Development and Characterization of Films for Food Application Incorporating Porphyran Extracted from Porphyra dioica

: Non-biodegradable plastic is one of the biggest environmental problems of our lifetime and, considering the present societal needs, it will get worse. Consequently, there is an urgent need to develop sustainable and renewable alternatives to plastic, such as plastic-like materials obtained from biodegradable polymers, namely sulfated polysaccharides, considered one of the most viable alternatives. There is also a need to obtain these materials in an environmentally and economically sustainable way. The hereby developed process of obtaining ﬁlm-forming solutions from semi-reﬁned porphyran (PorphSR) uses a green solvent (hot water) with a high extraction yield of semi-reﬁned porphyran (26.66 ± 0.27%) in a reproducible way and with low levels of contaminants. The obtained semi-reﬁned porphyran showed good antioxidant potential in all tests performed: HPSA ( ∆ 0.066 ± 0.002), DPPH (2.23 ± 0.78%), FRAP (0.420 ± 0.014 eq. ascorbic acid µ g mg − 1 of extract) and ABTS (20.46 ± 0.90%). After being cast into ﬁlms, the most notable antioxidant properties were those of the semi-reﬁned porphyran in the DPPH, FRAP and ABTS assays and of the pectin, (PorphSR_PcT and PorphSR_PcT_Gly) in the HPSA assay. Morphologically, the ﬁlms showed relatively homogeneous and low roughness surfaces. It is concluded that the described method to obtain semi-reﬁned porphyran is feasible and reproducible, and that the developed ﬁlms, mainly PorfP2_PcT_Gly, proved to be a potential candidate for non-biodegradable plastic substitutes.


Introduction
Petroleum-derived plastic is a virtually non-degradable anthropogenic compound, and its residues constitute one of the biggest environmental problems of our time [1]. It is non-biodegradable due to its long-chain polymeric structure, lacking a functional group susceptible to microbial degradation, high molecular weight, hydrophobicity and crystallinity [2].
Due to its diverse applications, there has been a 20-fold increase in production over five decades since 1964, reaching 335 million tons in 2015 [2], with a forecast of doubling by 2038 and nearly quadrupling by 2050 [3]. The largest consumption sector is packaging, with special relevance to the food industry [4].
Plastic debris is a threat to marine life and a growing environmental problem that occurs on a global scale [5,6]. The main threats of macroplastics arise from ingestion, leading to the obstruction of the digestive and/or respiratory systems, and entanglement in plastic Porphyra dioica J. Brodie and L. M. Irvine 1997 is a species native to the North Atlantic coast that occurs from the northeast coast of the United States of America to the northwest of Portugal in the intertidal zone [34,35]. It grows in a relatively wide range of conditions, such as temperature, photoperiod and light intensity [36], and due to its fast growth and high absorption of nitrates, phosphates and carbon dioxide, this species has a high potential for bioremediation, allowing its use in multitrophic culture systems [37,38] with fast biomass production at a low cost [39].
Structurally, porphyran ( Figure 1) consists of (1,3-β) D-galactose residues alternating with (1,4-α) L-galactose-6-sulfate or 3,6-anhydrous-α-L-galactose, and substitutions with sulfate ester residues may occur [40]. Sulfate groups represent 10-11% of dry biomass weight [41]. Like alginate and carrageenan, porphyran is an anionic hydrocolloid, from which it is possible to obtain films from filmogenic solutions using water as a solvent; however, according to the published results, its application in food packaging is still underexploited, as shown by the limited number of reports in the literature. As stated, the present study develops a new method of porphyran extraction from Porphyra dioica, using a small volume of water, with a high yield and ease of scaling up, resulting in biodegradable porphyran-based films with antioxidants properties that can be used in dry food with high lipid content packaging, such as chocolate cereals, in which lipid oxidation and water absorption are the main factors responsible for shelf life reduction.
About 15 g of dry powdered Porphyra dioica (≤0.25 mm) (ALGAplus, Ílhavo, Aveiro, Portugal) were distributed on three sheets of absorbent laboratory paper and rolled up to form a cartridge. These were moistened and placed in the Soxhlet extractor. In a 1000 mL collector, 500 mL of distilled water and ceramic chips were placed. The extraction solvent was heated to boiling point with a heating mantle set to about 200 °C at 7-h intervals, with rest periods overnight. After this rest period, the contents of the collector were recovered, and this process was repeated for two days. The contents of the collector corresponding to the first 1-h extraction were discarded.
The contents recovered from the collector were heated to approximately 100 °C and filtered with a 90 mm quantitative 2240 filter paper (Filter-Lab, Laval, QC, Canada) under vacuum and evaporated in a rotary evaporator at 60 °C, 260 rpm and 20 mbar until a thick, very viscous mass is formed. Then, 400 mL of 90% isopropanol was added, allowed to precipitate, decanted, and 200 mL of 99.9% isopropanol were added (Carlo Erba, Milan, Italy). The contents were fragmented in a blender and filtered with a 90 mm quantitative 2240 paper filter under vacuum. The content present in the filter was washed with the addition of small volumes of isopropanol, recovered and placed in an oven at 60 °C for 24 h to remove all solvent residues.

