<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">NS</journal-id><journal-title-group><journal-title>Natural Science</journal-title></journal-title-group><issn pub-type="epub">2150-4091</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ns.2016.86029</article-id><article-id pub-id-type="publisher-id">NS-67478</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Chemistry&amp;Materials Science</subject><subject> Earth&amp;Environmental Sciences</subject><subject> Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  Phenolic Contents and Antioxidant Activities of Green Tea with and without Lemon
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ayat</surname><given-names>B. Al-Ghafari</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ayat</surname><given-names>M. Shorbaji</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lamya</surname><given-names>A. AL-Sarori</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Eman</surname><given-names>O. Baduwailan</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aisha</surname><given-names>A. Basaar</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Huda</surname><given-names>A. Al Doghaither</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hala</surname><given-names>F. Al-Marzouki</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ulfat</surname><given-names>M. Omar</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, KSA</addr-line></aff><pub-date pub-type="epub"><day>17</day><month>06</month><year>2016</year></pub-date><volume>08</volume><issue>06</issue><fpage>247</fpage><lpage>255</lpage><history><date date-type="received"><day>3</day>	<month>March</month>	<year>2016</year></date><date date-type="rev-recd"><day>accepted</day>	<month>14</month>	<year>June</year>	</date><date date-type="accepted"><day>17</day>	<month>June</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Tea is the most widely consumed beverage throughout the world, after water and is considered as a good antioxidant nutrient against free radical reactions. Lemons are citrus fruits that are very common in many parts of the world and are well known for their health benefits. In this study, different assays were used to evaluate total phenolic content and antioxidant activities of green tea with and without lemon. Our results showed that green tea with lemon has higher phenolic content, stronger reducing power than green tea without lemon; and exhibits a significant inhibition of 2,2-Diphenyl-1-picrylhydrazyl (DPPH) and hydrogen peroxide (H
  <sub>2</sub>O
  <sub>2</sub>). However, both samples exhibited high ferrous chelating activity with no significant difference among each other indicating a good antioxidant potential for both. This is a comparative study between green tea and green tea supplemented with lemon. The study contributes to a better understanding about how the addition of supplements like lemon might influence the antioxidant activity of tea.
 
</p></abstract><kwd-group><kwd>Antioxidant Activity</kwd><kwd> Green Tea</kwd><kwd> Lemon</kwd><kwd> Metal Chelation</kwd><kwd> Phenolic Compounds</kwd><kwd> Radical Scavenging Component</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Tea is one of the most widely used beverages in the world and can be grouped into green, black, white, yellow, oolong and mate. It contains polyphenols, amino acids, proteins, carbohydrates, minerals, caffeine and other volatile compounds. Among the different types of tea, green tea (Camellia sinesis) is the most preferred type as it has many benefits for human health [<xref ref-type="bibr" rid="scirp.67478-ref1">1</xref>] - [<xref ref-type="bibr" rid="scirp.67478-ref3">3</xref>] . Polyphenol, the main component of tea, consists of various types of catechin (C) [<xref ref-type="bibr" rid="scirp.67478-ref3">3</xref>] , in particular, epicatechin (EC), epigallocatechin (EGC), epicatechin-3-gallate (ECG) and epigallocatechin-3-gallate (EGCG), which is the most active catechin in green tea [<xref ref-type="bibr" rid="scirp.67478-ref3">3</xref>] - [<xref ref-type="bibr" rid="scirp.67478-ref5">5</xref>] . Catechin compounds in fresh green tea leaves have been reported to have strong antioxidant activity in comparison with oolong and black tea leaves [<xref ref-type="bibr" rid="scirp.67478-ref4">4</xref>] . This is because green tea leaves are not fermented and catechin oxidation by polyphenol oxidase is prevented, while the oolong tea and the black tea leaves are either fermented to a limited extent or fully fermented, respectively [<xref ref-type="bibr" rid="scirp.67478-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.67478-ref4">4</xref>] .