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Characterization of Bioactive Compounds in Tunisian Bitter Orange (Citrus aurantium L.) Peel and Juice and Determination of Their Antioxidant Activities

Identifieur interne : 000B29 ( Pmc/Checkpoint ); précédent : 000B28; suivant : 000B30

Characterization of Bioactive Compounds in Tunisian Bitter Orange (Citrus aurantium L.) Peel and Juice and Determination of Their Antioxidant Activities

Auteurs : Iness Jabri Karoui [Tunisie] ; Brahim Marzouk [Tunisie]

Source :

RBID : PMC:3697287

Abstract

Citrus aurantium peel and juice aroma compounds were investigated by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS), whereas phenolic compounds analysis was performed by reversed-phase high-performance liquid chromatography (RP-HPLC). Limonene was the major volatile compound of bitter orange peel (90.25%) and juice (91.61%). HPLC analysis of bitter orange peel and juice methanolic extracts indicated that phenolic acids constitute their main phenolic class representing 73.80% and 71.25%, respectively, followed by flavonoids (23.02% and 23.13%, resp.). p-Coumaric and ferulic acids were the most abundant phenolic compounds representing 24.68% and 23.79%, respectively, in the peel, while the juice contained 18.02% and 19.04%, respectively. The antioxidant activities of bitter orange peel and juice methanolic extracts have been evaluated using four in vitro assays, and the results were compared with the standard antioxidants (BHT, BHA, and ascorbic acid). Our findings demonstrated that Citrus aurantium peel and juice possess antioxidant activities which were less effective than those of antioxidant standards. Both extracts may be suggested as a new potential source of natural antioxidant.


Url:
DOI: 10.1155/2013/345415
PubMed: 23841062
PubMed Central: 3697287


Affiliations:


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PMC:3697287

Le document en format XML

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<name sortKey="Jabri Karoui, Iness" sort="Jabri Karoui, Iness" uniqKey="Jabri Karoui I" first="Iness" last="Jabri Karoui">Iness Jabri Karoui</name>
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<italic>Citrus aurantium</italic>
peel and juice aroma compounds were investigated by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS), whereas phenolic compounds analysis was performed by reversed-phase high-performance liquid chromatography (RP-HPLC). Limonene was the major volatile compound of bitter orange peel (90.25%) and juice (91.61%). HPLC analysis of bitter orange peel and juice methanolic extracts indicated that phenolic acids constitute their main phenolic class representing 73.80% and 71.25%, respectively, followed by flavonoids (23.02% and 23.13%, resp.).
<italic>p</italic>
-Coumaric and ferulic acids were the most abundant phenolic compounds representing 24.68% and 23.79%, respectively, in the peel, while the juice contained 18.02% and 19.04%, respectively. The antioxidant activities of bitter orange peel and juice methanolic extracts have been evaluated using four
<italic> in vitro</italic>
assays, and the results were compared with the standard antioxidants (BHT, BHA, and ascorbic acid). Our findings demonstrated that
<italic>Citrus aurantium</italic>
peel and juice possess antioxidant activities which were less effective than those of antioxidant standards. Both extracts may be suggested as a new potential source of natural antioxidant.</p>
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</author>
<author>
<name sortKey="Tarnus, E" uniqKey="Tarnus E">E Tarnus</name>
</author>
<author>
<name sortKey="Aruoma, Oi" uniqKey="Aruoma O">OI Aruoma</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Biomed Res Int</journal-id>
<journal-id journal-id-type="iso-abbrev">Biomed Res Int</journal-id>
<journal-id journal-id-type="publisher-id">BMRI</journal-id>
<journal-title-group>
<journal-title>BioMed Research International</journal-title>
</journal-title-group>
<issn pub-type="ppub">2314-6133</issn>
<issn pub-type="epub">2314-6141</issn>
<publisher>
<publisher-name>Hindawi Publishing Corporation</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">23841062</article-id>
<article-id pub-id-type="pmc">3697287</article-id>
<article-id pub-id-type="doi">10.1155/2013/345415</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Research Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Characterization of Bioactive Compounds in Tunisian Bitter Orange (
<italic>Citrus aurantium</italic>
L.) Peel and Juice and Determination of Their Antioxidant Activities</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Jabri karoui</surname>
<given-names>Iness</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
<xref ref-type="corresp" rid="cor1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Marzouk</surname>
<given-names>Brahim</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
</contrib>
</contrib-group>
<aff id="I1">Laboratoire des Substances Bioactives, Centre de Biotechnologie à la Technopole de Borj-Cédria (CBBC), BP 901, 2050 Hammam-lif, Tunisia</aff>
<author-notes>
<corresp id="cor1">*Iness Jabri karoui:
<email>iness.karoui@yahoo.fr</email>
</corresp>
<fn fn-type="other">
<p>Academic Editor: Jose R. Botella</p>
</fn>
</author-notes>
<pub-date pub-type="ppub">
<year>2013</year>
</pub-date>
<pub-date pub-type="epub">
<day>13</day>
<month>6</month>
<year>2013</year>
</pub-date>
<volume>2013</volume>
<elocation-id>345415</elocation-id>
<history>
<date date-type="received">
<day>16</day>
<month>4</month>
<year>2013</year>
</date>
<date date-type="rev-recd">
<day>18</day>
<month>5</month>
<year>2013</year>
</date>
<date date-type="accepted">
<day>22</day>
<month>5</month>
<year>2013</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2013 I. Jabri karoui and B. Marzouk.</copyright-statement>
<copyright-year>2013</copyright-year>
<license license-type="open-access">
<license-p>This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract>
<p>
<italic>Citrus aurantium</italic>
peel and juice aroma compounds were investigated by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS), whereas phenolic compounds analysis was performed by reversed-phase high-performance liquid chromatography (RP-HPLC). Limonene was the major volatile compound of bitter orange peel (90.25%) and juice (91.61%). HPLC analysis of bitter orange peel and juice methanolic extracts indicated that phenolic acids constitute their main phenolic class representing 73.80% and 71.25%, respectively, followed by flavonoids (23.02% and 23.13%, resp.).
