Study of Polyphenol Content and Antioxidant Properties of Various Mix of Chocolate Milk Masses with Different Protein Content.

The aim of the study was to analyze the antioxidant character of conched chocolate milk masses, taking into account different protein content in milk. For the study, cocoa liquor obtained from roasted and unroasted cocoa beans from different regions, as well as milk powder obtained by spray and cylindrical drying were used. The analysis that was carried out showed that the protein content of powdered milk products ranged from about 11.6% (w/w) to over 31% (w/w). Lower content of polyphenols and lower antioxidant activity were shown in the masses to which the addition of milk with higher protein content was applied. The analysis of antioxidant character of chocolate milk masses showed higher total polyphenols content in masses prepared from unroasted cocoa beans liquor.


Introduction
Cocoa beans are seeds of the tropical Theobroma cacao tree. There are three best known varieties of this plant: Forastero, which covers about 95% of the world's cocoa production and is most commonly used to produce chocolate; Criollo, which is the most exclusive but at the same time the least cultivated variety due to its susceptibility to diseases; and Trinitario, a hybrid combining the characteristics of Criollo and Forastero, with an intense chocolate aroma, with a hint of wine, more resistant to diseases and pests [1,2].
Many studies and numerous publications confirm that cocoa beans are a raw material carrying a powerful load of antioxidants, valued in today's diets mainly for their antiatherogenic, antiradical, and anticancer properties [3][4][5][6]. The genotype of cocoa beans, the region in which they are grown, the environmental conditions, as well as the conditions and parameters of applied technological operations, especially fermentation, drying, roasting, and conching, have a significant influence on the formation of sensory characteristics and antioxidant properties of cocoa bean processing products [7][8][9][10]. As numerous studies have shown, the most degrading content of phenolic compounds is the roasting stage-high-temperature heating of beans or cocoa shots, which significantly affects the antioxidant potential of chocolates [11][12][13][14][15]. The use of less processed cocoa beans (omitting the roasting process) for the production of chocolate mass may result in a product with a higher content of polyphenols and higher antiradical activity, as well as positively change the nutritional and health value. Therefore, interest in cocoa mass obtained from unroasted cocoa beans [2] has increased in recent years.
Conching is one of the main and most important stages in the chocolate production process. It consists of stirring and aerating the chocolate mass with simultaneous heating at a certain temperature results [22]. As shown by the results of the work involving the evaluation of consumer preference for chocolate, consumers are most likely to reach for milk chocolates.
However, research on milk chocolates is not conducted on a large scale, especially in terms of evaluating their antioxidant potential. They are mainly produced using milk obtained from spray drying and such products are the subject of most studies and publications. Moreover, chocolates called "raw"-produced without roasting-have appeared on the market. There is little research into these products. As well as few studies on the effect of conching on antioxidant properties have been published. Therefore, it seems reasonable to attempt to assess the effect of conching on the antioxidant potential of chocolate milk masses, taking into account the protein content of milk powder obtained by spray or cylindrical drying, as well as to analyze the subject of research after using roasted and unroasted cocoa pulp.
The aim of the study was to investigate the relationship between the protein content of milk powder and cocoa mass and the antioxidant potential of chocolate milk masses after conching.

Test Material
The research material was 19 milk powders differing in production technologies (Table 1) and the raw materials used to prepare chocolate milk masses-cocoa liquors from 3 manufacturers, differing the country of origin and in the process of processing the beans from which they were made and selected powdered milk ( Table 2). The results of the protein content and dry weight given in grams in 100 g of product (g 100 g −1 ) were expressed in (%)-(w/w). Whole-milk powder-WMP, Whey powder-WP, Milk preparation-MP, manufacturer X-MX, manufacturer Y-MY, manufacturer Z-MZ, drying technique-D, cylindrical drying technique-C. Milk powders and cocoa masses were obtained from the chocolate products manufacturers. The first stage of the research was to carry out the analysis of dry matter and protein content in powdered milk according to the research methodology described in the subchapter of analytical methods 3.1 and 3.2, respectively.
The samples marked with the codes Ml_1, Ml_2, Ml_3, Ml_6, and Ml_7 were spray-dried whole milk powders, differing in protein content (Table 1). On the other hand, the milk Ml_4 and Ml_5 differed from the other compositions (they were mixtures of milk with sugar) and were produced using the cylindrical method.