</p><p>Lemon fruits (Citrus lemon) contain several kinds of flavonoids―a group of polyphenolic compound―such as flavone glycoside, flavanone glycoside and polymethoxyflavone [<xref ref-type="bibr" rid="scirp.67478-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.67478-ref7">7</xref>] . Moreover, it is an excellent source of vitamin C, an antioxidant that improves immune system and prevents oxidative stress related diseases [<xref ref-type="bibr" rid="scirp.67478-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.67478-ref9">9</xref>] .</p><p>There are two methods to determine antioxidant capacity: the electron transfer and the hydrogen atom transfer. Folin-Ciocalteu, DPPH, hydrogen peroxide and reducing power are classified as electron transfer methods [<xref ref-type="bibr" rid="scirp.67478-ref10">10</xref>] . In this study, we aimed to compare the antioxidant activity of polyphenols in green tea and green tea supplemented with lemon using different spectrophotometric assays, to estimate the best type of tea that provides a better antioxidant effect. As far as we are aware, there are no studies that have been done on local Saudi green tea brand supplemented with lemon, to evaluate the total phenolic content and the antioxidant activity using five different mechanisms.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Materials</title><p>Classic green tea and green tea supplemented with lemon were obtained from Local Saudi Market, Folin-Cio- calteu’s phenol reagent, anhydrous sodium carbonate, 2,2-Diphenyl-1-picrylhydrazyl (DPPH), ethanol, hydrogen peroxide, phosphate buffer saline (PBS), ascorbic acid, potassium ferricyanide, trichloroacetic acid (TCA), ferric chloride, ferrous chloride, Ferrozin and ethylenediaminetetraacetic acid (EDTA) were purchased from Sigma-Aldrich Chemical Co. (Pool, UK).</p></sec><sec id="s2_2"><title>2.2. Sample Preparation</title><p>The experimental tea samples were prepared as traditionally consumed by Saudi people. A 10 mg/ml of each sample was prepared by adding hot boiling water to tea samples. The mixture was left for 10 minutes at room temperature, after that the antioxidant mechanisms were evaluated. Three different concentrations (2.5, 5 and 10 mg/ml) were prepared, to estimate the ability of different concentrations as reducing agents.</p></sec><sec id="s2_3"><title>2.3. Determination of Polyphenol by Follin Reagent</title><p>The amount of total phenolic content was quantified according to Folin-Ciocalteu method [<xref ref-type="bibr" rid="scirp.67478-ref11">11</xref>] . First, 0.5 ml of each sample was transferred into test tubes and 5 ml of deionized water was added to each sample. Then 0.5 ml of Folin’s reagent was added. The mixtures were left for 5 minutes at room temperature. After that, 1 ml of 2% sodium carbonate solution was added to the mixtures and incubated for 1 hour in dark room. The color formed was measured at 750 nm.</p></sec><sec id="s2_4"><title>2.4. DPPH Radical Scavenging Activity</title><p>DPPH radical scavenging activity was measured by [<xref ref-type="bibr" rid="scirp.67478-ref12">12</xref>] method. First, 250 &#181;l of each sample was added to 99.5% ethanol. Then, 62.5 &#181;l of DPPH was added to the previous mixture and then incubated for 1 hour in dark place. The absorbance was measured at 517 nm. Radical scavenging activity was expressed as inhibition percentage and was calculated using the following formula:</p><disp-formula id="scirp.67478-formula363"><graphic  xlink:href="http://html.scirp.org/file/3-8302732x7.png"  xlink:type="simple"/></disp-formula><p>where (AB) = absorption of blank sample and (AA) = absorption of sample.</p></sec><sec id="s2_5"><title>2.5. Hydrogen Peroxide Radical Scavenging Activity</title><p>Scavenging activity of hydrogen peroxide was measured according to [<xref ref-type="bibr" rid="scirp.67478-ref13">13</xref>] . First, 1 ml of the sample was added to 0.6 ml of 40 mM hydrogen peroxide. The absorbance value of the reaction mixture was recorded at 230 nm. Radical scavenging activity was expressed as inhibition percentage and was calculated by the following equation:</p><disp-formula id="scirp.67478-formula364"><graphic  xlink:href="http://html.scirp.org/file/3-8302732x8.png"  xlink:type="simple"/></disp-formula><p>where (AB) = absorption of blank sample and (AA) = absorption of sample.</p></sec><sec id="s2_6"><title>2.6. Reducing Power</title><p>The reducing power assay was performed as described by [<xref ref-type="bibr" rid="scirp.67478-ref14">14</xref>] . First, 2.5 ml of 0.2 M phosphate buffer pH 6.6 and 2.5 ml of 1% potassium ferric cyanide were added to 1 ml of the sample and mixed well then incubated for 30 minutes at 50˚C. Then, 2.5 ml of 10% Trichromoacetic acid was added to the previous mixture and centrifuged at 4˚C for 10 minutes at 1600 rpm. After that, 2.5 ml of the supernatant was mixed with 2.5 ml deionized water and 0.5 ml of 1% ferric chloride. The absorbance was measured at 700 nm.