<?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">FNS</journal-id><journal-title-group><journal-title>Food and Nutrition Sciences</journal-title></journal-title-group><issn pub-type="epub">2157-944X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/fns.2015.611103</article-id><article-id pub-id-type="publisher-id">FNS-58815</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></subj-group></article-categories><title-group><article-title>
 
 
  Phytochemical Composition of &lt;i&gt;Tridax procumbens&lt;/i&gt; Linn Leaves: Potential as a Functional Food
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>atherine</surname><given-names>C. Ikewuchi</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>Jude</surname><given-names>C. Ikewuchi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mercy</surname><given-names>O. Ifeanacho</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 Biological and Chemical Sciences, College of Natural and Applied Sciences, University of Port Harcourt, Port Harcourt, Nigeria</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>ecoli240733@yahoo.com(JCI)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>11</day><month>08</month><year>2015</year></pub-date><volume>06</volume><issue>11</issue><fpage>992</fpage><lpage>1004</lpage><history><date date-type="received"><day>21</day>	<month>February</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>12</month>	<year>August</year>	</date><date date-type="accepted"><day>17</day>	<month>August</month>	<year>2015</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>
 
 
  The leaves of 
  Tridax procumbens were screened for the presence of bioactive molecules. They had high flavonoids, alkaloids, hydroxycinnamates, tannins and phytosterols, moderate benzoic acid derivatives and lignans, and low carotenoids contents. Thirty nine known alkaloids (mainly akuammidine, 68.756%), twenty three known flavonoids (mainly 17.593% kaempferol and 12.538% (-)-epicatechin), five known carotenoids (mainly lutein, 62.608%), four known benzoic acid derivatives (mainly ferulic acid, 46.091%), two phytosterols (mainly stigmasterol, 80.853%) and six known lignans (mainly galgravin, 77.326%) were detected. Also detected were caffeic acid and tannic acid. The medicinal properties of the flavonoids, phytosterols, alkaloids, tannins, hydroxicinnamates, carotenoids, benzoic acid derivatives and lignans that were present in the leaves were discussed herein and proposed to be explored for their potential medicinal values. The great number of potentially active nutrients and their multifunctional properties make 
  Tridax procumbens a perfect candidate for the production of health-promoting food and food supplements.
 
</p></abstract><kwd-group><kwd>Flavonoids</kwd><kwd> Hydroxycinnmates</kwd><kwd> Lignans</kwd><kwd> Nutraceuticals</kwd><kwd> Phytosterol</kwd><kwd> Tannins</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Natural products and health foods have recently received a lot of attention both by health professionals and the common population for improving overall well-being, as well as in the prevention of diseases. Epidemiological evidence has associated the frequent consumption of vegetables with decreased disease risk [<xref ref-type="bibr" rid="scirp.58815-ref1">1</xref>] -[<xref ref-type="bibr" rid="scirp.58815-ref3">3</xref>] . In line with this, different types of vegetables have been re-evaluated for recognition for possible candidature as functional foods, and as valuable sources of nutraceuticals. Functional foods refer to those whole, fortified, enriched or enhanced foods that provide health benefits beyond the provision of essential nutrients (e.g., vitamins and minerals), when they are consumed at efficacious levels as part of a varied diet on a regular basis [<xref ref-type="bibr" rid="scirp.58815-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref4">4</xref>] . The term nutraceutical, which combines the word nutrition and pharmaceutical, is defined as a food that contains a medical health benefit beyond that of basic nutrition [<xref ref-type="bibr" rid="scirp.58815-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref4">4</xref>] .