p-Benzoquinone Assay
Protein quantification was performed using the p-Benzoquinone method, adapted from Amin and El-Didamony (2003) [42]. The reaction was mediated by phosphate buffer Like alginate and carrageenan, porphyran is an anionic hydrocolloid, from which it is possible to obtain films from filmogenic solutions using water as a solvent; however, according to the published results, its application in food packaging is still under-exploited, as shown by the limited number of reports in the literature. As stated, the present study develops a new method of porphyran extraction from Porphyra dioica, using a small volume of water, with a high yield and ease of scaling up, resulting in biodegradable porphyranbased films with antioxidants properties that can be used in dry food with high lipid content packaging, such as chocolate cereals, in which lipid oxidation and water absorption are the main factors responsible for shelf life reduction.
About 15 g of dry powdered Porphyra dioica (≤0.25 mm) (ALGAplus, Ílhavo, Aveiro, Portugal) were distributed on three sheets of absorbent laboratory paper and rolled up to form a cartridge. These were moistened and placed in the Soxhlet extractor. In a 1000 mL collector, 500 mL of distilled water and ceramic chips were placed. The extraction solvent was heated to boiling point with a heating mantle set to about 200 • C at 7-h intervals, with rest periods overnight. After this rest period, the contents of the collector were recovered, and this process was repeated for two days. The contents of the collector corresponding to the first 1-h extraction were discarded.
The contents recovered from the collector were heated to approximately 100 • C and filtered with a 90 mm quantitative 2240 filter paper (Filter-Lab, Laval, QC, Canada) under vacuum and evaporated in a rotary evaporator at 60 • C, 260 rpm and 20 mbar until a thick, very viscous mass is formed. Then, 400 mL of 90% isopropanol was added, allowed to precipitate, decanted, and 200 mL of 99.9% isopropanol were added (Carlo Erba, Milan, Italy). The contents were fragmented in a blender and filtered with a 90 mm quantitative 2240 paper filter under vacuum. The content present in the filter was washed with the addition of small volumes of isopropanol, recovered and placed in an oven at 60 • C for 24 h to remove all solvent residues.

p-Benzoquinone Assay
Protein quantification was performed using the p-Benzoquinone method, adapted from Amin and El-Didamony (2003) [42]. The reaction was mediated by phosphate buffer at pH 9.2, composed of anhydrous monobasic sodium phosphate (Amresco, Solon, OH, USA) and pH adjusted with NaOH. A solution of p-benzoquinone (Sigma-Aldrich, St. Louis, MO, USA) to 1 mg·mL −1 (p-BQ) in phosphate buffer at pH 9.2. The external standard was obtained by diluting a solution of an amino acid, in this case L-alanine (PanReac AppliChem, Castellar del Vallès, Barcelona, Spain), to 0.3 mg·mL −1 in phosphate buffer at pH 9.2. The samples were prepared in phosphate buffer at pH 9.2 at a concentration of 0.6 mg·mL −1 . The HCl (VWR Chemicals, Radnor, PA, USA) solution 2.5 M was prepared in ethanol 96%. The calibration concentrations were 30-5 µg·mL −1 and 0 µg·mL −1 . Samples were prepared at an initial concentration of 0.6 mg·mL −1 . Then, 1 mL of p-BQ was added to 2 mL of the sample or standard solution that immediately after was kept in a 50 • C bath for 15 min. Finally, 3 mL of 2.5 M HCl were then added, and the absorbance at 467 nm was read. All measurements were performed in three independent trials and triplicate. Sample results were interpreted based on the L-alanine standard calibration curve.