</p></sec><sec id="s2_7"><title>2.7. Iron Chelating Activity</title><p>The iron chelating activity was determined according to the procedure mentioned by [<xref ref-type="bibr" rid="scirp.67478-ref15">15</xref>] . A sample 500 &#181;l was added to 50 &#181;l of 2 mM ferrous chloride and 1.5 ml distilled, and then the mixture was vortexed for 30. A 100 &#181;l of 5 mM Ferrozin was added to the previous mixture and was incubated for 10 minutes at room temperature. The absorbance was measured at 562 nm. Ferrous ion chelating capacity was calculated using the following formula:</p><disp-formula id="scirp.67478-formula365"><graphic  xlink:href="http://html.scirp.org/file/3-8302732x9.png"  xlink:type="simple"/></disp-formula></sec><sec id="s2_8"><title>2.8. Statistical Analysis</title><p>The data were statistically analyzed using GraphPad Prism 6. Results with p &lt; 0.05 were considered statistically significant. All experiments were performed in triplicate and the values were expressed as mean &#177; SD. The differences between the samples were assessed using unpaired t-test.</p></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Total Polyphenol Content</title><p>Total polyphenol content was estimated by Folin-Ciocalteu’s method. Gallic acid was used as a standard. The content of polyphenols for green tea and green tea supplemented with lemon were 678.7 and 957.3 &#181;g of Gallic acid/10mg of tea, respectively showing that green tea supplemented with lemon has higher polyphenol contents than green tea.</p></sec><sec id="s3_2"><title>3.2. DPPH Radical Scavenging Activity</title><p>Scavenging of DPPH is done by hydrogen/electron Transfer from a given antioxidant to DPPH [<xref ref-type="bibr" rid="scirp.67478-ref16">16</xref>] . The method is based on the reduction of alcoholic solution of the stable free radical DPPH by providing hydrogen atoms from antioxidant molecules to convert DPPH from radical form to non-radical form DPPH-H [<xref ref-type="bibr" rid="scirp.67478-ref17">17</xref>] . The percentages of inhibition caused by green tea and green tea supplement with lemon were 91% and 99% respectively. In this experiment, a significant reduction in the absorbance of DPPH radical was observed. <xref ref-type="fig" rid="fig1">Figure 1</xref> shows that green tea with lemon has more effect in reducing DPPH radicals than green tea at the same concentration (10 mg∙ml<sup>−1</sup>).</p></sec><sec id="s3_3"><title>3.3. Hydrogen Peroxide Radical Scavenging Activity</title><p>The ability of green tea and lemon to scavenge H<sub>2</sub>O<sub>2 </sub>was measured at 320 nm. Since the samples contain phenolic compounds, H<sub>2</sub>O<sub>2</sub> can be converted into H<sub>2</sub>O by donating electrons [<xref ref-type="bibr" rid="scirp.67478-ref17">17</xref>] . At 10 mg∙ml<sup>−1</sup> concentration, green tea with lemon showed a significant H<sub>2</sub>O<sub>2</sub> scavenging activity compared with green tea alone as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>. The percent of inhibition activity of H<sub>2</sub>O<sub>2</sub> of green tea and green tea with lemon were 67% and 93%, respectively.</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Radical scavenging activity of green tea without and with lemon. The value expressed as mean &#177; SD (n = 3) of triplicate measurements. Comparisons of means were ma- de using unpaired t-test (*p &lt; 0.05)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-8302732x10.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> H<sub>2</sub>O<sub>2</sub> scavenging activity of green tea without and with lemon. The value expressed as mean &#177; SD (n = 3) of triplicate measurements. Comparisons of means were made using unpaired t-test (**p &lt; 0.005)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-8302732x11.png"/></fig></sec><sec id="s3_4"><title>3.4. Reducing Power</title><p>In this experiment, the antioxidant compounds convert the oxidation form of iron (Fe<sup>+3</sup>) in ferric chloride to ferrous (Fe<sup>+2</sup>). The reducing powers of green tea and green tea supplemented with lemon were presented in <xref ref-type="fig" rid="fig3">Figure 3</xref>, and it is clearly shown that, with increased concentrations, the reducing power will also be increased. At all the tested concentrations, the reducing activity of green tea supplemented with lemon was significantly higher than that of green tea. The p values were 0.03, 0.0003 and 0.03 for 2.5, 5 and 10 mg∙ml<sup>−1</sup> respectively.