membrane and cytoplasm (38, 74). In particular, G- bacteria have higher resistance than G+ ones due to the cell membrane structure is based on complex lipopolysaccharides that restrict the diffusion rate of hydrophobic compounds of essential oils across the cell membranes. Besides, the solubility rate and the concentration of antimicrobial agents in the lipid moiety of the cell membranes, along with the hydrophobicity of the membrane surfaces, can all influence in the resistance of G- bacteria against these active compounds (7577).

TABLE 2
www.frontiersin.org

Table 2. Antibacterial reduction (R) for Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) of the electrospun monolayers of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing different amounts of eugenol in the open system for 24 h.

Based on the antimicrobial reduction attained for both strains and also taken into account the morphological and thermal stability results described above, one can consider that the best concentration of eugenol in the electrospun monolayer of PHBV is 15 wt.%. Hence, the PHBV monolayer films containing 15 wt.% were evaluated against S. aureus and E. coli strains in an open a closed system for a longer period, that is, up to 15 days. These conditions resemble better those found in actual packaging systems in terms of design and time so that the antimicrobial performance of the active materials can be more accurately determined. As one can observe in Table 3, the electrospun PHBV monolayers presented a strong inhibition (R ≥ 3) against S. aureus and a significant inhibition (R ≥ 1 and < 3) against E. coli during the 15 days of evaluation, showing lower antibacterial performance in the open system. The different results obtained for the two tested systems, that is, the open system and the close one (actual packaging) are related with the expected accumulation of the volatile compounds in the headspace of the closed chamber, which can contribute to inhibiting the bacteria growth on the film surfaces. In this regard, Navikaite-Snipaitienea et al. (78) demonstrated that the release of eugenol to the headspace of sealed containers was very rapidly within 1 day and saturation in the packaging headspace was reached after 3 days. The coatings containing the highest amount of eugenol also showed the highest saturation concentration of active substance in the headspace. Similar results were reported in our previous study using oregano essential oil (OEO) and rosemary and green tea natural extracts, in which a slightly higher inhibition was achieved in the closed system in comparison with the open one after 15 days of storage against S. aureus and E. coli (59). Therefore, the here-attained release and accumulation of volatiles compounds from the developed packaging system can be regarded as an advantage to better preserve food products during their shelf life period.

TABLE 3
www.frontiersin.org

Table 3. Antibacterial reduction (R) for Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) of the electrospun monolayers of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing 15 wt.% of eugenol in the open and closed systems for 1, 8, and 15 days.

Characterization of the Active Multilayer

Morphology

Figure 6 shows the SEM micrographs in the top view and cross-section of the multilayer structures prepared with the electrospun interlayer of PHBV containing 15 wt.% of eugenol. The selected electrospun monolayer was incorporated in a sandwich-type structure between the cast-extruded PHB sheet (structural layer) and the 25-μm PHBV film (food contact layer). One can observe that both the PHB sheet (Figure 6A) and PHBV film (Figure 6B), which constitute the external layers of the multilayer structure, exhibited a smooth and homogenous surface. Figure 6C shows the cross-section of the multilayer system, where the electrospun PHBV monolayer can be seen as an interlayer effectively adhered to both external layers. The high adhesion achieved can be ascribed to the high surface-to-volume ratio of the electrospun fibers, in the submicron range, which efficiently adhered to the contact layer during the thermal post-treatment (annealing). Other recent studies have reported the potential of the electrospinning technology to develop multilayer structures based on the particular morphology of the fibers, even though different materials were employed to produce the layers. For instance, Cherpinski et al. (55) developed multilayer packaging structures based on paper/poly(vinyl alcohol) (PVOH)/PHB. It was observed that the multilayer structures self-adhered to the paper substrate during annealing and the applied electrospun biopolymer coatings yielded a significant improvement of the paper barrier properties to water and limonene vapors. In another study, Fabra et al. (79) studied the effect of different electrospun biopolyester coatings of poly(ε-caprolactone) (PCL), PLA, and PHB on the properties of thermoplastic corn starch (TPCS) films. The multilayers developed showed that the addition of electrospun biopolyester coatings led to an exponential oxygen gas and water vapor permeability reduction as the thickness of the electrospun coating increased. Fabra et al. (53) also obtained multilayer structures based on PHBV prepared by compression-molding and casting, which contained a high barrier interlayer made of electrospun zein nanofibers, concluding that the addition of a zein interlayer significantly improved oxygen barrier properties of the multilayer films prepared by both processing technologies. Similar results were formerly obtained by the use of multilayers of PLA film/electrospun zein fibers/PLA film, in which the introduction of the electrospun zein mat enhanced the barrier properties due to the large aspect ratio of the electrospun fibers by establishing a tortuous pathway for the diffusion of the oxygen gas molecules (51, 52). In another study, Wan et al. (80) developed bacterial cellulose multilayer films by incorporating interlayers of electrospun zein fibers, which enhanced water resistance properties of the multilayer films.

FIGURE 6
www.frontiersin.org

Figure 6. Scanning electron microscopy (SEM) micrographs of the multilayer structure of poly(3-hydroxybutyrate) (PHB) sheet/electrospun poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) interlayer containing eugenol/PHBV film: (A) bottom view of the structural layer of PHB: (B) top view of the food contact layer of PHBV; (C) multilayer cross-section.

Water Contact Angle

The WCA values of the electrospun PHBV monolayers with different eugenol contents and the multilayer containing 15 wt.% of eugenol are presented in Figure 7. Figure 7A shows the contact angle for the electrospun PHBV monolayer without eugenol, showing a value of 86.77°. A similar WCA value, that is, 86°, was reported by Yoon et al. (81) for PHBV surfaces prepared by the electrospinning technique. As one can observe in Figures 7B–E, the values of WCA of the monolayers containing 2.5 wt.% (85.39°), 5 wt.% (85.21°), 10 wt.% (85.12°), and 15 wt.% of eugenol (85.08°) were very similar and slightly lower than that of PHBV without eugenol. The lower values can be ascribed to the reduction of the surface tension of the water drops on the film surface by the oily molecules of eugenol. It can also be observed that the food contact layer showed an WCA value of 70.91° (Figure 7F), whereas the structural layer of PHB presented a value of 72.68° (Figure 7G). The difference observed in hydrophobicity between the homopolyester and copolyester films are slight, being both hydrophobic polyesters, since the molar content of 3HV in the commercial copolyester is relatively low (8284). In an application context, Chang et al. (85) studied the WCA of plasma-treated and untreated PHB and PHBV films fabricated by solvent casting. It was observed that the untreated PHB and PHBV films led to WCA values of 76.0 and 72.5°, respectively, and the value decreased in the CH4/O2 plasma-treated PHB (23.0°) and PHBV (18.5°) films. Finally, the active multilayer containing 15 wt.% eugenol in the electrospun interlayer of PHBV presented a WCA value of 75.53° (Figure 7H). This intermediate value between the external layers of the commercial PHAs and the other electrospun monolayers can be explained in terms of the high eugenol content present in the interlayer, in which some essential oil could diffuse to the external food contact layer of PHBV and decreased its surface tension. In any case, all the samples yielded angles characteristic of hydrophobic materials according to the classification reported by Medina-Jaramillo et al. (86), where ‘hydrophobic’ and ‘hydrophilic’ are defined for angles >65 and < 65°, respectively.

