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<article xml:lang="en" article-type="research-article" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">
    <front>
        <journal-meta>
            <journal-id journal-id-type="publisher-id">PSJFS</journal-id>
            <journal-title-group>
                <journal-title>Potravinarstvo Slovak Journal of Food Sciences</journal-title>
                <abbrev-journal-title abbrev-type="pubmed">Potr. S. J. F. Sci.</abbrev-journal-title>
            </journal-title-group>
            <issn pub-type="ppub">1338-0230</issn>
            <issn pub-type="epub">1337-0960</issn>
            <publisher>
                <publisher-name>Association HACCP Consulting</publisher-name>
            </publisher>
        </journal-meta>
        <article-meta>
            <article-id pub-id-type="publisher-id">PSJFS-15-1-445</article-id>
            <article-id pub-id-type="doi">10.5219/1623</article-id>
            <article-categories>
                <subj-group subj-group-type="heading">
                    <subject>ARTICLE</subject>
                </subj-group>
            </article-categories>
            <title-group>
                <article-title>BASIL – A COMPARISON OF THE TOTAL PHENOLIC CONTENT AND ANTIOXIDANT ACTIVITY IN SELECTED CULTIVARS</article-title>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author">
                    <name>
                        <surname>Adámek</surname>
                        <given-names>Martin</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff1" />
                    <xref ref-type="corresp" rid="cor1">&#x002A;</xref>
                </contrib>
                <contrib contrib-type="author">
                    <name>
                        <surname>Mlček</surname>
                        <given-names>Jiří</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff2" />
                </contrib>
                <contrib contrib-type="author">
                    <name>
                        <surname>Adámková</surname>
                        <given-names>Anna</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff3" />
                </contrib>
                <contrib contrib-type="author">
                    <name>
                        <surname>Mišurec</surname>
                        <given-names>Vít Guiglielmo</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff4" />
                </contrib>
                <contrib contrib-type="author">
                    <name>
                        <surname>Orsavová</surname>
                        <given-names>Jana</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff5" />
                </contrib>
                <contrib contrib-type="author">
                    <name>
                        <surname>Bučková</surname>
                        <given-names>Martina</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff6" />
                </contrib>
                <contrib contrib-type="author">
                    <name>
                        <surname>Búran</surname>
                        <given-names>Martin</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff7" />
                </contrib>
                <contrib contrib-type="author">
                    <name>
                        <surname>Plášková</surname>
                        <given-names>Anna</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff8" />
                </contrib>
                <contrib contrib-type="author">
                    <name>
                        <surname>Kouřimská</surname>
                        <given-names>Lenka</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff9" />
                </contrib>
                <aff id="aff1">
                    <institution>Martin Adámek, Brno University of Technology, Faculty of Electrical Engineering and Communication, Department of Microelectronics, Technická 3058/10, 616 00 Brno, the Czech Republic, Tel.: +420541146136; Tomas Bata University in Zlin, Faculty of Technology, Department of Physics and Materials Engineering, Vavreckova 275, 760 01 Zlín, the Czech Republic, Tel.: +420576035105, E-mail: adamek@feec.vutbr.cz, m2adamek@utb.cz</institution>
                </aff>
                <aff id="aff2">
                    <institution>Jiří Mlček, Tomas Bata University in Zlin, Faculty of Technology, Department of Food Analysis and Chemistry, Vavreckova 275, 760 01 Zlín, the Czech Republic, Tel.: +420576033030, E-mail: mlcek@ft.utb.cz</institution>
                </aff>
                <aff id="aff3">
                    <institution>Anna Adámková, Tomas Bata University in Zlin, Faculty of Technology, Department of Food Analysis and Chemistry, Vavreckova 275, 760 01 Zlín, the Czech Republic, Tel.: +420576031592, E-mail: aadamkova@ft.utb.cz</institution>
                </aff>
                <aff id="aff4">
                    <institution>Vít Guiglielmo Mišurec, Tomas Bata University in Zlin, Faculty of Technology, Department of Food Analysis and Chemistry, Vavreckova 275, 760 01 Zlín, the Czech Republic, Tel.: +420576033030, E-mail: v_misurec@utb.cz</institution>
                </aff>
                <aff id="aff5">
                    <institution>Jana Orsavová, Tomas Bata University in Zlin, Faculty of Humanities, Language Centre, Štefánikova 5670, 760 01 Zlín, Czech Republic,Tel.: +420576038158 E-mail: orsavova@utb.cz</institution>
                </aff>
                <aff id="aff6">
                    <institution>Martina Bučková, Tomas Bata University in Zlin, Faculty of Technology, Department of Food Analysis and Chemistry, Vavreckova 275, 760 01 Zlín, the Czech Republic, Tel.: +420734796959 E-mail: buckova@utb.cz</institution>
                </aff>
                <aff id="aff7">
                    <institution>Martin Búran, Brno University of Technology, Faculty of Electrical Engineering and Communication, Department of Microelectronics, Technická 3058/10, 616 00 Brno, the Czech Republic, Tel.: +420541146106, E-mail: xburan02@stud.feec.vutbr.cz</institution>
                </aff>
                <aff id="aff8">
                    <institution>Anna Plášková, Tomas Bata University in Zlin, Faculty of Technology, Department of Food Analysis and Chemistry, Vavreckova 275, 760 01 Zlín, the Czech Republic, Tel.: +420734796959 E-mail: plaskova@utb.cz</institution>
                </aff>
                <aff id="aff9">
                    <institution>Lenka Kouřimská, Czech University of Life Sciences Prague, Faculty of Agrobiology, Food and Natural Resources, Department of Microbiology, Nutrition and Dietetics, Kamýcká 129, 165 00 Praha, Czech Republic, Tel.: +420224383507, E-mail: kourimska@af.czu.cz</institution>
                </aff>
            </contrib-group>
            <author-notes>
                <corresp id="cor1">
                    <label>&#x002A;</label>
                    <email xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="adamek@feec.vutbr.cz">adamek@feec.vutbr.cz</email>, <email xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="m2adamek@utb.cz">m2adamek@utb.cz</email>
                </corresp>
            </author-notes>
            <pub-date pub-type="epub">