</p><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Reducing power of different concentrations of green tea without and with lemon. The value expressed as mean &#177; SD (n = 3) of triplicate measurements. Comparisons of means were made using unpaired t-test (*p &lt; 0.05 and ***p &lt; 0.005)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-8302732x12.png"/></fig></sec><sec id="s3_5"><title>3.5. Iron Chelating Activity</title><p>One of the mechanisms of antioxidant action is the chelation of transition metals that prohibiting stimulation of hydrogen peroxide dissociation [<xref ref-type="bibr" rid="scirp.67478-ref18">18</xref>] . This method is based on the inhibition of ferrous-ferrozin complex formation by the antioxidant compound present in the green tea and lemon. By comparing the two results, it can be seen that there is no significant difference in iron chelating activity at the same concentration (10 mg∙ml<sup>−1</sup>) in both samples (<xref ref-type="fig" rid="fig4">Figure 4</xref>).</p><p>The standard metal chelator agent used in this experiment was EDTA. Ferrous chelating activity of EDTA was 97% while for green tea and green tea with lemon, chelating activity were lower 83% and 84%, respectively (<xref ref-type="fig" rid="fig5">Figure 5</xref>).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>Green, black and oolong tea are three different types of tea that different from each other by fermentation processing [<xref ref-type="bibr" rid="scirp.67478-ref4">4</xref>] . Black tea and oolong tea are fully fermented or semi fermented, respectively during fermentation process [<xref ref-type="bibr" rid="scirp.67478-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.67478-ref19">19</xref>] . However, green tea is not fermented. It is processed by preventing oxidation of catechin [<xref ref-type="bibr" rid="scirp.67478-ref19">19</xref>] . As a result, the flavanol group of polyphenols called catechins, the major bioactive compounds of green tea, are found in higher concentrations compared to black and oolong tea [<xref ref-type="bibr" rid="scirp.67478-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.67478-ref20">20</xref>] - [<xref ref-type="bibr" rid="scirp.67478-ref22">22</xref>] . Therefore, the order of antioxidant activity is: green tea &gt; oolong tea &gt; black tea [<xref ref-type="bibr" rid="scirp.67478-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.67478-ref21">21</xref>] . Based on that, green tea has powerful antioxidantactivity which is responsible for important biological activity and have many health advantages [<xref ref-type="bibr" rid="scirp.67478-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.67478-ref23">23</xref>] . In general, many studies, reported the efficiency of green tea to scavenge free radicals. One study [<xref ref-type="bibr" rid="scirp.67478-ref24">24</xref>] reported that green tea has high radical scavenging ability by using DPPH free radical scavenging method. Previous studies showed that many bioactive compounds have been found in lemon such as phenolic acid, ascorbic acid, citric acid, limonoids, carotenoids, minerals and flavanone (hesperidin and naringin) [<xref ref-type="bibr" rid="scirp.67478-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.67478-ref26">26</xref>] . The benefits of polyphenols came from their high antioxidant capacity which prevents the development of many diseases associated with oxidative stress [<xref ref-type="bibr" rid="scirp.67478-ref27">27</xref>] . In our results, green tea with lemon showed more polyphenol contents than green tea and this might be due to the presence of additional phenolic compounds in lemon that increase the amount of antioxidantsin our body.</p><p>Flavonoids have a direct role in scavenging free radicals produced mostly as reactive oxygen species (ROS). [<xref ref-type="bibr" rid="scirp.67478-ref28">28</xref>] found that naringin, which is a part of lemon flavanone, can stimulate the immune system defenses to avoid oxidative damage caused by oxidation, by increasing the activity of the body’s antioxidant enzymes including catalase, glutathione peroxidase and superoxide dismutase. These enzymes catalyze the dismutation of superoxide radical, which is the most common free radical in the body, into hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>). As a result, the addition of lemon might increase the ability of samples to reduce the amount of H<sub>2</sub>O<sub>2</sub> [<xref ref-type="bibr" rid="scirp.67478-ref20">20</xref>] . A study performed by [<xref ref-type="bibr" rid="scirp.67478-ref29">29</xref>] showed that there is a relationship between flavonoid structure and their radical scavenging. The powerful</p><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Ferrous chelating activity of green tea without and with lemon. The value expressed as mean &#177; SD (n = 3) of triplicate measurements. Compression of means was made using unpaired t-test</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-8302732x13.png"/></fig><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> Ferrous chelating activity of green tea without and with lemon compared with EDTA at 0.1 mg∙ml<sup>−1</sup>. The value expressed as mean &#177; SD (n = 3) of triplicate measurements. Comparisons of means were made using a one-way ANOVA followed by Bonferroni’s test (***p &lt; 0.0005)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-8302732x14.png"/></fig><p>radical scavenging of lemon flavonoids is due to the presence of the ortho-dihydroxy structure in either ring A or ring B, the hydroxyl moiety on position 3 in combination with the oxo group at position 4 and the presence of a C2-C3 double bond in ring C as shown in <xref ref-type="fig" rid="fig6">Figure 6</xref>.