FIGURE 7
www.frontiersin.org

Figure 7. Water contact angle (WCA) of electrospun monolayer films of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing eugenol: (A) Neat PHBV; (B) 2.5 wt.%; (C) 5 wt.%; (D) 10 wt.%; (E) 15 wt.%; (F) Food contact layer of PHBV, (G) Structural layer of poly(3-hydroxybutyrate) (PHB); (H) Multilayer containing 15 wt.% eugenol measured on the food contact layer side. (ae) Different superscripts indicate significant differences among samples (p < 0.05).

Mechanical Adhesion

Table 4 shows the mechanical parameters in terms of tensile modulus (E), tensile strength at yield (σy), and elongation at break (εb) of the electrospun PHBV monolayer films containing eugenol. The table also includes the tensile properties of the cast-extruded sheet of PHBV, which constitutes the structural layer and, at the end, determines the whole mechanical properties of the multilayer. The tensile parameters of the structural layer were similar to those reported earlier for PHB films prepared by extrusion and thermo-compression, that is, ~2,900 MPa, 37 MPa, and 4% (25). Alternatively, the neat PHBV monolayer obtained by electrospinning and subsequent annealing presented E, σy, and εb values of 1,252 MPa, 18.1 MPa, and 2%, respectively, which are in the range of the values reported by Corre et al. (87) for melt-extruded films. The incorporation of low contents of eugenol into the electrospun monolayers slightly improved all the mechanical properties, more notably the film elasticity. In particular, the electrospun PHBV monolayer film containing 2.5 wt.% of eugenol presented the highest E value, that is, 2,884 MPa. Lower values were attained, however, at the highest content of eugenol, that is, 15 wt.%, which correlates well with the thermal properties reported above and suggests that the oil particles agglomerated in the biopolymer matrix and induced a plasticizing effect. Furthermore, the differences attained among the electrospun monolayers can also be ascribed to interactions between the coalesced fibers in the electrospun film sample such as slip of fibers over one another, point bonding, alignment, etc. (88). In comparison to PHA films containing essential oils prepared by solvent casting and melting routes, the here-attained electrospun PHBV films were more ductile but less mechanical resistant. For instance, melt-mixed PHB films prepared by Arrieta et al. (89) showed an E value of 1,390 MPa, also showing a significant reduction after the incorporation of 15 wt.% of limonene since it is a strong plasticizer that contributes to reducing the intramolecular bonds of the biopolymer. In the work performed by Narayanan et al. (90), solvent-casted PHB films with different amounts of eugenol showed a σy reduction from 40 MPa, for neat PHB, to 23.5 MPa after the incorporation of the essential oil. In another study, compression-molded bilayer structures based on PHBV containing different essential oils at 15 wt% were produced by Requena et al. (91), showing that the E and σy values ranged between 1,141–773 MPa and 27.6–17 MPa, respectively. These results confirm that the electrospun film show lower mechanical strength due to they consist of coalesced fibers and also show higher porosity (92). In any case, all the developed monolayers showed sufficient strength to be successfully applied as interlayers in packaging applications.

TABLE 4
www.frontiersin.org

Table 4. Mechanical properties of the cast-extruded poly(3-hydroxybutyrate) (PHB) sheet and electrospun monolayer films of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing eugenol in terms of tensile modulus (E), tensile strength at yield (σy), and elongation at break (εb).

Furthermore, the adhesion capacity of the electrospun PHBV layer to the structural and food contact layers was assessed by T-peel adhesion tests. For all the samples studied, the PHB film broke before the detachment of the adhesive union, thus revealing an excellent performance of the electrospun PHBV interlayers as tie-layers. A maximum stress of ~10 N/cm was reached at break of the PHB film, thus proving an adhesion force above that value.

Barrier Performance

The WVP and LP values of the electrospun PHBV monolayers containing eugenol, food contact PHBV film, and structural PHB sheet are shown in Table 5. In the case of the food contact film, the permeability values were 6.27 × 10−14 and 5.17 × 10−14 Kg· m·m−2·s−1·Pa−1 for water and limonene vapors, respectively. These values were higher than those observed for both the electrospun PHBV monolayer without eugenol, that is, 4.05 × 10−14 and 3.75 × 10−14 Kg·m·m−2·s−1·Pa−1, respectively, and also for the structural layer of PHB, that is, 1.75 × 10−15 and 1.95 × 10−15 Kg·m·m−2·s−1·Pa−1. This observation is related to the higher 3HV molar content of the biopolyester in the food contact layer, that is, 8 mol.%. In a context of packaging applications for food preservation, the present PHAs showed values of permeability relatively close to petroleum derived thermoplastics such as polyethylene terephthalate (PET), with WVP value around 5.2 × 10−15 Kg·m·m−2·s−1·Pa−1 (54, 87). As described during the mechanical analysis, the differences attained can be ascribed to the remaining porosity and, thus, lower continuity of the annealed fiber-based material (92). One can also observe that the incorporation of eugenol into the PHBV monolayers decreased the permeability of both vapors whereas there were also significant differences for the electrospun monolayers containing eugenol. The monolayer PHBV films containing 2.5 and 5 wt.% of eugenol presented WPV values of 3.59 × 10−14 and 2.79 × 10−14 Kg·m·m−2·s−1·Pa−1 and LP values of 2.86 × 10−14 and 2.13 × 10−14 Kg·m·m−2·s−1·Pa−1. For the monolayer PHBV films containing 10 wt.% and 15 wt.% of eugenol, the WVP values decreased to 1.98 × 10−14 and 0.95 × 10−14 Kg·m·m−2·s−1·Pa−1, respectively. In the case of LP, values were respectively 1.83 × 10−14 and 0.81 × 10−14 Kg·m·m−2·s−1·Pa−1. Since water vapor is mainly a diffusivity-driven property in PHAs due to their low water sorption nature (93), the decrease in permeability to water vapor can be ascribed to the hydrophobic character of eugenol, where the presence of the oily molecules dispersed in PHA matrix impaired the mobility of water molecules (61, 67, 94). For limonene, as opposed to moisture, the aroma molecules are known to plasticize PHAs and, then, solubility plays a more important role in permeability than diffusion. Therefore, the lower permeability values attained indicate that eugenol also reduced the sorption of limonene in the PHBV matrix. Similar barrier improvements were reported by Melendez-Rodriguez et al. (67) when incorporated eugenol encapsulated in mesoporous silica nanoparticles in PHBV monolayers, though the barrier effect was mainly ascribed to the mineral nanofillers. Likewise, Hasheminya et al. (95) showed that Kefiran/carboxymethyl cellulose composite films incorporating Satureja Khuzestanica essential oil by solvent casting decreased significantly the WVP values due to interactions between the hydrophobic compounds and the biopolymer. This phenomenon was explained by a reduction of the number of hydrophilic groups available that could diffuse into the continuous biopolymer phase.