                <day>28</day>
                <month>5</month>
                <year>2021</year>
            </pub-date>
            <pub-date pub-type="ppub">
                <month>5</month>
                <year>2021</year>
            </pub-date>
            <volume>15</volume>
            <issue>1</issue>
            <fpage>445</fpage>
            <lpage>452</lpage>
            <history>
                <date date-type="received">
                    <day>22</day>
                    <month>3</month>
                    <year>2021</year>
                </date>
                <date date-type="accepted">
                    <day>3</day>
                    <month>5</month>
                    <year>2021</year>
                </date>
            </history>
            <permissions>
                <copyright-statement>&#x00A9; Association HACCP Consulting. All rights reserved.</copyright-statement>
                <copyright-year>2021</copyright-year>
                <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">
                    <license-p>This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<uri xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">http://creativecommons.org/licenses/by-nc/3.0</uri>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
                </license>
            </permissions>
            <abstract>
                <p>During the lifetime, the human body forms a considerable amount of free radicals damaging DNA, cell membranes, and their components. A wider application of basil (<italic>Ocimum basilicum</italic>), an aromatic plant and one of the common gastronomic commodities in the human diet could help to prevent the formation of free radicals and to remove them from the human body. Therefore, determination of antioxidant activity and total content of phenolic substances in selected cultivars of basil (Ohře, Sweet green, Salad leaf, Purple opal, Thai) in a fresh and frozen state and the mixture with another plant (garlic, mint, rocket, spinach) in the fresh and refrigerated state was performed. The total content of phenolic substances in basil was established by the spectrophotometric Folin-Ciocalteu method. DPPH spectrophotometric method was used to analyze the antioxidant activity. The results have shown statistically significant differences between basil cultivars under the same growing conditions. The values of antioxidant activity in frozen samples ranged from 5.1 ±0.4 mg.g<sup>-1</sup> AA FW to 11.71 ±0.18 mg.g<sup>-1</sup> AA FW and the total phenolic content varied between 2.77 ±0.16 mg.g<sup>-1</sup> GAE FW in TH and 8.93 ±0.13 mg.g<sup>-1</sup> GAE FW. A statistically significant difference between fresh and frozen samples was established only in the “Ohře” cultivar. After the storage in cold temperatures, all mixtures showed a reduction in the antioxidant activity and total content of phenolic substances. The mixture of basil and mint performed the highest values of antioxidant activity and total content of phenolic substances and significantly differed from the other mixtures most often. The addition of basil and its mixtures to food and beverages can substantially increase their biological value and subsequently also the quality of human nutrition.</p>
                <p>
                    <bold>Keywords:</bold> Basil; <italic>Ocimum basilicum</italic>; total phenolic content; antioxidant activity; cultivar</p>
            </abstract>
        </article-meta>
    </front>
    <body>
        <sec sec-type="intro">
            <title>INTRODUCTION</title>
            <p>Basil is one of the basic commodities of world gastronomy, particularly Italian. It also plays an important role in Thai, Indonesian, French and Brazilian cuisine. The spread of basil all over the world has driven the development of an immense number of cultivars differing in shape, color, and size of leaves, plant height, taste, and aroma. The place of origin affects the resistance of the plant to higher or lower temperatures or temperature changes. Furthermore, the plants may differ, for example, also in their resistance to infestation. These properties influence the content of chemical substances including phenolic substances or other non-phenolic antioxidants with positive effects on human health.</p>
            <p>Basil leaves rich in essential oils are mainly used to add flavor to food and drinks. These essential oils extracted from leaves show many positive impacts on human health. They can lower blood cholesterol, help to lower blood sugar in diabetic patients, and protect the stomach from ulcers (<xref ref-type="bibr" rid="b13">Dzida, 2010;</xref> <xref ref-type="bibr" rid="b14">Ezeani et al., 2017</xref>). Recently, in connection to the great success of sage seeds (known by its Mayan name chia), basil seeds have also emerged on the market. They are a good source of polyunsaturated fatty acids. Regular consumption of basil, both leaves, and seeds, provides many health benefits.</p>
            <p>Basil (<italic>Ocimum basilicum</italic>, OB), also known as great basil, is one of the most common and available species of basil. It is usually an annual plant with a height of up to 60 cm. Apart from a few subspecies that are purple, it is a brightly green plant (<xref ref-type="bibr" rid="b16">Hiltunen and Holm, 1999</xref>). Basil has a large number of cultivars and subspecies.</p>
            <p>Basil leaves contain over 92% of free or bound water, approximately 5% of tannins and sitosterols, up to 1% of fats, 0.5 – 1.5% of essential oils, 0.17% of oleanolic acid; ursolic acid is present as well.</p>
            <p>The composition of seeds is also remarkable, they contain 25% of fat, more than half of which consists of &#x3B1;-linolenic acid, furthermore, minerals, vitamins, antioxidants, and phenolic substances (<xref ref-type="bibr" rid="b16">Hiltunen and Holm, 1999;</xref> <xref ref-type="bibr" rid="b25">Nirali et al., 2017</xref>).</p>
            <p>Antioxidants are a very important group of substances with promising properties that prevent oxidation not only in food but also in the human body. The main groups of antioxidants in basil occurring primarily in its essential oils are phenolic antioxidants and endiols (<xref ref-type="bibr" rid="b38">Vel&#xED;&#x161;ek and Haj&#x161;lov&#xE1;, 2009</xref>). Endiol antioxidants are principally represented by ascorbic acid and its salts and derivatives. As part of its antioxidant activity, ascorbic acid reacts with reactive oxygen species, which slows down the oxidation of lipids, or with fatty acid radicals and alkoxy radicals. The efficiency of reactions with lipid radicals can be increased by the presence of tocopherols, which, in contrast to ascorbic acid, are fat-soluble (<xref ref-type="bibr" rid="b38">Vel&#xED;&#x161;ek and Haj&#x161;lov&#xE1;, 2009</xref>).</p>
            <p>Phenolic compounds can be generally defined as substances containing at least one benzene ring bonding at least one hydroxyl group or their functional derivatives. This group is extensive and diverse with several characteristics in common. Phenolic substances are often secondary metabolites of plants with antioxidant properties which are desirable and valued for a healthy human diet. Hydroxyl group of phenolic substances binds to hydroxy peroxide, superoxide, or hydroxyl radicals and thus prevents radicals from degenerative changes in the body (<xref ref-type="bibr" rid="b38">Vel&#xED;&#x161;ek and Haj&#x161;lov&#xE1;, 2009;</xref> <xref ref-type="bibr" rid="b32">Skinner and Hunter, 2013</xref>).</p>