</p><p>For that, this flavonoid has the ability to scavenge DPPH free radicals by rapidly donating hydrogen atom from hydroxyl group to radicals and it is visually noticeable by the change in the color from purple to yellow as shown in <xref ref-type="fig" rid="fig7">Figure 7</xref>.</p><p>Furthermore, several studies reported that lemon has other important natural chemical components including limonoids, carotenoids, phenolic acid and pectin that also have different levels of free radical scavenging. These components can neutralize free radicals and therefore prevent some of the damages caused by free radicals</p><fig id="fig6"  position="float"><label><xref ref-type="fig" rid="fig6">Figure 6</xref></label><caption><title> Structural features of flavonoid with a high radical scavenging activity [<xref ref-type="bibr" rid="scirp.67478-ref29">29</xref>] </title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-8302732x15.png"/></fig><fig id="fig7"  position="float"><label><xref ref-type="fig" rid="fig7">Figure 7</xref></label><caption><title> Scavenging of DPPH free radical by a flavonoid [<xref ref-type="bibr" rid="scirp.67478-ref29">29</xref>] </title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-8302732x16.png"/></fig><p>[<xref ref-type="bibr" rid="scirp.67478-ref30">30</xref>] - [<xref ref-type="bibr" rid="scirp.67478-ref32">32</xref>] . From all these studies, we noticed that there is a relationship between the scavenging activity and the flavonoid content of lemon [<xref ref-type="bibr" rid="scirp.67478-ref28">28</xref>] . This explains to some degree why green tea supplemented with lemon has more ability to scavenge free radical than green tea alone. Reducing power of bioactive compounds may serve as a significant reflection of its potential antioxidant activity [<xref ref-type="bibr" rid="scirp.67478-ref8">8</xref>] . Compounds with reducing power can act as electron givers and can react with free radicals to become steady and prevent radical chain reaction [<xref ref-type="bibr" rid="scirp.67478-ref33">33</xref>] . Therefore, the reducing activity of green tea supplemented with lemon was significantly higher than that of green tea.</p><p>Our results in iron chelating activity assay showed that the ability of lemon to chelate iron was weak. In agreement with our results, the study by [<xref ref-type="bibr" rid="scirp.67478-ref34">34</xref>] , indicated that naringin did not chelate iron completely because it was incapable to overrun all active sites of iron. Moreover, a study by [<xref ref-type="bibr" rid="scirp.67478-ref35">35</xref>] indicated that citric acid, which is the main component of lemon, was not a good chelating agent for ferrous ion and its chelating ability was low. The high chelating iron activity in our results derived from green tea might be due to the specific functional group in its catechin flavanols structure [<xref ref-type="bibr" rid="scirp.67478-ref35">35</xref>] .</p></sec><sec id="s5"><title>5. Conclusion</title><p>In conclusion, our results indicated that green tea supplemented with lemon has a better antioxidant activity compared to green tea without lemon supplementation, due to the presence of additional phenolic compound in lemon. Further researches are needed using different tea brands with different supplements, in order to estimate the best type of tea supplementation that provides the optimal antioxidants for potential health benefits.</p></sec><sec id="s6"><title>Acknowledgements</title><p>The research team would like to thank Science Research &amp; Innovation Unit at the Faculty of Science, King Abdulaziz University for supporting this work</p></sec><sec id="s7"><title>Cite this paper</title><p>Ayat B. Al-Ghafari,Ayat M. Shorbaji,Lamya A. AL-Sarori,Eman O. Baduwailan,Aisha A. Basaar,Huda A. Al Doghaither,Hala F. Al-Marzouki,Ulfat M. Omar, (2016) Phenolic Contents and Antioxidant Activities of Green Tea with and without Lemon. Natural Science,08,247-255. doi: 10.4236/ns.2016.86029</p></sec><sec id="s8"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.67478-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Jiang, H., Engelhardt, U.H., Thr&amp;auml;ne, C., Maiwald, B. and Stark, J. (2015) Determination of Flavonol Glycosides in Green Tea, Oolong Tea and Black Tea by UHPLC Compared to HPLC. Food Chemistry, 183, 30-35. 
