CC BY
204
Marina Ramos, Ana Beltran, Arancha Valdes, Mercedes A. Peltzer,
Alfonso Jimenez, Marfa C. Garrigos, A. M. Kochnev, G. E. Zaikov
CARVACROL AND THYMOL FOR FRESH FOOD PACKAGING
Keywords: active packaging, carvacrol, thymol, strawberries, bread, thermal properties, volatile profile.
Active packaging is becoming an emerging food technology to improve quality and safety offood products. One of the most common approaches is based on the release of antioxidant/antimicrobial compounds from the packaging material. In this work an antifungal active packaging system based on the release of carvacrol and thymol was optimized to increase the post-harvest shelf life offresh strawberries and bread during storage. Thermal properties of the developed packaging material were determined by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Volatile compounds in food samples contained in active packaging systems were monitored by using headspace solid phase microextraction followed by gas chromatography analysis (HS-SPME-GC-MS) at controlled conditions. The obtained results provided evidences that exposure to carvacrol and thymol is an effective way to enlarge the quality of strawberries and bread samples during distribution and sale.
Ключевые слова: активная упаковка, карвакрол, тимол, клубника, хлеб, термические свойства, летучий профиль.
Активная упаковка становится передовой технологией, используемой для повышения качества и безопасности пищевых продуктов. Один из наиболее распространенных подходов основан на миграции антиоксидантно - антимикробных соединений из упаковочного материала. В данной работе для увеличения послеуборочного срока хранения свежей клубники и хлеба была оптимизирован состав противогрибковой активной упаковочной системы, основанной на миграции карвакрола и тимола. При помощи дифференциальной сканирующей калориметрии (ДСК) и термогравиметрического анализа (ТГА) определены термические свойства разработанного упаковочного материала. Наличие летучих соединений в пищевых образцах, мигрирующих из активной упаковочной системы, контролировались при помощи микроэкстракции свободного пространства твердой фазы с последующим анализом методом газовой хроматографии в контролируемых условиях (метод HS-SPME-GC-MS). Полученные результаты свидетельствуют, что воздействие карвакрола и тимола является эффективным способом повышения качества образцов клубники и хлеба в процессе их хранения и реализации.
Introduction
Active packaging is the one of most relevant approaches to increase the protection and shelf-life of fresh food [1]. Active packaging is broad concept that can be defined as a system in which the product, the packaging material and the environment interact in a positive way to extend food shelf-life [2]. Many different active agents can be incorporated into the packaging material to improve its functionality. The migration of the active compound may be achieved by direct contact between food and the packaging material or through gas phase diffusion from the inner packaging layer to the food surface [3,4,5,6].
Food can be subjected to microbial contamination that is mainly caused by bacteria, yeasts and fungi. Many of these microorganisms can cause undesirable reactions and can deteriorate organoleptic and nutritional properties of foods [7]. Different antimicrobial (AM) agents (most of them synthetic) are commonly incorporated directly into the food to diminish food spoilage by microorganisms. But this strategy has several disadvantages such as: the rising consumer refusal for food with synthetic additives; the useless addition of these agents to the food bulk when spoilage occurs primarily on the surface and the undesirable modification of food flavor. Therefore, antimicrobial packaging is a promising method to protect food from microbial contamination with no need of using synthetic additives in food compostion
[8].
Natural AM agents (AMs) have attracted much attention from food and packaging industries by their potential action in food preservation. According to Da-
vidson and Zivanovic, natural AM agents can be classified by their sources in vegetal (herbs and essential oils (EOs)), animals (lysozyme, lactoferrin), microbials (nisin, natamycin) or antimicrobial polymers (chitosan)
[9]. In these sense, many studies have focused on the AMs present in EOs extracted from plants (basil, thyme, oregano, cinnamon, clove, rosemary) consisting on complex mixtures of different compounds including terpenoids, esters, aldehydes, ketones, acids and alcohols [10]. These plant EOs are volatile liquids characterized by a strong odor [11]. Extracts derived from herbs and EOs contain many natural compounds such as thymol, linalool and carvacrol with a broad AM range against different pathogenic and spoilage microorganisms including Gram-negative [12,13] and Gram-positive species [14,15]; as well as against yeast [16] and molds [17]. In general, these additives are considered to be safe and they have been classified as GRAS (Generally Recognized As Safe) by the American Food and Drug Administration [7].