Technological Process
Chocolate milk masses were prepared by mixing (Table 3)  Chocolate milk masses were prepared from ingredients weighed and mixed at controlled temperature and time conditions in the Termomix device (Vorweck, Germany)-the household appliances. The first step was to liquefy a weighed portion of cocoa butter at 45 • C. Then the fat was poured into another container. The cocoa liquor was liquefied at 55 • C. The sugar, milk powder, whey, and 10% cocoa butter were added to the liquefied cocoa liquor. The ingredients were mixed for 10 min at a constant temperature of 45 • C, then residual cocoa fat and lecithin were added. The final stage was the proper conching, i.e., slow mixing of the mass at 55 • C for 1 h.

Analytical Methods
The reagents used for the analyses were purchased from Sigma Aldrich Company.

Determination of Dry Matter Content
The dry matter content was determined in all samples of milk powder and cocoa liquor. This analysis consisted in the evaporation of water from the material tested during the drying process, followed by weight determination of the residue (dry matter).
The weight of test material was dried to constant mass at 105 • C for 3 h in the laboratory chamber oven type SUP-65 WG manufacturer WAMED. Samples of cocoa liquor and chocolate masses were dried with sand to increase the evaporation surface. The dry matter content was calculated from the difference of sample weight before and after drying. The arithmetic mean of three parallel repetitions for each sample was taken as the final result.

Determination of Protein Content
The determination of protein content was performed in all samples of milk powder and cocoa liquor. The protein content was determined by the Kjeldahl method. The principle of the method consisted in mineralization of samples with concentrated sulphuric acid (VI) in the presence of a catalyst (selenium-copper mixture) in the Buchi 426 Dugestion Unit. Under these conditions, the protein nitrogen was converted to an ammonium ion, which after alkalization was distilled in the form of ammonia and bound in excess boric acid in Buchi's distillation unit B-316. The ammonia solution was determined by potentiometric titration with 0.1 N hydrochloric acid standard solution. The nitrogen content in the sample was calculated on the basis of the volume of 0.1 N of hydrochloric acid standard solution used for titration, knowing that 1 cm 3 of 0.1 N of hydrochloric acid solution corresponds to 0.0014 g of nitrogen. Nitrogen was converted into protein using a multiplier calculated from the average nitrogen content in proteins, which is 16% (100:16 = 6.25). The determination was carried out in three consecutive repetitions.

Determination of Total Polyphenols Content by the Folin-Ciocalteu Method
Total polyphenol content was determined by Folin-Ciocalteu's method [31,32]. Based on preliminary tests, a 70% acetone solution was used as a solvent to prepare extracts. The extracts were prepared by weighing about 5 g of crushed test material into 300 mL grinding conical flasks and adding 100 mL of 70% acetone (v/v). The samples were then shaken for 30 min in a Multi-Shaker PSU 20 Biosan shaker. Following this procedure, the solutions were filtered through the corrugated filters into 100 mL grinding flasks. In order to determine the total polyphenol content, 300 µL of the extract was taken from the tubes, and 4.15 mL of deionized water, 500 µL of 20% sodium carbonate solution, and 50 µL of the Folin-Ciocalteu reagent were added. The blank sample was prepared by sampling: 300 µL of the extraction solution, 4.15 mL of deionized water, 500 µL of the 20% sodium carbonate solution, and 50 µL of the Folin-Ciocalteu reagent. Absorbance was measured at 700 nm on a Shimadzu UV-160A spectrophotometer. The apparatus was zeroed to a blank. In order to calculate the total polyphenol content, a standard curve was prepared. The standard curve was plotted for chlorogenic acid for various concentrations (0, 25, 50, 75, and 100 µL) used in absorbance measurements. Based on the results obtained, the graphical dependence of the absorbance of the solution on the amount of gallic acid contained in it was plotted. The total polyphenol content was calculated on the basis of the calibration curve and expressed in gallic acid equivalent in mg per 100 g d.m. (mg GAE·100 g −1 of the product Two extracts from each mass were made and polyphenols content was determined in three parallel repetitions for each extract. The average of six repetitions for each mass was considered the final result.