TABLE 5
www.frontiersin.org

Table 5. Permeance of water and limonene vapors and limonene of the structural poly(3-hydroxybutyrate) (PHB) layer, food-contact poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) layer, electrospun PHBV interlayers with different contents of eugenol, and multilayer with 15 wt.% eugenol.

The permeance of all the monolayers and multilayer was also determined by dividing the permeability values by each sample thickness. Permeance is the time it takes the vapor to transmit through a unit area of film that has a vapor pressure difference between the two exposed surfaces of the film, therefore, the lower the permeance the higher the barrier of the film or sheet. One can observe that the water vapor and limonene permeances of the active multilayer were 0.03 × 10−10 and 0.02 × 10−10 Kg·m−2·s−1·Pa−1, respectively. These values were slightly lower than those attained for the structural PHB sheet due to the presence of electrospun interlayers of PHBV containing eugenol and the higher thickness of the sample. The present multilayers can be compared with the multilayers prepared by Akinalan Balik et al. (58), who evaluated the water permeance of multilayer films that consisted of an electrospun pectin-based interlayer sandwiched between two electrospun PHBV films. The previous study reported higher permeance values for the neat PHBV/PHBV film (5 × 10−10 Kg·m−2·s−1·Pa−1) mainly due to the lower total thickness of the multilayer (72 μm). In the case of PHBV/electrospun pectin/PHBV multilayer, the permeance value was also lower (1.75 × 10−10 kg·m−2·Pa−1·s−1) even though the electrospun pectin highly improved the barrier performance of PHBV. Therefore, the here-prepared multilayers can be applied to medium barrier applications or even medium-to-high barrier applications at the current thickness.

Antimicrobial Activity

Table 6 shows the antimicrobial properties of the multilayer system against S. aureus and E. coli strains in an open a closed system for up to 15 days. It can be observed that the multilayer presented a significant inhibition reduction (R ≥ 1 and < 3) against both bacterial strains in the all days of evaluation, reaching at day 15 R values of 1.84 for S. aureus and 1.47 for E. coli. Compared with the monolayer materials, lower values were obtained since the release rate was slower due to the presence of the food contact layer, which potentially hindered the diffusion of eugenol (96). In any case, the R values obtained for these multilayers systems, ranging between 1.24 and 2.19, were still significant (R ≥ 1 and < 3) against both bacteria and in both tested systems. Similarly, Cerqueira et al. (61) developed active multilayers based on bilayers of PHBV/zein and PHBV containing cinnamaldehyde by electrospinning, achieving a good antimicrobial activity against L. monocytogenes with a logarithmic reduction around of 2.18 Log10 CFU/mL after 30 days of storage. Figueroa-Lopez et al. (42) also achieved a high reduction of S. aureus [3.9 Log10 (CFU/mL)] using active multilayer films based on gelatin, PCL, and black pepper oleoresin prepared by electrospinning. It is also worthy to note that the inhibition had a slight increase in the closed system at days 8 and 15 of evaluation, which is related to the accumulation of eugenol released from the multilayer in the headspace. Therefore, development of active packaging are foreseen to preserve food products for up to 15 days, maintaining their physical and microbiological quality (97). Thus, the design of multilayer active systems can successfully allow the controlled release of the bioactive compounds.

TABLE 6
www.frontiersin.org

Table 6. Antibacterial activity for S. aureus and E. coli of the multilayer structure of poly(3-hydroxybutyrate) (PHB) sheet/electrospun poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) interlayer containing eugenol/PHBV film in the open and closed systems for 15 days.

In a food packaging content, it is also worthy to mention that a slow or sustained release supposes an advantage because, in some cases, the excess of volatiles substances can be affect the organoleptic food properties and result in consumer rejection. As reported by Ribes et al. (98), the presence of active compounds such as eugenol, carvacrol, and vanillin altered the sensory acceptance of fruit juices. It was observed that active compounds immobilized in silica supports induced a change on the aroma of juice samples, particularly for the samples containing eugenol. Thus, the use of multilayers can also successfully contribute to reducing the organoleptic impact of essential oils on the original aroma of food products.

Conclusion

A novel multilayer structure fully based on PHA with antibacterial properties was successfully produced by the electrospinning of PHBV fibers containing eugenol on a cast-extruded PHB sheet (structural layer) followed by the deposition of a PHBV film (food contact layer) and thereafter the application of annealing to the whole assembly at mild temperature. The amount of eugenol in the electrospun monolayer was optimal at 15 wt.% since it yielded high electrospinnability and provided the highest antibacterial properties against bacteria strains of S. aureus and E. coli as well as sufficient thermal stability. The resultant multilayer showed high hydrophobicity to be used in high humidity packaging environments, sufficient interlayer adhesion, a mechanical performance similar to the structural layer, and improved barrier properties against water and aroma vapors. The antimicrobial tests finally showed that the multilayer is very effective to reduce and control the growth of food-borne bacteria in both open and closed systems for up to 15 days. Moreover, through the multilayer design, the release of eugenol was sustained and it can be prolonged so that the organoleptic properties would be less affected. Further studies will be focused on analyzing the migration of eugenol from the multilayer active system into food simulants and the practical application of the multilayer in the form of packaging articles such as trays or lids to study the shelf life of food products and also their impact on the organoleptic properties.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Author Contributions

KF-L performed all experiments, measurements, data analysis, and wrote the manuscript. LC realized the mechanical test of the materials. JL and ST-G proposed, planned, guided the execution of the research work, and co-wrote the manuscript. All authors contributed to the article and approved the submitted version.

Funding

This research was funded by the Spanish Ministry of Science and Innovation (MICI) through the RTI2018-097249-B-C21 program number and the H2020 EU project YPACK (reference number 773872).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

KF-L is a recipient of a Santiago Grisolía (Ref. 0001426013N810001A201) research contract of the Valencian Government (GVA) whereas ST-G holds a Juan de la Cierva–Incorporación contract (IJCI-2016-29675) from MICI. The authors would also like to thank the Unidad Asociada IATA-UJI Plastics Technology.

