Sustainability Journal (MDPI)

2009 | 1,010,498,008 words

Sustainability is an international, open-access, peer-reviewed journal focused on all aspects of sustainability—environmental, social, economic, technical, and cultural. Publishing semimonthly, it welcomes research from natural and applied sciences, engineering, social sciences, and humanities, encouraging detailed experimental and methodological r...

Optimization of A Procedure to Improve the Extraction Rate of Biologically...

Author(s):

Alina Maier
Faculty of Food and Tourism, Transilvania University of Brasov, Castelului 148, 500014 Brasov, Romania
Vasile Padureanu
Faculty of Food and Tourism, Transilvania University of Brasov, Castelului 148, 500014 Brasov, Romania
Mirabela Ioana Lupu
Faculty of Food and Tourism, Transilvania University of Brasov, Castelului 148, 500014 Brasov, Romania
Cristina Maria Canja
Faculty of Food and Tourism, Transilvania University of Brasov, Castelului 148, 500014 Brasov, Romania
Carmen Badarau
Faculty of Food and Tourism, Transilvania University of Brasov, Castelului 148, 500014 Brasov, Romania
Cristina Padureanu
Faculty of Food and Tourism, Transilvania University of Brasov, Castelului 148, 500014 Brasov, Romania
Ersilia Alexa
Faculty of Food Engineering, University of Life Sciences “King Mihai I” from Timisoara, Calea Aradului 119, 300645 Timisoara, Romania
Mariana-Atena Poiana
Faculty of Food Engineering, University of Life Sciences “King Mihai I” from Timisoara, Calea Aradului 119, 300645 Timisoara, Romania


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Year: 2023 | Doi: 10.3390/su15086697

Copyright (license): Creative Commons Attribution 4.0 International (CC BY 4.0) license.


[Full title: Optimization of A Procedure to Improve the Extraction Rate of Biologically Active Compounds in Red Grape Must Using High-Power Ultrasound]

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[Summary: This page is the title page of a study on optimizing ultrasound to improve extraction of bioactive compounds from red grape must. It lists the authors, affiliations, publication details, and an abstract summarizing the study's aims, methods (RSM, CCD), results (increased TPC, MA, FRAP, DPPH), and optimized conditions.]

Citation: Maier, A.; Padureanu, V.; Lupu, M.I.; Canja, C.M.; Badarau, C.; Padureanu, C.; Alexa, E.; Poiana, M.-A. Optimization of A Procedure to Improve the Extraction Rate of Biologically Active Compounds in Red Grape Must Using High-Power Ultrasound Sustainability 2023 , 15 , 6697. https://doi.org/10.3390/ su 15086697 Academic Editors: Facundo Joaqu í n M á rquez Rocha, Izabela Michalak, Katarzyna Chojnacka, Jorge S. Olmos-Soto and Antoni S á nchez Received: 11 February 2023 Revised: 7 April 2023 Accepted: 13 April 2023 Published: 15 April 2023 Copyright: © 2023 by the authors Licensee MDPI, Basel, Switzerland This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/) sustainability Article Optimization of A Procedure to Improve the Extraction Rate of Biologically Active Compounds in Red Grape Must Using High-Power Ultrasound Alina Maier 1 , Vasile Padureanu 1, *, Mirabela Ioana Lupu 1 , Cristina Maria Canja 1 , Carmen Badarau 1 , Cristina Padureanu 1 , Ersilia Alexa 2 and Mariana-Atena Poiana 2, * 1 Faculty of Food and Tourism, Transilvania University of Brasov, Castelului 148, 500014 Brasov, Romania 2 Faculty of Food Engineering, University of Life Sciences “King Mihai I” from Timisoara, Calea Aradului 119, 300645 Timisoara, Romania * Correspondence: padu@unitbv.ro (V.P.); marianapoiana@usab-tm.ro (M.-A.P.); Tel.: +40-745-080-149 (V.P.); +40-726-239-838 (M.-A.P.) Abstract: The primary focus in the production of quality red wine is the extraction of grape components, which can be achieved in a variety of ways. This work investigates the extraction yield of biologically active compounds from crushed Merlot grapes, as a result of ultrasound treatment applied before maceration, and optimizes the process parameters of a laboratory scale using response surface methodology (RSM) within a central composite design (CCD) model. The two factors whose response was studied were amplitude (A) % and treatment time (t), while the dependent variables were the total phenolic compounds (TPC), monomeric anthocyanins (MA), and antioxidant activity expressed as ferric reducing antioxidant power (FRAP) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity. The results showed that the application of high-power ultrasound treatment to crushed grapes for a few minutes increased both the extraction rate of bioactive compounds and the antioxidant activity by a maximum of 12 times for the TPC, 14 times for the MA, 3.6 times for the FRAP value, and 18.77% for the DPPH. The optimized solution had an amplitude of 90% and a treatment time of 4 min and 24 s. The validation experiments yielded errors between—8.70% and 3.14%, confirming the proposed model. Thus, the RSM model is recommended as a tool to optimize a procedure for enhancing both the extraction rate of the bioactive compounds from grapes and the antioxidant properties of grape must. Our results demonstrate the ultimate benefits of using ultrasonic treatment on crushed grapes at the beginning of the winemaking process, as a highly effective technique for improving the extraction of high-value bioactive chemicals, with significant application potential Keywords: red grapes; bioactive compounds; antioxidant activity; ultrasound; extraction optimization procedure 1. Introduction Wine is a cultural emblem, whose function has evolved over time from being a vital source of sustenance to becoming a social and cultural accompaniment to food. The production of wine grapes of 33.8 million tons and the volume of wine produced globally in 2022, which was between 257.5 and 262.3 million hectoliters of wine, with a midpoint estimate of 259.9 million hectoliters, is anticipated to be comparable to the level seen in 2021. The worldwide output level can be regarded as somewhat below average for the fourth year in a row [ 1 ]. To satisfy the varied sensory preferences of consumers, it is essential to be able to manufacture several red wine types, and wine producers are continually changing their winemaking techniques to this end. When making high-quality red wine, the extraction of grape components, which can be conducted in a variety of ways, is the major focus [ 2 ]. Sustainability 2023 , 15 , 6697. https://doi.org/10.3390/su 15086697 https://www.mdpi.com/journal/sustainability

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[Summary: This page discusses the health benefits of phenolic compounds and anthocyanins in red wine. It highlights the limitations of conventional extraction methods and introduces ultrasound as a green technology. It explains the different categories of ultrasound and its applications in the enological sector, including improving wine quality and microbial control.]

Sustainability 2023 , 15 , 6697 2 of 22 Due to their numerous positive health benefits, including antioxidant properties, neuroprotective action, anti-inflammation, antiaging antimicrobial activity, and lowering arterial blood pressure, phenolic compounds have attracted a lot of interest by the scientific community and the general public in recent years [ 3 – 7 ]. Moreover, customers place a high value on the sensory quality of red wine’s color, preferring it to be a deep red. The primary pigments responsible for the young wines’ vivid red color are called anthocyanins, the main polyphenolics in red grapes [ 8 ]. The initial monomeric anthocyanin profile is an element that affects the ultimate color of the wine and, additionally, might have anti-cancer and anti-glycemic properties [ 9 ]. Because of the inherent drawbacks to conventional extraction techniques, the effective extraction of these chemicals from natural sources continues to be a significant issue. The rising need for novel technical solutions that can deliver the highest extraction yields, guarantee the stability of the target compounds, and also satisfy environmental requirements, has been sparked by the growing interest in natural antioxidants [ 10 ]. Due to its eco-friendly nature, non-toxic behavior, and low energy usage, ultrasound (US) may be regarded as a sustainable, green, and innovative technology [ 11 , 12 ]. There are several uses for it in food technology, including analysis, preservation, and homogenization, extraction, filtering, and drying. In order to achieve these objectives, ultrasound principally employs acoustic waves, which cause mechanical and chemical reactions. These reactions are fundamentally different from those produced by conventional methods. The main goals of this technology are to speed up processing, save energy, and improve the quality, safety, and shelf life of food products [ 12 , 13 ]. To sum up, this technique is a green alternative for this industry, as it does not use toxic solvents. Additionally, it supports economic sustainability through its use in efficient extraction procedures [ 14 ]. Ultrasound is divided into three categories: high frequency–low power US (between 1 and 10 MHz), intermediate frequency–medium power US (between 100 kHz and 1 MHz), and low frequency–high power US (between 20 and 100 kHz). Strong physical effects are primarily produced at a US frequency of about 20 kHz by fragmentary transitory cavitation, promoting bioactive chemical release from plant matrices during cell disruption [ 15 – 17 ]. The effect of low frequency may be related, not only to cavitation bubble size, but also to its effect on mass transfer resistance [ 13 ]. High-power US treatment on food matrices can cause physical, chemical, and biological changes, and a variety of uses have been documented [ 18 , 19 ]. Numerous studies have demonstrated that high-power ultrasound is becoming more prevalent in the enological sector due to its ability to enhance a wine’s organoleptic qualities, shorten processing times, and provide better microbial control in wines [ 20 – 22 ]. Furthermore, the International Organization of Vine and Wine has included ultrasonic treatment among the methods that can be used during winemaking [ 23 ]. Currently, adopting all the techniques designed to make color extraction and fragrance dissolution easier, throughout the winemaking process, is desired. Through the application of ultrasonic technology, the potential for the continuous extraction of qualitatively significant substances from the exocarp is explored. This is conducted by taking advantage of the phenomena caused by the transmission of ultrasound in a solid–liquid environment, such as grape must [ 13 ]. However, taking into account the fact that most research was carried out at the laboratory scale, and that the grape skins’ total phenolic content varies according to the cultivar, soil type, climate, region of origin, and cultivation techniques, we consider that it is vital to optimize the factors involved in this form of extraction in order to build a workable ultrasound-assisted large-scale procedure. The extraction efficiency using high-power US is significantly influenced by a variety of factors, such as the temperature of the samples, the power of the ultrasonic device, the process frequency, the treatment’s intensity, as well as the shape and size of the ultrasonic reactor [ 24 ]. Thanks to its reliable design, the statistical method known as response surface methodology (RSM) is currently widely utilized for optimization. The RSM is a collection of mathematical and statistical methods that are used to investigate the relationship between

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[Summary: This page continues discussing response surface methodology (RSM) for optimization. It states the objective of the study, which is to investigate the extraction yield of biologically active compounds from crushed grapes using ultrasound before maceration. It also lists the phytochemicals being tested such as TPC and MA, and the antioxidant activity.]