            <p>The proportion of individual substances in plant material obtained from basil (<italic>Ocimum basilicum</italic>) is influenced not only by growing conditions and cultivar but also by other factors, such as the method of treatment and storage time. This work aimed to determine the antioxidant activity and total content of phenolic substances in selected cultivars in fresh and frozen leaves of basil (<italic>Ocimum basilicum</italic>).</p>
            <sec>
                <title>Scientific hypothesis</title>
                <list list-type="simple">
                    <list-item>
                        <p>
                            <bold>Hypothesis 1</bold> – Individual basil cultivars differ in the total content of phenolic substances and antioxidant activity.</p>
                    </list-item>
                    <list-item>
                        <p>
                            <bold>Hypothesis 2</bold> – the value of the total content of phenolic substances and antioxidant activity differs in the case of direct processing and within the processing after the storage in a freezer at the temperature of -18 &#xB0;C.</p>
                    </list-item>
                    <list-item>
                        <p>
                            <bold>Hypothesis 3</bold> – the total content of phenolic substances and antioxidant activity differ between the mixtures prepared from basil (<italic>Ocimum basilicum</italic>) and other plant material (garlic, mint, rocket, spinach).</p>
                        </list-item>
                    </list>
                </sec>
            </sec>
            <sec sec-type="materials|methods">
                <title>MATERIAL AND METHODOLOGY</title>
                <sec>
                    <title>Samples</title>
                    <p>The following basil cultivars were used for the research (<italic>Ocimum basilicum</italic>):</p>
                    <list list-type="simple">
                        <list-item>
                            <p>&#x2A;Oh&#x159;e (marked as OH) – Czechoslovak cultivar (Figure <xref ref-type="fig" rid="F1">1</xref>), bright green, pleasant, and typically aromatic, with larger leaves and white flowers (<xref ref-type="bibr" rid="b24">Mur&#xE1;rikov&#xE1; and Neugebauerov&#xE1;, 2018;</xref> <xref ref-type="bibr" rid="b15">GRIN Czech, 2021</xref>).</p>
                        </list-item>
                        <list-item>
                            <p>&#x2A;Sweet green (marked as SG) – cultivar similar to the cultivar Oh&#x159;e, medium-sized, shiny, and convex leaves, tastes sweeter, typical.</p>
                        </list-item>
                        <list-item>
                            <p>&#x2A;Salad leaf (marked as SL) – very broad leaves with a typical green color and taste. However, compared to the Oh&#x159;e and Sweet Green cultivars, the intensity of the taste is lower.</p>
                        </list-item>
                        <list-item>
                            <p>&#x2A;Purple opal (marked as PO) – purple color (high content of anthocyanins in leaves (<xref ref-type="bibr" rid="b31">Simon et al., 1999</xref>)), it is used more for aesthetic purposes than taste (Figure <xref ref-type="fig" rid="F2">2</xref>).</p>
                        </list-item>
                        <list-item>
                            <p>&#x2A; Thai (marked as TH)the – different shape of leaves, the coloring of stems red, taste and smell similar to anise or licorice, with better resistance to higher temperatures, but worse resistance to cold (<xref ref-type="bibr" rid="b3">Asijsk&#xE9; bylinky, 2020;</xref> <xref ref-type="bibr" rid="b29">Semena.cz, 2020</xref>).</p>
                        </list-item>
                    </list>
                    <fig id="F1" position="float">
                        <label>Figure 1</label>
                        <caption>
                            <p>
                                <italic>Ocimum basilicum</italic> – cultivar Ohře.</p>
                        </caption>
                        <graphic xlink:href="PSJFS-15-1-445_F1.jpg"/>
                    </fig>
                    <fig id="F2" position="float">
                        <label>Figure 2</label>
                        <caption>
                            <p>
                                <italic>Ocimum basilicum</italic> – cultivar Purple opal.</p>
                        </caption>
                        <graphic xlink:href="PSJFS-15-1-445_F2.jpg"/>
                    </fig>
                    <p>For selected cultivars, a difference in the analyzed values depending on the type of cultivar was expected.</p>
                    <p>These samples originated from the same locality, were grown under the same conditions (the same soil composition, amount of sunshine,&#x2026;) and agrotechnical treatments. For this reason, the dependence of these samples on different growing conditions for different sample origins was not expected.</p>
                    <p>The samples of basil of unknown variety marked as &#x201C;XX1&#x201D; and &#x201C;XX2&#x201D;, were used for the research as well.</p>
                    <p>Furthermore, the mixtures of basil, cultivar &#x201C;Oh&#x159;e&#x201D;, with other plant material were produced with the following composition:</p>
                    <list list-type="simple">
                        <list-item>
                            <p>- mix 1 – basil, cultivar &#x201C;Oh&#x159;e&#x201D; (92 wt. %) + garlic (<italic>Allium sativum</italic>) (8 wt. %) (marked as OHG)</p>
                        </list-item>
                        <list-item>
                            <p>- mix 2 – basil, cultivar &#x201C;Oh&#x159;e&#x201D; (95 wt. %) + peppermint (<italic>Mentha peperita</italic>) (5 wt. %) (marked as OHM)</p>
                        </list-item>
                        <list-item>
                            <p>- mix 3 – basil, cultivar &#x201C;Oh&#x159;e&#x201D; (95 wt. %) + rocket (<italic>Eruca vesicaria</italic>) (5 wt. %) (marked as OHR)</p>
                        </list-item>
                        <list-item>
                            <p>- mix 4 – basil, cultivar &#x201C;Oh&#x159;e&#x201D; (90 wt. %) + spinach (<italic>Spinacia oleracea</italic>) (10 wt. %) (labelled as OHS)</p>
                        </list-item>
                    </list>
                </sec>
                <sec>
                    <title>Chemicals</title>
                    <p>To prepare samples, an extraction solution in the composition of demineralized water and methanol was used (Methyl alcohol p.a., CH<sub>3</sub>OH, CAS: 67-56-1, Penta, Chrudim, Czech Republic) in a ratio of 30:70.</p>
                    <p>The following chemicals were used to determine the total phenolic content:</p>
                    <p>Folin-Ciocalteu&#x2019;s reagent, (Sigma-Aldrich, St Louis, MO, USA)</p>
