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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">GYA</journal-id>
<journal-title-group>
<journal-title>Grasas y Aceites</journal-title>
</journal-title-group>
<issn pub-type="epub">0017-3495</issn>
<publisher>
<publisher-name>Consejo Superior de Investigaciones Cientificas</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">GYA201934_e317-0927182</article-id>
<article-id pub-id-type="doi">10.3989/gya.0927182</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Articles</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Composition and characterization by GC-MS of the essential oil extracted from <italic>Nicotiana glauca</italic> Graham</article-title>
<trans-title-group xml:lang="es">
<trans-title><italic>Composici&#x00F3;n y caracterizaci&#x00F3;n mediante GC-MS de aceite esencial extra&#x00ED;do de</italic> Nicotiana glauca <italic>Graham</italic></trans-title>
</trans-title-group>
<alt-title alt-title-type="running-head">Composition and characterization by GC-MS of the essential oil extracted from <italic>Nicotiana glauca</italic> Graham</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Cherif</surname>
<given-names>A.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">a</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ammar</surname>
<given-names>S.</given-names>
</name>
<xref ref-type="aff" rid="aff0002">b</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Boukhchina</surname>
<given-names>S.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">a</xref>
</contrib>
</contrib-group>
<aff id="aff0001"><label>a</label>Department of Biology, Faculty of Sciences, University of Tunis El-Manar, Tunis 2092, Tunisia</aff>
<aff id="aff0002"><label>b</label>Department of Chemistry, Faculty of Sciences of Gabes, Erriadh city, 6072 Zrig, Tunisia</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Corresponding author: <email xlink:href="cherif.ammar@yahoo.com">cherif.ammar@yahoo.com</email></corresp>
<fn><p><bold>ORCID ID</bold>: Cherif A <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0003-4924-0120">https://orcid.org/0000-0003-4924-0120</ext-link>, Ammar S <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0002-5571-9851">https://orcid.org/0000-0002-5571-9851</ext-link>, Boukhchina S <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0003-1215-2813">https://orcid.org/0000-0003-1215-2813</ext-link></p></fn>
</author-notes>
<pub-date pub-type="epub">
<day>30</day>
<month>09</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="collection">
<year>2019</year>
</pub-date>
<volume>70</volume>
<issue>3</issue>
<elocation-id content-type="doi">10.3989/gya.0927182</elocation-id>
<history>
<date date-type="received">
<day>01</day>
<month>09</month>
<year>2018</year>
</date>
<date date-type="accepted">
<day>10</day>
<month>12</month>
<year>2018</year>
</date>
<date date-type="published online">
<day>07</day>
<month>05</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>&#x00A9; 2019 CSIC</copyright-statement>
<copyright-year>2019</copyright-year>
<license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) License.</license-p>
</license>
</permissions>
<abstract>
<title>SUMMARY</title>
<p>Fresh leaves of <italic>N. glauca</italic> were collected from the northern region of Tunisia. The leaves were submitted to water distillation for 4 h, using a Clevenger-type apparatus. The obtained essential oils were dried over anhydrous sodium sulphate and after filtration, stored at 4 &#x00B0;C until use. The chemical composition of the isolated essential oil was analyzed by gas chromatography&#x2013;mass spectrometry (GC&#x2013;MS). Eighteen compounds were identified: eugenol, the major compound in the essential oil, was present at a high level (58.49%), followed by nonadecane, eugenyl acetate and tridecane, 3-methyl at 6.38; 5.57 and 5.19%, respectively. The percentage of compounds dodecane, 2, 6, 11 trimethyl, tetradecane, docosane, tricosane and 1, 2-benzene dicarboxilic, dibutyl ester varied between 1 and 2%; whereas the other compounds (including limonene, and saturated hydrocarbons) remained at low percentages, not exceeding 1%. This study could be very useful for the characterization, pharmaceutical and therapeutic applications of the essential oil from <italic>N. glauca</italic>.</p>