Sustainability 2023 , 15 , 6697 3 of 22 process input variables and outputs (responses). The methodology can be used for process optimization in a variety of circumstances and is relatively affordable, practical, and effective [ 25 ]. The objective of this work was to investigate the extraction yield of biologically active compounds from crushed grapes, as a result of an ultrasonic treatment applied during the first stages of the winemaking process, before maceration. In addition, the aim was to identify the optimized process parameters in terms of amplitude (A) % and treatment time (t) at the laboratory scale, as well as to develop a procedure that improves both the extraction rate of bioactive compounds from grapes and the antioxidant properties of grape must. To this end, we first evaluated the high-value phytochemicals, such as the total phenolic compounds (TPC), which are generally associated with the organoleptic properties of finished wines and (with) their stability. We also quantified the monomeric anthocyanins (MA), which are responsible for the red color of red wines. In addition, the antioxidant activity was assessed, from all the possible biological functions performed by V. vinifera compounds, both the ferric reducing antioxidant power (FRAP) and the 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity assays are probably the most important regarding human health 2. Materials and Methods 2.1. Grapes The Merlot variety employed for the experimental research is the second most planted grape variety in the world, well-known for producing high-quality wines [ 26 ]. The red grapes, vintage 2019, were hand-harvested (approximately 100 kg) from a vineyard in Prahova, Romania (Pietroasa-Istrita Viticulture and Winemaking Research and Development Station). The grapes were harvested at technological maturation when they reached 29.8 ◦ Brix, then quickly transported to the laboratory for processing. Only healthy, selected bunches of grapes were used for the experimental research 2.2. Ultrasonic Equipment The sonication of all the experimental tests was performed using a probe-type ultrasonic device (Sonics VCX-750, Sonics and Materials Inc., Newtown, CT, USA). The amplitude can be set as a percentage, between 10% and 100%. The device produces an ultrasonic power of 750 W and frequency of 20 kHz. The most typical frequencies utilized in the extraction procedures were between 20 and 100 kHz 2.3. Optimization Design The experimental design was developed with Design Expert ® software version 13 (Stat-Ease, Inc., Minneapolis, MN, USA, 2022), to optimize the number of experiments and operating conditions Based on the results of the single factor experiment, an optimization design was created. For these experiments, the RSM was used within a central composite design (CCD) model. The two factors whose response was studied were amplitude (A) % and treatment time (t). The high and low levels of each variable were determined by preliminary research that took place before carrying out of these experiments. The limits of the instrument were also taken into account when choosing the ranges for all the variables. The intensity and frequency of the waves were two of the most important operating parameters that affect the performance of ultrasound technology in extracting bioactive chemicals. The results of some studies indicated that the sonochemical effects in the treated fluids increase as the amplitude increases. Moreover, the amplitude varies over a wide range, from 20% to 90% [ 27 ], to determine the ideal extraction configuration, while other studies used treatment durations ranging from 2 to 10 min [ 28 , 29 ]. Furthermore, according to our preliminary research, there were no significant differences in the extraction of biologically active compounds between the control sample and the ultrasound-treated samples, when ultrasound was applied at low amplitude levels

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[Summary: This page details the materials and methods used in the study, including grape variety, ultrasonic equipment, and optimization design. It specifies the levels of independent variables (amplitude and sonication time) and dependent variables (TPC, MA, FRAP, DPPH). It also presents the equation used to choose the best statistical model.]

Sustainability 2023 , 15 , 6697 4 of 22 (from 30% to 50%) for a maximum treatment time of 5 min. The extraction temperature during ultrasound extraction was shown to be closely related to the extraction time, as it was found that longer extraction times resulted in higher extraction temperatures. Therefore, the extraction time selected should be within the appropriate range. However, it was found that a maximum extraction time of 5 min was necessary because high temperatures promote the oxidation and destruction of phenolic compounds Taking into account the aforementioned factors, the levels of the independent variables, such as percent amplitude (A) and sonication time (t), were selected at 50%, 70%, and 90% for the ultrasound time of 3, 4, and 5 min (Table 1 ), respectively. The dependent variables were the TPC, MA, and antioxidant activity, expressed as the FRAP and DPPH free radical scavenging activity Table 1. Ultrasonic extraction test treatment options Independent Variables Dependent Variables Probe Diameter (mm) Frequency (kHz) Amplitude (A) % Treatment Time (t) min 13 20 50 3 TPC 70 4 MA 90 5 FRAP DPPH To choose the best statistical model, such as linear, quadratic, and cubic models, the experimental data were examined based on the second-degree polynomial equation (Equation (1)): Y k = α 0 + n ∑ i = 1 α i X I + n ∑ i = 1 I X i + n ∑ i < j α ij X i X j (1) where Y k is the dependent variable, α 0 , α i , α ii , and α ij are the regression coefficients of the model, which are constants, and X i and X j are the independent variables of the model. Response surface plots were generated using the expected values from the fitted model. To illustrate the influence of the independent variables on each response, twoand three-dimensional contour plots were generated for each response 2.4. Sample Preparation For the laboratory tests, randomly collected grape samples (100 g) were destemmed, hand-crushed, and then treated using a probe-type ultrasonic device. The control sample (C) that was not subjected to ultrasound treatment was evaluated separately. The samples were treated in a 100 mL Pyrex glass beaker fitted with a counter-current water-cooling jacket The water used for cooling was kept at a constant temperature of 19 ◦ C. The positioning of the acoustic amplifier in the container was standardized at a distance of 20 mm from the bottom. At the end of the ultrasonic treatment, the samples were vacuum filtered (Nalgene Rapid-Flow Filter Units, 0.45 µ m PES membrane). The filtrate was collected in a vial and stored in a refrigerator at 4 ◦ C for further use. All extraction experiments were conducted in this manner 2.5. Total Polyphenolic Content and Anthocyanins Determination The total polyphenolic content (TPC) was determined by using the Folin–Ciocalteu spectrophotometric method, with gallic acid as a reference and expressed as micrograms of gallic acid equivalents per milliliter ( µ g GAE/mL) [ 30 ]. A 0.5 mL sample was treated with 1.25 mL of Folin–Ciocalteu reagent (Merck, Darmstadt, Germany), previously diluted 1:10 ( v / v ) with distilled water. After incubation for 5 min at room temperature, 1 mL Na 2 CO 3 60 g/L was added. A UV–VIS spectrophotometer (Specord 205, Analytik Jena Inc., Jena, Germany) was used to detect sample absorbance at 750 nm after 30 min of incubation at

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[Summary: This page continues the materials and methods section, describing sample preparation, including destemming, crushing, and ultrasonic treatment. It also details the methods used to determine total polyphenolic content (TPC), monomeric anthocyanins (MA), and antioxidant activity (FRAP and DPPH assays).]

Sustainability 2023 , 15 , 6697 5 of 22 50 ◦ C. The calibration curve was established using gallic acid as standard, at concentrations ranging from 5 to 250 µ g GAE/mL The monomeric anthocyanins (MA) were determined by the pH differential method [ 31 ]. Briefly, two dilutions of the same sample were prepared by adding 1 mL of wine to 14 mL of potassium chloride buffer (0.025 M, pH 1.0) and 14 mL of sodium acetate buffer (0.4 M, pH 4.5). After incubation for 15 min at room temperature, the absorbance was measured at 520 and 700 nm against deionized water. The results were expressed in milligrams of cyanidin-3-glucoside equivalents per liter (mg CGE/L). The total anthocyanin content of the samples was calculated using a molar absorption coefficient of 26,900 L/mol × cm and a molecular weight of 449.2 g/mol 2.6. Antioxidant Activity The antioxidant activity of the investigated samples was evaluated by FRAP and DPPH assays 2.6.1. FRAP Assay The protocol for the FRAP test was based on the method of Benzie and Strain [ 32 ]. For this purpose, 300 mM acetate buffer (pH = 3.6), 10 mM of 2,4,6-tris(2-pyridyl)-s-triazine (TPTZ) solution in 40 mM HCl, and 20 mM FeCl 3 × 6 H 2 O solution were used as stock solutions. The working solution was prepared by mixing 100 mL acetate buffer, 10 mL TPTZ solution, and 10 mL FeCl 3 × 6 H 2 O solution, which was then heated to 37 ◦ C before use. Prior to analysis, the wine samples were diluted 1:50 ( v / v ) with distilled water, then a 0.5 mL aliquot of diluted samples was allowed to react with 2.5 mL of working solution for 30 min at 37 ◦ C. The absorbance of the mixture was read at 593 nm against a blank sample obtained under the same working conditions. The results were expressed in µ mol of Fe 2+ equivalents per milliliter of grape must ( µ mol Fe 2+ /mL) 2.6.2. DPPH Assay The 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity of the samples was measured following the procedure described by Kalita et al. [ 33 ], with some minor adjustments. For this purpose, 20 µ L of each investigated sample was mixed in a microplate with 20 µ L of distilled water, after which the resulting mixture was combined with 200 µ L of a 120 mg/L DPPH radical solution prepared in 96% ( v / v ) ethanol. The microplate was left in the dark for 30 min, and the absorbance value (A sample) at 515 nm was measured against a blank of 96% ( v / v ) ethanol, using a plate reader (Tecan SunRiseTM, software MagellanTM, Tecan Group Ltd., Männedorf, Switzerland). The control was prepared under the same working conditions, containing 20 µ L of 96% ( v / v ) ethanol instead of the investigated sample. The absorbance of the control (A control) was read against 96% ( v / v ) ethanol The DPPH scavenging activity (%) was calculated according to Equation (2), as follows: DPPH scavenging activity (%) = [(A control − A sample )/A control ] × 100 (2) 2.7. Total Soluble Content and Acidity The total soluble solids (TSS, ◦ Brix) and the titratable acidity (TA, g/L of tartaric acid) were analyzed according to the standard procedure of Council Regulation EEC 2676/90 [ 34 ]. 2.8. Statistical Analysis All the measurements were performed in triplicate and the results are presented as mean ± standard deviation (SD). The Design Expert ® software version 13 (Stat-Ease, Inc., Minneapolis, USA, 2022) was used for the statistical analysis. Significant differences between the samples were assessed using a one-way ANOVA, with post-hoc analysis using the HSD Tukey test.