References

1. Fu Y, Sarkar P, Bhunia AK, Yao Y. Delivery systems of antimicrobial compounds to food. Trends Food Sci Technol. (2016) 57:165–77. doi: 10.1016/j.tifs.2016.09.013

CrossRef Full Text | Google Scholar

2. Petersen K, Væggemose Nielsen P, Bertelsen G, Lawther M, Olsen MB, Nilsson NH, et al. Potential of biobased materials for food packaging. Trends Food Sci Technol. (1999) 10:52–68. doi: 10.1016/S0924-2244(99)00019-9

CrossRef Full Text | Google Scholar

3. Arena U, Di Gregorio F. A waste management planning based on substance flow analysis. Resources Conservat Recycling. (2014) 85:54–66. doi: 10.1016/j.resconrec.2013.05.008

CrossRef Full Text | Google Scholar

4. Kumar G, Ponnusamy VK, Bhosale RR, Shobana S, Yoon JJ, Bhatia SK, et al. A review on the conversion of volatile fatty acids to polyhydroxyalkanoates using dark fermentative effluents from hydrogen production. Bioresource Technol. (2019) 287:121427. doi: 10.1016/j.biortech.2019.121427

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Shen M, Huang W, Chen M, Song B, Zeng G, Zhang Y. (Micro)plastic crisis: un-ignorable contribution to global greenhouse gas emissions and climate change. J Clean Prod. (2020) 254:120138. doi: 10.1016/j.jclepro.2020.120138

CrossRef Full Text | Google Scholar

6. Mannina G, Presti D, Montiel-Jarillo G, Carrera J, Suárez-Ojeda ME. Recovery of polyhydroxyalkanoates (PHAs) from wastewater: a review. Bioresource Technol. (2020) 297:122478. doi: 10.1016/j.biortech.2019.122478

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Costa SS, Miranda AL, de Morais MG, Costa JAV, Druzian JI. Microalgae as source of polyhydroxyalkanoates (PHAs)—a review. Int J Biol Macromol. (2019) 131:536–47. doi: 10.1016/j.ijbiomac.2019.03.099

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Nielsen C, Rahman A, Rehman AU, Walsh MK, Miller CD. Food waste conversion to microbial polyhydroxyalkanoates. Microbial Biotechnol. (2017) 10:1338–52. doi: 10.1111/1751-7915.12776

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Bhatia SK, Gurav R, Choi TR, Jung HR, Yang SY, Moon YM, et al. Bioconversion of plant biomass hydrolysate into bioplastic (polyhydroxyalkanoates) using Ralstonia eutropha 5119. Bioresource Technol. (2019) 271:306–15. doi: 10.1016/j.biortech.2018.09.122

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Bhatia SK, Shim YH, Jeon JM, Brigham CJ, Kim YH, Kim HJ, et al. Starch based polyhydroxybutyrate production in engineered Escherichia coli. Bioprocess Biosystems Eng. (2015) 38:1479–84. doi: 10.1007/s00449-015-1390-y

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Park YL, Bhatia SK, Gurav R, Choi TR, Kim HJ, Song HS, et al. Fructose based hyper production of poly-3-hydroxybutyrate from Halomonas sp. YLGW01 and impact of carbon sources on bacteria morphologies. Int J Biol Macromol. (2020) 154:929–36. doi: 10.1016/j.ijbiomac.2020.03.129

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Hong JW, Song HS, Moon YM, Hong YG, Bhatia SK, Jung HR, et al. Polyhydroxybutyrate production in halophilic marine bacteria Vibrio proteolyticus isolated from the Korean peninsula. Bioprocess Biosystems Eng. (2019) 42:603–10. doi: 10.1007/s00449-018-02066-6

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Vu DH, Åkesson D, Taherzadeh MJJ, Ferreira A. Recycling strategies for polyhydroxyalkanoate-based waste materials: an overview. Bioresource Technol. (2020) 298:122393. doi: 10.1016/j.biortech.2019.122393

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Mozejko-Ciesielska J, Kiewisz R. Bacterial polyhydroxyalkanoates: still fabulous? Microbiol Res. (2016) 192:271–82. doi: 10.1016/j.micres.2016.07.010

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Torres-Giner S, Hilliou L, Melendez-Rodriguez B, Figueroa-Lopez KJ, Madalena D, Cabedo L, et al. Melt processability, characterization, and antibacterial activity of compression-molded green composite sheets made of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) reinforced with coconut fibers impregnated with oregano essential oil. Food Packaging Shelf Life. (2018) 17:39–49. doi: 10.1016/j.fpsl.2018.05.002

CrossRef Full Text | Google Scholar

16. Vahabi H, Rohani Rad E, Parpaite T, Langlois V, Saeb MR. Biodegradable polyester thin films and coatings in the line of fire: the time of polyhydroxyalkanoate (PHA)? Progr Organ Coatings. (2019) 133:85–9. doi: 10.1016/j.porgcoat.2019.04.044

CrossRef Full Text | Google Scholar

17. Jung HR, Jeon JM, Yi DH, Song HS, Yang SY, Choi TR, et al. Poly(3-hydroxybutyrate-co-3-hydroxyvalerate-co-3-hydroxyhexanoate) terpolymer production from volatile fatty acids using engineered Ralstonia eutropha. Int J Biol Macromol. (2019) 138:370–8. doi: 10.1016/j.ijbiomac.2019.07.091

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Rehm BHA, Steinbüchel A. Biochemical and genetic analysis of PHA synthases and other proteins required for PHA synthesis. Int J Biol Macromol. (1999) 25:3–19. doi: 10.1016/S0141-8130(99)00010-0

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Braunegg G, Lefebvre G, Genser KF. Polyhydroxyalkanoates, biopolyesters from renewable resources: physiological and engineering aspects. J Biotechnol. (1998) 65:127–61. doi: 10.1016/S0168-1656(98)00126-6

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Bhatia SK, Gurav R, Choi TR, Jung HR, Yang SY, Song HS, et al. Poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) production from engineered Ralstonia eutropha using synthetic and anaerobically digested food waste derived volatile fatty acids. Int J Biol Macromol. (2019) 133:1–10. doi: 10.1016/j.ijbiomac.2019.04.083

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Tarawat S, Incharoensakdi A, Monshupanee T. Cyanobacterial production of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) from carbon dioxide or a single organic substrate: improved polymer elongation with an extremely high 3-hydroxyvalerate mole proportion. J Appl Phycol. (2020) 32:1095–102. doi: 10.1007/s10811-020-02040-4

CrossRef Full Text | Google Scholar

22. Bhatia SK, Yoon JJ, Kim HJ, Hong JW, Gi Hong Y, Song HS, et al. Engineering of artificial microbial consortia of Ralstonia eutropha and Bacillus subtilis for poly(3-hydroxybutyrate-co-3-hydroxyvalerate) copolymer production from sugarcane sugar without precursor feeding. Bioresource Technol. (2018) 257:92–101. doi: 10.1016/j.biortech.2018.02.056