</abstract>
<trans-abstract xml:lang="es">
<title>RESUMEN</title>
<p><bold><italic>Composici&#x00F3;n y caracterizaci&#x00F3;n mediante GC-MS de aceite esencial extra&#x00ED;do de</italic> Nicotiana glauca <italic>Graham</italic>.</bold> Las hojas frescas de <italic>N. glauca</italic> se recolectaron en la regi&#x00F3;n norte de T&#x00FA;nez. Las hojas se sometieron a destilaci&#x00F3;n en agua durante 4 h, utilizando un aparato de destilaci&#x00F3;n tipo Clevenger. Los aceites esenciales obtenidos se secaron y filtraron sobre sulfato de sodio anhidro y se almacenaron a 4 &#x00B0;C hasta su uso. La composici&#x00F3;n qu&#x00ED;mica del aceite esencial aislado se analiz&#x00F3; mediante cromatograf&#x00ED;a de gases y espectrometr&#x00ED;a de masas (GC-MS). Se identificaron dieciocho compuestos: eugenol es el compuesto mayoritario (58,49%), seguido por nonadecano, acetato de eugenilo y tridecano, 3-metilo con 6,38%; 5,57% y 5,19% respectivamente. El porcentaje de los compuestos: dodecano, 2,6,11 trimetil, tetradecano, docosano, tricosano y 1,2-benceno dicarbox&#x00ED;lico, dibutil &#x00E9;ster vari&#x00F3; entre 1 y 2%, mientras que el resto de compuestos (incluido el limoneno e hidrocarburos saturados) permanecieron en cantidades que no superan el 1%. Este estudio de caracterizaci&#x00F3;n podr&#x00ED;a ser de gran utilidad para aplicaciones farmac&#x00E9;uticas y terap&#x00E9;uticas del aceite esencial de <italic>N. glauca</italic>.</p>
</trans-abstract>
<kwd-group xml:lang="en">
<title>KEYWORDS</title>
<kwd>Essential oil</kwd>
<kwd>Eugenol</kwd>
<kwd>GC-MS</kwd>
<kwd>Hydrodistillation</kwd>
<kwd><italic>N. glauca</italic></kwd>
</kwd-group>
<kwd-group xml:lang="es">
<title>PALABRAS CLAVE</title>
<kwd>Aceite esencial</kwd>
<kwd>Eugenol</kwd>
<kwd>GC-MS</kwd>
<kwd>Hidrodestilaci&#x00F3;n</kwd>
<kwd><italic>N. glauca</italic></kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="sec1" sec-type="intro">
<title>1. INTRODUCTION</title>
<p>The genus Nicotiana of the family Solanaceae contains more than 40 species. <italic>Nicotiana tabacum</italic> L. and <italic>Nicotiana rustica</italic> L. are the well-known species spread throughout the world (Pandey and Chada <xref ref-type="bibr" rid="cit0014">1998</xref>). The leaves of these species yield tobacco and are commonly cultivated as crops. However, <italic>N. glauca</italic>, also called wild tobacco or tree tobacco, is considered the most powerful of the Nicotiana species, due to its potential for exploitation in the therapeutic field. Like all Nicotiana, it was used for many medical treatments (Watt and Breyer-Brandwijk <xref ref-type="bibr" rid="cit0025">1962</xref>); it is used to treat burns and inflammatory diseases in some countries (Morel <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0012">1998</xref>). Warmed leaves are applied to the head to relieve headache, on the throat to relieve pain and put in shoes for painful feet (Van Wyk and Gericke <xref ref-type="bibr" rid="cit0024">2000</xref>). <italic>N. glauca</italic> is also known as a highly toxic and teratogenic plant (Panter <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0015">1999</xref>). The recorded death in humans was due to poisoning by accidental ingestion of the leaves of <italic>N. glauca</italic> (Sims <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0020">1999</xref>; Manoguerra and Freeman <xref ref-type="bibr" rid="cit0009">1982</xref>). A considerable amount of work has been carried out on the metabolism of nicotine in Nicotiana species (Leete and Chedekel <xref ref-type="bibr" rid="cit0008">1973</xref>) and other works have been conducted on the total alkaloid or nicotine content, which was determined by steam distillation and spectrophotometry. Among the alkaloids in Nicotiana, nicotine was the dominant alkaloid in the leaves of 33 species, nornicotine of 24 species, and anabasine of 2 species <italic>(N. glauca</italic> and <italic>N. debneyi);</italic> whereas in the roots of Nicotiana, anabasine predominated in 7 species of Nicotiana including <italic>N. glauca.</italic> According to (Skliar <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0021">2000</xref>), results show that <italic>N. glauca</italic> contains 7-dehydrocholesterol, vitamin D3 and its hydroxylated metabolites. Recently, (Tabana <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0022">2016</xref>) reported the anti neovascularization effect of scopoletin, an active principle extract from <italic>N. glauca</italic>, and its antitumorigenic activity on human tumors in xenograft models.</p>
<p>But, to our knowledge no information is available on the essential oil (EO) composition of <italic>N. glauca</italic>. Essential oils of plants and other products from secondary metabolism have been widely used in traditional medicine, food flavoring, pharmaceutical industries, perfumes and cosmetics (Bauer K, Garbe D, Surburg H. <xref ref-type="bibr" rid="cit0003">2008</xref>; Price <xref ref-type="bibr" rid="cit0017">1998</xref>; Satil <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0018">2003</xref>) and some plant secondary metabolites were implied in the protection against herbivore attack (Kaczorowski and Markman <xref ref-type="bibr" rid="cit0007">2016</xref>). Some biological activities of essential oils have been known for long time (Digrak <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0005">1999</xref>; Dang <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0004">2001</xref>; Grassmann <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0006">2000</xref>). On the other hand the quantitative composition of the essential oils of many aromatic plants is greatly influenced by genotype and agronomic conditions, such as harvesting time, plant age and crop density (Marotti <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0011">1996</xref>).</p>
<p>The present study performed on <italic>N. glauca</italic>, which was harvested from the northern region of Tunisia, provides the content and chemical composition of the essential oil analyzed by GC-MS.</p>
</sec>
<sec id="sec2" sec-type="materials|methods">
<title>2. MATERIALS AND METHODS</title>
<sec id="sec2.1">
<title>2.1. Plant material</title>
<p>Fresh leaves of <italic>N. glauca</italic> were submitted to hydro distillation for 4 h using a Clevenger type apparatus. Then, the extract of EO was obtained by petroleum ether extraction (Nakamura <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0013">1999</xref>). The solvent was evaporated; the extract of EO was dried with anhydrous sodium sulphate. The essential oils were stored in dark glass bottles at 4 &#x00BA;C (Marotti <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0010">1994</xref>) until analysis.</p>
</sec>
<sec id="sec2.2">
<title>2.2. Gas chromatography-mass spectrometry (GC-MS) analysis</title>