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[Summary: This page further describes the methods, focusing on the FRAP and DPPH assays for antioxidant activity. It includes equations for calculating DPPH scavenging activity. It also mentions the analysis of total soluble content and acidity, and the statistical analysis methods used (ANOVA, Tukey test, Pearson correlation). It then begins to present the results and discussion.]

Sustainability 2023 , 15 , 6697 6 of 22 The Pearson correlation coefficient between the total phenolic content, monomeric anthocyanins, and antioxidant activity was calculated using JASP software, version 0.17.1 (JASP Team, Amsterdam, The Netherlands, 2023) 3. Results and Discussion The effects of an ultrasonic pre-treatment to improve the extraction rate of polyphenols and, subsequently, to increase the antioxidant activity of several samples, with three replicates each, all from red grapes, the Merlot variety, vintage 2019, were followed in the laboratory. The experimental design provided for the randomized treatment of 13 samples with 3 repetitions each, with 5 central points, as shown in Table 2 . Table 2. Design of the central composite experimental model and results Std Order Run Order Factors Responses A (%) B (min) TPC ( µ g GAE/mL) MA (mg CGE/L) FRAP ( µ mol Fe 2+ /mL) DPPH Scavenging Activity (%) 2 1 90 3 1396.06 ± 5.23 223.46 ± 2.32 41.78 ± 2.25 74.5 ± 0.2 9 2 70 4 947.92 ± 3.79 167.05 ± 1.46 27.52 ± 1.21 73.3 ± 0.6 1 3 50 3 124.5 ± 1.01 20.67 ± 0.72 15.02 ± 0.83 66.8 ± 0.5 6 4 90 4 1177.85 ± 4.87 214.97 ± 2.36 42.96 ± 1.98 75.9 ± 0.6 11 5 70 4 948.05 ± 4.56 169.7 ± 1.55 28.85 ± 1.09 73.2 ± 0.3 5 6 50 4 136.4 ± 1.08 25.49 ± 0.65 16.09 ± 0.78 68.2 ± 0.2 7 7 70 3 482.31 ± 3.82 108.37 ± 1.02 27.17 ± 0.94 72.1 ± 0.5 4 8 90 5 1172.1 ± 3.75 176.29 ± 2.45 48.32 ± 2.23 77.2 ± 1.0 12 9 70 4 949.23 ± 3.98 166.6 ± 1.47 28.02 ± 0.74 73.2 ± 0.9 10 10 70 4 951.19 ± 4.56 168.15 ± 1.62 29.15 ± 1.16 73.3 ± 0.8 3 11 50 5 148.3 ± 2.04 26.22 ± 1.23 18.68 ± 0.43 71.1 ± 0.6 13 12 70 4 950.24 ± 4.21 167.24 ± 1.74 27.97 ± 0.54 73.4 ± 0.5 8 13 70 5 1126.11 ± 2.01 137.74 ± 1.03 29.97 ± 0.81 73.5 ± 0.7 Amplitude (A); time (B); total polyphenol content (TPC); monomeric anthocyanins content (MA); antioxidant activity: FRAP and DPPH. The results are expressed as the mean value of the three replicates ± the standard deviation (SD) In terms of the content of bioactive compounds, such as the TPC and MA, as well as the antioxidant activity measured by the FRAP and DDPH assays, the effects of the high-power ultrasonic treatment on extraction kinetics were explored. All the above parameters were studied in untreated red grapes must as a control sample (C) and on the samples subjected to ultrasound treatment at 50, 70, and 90% amplitude for 3, 4, and 5 min, respectively, as follows: SM 50/3 (A: 50%, t: 3 min), SM 50/4 (A: 50%; t: 4 min), SM 50/5 (A: 50%; t: 5 min), SM 70/3 (A: 70%; t: 3 min), SM 70/4 (A: 70%; t: 4 min), SM 70/5 (A: 70%; t: 5 min), SM 90/3 (A: 90%; t: 3 min), SM 90/4 (A: 90%; t: 4 min), and SM 90/5 (A: 90%, t: 5 min) Analytical determinations were performed immediately after crushing for the control sample and immediately after treatment for the ultrasound-treated samples Two factors, the amplitude level and the duration of the ultrasound treatment, were found to have an effect on the parameters studied, with single or interaction effects. The ANOVA analysis of variance performed on the analytical parameters, in relation to the different conditions of amplitude and treatment time, revealed significant differences in the total polyphenolic content, the monomeric anthocyanins, and the antioxidant activity. Using the RSM and ANOVA, the best extraction parameters were statistically examined The process of sonication results in the development of cavitation bubbles, which have the potential to violently collapse, releasing energy and increasing the temperature and pressure. These bubbles may burst close to a solid surface or interact chemically with molecules, harming cell structures and altering the selectivity or permeability of cell membranes [ 20 ].

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[Summary: This page presents the results and discussion, focusing on the effects of ultrasonic pre-treatment on polyphenol extraction and antioxidant activity. It discusses the role of cavitation bubbles in cell disruption and the monitoring of temperature rise during sonication. It also includes a figure showing the changes in temperature of the samples.]

Sustainability 2023 , 15 , 6697 7 of 22 To monitor the corresponding temperature rise, the temperature of the sonicated samples was measured at 1 min intervals, using a thermovision camera. The mean value of the untreated sample (C), and the mean values recorded by a forward-looking infrared (FLIR) camera for each sample when the sonication treatment ended are illustrated in Figure 1 . Sustainability 2023 , 15 , x FOR PEER REVIEW 7 of 22 Amplitude (A); time (B); total polyphenol content (TPC); monomeric anthocyanins content (MA); antioxidant activity: FRAP and DPPH. The results are expressed as the mean value of the three replicates ± the standard deviation (SD) Two factors, the amplitude level and the duration of the ultrasound treatment, were found to have an effect on the parameters studied, with single or interaction effects. The ANOVA analysis of variance performed on the analytical parameters, in relation to the different conditions of amplitude and treatment time, revealed significant differences in the total polyphenolic content, the monomeric anthocyanins, and the antioxidant activity. Using the RSM and ANOVA, the best extraction parameters were statistically examined The process of sonication results in the development of cavitation bubbles, which have the potential to violently collapse, releasing energy and increasing the temperature and pressure. These bubbles may burst close to a solid surface or interact chemically with molecules, harming cell structures and altering the selectivity or permeability of cell membranes [20] To monitor the corresponding temperature rise, the temperature of the sonicated samples was measured at 1 min intervals, using a thermovision camera. The mean value of the untreated sample (C), and the mean values recorded by a forward - looking infrared (FLIR) camera for each sample when the sonication treatment ended are illustrated in Figure 1. Figure 1. Changes in the temperature of the samples treated with US compared to the control sample (C) An increase in the temperature of the samples following the ultrasound treatment was evident, compared to the reference sample, C (20 °C), correlated with the intensity and time of the treatment. The minimum and maximum average temperatures reached in the samples were 26.20 °C for SM 50/3 and 60.17 °C for SM 90/5, respectively. The results confirmed the fact that the increasing temperature of the must samples depends on the operating parameters used during the ultrasound treatments, as it was established that the device’s real input power was transformed into heat that was released into the medium [26]. It can be observed that the increasing temperature in the sonicated samples was influenced to a higher measure by increasing the amplitude compared with the treatment time. Thereby, the temperature reached in SM 70/5 (54.23 °C), treated with a lower am- Figure 1. Changes in the temperature of the samples treated with US compared to the control sample (C) An increase in the temperature of the samples following the ultrasound treatment was evident, compared to the reference sample, C (20 ◦ C), correlated with the intensity and time of the treatment. The minimum and maximum average temperatures reached in the samples were 26.20 ◦ C for SM 50/3 and 60.17 ◦ C for SM 90/5, respectively. The results confirmed the fact that the increasing temperature of the must samples depends on the operating parameters used during the ultrasound treatments, as it was established that the device’s real input power was transformed into heat that was released into the medium [ 26 ]. It can be observed that the increasing temperature in the sonicated samples was influenced to a higher measure by increasing the amplitude compared with the treatment time Thereby, the temperature reached in SM 70/5 (54.23 ◦ C), treated with a lower amplitude but the maximum time (5 min), was close to that of SM 90/3 (51.53 ◦ C) treated with a higher amplitude but the minimum time (3 min) Increased temperature often results in higher extraction yields. Temperature optimization can be performed to obtain the best yield of the target compounds without degradation, as this parameter can vary depending on the type of product [ 35 ]. It was also concluded that the intensity of the ultrasound was directly related to the amplitude of the transducer. Increasing the amplitude increased the ultrasound intensity and resulted in an increase in the sonochemical effects [ 36 ]. Using different levels of device power, intensity, frequency, amplitude, and treatment time, previous research on red grapes and wines of various types has yielded very encouraging findings on the ability of ultrasound to extract and improve the physicochemical quality of wines, as well as its ability to accelerate wine aging or control microorganisms [ 37 – 41 ]. In addition, other authors reported that the application of US produced interesting findings on the recovery of bioactive compounds from marc and lees, and the extraction of various aromatic compounds from wines [ 42 – 44 ].