http://dx.doi.org/10.1016/j.foodchem.2015.03.024</mixed-citation></ref><ref id="scirp.67478-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Majchrzak, D., Mitter, S. and Elmadfa, I. (2004) The Effect of Ascorbic Acid on Total Antioxidant Activity of Black and Green Teas. Food Chemistry, 88, 447-451. http://dx.doi.org/10.1016/j.foodchem.2004.01.058</mixed-citation></ref><ref id="scirp.67478-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Quan, P.T., Hang, T.V., Ha, N.H. and Giang, B.L. (2007) Total Polyphenols, Total Catechins Content and DPPH Free Radical Scavenger Activity of Several Types of Vietnam Commercial Green Tea. Science Technology Development, 10, 5-11.</mixed-citation></ref><ref id="scirp.67478-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Anesini, C., Ferraro, G.E. and Filip, R. (2008) Total Polyphenol Content and Antioxidant Capacity of Commercially Available Tea (Camellia sinensis) in Argentina. Journal of Agricultural and Food Chemistry, 56, 9225-9229. 
http://dx.doi.org/10.1021/jf8022782</mixed-citation></ref><ref id="scirp.67478-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Taheri, M., Giahi, M., Shahmohamadi, R., Ghafoori, H., Aghamaali, M.R. and Sariri, R. (2011) Screening Antioxidant Activity of Extracts from Different Tea Samples. Pharmacologyonline, 3, 442-448.</mixed-citation></ref><ref id="scirp.67478-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Fukuchi, Y., Hiramitsu, M., Okada, M., Hayashi, S., Nabeno, Y., Osawa, T. and Naito, M. (2008) Lemon Polyphenols Suppress Diet-Induced Obesity by Up-Regulation of mRNA Levels of the Enzymes Involved in β-Oxidation in Mouse White Adipose Tissue. Journal of Clinical Biochemistry and Nutrition, 43, 201-209.  
http://dx.doi.org/10.3164/jcbn.2008066</mixed-citation></ref><ref id="scirp.67478-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Shaghaghi, M., Manzoori, J.L. and Jouyban, A. (2008) Determination of Total Phenols in Tea Infusions, Tomato and Apple Juice by Terbium Sensitized Fluorescence Method as an Alternative Approach to the Folin-Ciocalteu Spectrophotometric Method. Food Chemistry, 108, 695-701. http://dx.doi.org/10.1016/j.foodchem.2007.11.008</mixed-citation></ref><ref id="scirp.67478-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Kanatt, S.R., Chawla, S.P. and Sharma, A. (2014) Antioxidant and Radio-Protective Activities of Lemon Grass and Star Anise Extracts. Food Bioscience, 6, 24-30. http://dx.doi.org/10.1016/j.fbio.2014.03.002</mixed-citation></ref><ref id="scirp.67478-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Kim, J., Jayaprakasha, G.K. and Patil, B.S. (2013) Limonoids and Their Anti-Proliferative and Anti-Aromatase Properties in Human Breast Cancer Cells. Food &amp; Function, 4, 258-265. http://dx.doi.org/10.1039/C2FO30209H</mixed-citation></ref><ref id="scirp.67478-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Gorjanovic, S., Komes, D., Pastor, F., Belsak-Cvitanovic, A., Pezo, L., Heimovic, I. and Suznjevic, D. (2012) Antioxidant Capacity of Teas and Herbal Infusions: Polarographic Assessment. Journal of Agricultural and Food Chemistry, 60, 9573-9580. http://dx.doi.org/10.1021/jf302375t</mixed-citation></ref><ref id="scirp.67478-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Kim, D., Chun, O.K., Kim, Y.J., Moon, H. and Lee, C.Y. (2003) Quantification of Polyphenolics and Their Antioxidant Capacity in Fresh Plums. Journal of Agricultural and Food Chemistry, 51, 6509-6515. 