Phenol-Sulfuric Acid Method
The quantification of galactose was performed using the phenol-sulfuric acid method, adapted from Rao and Pattabiraman (1989) [43]. The initial concentration of the phenol solution, 10 mg·mL −1 , was prepared from phenol crystals (Fisher Scientific, Waltham, MA, USA). The external standard was obtained throughout dilutions of D-galactose (VWR, Radnor, PA, USA) 0.6 mg·mL −1 in distilled water. Samples were prepared in distilled water at 0.6 mg·mL −1 . The calibration concentrations were 45-7.5 µg·mL −1 and 0 µg·mL −1 . To 0.6 mL of samples or of standard solution, 1.8 mL of 95% sulfuric acid (VWR, Radnor, PA, USA) and 0.6 mL of phenol solution were added, and then, after the exothermic reaction ended, 5 mL of distilled water were added, and the resulting solution was read at 495 nm absorbance. The 495 nm absorbance of the samples was also measured with H 2 SO 4 and distilled water in the proportions described, replacing the phenol solution with distilled water, and this absorbance was subtracted from the previous values. All measurements were performed in three independent trials and in quadruplicate. Sample results were interpreted based on the D-galactose standard calibration curve.

Quantification of Total Phenols (QTP)
The quantification of total phenols (QTP) was determined with the Folin-Ciocalteu (F-C) reagent (AppliChem, Darmstadt, Germany) based on the method by Fu et al. (2010) [44]. Calibration was obtained using a solution of gallic acid (Merck KGaA, Darmstadt, Germany) at 0.1 mg·mL −1 with the following concentrations: 6-1 µg·mL −1 and 0 µg·mL −1 . Sample solutions at 2 mg·mL −1 in distilled water were prepared. The F-C reagent was diluted 1:10 in water, and the sodium carbonate solution (Scharlau, Sentmenat, Barcelona, Spain) was saturated to 75 mg·mL −1 . The analysis was performed by mixing 0.5 mL of the sample or standard solution and 2.5 mL of diluted FC reagent, followed by the addition of 2 mL of sodium carbonate to the mixture after 4 min. The reaction allowed to run for 2 h at room temperature. After this period, the absorbance at 760 nm was read. All measurements were performed in three independent trials and in triplicate. Sample results were interpreted based on the gallic acid standard calibration curve.

Hydrogen Peroxide Scavenging Assay (HPSA)
The hydrogen peroxide scavenging assay was adapted from Bektaşoǧlu et al. (2008) [45]. A solution of sodium iron(III) ethylenediaminetetraacetate (NaFeEDTA) and methyl red was prepared by dissolving 0.251 g of NaFeEDTA, formed by the addition of ethylenediaminetetraacetic acid disodium salt dihydrate (VWR Chemicals, Radnor, PA, USA) and chloride of Iron (III) (Labkem, Barcelona, Spain) in a saturated solution of methyl red (Ika, Radnor, PA, USA), 12 mg in 500 mL of distilled water and 0.2 mL of acetic acid (VWR Chemicals, Radnor, PA, USA), which was filtered with a quantitative paper filter 2240.
The preparation of the samples for analysis consisted of mixing 1 mL of the polysaccharide stock solution at 0.6 mg·mL −1 and 1.8 mL of the NaFeEDTA/methyl red/acetic acid solution with 0.2 mL of 30% hydrogen peroxide (Chem-Lab, Zedelgem, Belgium). The sample was homogenized, and the absorbance at 524 nm was measured immediately at t = 0 min and t = 10 min. The change in absorbance after 10 min was determined by subtracting the referred values. All measurements were performed in three independent trials and in quadruplicate.
Then, 2 mL of DPPH were added to 0.05 mL of samples or standard solution. The reaction took place in the dark at room temperature, and after 30 min the absorbance at 517 nm was read. All measurements were performed in three independent trials and in triplicate. The %Inhibition (mg −1 of the sample) was determined using the equation %Inhibition mg −1 of sample = Abs t0min 517nm −Abs t30min 517mn Abs t0min 517nm × 100 m Sample mg (1)