<italic>p</italic>
-Coumaric and ferulic acids were the most abundant phenolic compounds representing 24.68% and 23.79%, respectively, in the peel, while the juice contained 18.02% and 19.04%, respectively. The antioxidant activities of bitter orange peel and juice methanolic extracts have been evaluated using four
<italic> in vitro</italic>
assays, and the results were compared with the standard antioxidants (BHT, BHA, and ascorbic acid). Our findings demonstrated that
<italic>Citrus aurantium</italic>
peel and juice possess antioxidant activities which were less effective than those of antioxidant standards. Both extracts may be suggested as a new potential source of natural antioxidant.</p>
</abstract>
</article-meta>
</front>
<floats-group>
<fig id="fig1" orientation="portrait" position="float">
<label>Figure 1</label>
<caption>
<p>RP-HPLC chromatographic profiles of phenolic acids, flavonoids, and phenolic monoterpenes standards and
<italic>Citrus aurantium </italic>
peel and juice extracts monitored at 280 nm. *The peak numbers correspond to the following: 1. caffeic acid; 2. gallic acid; 3.
<italic>p</italic>
-hydroxybenzoic acid; 4. chlorogenic acid; 5. syringic acid; 6. vanillic acid; 7.
<italic>p</italic>
-coumaric acid; 8. ferulic acid; 9. trans-2-hydroxycinnamic acid; 10. rosmarinic acid; 11.
<italic>o</italic>
-coumaric acid; 12. cinnamic acid; 13. trans-cinnamic acid; 14. epicatechin gallate; 15. catechin; 16. rutin; 17. naringin; 18. quercetrin; 19. luteolin; 20. quercetin; 21. apigenin; 22. amentoflavone; 23. flavone; 24. tyrosol; 25. thymol; S1. resorcinol. </p>
</caption>
<graphic xlink:href="BMRI2013-345415.001"></graphic>
</fig>
<table-wrap id="tab1" orientation="portrait" position="float">
<label>Table 1</label>
<caption>
<p>Essential oil composition of
<italic>Citrus aurantium </italic>
peel and juice
<sup>A</sup>
.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Volatile compounds</th>
<th align="center" rowspan="1" colspan="1">RI
<sup>a</sup>
</th>
<th align="center" rowspan="1" colspan="1">RI
<sup>b</sup>
</th>
<th align="center" rowspan="1" colspan="1">Peel</th>
<th align="center" rowspan="1" colspan="1">Juice</th>
<th align="center" rowspan="1" colspan="1">Identification</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">
<italic>α</italic>
-thujene</td>
<td align="center" rowspan="1" colspan="1">928</td>
<td align="center" rowspan="1" colspan="1">1035</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">1.03 ± 0.04
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Tricyclen</td>
<td align="center" rowspan="1" colspan="1">930</td>
<td align="center" rowspan="1" colspan="1">1015</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">0.68 ± 0.18
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. Co-CG. SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">
<italic>α</italic>
-Pinene</td>
<td align="center" rowspan="1" colspan="1">939</td>
<td align="center" rowspan="1" colspan="1">1032</td>
<td align="center" rowspan="1" colspan="1">0.55 ± 0.06
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.55 ± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. Co-CG. SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">β-Pinene</td>
<td align="center" rowspan="1" colspan="1">980</td>
<td align="center" rowspan="1" colspan="1">1118</td>
<td align="center" rowspan="1" colspan="1">0.44 ± 0.04
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Sabinene</td>
<td align="center" rowspan="1" colspan="1">975</td>
<td align="center" rowspan="1" colspan="1">1132</td>
<td align="center" rowspan="1" colspan="1">0.48 ± 0.16
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Myrcene</td>
<td align="center" rowspan="1" colspan="1">991</td>
<td align="center" rowspan="1" colspan="1">1174</td>
<td align="center" rowspan="1" colspan="1">0.04 ± 0.00
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.68 ± 0.16
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">
<italic>α</italic>
-Phellandrene</td>
<td align="center" rowspan="1" colspan="1">1006</td>
<td align="center" rowspan="1" colspan="1">1176</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">1.84 ± 0.04
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">
<italic>α</italic>
-Terpinene</td>
<td align="center" rowspan="1" colspan="1">1018</td>
<td align="center" rowspan="1" colspan="1">1188</td>
<td align="center" rowspan="1" colspan="1">1.10 ± 0.27
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">IR. CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Limonene</td>
<td align="center" rowspan="1" colspan="1">1030</td>
<td align="center" rowspan="1" colspan="1">1203</td>
<td align="center" rowspan="1" colspan="1">
<bold>90.25</bold>
  