Determination the Ability of Extracts to Inactivate Stable DPPH Radicals
The extracts were prepared by weighing 5 g test material to conical flasks (300 mL) and adding 100 mL of 70% acetone (v/v). The samples were then shaken for 30 min in a Multi-Shaker PSU 20 Biosan shaker. Following that, the solutions were filtered through the corrugated filters into 100 mL flasks. Acetone extract (1 mL), acetone solution (3 mL), and added DPPH solution (1 mL) were taken to determine the appropriate sample. Acetone solution (4 mL) and DPPH solution (1 mL) were collected for the control sample. The samples were mixed and left to stand for 30 min, then absorbance was measured on the NOVASPEC II Pharmacia spectrophotometer (apparatus were zeroed for the blank test) at a wavelength of 517 nm in glass cuvettes with a diameter of 1 cm [33,34].
The antioxidant activity of the extracts against DPPH was calculated using the formula: where Act.-antioxidant activity (%); Ak-the absorbance of the control sample; and As-absorption of the specific sample.

The Statistical Analysis
The statistical analysis of results was performed in the Statistica 13.0. Program by using oneand two-factor analysis of variance at significance level α = 0.05 to determine differences between the content of polyphenolic compounds and the antioxidant ability the test samples of chocolate milk masses, taking into account the effect of the protein content of milk powder. Significant differences between means were determined through Tukey's tests. The correlation matrix was analyzed to determine the relationship between polyphenol content and antioxidant activity.

Selection of Raw Materials for Chocolate Milk Masses Production
The selection of components differentiating the mixtures was carried out on the basis of their own characteristics and the results of analyses to which they were subjected (Tables 1 and 4). For preparation of milk masses three cocoa liquor were used: Ch_1, Ch_2, and Ch_3 ( Table 4) and seven of tested powdered milk: Ml_1, Ml_2, Ml_3, Ml_4, Ml_5, Ml_6, and Ml_7 (Tables 1 and 2). The remaining part of the composition consisted of ingredients such as cocoa fat, sugar, whey, and lecithin.
The protein content in the tested cocoa masses oscillated around 13.6-14.6% (w/w). The values obtained in this study are also presented by the studies of Jumnongpon, et al. [35] and Torres-Moreno, et al. [36], who determined the protein content in cocoa beans from which cocoa mass is produced at the level of 13-20% (w/w). Selected pulp differed in producer, origin, and type of grain from which they were prepared, while in the case of dry substance and protein content they had similar parameters (Table 4).
Proteins are important bioactive food ingredients, but the potential biological activity of oligopeptides found in cocoa is insufficiently researched. Biologically active or functional proteins come primarily from food and have, in addition to their nutritional value, a physiological effect on the body [37].
In cocoa, peptides are formed naturally during the fermentation of cocoa beans and are considered important flavor precursors. The peptides come from two main protein fractions-globules, consisting of a storage protein resembling vicilin and albumin, which exhibit trypsin inhibitory properties. Cocoa proteins during natural cocoa fermentation are split into hydrophilic and hydrophobic peptides as well as amino acids by autolysis of two endogenous enzymes: aspartic endoprotease and carboxypeptidase activated by microbial metabolites such as acetic acid [38]. Milk proteins include complex groups of proteins: caseins (αs1-, αs2-, β-, and κcasein), whey proteins (β-lactoglobulin, α-lacto-albumin, albumin serum, and immunoglobulin), and protein envelopes of fat globules. Structural differences within milk protein molecules affect their properties [39]. It is assumed that β-casein is the most effective stabilizer among milk proteins as it reduces the surface tension most [40].
According to Christian Vásquez, et al. [41] milk proteins can act as surfactants and stabilizers that are able to induce the formation of spherical micellar aggregates in the chocolate structure. Moreover, spray drying technology can induce changes in proteins that affect hydrophobicity, solubility, and denaturation [42][43][44]. Milk selected for preparation of milk chocolate masses contained from 11.61 to 31.1 mg of protein in 100 g of powder ( Table 1). The selection was made in such a way that protein content in the analyzed milk was differentiated. This allowed for comparative analysis and evaluation of the dependence between phenol potential and protein content.
Antioxidants prevent formation of free radicals or support their removal. The milk contains several antioxidant factors such as vitamins and enzymes. Possible antioxidant activity of milk proteins and their hydrolysates has also been shown. It has been reported that peptides produced from milk protein digestion have an antioxidant effect. According to Pihlanto [45], antioxidant peptides derived from milk consist of 5-11 amino acids, including hydrophobic amino acids, proline, histidine, tyrosine, or tryptophan in the sequence.
The cocoa liquor and milk used in the study were subjected to a technological process to obtain 21 chocolate milk masses, which were tested for polyphenols content and antioxidant activity against free radicals of DPPH.