Rodriguez et al studied the addition of EOs to a wax coating in order to develop an antimicrobial active packaging and they assessed their ability to preserve strawberries from microorganism contamination by the release of AMs from the coating [18]. During this study, there was no direct contact between the EOs and the food product. Therefore, the chemicals responsible for the inhibition of the pathogen growth must have been the natural volatile compounds (eugenol, carvacrol, thymol) present in the headspace packaging. In other study, carvacrol was added to chitosan-based films for active packaging and its antimicrobial efficiency against food spoilage microorganisms was demonstrated by
using a headspace chromatographic technique [19]. Gutierrez et al used a cinnamon-based active material to increase more than three times the shelf-life of a complex bakery product with minimal changes in the packaging and no additional manipulation steps [20].
In addition to microbial contamination, there are changes in the food macroscopic properties that also induced biochemical reactions and chemical alterations in tissues, such as changes in the volatile profile [21] and development of undesirable chemicals (i.e. ethanol or acetaldehyde) associated with changes in the respiratory paths [22]. Flavor is one of the main factors influencing consumer’s food choice [23]. Volatile compounds are important contributors to flavor and odor of fruits, being aroma a very important quality attribute of strawberries. The flavor of strawberries is comprised of a complex mixture of esters, aldehydes, alcohols, furans and sulfur compounds. Esters are the main headspace volatiles. Methyl esters amount increases with the plant maturation, while ethyl esters amount do not change significantly during the fruit growth [24].
In the case of bread, aroma has been largely studied and many methods have been developed to identify the compounds responsible of flavor [25]. More than 540 different compounds have been described in the complex volatile fraction of bread [26], being alcohols, aldehydes, esters, ketones, acids, pyrazines and pyrrolines the most important quantitatively, but furans, hydrocarbons and lactones were also identified [27].
Solid Phase Microextraction (SPME) has become one of the preferred techniques in aroma analysis, offering solvent free, rapid sampling with low cost and easy preparation. Also, it is sensitive, selective and compatible with low detection limits [28]. Placed in the sample headspace, SPME is a non-destructive and non-invasive method to evaluate volatile and semi-volatile compounds. In this sense, the extraction of volatile compounds released from a great number of foods has been carried out by using HS-SPME technique [27, 29].
Besides the increasing concern in recent years about the use of synthetic polymers due to their poor biodegradability and high permanence in the environment after their use, these materials are still highly competitive by their many advantages including low cost, good processability and excellent mechanical and physical properties. Therefore, the development of antimicrobial packaging materials manufactured from synthetic polymers, such as low-density polyethylene (LDPE), high-density polyethylene (HDPE), polystyrene (PS), polyethylene terephthalate (PET) and polypropylene (PP) is important by their commercial benefits for food packaging [7].
This study focuses on the optimization of anti-fungal active systems based on the controlled release of carvacrol and thymol from polypropylene (PP) films. The effectiveness of the developed active films was evaluated by studying the headspace volatile composition of two food samples (bread and strawberries) stored at different conditions. This study was carried out by headspace Solid Phase Micro-Extraction (SPME) followed by gas chromatography analysis (HS-SPME-GC-MS). Results were correlated with the antimicrobial activity by visual observation of the fungal growth in
the studied food (bread and strawberries). In addition, the effect of the studied additives on the thermal properties of the developed active films was also carried out.
Experimental
Materials
The polymer used in this work was polypropylene (PP) ECOLEN HZ10K (Hellenic Petroleum, Greece), kindly supplied in pellets by Ashland Chemical Hispania (Barcelona, Spain). Melt flow index (MFI) was 3.2 g 10 min-1 determined according to ASTM-D1238 standard (230 °C, 2.16 Kg), and density 0.9 g cm-3. Carvacrol (98 %) and thymol (99.5 %) were obtained from Sigma-Aldrich (Madrid, Spain).