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Quillaguamán J, Guzmán H, Van-Thuoc D, Hatti-Kaul R. Synthesis and production of polyhydroxyalkanoates by halophiles: current potential and future prospects. Appl Microbiol Biotechnol. (2010) 85:1687–96. doi: 10.1007/s00253-009-2397-6

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Cinelli P, Seggiani M, Mallegni N, Gigante V, Lazzeri A. Processability and degradability of PHA-based composites in terrestrial environments. Int J Mol Sci. (2019) 20:284. doi: 10.3390/ijms20020284

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Melendez-Rodriguez B, Torres-Giner S, Aldureid A, Cabedo L, Lagaron V. Reactive melt mixing of poly(3-hydroxybutyrate)/rice husk flour composites with purified biosustainably produced poly(3-hydroxybutyrate-co-3-hydroxyvalerate). Materials. (2019) 12:2152. doi: 10.3390/ma12132152

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Torres-Giner S, Montanes N, Fombuena V, Boronat T, Sanchez-Nacher L. Preparation and characterization of compression-molded green composite sheets made of poly(3-hydroxybutyrate) reinforced with long pita fibers. Adv Polym Technol. (2018) 37:1305–15. doi: 10.1002/adv.21789

CrossRef Full Text | Google Scholar

27. Cherpinski A, Torres-Giner S, Cabedo L, Lagaron JM. Post-processing optimization of electrospun submicron poly(3-hydroxybutyrate) fibers to obtain continuous films of interest in food packaging applications. Food Additives Contaminants. (2017) 34:1817–30. doi: 10.1080/19440049.2017.1355115

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Melendez-Rodriguez B, Torres-Giner S, Figueroa-Lopez KJ, Castro-Mayorga JL, Lagaron JM, Cabedo L. On the use of high-throughput electrospinning to produce optimized packaging films from polyhydroxyalkanoates. In: Annual Technical Conference—ANTEC, Conference Proceedings (Orlando, FL), (2018).

Google Scholar

29. Radusin T, Torres-Giner S, Stupar A, Ristic I, Miletic A, Novakovic A, et al. Preparation, characterization and antimicrobial properties of electrospun polylactide films containing Allium ursinum L. extract. Food Packaging Shelf Life. (2019) 21:357. doi: 10.1016/j.fpsl.2019.100357

CrossRef Full Text | Google Scholar

30. Tariq S, Wani S, Rasool W, Shafi K, Bhat MA, Prabhakar A, et al. A comprehensive review of the antibacterial, antifungal and antiviral potential of essential oils and their chemical constituents against drug-resistant microbial pathogens. Microbial Pathogenesis. (2019) 134:103580. doi: 10.1016/j.micpath.2019.103580

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Dorman HJD, Deans SG. Antimicrobial agents from plants: antibacterial activity of plant volatile oils. J Appl Microbiol. (2000) 88:308–16. doi: 10.1046/j.1365-2672.2000.00969.x

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Cao D, Jia C, Ji S, Zhang X, Muhoza B. Tannic acid-assisted cross-linked nanoparticles as a delivery system of eugenol: the characterization, thermal degradation and antioxidant properties. Food Hydrocolloids. (2020) 104:105717. doi: 10.1016/j.foodhyd.2020.105717

CrossRef Full Text | Google Scholar

33. Kim J, Marshall MR, Wei C-i. Antibacterial activity of some essential oil components against five foodborne pathogens. J Agri Food Chem. (1995) 43:2839–45. doi: 10.1021/jf00059a013

CrossRef Full Text | Google Scholar

34. Walsh SE, Maillard JY, Russell AD, Catrenich CE, Charbonneau DL, Bartolo RG. Activity and mechanisms of action of selected biocidal agents on Gram-positive and -negative bacteria. J Appl Microbiol. (2003) 94:240–7. doi: 10.1046/j.1365-2672.2003.01825.x

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Elgayyar M, Draughon FA, Golden DA, Mount JR. Antimicrobial activity of essential oils from plants against selected pathogenic and saprophytic microorganisms. J Food Protect. (2001) 64:1019–24. doi: 10.4315/0362-028X-64.7.1019

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Devi KP, Nisha SA, Sakthivel R, Pandian SK. Eugenol (an essential oil of clove) acts as an antibacterial agent against Salmonella typhi by disrupting the cellular membrane. J Ethnopharmacology. (2010) 130:107–15. doi: 10.1016/j.jep.2010.04.025

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Kohanski MA, Dwyer DJ, Collins JJ. How antibiotics kill bacteria: from targets to networks. Nat Rev Microbiol. (2010) 8:423–35. doi: 10.1038/nrmicro2333

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Khameneh B, Iranshahy M, Soheili V, Fazly Bazzaz BS. Review on plant antimicrobials: a mechanistic viewpoint. Antimicrob Resistance Infect Control. (2019) 8:118–8. doi: 10.1186/s13756-019-0559-6

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Li Y, Dong Q, Chen J, Li L. Effects of coaxial electrospun eugenol loaded core-sheath PVP/shellac fibrous films on postharvest quality and shelf life of strawberries. Postharvest Biol Technol. (2020) 159:111028. doi: 10.1016/j.postharvbio.2019.111028

CrossRef Full Text | Google Scholar

40. Celebioglu A, Yildiz ZI, Uyar T. Fabrication of electrospun eugenol/cyclodextrin inclusion complex nanofibrous webs for enhanced antioxidant property, water solubility, and high temperature stability. J Agri Food Chem. (2018) 66:457–66. doi: 10.1021/acs.jafc.7b04312

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Soares RMD, Siqueira NM, Prabhakaram MPS. Ramakrishna: electrospinning and electrospray of bio-based and natural polymers for biomaterials development. Mater Sci Eng C. (2018) 92:969–82. doi: 10.1016/j.msec.2018.08.004

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Figueroa-Lopez KJ, Castro-Mayorga JL, Andrade-Mahecha MM, Cabedo L, Lagaron JM. Antibacterial and barrier properties of gelatin coated by electrospun polycaprolactone ultrathin fibers containing black pepper oleoresin of interest in active food biopackaging applications. Nanomaterials. (2018) 8:1–13. doi: 10.3390/nano8040199

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Marangoni Júnior L, Oliveira LMd, Bócoli PFJ, Cristianini M, Padula M, Anjos CAR. Morphological, thermal and mechanical properties of polyamide and ethylene vinyl alcohol multilayer flexible packaging after high-pressure processing. J Food Eng. (2020) 276:109913. doi: 10.1016/j.jfoodeng.2020.109913