Results of Polyphenols Content Determination in Chocolate Milk Masses
The presence of polyphenols in milk depends on the animal's diet and may affect the preservative effect of milk components [46].
In milk masses made on the basis of cocoa liquor obtained from unroasted beans from Peru (Ch_1) and seven milk/milk powder mixes, the polyphenols content was obtained from about 1525 to about 1685 mg calculated as gallic acid in 100 g of product ( Figure 1). The highest content of phenolic compounds was achieved by the T-5 sample with the addition of milk Ml_5 (protein content 13.19%) and the lowest by T1 based on whole milk powder Ml_1 (protein content 30.35%). The differences in the content of polyphenols were statistically significant, as indicated by five homogeneous groups.
1 Figure 1. Polyphenols content in chocolate milk masses prepared from cocoa liquor from Peru (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).

Figure 2.
Polyphenols content in chocolate masses prepared from Ivory Coast cocoa liquor (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).

Figure 1.
Polyphenols content in chocolate milk masses prepared from cocoa liquor from Peru (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
In the investigated milk masses prepared on the basis of cocoa liquor bean from the Ivory Coast (Ch_2) in combination with seven different milk powders the results of polyphenols content on the level from about 838 to almost 1071 mg per 100 g of product were obtained (Figure 2).

Figure 1.
Polyphenols content in chocolate milk masses prepared from cocoa liquor from Peru (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).

Figure 2.
Polyphenols content in chocolate masses prepared from Ivory Coast cocoa liquor (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3). Polyphenols content in chocolate masses prepared from Ivory Coast cocoa liquor (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
The highest content of polyphenols was determined for the mass of T-12, to which the milk mixture Ml_5 (dried by cylinders method) was used, whereas the lowest for the mass of T-8, to which spray-dried whole milk was applied (Ml_1). All masses formed six homogeneous groups, which prove their statistically significant differentiation in terms polyphenols content. Only T-14 masses did not differ significantly from T-9 and T-13 samples. In the presented values a specific order of increase in the content of phenolic compounds from T-8, through T-10, T-9, T-14, T-13, T-11, to T-12 chocolate was observed. It is worth emphasizing that T4 and T5, as well as T11 and T12 masses were characterized by the highest content of polyphenols, and Ml_4 (protein content 18.9%) and Ml_5 (protein content 13.19%) milk with the lowest protein content was used to produce them. Figure 3 shows the results of the determination of polyphenols content in masses obtained with the use of cocoa liquor made from cocoa beans grown in Ghana (Ch_3). Invariably, the mass with the highest content of the determined compounds remained the one with the addition of milk Ml_5 (T5 and T12 on Figures 1 and 2) and the one with the lowest one with the addition of whole milk powder Ml_1. A similar tendency to the polyphenol content was found as in the samples with the addition of cocoa liquor from the Ivory Coast. However, the differences between the masses were much less pronounced, but nevertheless formed six homogeneous groups. By comparing the results of the masses in Figure 3 with those produced from Ch_2 cocoa liquor (Ivory Coast), an average of 3-5% higher total polyphenol content could be observed in each sample in favor of those produced from beans from Ghana, regardless of the milk used. However, it is noteworthy that Ghanaian cocoa liquor beans were found to have a lower polyphenol content of approximately 6% compared to the values determined for Ivory Coast cocoa liquor bean. However, the protein content of the Ch_2 cocoa liquor was about 3% higher than that of the Ch_3 cocoa liquor ( Table 4). The results obtained may confirm the literature data describing interactions between polyphenols and proteins present in the chocolate matrix. This is mainly due to the induction by proteins of the formation of spherical micellar aggregates, which close polyphenolic compounds limiting their availability.  Table 3).