Strawberries and sliced bread were purchased from a local market. Damaged, non-uniform, unripe or overripe strawberries were removed and the selected fruits were stored for at least 2 h at 3 °C to ensure their thermal equilibrium. Strawberries were selected for this study due to their rapid post-harvest deterioration, which constitutes a problem on their commercial distribution. Sliced bread was selected due to the increasing consumer demand for fresh bread with long shelf-life.
Preparation of active films
Active films were prepared by melt-blending followed by compression molding by using a method previously reported [30]. A Haake Poly lab QC mixer (ThermoFischer Scientific, Walham, USA) at 190 °C for 6 min at rotation speed of 50 rpm was used. Both additives were introduced in the mixer once the polymer was already in the melt state to avoid unnecessary losses and to ensure their presence in the final materials. The active antimicrobial films were obtained at 190 °C in a hot press (Carver Inc, Model 3850, USA) for 12 minutes. The average thickness of the films was around 200 ^m measured with a Digimatic Micrometer Series 293 MDC-Lite (Mitutoyo, Japan) at five random positions around the film. The final appearance of the films was completely transparent and homogenous.
Two active formulations were prepared: PP containing 8 wt% of thymol (PPT8) and PP with 8 wt% of carvacrol (PPC8). An additional sample without any active compound was also prepared and used as control (PP0).
Thermal characterization of active films
Thermogravimetric analysis (TGA)
TGA tests were performed in a TGA/SDTA 851 Mettler Toledo thermal analyzer (Schwarzenbach, Switzerland). Approximately 5 mg samples were weighed in alumina pans (70 ^L) and were heated from 30 °C to 700 °C at a heating rate of 10 °C min-1-1 under inert nitrogen atmosphere (flow rate 50 mL min-1).
Differential scanning calorimetry (DSC)
Determination of thermal parameters in inert atmosphere
DSC tests were conducted in a TA DSC Q-2000 instrument (New Castle, DE, USA) under inert nitrogen atmosphere. 3 mg samples were introduced in aluminium pans (40^L) and were submitted to the following thermal program: heating from 0 °C to 180 °C at 10 °C min-1 (3 min hold), cooling at 10 °C min-1 to 0 °C
(3 min hold) and heating to 180 °C at 10 °C min-1. The percentage of crystallinity (x %) for each material was calculated according to the following equation,
(1)
where AHm (J g-1) is the latent heat of fusion of the sample, W is the PP weight fraction in the sample, and AHm° is the theoretical latent heat of fusion for 100 % crystalline PP, 138 J g-1 [31].
Evaluation of oxidation induction time
The antioxidant performance of carvacrol and thymol in the developed active films was also studied by DSC by determining their oxidation induction time, OIT (min) [32, 33]. The OIT value is defined as the time to the onset of an exothermic oxidation peak in oxidative atmosphere and it was determined by using oxygen and air, as the results obtained can be dependent on the type of atmosphere used for the analysis.
OIT tests were carried out by heating samples at 100 °C min-1 under nitrogen (flow rate 50 mL min-1) to the set temperature (200 °C) according to ASTM-D3895-07 Standard. After 5 min, the atmosphere was switched to pure oxygen or air (50 mL min-1). The heat flow was then recorded in isothermal conditions up to the detection of the exothermic peak indicating the beginning of the oxidation reaction. All tests were performed in triplicate for each formulation.
Study of the effectiveness of the active films to preserve perishable food
Observation of fungal growth
The effectiveness of the developed active films was evaluated by putting them in contact with sliced bread and strawberries and further observing the occurrence of fungal growth on food samples with time. For this purpose, food samples were appropriately cut to be placed on the base of disposable polypropylene Petri dishes (inside dimensions: 88 mm diameter x 12 mm high). An additional test was carried out with uncut strawberries which were placed into a polyethylene suitable food container (250 mL, 4 cm high x 13 cm opening diameter) as shown in Figure 1.
Active films were cut with the appropriate dimensions to match the top of the lid of the used containers in order to release the antimicrobial studied agents (carvacrol and thymol) into the packaging headspace. The final containers were then sealed with "Parafilm" in order to avoid losses of volatile compounds and were incubated at 25 °C and 50% RH in a CM 0/81 climatic chamber (Dycometal, Barcelona, Spain) during 15 days. Food samples stored with the control film (without active compounds) were also studied for comparison.