                    <p>Sodium carbonate anhydrous p.a. (Na<sub>2</sub>CO<sub>3</sub>, Sigma Aldrich, St Louis, MO, USA)</p>
                    <p>Gallic acid (GAE) (Sigma Aldrich, St Louis, MO, USA)</p>
                    <p>Determination of antioxidant activity was performed using the following chemicals:</p>
                    <p>DPPH (2,2-diphenyl-1-picrylhydrazyl) (Sigma Aldrich, St Louis, MO, USA)</p>
                    <p>methanol (Methylalkohol p.a., CH<sub>3</sub>OH, CAS: 67-56-1, Penta, Chrudim, &#x10C;R).</p>
                    <p>All chemicals were of analytical reagent grade or equivalent analytical purity.</p>
                    <p>Demineralized water – 18.2 MOhm.cm, Milli-Q, Millipore was used throughout the experiment.</p>
                </sec>
                <sec>
                    <title>Animals and Biological Material:</title>
                    <p>Samples of cultivars Oh&#x159;e, Purple opal, Sweet green, Salad leaf, and Thai were supplied by the Faculty of Horticulture of Mendel University in Brno, Czech Republic.</p>
                    <p>The samples were grown in the gene pool areas of this university in Lednice, Czech Republic (approximate GPS 48.79353068254463, 16.798598359226208). The location is in a temperate climate zone. The climate is continental with an average annual temperature of above 9 &#xB0;C and average annual rainfall of around 520 mm (<xref ref-type="bibr" rid="b10">&#x10C;S&#xDA;, 2016</xref>).</p>
                    <p>All other plant materials (samples of basil of unknown variety, garlic, peppermint, rocket, spinach) were purchased in a regular retail chain in Zl&#xED;n, Czech Republic.</p>
                </sec>
                <sec>
                    <title>Instruments</title>
                    <p>The following instruments were used for the measurements:</p>
                    <p>Spectrophotometer Libra S6, Biochrom, Cambridge, UK (Determination of AA),</p>
                    <p>Spectrophotometer Specord 50 Plus, Analytik Jena, Jena, Germany (Determination of TPC),</p>
                    <p>Analytical scale Voyager PRO VP214C (Ohaus corporation, Pine Brook USA)</p>
                </sec>
                <sec>
                    <title>Laboratory Methods</title>
                    <sec>
                        <title>Determination of the total phenolic content</title>
                        <p>Folin-Ciocalteu spectrophotometric method was selected to determine the total phenolic content (<xref ref-type="bibr" rid="b7">Cicco et al., 2009</xref>). The principle of this method is based on the reaction of the Folin-Ciocalteu reagent with phenolic substances (it reduces itself to a blue-colored mixture). The concentration of the reduced reagent is proportional to the amount of absorbed blue light at the wavelength &#x3BB; = 765 nm (<xref ref-type="bibr" rid="b8">Costa et al., 2019;</xref> <xref ref-type="bibr" rid="b2">Albergamo et al., 2020</xref>).</p>
                    </sec>
                    <sec>
                        <title>Determination of the antioxidant activity</title>
                        <p>DPPH spectrophotometric method modified according to Brand-Williams was used to establish the antioxidant activity (<xref ref-type="bibr" rid="b6">Brand-Williams, Cuvelier and Berset, 1995</xref>). The principle of this method is based on the reaction of the stable free radical 1,1-diphenyl-2-picrylhydrazyl (DPPH). In the reaction of DPPH with an antioxidant, a radical is eliminated, and colorless products are formed from purple DPPH. The concentration of antioxidants and their activity is proportional to the decrease of absorbance.</p>
                        <p>The measurement was performed at the wavelength &#x3BB; = 515 nm (<xref ref-type="bibr" rid="b6">Brand-Williams, Cuvelier and Berset, 1995;</xref> <xref ref-type="bibr" rid="b20">Lee et al., 2005;</xref> <xref ref-type="bibr" rid="b36">Thaipong et al., 2006</xref>).</p>
                    </sec>
                </sec>
                <sec>
                    <title>Description of the Experiment</title>
                    <p>
                        <bold>Sample preparation:</bold> Leaves with a minimal petiole part were separated from the plants and crushed in a ceramic mortar as it maximally prevents the loss of antioxidants.</p>
                    <p>It is also a traditional method. The crushed biological material was processed immediately, stored in the freezer (-18 &#xB0;C to -20 &#xB0;C) for approximately 60 days or in the refrigerator (+4 &#xB0;C to +7 &#xB0;C) for 4 days. The storage was airtight. After crushing and potential storage, approximately 1 g of the sample was placed into 2 vials and weighted precisely using analytical scales. Then, 10 mL of extraction solution (30% water : 70% methanol) was immediately added to the vials. The sealed vials were placed in a 50 &#xB0;C water bath for 60 min. After being filtrated, the samples were stored in the refrigerator until the analysis. Due to a technical refrigeration error, it was impossible to analyze some fresh samples.</p>
                    <p>The parameters of the determination of the differences between the cultivars were as follows:</p>
                    <p>
                        <bold>Number of samples analyzed:</bold> 4 (fresh), 5 (frozen)</p>
                    <p>
                        <bold>Number of repeated analyses:</bold> 8x</p>
                    <p>
                        <bold>Number of experiment replication:</bold> 1x</p>
                    <p>The parameters of the determination of the differences between the mixtures were as follows:</p>
                    <p>
                        <bold>Number of samples analyzed:</bold> 4 (fresh), 4 (refrigerated)</p>
                    <p>
                        <bold>Number of repeated analyses:</bold> 4x</p>
                    <p>
                        <bold>Number of experiment replication:</bold> 1x</p>
                    <sec>
                        <title>Determination of the total phenolic content</title>
                        <p>Before the analysis, 20% sodium carbonate solution was prepared. Then, 0.1 mL of basil extract was added to a 10 mL volumetric flask with 5 mL of deionized water. 0.5 mL of Folin-Ciocalteu reagent was added to the mixture and shaken. 1.5 mL of 20% Na<sub>2</sub>CO<sub>3</sub> was added after three minutes and shaken. Demineralized water was added to an overall volume of 10 mL. After the incubation for 30 min at room temperature, the absorbance at 765 nm was determined using a spectrophotometer. To express the results, unit milligrams of Gallic acid (GAE) per 100 grams of fresh weight of the sample <italic>m<sub>g</sub></italic> were used.</p>
                    </sec>
                    <sec>
                        <title>Determination of the antioxidant activity</title>
                        <p>First, a stock methanol solution of DPPH is prepared. For the analysis, 4 mL of the stock solution and 20 &#x3BC;L of the extract are placed into a test tube. If the samples contained a small amount of antioxidants, their volume was increased to either 70 or 210 &#x3BC;L. After 60-min rest in the dark, the absorbance of the sample was measured using a spectrophotometer. The results are expressed as the equivalent of ascorbic acid measured in g per 100 g of fresh weight of the sample <italic>m<sub>a</sub></italic> using a standard calibration curve.</p>