<p>The gas chromatography-mass spectrometry analysis was carried out using a capillary column HP-5MS (30 m x 0.25i.d, film thickness: 0.25mm). The carrier gas was helium at a flow velocity of 1.2 ml/min; and the splitter used a 1:5 ratio. Oven temperature was kept at 50 &#x00BA;C for 3 min and programmed from 50 &#x00BA;C to 220 &#x00BA;C at a rate of 7 &#x00BA;C/min, then isothermal at 250 &#x00BA;C for 5 min. The injector temperature was 240 &#x00BA;C. For GC&#x2013;MS detection an electron ionization system was used. Mass spectra were taken at 70 eV. The source of impact electronic ionization was set at 230 &#x00BA;C. The essential oil was diluted in hexane and 1&#x00B5;l was injected for analysis.</p>
<p>The identification of compounds was determined by comparison of their mass spectra with those of the database in the Wiley GC-MS Library and those in the literature (Adams <xref ref-type="bibr" rid="cit0001">2007</xref>) where the components were listed according to their elution on the a polar column.</p>
</sec>
</sec>
<sec id="sec3" sec-type="result|discussion">
<title>3. RESULT AND DISCUSSION</title>
<p>To our knowledge, no investigations have been previously performed on the chemical composition of the essential oil from <italic>N. glauca</italic>. The essential oil isolated from the leaves of <italic>N. glauca</italic> by hydro distillation (yield &#x003C; 1 %, on dry weight basis) was analyzed by GC and GC-MS. The content and distribution of EO in the green leaves of <italic>N. glauca</italic> are summarized in <xref ref-type="table" rid="t0001">Table 1</xref>. A total of 18 compounds representing almost 93.33% of the essential oil were characterized. Seven compounds were detected but not identified (NI) (<xref ref-type="fig" rid="f0001">Figure 1</xref>).</p>
<table-wrap id="t0001">
<label>Table 1</label>
<caption>
<p>Composition of the essential oils from leaves of a Tunisian variety of Nicotiana (<italic>Nicotiana glauca Glauca</italic>).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Pic number</th>
<th align="center">Rt<sup><xref ref-type="table-fn" rid="tf1-1">a</xref></sup> (min)</th>
<th align="left">Compound</th>
<th align="center">Chemical formula</th>
<th align="center">Content %</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">1</td>
<td align="center">9.35</td>
<td align="left">Heptane,2,2,4,6,6-Pentamethyl</td>
<td align="center">C<sub>12</sub>H<sub>26</sub></td>
<td align="center">0.50</td>
</tr>
<tr>
<td align="left">2</td>
<td align="center">10.28</td>
<td align="left">Limonene</td>
<td align="center">C<sub>10</sub>H<sub>16</sub></td>
<td align="center">0.33</td>
</tr>
<tr>
<td align="left">3</td>
<td align="center">10.86</td>
<td align="left">NI<sup><xref ref-type="table-fn" rid="tf1-2">b</xref></sup></td>
<td align="center"/>
<td align="center">1.84</td>
</tr>
<tr>
<td align="left">4</td>
<td align="center">11.85</td>
<td align="left">NI</td>
<td align="center"/>
<td align="center">0.44</td>
</tr>
<tr>
<td align="left">5</td>
<td align="center">15.61</td>
<td align="left">Heptadecane,8-methyl</td>
<td align="center">C<sub>18</sub>H<sub>38</sub></td>
<td align="center">4.19</td>
</tr>
<tr>
<td align="left">6</td>
<td align="center">16.51</td>
<td align="left">Dodecane,2,6,11 trimethyl</td>
<td align="center">C<sub>15</sub>H<sub>32</sub></td>
<td align="center">1.08</td>
</tr>
<tr>
<td align="left">7</td>
<td align="center">17.34</td>
<td align="left">Eugenol</td>
<td align="center">C<sub>12</sub>H<sub>12</sub>O<sub>2</sub></td>
<td align="center">58.49</td>
</tr>
<tr>
<td align="left">8</td>
<td align="center">17.91</td>
<td align="left">Tetradecane</td>
<td align="center">C<sub>14</sub>H<sub>30</sub></td>
<td align="center">1.20</td>
</tr>
<tr>
<td align="left">9</td>
<td align="center">19.67</td>
<td align="left">Nonadecane</td>
<td align="center">C<sub>19</sub>H<sub>40</sub></td>
<td align="center">6.38</td>
</tr>
<tr>
<td align="left">10</td>
<td align="center">19.83</td>
<td align="left">Heneicosane</td>