Headspace analysis by HS-SPME-GC-MS
Food samples (whole strawberries and sliced bread) were placed into the polyethylene container described in the previous section in direct contact with the PP films and samples were extracted at selected times to determine the headspace composition. Containers were sealed and a PTFE/silicone septum was placed on their top part to allow the insertion of the SPME fibre for volatiles extraction (Figure 1). Samples were then stored
in a climatic chamber and tested at different temperatures and days of storage according to the conditions shown in Table 1. In this sense, 25°C and 4°C were selected in order to simulate ambient and refrigerated storage conditions, respectively. Three replicates were performed for each food sample and day of study.
HS-SPME analysis of volatile compounds for food samples was performed according to a previously reported method applied to bread samples [34] with slight modifications. Similar conditions to those proposed by G. Blanda et al. Were used in the study with strawberries [35]. The SPME fibre used was divinylbenzene/carboxen/polydimethylsiloxane (DVB/CAR/PDMS) 50/30 ^m, StableFlex, 1 cm long mounted to an SPME manual holder assembly from Supelco (Bellefonte, PA) (Figure 1). Prior to use, the fibre was conditioned by following the manufacturer’s recommendations. The needle of the SPME device was inserted into the container through the septum and the fibre was exposed to the food sample headspace for 30 min at room temperature. The fibre was then retracted into the needle assembly, removed from the container, transferred to the injection port of the GC unit and immediately desorbed.
Table 1 - Storage and testing conditions in the headspace study of food by HS-SPME-GC-MS
Food sample Temperature (°C) Days of study
Slice bread 25 0 2 5 10 15 -
Whole 25 0 2 4 7 10 -
strawberries
Whole strawberries 4 0 2 4 7 10 15
PP0 PPT PPC
Fig. 1 - Experimental assembly used for headspace analysis of whole strawberries by HS-SPME
Analysis of volatiles produced in the headspace of bread and strawberries packed samples was performed by using a Perkin Elmer TurboMass Gold GC-MS (Boston, MA, USA) equipped with a split/splitless injector and a quadrupole mass spectrometer operating in electronic impact (EI) ionisation mode (70 eV). A SPB-5 capillary column (30 m x 0.25 mm x 0.25 |am; Supelco, Bellefonte, PA, USA) was used. The column temperature was programmed from 40 °C (hold 10 min) to 120 °C (hold 1 min) at 5 °C min-1, to 140 °C at 2 °C
min"1 (hold 0 min) and to 230 °C at 5 °C min"1 (hold 8 min). Helium was used as carrier gas at a flow rate of 1 mL min"1. Ion source and GC/MS transfer line temperatures were 250 and 270 °C, respectively. Injector temperature was 270 °C and time for fibre desorption was fixed at 5 min in the splitless mode (1.5 min splitless-period). After every run, the SPME fibre was conditioned for 30 min at 270 °C in the injector of the gas chromatograph followed by a blank analysis to avoid carryover of the fibre.
Identification of volatile compounds in strawberries and sliced bread headspace was performed in full scan mode (m/z 30-550). Carvacrol and thymol were identified by a combination of the NIST mass spectral library and gas chromatographic retention times of standard compounds. The rest of volatiles were tentatively identified by their GC/MS spectra. In this sense, the compounds having < 90% similarity with spectra in the NIST library were not taken into consideration. Chromatographic responses of detected volatile compounds (peak area counts) were monitored for comparative measurements of each compound in the studied samples.
Results and discussion
Thermogravimetric Analysis (TGA)
The effect of carvacrol and thymol on the thermal stability of PP films was studied by TGA under nitrogen atmosphere. The TGA patterns obtained for PP films showed a first degradation step at low temperatures (about 115 °C) observed only for active films, which was associated to the thermal decomposition of carvacrol and/or thymol and a second step corresponding to the thermal degradation of the polymer matrix [30](Ramos et al., 2012). The first degradation step observed for active films was considered as an indirect confirmation of the presence of the active compounds (thymol and carvacrol) in the polymer matrix after processing and consequently their ability to act as active agents in these materials as it has been reported by other authors [36].