                    </sec>
                </sec>
                <sec>
                    <title>Statistical Analysis</title>
                    <p>Excel 2013 (Microsoft Corporation, USA) and STATISTICA CZ version 12 (StatSoft, Inc., USA) were used for data analysis. The results were expressed by mean &#xB1; standard deviation. Shapiro-Wilk test of normality was performed within all monitored samples.</p>
                    <p>To establish statistically significant differences between individual basil cultivars, Levene&#x27;s test of homogeneity of variances was performed. Since the conditions for the calculation by ANOVA analysis did not comply in any of the monitored data sets, a non-parametric Kruskal-Wallis test (&#x3B1; = 0.05) and multiple comparisons of p values (twosided) (&#x3B1; = 0.05) based on Mann-Whitney U test were performed.</p>
                    <p>Considering fresh samples, there were only 2 cultivars (TH and OH) to compare, Levene&#x2019;s test of homogeneity was performed after applying the Shapiro-Wilk test of normality. If the conditions for a t-test complied, F-test and a two-tailed t-test (&#x3B1; = 0.05) were executed. Otherwise, the Mann-Whitney U test (&#x3B1; = 0.05) was used. The same procedure was applied to compare fresh and frozen samples.</p>
                    <p>To determine statistically significant differences between the mixtures, Levene&#x2019;s test of homogeneity was performed after the test of normality. Due to non-compliance with the conditions of normality and homogeneity, the results were further calculated using the nonparametric Kruskal-Wallis test (&#x3B1; = 0.05) and the differences between the groups were monitored using multiple comparisons of p values (twosided) (&#x3B1; = 0.05).</p>
                    <p>Levene&#x2019;s test of homogeneity of variances was performed to establish differences between the group processed immediately and the group stored for 4 days in the refrigerator. If the conditions of normality and homogeneity were fulfilled, F-test and the two-tailed t-test were used. Otherwise, the Mann-Whitney U test (&#x3B1; = 0.05) was applied.</p>
                </sec>
            </sec>
            <sec sec-type="results|discussion">
                <title>RESULTS AND DISCUSSION</title>
                <sec>
                    <title>AA and TPC in the cultivars</title>
                    <p>As can be seen in Table <xref ref-type="table" rid="T1">1</xref> shows the measurement of fresh cultivars, only OH and TH cultivars could be used for the analysis. There was a statistically significant difference between cultivars for both AA determination using t-test (t = 11.754; sv = 6; <italic>p</italic> &#x003C;0.05) and TPC analysis, where it was necessary to employ a non-parametric U-test (U = 10.00; <italic>p</italic> &#x003C;0.05). Regarding AA, the OH cultivar performed almost twice the value established in TH. What is more, it showed 15 times higher values if compared to groups purchased in the retail chain. Similar results were achieved in TPC determination. Even though the differences were less considerable, the OH cultivar reached higher values than TH. If compared to the groups purchased in the retail chain, the OH cultivar showed up to 4 times higher values.</p>
                    <table-wrap id="T1" position="float">
                        <label>Table 1</label>
                        <caption>
                            <p>Antioxidant activity (AA) and total phenolic content (TPC) in cultivars of brasil (<italic>Ocimum basilicum</italic>) in fresh and frozen state.</p>
                        </caption>
                        <table frame="hsides" rules="none" width="100%">
                            <thead>
                                <tr>
                                    <th rowspan="3">Cultivars</th>
                                    <th colspan="2">AA (mg.g<sup>-1</sup> AA &#x00B1;<italic>S D</italic>)</th>
                                    <th colspan="2">TPC (mg.g<sup>-1</sup> GAE &#x00B1;<italic>S D</italic>)</th>
                                </tr>
                                <tr>
                                    <th colspan="4">
                                        <hr/>
                                    </th>
                                </tr>
                                <tr>
                                    <th>Fresh</th>
                                    <th>Frozen</th>
                                    <th>Fresh</th>
                                    <th>Frozen</th>
                                </tr>
                                <tr>
                                    <th colspan="5">
                                        <hr/>
                                    </th>
                                </tr>
                            </thead>
                            <tbody>
                                <tr align="center">
                                    <td><bold>SG</bold>
</td>
                                    <td/>
                                    <td>6.9 &#x00B1;0.4</td>
                                    <td/>
                                    <td>5.49 &#x00B1;0.09<sup>a</sup></td>
                                </tr>
                                <tr align="center">
                                    <td><bold>SL</bold>
</td>
                                    <td/>
                                    <td>11.71 &#x00B1;0.18<sup>a</sup></td>
                                    <td/>
                                    <td>8.93 &#x00B1;0.13<sup>a, b, c</sup></td>
                                </tr>
                                <tr align="center">
                                    <td><bold>TH</bold>
</td>
                                    <td>4.2 &#x00B1;0.3<sup>&#x2021;</sup></td>
                                    <td>5.1 &#x00B1;0.4<sup>a, b</sup></td>
                                    <td>3.3 &#x00B1;0.3<sup>&#x2021;U</sup></td>
                                    <td>2.77 &#x00B1;0.16<sup>b, d</sup></td>
                                </tr>
                                <tr align="center">
                                    <td><bold>PO</bold>
</td>
                                    <td/>
                                    <td>8.34 &#x00B1;0.18<sup>b</sup></td>
                                    <td/>
                                    <td>7.00 &#x00B1;0.11<sup>d</sup></td>
                                </tr>
                                <tr align="center">
                                    <td><bold>OH</bold>
</td>
                                    <td>8.2 &#x00B1;0.2<sup>&#x002A;U,&#x2021;</sup></td>
                                    <td>6.22 &#x00B1;0.17<sup>&#x002A;U</sup></td>
                                    <td>4.23 &#x00B1;0.16<sup>&#x2021;U</sup></td>
                                    <td>4.7 &#x00B1;0.3<sup>c</sup></td>
                                </tr>
                                <tr align="center">