</p><p>One such vegetables with a potential for use as functional food is Tridax procumbens Linn (family Asteraceae), which is commonly called coat buttons. Its leaves are cooked and eaten as vegetable, and are also used as fodders [<xref ref-type="bibr" rid="scirp.58815-ref5">5</xref>] -[<xref ref-type="bibr" rid="scirp.58815-ref8">8</xref>] . Consequent upon this, Ikewuchi and colleagues investigated the nutritional potential of the leaves [<xref ref-type="bibr" rid="scirp.58815-ref9">9</xref>] -[<xref ref-type="bibr" rid="scirp.58815-ref11">11</xref>] . The leaves are also commonly used for medicinal purposes, because of their myriad of pharmacological properties. These include analgesic [<xref ref-type="bibr" rid="scirp.58815-ref12">12</xref>] , anti-anemic [<xref ref-type="bibr" rid="scirp.58815-ref13">13</xref>] , anti-arthritic [<xref ref-type="bibr" rid="scirp.58815-ref14">14</xref>] , anti-diabetic [<xref ref-type="bibr" rid="scirp.58815-ref15">15</xref>] -[<xref ref-type="bibr" rid="scirp.58815-ref17">17</xref>] , antihypertensive [<xref ref-type="bibr" rid="scirp.58815-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref19">19</xref>] , anti-inflammatory, antioxidant [<xref ref-type="bibr" rid="scirp.58815-ref20">20</xref>] , antimicrobial [<xref ref-type="bibr" rid="scirp.58815-ref21">21</xref>] , antipyretic [<xref ref-type="bibr" rid="scirp.58815-ref6">6</xref>] , hepatoprotective [<xref ref-type="bibr" rid="scirp.58815-ref22">22</xref>] , hypocholesterolemic and weight reducing [<xref ref-type="bibr" rid="scirp.58815-ref23">23</xref>] properties. The present study reports the phytochemical composition of the leaves of Tridax procumbens, and in addition discusses the bioactivities of the detected compounds, with a view to highlighting the possibilities of the use of the leaves as a functional food, or as a source of nutraceuticals.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Collection of Plant Samples</title><p>Samples of fresh Tridax procumbens plants were collected from within the Choba and Abuja Campuses of University of Port Harcourt, Nigeria. Their identity was confirmed by Dr. M.C. Dike of Taxonomy Unit, Department of Forestry and Environmental Management, Michael Okpara University of Agriculture, Umudike, Abia State, Nigeria; and Mr. John Ibe, the Herbarium Manager of the Forestry Department, National Root Crops Research Institute, Umuahia, Nigeria. They were cleaned and their leaves were removed, oven dried at 55˚C and grounded into powder, which was stored in an air tight container, for subsequent use.</p></sec><sec id="s2_2"><title>2.2. Determination of the Phytochemical Content of the Leaves</title><sec id="s2_2_1"><title>2.2.1. General Experimental Procedures</title><p>Analyses were carried out at Multi Environmental Management Consultants Limited, Igbe Road, Ikorodu, Lagos, Nigeria, with a Hewlett Packard HP 6890, GC apparatus, fitted with flame ionization detector, powered with HP Chemstation Rev. A 09.01 (1206) software, to identify and quantify compounds. Standard solutions were prepared in methanol for alkaloids, flavonoids, tannins and simple benzoic acid derivatives; acetone for carotenoids and lignans, methylene chloride for phytosterols; and ethanol for hydroxycinnamates. The linearity of the dependence of response on concentration was verified by regression analysis. Identification was based on comparison of retention times and spectral data with standards. Quantification was performed by establishing calibration curves for each compound determined, using the standards.</p></sec><sec id="s2_2_2"><title>2.2.2. Determination of Alkaloid Composition</title><p>Extraction was carried out according to the method of Tram et al. [<xref ref-type="bibr" rid="scirp.58815-ref24">24</xref>] . The extract was subjected to gas chromatography on a capillary DB-5MS column (30 m &#215; 0.25 mm &#215; 0.25 μm film thickness). The inlet and detection temperatures were 250˚C and 320˚C. Split injection (split ratio of 20:1) was adopted. The carrier gas was nitrogen. The hydrogen and compressed air pressures were 1.97 and 2.67 kg/cm<sup>2</sup>. The oven was programmed initially at 60˚C for 5 min, ramped at 10˚C/min for 20 min, before ramping again at 15˚C/min for 4 min.</p></sec><sec id="s2_2_3"><title>2.2.3. Determination of Carotenoid Composition</title><p>The extraction was carried out by a modification of the method of Rodriguez-Amaya and Kimura [<xref ref-type="bibr" rid="scirp.58815-ref25">25</xref>] . The carotenoids were successively extracted with acetone and a (1:1) mixture of diethyl ether and petroleum ether, were concentrated and re-dissolved in acetone before saponifying and re-extracting with a (1:1) mixture of diethyl ether and petroleum ether. The resultant extracts were dried and re-dissolved in petroleum ether and subjected to gas chromatography on a capillary ZP-5 column (30 m &#215; 0.32 mm &#215; 0.25 μm film thickness). The oven was programmed initially at 45˚C, held for 6 min, and ramped at 38˚C/min to 250˚C. Initial column head pressure at a constant flow mode was 0.243 kg/cm<sup>2</sup>.