CrossRef Full Text | Google Scholar

44. Gómez Ramos MJ, Lozano A, Fernández-Alba AR. High-resolution mass spectrometry with data independent acquisition for the comprehensive non-targeted analysis of migrating chemicals coming from multilayer plastic packaging materials used for fruit purée and juice. Talanta. (2019) 191:180–92. doi: 10.1016/j.talanta.2018.08.023

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Wang L, Chen C, Wang J, Gardner DJ, Tajvidi M. Cellulose nanofibrils versus cellulose nanocrystals: comparison of performance in flexible multilayer films for packaging applications. Food Packaging Shelf Life. (2020) 23:100464. doi: 10.1016/j.fpsl.2020.100464

CrossRef Full Text | Google Scholar

46. Garrido-López ÁM, Tena T. Study of multilayer packaging delamination mechanisms using different surface analysis techniques. Appl Surface Sci. (2010) 256:3799–805. doi: 10.1016/j.apsusc.2010.01.029

CrossRef Full Text | Google Scholar

47. Úbeda S, Aznar M, Vera P, Nerín C, Henríquez L, Taborda L, et al. Overall and specific migration from multilayer high barrier food contact materials—kinetic study of cyclic polyester oligomers migration. Food Additives Contaminants A. (2017) 34:1784–94. doi: 10.1080/19440049.2017.1346390

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Anukiruthika T, Sethupathy P, Wilson A, Kashampur K, Moses JA, Anandharamakrishnan C. Multilayer packaging: advances in preparation techniques and emerging food applications. Comprehensive Rev Food Sci Food Safety. (2020) 19:1156–86. doi: 10.1111/1541-4337.12556

CrossRef Full Text | Google Scholar

49. Mount E. Chapter 6—Coextrusion equipment for multilayer flat films sheets. In: Wagner JR, editor. Multilayer Flexible Packaging. Boston: William Andrew Publishing. (2010) 75–95. doi: 10.1016/B978-0-8155-2021-4.10006-1

CrossRef Full Text | Google Scholar

50. Torres-Giner S, Pérez-Masiá R, Lagaron JM. A review on electrospun polymer nanostructures as advanced bioactive platforms. Polym Eng Sci. (2016) 56:500–27. doi: 10.1002/pen.24274

CrossRef Full Text | Google Scholar

51. Busolo MA, Torres-Giner S, Lagaron JM. Enhancing the gas barrier properties of polylactic acid by means of electrospun ultrathin zein fibers. In: Annual Technical Conference—ANTEC, Conference Proceedings (Chicago, IL). (2009).

Google Scholar

52. Torres-Giner S, Martinez-Abad A, Lagaron JM. Zein-based ultrathin fibers containing ceramic nanofillers obtained by electrospinning. II. Mechanical properties, gas barrier, and sustained release capacity of biocide thymol in multilayer polylactide films. J Appl Polym Sci. (2014) 131:9270–6. doi: 10.1002/app.40768

CrossRef Full Text | Google Scholar

53. Fabra MJ, Lopez-Rubio A, Lagaron JM. High barrier polyhydroxyalcanoate food packaging film by means of nanostructured electrospun interlayers of zein. (2013) 32:106–14. doi: 10.1016/j.foodhyd.2012.12.007

CrossRef Full Text | Google Scholar

54. Fabra MJ, Lopez-Rubio A, Lagaron JM. Nanostructured interlayers of zein to improve the barrier properties of high barrier polyhydroxyalkanoates and other polyesters. J Food Eng. (2014) 127:1–9. doi: 10.1016/j.jfoodeng.2013.11.022

CrossRef Full Text | Google Scholar

55. Cherpinski A, Torres-Giner S, Cabedo L, Méndez JA, Lagaron JM. Multilayer structures based on annealed electrospun biopolymer coatings of interest in water and aroma barrier fiber-based food packaging applications. J Appl Polym Sci. (2017) 135:45501. doi: 10.1002/app.45501

CrossRef Full Text | Google Scholar

56. Cherpinski A, Torres-Giner S, Vartiainen J, Peresin MS, Lahtinen P, Lagaron JM. Improving the water resistance of nanocellulose-based films with polyhydroxyalkanoates processed by the electrospinning coating technique. Cellulose. (2018) 25:1291–307. doi: 10.1007/s10570-018-1648-z

CrossRef Full Text | Google Scholar

57. Quiles-Carrillo L, Montanes N, Lagaron JM, Balart R, Torres-Giner S. Bioactive multilayer polylactide films with controlled release capacity of gallic acid accomplished by incorporating electrospun nanostructured coatings and interlayers. Appl Sci. (2019) 9:30533. doi: 10.3390/app9030533

CrossRef Full Text | Google Scholar

58. Akinalan Balik B, Argin S, Lagaron JM, Torres-Giner S. Preparation and characterization of electrospun pectin-based films and their application in sustainable aroma barrier multilayer packaging. Appl Sci. (2019) 9:5136. doi: 10.3390/app9235136

CrossRef Full Text | Google Scholar

59. Figueroa-Lopez KJ, Vicente AA, Reis MAM, Torres-Giner S, Lagaron JM. Antimicrobial and antioxidant performance of various essential oils and natural extracts and their incorporation into biowaste derived poly(3-hydroxybutyrate-co-3-hydroxyvalerate) layers made from electrospun ultrathin fibers. Nanomaterials. (2019) 9:144. doi: 10.3390/nano9020144

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Castro-Mayorga JL, Fabra MJ, Pourrahimi AM, Olsson RT, Lagaron JM. The impact of zinc oxide particle morphology as an antimicrobial and when incorporated in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) films for food packaging and food contact surfaces applications. Food Bioproducts Proces. (2017) 101:32–44. doi: 10.1016/j.fbp.2016.10.007

CrossRef Full Text | Google Scholar

61. Cerqueira MA, Fabra MJ, Castro-Mayorga JL, Bourbon AI, Pastrana LM, Vicente AA, et al. Use of electrospinning to develop antimicrobial biodegradable multilayer systems: encapsulation of cinnamaldehyde and their physicochemical characterization. Food Bioprocess Technol. (2016) 9:1874–84. doi: 10.1007/s11947-016-1772-4

CrossRef Full Text | Google Scholar

62. Torres-Giner S, Torres A, Ferrandiz M, Fombuena V, Balart R. Antimicrobial activity of metal cation-exchanged zeolites and their evaluation on injection-molded pieces of bio-based high-density polyethylene. J Food Safety. (2017) 37:1–12. doi: 10.1111/jfs.12348

CrossRef Full Text | Google Scholar

63. Jouki M, Yazdi FT, Mortazavi SA, Koocheki A. Quince seed mucilage films incorporated with oregano essential oil: physical, thermal, barrier, antioxidant and antibacterial properties. Food Hydrocolloids. (2014) 36:9–19. doi: 10.1016/j.foodhyd.2013.08.030