http://dx.doi.org/10.1021/jf0343074</mixed-citation></ref><ref id="scirp.67478-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Bersuder, P., Hole, M. and Smith, G. (1998) Antioxidants from a Heated Histidine-Glucose Model System. I: Investigation of the Antioxidant Role of Histidine and Isolation of Antioxidants by High-Performance Liquid Chromatography. Journal of the American Oil Chemists’ Society, 75, 181-187. http://dx.doi.org/10.1007/s11746-998-0030-y</mixed-citation></ref><ref id="scirp.67478-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Gülin, I., Alici, H.A. and Cesur, M. (2005) Determination of in Vitro Antioxidant and Radical Scavenging Activities of Propofol. Chemical &amp; Pharmaceutical Bulletin, 53, 281-285. http://dx.doi.org/10.1248/cpb.53.281</mixed-citation></ref><ref id="scirp.67478-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Yildirim, A., Mavi, A., Oktay, M., Kara, A.A., Algur, &amp;Ouml;.F. and Bilaloglu, V. (2000) Comparison of Antioxidant and Antimicrobial Activities of Tilia (Tiliaargentea desf ex DC), Sage (Salvia triloba L.), and Black Tea (Camellia sinensis) Extracts. Journal of Agricultural and Food Chemistry, 48, 5030-5034. http://dx.doi.org/10.1248/cpb.53.281</mixed-citation></ref><ref id="scirp.67478-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Dinis, T.C.P., Maderia, V.M.C. and Almeida, L.M. (1994) Action of Phenolic Derivatives (Acetaminophen, Salicylate, and 5-Aminosalicylate) as Inhibitors of Membrane Lipid Peroxidation and as Peroxyl Radical Scavengers. Archives of Biochemistry and Biophysics, 315, 161-169. http://dx.doi.org/10.1006/abbi.1994.1485</mixed-citation></ref><ref id="scirp.67478-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Anissi, J., El Hassouni, M., Ouardaoui, A. and Sendide, K. (2014) A Comparative Study of the Antioxidant Scavenging Activity of Green Tea, Black Tea and Coffee Extracts: A Kinetic Approach. Food Chemistry, 150, 438-447. 
http://dx.doi.org/10.1016/j.foodchem.2013.11.009</mixed-citation></ref><ref id="scirp.67478-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Shon, M.Y., Kim, T.H. and Sung, N.J. (2003) Antioxidants and Free Radical Scavenging Activity of Phellinus baumii (Phellinus of Hymenochaetaceae) Extracts. Food Chemistry, 82, 593-597.  
http://dx.doi.org/10.1016/S0308-8146(03)00015-3</mixed-citation></ref><ref id="scirp.67478-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Dastmalchi, K., Dorman, H.J.D., Oinonen, P.P., Darwis, Y., Laakso, I. and Hiltunen, R. (2008) Chemical Composition and in Vitro Antioxidative Activity of a Lemon Balm (Melissa officinalis L.) Extract. LWT-Food Science and Technology, 41, 391-400. http://dx.doi.org/10.1016/j.lwt.2007.03.007</mixed-citation></ref><ref id="scirp.67478-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Tran, J. (2013) Green Tea: A Potential Alternative Anti-Infectious Agent Catechins and Viral Infections. Advances in Anthropology, 3, 198-202. http://dx.doi.org/10.4236/aa.2013.34028</mixed-citation></ref><ref id="scirp.67478-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Ayabe, S. and Aoshima, H. (2007) Aqueous Extract of Citrus Peel Reduces Production of Hydrogen Peroxide in Catechin-Enriched Green Tea. Food Chemistry, 104, 1594-1598. http://dx.doi.org/10.1016/j.foodchem.2007.03.009</mixed-citation></ref><ref id="scirp.67478-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Carloni, P., Tiano, L., Padella, L., Bacchetti, T., Customu, C., Kay, A. and Damiani, E. (2013) Antioxidant Activity of White, Green and Black Tea Obtained from the Same Tea Cultivar. Food Research International, 53, 900-908. 
http://dx.doi.org/10.1016/j.foodres.2012.07.057</mixed-citation></ref><ref id="scirp.67478-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Sutherland, B.A., Rahman, R.M. and Appleton, I. (2006) Mechanisms of Action of Green Tea Catechins, with a Focus on Ischemia-Induced Neurodegeneration. Journal of Nutritional Biochemistry, 17, 291-306. 
http://dx.doi.org/10.1016/j.jnutbio.2005.10.005</mixed-citation></ref><ref id="scirp.67478-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Takumi-Kobayashi, A., Ogura, R., Morita, O., Nishiyama, N. and Kasamatsu, T. (2008) Involvement of Hydrogen Peroxide in Chromosomal Aberrations Induced by Green Tea Catechins in Vitro and Implications for Risk Assessment. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 657, 13-18. 