Table 2 summarizes the temperatures obtained for the main degradation step (Tmax), ascribed to the PP thermal degradation. No significant differences were observed for Tmax values in all samples. These results showed that the addition of carvacrol and thymol to the polymer matrix did not significantly affect its thermal degradation profile in inert nitrogen atmosphere. However, it would be expectable that a certain amount of carvacrol and thymol would be lost during processing, since materials are submitted to temperatures above the decomposition point of these additives. Therefore, the processing parameters, in particular temperature and time, should be optimized to avoid the excessive evaporation and consequent loss of these additives incorporated to PP [37].
Differential Scanning Calorimetry (DSC)
Determination of thermal parameters in inert atmosphere
Four parameters were determined for the thermal caharacterization of these materials by DSC (Table 2): cold-crystallization temperature, Tcc (°C); melting temperature, Tm (°C); crystallization enthalpy, AHc (J g-
1) and melting enthalpy, AHm (J g-1). As can be seen in Table 2, melting and cold-crystallization temperatures as well as crystallization enthalpy did not show important differences for all the studied materials. Nevertheless, it should be highlighted that the melting enthalpy of PP0 sample was clearly higher than those obtained for the active materials. In this sense, crystallinity, % (%), of samples was calculated according to equation (1) to evaluate if the addition of thymol and carvacrol could alter the crystallization behavior of PP. A higher value for %(%) was determined for the PP0 sample. Therefore, it could be concluded that the PP crystallinity decreases significantly with the addition of thymol and carvacrol. This decrease in crystallinity could be due to the interactions between the polymer matrix and the additive molecules in the PP macromolecular network. A similar effect was reported for PP with the addition of some commercial synthetic antioxidants, such as Irgafos 168 and Irganox 1010 [38].
Table 2 - TGA, DSC and OIT parameters obtained for all samples
Sample Tmax (°C) Tc (°C) Tm (°C) AHc (J g-1)
PP0 461 119 161 95.2
PPC8 462 118 161 89.2
PPT8 462 115 159 88.9
AHm (J g-1) % (%) OIT OIT
Sample (min) Oxygena (min) Aira
PP0 99.1 72 0.9 ± 0.3 1.3 ± 0.4
PPC8 48.1 38 8.5 ± 1.0 20.7 ± 2.8
PPT8 49.5 39 15.4 ± 1.7 38.8 ± 0.6
a mean ± SD (n = 3).
Evaluation of the oxidation induction time (OIT)
The determination of OIT is considered a simple, reliable and fast method for the evaluation of the antioxidants efficiency [39], corresponding to relative measurements of the materials stability against oxidation. The evaluation of the antioxidant performance of carvacrol and thymol in PP is important since they are supposed not only to play the role of active additives for food, but also to protect the polymer to oxidative degradation during processing and use.
The evaluation of OIT was carried out in two different atmospheres. Air was selected to get a similar situation to the real conditions during materials processing or food shelf-life, while the use of pure oxygen would represent the most aggressive conditions for oxidative degradation. Table 2 shows the results obtained for OIT in both atmospheres.
In both cases it was confirmed the higher efficiency of thymol as an antioxidant when compared to carvacrol. This behavior was also reported by other authors who demonstrated that the antioxidant efficiency of thymol was higher in sunflower oil samples [40]. In the case of air atmosphere, as expected, OIT
values were higher than those obtained in pure oxygen atmosphere, since the experiment under air is less aggressive to materials [41].
In all cases, the increase in OIT values for PP with additives showed the existence of certain antioxidant effect after processing. These results are an additional confirmation that certain amounts of thymol and carvacrol are still remaining in all formulations after processing and they would be able to be released from the material to foodstuff as active additives.
Study of the effectiveness of the active films to preserve perishable food
Observation of fungal growth
This study was conducted to evaluate the antimicrobial activity of the developed films and their ability to act in active packaging formulations to increase the fresh food shelf-life. It was based on the visual observation of the inhibition of the fungal growth on food samples by the action of the volatile active additives, carva-crol and thymol. In this sense, some studies by other authors showed the effectiveness of these compounds against different fungal strains of particular interest in the food industry [15].