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Vieira MGA, da Silva MA, dos Santos LO, Beppu MM. Natural-based plasticizers and biopolymer films: a review. Eur Polym J. (2011) 47:254–63. doi: 10.1016/j.eurpolymj.2010.12.011

CrossRef Full Text | Google Scholar

65. Torres-Giner S, Gimenez E, Lagaron JM. Characterization of the morphology and thermal properties of Zein Prolamine nanostructures obtained by electrospinning. Food Hydrocolloids. (2008) 22:601–14. doi: 10.1016/j.foodhyd.2007.02.005

CrossRef Full Text | Google Scholar

66. Torres-Giner S, Ocio MJ, Lagaron JM. Development of active antimicrobial fiber-based chitosan polysaccharide nanostructures using electrospinning. Eng Life Sci. (2008) 8:303–14. doi: 10.1002/elsc.200700066

CrossRef Full Text | Google Scholar

67. Melendez-Rodriguez B, Figueroa-Lopez KJ, Bernardos A, Martínez-Máñez R, Cabedo L, Torres-Giner S, et al. Electrospun antimicrobial films of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) containing eugenol essential oil encapsulated in mesoporous silica nanoparticles. Nanomaterials. (2019) 9:227. doi: 10.3390/nano9020227

PubMed Abstract | CrossRef Full Text | Google Scholar

68. Shen ZD, Kamdem P. Development and characterization of biodegradable chitosan films containing two essential oils. Int J Biol Macromol. (2015) 74:289–96. doi: 10.1016/j.ijbiomac.2014.11.046

PubMed Abstract | CrossRef Full Text | Google Scholar

69. Haghighi H, Biard S, Bigi F, De Leo R, Bedin E, Pfeifer F, et al. Comprehensive characterization of active chitosan-gelatin blend films enriched with different essential oils. Food Hydrocolloids. (2019) 95:33–42. doi: 10.1016/j.foodhyd.2019.04.019

CrossRef Full Text | Google Scholar

70. Shao Y, Wu C, Wu T, Li Y, Chen S, Yuan C, et al. Eugenol-chitosan nanoemulsions by ultrasound-mediated emulsification: formulation, characterization and antimicrobial activity. Carbohydrate Polymers. (2018) 193:144–52. doi: 10.1016/j.carbpol.2018.03.101

PubMed Abstract | CrossRef Full Text | Google Scholar

71. Piletti R, Bugiereck AM, Pereira AT, Gussati E, Dal Magro J, Mello JMM, et al. Microencapsulation of eugenol molecules by β-cyclodextrine as a thermal protection method of antibacterial action. Mater Sci Eng: C. (2017) 75:259–71. doi: 10.1016/j.msec.2017.02.075

PubMed Abstract | CrossRef Full Text | Google Scholar

72. da Silva CG, Kano FS, dos Santos Rosa D. Thermal stability of the PBAT biofilms with cellulose nanostructures/essential oils for active packaging. J Thermal Anal Calorimetry. (2019) 138:2375–86. doi: 10.1007/s10973-019-08190-z

CrossRef Full Text | Google Scholar

73. Figueroa-Lopez KJ, Enescu D, Torres-Giner S, Cabedo L, Cerqueira MA, Pastrana L, et al. Development of electrospun active films of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) by the incorporation of cyclodextrin inclusion complexes containing oregano essential oil. Food Hydrocolloids. (2020) 108:106013. doi: 10.1016/j.foodhyd.2020.106013

CrossRef Full Text | Google Scholar

74. de Souza Moura W, de Souza SR, Campos FS, Sander Rodrigues Cangussu A, Macedo Sobrinho Santos E, Silva Andrade B, et al. Antibacterial activity of Siparuna guianensis essential oil mediated by impairment of membrane permeability and replication of pathogenic bacteria. Indus Crops Products. (2020) 146:112142. doi: 10.1016/j.indcrop.2020.112142

CrossRef Full Text | Google Scholar

75. Alizadeh Behbahani B, Noshad M, Falah F. Cumin essential oil: phytochemical analysis, antimicrobial activity and investigation of its mechanism of action through scanning electron microscopy. Microbial Pathogenesis. (2019) 136:103716. doi: 10.1016/j.micpath.2019.103716

PubMed Abstract | CrossRef Full Text | Google Scholar

76. Nazzaro F, Fratianni F, De Martino L, Coppola R, De Feo V. Effect of essential oils on pathogenic bacteria. Pharmaceuticals. (2013) 6:1451–74. doi: 10.3390/ph6121451

PubMed Abstract | CrossRef Full Text | Google Scholar

77. Figueroa-Lopez KJ, Torres-Giner S, Enescu D, Cabedo L, Cerqueira MA, Pastrana LM, et al. Electrospun active biopapers of food waste derived poly(3-hydroxybutyrate-co-3-hydroxyvalerate) with short-term and long-term antimicrobial performance. Nanomaterials. (2020) 10:506. doi: 10.3390/nano10030506

PubMed Abstract | CrossRef Full Text | Google Scholar

78. Navikaite-Snipaitiene V, Ivanauskas L, Jakstas V, Rüegg N, Rutkaite R, Wolfram E, et al. Development of antioxidant food packaging materials containing eugenol for extending display life of fresh beef. Meat Sci. (2018) 145:9–15. doi: 10.1016/j.meatsci.2018.05.015

PubMed Abstract | CrossRef Full Text | Google Scholar

79. Fabra MJ, López-Rubio A, Cabedo L, Lagaron JM. Tailoring barrier properties of thermoplastic corn starch-based films (TPCS) by means of a multilayer design. J Colloid Interface Sci. (2016) 483:84–92. doi: 10.1016/j.jcis.2016.08.021

PubMed Abstract | CrossRef Full Text | Google Scholar

80. Wan Z, Wang L, Yang X, Guo J, Yin S. Enhanced water resistance properties of bacterial cellulose multilayer films by incorporating interlayers of electrospun zein fibers. Food Hydrocolloids. (2016) 61:269–76. doi: 10.1016/j.foodhyd.2016.05.024

CrossRef Full Text | Google Scholar

81. Yoon YI, Moon HS, Lyoo WS, Lee TS, Park WH. Superhydrophobicity of PHBV fibrous surface with bead-on-string structure. J Colloid Interface Sci. (2008) 320:91–5. doi: 10.1016/j.jcis.2008.01.029

PubMed Abstract | CrossRef Full Text | Google Scholar

82. Sombatmankhong K, Suwantong O, Waleetorncheepsawat S, Supaphol P. Electrospun fiber mats of poly(3-hydroxybutyrate), poly(3-hydroxybutyrate-co-3-hydroxyvalerate), and their blends. J Polym Sci B. (2006) 44:2923–33. doi: 10.1002/polb.20915