Ferric-Reducing Antioxidant Power (FRAP)
The ferric-reducing antioxidant power assay was adapted from Berker et al. (2007) [47]. In preparing the standard, a solution of ascorbic acid (Villassar de Dalt, Barcelona, Spain) at 0.292 mg·mL −1 in distilled water was used. The samples were prepared in distilled water at a concentration of 0.6 mg·mL −1 .
The calibration concentrations changed from 2.60 µg·mL −1 to 0.65 µg·mL −1 and 0.00 mg·mL −1 . The reaction was carried out using 1 mL of samples or standard solution, 1.5 mL of distilled water and 0.5 mL of Fe(1,10-phenanthroline) 3 Cl 3 reagent, (1,10phenanthroline monohydrate, Sigma-Aldrich, St. Louis, MO, USA, FeCl 3 ·6H 2 O, Sigma-Aldrich, St. Louis, MO, USA) at 3.3 mM. The reaction took place in the dark at room temperature, and after 30 min, 6 mL of distilled water was added and the absorbance at 510 nm was read. All measurements were performed in three independent trials and in triplicate. Sample results were interpreted based on the ascorbic acid standard calibration curve.
The reaction medium consisted of 2 mL of ABTS reagent, 2 mL of sample or standard solution and 2 mL of distilled water. The reaction occurred in 1 min and its absorbance spectra from 500 to 850 nm was read immediately after this period; the procedure was modified from Pellegrini et al. (1999) [48]. All measurements were performed in three independent trials and in triplicate. The %Inhibition·mg −1 of the sample was determined using the equation Abs t0min 734nm × 100 m Sample mg (2)

Film Formulation
The films were produced by a casting process adapted from (Nieto, 2009) [49]. Filmogenic solutions were developed from the semi-refined porphyrane (PorphSR) described above, sodium carboxymethylcellulose (CMC) (Fluka, Buchs, St. Gallen, Switzerland), food pectin (PcT) (Sosa, Moià, Barcelona, Spain), sodium alginate (AL) (VWR, Radnor, PA, USA), 86-88% glycerol (Scharlau Chemie SA, Sentmenat, Barcelona, Spain) and calcium chloride (CaCl 2 ) (Chem-Lab, Zedelgem, East Flanders, Belgium) in the proportion described in Table 1 and dissolved in distilled water at 100 • C. After complete dissolution the solutions were filtered with quantitative 2240 paper filter under vacuum, and, as applicable, glycerol was added. After filtration, the filmogenic solution remained for 1-2 h at approximately 100 • C with constant agitation, after which 25 mL of filmogenic solution was applied to the molds of 56.74 cm 2 (25 mL, 0.44 mL·cm −2 ). The molds with the solution remained under vacuum for 20-60 min and then were placed in a UF 110 oven (Memmert, Büchenbach, Roth, Germany) at 40 • C and 10% ventilation capacity for 18-20 h. Afterwards the mold was placed on a surface at approximately 60 • C, and the film was removed. Table 1. Composition of film-forming solutions by components, semi-refined porphyran extracted by the Sohxlet method, sodium carboxymethylcellulose (CMC), pectin (PcT), sodium alginate (AL) and glycerol (Gly).

Electron Microscopy
The films were analyzed by field emission scanning electron microscopy (FEG-SEM, JSM-7001F, JEOL, Tokyo, Japan). Samples were previously coated with an Au-Pd alloy to avoid an accumulation of electrical charge during observation.