Figure 2 shows the appearance of sliced strawberries and bread samples at the beginning of the experiment (day 0) and after the observation of microbial growth. Regarding strawberries, satisfactory results were obtained for samples in contact with the films with additives, since no fungal growth was observed until six days of storage. In the case of strawberries in contact with the pure PP film (PP0), a rapid growth of microorganisms was observed at the third day of treatment.
On the other hand, the presence of microorganisms was observed in bread samples in contact with the PP0 film after 13 days of storage, in contrast with bread with the films with additives where no evidence of microbial contamination after 45 days of storage was observed.
However, it was noticed that strawberries lost their organoleptic properties in a few days, even before the visual evidence of fungal growth, when they were cut and stored. For this reason this study was also conducted for uncut strawberries (Figure 3). For the PP0 film microbial growth was observed after 6 days of storage. However, strawberries in contact with the film containing 8 wt% of thymol (PPT8) remained unaltered after 13 days. At this storage time strawberries presented a physical deterioration due to the experimental storage conditions, but it is important to highlight that microbial growth was not observed until the end of the study (15 days).
Similar studies were performed with uncut strawberries by other authors, getting satisfactory results for samples in contact with films treated with essential oils, such as cinnamon, oregano and thyme [18]. Regarding thyme and oregano essential oils, their antimicrobial activity is due to the high amount of carvacrol and thymol in their composition [42]. Other studies conducted in different fruits and vegetables also demonstrated the effectiveness of the constituents of different essential oils (eugenol, thymol, menthol or eucalyptol) to improve the organoleptic quality of food as well as to
reduce the microbial growth, by using also a modified atmosphere [43].
Fig. 2 - Study of the effectiveness of PPO and active films containing 8 wt% of thymol (PPT8) to preserve cut bread and strawberries by observation of fungal growth
In conclusion, results obtained from food samples in contact with PP films containing carvacrol and thymol evidenced the effectiveness of these compounds to improve the shelf-life of perishable food, such as strawberries and bread. Accordingly, these results also indicated the potential to use the developed films in active packaging systems to replace the direct addition of preservatives in food formulations.
Fig. 3 - Evaluation of the effectiveness of PPO and active film containing 8 wt% of thymol (PPT8) to preserve uncut strawberries by observation of fungal growth
Headspace analysis by HS-SPME-GC-MS
Figure 4 shows the levels of carvacrol, in terms of peak area counts, reached in the headspace of the
containers with bread slices after 0, 2, 5, 10 and 15 days of storage at room temperature. As it can be seen, an increase in the amount of carvacrol released from the PP films was observed with time for the bread samples. A high release of carvacrol was observed at 2 days, being released more slowly after 5, 10 and 15 days of storage. This mechanism of controlled release could lead to shelf-life improvement of the stored samples retarding the post-harvest deterioration. This behavior was also observed for strawberries. Regarding the thymol release, a similar trend was shown for both test food samples.
Equilibrium modified atmosphere packaging (EMAP) is the most commonly used packaging technology to reduce the high respiration rate of strawberries. It is known that a suitable atmosphere composition can reduce the respiration rate of fruits and fungal growth with minimal alteration of organoleptic properties [24]. In this sense, Table 3 shows the compounds identified in the headspace of strawberries with PP0 films after 4 days. One of the most important processes occurring during fruit ripening is the increase in volatiles contributing to fruit aroma and flavor. The major volatiles identified for strawberries stored at room temperature include methyl-isopentanoate, 2-methyl-butylacetate, methyl-hexanoate and hexyl-acetate. The compounds methyl-butanoate and methyl-hexanoate were also found in the headspace composition of refrigerated strawberries at 4 °C. These results are in accordance with those obtained by other authors when studying volatile compounds in the same food samples [24, 35].
The addition of thymol and carvacrol to PP films significantly modified the initial atmosphere composition inside packages during the storage of food samples due to their release from the film. This fact could be related to the inhibition of the volatile identified compounds (Table 3) that did not were detected in samples in contact with PPT8 and PPC8 films after 4 days of storage.