CrossRef Full Text | Google Scholar

83. Li X, Liu KL, Wang M, Wong SY, Tjiu WC, He CB, et al. Improving hydrophilicity, mechanical properties and biocompatibility of poly[(R)-3-hydroxybutyrate-co-(R)-3-hydroxyvalerate] through blending with poly[(R)-3-hydroxybutyrate]-alt-poly(ethylene oxide). Acta Biomaterialia. (2009) 5:2002–12. doi: 10.1016/j.actbio.2009.01.035

PubMed Abstract | CrossRef Full Text | Google Scholar

84. Han J, Wu LP, Hou J, Zhao D, Xiang H. Biosynthesis, characterization, and hemostasis potential of tailor-made poly(3-hydroxybutyrate-co-3-hydroxyvalerate) produced by Haloferax mediterranei. Biomacromolecules. (2015) 16:578–88. doi: 10.1021/bm5016267

PubMed Abstract | CrossRef Full Text | Google Scholar

85. Chang CK, Wang H-MD, Lan JC-W. Investigation and characterization of plasma-treated poly(3-hydroxybutyrate) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) biopolymers for an in vitro cellular study of mouse adipose-derived stem cells. Polymers. (2018) 10:355. doi: 10.3390/polym10040355

PubMed Abstract | CrossRef Full Text | Google Scholar

86. Medina-Jaramillo C, Ochoa-Yepes O, Bernal C, Famá L. Active and smart biodegradable packaging based on starch and natural extracts. Carbohydrate Polymers. (2017) 176:187–94. doi: 10.1016/j.carbpol.2017.08.079

PubMed Abstract | CrossRef Full Text | Google Scholar

87. Corre YM, Bruzaud S, Audic JL, Grohens Y. Morphology and functional properties of commercial polyhydroxyalkanoates: a comprehensive and comparative study. Polymer Testing. (2012) 31:226–35. doi: 10.1016/j.polymertesting.2011.11.002

CrossRef Full Text | Google Scholar

88. Kim GH, Han H, Park JH, Kim WD. An applicable electrospinning process for fabricating a mechanically improved nanofiber mat. Polym Eng Sci. (2007) 47:707–12. doi: 10.1002/pen.20744

CrossRef Full Text | Google Scholar

89. Arrieta MP, López J, Hernández A, Rayón E. Ternary PLA–PHB–Limonene blends intended for biodegradable food packaging applications. Eur Polym J. (2014) 50:255–70. doi: 10.1016/j.eurpolymj.2013.11.009

CrossRef Full Text | Google Scholar

90. Narayanan A, Neera Mallesha K. Ramana V. Synergized antimicrobial activity of eugenol incorporated polyhydroxybutyrate films against food spoilage microorganisms in conjunction with pediocin. Appl Biochem Biotechnol. (2013) 170:1379–88. doi: 10.1007/s12010-013-0267-2

CrossRef Full Text | Google Scholar

91. Requena R, Jiménez A, Vargas M, Chiralt A. Poly[(3-hydroxybutyrate)-co-(3-hydroxyvalerate)] active bilayer films obtained by compression moulding and applying essential oils at the interface. Polym Int. (2016) 65:883–91. doi: 10.1002/pi.5091

CrossRef Full Text | Google Scholar

92. Alp-Erbay E, Figueroa-Lopez KJ, Lagaron JM, Çaglak E, Torres-Giner S. The impact of electrospun films of poly(ε-caprolactone) filled with nanostructured zeolite and silica microparticles on in vitro histamine formation by Staphylococcus aureus and Salmonella Paratyphi A. Food Packaging Shelf Life. (2019) 22:100414. doi: 10.1016/j.fpsl.2019.100414

CrossRef Full Text | Google Scholar

93. Razumovskii LP, Iordanskii AL, Zaikov GE, Zagreba ED, McNeill IC. Sorption and diffusion of water and organic solvents in poly(β-hydroxybutyrate) films. Polym Degradation Stabil. (1994) 44:171–5. doi: 10.1016/0141-3910(94)90161-9

CrossRef Full Text | Google Scholar

94. Figueroa-Lopez KJ, Andrade-Mahecha MM, Torres-Vargas OL. Development of antimicrobial biocomposite films to preserve the quality of bread. Molecules. (2018) 23:10212. doi: 10.3390/molecules23010212

PubMed Abstract | CrossRef Full Text | Google Scholar

95. Hasheminya SM, Mokarram RR, Ghanbarzadeh B, Hamishekar H, Kafil HS, Dehghannya J. Development and characterization of biocomposite films made from kefiran, carboxymethyl cellulose and Satureja Khuzestanica essential oil. Food Chem. (2019) 289:443–52. doi: 10.1016/j.foodchem.2019.03.076

PubMed Abstract | CrossRef Full Text | Google Scholar

96. Requena R, Vargas M, Chiralt A. Obtaining antimicrobial bilayer starch and polyester-blend films with carvacrol. Food Hydrocolloids. (2018) 83:118–33. doi: 10.1016/j.foodhyd.2018.04.045

CrossRef Full Text | Google Scholar

97. Al-Tayyar NA, Youssef AM, Al-hindi R. Antimicrobial food packaging based on sustainable Bio-based materials for reducing foodborne Pathogens: a review. Food Chem. (2020) 310:125915. doi: 10.1016/j.foodchem.2019.125915

PubMed Abstract | CrossRef Full Text | Google Scholar

98. Ribes S, Ruiz-Rico M, Pérez-Esteve E, Fuentes A, Barat JM. Enhancing the antimicrobial activity of eugenol, carvacrol and vanillin immobilised on silica supports against Escherichia coli or Zygosaccharomyces rouxii in fruit juices by their binary combinations. LWT. (2019) 113:108326. doi: 10.1016/j.lwt.2019.108326

CrossRef Full Text | Google Scholar

Keywords: PHA, essential oils, multilayer, antimicrobial activity, electrospinning

Citation: Figueroa-Lopez KJ, Cabedo L, Lagaron JM and Torres-Giner S (2020) Development of Electrospun Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) Monolayers Containing Eugenol and Their Application in Multilayer Antimicrobial Food Packaging. Front. Nutr. 7:140. doi: 10.3389/fnut.2020.00140

Received: 25 May 2020; Accepted: 20 July 2020;
Published: 03 September 2020.

Edited by:

Javier Raso, University of Zaragoza, Spain

Reviewed by:

Shashi Kant Bhatia, Konkuk University, South Korea
Houyong Yu, Zhejiang Sci-Tech University, China

Copyright © 2020 Figueroa-Lopez, Cabedo, Lagaron and Torres-Giner. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jose M. Lagaron, lagaron@iata.csic.es; Sergio Torres-Giner, storresginer@iata.csic.es

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.