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[Summary: This page discusses the effects of temperature on extraction yields and the potential degradation of phenolic compounds at high temperatures. It presents the characteristics of the untreated red grape must and discusses the total polyphenolic content (TPC) in sonicated samples, comparing it to the control sample.]

Sustainability 2023 , 15 , 6697 8 of 22 Table 3 depicts the results for the physicochemical and analytical determinations of the untreated red grape must Table 3. Characteristics of the red grape must Sample TSS ( Brix) TA (g Tartaric Acid/L) TPC ( µ g GAE/mL) MA (mg CGE/L) FRAP ( µ mol Fe 2+ /mL) DPPH Scavenging Activity (%) C 29.9 ± 0.1 3.4 ± 0.03 114.42 ± 2.67 16.06 ± 0.9 13.43 ± 1.02 65.0 ± 0.4 Untreated red grape must (C); total soluble solids (TSS); total acidity (TA); total polyphenolic content (TCP); monomeric anthocyanins content (MA); antioxidant activity: FRAP and DPPH. The results are expressed as the mean value of the three replicates ± the standard deviation (SD) 3.1. Total Polyphenolic Content The TPC extraction yields were observed to rise with any increase in temperature This impact might primarily be ascribed to the cavitation phenomenon, which is preferred at lower temperatures, and which makes it easier to release extractable chemicals and enhances mass movement via diffusion or by rupturing plant cell walls [ 23 , 32 , 45 ]. The TPC for sonicated samples varied from 124.5 micrograms of gallic acid equivalents per milliliter (GAE/mL) to 1396.06 µ g GAE/mL, as shown in Table 2 . The lowest amount of TPC was found in the SM 50/3 sample (run order three) using 50% amplitude for 3 min, while the higher TPC content was found for the SM 90/3 sample (run order one) using 90% amplitude for 3 min. It can be seen that there was an increase, generally proportional with the treatment conditions, of 9% to 12 times for the total polyphenol content of the sonicated samples compared with untreated sample (C). These findings indicate that amplitude is a significant factor in the extraction of total phenols Previous studies have shown a higher extraction yield of TPC when high-power ultrasound was applied to grapes or during winemaking [ 27 , 46 ]. Other authors have reported that no degradation of the polyphenols was observed after the sonication of red wine [ 29 ]. Moreover, the ultrasound treatment with an amplitude of 90% for 3 min determined the highest extraction of TPC in the sample SM 90/3, while lower values were recorded when applied at the same amplitude of 90% for 4 min and 5 min, by 15.63% in the sample SM 90/4 and 16.04% in the sample SM 90/5, respectively. The possible explanation for this decrease might be the high temperatures reached in the immediate vicinity of the ultrasonic probe, as well as the average temperatures of 55.71 ◦ C and 60.17 ◦ C reached in samples SM 90/4 and SM 90/5, respectively, that could lead to the degradation of phenolic compounds. Other research has shown that polyphenol can be protected against thermal breakdown processes at temperatures as high as 50 degrees Celsius [ 47 ]. Despite their benefits, many phenolic compounds quickly hydrolyze and oxidize at higher temperatures, particularly when extracted for extended periods of time [ 48 , 49 ]. At extraction temperatures over 60 ◦ C, Akowuah, Mariam, and Chin demonstrated that the total polyphenol content of the extracts reduced as a result of oxidative degradation [ 50 ]. The vulnerability of phenolic compounds to high temperatures was demonstrated, as early as three decades ago, by Havlikova and Mikova [ 51 ]. They demonstrated that high temperatures and prolonged extraction times enhanced the rate at which phenolic components oxidized and lowered the yield of the extracts. For instance, during maceration, the extraction of polyphenols is typically carried out between 20 and 50 ◦ C, never over this range [ 52 ]. Furthermore, it is important to remember that the sensitivity of a sample to temperatureinduced polyphenol degradation is influenced by the types of polyphenolic compounds present in the plant extract or matrix, as well as their physicochemical and biochemical properties [ 47 ].

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[Summary: This page continues discussing the total polyphenolic content (TPC), explaining that high temperatures can lead to degradation of phenolic compounds. It presents the ANOVA and coefficient table for the quadratic model used to statistically investigate the optimal extraction parameters for the TPC.]

Sustainability 2023 , 15 , 6697 9 of 22 However, additional variables such as plant species, geographical origin, or cultivars may also have an impact on the quantity of phenolic chemicals recovered using an ultrasound-assisted approach [ 10 ]. The optimal extraction parameters for the TPC were statistically investigated using the RSM and ANOVA (Table 4 ). Table 4. ANOVA and coefficient table for the quadratic model. Response 1: total phenolic compounds Source F-Value p -Value R 2 Adjusted R 2 Coefficients Model 13.40 0.0018 0.9054 0.8378 Intercept 921.98 A 60.33 0.0001 556.13 B 1.07 0.3361 73.94 AB 0.4989 0.5028 61.94 A 2 3.47 0.1049 − 196.5 B 2 0.2193 0.6538 − 49.42 Lack of fit 36229.38 <0.0001 Amplitude (A); time (B) As Table 4 shows, the amplitude term is significant for the enhanced extraction of polyphenols. The model F-value of 13.40 means that the model is significant. Due to the noise, there is only a 0.18% chance that such a large F-value could occur. Moreover, p -values less than 0.0500 indicate that the model terms are significant. In this case, amplitude is a significant model term. Values greater than 0.1000 indicate that the model terms are not significant. A high R 2 value (0.9054) indicates a good level of model fit. The lack of fit F-value of 36,229.38 indicates that the lack of fit is significant. There is only a 0.01% chance that such a large lack of fit F-value could occur due to noise The final equation in terms of the actual factors for the TPC is shown in Equation (3) The equation can be used to make predictions about the response for given levels of each factor Y TPC = − 5385.266 + 108.970 × A + 686.076 × B − 3.097 × A × B − 0.491 × A 2 − 49.418 × B 2 (3) where A is the amplitude and B represents the time The influence of the process parameters A and B on the extraction rate of the TPC in samples treated with US is shown in Figure 2 . Figure 2 clearly illustrates that the amplitude of ultrasonic waves has a greater impact on the outcomes than the time of the treatment. A higher treatment time with smaller amplitudes (50%) has a detrimental effect, and less TPC is extracted. Higher amplitude values (90%), on the other hand, greatly improve the TPC extraction yield The potential of ultrasonic waves to have a detrimental effect on biomass, aiding the extraction of cell contents, has been ascribed to ultrasound assisted extraction, having an improving influence on extracting phenolics from plants. Using ultrasound and different operating conditions, previous studies have shown increased yields of phenolic extracts as plant bioactive compounds, when applied to blueberry pomace, mango peels, or coffee beans [ 53 – 55 ]. In addition, it was observed that heat breakdown of the polyphenols may take place at high temperatures. A reduction in the extraction yield owing to temperature might be attributed to phenolic components degrading at high temperatures [ 56 ]. In the described situation, the optimal circumstances would be a higher amplitude, and a reduced duration of the treatment.

[[[ p. 10 ]]]

[Summary: This page further discusses the effects of ultrasound on phenolic extraction, attributing it to the potential of ultrasonic waves to aid in extracting cell contents. It presents figures showing the influence of process parameters on the TPC and begins to discuss monomeric anthocyanins, highlighting their increased concentration with the treatment.]