Mechanical Tests
Tensile tests were performed on a universal electromechanical testing machine (IN-STRON, 5544, Norwood, MA, USA), equipped with a 100 N load cell (INSTRON) and a video strain gauge (INSTRON, SVE I, Norwood, MA, USA). Tests were carried out until sample fracture with a speed of 1 mm/min. Both the Young's modulus and the sample ultimate tensile stress (UTS) were calculated according to ASTM D638 (Standard Test Method for Tensile Properties of Plastics). At least 3 (n = 3 . . . 6) samples with 15 mm width and 55 mm gauge length (over 95 mm long) were used per film composition. Sample thickness (between 25 and 59 µm) was determined using the Archimedes method.

Sensory Analysis
In the present study, chocolate cereal balls (Dia, Las Rozas, Madrid, Espanha), which have high lipid content as intended, were packaged in the test films (PorphP2_AL_Gly, PorfP2_PcT_Gly e PorfP2_CMC_Gly) and in the control film (polyethylene) for 2 months. The samples were subsequently submitted to a triangular sensory analysis test in which 12 untrained tasters have participated. This was followed by the methodology described by Meilgaard, Carr e Civille (1999) [50]. Each participant was asked to taste sets of 3 samples, two being the same and one different, to determine differences between samples. Six replicates were used with porphyran films per taster with random order and three replicates with the control. All samples were compared with each other and with the control.

Statistical Treatment
Statistical analysis was performed using ANOVA tests with one factor; in the case of statistically significant differences, the Tukey multiple comparison test was performed. The tests have a significance of 5% and were analysed by the GraphPad Prism 8.0.2 software. The graphical representations were made using the GraphPad Prism 8.0.2. Lowercase letters represent statistically significant differences; data with the same letters do not show Coatings 2022, 12, 148 7 of 16 statistically significant differences from each other and data that do not contain a letter do not show statistically significant differences with the negative control. Table 2 shows the porphyran extraction yield obtained by applying the extraction method developed from Porphyra dioica and the main components present. The yield obtained was 26.66% in algae dry weight; the protein content was below the detection limit; the concentration of D-galactose corresponded to 67.74% of the dry weight of the extract, and the presence of phenols was detected in 0.616 gallic acid equivalent µg·mg −1 of sample.

Antioxidant Potential
The antioxidant properties, determined by the described HPSA, DPPH, FRAP and ABTS methods, of the extract, PorphSR, of the remaining components of the films, food pectin (PcT), sodium carboxymethylcellulose (CMC), sodium alginate (AL) and glycerol 86-88% (Gly) and of the films produced (Table 1) are presented in Table 3, with all the samples being compared to a negative control. Lowercase letters represent statistically significant differences; data with the same letters do not show statistically significant differences from each other and data that do not contain a letter do not show statistically significant differences with the negative control.  Figure 2 shows surface features of the developed films.

Mechanical Tests
The mechanical properties (Young's Modulus and UTS), determined by the described methods, are presented in Table 4.

Mechanical Tests
The mechanical properties (Young's Modulus and UTS), determined by the described methods, are presented in Table 4.    Figure 3 shows the chocolate cereal balls packed with different films, namely PorphSR_CMC_Gly, PorphSR_PcT_Gly, PorphSR_AL_Gly and polyethylene (control). The data obtained was analyzed according to Meilgaard et al. (1999) [50]. Figure 4 represents, on the left, the number of correct answers in the identification of the different chocolate cereal ball originating from packages made with the produced films (different films between themselves) and, on the right, the number of correct answers in the identification of the different chocolate cereal ball originating from packages made with the produced films and the control (different films against the control), as well as the critical number of correct answers in the black column, which represents the number of correct answers from which the existence of perception of difference is identified with a significance of 5%.  Figure 3 shows the chocolate cereal balls packed with different films, namely PorphSR_CMC_Gly, PorphSR_PcT_Gly, PorphSR_AL_Gly and polyethylene (control). The data obtained was analyzed according to Meilgaard et al. (1999) [50]. Figure 4 represents, on the left, the number of correct answers in the identification of the different chocolate cereal ball originating from packages made with the produced films (different films between themselves) and, on the right, the number of correct answers in the identification of the different chocolate cereal ball originating from packages made with the produced films and the control (different films against the control), as well as the critical number of correct answers in the black column, which represents the number of correct answers from which the existence of perception of difference is identified with a significance of 5%.