<bold>±</bold>
  
<bold>0.81</bold>
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">
<bold>91.61</bold>
  
<bold>±</bold>
  
<bold>0.97</bold>
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">1-8 Cineole</td>
<td align="center" rowspan="1" colspan="1">1033</td>
<td align="center" rowspan="1" colspan="1">1213</td>
<td align="center" rowspan="1" colspan="1">0.87 ± 0.06
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.31 ± 0.04
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">E-β-Ocimene</td>
<td align="center" rowspan="1" colspan="1">1050</td>
<td align="center" rowspan="1" colspan="1">1266</td>
<td align="center" rowspan="1" colspan="1">0.36 ± 0.00
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">IR. CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Terpinolene</td>
<td align="center" rowspan="1" colspan="1">1088</td>
<td align="center" rowspan="1" colspan="1">1290</td>
<td align="center" rowspan="1" colspan="1">0.28 ± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Cis-linalool oxide</td>
<td align="center" rowspan="1" colspan="1">1074</td>
<td align="center" rowspan="1" colspan="1">1478</td>
<td align="center" rowspan="1" colspan="1">0.23 ± 0.03
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.49 ± 0.23
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Trans-linalool oxide</td>
<td align="center" rowspan="1" colspan="1">1088</td>
<td align="center" rowspan="1" colspan="1">1450</td>
<td align="center" rowspan="1" colspan="1">0.13 ± 0.01
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.21 ± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Linalool</td>
<td align="center" rowspan="1" colspan="1">1098</td>
<td align="center" rowspan="1" colspan="1">1553</td>
<td align="center" rowspan="1" colspan="1">1.56 ± 0.08
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Linalyl acetate</td>
<td align="center" rowspan="1" colspan="1">1257</td>
<td align="center" rowspan="1" colspan="1">1556</td>
<td align="center" rowspan="1" colspan="1">0.29 ± 0.02
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Bornyl acetate</td>
<td align="center" rowspan="1" colspan="1">1270</td>
<td align="center" rowspan="1" colspan="1">1590</td>
<td align="center" rowspan="1" colspan="1">0.14 ± 0.05
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Terpinene-4-ol</td>
<td align="center" rowspan="1" colspan="1">1419</td>
<td align="center" rowspan="1" colspan="1">1612</td>
<td align="center" rowspan="1" colspan="1">0.06 ± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">β-Caryophyllene</td>
<td align="center" rowspan="1" colspan="1">1178</td>
<td align="center" rowspan="1" colspan="1">1611</td>
<td align="center" rowspan="1" colspan="1">0.05 ± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">
<italic>γ</italic>
-Elemene</td>
<td align="center" rowspan="1" colspan="1">1492</td>
<td align="center" rowspan="1" colspan="1">1623</td>
<td align="center" rowspan="1" colspan="1">0.05 ± 0.00
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Neral</td>
<td align="center" rowspan="1" colspan="1">1240</td>
<td align="center" rowspan="1" colspan="1">1694</td>
<td align="center" rowspan="1" colspan="1">0.13 ± 0.00
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">β-Farnesene</td>
<td align="center" rowspan="1" colspan="1">1456</td>
<td align="center" rowspan="1" colspan="1">1696</td>
<td align="center" rowspan="1" colspan="1">0.15 ± 0.15
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">
<italic>α</italic>
-Terpineol</td>
<td align="center" rowspan="1" colspan="1">1189</td>
<td align="center" rowspan="1" colspan="1">1709</td>
<td align="center" rowspan="1" colspan="1">0.56 ± 0.03
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.38 ± 0.08
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Neryl acetate</td>
<td align="center" rowspan="1" colspan="1">1385</td>
<td align="center" rowspan="1" colspan="1">1733</td>
<td align="center" rowspan="1" colspan="1">0.23 ± 0.03
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.36 ± 0.06
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Δ-Cadinene</td>
<td align="center" rowspan="1" colspan="1">1523</td>
<td align="center" rowspan="1" colspan="1">1755</td>
<td align="center" rowspan="1" colspan="1">0.28 ± 0.02
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Geranyl acetate</td>
<td align="center" rowspan="1" colspan="1">1383</td>
<td align="center" rowspan="1" colspan="1">1765</td>
<td align="center" rowspan="1" colspan="1">0.11 ± 0.00
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Nerol</td>
<td align="center" rowspan="1" colspan="1">1228</td>
<td align="center" rowspan="1" colspan="1">1797</td>
<td align="center" rowspan="1" colspan="1">0.08 ± 0.00
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Geraniol</td>
<td align="center" rowspan="1" colspan="1">1255</td>
<td align="center" rowspan="1" colspan="1">1857</td>
<td align="center" rowspan="1" colspan="1">0.16 ± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">IR. SM. Co-CG</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">E-Nerolidol</td>
<td align="center" rowspan="1" colspan="1">1566</td>
<td align="center" rowspan="1" colspan="1">2030</td>
<td align="center" rowspan="1" colspan="1">0.35 ± 0.04
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Oxyde de caryophyllène</td>
<td align="center" rowspan="1" colspan="1">1581</td>
<td align="center" rowspan="1" colspan="1">2008</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">1.42 ± 0.51