Sustainability 2023 , 15 , 6697 10 of 22 Sustainability 2023 , 15 , x FOR PEER REVIEW 10 of 22 The potential of ultrasonic waves to have a detrimental effect on biomass, aiding the extraction of cell contents, has been ascribed to ultrasound assisted extraction, having an improving influence on extracting phenolics from plants. Using ultrasound and different operating conditions, previous studies have shown increased yields of phenolic extracts as plant bioactive compounds, when applied to blueberry pomace, mango peels, or coffee beans [53–55] ( a ) ( b ) Figure 2. Influence of the process parameters on the TPC: ( a ) amplitude (A) and time (B) as contour graph; ( b ) amplitude (A) and time (B) as 3 D surface In addition, it was observed that heat breakdown of the polyphenols may take place at high temperatures. A reduction in the extraction yield owing to temperature might be attributed to phenolic components degrading at high temperatures [56] In the described situation, the optimal circumstances would be a higher amplitude, and a reduced duration of the treatment 3.2. Monomeric Anthocyanins Anthocyanins are a major family of phenolic compounds found in red wine. The treatment tests showed a strong interaction of the cavitation phenomena with the cells of the exocarp, with an increase in the concentration of anthocyanins. Our results were consistent with others that include ultrasound - assisted extraction on the list of new technologies that have been developed with the goal of reducing extraction times and enhancing yields [57] The MA content for the sonicated samples varied from 20.67 mg cyanidin 3 - glucoside equivalents (CGE)/L to 223.46 mg CGE/L, as shown in Table 2. Similar to the TPC, the lowest amount of MA was found for the SM 50/3 sample (run order three) using 50% amplitude for 3 min, while the higher MA content was found for the SM 90/3 sample (run order one) using 90% amplitude for 3 min. It can be observed that there was an increase, generally proportional with the treatment conditions, of 28.7% to about 14 times for the MA of the sonicated samples compared with untreated sample (C) Regarding the extraction of MA, US treatment with A 90% for 3 min led to the highest extraction (sample SM 90/3), while slightly lower values of 3.8% (sample SM 90/4) and significant lower values of 21.11% (sample SM 90/5) were recorded when we used an Figure 2. Influence of the process parameters on the TPC: ( a ) amplitude (A) and time (B) as contour graph; ( b ) amplitude (A) and time (B) as 3 D surface 3.2. Monomeric Anthocyanins Anthocyanins are a major family of phenolic compounds found in red wine. The treatment tests showed a strong interaction of the cavitation phenomena with the cells of the exocarp, with an increase in the concentration of anthocyanins. Our results were consistent with others that include ultrasound-assisted extraction on the list of new technologies that have been developed with the goal of reducing extraction times and enhancing yields [ 57 ]. The MA content for the sonicated samples varied from 20.67 mg cyanidin 3-glucoside equivalents (CGE)/L to 223.46 mg CGE/L, as shown in Table 2 . Similar to the TPC, the lowest amount of MA was found for the SM 50/3 sample (run order three) using 50% amplitude for 3 min, while the higher MA content was found for the SM 90/3 sample (run order one) using 90% amplitude for 3 min. It can be observed that there was an increase, generally proportional with the treatment conditions, of 28.7% to about 14 times for the MA of the sonicated samples compared with untreated sample (C) Regarding the extraction of MA, US treatment with A 90% for 3 min led to the highest extraction (sample SM 90/3), while slightly lower values of 3.8% (sample SM 90/4) and significant lower values of 21.11% (sample SM 90/5) were recorded when we used an amplitude of 90% for 4 min and 90% for 5 min, respectively. It is observed that the extraction of monomeric anthocyanins increases by a maximum value and then start to decrease, probably also due to the influence of the final temperature reached in the treated samples The anthocyanin content of grape juice was negatively impacted by higher amplitude levels and longer treatment times, as other authors have shown [ 28 ]. Moreover, it was observed that anthocyanins are susceptible to degradation due to a variety of variables such as pH, temperature, oxygen, water activity, and co-pigments [ 58 ]. Other researchers revealed that the temperature has a substantial impact on anthocyanin extraction, with maximal extraction occurring at roughly 30 to 35 ◦ C. However, temperature increases enhance extraction by increasing the solubility of anthocyanins and the diffusion coefficient. However, temperatures over a particular point resulted in a reduction in anthocyanin output, e.g., at temperatures above 45 ◦ C, anthocyanins decrease dramatically [ 59 ].

[[[ p. 11 ]]]

[Summary: This page discusses monomeric anthocyanins (MA) and their extraction yields, noting that the highest extraction occurs at 90% amplitude for 3 minutes. It explains the potential degradation of anthocyanins at higher temperatures. It also presents the ANOVA and coefficient table for the quadratic model for monomeric anthocyanins.]

Sustainability 2023 , 15 , 6697 11 of 22 As it can be noticed, for the highest extraction of both the TPC and MA ultrasound amplitude and treatment time are the same: 90% amplitude for 3 min The difference in behavior between the total phenolics and anthocyanins might be explained by anthocyanins’ greater vulnerability to high temperatures [ 56 ]. According to Table 5 , model terms for the monomeric anthocyanins A, A 2 , and B 2 are significant since their p -values are less than 0.0500, as shown. If the value is higher than 0.1000, the model terms are not considered relevant. An F-value this large might be caused by noise just 0.01% of the time, but the model’s F-value of 44.35 suggests that the model is important. The lack of fit is implied to be significant by the lack of fit F-value of 396.80 Table 5. ANOVA and coefficient table for the quadratic model. Response 2: monomeric anthocyanins Source F-Value p -Value R 2 Adjusted R 2 Coefficients Model 44.35 <0.0001 0.9694 0.9475 Intercept 162.77 A 190.42 <0.0001 90.39 B 0.0972 0.7644 2.04 AB 2.70 0.1444 –13.18 A 2 9.71 0.0169 –30.08 B 2 7.97 0.0257 –27.25 Lack of fit 396.80 <0.0001 Amplitude (A); time (B) The adjusted R 2 of 0.9475 and the predicted R 2 of 0.8878 are in fair agreement (i.e., the difference is less than 0.2), indicating that the model makes accurate predictions. Equation (4) displays the final equation in terms of the actual factors for monomeric anthocyanins. For specific levels of each element, predictions regarding the response can be made using the equation Y MA = − 1134.49 + 17.683 × A + 262.123 × B − 0.659 × A × B − 0.075 × A 2 − 27.254 × B 2 (4) where A is the amplitude and B represents the time The effect of the process parameters A and B on the extraction rate of the MA in samples that underwent US treatment is shown in Figure 3 . According to Figure 3 , which compares the effects of the treatment duration and ultrasonic wave amplitude on the extraction of the monomeric anthocyanins from red grape exocarp, the extraction yield of the MA increases with both up to a certain point before starting to decline. However, as the treatment time increases over 3 min using the ultrasound wave amplitude at the maximum level (90%), the extraction rate of the MA decreases. Excessive cavitation occurs at high amplitudes, raising the temperature around the probe, creating more hydroxyl radicals, and resulting in excessive degradation [ 60 ]. Moreover, as a smaller amplitude may not deliver enough energy to break the cell wall, the lowest extraction yields of the MA were observed in the samples where the minimum amplitude level was used (A = 50%) Using ultrasound and different working conditions, previous studies have also shown increased yields for anthocyanin extractions from blueberry marc, mulberry wine residues, or purple sweet potatoes [ 61 – 63 ]. Similar to the TPC, the optimal circumstances for the MA enhanced extraction would be a higher amplitude, and a reduced duration of the treatment.

[[[ p. 12 ]]]

[Summary: This page continues the discussion of monomeric anthocyanins (MA), explaining how excessive cavitation at high amplitudes can lead to degradation. It presents figures showing the influence of process parameters on MA. It transitions to discussing antioxidant activity, noting the antioxidant properties of phenolic compounds.]

Sustainability 2023 , 15 , 6697 12 of 22 Sustainability 2023 , 15 , x FOR PEER REVIEW 12 of 22 ( a ) ( b ) Figure 3. Influence of the process parameters on the MA: ( a ) amplitude (A) and time (B) as contour graph; ( b ) amplitude (A) and time (B) as 3 D surface According to Figure 3, which compares the effects of the treatment duration and ultrasonic wave amplitude on the extraction of the monomeric anthocyanins from red grape exocarp, the extraction yield of the MA increases with both up to a certain point before starting to decline. However, as the treatment time increases over 3 min using the ultrasound wave amplitude at the maximum level (90%), the extraction rate of the MA decreases. Excessive cavitation occurs at high amplitudes, raising the temperature around the probe, creating more hydroxyl radicals, and resulting in excessive degradation [60]. Moreover, as a smaller amplitude may not deliver enough energy to break the cell wall, the lowest extraction yields of the MA were observed in the samples where the minimum amplitude level was used (A = 50%) Using ultrasound and different working conditions, previous studies have also shown increased yields for anthocyanin extractions from blueberry marc, mulberry wine residues, or purple sweet potatoes [61–63] Similar to the TPC, the optimal circumstances for the MA enhanced extraction would be a higher amplitude, and a reduced duration of the treatment 3.3. Antioxidant Activity The antioxidant properties of the phenolic compounds from grapes have been extensively researched, including the scavenging of free radicals, the suppression of lipid oxidation, the decrease of hydroperoxide production, and so on. These properties are especially significant in terms of bioactivity. Moreover, antioxidants can stop the oxidation process by preferentially interacting with an oxidizing agent, rather than the desired target molecules or cells [64] In addition to the FRAP assay, the DPPH scavenging activity was evaluated to further support our research findings. Both the DPPH and FRAP assays could be used to determine the antioxidant activity, as both showed high reproducibility [65] The maximum antioxidant activity, 48.32 µmol Fe 2+ /mL and 77.2%, as measured by the FRAP and DDPH assays, respectively, was observed in the sonicated samples of run order 8, acquired at 90% amplitude for 5 min (sample SM 90/5) (Table 2). The lowest ac- Figure 3. Influence of the process parameters on the MA: ( a ) amplitude (A) and time (B) as contour graph; ( b ) amplitude (A) and time (B) as 3 D surface 3.3. Antioxidant Activity The antioxidant properties of the phenolic compounds from grapes have been extensively researched, including the scavenging of free radicals, the suppression of lipid oxidation, the decrease of hydroperoxide production, and so on. These properties are especially significant in terms of bioactivity. Moreover, antioxidants can stop the oxidation process by preferentially interacting with an oxidizing agent, rather than the desired target molecules or cells [ 64 ]. In addition to the FRAP assay, the DPPH scavenging activity was evaluated to further support our research findings. Both the DPPH and FRAP assays could be used to determine the antioxidant activity, as both showed high reproducibility [ 65 ]. The maximum antioxidant activity, 48.32 µ mol Fe 2+ /mL and 77.2%, as measured by the FRAP and DDPH assays, respectively, was observed in the sonicated samples of run order 8, acquired at 90% amplitude for 5 min (sample SM 90/5) (Table 2 ). The lowest activity, 15.02 µ mol Fe 2+ /mL or 66.8% (run order 3) was observed at 50% amplitude for 3 min (sample SM 50/3) It was noted that the greatest extraction of antioxidants required the same ultrasonic amplitude (90%) as for the TPC and MA, but the maximum time was 5 min, not 3 min as for the TPC and MA. Moreover, the fact that antioxidants also include non-phenolic chemicals, which may require a higher temperature for extraction, may help to explain a slightly higher extraction temperature of 60.17 ◦ C for the maximum value of antioxidant compounds. Previous studies that claimed antioxidants required a higher temperature for extraction are consistent with this conclusion [ 25 ]. Moreover, the results might suggest that the antioxidant activity of the samples was significantly influenced by the TPC levels It can be seen that the antioxidant activity of the sonicated samples increases in proportion to the treatment conditions, from 11.84% to about 3.6 times as measured by the FRAP and from 2.77 to 18.77% as measured by the DPPH free radical scavenging assay, compared to the untreated sample (C) According to the mechanism of action exhibited by antioxidant compounds, the methods used to measure antioxidant activity evaluate the ability of antioxidant species to scavenge free radicals or the ability of antioxidants to reduce an oxidant compound [ 65 ].