                                    <td colspan="5"><hr/></td>
                                </tr>
                                <tr align="center">
                                    <td><bold>XX1</bold>
</td>
                                    <td>0.630 &#x00B1;0.007</td>
                                    <td/>
                                    <td>1.06 &#x00B1;0.16</td>
                                    <td/>
                                </tr>
                                <tr align="center">
                                    <td><bold>XX2</bold>
</td>
                                    <td>0.519 &#x00B1;0.010</td>
                                    <td/>
                                    <td>1.0 &#x00B1;0.3</td>
                                    <td/>
                                </tr>
                            </tbody>
                        </table>
                        <table-wrap-foot>
                            <fn id="T1FN1">
                                <p>Note: <sup>a, b, c, d</sup> - the same superscipts indicate a statistically significant difference between the cultivars (frozen samples, Multiple comparison of p values - two-sided),</p>
                                <p>
                                    <sup>&#x2021;</sup> - indicates a statistically significant difference between the cultivars (fresh samples, t-test - two-sided),</p>
                                <p>
                                    <sup>&#x2021;</sup>U - indicates a statistically significant difference between the cultivars (fresh samples, U-test),</p>
                                <p>
                                    <sup>&#x2A;</sup>U - indicates a statistically significant difference between the samples analysed on the day of processing and frozen samples (U-test).</p>
                            </fn>
                        </table-wrap-foot>
                    </table-wrap>
                    <p>As far as a comparison of fresh and frozen samples is concerned, a statistically significant difference was demonstrated only in the OH cultivar within the U-test (U = 0.00; <italic>p</italic> &#x003C;0.05). Nevertheless, the trends in the OH values showed a decrease in AA and rice in TPC during freezing. Considering the TH cultivar, contrasting trends were recorded. When comparing the differences in frozen samples, the highest values of TPC and AA were established within the SL cultivar and the lowest within the TH cultivar. The values of antioxidant activity in frozen samples ranged from 5.1 &#xB1;0.4 mg.g<sup>-1</sup> AA FW in TH to 11.71 &#xB1;0.18 mg.g<sup>-1</sup> AA FW in SL. The values of TPC varied between 2.77 &#xB1;0.16 mg.g<sup>-1</sup> GAE FW in TH and 8.93 &#xB1;0.13 mg.g<sup>-1</sup> GAE FW in SL.</p>
                    <p>
                        <xref ref-type="bibr" rid="b24">Mur&#xE1;rikov&#xE1; and Neugebauerov&#xE1; (2018)</xref> reported the values of the same cultivars OH (0.083 – 0.220 mg.g<sup>-1</sup> AA FW), PO (0.079 – 0.166 mg.g<sup>-1</sup> AA FW), and a similar cultivar Lettuce Leaf (0.047 – 0.139 mg.g<sup>-1</sup> AA FW) which are a magnitude smaller than the values recorded in this study. The reason may be a different method of cultivation, measuring method and agrotechnics applied.</p>
                    <p>
                        <xref ref-type="bibr" rid="b16">Hiltunen and Holm (1999)</xref> state that fresh basil generally contains a large amount of ascorbic acid. <xref ref-type="bibr" rid="b13">Dzida (2010)</xref> reported the value of 0.26 mg.g<sup>-1</sup> AA FW measured in the Polish variation of basil &#xB4;Kasia&#xB4; and the value of 0.204 mg.g<sup>-1</sup> AA FW established in the variance &#xB4;Wala&#xB4;. A lower value of ascorbic acid in basil (0.119 mg.g<sup>-1</sup> AA FW) is monitored by <xref ref-type="bibr" rid="b23">Martyniak-Przebyszewska and Wojciechowski (2004)</xref>. Comparing the vitamin C content in basil and rosemary leaves, <xref ref-type="bibr" rid="b12">Dumbrav&#x103; et al. (2012)</xref> declared a higher content of vitamin C in basil (0.271 mg.g<sup>-1</sup> FW) than in rosemary (0.185 mg.g<sup>-1</sup> FW).</p>
                    <p>
                        <xref ref-type="bibr" rid="b33">Szarowsk&#xE1; (2012)</xref> presented the antioxidant activity for various aromatic herbs. The highest antioxidant activity was found in the sample of lemon balm (both lyophilized and dried samples), oregano (dried sample), and basil (dried sample). The lowest antioxidant activity was determined in mint (fresh sample), lemon balm (fresh sample), basil (lyophilized sample), and oregano (lyophilized sample). Basil showed the average values depending on the temperature of the leachate and method of processing.</p>
                    <p>
                        <xref ref-type="bibr" rid="b17">Chrpov&#xE1; et al. (2010)</xref> examined the antioxidant activity of dried basil in the water extract (70 &#xB0;C). They determined a value of 55.5 mg.g<sup>-1</sup> AA DM. <xref ref-type="bibr" rid="b33">Szarowsk&#xE1; (2012)</xref> determined the values of antioxidant activity in the water extract higher than 92.3 mg.g<sup>-1</sup> AA DM.</p>
                    <p>
                        <xref ref-type="bibr" rid="b33">Szarowsk&#xE1; (2012)</xref> established TPC in selected varieties of aromatic plants, where the lowest TPC content was monitored in a sample of lavender (lyophilized sample), mint (frozen sample), oregano (lyophilized sample), and chamomile (dried samples). In contrast, the highest TPC was determined in oregano (dried samples), lemon balm (dried and lyophilized samples), and mint (lyophilized samples). The basil reached the average values depending on the temperature of the leachate and method of processing.</p>
                    <p>
                        <xref ref-type="bibr" rid="b41">Zheng and Wang (2001)</xref> recorded the value of TPC in the <italic>Ocimum basilicum</italic> of 2.23 mg.g<sup>-1</sup> GAE FW. The TPC content in the study by <xref ref-type="bibr" rid="b37">V&#xE1;bkov&#xE1; and Neugebauerov&#xE1; (2010)</xref> was higher in the monitored cultivars – &#xB4;Oh&#x159;e&#xB4; 3.63 mg.g<sup>-1</sup> GAE FW, &#xB4;Lettuce Leaf&#xB4; 3.47 mg.g<sup>-1</sup> GAE FW, &#xB4;Purple Opaal&#xB4; 3.43 mg.g<sup>-1</sup> GAE FW and &#xB4;Compakt&#xB4; 2.50 mg.g<sup>-1</sup> GAE FW. The TPC content was established to be higher in this study (more than twice when evaluating the &#x201C;Ohre&#x201D; cultivar). <xref ref-type="bibr" rid="b9">Cruz et al. (2020)</xref> compared colored basil cultivars Red Basil (25 &#xB1; 13 mg.g<sup>-1</sup> extract), Dark Opal (25 &#xB1;17 mg.g<sup>-1</sup> extract), Basilico Rosso (12 &#xB1;3 mg.g<sup>-1</sup> extract) and one green local landrace Mitikas (9 &#xB1;6 mg.g<sup>-1</sup> extract). Their results revealed a higher level of TPC in colored basil cultivars compared to the examined green local landrace (Mitikas).</p>
                    <p>
                        <xref ref-type="bibr" rid="b30">Shan et al. (2005)</xref> examined the TPC of 26 spice extracts, determining 36.4 mg.g<sup>-1</sup> GAE FW in basil. The highest TPC was established in cinnamon (119 mg.g<sup>-1</sup> GAE) and oregano (101.7 mg.g<sup>-1</sup> GAE). The samples of sage (53.2 mg.g<sup>-1</sup> GAE) and mint (51.5 mg.g<sup>-1</sup> GAE) contained the average CP values.</p>