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">IR. CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">E.Z farnesyl acetate</td>
<td align="center" rowspan="1" colspan="1">1818</td>
<td align="center" rowspan="1" colspan="1">2198</td>
<td align="center" rowspan="1" colspan="1">0.57 ± 0.02
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">CG-SM</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">NI</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">0.52 ± 0.03</td>
<td align="center" rowspan="1" colspan="1">0.44 ± 0.05</td>
<td align="center" rowspan="1" colspan="1"></td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>
<sup>A</sup>
Values are given as mean ± SD (
<italic>n</italic>
= 3). Values followed by the same letter did not share significant differences at
<italic>P</italic>
< 0.05 (Duncan's test). —: not detected.</p>
</fn>
<fn>
<p>
<sup>b</sup>
Components are listed in order of elution in apolar column (HP-5). </p>
</fn>
<fn>
<p>
<sup>c</sup>
RI
<sup>a</sup>
, RI
<sup>b</sup>
: retention indices calculated using, respectively, an apolar column (HP-5) and polar column (HP INNOWax). Volatile compound proportions were calculated from the chromatograms obtained on the HP INNOWax column. </p>
</fn>
</table-wrap-foot>
</table-wrap>
<table-wrap id="tab2" orientation="portrait" position="float">
<label>Table 2</label>
<caption>
<p>Contents (mg/g) and percentages (%) of phenolic compounds of bitter orange peel and juice
<sup>A</sup>
.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="2" colspan="1">Phenolic compounds</th>
<th align="center" colspan="2" rowspan="1">Peel</th>
<th align="center" colspan="2" rowspan="1">Juice</th>
</tr>
<tr>
<th align="center" rowspan="1" colspan="1">%</th>
<th align="center" rowspan="1" colspan="1">Mg/g</th>
<th align="center" rowspan="1" colspan="1">%</th>
<th align="center" rowspan="1" colspan="1">Mg/L</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">Phenolic acids</td>
<td align="center" rowspan="1" colspan="1">
<bold>73.80</bold>
<bold>± 3.33</bold>
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">
<bold>1.03</bold>
<bold>± 0.02</bold>
</td>
<td align="center" rowspan="1" colspan="1">
<bold>71.25</bold>
   ± 0.25
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">
<bold>473.89</bold>
<bold> ± 0.30</bold>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Gallic acid</td>
<td align="center" rowspan="1" colspan="1">1.84 ± 0.25
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.03 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">
<bold>13.05</bold>
± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">84.53 ± 0.07</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Hydroxybenzoic acid</td>
<td align="center" rowspan="1" colspan="1">1.13 ± 0.65
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.02 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">4.05 ± 0.11
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">27.88 ± 0.05</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Chlorogenic acid</td>
<td align="center" rowspan="1" colspan="1">8.63 ± 0.13
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.12 ± 0.01</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1"></td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Syringic acid</td>
<td align="center" rowspan="1" colspan="1">1.69 ± 0.46
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.02 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">2.24 ± 0.00
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">13.75 ± 0.1</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Vanillic acid</td>
<td align="center" rowspan="1" colspan="1">1.75 ± 0.57
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.02 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">2.61 ± 0.04
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">17.19 ± 0.01</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Rosmarinic acid</td>
<td align="center" rowspan="1" colspan="1">5.58 ± 0.65
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.08 ± 0.02</td>
<td align="center" rowspan="1" colspan="1">5.43 ± 0.10
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">36.84 ± 0.02</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Trans-2-hydroxycinnamic acid</td>
<td align="center" rowspan="1" colspan="1">3.15 ± 0.28
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.04 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">4.56 ± 0.05
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">30.69
<bold>± </bold>
0.20</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Trans-cinnamic acid</td>
<td align="center" rowspan="1" colspan="1">1.56 ± 0.65
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.02 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">2.58 ± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">15.64 ± 0.09</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">
<italic>p</italic>
-Coumaric acid</td>
<td align="center" rowspan="1" colspan="1">
<bold>24.68</bold>
<bold>± 2.64</bold>
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.34 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">
<bold>18.02</bold>
± 0.22
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">116.13 ± 0.18 </td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Ferulic acid</td>
<td align="center" rowspan="1" colspan="1">
<bold>23.79</bold>
<bold>± 3.27</bold>
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.33 ± 0.02 </td>
<td align="center" rowspan="1" colspan="1">
<bold>19.04</bold>
± 0.22
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">131.24 ± 0.21</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Flavonoids</td>