Figure 3. Polyphenols in chocolate milk masses prepared from
Ghana cocoa liquor (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
Analyzing the results obtained for all 21 chocolate milk masses, it was noted that the amount of polyphenols contained in them oscillated between 35% and 50% of the values obtained for the cocoa liquor from which they were obtained. This is mainly due to the recipe in which cocoa mass constitutes less than 2/3 of the raw material composition of the finished chocolate milk mass. Additionally, not only the cocoa liquor (although certainly in the majority) brings an additional antioxidant character to the chocolate milk masses, because, as indicated by the studies of Ertan, et al. [47], whole milk powder may contain from about 50 to even 100 mg of polyphenols converted into gallic acid in 100 g of product. Summarizing these values in the finished product, which is a milk mass, it is possible to explain a polyphenol content of 1000-1500 mg in chocolates based on roasted cocoa liquor bean and correspondingly more in chocolates prepared from unroasted cocoa liquor bean. While the values for dairy products based on unroasted cocoa liquor bean were within the assumed range, this was not the case for roasted cocoa liquor bean. This could result in a small extent from the treatments (in the process of conching) to which the milk mass was subjected, losing between 5% and 10% of phenolic compounds as indicated by Di Mattia, et al. [1]. However, in the majority of cases, this loss was probably the result of possible interactions between polyphenols and proteins contained in milk and whey powder, intensified mixing time to which chocolate masses are subjected. As Gallo, et al. [48] points out, polyphenol-protein interactions may occur in milk chocolates, resulting in compounds that are inaccessible to the components of the reaction, while limiting their availability and in vitro oxidative potential. These studies showed a 15% decrease in the assay of polyphenols combined with casein, a 25% decrease in combination with whey proteins and almost 40% decrease in combination with pure ß-lactoglobulin (the main whey protein of milk). The results of these studies may explain the trends obtained in the studies carried out in this study, considering that the results obtained after statistical analysis confirmed a correlation of −0.66 between protein and polyphenol content in chocolate milk masses.
The comparative analysis of polyphenol content in all analyzed milk chocolate masses was 13 homogeneous groups, which indicates a large diversity of tested samples ( Table 5). Considering that the protein content in chocolate pulp used to make the masses was at a similar level, and every third sample contained the addition of the same milk, such a large number of homogeneous groups indicate the complexity of factors shaping the antioxidant potential. Table 5. Results of statistical analysis of polyphenols content and antiradical activity of all analyzed milk chocolate masses (code explanation in Table 3).

Codes of Masses
Polyph. DPPH Codes of Masses Polyph. DPPH Codes of Masses Polyph. DPPH The same letter A, B or a, b means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3.