http://dx.doi.org/10.1016/j.mrgentox.2008.08.016</mixed-citation></ref><ref id="scirp.67478-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Gramza, A., Pawlak-Lemańska, K., Korczak, J., Wasowicz, E. and Rudzinska, M. (2005) Tea Extracts as Free Radical Scavengers. Polish Journal of Environmental Studies, 14, 861-867.</mixed-citation></ref><ref id="scirp.67478-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Del Rio, J.A., Fuster, M.D., Gomez, P., Porras, I., Garcia-Lidon, A. and Ortuno, A. (2004) Citrus Limon: A Source of Flavonoids of Pharmaceutical Interest. Food Chemistry, 84, 457-461.  
http://dx.doi.org/10.1016/S0308-8146(03)00272-3</mixed-citation></ref><ref id="scirp.67478-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Sun, Y., Shen, Y., Liu, D. and Ye, X. (2015) Effects of Drying Methods on Phytochemical Compounds and Antioxidant Activity of Physiologically Dropped Un-Matured Citrus Fruits. LWT—Food Science and Technology, 60, 1269-1275. http://dx.doi.org/10.1016/j.lwt.2014.09.001</mixed-citation></ref><ref id="scirp.67478-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Cyboran, S., Strugala, P., Wloch, A., Oszmianski, J. and Kleszczynska, H. (2015) Concentrated Green Tea Supplement: Biological Activity and Molecular Mechanisms. Life Sciences, 126, 1-9. http://dx.doi.org/10.1016/j.lfs.2014.12.025</mixed-citation></ref><ref id="scirp.67478-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Zou, Z., Xi, W., Hu, Y., Nie, C. and Zhou, Z. (2015) Antioxidant Activity of Citrus Fruits. Food Chemistry, 196, 885-896. http://dx.doi.org/10.1016/j.foodchem.2015.09.072</mixed-citation></ref><ref id="scirp.67478-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Seyoum, A., Asres, K. and El-Fiky, F.K. (2006) Structure-Radical Scavenging Activity Relationships of Flavonoids. Phytochemistry, 67, 2058-2070. http://dx.doi.org/10.1016/j.phytochem.2006.07.002</mixed-citation></ref><ref id="scirp.67478-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Dai, J. and Mumper, R.J. (2010) Plant Phenolics: Extraction, Analysis and Their Antioxidant and Anticancer Properties. Molecules, 15, 7313-7352. http://dx.doi.org/10.3390/molecules15107313</mixed-citation></ref><ref id="scirp.67478-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Di Mascio, P., Kaiser, S. and Sies, H. (1989) Lycopene as the Most Efficient Biological Carotenoid Singlet Oxygen Quencher. Archives of Biochemistry and Biophysics, 274, 532-538. http://dx.doi.org/10.1016/0003-9861(89)90467-0</mixed-citation></ref><ref id="scirp.67478-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Koriem, K.M.M., Arbid, M.S. and Emam, K.R. (2014) Therapeutic Effect of Pectin on Octylphenol Induced Kidney Dysfunction, Oxidative Stress and Apoptosis in Rats. Environmental Toxicology and Pharmacology, 38, 14-23. 
http://dx.doi.org/10.1016/j.etap.2014.04.029</mixed-citation></ref><ref id="scirp.67478-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Kamdem, J.P., Adeniran, A., Boligon, A.A., Klimaczewski, C.V., Elekofehinti, O.O., Hassan, W., Ibrahim, M., Waczuk, E.P., Meinerz, D.F. and Athayde, M.L. (2013) Antioxidant Activity, Genotoxicity and Cytotoxicity Evaluation of Lemon Balm (Melissa officinalis L.) Ethanolic Extract: Its Potential Role in Neuroprotection. Industrial Crops and Products, 51, 26-34. http://dx.doi.org/10.1016/j.indcrop.2013.08.056</mixed-citation></ref><ref id="scirp.67478-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Jagetia, G.C. and Reddy, T.K. (2011) Alleviation of Iron Induced Oxidative Stress by the Grape Fruit Flavano nenaringin in Vitro. Chemico-Biological Interactions, 190, 121-128. http://dx.doi.org/10.1016/j.cbi.2011.02.009</mixed-citation></ref><ref id="scirp.67478-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Lin, S.D., Liu, E.H. and Mau, J.L. (2008) Effect of Different Brewing Methods on Antioxidant Properties of Steaming Green Tea. LWT—Food Science and Technology, 41, 1616-1623. http://dx.doi.org/10.1016/j.lwt.2007.10.009</mixed-citation></ref></ref-list></back></article>