[[[ p. 13 ]]]

[Summary: This page discusses antioxidant activity, presenting the maximum activity observed in samples treated at 90% amplitude for 5 minutes. It discusses the mechanisms of action of antioxidant compounds and the FRAP and DPPH assays. It also presents the ANOVA and coefficient table for the quadratic model for antioxidant activity.]

Sustainability 2023 , 15 , 6697 13 of 22 FRAP values quantify the ability of the antioxidant compounds contained in red grape must samples to donate electrons and, thus, reduce the oxidized species. A relevant indicator of a compound possessing potential antioxidant activity may be its reducing power [ 66 ]. It can be observed that the presence of a significant amount of phenolic compounds in red grape must, as a result of US treatment, led to high FRAP values The DPPH radical scavenging activity reflects the hydrogen-donating capacity of the samples, thanks to the presence of bioactive substances. When the DPPH radical scavenging activity of the samples was examined, the same conclusion was reached as in the FRAP evaluation, namely that the antioxidant potential was higher after treatment with ultrasound A closer examination of the results obtained from the FRAP and DPPH tests revealed that the increase in the electron-donating capacity or reducing power of the samples in response to US treatment was greater than that recorded for their free radical scavenging capacity The study performed by Rajurkar and Hande [ 67 ] revealed that the phenolic compounds exhibited a much higher correlation with the reducing power than with the DPPH free radical scavenging activity. Thus, it is estimated that the phenolic compounds extracted from red grapes provide antioxidant protection directly through the mechanism of reducing the oxidized intermediates in the chain reaction Our results suggest that the FRAP and DPPH assays could be used to distinguish the dominant mechanism, by which polyphenolic compounds from grape must act as antioxidants Other results showed that the antioxidant activity of phenolic compounds may have a concentration saturation limit, beyond which the activity cannot be increased by concentration. However, some results showed that there are factors other than concentration that influence the antioxidant properties of phenolic compounds, as the relationship between the phenolic compounds and the antioxidant activity was inconsistent [ 8 , 68 ]. Furthermore, other research showed a significant relationship between the polyphenolic compounds assessed in the various samples and the outcomes of the antioxidant activity tests [ 69 ]. As their p-values are less than 0.0500, Table 6 shows that the model parameters A, B, and A 2 are significant for the antioxidant activity measured by both the FRAP and DPPH assays. Values greater than 0.1000 indicate that the model terms are not decisive The model significance is indicated by the model F-value of 330.16 and 58.81, respectively. The F-values for lack of fit, 2.40 and 102.78, respectively, indicate that the lack of fit is not significant Table 6. ANOVA and coefficient table for the quadratic model. Response 3: antioxidant activity Source F-Value p -Value R 2 Adjusted R 2 Coefficients FRAP DPPH FRAP DPPH FRAP DPPH FRAP DPPH FRAP DPPH Model 330.16 58.81 <0.0001 <0.0001 0.9958 0.9767 0.9928 0.9601 Intercept 28.14 73.17 A 1587.16 246.65 <0.0001 <0.0001 13.88 3.58 B 33.68 37.65 0.0004 0.0005 2.17 1.40 AB 2.85 2.05 0.1354 0.1954 0.7200 –0.4000 A 2 12.04 6.08 0.0104 0.0431 1.78 –0.8293 B 2 2.59 0.0556 0.1515 0.8203 0.8266 –0.0793 Lack of fit 2.40 102.78 0.2085 0.0003 Amplitude (A); time (B) The predicted R 2 (0.9727 FRAP and 0.7829 DPPH) and the adjusted R 2 (0.9928 FRAP and 0.9601 DPPH) are in good agreement (i.e., the difference is less than 0.2), indicating that the model makes accurate predictions.

[[[ p. 14 ]]]

[Summary: This page continues the discussion of antioxidant activity, presenting the final equations for FRAP and DPPH in terms of actual factors. It includes figures showing the kinetics of antioxidant activity in samples treated with ultrasound. It also mentions other researchers' findings on the relationship between phenolic compounds and antioxidant activity.]

Sustainability 2023 , 15 , 6697 14 of 22 Equations (5) and (6) display the final equations in terms of the actual factors for the antioxidant activity as measured by the FRAP and DPPH assays. For specific levels of each element, the equation can be used to predict the response Y FRAP = 16.030 − 0.074 × A − 6.965 × B + 0.036 × A × B + 0.004 × A 2 + 0.826 × B 2 (5) Y DPPH = 37.996 + 0.549 × A + 3.434 × B − 0.020 × A × B − 0.002 × A 2 − 0.079 × B 2 (6) where A is the amplitude and B represents the time Figure 4 shows the kinetics of the antioxidant activity in samples treated with US, as well as the 3 D response surfaces and contour plots From Figure 4 , which compares the effects of the treatment time and ultrasonic wave amplitude on the antioxidant activity of the samples, it can be seen that both the FPAP and DPPH values increase with both factors, up to a maximum value of 48.32 µ mol Fe 2+ /mL and 77.2% in sample SM 90/5 Other researchers came to the conclusion that the antioxidant activity of wines is more closely related to the type of individual phenolic compounds found in the wines than to the TPC. It has also been proposed that the antioxidant activity is mostly attributed to the flavan-3-ol fraction, rather than anthocyanins [ 70 ]. However, the grapes and wines showed a strong link between their phenolic composition and the antioxidant activity. The main substances involved in this bioactivity varied depending on the type of sample examined. The primary category, with a significant contribution to this feature, was identified as anthocyanins. Additionally, variations in the phenolic component quantities may account for the variations in the antioxidant efficacy between grape cultivars [ 71 ]. In the situation described, the optimal circumstances for antioxidant activity would be a higher amplitude and a longer duration of treatment compared to the TPC and MA Sustainability 2023 , 15 , x FOR PEER REVIEW 14 of 22 The F - values for lack of fit, 2.40 and 102.78, respectively, indicate that the lack of fit is not significant Table 6. ANOVA and coefficient table for the quadratic model. Response 3: antioxidant activity Source F - Value p - Value R 2 Adjusted R 2 Coefficients FRAP DPPH FRAP DPPH FRAP DPPH FRAP DPPH FRAP DPPH Model 330.16 58.81 ˂ 0.0001 ˂ 0.0001 0.9958 0.9767 0.9928 0.9601 Intercept 28.14 73.17 A 1587.16 246.65 ˂ 0.0001 ˂ 0.0001 13.88 3.58 B 33.68 37.65 0.0004 0.0005 2.17 1.40 AB 2.85 2.05 0.1354 0.1954 0.7200 –0.4000 A 2 12.04 6.08 0.0104 0.0431 1.78 –0.8293 B 2 2.59 0.0556 0.1515 0.8203 0.8266 –0.0793 Lack of fit 2.40 102.78 0.2085 0.0003 Amplitude (A); time (B) The predicted R 2 (0.9727 FRAP and 0.7829 DPPH) and the adjusted R 2 (0.9928 FRAP and 0.9601 DPPH) are in good agreement (i.e., the difference is less than 0.2), indicating that the model makes accurate predictions Equations (5) and (6) display the final equations in terms of the actual factors for the antioxidant activity as measured by the FRAP and DPPH assays. For specific levels of each element, the equation can be used to predict the response Y FRAP = 16.030 − 0.074 × A − 6.965 × B + 0.036 × A × B + 0.004 × A 2 + 0.826 × B 2 (5) Y DPPH = 37.996 + 0.549 × A + 3.434 × B − 0.020 × A × B − 0.002 × A 2 − 0.079  B 2 (6) where A is the amplitude and B represents the time Figure 4 shows the kinetics of the antioxidant activity in samples treated with US, as well as the 3 D response surfaces and contour plots ( a ) ( b ) Figure 4. Cont .

[[[ p. 15 ]]]

[Summary: This page continues the discussion of antioxidant activity, noting the correlation between TPC, MA, and antioxidant activity. It includes figures showing the influence of process parameters on antioxidant activity. It highlights the improved values that confirm the influence of phenolics and anthocyanins on antioxidant activity.]