<td align="center" rowspan="1" colspan="1">
<bold>23.02</bold>
<bold> ± 3.83</bold>
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">
<bold>0.33</bold>
<bold>± 0.07</bold>
</td>
<td align="center" rowspan="1" colspan="1">
<bold>23.13</bold>
  ± 1.11
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">
<bold>136.91</bold>
± 0.17</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Epicatechin</td>
<td align="center" rowspan="1" colspan="1">2.77 ± 0.83
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.04 ± 0.02</td>
<td align="center" rowspan="1" colspan="1">5.36 ± 0.15
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">36.47 ± 0.05</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Catechin</td>
<td align="center" rowspan="1" colspan="1">3.17 ± 0.27
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.04 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">3.16 ± 0.08
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">20.24 ± 0.09</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Rutin</td>
<td align="center" rowspan="1" colspan="1">9.91 ± 1.18
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.14 ± 0.03</td>
<td align="center" rowspan="1" colspan="1">5.98 ± 0.19
<sup>b</sup>
</td>
<td align="center" rowspan="1" colspan="1">37.21 ± 0.10</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Naringin</td>
<td align="center" rowspan="1" colspan="1">5.23 ± 1.15
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.07 ± 0.02</td>
<td align="center" rowspan="1" colspan="1">5.59 ± 0.04
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">35.05 ± 0.12</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Flavone</td>
<td align="center" rowspan="1" colspan="1">1.95 ± 1.98
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">0.03 ± 0.03</td>
<td align="center" rowspan="1" colspan="1">1.19 ± 0.01
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">7.96 ± 0.01</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Phenolic monoterpenes</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">
<bold>3.51</bold>
± 0.17
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">
<bold>23.54</bold>
± 0.03</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Tyrosol</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">3.51 ± 0.17
<sup>a</sup>
</td>
<td align="center" rowspan="1" colspan="1">23.54 ± 0.03</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Unknown</td>
<td align="center" rowspan="1" colspan="1">3.18 ± 0.50</td>
<td align="center" rowspan="1" colspan="1">0.04 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">3.62</td>
<td align="center" rowspan="1" colspan="1">22.79 ± 0.08</td>
</tr>
<tr>
<td align="left" colspan="5" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Total</td>
<td align="center" rowspan="1" colspan="1">100</td>
<td align="center" rowspan="1" colspan="1">1.40 ± 0.09</td>
<td align="center" rowspan="1" colspan="1">100</td>
<td align="center" rowspan="1" colspan="1">657.13 ± 0.27</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>
<sup>A</sup>
Values are given as mean ± SD (
<italic>n</italic>
= 3). Values followed by the same letter did not share significant differences at
<italic>P</italic>
< 0.05 (Duncan's test). —: not detected.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<table-wrap id="tab3" orientation="portrait" position="float">
<label>Table 3</label>
<caption>
<p>Antioxidant activities of bitter orange peel and juice methanolic extracts
<sup>A</sup>
.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1"></th>
<th align="center" rowspan="1" colspan="1">Total antioxidant capacity
<break></break>
(mg GAE/g FW: peel)
<break></break>
(mg GAE/L: juice)</th>
<th align="center" rowspan="1" colspan="1">DPPH
<break></break>
(IC
<sub>50</sub>
,
<italic>µ</italic>
g mL
<sup>−1</sup>
: peel)
<break></break>
(%
<italic>I</italic>
: juice)</th>
<th align="center" rowspan="1" colspan="1">β-Carotene bleaching
<break></break>
(IC
<sub>50</sub>
, mg mL
<sup>−1</sup>
: peel)
<break></break>
(%
<italic>I</italic>
: juice)</th>
<th align="center" rowspan="1" colspan="1">Reducing power
<break></break>
(EC
<sub>50</sub>
, mg mL
<sup>−1</sup>
: peel)
<break></break>
</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">Peel</td>
<td align="center" rowspan="1" colspan="1">5.23 ± 0.05</td>
<td align="center" rowspan="1" colspan="1">190 ± 0.01</td>
<td align="center" rowspan="1" colspan="1">5.81 ± 0.03</td>
<td align="center" rowspan="1" colspan="1">1.88 ± 0.05</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Juice</td>
<td align="center" rowspan="1" colspan="1">823.13 ± 17.18</td>
<td align="center" rowspan="1" colspan="1">97.05 ± 0.38</td>
<td align="center" rowspan="1" colspan="1">15.92 ± 0.66</td>
<td align="center" rowspan="1" colspan="1"></td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>
<sup>A</sup>
Values are given as mean ± SD (
<italic>n</italic>
= 3). —: not detected.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</floats-group>
</pmc>
<affiliations>
<list>
<country>
<li>Tunisie</li>
</country>
</list>
<tree>
<country name="Tunisie">
<noRegion>
<name sortKey="Jabri Karoui, Iness" sort="Jabri Karoui, Iness" uniqKey="Jabri Karoui I" first="Iness" last="Jabri Karoui">Iness Jabri Karoui</name>
</noRegion>
<name sortKey="Marzouk, Brahim" sort="Marzouk, Brahim" uniqKey="Marzouk B" first="Brahim" last="Marzouk">Brahim Marzouk</name>
</country>
</tree>
</affiliations>
</record>

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