                    <p>
                        <xref ref-type="bibr" rid="b21">Marcin&#x10D;&#xE1;k, Popelka and &#x160;oltysov&#xE1; (2008)</xref> determined TPC spectrophotometrically in methanol extracts of 10 selected herbs. The highest TPC was found in the sample of oregano (262.12 mg.g<sup>-1</sup> GAE DM), basil (249.852 mg.g<sup>-1</sup> GAE DM) and rapeseed (179.22 mg.g<sup>-1</sup> GAE DM).</p>
                    <p>
                        <xref ref-type="bibr" rid="b17">Chrpov&#xE1; et al. (2010)</xref>, <xref ref-type="bibr" rid="b30">Shan et al. (2005)</xref> and <xref ref-type="bibr" rid="b21">Marcin&#x10D;&#xE1;k, Popelka and &#x160;oltysov&#xE1; (2008)</xref> emphasize the fact that basil is a rich source of TPC. However, as it is consumed only occasionally in small quantities, it has rather insignificant effects on the TPC daily dose (<xref ref-type="bibr" rid="b38">Vel&#xED;&#x161;ek and Haj&#x161;lov&#xE1;, 2009</xref>).</p>
                </sec>
                <sec>
                    <title>AA and TPC in the mixtures</title>
                    <p>Examining the antioxidant activity, the effect of added plant raw materials (garlic, mint, rocket, and spinach) to the cultivar &#x201C;Oh&#x159;e&#x201D; in the fresh state was negative in all. The antioxidant activity of the mixtures decreased by more than 50% - in the mixture with garlic by 54% and in the mixture with rocket by 57%. A decrease of 41% was recorded in the mixture with spinach. The smallest decline in the antioxidant activity was recorded in the mixture with mint (30%), where the smallest decrease in TPC content was determined (11%) as well. The other mixtures showed a significant decrease of more than 45% (OHG mixture 49%, OHR mixture 53%). <xref ref-type="bibr" rid="b11">Dobrinas, Stanciu and Lupsor (2017)</xref> reported a higher TPC content in the rocket (<italic>Eruca sativa</italic>) (6.20 mg.g<sup>-1</sup> GAE) than in the cultivar &#x201C;Oh&#x159;e&#x201D;; therefore, an increase in the TPC content of the mixture was expected. The reason for such a drop may be due to differences in the growing and processing conditions. The most significant decline was monitored in the mixture with spinach (61%).</p>
                    <p>As Table <xref ref-type="table" rid="T2">2</xref> shows, the effect of the storage in the refrigerator for 4 days was significantly reflected in the values of the antioxidant activity.</p>
                    <table-wrap id="T2" position="float">
                        <label>Table 2</label>
                        <caption>
                            <p>Antioxidant activity (AA) and total phenolic content (TPC) in mixtures of basil (<italic>Ocimum basilicum</italic>) of &#x201E;Oh&#x159;e&#x201C; cultivar with other raw materials on the day of processing and after 4 days of the storage of the samples in the refrigerator.</p>
                        </caption>
                        <table frame="hsides" rules="none" width="100%">
                            <thead>
                                <tr>
                                    <th rowspan="3">Cultivars</th>
                                    <th colspan="2">AA (mg.g<sup>-1</sup>AA &#x00B1;<italic>SD</italic>)</th>
                                    <th colspan="2">TPC (mg.g<sup>-1</sup>GAE &#x00B1;<italic>SD</italic>)</th>
                                </tr>
                                <tr>
                                    <th colspan="4">
                                        <hr/>
                                    </th>
                                </tr>
                                <tr>
                                    <th>Fresh</th>
                                    <th>Refrigerated</th>
                                    <th>Fresh</th>
                                    <th>Refrigerated</th>
                                </tr>
                                <tr>
                                    <th colspan="5">
                                        <hr/>
                                    </th>
                                </tr>
                            </thead>
                            <tbody>
                                <tr align="center">
                                    <td><bold>OHG</bold></td>
                                    <td>3.80&#x00B1;0.13<sup>&#x002A;</sup></td>
                                    <td>2.33&#x00B1;0.16<sup>&#x002A;</sup></td>
                                    <td>2.2&#x00B1;0.3<sup>a</sup></td>
                                    <td>1.3&#x00B1;0.3<sup>a</sup></td>
                                </tr>
                                <tr align="center">
                                    <td><bold>OHM</bold></td>
                                    <td>5.7&#x00B1;0.3<sup>&#x002A;, a</sup></td>
                                    <td>3.98&#x00B1;0.07<sup>&#x002A;, a, b</sup></td>
                                    <td>3.75&#x00B1;0.12<sup>a, b</sup></td>
                                    <td>3.6&#x00B1;0.3<sup>a, b</sup></td>
                                </tr>
                                <tr align="center">
                                    <td><bold>OHR</bold></td>
                                    <td>3.49&#x00B1;0.09<sup>&#x002A;, a</sup></td>
                                    <td>1.25&#x00B1;0.12<sup>&#x002A;, a</sup></td>
                                    <td>1.97&#x00B1;0.07<sup>&#x002A;U</sup></td>
                                    <td>1.31&#x00B1;0.8<sup>&#x002A;U</sup></td>
                                </tr>
                                <tr align="center">
                                    <td><bold>OHS</bold></td>
                                    <td>4.84&#x00B1;0.05<sup>&#x002A;</sup></td>
                                    <td>1.44&#x00B1;0.02<sup>&#x002A;, b</sup></td>
                                    <td>1.63&#x00B1;0.02<sup>&#x002A;, b</sup></td>
                                    <td>0.813&#x00B1;0.011<sup>&#x002A;, b</sup></td>
                                </tr>
                            </tbody>
                        </table>
                        <table-wrap-foot>
                            <fn id="T2FN1">
                                <p>Note: &#x2A; &#x2013; indicates a statistically significant difference between the samples analysed on the day of processing and samples stored for 4 days in the refrigerator (t-test),</p>
                                <p>&#x2A;U &#x2013; indicates a statistically significant difference between the samples analysed on the day of processing and samples stored for 4 days in the refrigerator (U-test),</p>
                                <p> a, b &#x2013; the superscripts indicate a statistically significant difference between the samples of the mixtures (Multiple comparison of p values - two-sided).</p>
                            </fn>
                        </table-wrap-foot>
                    </table-wrap>