Results of Determination of Antioxidant Activity in Chocolate Milk Masses
Whey proteins may have an antioxidant activity, while heat treatment at very high temperature has no clear effect on the antioxidant potential of milk [49].
Antioxidant potential (AP) is an important nutritional property of food, as increased oxidative stress has an effect on most diet-related chronic diseases. In dairy products the protein fraction shows antioxidant activity, especially casein. Pihlanto study [45] reported that peptides produced from milk protein digestion have an antioxidant effect. Antioxidant peptides derived from milk consist of 5-11 amino acids, including hydrophobic amino acids, proline, histidine, tyrosine, and tryptophan in sequence.
The milk contains several antioxidants: naturally occurring vitamins (i.e., E and C), β-carotene, enzymatic systems, serum albumin, and lactoferrin, which act as chelating agents, iron-binding glycoprotein, and the activity of free radical scavenging by amino acids such as tyrosine and cysteine [45]. Therefore, polyphenols may be the main contributor to the antioxidant capacity of the food matrix [44].
The solubility of milk protein in water may be closely related to the oxidative status as oxidation improves interactions and protein aggregation [50], which reduces the solubility of milk powder [51].
In these studies, the antioxidant activity remained in the same upward trend as polyphenols. The results of the phenolic potential expressed as antioxidant activity in the masses obtained from unroasted cocoa beans are shown in Figure 4. However, it was noticeable, as in the case of the determination of phenolic compounds, that higher values, on average by 8-10%, were obtained for the masses obtained from unroasted cocoa beans. The obtained values were subjected to statistical analysis, on the basis of which the masses were assigned to seven homogeneous groups. No significant differences were observed between T2 and T3 masses, prepared successively from whole milk powder Ml_2 and Ml_3, containing 27.44% and 29.14% (w/w) protein, respectively. Antioxidants 2020, 9, x FOR PEER REVIEW 11 of 17 The solubility of milk protein in water may be closely related to the oxidative status as oxidation improves interactions and protein aggregation [50], which reduces the solubility of milk powder [51].
In these studies, the antioxidant activity remained in the same upward trend as polyphenols. The results of the phenolic potential expressed as antioxidant activity in the masses obtained from unroasted cocoa beans are shown in Figure 4. However, it was noticeable, as in the case of the determination of phenolic compounds, that higher values, on average by 8%-10%, were obtained for the masses obtained from unroasted cocoa beans. The obtained values were subjected to statistical analysis, on the basis of which the masses were assigned to seven homogeneous groups. No significant differences were observed between T2 and T3 masses, prepared successively from whole milk powder Ml_2 and Ml_3, containing 27.44% and 29.14% (w/w) protein, respectively.  Table 3).
In chocolate milk masses prepared from unroasted cocoa liquor bean from Peru, the results of determination of antioxidant activity against free radicals of DPPH were 70%-80% ( Figure 5). The highest activity was characterized by T12 mass with the addition of milk mixture Ml_5, while the lowest T-8 mass with addition of whole milk powder Ml_1, which coincides with the dependence obtained during polyphenols determination. Similar observations were also observed in the significance of differences in the levels of antioxidant activity as, as well as in the case of polyphenols content. Chocolate milk masses from the Ivory Coast cocoa liquor bean formed six homogeneous groups from which no significant differences between the T14 and T9 and T13 mixture were found.
In chocolate milk masses prepared from roasted cocoa liquor bean from Ivory Coast the results of determination of antioxidant activity against free radicals of DPPH were 70%-80% ( Figure  5). The highest activity was characterized by T12 mass with addition of milk mixture Ml_5, while the lowest T-8 mass with addition of whole milk powder Ml_1, which coincides with the dependence obtained during polyphenols determination. Similar observations were also observed in the significance of differences in the levels of antioxidant activity as well as in the case of polyphenols content. Milk masses from the Ivory Coast cocoa liquor bean formed six homogeneous groups from which no significant differences between T14 and T9 and T13 mixture resulted (Figure 5?). . Antioxidant activity in chocolate milk masses prepared from unroasted cocoa liquor from Peru (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
In chocolate milk masses prepared from unroasted cocoa liquor bean from Peru, the results of determination of antioxidant activity against free radicals of DPPH were 70-80% ( Figure 4). The highest activity was characterized by T5 mass with the addition of milk mixture Ml_5, while the lowest T-8 mass with addition of whole milk powder Ml_1, which coincides with the dependence obtained during polyphenols determination. Similar observations were also observed in the significance of differences in the levels of antioxidant activity as, as well as in the case of polyphenols content. Chocolate milk masses from the Ivory Coast cocoa liquor bean formed six homogeneous groups from which no significant differences between the T14 and T9 and T13 mixture were found.
In chocolate milk masses prepared from roasted cocoa liquor bean from Ivory Coast the results of determination of antioxidant activity against free radicals of DPPH were 70-80% ( Figure 5). The highest activity was characterized by T12 mass with addition of milk mixture Ml_5, while the lowest T-8 mass with addition of whole milk powder Ml_1, which coincides with the dependence obtained during polyphenols determination. Similar observations were also observed in the significance of differences in the levels of antioxidant activity as well as in the case of polyphenols content. Milk masses from the Ivory Coast cocoa liquor bean formed six homogeneous groups from which no significant differences between T14 and T9 and T13 mixture resulted ( Figure 5).