Sustainability 2023 , 15 , 6697 15 of 22 Sustainability 2023 , 15 , x FOR PEER REVIEW 15 of 22 ( c ) ( d ) Figure 4. Influence of the process parameters on the antioxidant activity: ( a ) amplitude (A) and time (B) as contour graph for the FRAP values; ( b ) amplitude (A) and time (B) as the 3 D surface for the FRAP values; ( c ) amplitude (A) and time (B) as the contour graph for the DPPH values; ( d ) amplitude (A) and time (B) as the 3 D surface for the DPPH values From Figure 4, which compares the effects of the treatment time and ultrasonic wave amplitude on the antioxidant activity of the samples, it can be seen that both the FPAP and DPPH values increase with both factors, up to a maximum value of 48.32 µmol Fe 2+ /mL and 77.2% in sample SM 90/5 Other researchers came to the conclusion that the antioxidant activity of wines is more closely related to the type of individual phenolic compounds found in the wines than to the TPC. It has also been proposed that the antioxidant activity is mostly attributed to the flavan - 3 - ol fraction, rather than anthocyanins [70] However, the grapes and wines showed a strong link between their phenolic composition and the antioxidant activity. The main substances involved in this bioactivity varied depending on the type of sample examined. The primary category, with a significant contribution to this feature, was identified as anthocyanins. Additionally, variations in the phenolic component quantities may account for the variations in the antioxidant efficacy between grape cultivars [71] In the situation described, the optimal circumstances for antioxidant activity would be a higher amplitude and a longer duration of treatment compared to the TPC and MA 3.4. Correlations between Total Phenolic Content, Monomeric Anthocyanins and Antioxidant Activity The results of our study show that the higher the amplitude and the longer the duration of the ultrasound treatment, the higher the antioxidant activity, expressed both as the FRAP or DPPH free radical scavenging activity, as the maximum values for the antioxidant activity were found when an ultrasonic amplitude of 90% was applied for 5 min (sample SM 90/5): 48.32 µmol Fe 2+/ mL and 77.2%, respectively It can also be observed that the antioxidant activity of the sonicated samples, expressed by both the FRAP and DPPH tests, increased in proportion to the total polyphenol and monomeric anthocyanin content Figure 4. Influence of the process parameters on the antioxidant activity: ( a ) amplitude (A) and time (B) as contour graph for the FRAP values; ( b ) amplitude (A) and time (B) as the 3 D surface for the FRAP values; ( c ) amplitude (A) and time (B) as the contour graph for the DPPH values; ( d ) amplitude (A) and time (B) as the 3 D surface for the DPPH values 3.4. Correlations between Total Phenolic Content, Monomeric Anthocyanins and Antioxidant Activity The results of our study show that the higher the amplitude and the longer the duration of the ultrasound treatment, the higher the antioxidant activity, expressed both as the FRAP or DPPH free radical scavenging activity, as the maximum values for the antioxidant activity were found when an ultrasonic amplitude of 90% was applied for 5 min (sample SM 90/5): 48.32 µ mol Fe 2+ /mL and 77.2%, respectively It can also be observed that the antioxidant activity of the sonicated samples, expressed by both the FRAP and DPPH tests, increased in proportion to the total polyphenol and monomeric anthocyanin content For the maximum values observed for the total polyphenol content (1396.06 µ g GAE/mL) and the monomeric anthocyanins (223.4 mg CGE/L), when an ultrasonic amplitude of 90% was applied for 3 min (sample SM 90/3), the antioxidant activity was 3.11 times higher when measured with the FRAP test and 14.62% higher when measured as DPPH radical scavenging activity (%) compared to the control sample (C). These improved values confirmed the greatest influence of phenolics and anthocyanins on the antioxidant activity These results are in agreement with those reported by some authors who have shown a positive correlation between the TPC and the antioxidant activity evaluated by DPPH [ 72 ], or who have linked the high antiradical power of the samples to their anthocyanin concentration [ 73 ], but are in contrast to others [ 74 , 75 ]. The current analysis shows a very good correlation ( p < 0.01) between the TPC and antioxidant activity as the FRAP (Pearson’s r = 0.917) and as the DPPH radical scavenging activity (%) (Pearson’s r = 0.878). The same, very good, Pearson correlations were found between the MA and the antioxidant activity as the FRAP (Pearson’s r = 0.928) and as the DPPH radical scavenging activity (%) (Pearson’s r = 0.888) Finally, our results showed that the antioxidant activity of the sonicated samples was influenced by the TPC and MA, although the samples with the highest TPC and MA did

[[[ p. 16 ]]]

[Summary: This page discusses the optimization of the experimental model to increase the extraction rate of biologically active compounds and antioxidant activity. It describes the numerical optimization process using Design Expert software and presents the optimal solution found which was 90% amplitude and 4 minutes and 24 seconds.]

Sustainability 2023 , 15 , 6697 16 of 22 not always show the highest values for antioxidant activity expressed either as the FRAP or as the free radical scavenging activity, DPPH % 3.5. Optimization of the Experimental Model for Increasing the Extraction Rate of Biologically Active Compounds and the Antioxidant Activity in Grape Must Aiming to maximize the extraction of biologically active compounds in grape must, as well as to enhance its antioxidant activity, we investigated the optimization function of the model made with the Design Expert ® software version 13, (Stat-Ease, Inc., Minneapolis, USA, 2022). For numerical optimization, any combination of one or more objectives was optimized. The goals we applied to either factors or responses were as follows: amplitude and treatment time in range; TPC, MA, FRAP, and DPPH maximized The optimization function of the software gave us 20 found solutions, indicating the solution with the highest value of desirability, which was 0.918 (Figure 5 ), namely an amplitude of 90% and a treatment time of 4 min and 24 s, as the solution selected to maximize the extraction of the TPC, MA, and antioxidant activity as the FRAP and DPPH scavenging activity Sustainability 2023 , 15 , x FOR PEER REVIEW 17 of 22 Figure 5. Graphical view of the optimal solution: the optimal factor settings are shown as red bars and the optimal response predictions are shown in blue To identify the factor settings that meet specified objectives, numerical optimization searches the design space using the models built during the analysis (Figure 6). Under certain conditions, the model can accurately predict the extraction rate of compounds ( a ) ( b ) Figure 5. Graphical view of the optimal solution: the optimal factor settings are shown as red bars and the optimal response predictions are shown in blue To identify the factor settings that meet specified objectives, numerical optimization searches the design space using the models built during the analysis (Figure 6 ). Under certain conditions, the model can accurately predict the extraction rate of compounds.

[[[ p. 17 ]]]

[Summary: This page shows a graphical view of the optimal solution, including optimal factor settings and response predictions. It also includes numerical optimization plots for the optimal solution, showing predicted values for TPC, MA, FRAP, and DPPH. It presents the overlay graph for the optimal solution.]

Sustainability 2023 , 15 , 6697 17 of 22 Sustainability 2023 , 15 , x FOR PEER REVIEW 17 of 22 Figure 5. Graphical view of the optimal solution: the optimal factor settings are shown as red bars and the optimal response predictions are shown in blue To identify the factor settings that meet specified objectives, numerical optimization searches the design space using the models built during the analysis (Figure 6). Under certain conditions, the model can accurately predict the extraction rate of compounds ( a ) ( b ) Sustainability 2023 , 15 , x FOR PEER REVIEW 18 of 22 ( c ) ( d ) Figure 6. The numerical optimization plots for the optimal solution: ( a ) predicted value for the TPC; ( b ) predicted value for the MA; ( c ) predicted value for the FRAP; ( d ) predicted value for the DPPH Figure 7 shows the optimization graph for the optimal displayed solution, highlighting the point at which the response criteria is met Figure 7. The overlay graph for the optimal solution: the bright yellow color defines the acceptable factor settings and grey color defines the unacceptable factor settings 3.6. Confirmation of the Model The optimization analysis was used to guide the validation trials, which were conducted using the same methodology at the ideal selected amplitude—90% and treatment Figure 6. The numerical optimization plots for the optimal solution: ( a ) predicted value for the TPC; ( b ) predicted value for the MA; ( c ) predicted value for the FRAP; ( d ) predicted value for the DPPH Figure 7 shows the optimization graph for the optimal displayed solution, highlighting the point at which the response criteria is met 3.6. Confirmation of the Model The optimization analysis was used to guide the validation trials, which were conducted using the same methodology at the ideal selected amplitude—90% and treatment of time 4 min and 24 s. The predicted data were found to be TPC—1278.52 ( µ g GAE/mL), MA—212.64 (mg/L), FRAP—45.09 ( µ mol Fe 2+ /mL) and DPPH—76.31%, as observed in Figures 6 and 7 . The observed response data and the predicted data from the modelled response were compared under the extraction conditions. The errors for the TPC, MA, FRAP, and DPPH were − 8.70%, − 0.99, 3.14 and 0.25%, respectively, as shown in Table 7 , indicating the confirmation of the model.

[[[ p. 18 ]]]

[Summary: This page discusses the confirmation of the model through validation trials. It compares the predicted data with the observed response data and presents the errors for TPC, MA, FRAP, and DPPH, indicating confirmation of the model. It also states that the model has potential for large-scale extraction.]