                    <p>All examined mixtures performed a statistically significant reduction in their antioxidant activity. The most significant influence was measured in the mixture of the cultivar &#x201C;Oh&#x159;e&#x201D; with spinach where the content of antioxidants decreased by 70% and a statistically significant difference was recorded (t = 63.215; sv = 6; <italic>p</italic> &#x003C;0.05). Leafy vegetables, such as spinach, are known to contain significant amounts of ascorbic acid together with polyphenols which increase the antioxidant effects and improve the sensory quality (<xref ref-type="bibr" rid="b18">Kopec, 2010;</xref> <xref ref-type="bibr" rid="b22">Mart&#xED;n-Belloso and Soliva-Fortuny, 2010</xref>). During the storage and processing, losses of antioxidants in the vegetable can occur, particularly by the heat treatment (blanching, pasteurization, cooking, sterilization, preservation, freezing) (<xref ref-type="bibr" rid="b26">Patras et al., 2009</xref>) or by the oxidation caused by atmospheric oxygen. That is why leaf vegetables should be consumed mostly fresh to preserve antioxidants and not to reduce them as in the OHS mixture.</p>
                    <p>Rocket, rich in substances with antioxidant effects, is an essential part of the human diet important for detoxication of the body and the protection against oxidative stress (<xref ref-type="bibr" rid="b4">Barillari et al., 2005;</xref> <xref ref-type="bibr" rid="b28">Sarwar et al., 2007;</xref> <xref ref-type="bibr" rid="b1">Abbasi et al., 2013</xref>). The rocket contains mainly vitamin C (<xref ref-type="bibr" rid="b39">Villatoro- Pulido et al., 2012</xref>). Similar to the basil-spinach mixture, the antioxidant activity in the OHR mixture decreased by 64%.</p>
                    <p>Considering fresh mixtures, the highest value of antioxidant activity was established in the OHM mixture (5.7 &#xB1;0.3 mg.g<sup>-1</sup> AA). Despite a statistically significant decrease (t = 5.934; sv = 6; <italic>p</italic> &#x003C;0.05), it was also the highest value measured after 4 days of storage in the refrigerator with losses of only 23%. Therefore, based on the analysis, the OHM mixture was evaluated as the most stable mixture. That may be caused by the fact that plants, such as mint, are rich in phenolic compounds, polyphenols, and flavonoids synthesized as defensive metabolites of the plant. It has been found that, apart from mint extracts, also mint essential oils perform antioxidative properties as they contain &#x3B1; and &#x3B2;-pinene, cineole, jasmone, isomenthol, isomentone, ledol, limonene, mentofuran, menthol, menton, menthyl acetate, neomenthol, piperitone, pulegone and viridiflorol (<xref ref-type="bibr" rid="b19">Koz&#x142;owska et al., 2015;</xref> <xref ref-type="bibr" rid="b27">Peter, 2006;</xref> <xref ref-type="bibr" rid="b40">Yadegarinia et al., 2006</xref>). The difference in the AA established in all extracts from fresh and stored mint samples can be attributed mainly to the species and growing conditions of the herbs (<xref ref-type="bibr" rid="b19">Koz&#x142;owska et al., 2015;</xref> <xref ref-type="bibr" rid="b35">Telci et al., 2010</xref>). Furthermore, the content of antioxidants in mint extracts is also affected by the applied solvent.</p>
                    <p>The last examined OHG mixture showed a statistically significant decrease (t = 7.154; sv = 6; <italic>p</italic> &#x003C;0.05) of approximately 43%. This decline was lower than in other mixtures of OHR and OHS. The slight decrease seems to be due to the content of antioxidant phytochemicals, which prevents oxidative damage. Also, garlic contains further biologically active substances (S-allyl cysteine (SAC), Sallyl mercapto cysteine (SAMC), allicin, alixin, and selenium) which eliminate hydroxyl radicals in the blood serum and increase the activity of some enzymes with antioxidant effects (<xref ref-type="bibr" rid="b34">&#x160;krov&#xE1;nkov&#xE1; et al., 2018</xref>). Generally, other influencing factors include the origin, soil conditions, variety, treatment, and thermal treatment (<xref ref-type="bibr" rid="b5">Borek, 2001</xref>).</p>
                    <p>Similarly to the antioxidant activity, the TPC values were reduced after storage in the refrigerator for 4 days. The smallest reduction of 4% occurred in the OHM mixture, the largest reduction of 50% was recorded in the OHS mixture. In this mixture, also a statistically significant difference (t = 30.670; sv = 14; <italic>p</italic> &#x003C;0.05) was determined. The difference (U = 0.00; <italic>p</italic> &#x003C;0.05) was recorded in the OHR mixture as well, where, however, the U-test had to be applied.</p>
                </sec>
            </sec>
            <sec sec-type="conclusion">
                <title>CONCLUSION</title>
                <p>This paper aimed to determine the total content of phenolic substances and antioxidant activity in selected cultivars of basil (<italic>Ocimum basilicum</italic>) in a fresh and frozen state and also in the mixture of basil with other plants in a fresh and refrigerated state. The values of antioxidant activity in frozen samples ranged from 5.1 &#xB1;0.4 mg.g<sup>-1</sup> AA FW to 11.71 &#xB1;0.18 mg.g<sup>-1</sup> AA FW and the total phenolic content varied between 2.77 &#xB1;0.16 mg.g<sup>-1</sup> GAE FW in TH and 8.93 &#xB1;0.13 mg.g<sup>-1</sup> GAE FW. Considering individual cultivars, statistically, significant differences were established between some cultivars in both AA and TPC determinations. Even though differences between cultivars were recorded in both fresh and frozen samples, a statistically significant difference between the fresh and frozen samples was established only in the OH cultivar in AA analysis (U-test; U = 0.00; <italic>p</italic> &#x003C;0.05).</p>
                <p>Fresh and refrigerated mixtures showed statistically significant differences in all mixtures considering AA; the mixture of OHR and OHS also in TPC determination. The most significant differences were found between OHM and other groups, with OHM showing the highest values.</p>
                <p>Wider usage of basil in human nutrition as a healthpromoting substance could help to suppress the formation of free radicals and their removal from the human body.</p>
            </sec>
        </body>
        <back>
            <ack>
                <title>Acknowledgments:</title>
                <p>We would like to special thank you to the Department of Vegetable Growing and Florticluture, Faculty of Horticulture of Mendel University in Brno, Czech Republic, for providing samples and photos of herbs.</p>
            </ack>
            <sec>
                <title>Funds:</title>
                <p>This work was supported by the internal grant of TBU in Zl&#xED;n [No. IGA/FT/2021/008], project BUT in Brno [No. FEKT-S-20-6215] and METROFOOD-CZ research infrastructure project (MEYS Grant No: LM2018100).</p>
            </sec>
            <sec>
                <title>Conflict of Interest:</title>
                <p>The authors declare no conflict of interest.</p>
            </sec>
            <sec>
                <title>Ethical Statement:</title>
                <p>This article does not contain any studies that would require an ethical statement.</p>
            </sec>
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