On the other hand, ethanol was the main volatile found in the headspace of bread in contact with the PP0 film and stored at room temperature for 4 days. This compound was resulting from fermentation and/or lipid oxidation as it has been reported by other authors [27](Poinot et al, 2007). In this sense, commercial bread samples in contact with PPT8 or PPC8 films after 4 days of storage were characterized by significantly lower amounts of ethanol, suggesting a reduction on the lipid oxidation reactions by the presence of thymol and carvacrol. The improvement on the oxidative stability of bread could be attributed to the release of carvacrol and thymol increasing the shelf-life of bread.
From these results, it can be concluded that the release of both additives from active films to the headspace of the studied packaged foodstuff increased with the storage time, as expected. The volatiles profile obtained by HS-SPME-GC-MS was found to be different for samples in contact with PP0 and those with PPT8 and PPC8, due to the modification of the food headspace composition by the presence of these additives. Therefore, the release of thymol and carvacrol from the active PP films has shown to be effective in maintaining the quality of strawberries and bread during different storage conditions. Finally, it can be concluded that PP
films with carvacrol and thymol could be a promising alternative to increase the shelf-life of different foodstuff.
Conclusions
Carvacrol and thymol have demonstrated their potential to be used as active additives in PP films for food packaging applications by their controlled antimicrobial release to foodstuff and also by the possibility to protect food from degradation processes. The addition of carvacrol and thymol did not significantly affect the thermal behavior of PP, but they modified the material cristallinity. PP films containing carvacrol and thymol showed a significant increase in OIT values, indicating that the polymer is well stabilized and a certain amount of these compounds remained in the polymer matrix after processing at relatively high temperatures. In this sense, these additives could be furthermore released from the material playing their role as antimicrobial additives. Therefore, it could be concluded that the addition of antimicrobial additives as carvacrol and thymol at 8 wt% to PP shows potential to improve the food quality and safety.
Acknowledgments
Authors would like to thank Ashland Chemical Hispania for kindly supplying ECOLEN HZ10K PP (Hellenic Petroleum). Marina Ramos would like to thank University of Alicante (Spain) for UAFPU2011-48539721Spredoctoral research grant.
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1E+10
9E+09
SE+09
7E+09
6E+09
5E+09
4E+09
3E409
2E+09
1E+09
0
20
Bread stored at 100111 temperature with PPC films
----DayO
----Day 2
----Day ?
----Day 10
----Day 15
Bread stored at room temperature with PPC8 films
Days of study Abundance*109
0 644
2 1086
5 1443
10 1616
15 2178007A
22
24 26
Time (mill)
2S
30
Fig. 4 - Release of carvacrol in the headspace of bread slices after 0, 2, 5, 10 and 15 days of storage at room temperature
Table 3 - Identified compounds present in the headspace of food samples packed with PP0 films after 4 days
Bread stored at room temperature Strawberries stored at room temperature Strawberries refrigerated at 4 °C
Time (min) Compound 1.4 Ethanol 5.7 2,4-dimethylheptane 6.6 2,4-dimethyl heptene 7.8 Isononane 13.0 4-methyloctane Time (min) Compound 3.2 Methyl isopentanoate 5.8 2-methyl butylacetate 7.4 Methyl hexanoate 10.6 Hexylacetate Time (min) Compound 1.9 Hexane 3.1 Methylbutanoate 3.9 Toluene 6.8 Isopropyl butyrate 12.2 Methyl hexanoate
© Marina Ramos - Analytical Chemistry, Nutrition & Food Sciences Department, University of Alicante, Alicante, Spain; Ana Beltran - Analytical Chemistry, Nutrition & Food Sciences Department, University of Alicante, Alicante, Spain; Arancha Valdes -Analytical Chemistry, Nutrition & Food Sciences Department, University of Alicante, Alicante, Spain; Mercedes A. Peltzer - Analytical Chemistry, Nutrition & Food Sciences Department, University of Alicante, Alicante, Spain; Alfonso Jimenez - Analytical Chemistry, Nutrition & Food Sciences Department, University of Alicante, Alicante, Spain; Maria C. Garrigos - Analytical Chemistry, Nutrition & Food Sciences Department, University of Alicante, Alicante, Spain; A. M. Kochnev - Kazan national research technological university, [email protected]; G. E. Zaikov - Institute of bio-chemical physics, Russian Academy of Science.