Sustainability 2023 , 15 , 6697 18 of 22 Sustainability 2023 , 15 , x FOR PEER REVIEW 18 of 22 ( c ) ( d ) Figure 6. The numerical optimization plots for the optimal solution: ( a ) predicted value for the TPC; ( b ) predicted value for the MA; ( c ) predicted value for the FRAP; ( d ) predicted value for the DPPH Figure 7 shows the optimization graph for the optimal displayed solution, highlighting the point at which the response criteria is met Figure 7. The overlay graph for the optimal solution: the bright yellow color defines the acceptable factor settings and grey color defines the unacceptable factor settings 3.6. Confirmation of the Model The optimization analysis was used to guide the validation trials, which were conducted using the same methodology at the ideal selected amplitude—90% and treatment Figure 7. The overlay graph for the optimal solution: the bright yellow color defines the acceptable factor settings and grey color defines the unacceptable factor settings Table 7. Confirmation table of the model Response Data TPC ( µ g GAE/mL) MA (mg CGE/L) FRAP ( µ mol Fe 2+ /mL) DPPH Scavenging Activity (%) Observed 1176.16 210.56 46.55 76.5 Predicted 1278.52 212.64 45.09 76.31 Error (%) –8.70 –0.99 3.14 0.25 Total polyphenol content (TPC); monomeric anthocyanins content (MA); antioxidant activity (FRAP) The small differences between the predicted and observed values showed that the extraction optimization model obtained with the RSM in this study had a high degree of fit, and has the potential to be used even for large-scale extraction of phenolics and other antioxidant compounds from grapes using high-power ultrasound 4. Conclusions The acceleration of extraction kinetics using a physical technique can be important when the levels of physiologically active compounds in grapes are high. The use of ultrasound reduces the extraction times, while intensifying and almost maximizing the extraction yield and antioxidant activity. Overall, the use of ultrasound in winemaking opens up the possibility to optimize and better manage the vinification of red grapes. Due to the relatively short time required for ultrasound exposure, the application of ultrasound can be considered as a continuous pre-treatment for crushed red grapes prior to filling the winemaking tank. High-power ultrasound treatment of crushed grapes for a few minutes increases both the extraction rate of the bioactive compounds and the antioxidant activity by 12 times for the TPC, 14 times for the MA, 3.6 times for the FRAP and by 18.77% for the free radical scavenging activity, DPPH. However, a treatment time of 5 min and an amplitude of 90% led to a decrease in the TPC and MA, while the FRAP and DPPH values

[[[ p. 19 ]]]

[Summary: This page presents the conclusions of the study, highlighting the benefits of using ultrasound in winemaking. It summarizes the increase in extraction rate of bioactive compounds and antioxidant activity achieved with ultrasound treatment. It also states the optimal solution for maximizing TPC, MA, and antioxidant activity.]

Sustainability 2023 , 15 , 6697 19 of 22 increased with the same operating parameters. The optimal solution to develop a procedure that maximizes the TPC and MA extraction rate and the antioxidant activity during the first stage of winemaking seems to be an A of 90% and a t of 4 min and 24 s. The use of high-power ultrasound in the winemaking process for the treatment of crushed grapes has proved to be a very promising and effective technique for the extraction of high-value bioactive compounds, with great potential for commercial use. For this reason, considering the optimal solution found in this study, our further research on the impact of ultrasound treatment will include an in-depth investigation related to the content of the individual polyphenolic compounds of samples during the winemaking process, namely grape must, maceration, fermentation and bottling, with the aim of reducing the maceration period and better managing the whole process Author Contributions: Conceptualization, A.M., V.P. and M.-A.P.; methodology, A.M. and V.P.; software, A.M.; validation, E.A, M.-A.P. and M.I.L.; formal analysis, M.-A.P., C.M.C., C.P., E.A. and C.B.; investigation, A.M., M.I.L., M.-A.P., C.M.C. and C.P.; resources, M.I.L.; data curation A.M., M.I.L. and C.M.C.; writing—original draft preparation, A.M., V.P., M.-A.P., M.I.L. and C.P.; writing—review and editing, A.M., E.A. and M.-A.P.; visualization, V.P.; supervision, A.M., E.A., M.-A.P. and V.P. All authors have read and agreed to the published version of the manuscript Funding: This research received no external funding Institutional Review Board Statement: Not applicable Informed Consent Statement: Not applicable Data Availability Statement: All related data and methods are presented in this paper. Additional inquiries should be addressed to the corresponding authors Acknowledgments: The authors acknowledge the technical support provided by the Transilvania University of Brasov, Faculty of Food and Tourism, and the Interdisciplinary Research Platform belonging to the University of Life Sciences “King Mihai I” from Timisoara Conflicts of Interest: The authors declare no conflict of interest References 1 OIV. World Wine Production Outlook—OIV First Estimates. no. November. International Organisation of Vine and Wine, 2022; p 1. Available online: https://www.oiv.int/public/medias/8553/en-oiv-2021-world-wine-production-first-estimates-to-update. pdf (accessed on 14 January 2023) 2 Ntuli, R.G.; Saltman, Y.; Ponangi, R.; Jeffery, D.W.; Bindon, K.; Wilkinson, K.L. Impact of skin contact time, oak and tannin addition on the chemical composition, color stability and sensory profile of Merlot wines made from flash d é tente treatment Food Chem 2023 , 405 , 134849. [ CrossRef ] 3 Zhang, Q.; Wang, T. Effect of ultrasound irradiation on the evolution of color properties and major phenolic compounds in wine during storage Food Chem 2017 , 234 , 372–380. [ CrossRef ] [ PubMed ] 4 Huang, G.; Chen, S.; Dai, C.; Sun, L.; Sun, W.; Tang, Y.; Xiong, F.; He, R.; Ma, H. Effects of ultrasound on microbial growth and enzyme activity Ultrason. Sonochem 2017 , 37 , 144–149. [ CrossRef ] 5 Zhang, X.; Zuo, Z.; Yu, P.; Li, T.; Guang, M.; Chen, Z.; Wang, L. Rice peptide nanoparticle as a bifunctional food-grade Pickering stabilizer prepared by ultrasonication: Structural characteristics, antioxidant activity, and emulsifying properties Food Chem 2021 , 343 , 128545. [ CrossRef ] 6 Aekthammarat, D.; Tangsucharit, P.; Pannangpetch, P.; Sriwantana, T.; Sibmooh, N. Moringa oleifera leaf extract enhances endothelial nitric oxide production leading to relaxation of resistance artery and lowering of arterial blood pressure Biomed Pharmacother 2020 , 130 , 110605. [ CrossRef ] 7 Brenes, A.; Viveros, A.; Chamorro, S.; Arija, I. Use of polyphenol-rich grape by-products in monogastric nutrition. A review Anim. Feed Sci. Technol 2016 , 211 , 1–17. [ CrossRef ] 8 Xia, E.Q.; Deng, G.F.; Guo, Y.J.; Bin Li, H. Biological activities of polyphenols from grapes Int. J. Mol. Sci 2010 , 11 , 622–646 [ CrossRef ] [ PubMed ] 9 Kumar, L.; Tian, B.; Harrison, R. Interactions of Vitis vinifera L. cv. Pinot Noir grape anthocyanins with seed proanthocyanidins and their effect on wine color and phenolic composition LWT 2022 , 162 , 113428. [ CrossRef ] 10 Yusoff, I.M.; Mat Taher, Z.; Rahmat, Z.; Chua, L.S. A review of ultrasound-assisted extraction for plant bioactive compounds: Phenolics, flavonoids, thymols, saponins and proteins Food Res. Int 2022 , 157 , 111268. [ CrossRef ] 11 Chemat, F.; Rombaut, N.; Meullemiestre, A.; Turk, M.; Perino, S.; Fabiano-Tixier, A.S.; Abert-Vian, M. Review of Green Food Processing techniques. Preservation, transformation, and extraction Innov. Food Sci. Emerg. Technol 2017 , 41 , 357–377. [ CrossRef ]

[[[ p. 20 ]]]

[Summary: This page continues the conclusion, stating that ultrasound is a promising technique for extracting bioactive compounds. It lists author contributions, funding information, and a conflict of interest declaration. It begins listing references used in the study.]

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Ma, Statistical analysis, Working condition, Temperature, Red Wine, Ultrasonic waves, Antioxidant activity, Experimental model, Antioxidant properties, P Value, Free radical scavenging activity, Radical Scavenging Activity, Plant species, DPPH scavenging activity, ANOVA, Total polyphenol content, DPPH, High temperature, Ferric reducing antioxidant power, Bioactive compound, DPPH radical scavenging activity, FRAP assay, Positive correlation, Statistical method, Design Expert software, Titratable acidity, Design space, Temperature optimization, Sonication time, Response-surface methodology, Sonication effect, Physicochemical quality, Total phenolic compound, Central composite design, Temperature rise, Biologically active compound, Extraction time, Extraction temperature, DPPH free radical scavenging activity, Analytical determination, Anthocyanin content, Natural antioxidant, Extraction conditions, Total phenol, Phenolic compound, Optimization, ANOVA analysis, Phenolic composition, Extraction kinetic, Antiradical power, Extraction yield, Extraction optimization, CELL WALL, Organoleptic qualities, Gallic acid equivalent, Ultrasound assisted extraction, Antioxidant compound, Pearson Correlation, Geographical Origin, Quadratic Model, FRAP, Cavitation, Ultrasonic technology, Food Matrices, Dependent variable, Independent variable, Treatment time, Model F-value, Untreated sample, Sonicated samples, R 2 value, Pearson's r, Optimal solution, Adjusted R 2, Polyphenol, TPC, Model fit, Total polyphenol, Amplitude, R 2, Ultrasound treatment, FRAP value, Plant bioactive compound, Phenolic, Optimal circumstances, Predicted data, Model parameter, Validation trials, Phenolic extract, Red grape juice, Physiologically active compound, Numerical optimization, Lack of fit, Predicted r 2, Model term, Grape must, Treatment condition, Cell Content, High power ultrasound, Total Soluble Solid, Extraction Rate.

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