Extraction Methods
The PorphSR yield obtained by the present process is very high, at 26.66%, as presented in Table 2, especially compared to other known methods with yields that vary from 6.24 to 17.6% of the initial dry weight [41,51,52]. The procedure for the extraction of PorphSR is reproducible, as the differences in yields, concentration of D-galactose and total phenols in the samples (Table 2) are not statistically significant.
Although the extraction process is reproducible, the extract has some contaminants. The presence of these substances in semi-refined porphyran extracts is due to the association of several compounds with porphyran molecules that make up the structure of the cell wall, as it has a complex and heterogeneous structure [29]. The presence of phenols was detected at a level of 0.616 equivalents of gallic acid µg·mg −1 of extract, however, the method used, QTP with Folin-Ciocalteu reagent, despite being widely used, is based on the oxidation of compounds with sufficient reducing character, thus not being a detection reaction unique to phenols and opening up the possibility of interference from other compounds [53]. The samples show a negligible degree of protein contamination, and when compared with the extraction procedure described by He et al., 2019, with a protein concentration between 1.1-0.4%, are lower. The D-galactose concentration of 67.74% in dry weight is close to the expected for pure porphyran [54], since this is the monomer of the porphyran structure (residues (1,3-β) D-galactose alternating with (1,4-α) L-galactose-6-sulfate or 3,6-anhydro-α-L-galactose) [40].

Antioxidant Potential
In the analysis of antioxidant activity of the polysaccharide extract, it was necessary to take into consideration the antioxidant activity against various types of oxidants, from reactive oxygen species (ROS) generated from hydrogen peroxide to milder single-electron oxidants such as the DPPH and ABTS radicals [55]. Alcohols and phenols can exhibit radical scavenging activity, with phenols being typically more effective reducing agents than aliphatic alcohols, thus being reactive towards milder oxidants such as DPPH and ABTS radicals [56]. Porphyran, being a polysaccharide, was expected to present some degree of antioxidant activity, on account of the alcohol groups that are part of the polymeric structure. The extent of the antioxidant activity of the porphyrans described herein was assessed by HPSA, DPPH, FRAP and ABTS methods (Table 3).
Some carbohydrates, such as carrageenan [57] and glucose [58], have antioxidant potential against ROS of H 2 O 2 origin. Regarding the tested porphyrans, it was observed that PorphSR, shows antioxidant potential when compared to the control. As mentioned earlier, this antioxidant activity can be assigned to the presence of alcohol functional groups on the polysaccharide structure and is analogous to the radical scavenging activity exhibited by simple alcohols [59]. The antioxidant action can be the result from the transfer of H + cations to OH• or the uptake of O 2 -• [60]. These are the main oxidation promoting species in organisms and greatly impact their health.
In the HPSA assays, it was observed that PorphSR, pectin and glycerol presented some antioxidant activity against ROS generated from the NaFeEDTA-promoted decomposition of H 2 O 2 when compared to the control reaction [61]. In the case of pectin, the antioxidant activity against ROS was superior to that of glycerol and porphyran; however, it should be noted that the pectin used was food grade, and it also contained glucose, sodium acid pyrophosphate and tricalcium phosphate, which can contribute to the overall radical scavenging potential [55]. In the case of sodium carboxymethylcellulose, sodium alginate and the respective composites with porphyran, oxidation was only slightly suppressed or even promoted. This was probably due to alkaline carboxylate groups that promote the deprotonation of hydrogen peroxide, increasing the formation of HOO -, resulting in an increased prevalence on uncontrolled Fenton reactions [62,63].

DPPH (2,2-Diphenyl-1-Picrylhydrazyl) Radical Scavenging Activity
In the DPPH method, the PorphSR extract showed antioxidant potential (2.23%). The remaining components and the films did not show statistically significant differences from the control.