Figure 5.
Antioxidant activity in chocolate milk masses prepared from Ivory Coast cocoa liquor (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
The levels of antiradical activity of milk masses prepared from cocoa liquor from Ghana also maintained very similar relationships as in the case of the previous variant and the results obtained during the determination of polyphenols content ( Figure 6). Again, the mixture with the addition of milk preparation Ml_5 (protein content 13.19%) was characterized by the highest value of the properties tested (in this case antiradical activity). A similar tendency of changes in antioxidant activity as in all previous determinations were shown on Figure 5 and Figure 6. . Antioxidant activity in chocolate milk masses prepared from cocoa liquor from Ghana (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
The antioxidant activity expressing the degree of reduction of free radicals by antioxidant compounds contained in the product is a valuable parameter of both the technological and health potential. The results obtained for all 21 milk masses allowed to determine in which of them the in  T15  T16  T17  T18  T19  T20  T21 Antyradical activity (%) Figure 5. Antioxidant activity in chocolate milk masses prepared from Ivory Coast cocoa liquor (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
The levels of antiradical activity of milk masses prepared from cocoa liquor from Ghana also maintained very similar relationships as in the case of the previous variant and the results obtained during the determination of polyphenols content ( Figure 6). Again, the mixture with the addition of milk preparation Ml_5 (protein content 13.19%) was characterized by the highest value of the properties tested (in this case antiradical activity). A similar tendency of changes in antioxidant activity as in all previous determinations were shown on Figures 5 and 6. Figure 5. Antioxidant activity in chocolate milk masses prepared from Ivory Coast cocoa liquor (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
The levels of antiradical activity of milk masses prepared from cocoa liquor from Ghana also maintained very similar relationships as in the case of the previous variant and the results obtained during the determination of polyphenols content ( Figure 6). Again, the mixture with the addition of milk preparation Ml_5 (protein content 13.19%) was characterized by the highest value of the properties tested (in this case antiradical activity). A similar tendency of changes in antioxidant activity as in all previous determinations were shown on Figure 5 and Figure 6. . Antioxidant activity in chocolate milk masses prepared from cocoa liquor from Ghana (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
The antioxidant activity expressing the degree of reduction of free radicals by antioxidant compounds contained in the product is a valuable parameter of both the technological and health potential. The results obtained for all 21 milk masses allowed to determine in which of them the in  T15  T16  T17  T18  T19  T20  T21 Antyradical activity (%) Figure 6. Antioxidant activity in chocolate milk masses prepared from cocoa liquor from Ghana (the same letter means that there are no statistically significant differences between the analyzed products at a confidence level of α = 0.05; the abbreviations used in the graph are described in Table 3).
The antioxidant activity expressing the degree of reduction of free radicals by antioxidant compounds contained in the product is a valuable parameter of both the technological and health potential. The results obtained for all 21 milk masses allowed to determine in which of them the in vitro antioxidant potential was highest and how it changed depending on the raw materials used and the process parameters.
In the studies of Da Silva Medeiros, et al. [30], as well as Todorović, et al. [52], chocolate milk masses with declared cocoa liquor content of about 30% were distinguished by almost six times lower antioxidant activity potential, as compared to the tested bitter chocolates with declared cocoa liquor content of 67-70%. Similarly, the studies of Serafini, et al. [53] on blueberry fruit extracts and Dubeau, et al. [54] on different types of tea proved to confirm the dependence of lowering the antioxidant activity of extracts prepared after mixing them with milk. However, these values, unlike in the case of chocolates, were characterized by only 5-20% lower results compared to the activity of extracts not enriched with milk. Differences may result mainly from different protein content in milk added to tea (liquid-about 5 g/100 mL) and content of this ingredient in dried milk (about 30 g/100 g), as well as the amount of milk added in the mentioned variants.
In the investigated milk masses similar relationships were noted, because after the addition of milk or milk preparations, they reached much lower inactivation capacity of free radicals DPPH. This characteristic tendency is caused mainly by the fact, as indicated by Vertuani, et al. [55], that these masses are mixtures of various components, of which the cocoa liquor, bringing the greatest antioxidant character, is only a part of their composition. It is noteworthy, however, that this decrease was not as large as in the case of studies comparing milk chocolates to bitter chocolates. The differences were closer to those recorded for blueberry or tea extracts. This may mean that further processing and more intense industrial conditions, which were not provided for in this study, may lead to an increase in the reduction of antioxidant activity in milk chocolate. Intensified and extended by the process of tempering, the mixing of milk chocolate components causes more frequent interactions in the mixture of polyphenols with proteins, which, as indicated by Belščak, et al. [56], form complexes no longer having the same antiradical properties under the conditions of the antioxidant activity determination reaction. Similar conclusions were also drawn by Dubeau, et al. [54], who determined that casein proteins and catechin molecules in tea are mainly responsible for complex formation.