<td align="center">C<sub>21</sub>H<sub>44</sub></td>
<td align="center">0.62</td>
</tr>
<tr>
<td align="left">11</td>
<td align="center">20.31</td>
<td align="left">Eugenyl acetate</td>
<td align="center">C<sub>12</sub>H<sub>14</sub>O<sub>3</sub></td>
<td align="center">5.57</td>
</tr>
<tr>
<td align="left">12</td>
<td align="center">20.61</td>
<td align="left">NI</td>
<td align="center"/>
<td align="center">0.34</td>
</tr>
<tr>
<td align="left">13</td>
<td align="center">21.43</td>
<td align="left">Hexadecane</td>
<td align="center">C<sub>16</sub>H<sub>34</sub></td>
<td align="center">0.47</td>
</tr>
<tr>
<td align="left">14</td>
<td align="center">23.37</td>
<td align="left">NI</td>
<td align="center"/>
<td align="center">0.33</td>
</tr>
<tr>
<td align="left">15</td>
<td align="center">23.91</td>
<td align="left">Docosane</td>
<td align="center">C<sub>22</sub>H<sub>46</sub></td>
<td align="center">1.40</td>
</tr>
<tr>
<td align="left">16</td>
<td align="center">26.44</td>
<td align="left">Tridecane,3-methyl</td>
<td align="center">C<sub>14</sub>H<sub>30</sub></td>
<td align="center">5.19</td>
</tr>
<tr>
<td align="left">17</td>
<td align="center">27.03</td>
<td align="left">Tricosane</td>
<td align="center">C<sub>23</sub>H<sub>48</sub></td>
<td align="center">1.33</td>
</tr>
<tr>
<td align="left">18</td>
<td align="center">27.09</td>
<td align="left">1,2-Benzene dicarboxilic, dibutyl ester</td>
<td align="center">C<sub>16</sub>H<sub>22</sub>o<sub>4</sub></td>
<td align="center">1.00</td>
</tr>
<tr>
<td align="left">19</td>
<td align="center">29.33</td>
<td align="left">NI</td>
<td align="center"/>
<td align="center">3.17</td>
</tr>
<tr>
<td align="left">20</td>
<td align="center">29.43</td>
<td align="left">NI</td>
<td align="center"/>
<td align="center">0.33</td>
</tr>
<tr>
<td align="left">21</td>
<td align="center">29.86</td>
<td align="left">NI</td>
<td align="center"/>
<td align="center">0.76</td>
</tr>
<tr>
<td align="left">22</td>
<td align="center">32.12</td>
<td align="left">Triacontane</td>
<td align="center">C<sub>30</sub>H<sub>62</sub></td>
<td align="center">2.62</td>
</tr>
<tr>
<td align="left">23</td>
<td align="center">32.74</td>
<td align="left">Hexacosane</td>
<td align="center">C<sub>26</sub>H<sub>54</sub></td>
<td align="center">0.78</td>
</tr>
<tr>
<td align="left">24</td>
<td align="center">32.82</td>
<td align="left">Eicosane</td>
<td align="center">C<sub>20</sub>H<sub>42</sub></td>
<td align="center">0.70</td>
</tr>
<tr>
<td align="left">25</td>
<td align="center">34.59</td>
<td align="left">Pentacosane</td>
<td align="center">C<sub>25</sub>H<sub>52</sub></td>
<td align="center">0.95</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="tf1-1"><label>a</label><p>Retention Time</p></fn>
<fn id="tf1-2"><label>b</label><p>Non Identified</p></fn>
</table-wrap-foot>
</table-wrap>
<fig id="f0001">
<label>Figure 1</label>
<caption>
<p>Total ion chromatogram of essential oil from <italic>Nicotiana glauca</italic> Graham<italic>.</italic> (For compound names see <xref ref-type="table" rid="t0001">Table 1</xref>).</p>
</caption>
<graphic xlink:href="GYA201934_e317-0927182-g001.tif" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</fig>
<p>The essential oil of <italic>N. glauca</italic> contains a complex mixture consisting of mainly phenol, saturated, cylic and terpenic compounds (<xref ref-type="table" rid="t0001">Table 1</xref>). It was dominated by eugenol (58.49%) followed by nonadecane, eugenyl acetate and tridecane,3-methyl at 6.38%; 5.57% and 5.19%, respectively. These compounds were considered as major in the EO; while the percentages of dodecane,2,6,11 trimethyl, tetradecane, docosane, tricosane and 1,2-benzene dicarboxilic, dibutyl ester varied between 1 and 2%. The remaining compounds (included limonene and saturated hydrocarbons (SH)) were only present in small percentage (&#x003C; 1%), with the exception of triacontane, which was found at 2.62%.</p>