Comparative Analysis of the Different Assays
In the DPPH, FRAP and ABTS tests, the only component that shows statistically significant differences, with a significance of 5% for the control, is porphyran, with a p-value less than 0.0001 in all tests. The other components (glycerol, CMC, sodium alginate and pectin) did not show discernible activity. The antioxidant potential of semi-refined porphyran stands out due to its observed antioxidant activity against DPPH, ABTS and the FRAP reagent. This bioactivity was not expected on sulfated polysaccharides such as porphyran, justifiable most probably by the presence of phenols and other secondary metabolites capable of undergoing single-electron transfer reactions [55]. Porphyran extracts are reported to have low antioxidant activity in one-electron donation assays such as DPPH, with less than a 2% inhibition rate at similar concentrations [64] and in ABTS an inhibition rate in the range of 1.5-2.8% [65]. Only in aqueous extracts with a high content of phenols was this activity found to be higher [66]. Thus, it is most likely that this action does not derive from porphyran itself but from other reducing molecules likely to be present in the extract, as porphyran has a complex and heterogeneous structure [29], as also noted above and as noted in the total quantification of phenols ( Table 2).
Another important point to emphasize is the importance of applying different tests to determine the antioxidant potential in order to account for all the different oxidation mechanisms occurring in each assay, the reaction stoichiometry, the reaction rate (DPPH and FRAP are slower than ABTS) and the method resolution (DPPH in different solvents). Therefore, by combining the different methods, a more complete antioxidant profile is obtained [67].
In accordance with the assays carried out with individual components, the films containing porphyran and pectin showed high antioxidant potential in HPSA.
The films prepared with CMC and AL exhibited antioxidant activities similar to the control reaction, which is consistent with the pro-oxidant activity of CMC and AL, mentioned earlier. The presence of glycerol had a negligible effect on the overall antioxidant activity. In DPPH scavenging assay, all samples presented low to no antioxidant activity. This contrasts with the activities observed in HPSA for porphyran, pectin and glycerol. There were no statistically significant differences between the control and the films PorphSR_PcT, PorphSR_PcT_Gly, PorphSR_CMC, PorphSR_CMC_Gly, PorphSR_AL and PorphSR_AL_Gly, in terms of DPPH scavenging activity. The low scavenging activity towards DPPH can be explained by the low reactivity of aliphatic alcohols towards this stable radical. For instance, methanol is a commonly used solvent in this type of assay. Since porphyran, Al, CMC and glycerol are also structurally alcohols, their lack of DPPH scavenging activity appears consistent with that exhibited by simpler alcohols.
It was observed that, in general, the films containing porphyran extract presented some antioxidant activity, although the composites presented a noticeably lower activity, most likely due to the lower porphyran content. Nevertheless, the antioxidant activity presented by PorphSR against ROS, ABTS and Fe(III), is sufficiently high so that composite films with a broad antioxidant activity could be successfully prepared.

Electron Microscopy
Porphyran films without added polysarides-PorphSR ( Figure 2a) and PorphSR_Gly ( Figure 2b) display a uniform microstructure and an apparently smoother surface. Observation at higher magnification shows that in the presence of glycerol the resulting structure consists in overlapping layers (Figure 2a). This probably results from differential drying shrinkage, caused by insufficient water in the matrix [68]. The addition of CMC to the semi-refined porphyran extract produces a uniform smooth film (Figure 2c). However, PorphSR_CMC_Gly displays biphasic microstructure (Figure 2d). The presence of a second phase is commonly associated with linear polymers: the simple and relatively short chains are able to wind, forming ordered crystallites in the amorphous martrix. This was possibly triggered by repulsion interactions with glycerol molecules [69]. Among the films without glycerol, PorphSR_PcT ( Figure 2e) and PorphSR_AL (Figure 2g) appear to display a higher surface roughness. This probably results from gas bubbles entrapped during drying of the high viscosity film-forming solutions. Scratches and small bubbles in PorphSR_CMC (Figure 2c), PorphSR_AL ( Figure 2g) and PorphSR (Figure 2a) films are probably due to irregularities in the moulds and to presence of small trapped gas bubbles, respectively.