By the use of ANOVA analysis the results of antioxidant activity obtained for particular chocolate milk masses were compared to their polyphenols content. The correlation was close to 96.5%, which is a very strong correlation. It shows a simultaneous proportional decrease in antioxidant activity with a decrease in polyphenols content and its high value is also confirmed by Miller, et al. [57] in which this correlation reached almost 98%. However, more interesting from the nutritional point of view was a strong correlation between the results of protein content in masses and the content of previously discussed polyphenols or antioxidant activity. Negative correlation at the level of 0.66 and 0.76, respectively, showed a gradual proportional decrease in polyphenols and antioxidant activity with increasing protein content in the mass. The possible formation of protein-polyphenol complexes, supported by the study results and quoted in the literature, may explain this relationship. It can also be a valuable indication for producers of milk chocolate, who, while making chocolate products, also want to ensure pro-healthy values by preserving as many polyphenol compounds as possible. This relationship may also explain the observations of Serafini, et al. [53], who stated in their research that the reduction of antioxidant potential may also be influenced by the fat content, because taking into account whole, semiskimmed and skimmed milk, they obtained for blueberry fruit extracts a similarly characteristic decrease in antioxidant activity with increasing fat content. However, this dependence may have been largely due to the decrease in potential due to the antioxidant products of fat oxidation as well as to the decreasing antioxidant potential due to their combination with milk proteins.
Statistical inference was carried out with a 95% confidence level, to which the results of antioxidant activity of all tested milk chocolate masses were subjected. Fourteen homogeneous groups were obtained-one group more than for the analysis of polyphenols content (Table 5). Noteworthy is the analysis of masses T-7, T-8, T-1, T-12, T-16, and T-21, which were in the same groups in both the content of polyphenols and DPPH. A similar inference arises, as described in the analysis of polyphenol content. The analytical analysis confirmed the large variation between the results obtained, despite the fact that the tested masses can be grouped into three areas in terms of the used milk chocolate mass and in seven groups in terms of the used milk powder. The results indicate the complexity of aspects related to antioxidant potential.
Regardless of the decreasing antioxidant reduction potential in vitro studies, in many works, among others, Serafini, et al. [53], Loffredo, et al. [58], and Di Mattia, et al. [1], the same trend is not observed in studies on living organisms. In all these studies, the results of the increase in the occurrence of specific antioxidants in plasma consumed in the vicinity of milk did not differ significantly from those of milk-free counterparts. Such dependence may mainly result from the conditions of the digestive process of living organisms and many transformations and changes of substances that may occur as a result. Decreases in the amount determined in the body of epicatechin patients were recorded in studies by Neilson, et al. [59] after consumption of cocoa products containing milk. In each case, however, these values, although lower, did not show statistically significant differences. This phenomenon was explained by the variability of intestinal capture of food components and their subsequent transport between cells in patients' organisms. It follows that lowering the antioxidant character of cocoa in a product with the addition of milk, such as milk chocolate, may be of primarily technological importance.

Conclusions
In this study, the highest content of polyphenols was determined in chocolate milk masses obtained from milk with the lowest protein content. This relationship is least evident in the masses obtained from cocoa liquor from Ghana, which also contained the least protein. Negative correlation between protein and polyphenol content in chocolate masses was observed.
A strong correlation was also shown for the decreasing ability of chocolate milk masses to scavenge DPPH radicals with increasing protein content of milk or milk preparations used to produce them. This correlation proves that the antioxidant potential of ready-made chocolate milk masses decreases with increasing content of milk proteins and consequently their ability to neutralize and inhibit the oxidation reaction of fats contained in chocolates decreases.
A strong correlation between the content of polyphenols in chocolate milk masses prepared for testing and their antioxidant activity was shown, which proves a proportional preservation of both values in the subject of the study.
In order to confirm this hypothesis, further studies should focus on the determination of fat oxidation products in masses and in vitro tests on the analyzed analytical matrix.