<p>Compared to our results, the same number of compounds was found in the essential oils of <italic>N. rustica;</italic> whereas twenty-seven EO were detected in <italic>N. forgetiana</italic> (Schlotzhauer <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0019">1995</xref>). According to Popova <italic>et al.,</italic> (<xref ref-type="bibr" rid="cit0016">2017</xref>) nineteen compounds in the essential oil of the leaves of <italic>N. alata</italic> were characterized, but different compounds in each species were detected by GC-MS. Our results showed the presence of 10 n-alkanes (saturated hydrocarbons). However, compared to the above authors, only two saturated hydrocarbons (tricosane and pentacosane) were identified in <italic>N. rustica</italic> and five SH were identified in <italic>N. forgetiana</italic>. The percentage of the EO composition was very different in the same genus. In fact, the percentages of tricosane in our study on <italic>N. glauca</italic> and in others on <italic>N. rustica</italic> and <italic>N. forgetiana</italic> were 1.33, 0.38, and 8.16%, respectively. In our research, the major compound was eugenol (58.49%). In contrast, phytol (38.82-48.53%) was the dominant compound in <italic>N. alata;</italic> nicotine (25.92%) and pentacosane (8.35%) were the major compounds in <italic>N. rustica</italic> and <italic>N. forgetiana,</italic> respectively.</p>
<p>The same major compounds in the EO can be found in different plants. Eugenol, the major component of the oil of <italic>N. glauca</italic>, was likewise present in a higher quantity (72-90%) in the EO fraction of <italic>Syzygium aromaticum</italic> (Bao <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0002">2012</xref>). This component varied between 3.1 and 21.1% in the essential oil of <italic>Ocimum basilicum</italic> cultivated in Turkey, and in the same species the percentage of methyl eugenol was detected at a high level (&#x02C3; 34%) (Telci <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0023">2006</xref>). However, the chemical composition of essential oils was specific to each species, regardless of its origin. In fact, the results showed that the EO of <italic>N. glauca</italic> (Tunisia) has a specific chemical composition compared to <italic>N. rustica, N. forgetiana</italic> (Oxford) and <italic>N. alata</italic> (Bulgaria). This information could be used as a fingerprint for this species.</p>
</sec>
<sec id="sec4" sec-type="conclusions">
<title>4. CONCLUSION</title>
<p>The content and distribution of EO in the green leaves of <italic>N. glauca</italic> are provided in this work. Eugenol was the dominant EO followed by nonadecane, eugenyl acetate and tridecane,3-methyl. In general, the <italic>N. glauca</italic> oil was characterized by a high percentage of the saturated hydrocarbons; while heneicosane, limonene and hexadecane were the minor constituents (&#x02C2; 0.5% for each compound) in the EO. This plant is therefore considered a potential source of eugenol (58.49%) and due to this high eugenol content, it can be exploited for medicinal purposes and other applications.</p>
</sec>
</body>
<back>
<ack>
<title>ACKNOWLEDGMENTS</title>
<p>The authors would like to thank the Arid Regions Institute (IRA) personnel (Medenine, Tunisia) for the availability of the GC-MS used to carry out this research.</p>
</ack>
<sec sec-type="COI-statement">
<title>DECLARATION OF FUNDING SOURCE AND CONFLICT OF INTEREST</title>
<p>This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.</p>
<p>The authors declare that they have no conflict of interest.</p>
</sec>
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