Mechanical Tests
The mechanical properties, summarized in Table 4, show that adding glycerol to the films compositions leads to a Young's modulus decrease. PorphSR_Gly, PorphSR_PcT_Gly and PorphSR_AL_Gly films show a 61 ± 2% Young's Modulus reduction when compared with their counterparts, without added glycerol. Porphyran films without added polysarides (PorphSR) also displayed a reduced Young's Modulus (minus 29 ± 3%) when compared with the PorphSR_PcT and PorphSR_AL films.
Regarding films' tensile strength, no statistically significant differences were found between ProphSR_Pct and ProphSR_AL films with or without glycerol. Therefore, glycerol, while reducing the films' Young's Modulus, will not affect their tensile strength significantly.
As an exception to this behavior, glycerol effectively reduced the PorphSR film tensile strength and Young's Modulus. Without the addition of other polysarides, ProphSR_Gly film tensile strength decreased to 4.34 ± 0.78 MPa, possibly due to large distance between chains [70]. Table 4 also shows no differences between PorphSR_CMC and PorphSR_CMC_Gly films Young's Modulus and a significant reduction of the PorphSR_CMC film tensile strength. As seen in Figure 2d, a biphasic microstructure points to an absent interaction between glycerol and CMC. PorphSR_CMC films might then be unable to provide the necessary interactions between matrix components, reducing their mechanical properties [71].
These results show that both semi-refined porphyran and glycerol can be used to reduce the films Young's Modulus while affecting the UTS. They contribute to ramified structures, where interactions (hydrogen bonds, electrostatic and van der Waals interactions) between matrix components increase tensile strength and elasticity [72][73][74].
Overall, the PorphSR_PcT_Gly film provided the best mechanical properties, with the Young's Modulus and the UTS reaching 1629.00 ± 142.41 and 26.00 ± 5.92 MPa, respectively.

Sensory Analysis
The analysis of the results was based on Meilgaard et al. (1999), in which a number of correct answers were established according to the number of total answers so that sensory differences could be considered as detected by the taster (critical number of correct answers), since there was not, in any of the cases studied, Figure 4, a number of correct answers greater than the critical number, it was considered that there was no detection of sensory differences between the cereals packed with any of the films developed between them and between the control. Thus, after 2 months, there is no perceptible difference, neither between the films among themselves, nor in the comparison of films with the control. The chocolate cereal balls maintain crispness and show no change in flavor indicating that lipid oxidation is minimal, which may be due either to the antioxidant activity of the films or the barrier effect of the film. The crispness of cereals after two months also allows us to conclude that the permeability of films to water vapor is low.
Based on these preliminary tests we can infer that the developed films have the potential to replace polyethylene in the packaging of chocolate cereals; however, further testing is needed in order to determine maximum shelf-life, as well as repeat the sensory trials with a larger group of trained tasters, increasing the representativeness of the results.

Conclusions
PorphSR extraction is a method that allows the extraction of semi-refined porphyran from an abundant and easy-to-grow algae, Porphyra dioica, using a green solvent, hot water, with a high yield of 26.66%, a 67.74% galactose content and undetectable protein contamination. Additionally, the extraction procedure is reproducible and shows scale-up potential. It presents itself as an efficient and low-polluting extraction method from available and renewable raw materials. In the development of the films, the same principle was applied, establishing a process that uses only thermal energy in its preparation, with no application of a cross-linking agent, keeping the filmogenic solution as minimally complex as possible, resulting in the resistance of these films to moisture and broadening its scope of application. The main films developed, PorphSR_CMC_Gly, PorphSR_PcT_Gly and PorphSR_AL_Gly, showed good durability over the time they were analyzed (2 months), maintaining their chemical and physical properties, even when subject to changing atmospheric conditions. The film with the best performance was PorphSR_PcT_Gly, because its bioactivities were equivalent (DPPH, ABTS and FRAP) or higher (HPSA) than other filmogenic solutions. This film also displayed the best mechanical performance, combining the highest tensile strength with a low Young's modulus. The sensory analysis showed that the films developed based on porphyran have the potential to be used in the packaging of dry foods with a high lipid content. In order to consider these films as substitutes for common plastics in food packaging, it is necessary to carry out more tests, such as migration tests, determination of the water vapor permeability rate, O 2 and CO 2 permeability rates, and extend the mechanical characterization.