</p></sec><sec id="s2_2_4"><title>2.2.4. Determination of Flavonoid Composition</title><p>The extraction was carried out according to the method of Millogo-Kone et al. [<xref ref-type="bibr" rid="scirp.58815-ref26">26</xref>] . The extract was subjected to gas chromatography on a capillary HP INNOWax column (30 m &#215; 0.25 mm &#215; 0.25 μm film thickness). The inlet and detection temperatures were 250˚C and 320˚C. Split injection (split ratio of 20:1) was adopted. The carrier gas was nitrogen. The hydrogen and compressed air pressures were 1.55 and 2.46 kg/cm<sup>2</sup>. The oven was programmed initially at 50˚C, ramped at 8˚C/min for 20 min, maintained for 4 min, ramped again at 12˚C/min for 4 min, and maintained for 4 min.</p></sec><sec id="s2_2_5"><title>2.2.5. Determination of Hydroxycinnamates Composition</title><p>The extraction was carried according to method of Ortan et al. [<xref ref-type="bibr" rid="scirp.58815-ref27">27</xref>] . The extract was subjected to gas chromatography on HP-5 column (30 m &#215; 0.32 mm &#215; 0.25 μm film thickness). It was introduced via an all-glass injector working in the split mode, with nitrogen as the carrier gas, at a flow rate of 1 mL/min. The injection and detector temperatures were 260˚C and 300˚C. The oven was programmed at the start of the run from 170˚C to 250˚C at 5˚C/min.</p></sec><sec id="s2_2_6"><title>2.2.6. Determination of the Lignans Composition</title><p>The extraction was carried out according to the method of Chapman et al. [<xref ref-type="bibr" rid="scirp.58815-ref28">28</xref>] . The extract was subjected to gas chromatography on a ZP-5 column (30 m &#215; 0.32 mm &#215; 0.25 μm film thickness). One microliter of sample was injected. The initial oven temperature was 40˚C, while the injector and transfer line temperatures were 250˚C and 280˚C. A solvent delay of 2.00 min was followed by ramping at 10˚C/min to a final temperature of 230˚C and held for 1.00 min.</p></sec><sec id="s2_2_7"><title>2.2.7. Determination of Benzoic Acid Derivatives Composition</title><p>The extraction was carried out according to the method of Ndoumou et al. [<xref ref-type="bibr" rid="scirp.58815-ref29">29</xref>] . The extract was subjected to gas chromatography on a capillary HP 1 column (30 m &#215; 0.25 mm &#215; 0.25 μm film thickness). The inlet and detection temperatures were 250˚C and 320˚C. Split injection (split ratio of 20:1) was adopted. The carrier gas was nitrogen, at a pressure of 2.11 kg/cm<sup>2</sup>. The hydrogen and compressed air pressures were 1.97 and 2.25 kg/cm<sup>2</sup>. The oven was programmed initially at 60˚C for 5 min, ramped at 15˚C/min for 15 min, maintained for 1 min, and then ramped again at 10˚C/min for 4 min.</p></sec><sec id="s2_2_8"><title>2.2.8. Determination of Phytosterols Composition</title><p>Extraction of oil was carried out according to AOAC method 999.02 [<xref ref-type="bibr" rid="scirp.58815-ref30">30</xref>] , while the analysis of sterols was carried out according to AOAC method 994.10 [<xref ref-type="bibr" rid="scirp.58815-ref30">30</xref>] . The resultant sterol derivatives were subjected to gas chromatography on a capillary HP INNOWax column (30 m &#215; 0.25 mm &#215; 0.25 μm film thickness). The inlet and detection temperatures were 250˚C and 320˚C. Split injection (split ratio of 20:1) was adopted. The carrier gas was nitrogen. The hydrogen and compressed air pressures were 1.55 and 2.46 kg/cm<sup>2</sup>. The oven was programmed initially at 60˚C, ramped at 10˚C/min for 20 min, maintained for 4 min, ramped again 15˚C/min for 4 min, and maintained for 10 min.</p></sec><sec id="s2_2_9"><title>2.2.9. Determination of Tannins Composition</title><p>Extraction was carried out according to the method of Luthar [<xref ref-type="bibr" rid="scirp.58815-ref31">31</xref>] . The extract was subjected to gas chromatography on HP 5 column (30 m &#215; 0.25 mm &#215; 0.25 μm film thickness). The inlet and detection temperatures were 250˚C and 320˚C. Split injection (split ratio of 20:1) was adopted. The carrier gas was nitrogen. The hydrogen and compressed air pressures were 1.97 and 2.81 kg/cm<sup>2</sup>. The oven was programmed initially at 120˚C, before ramping at 10˚C/min for 20 min.</p></sec></sec><sec id="s2_3"><title>2.3. Derivation of Composition per Wet Weight from the Composition per Dry Weight</title><p>The compositions per wet weight of the determined parameters were derived from the compositions per dry weight and vice versa, using the following formula, adapted from Health Canada Official Methods [<xref ref-type="bibr" rid="scirp.58815-ref32">32</xref>] .</p><disp-formula id="scirp.58815-formula1073"><graphic  xlink:href="http://html.scirp.org/file/6-2701538x6.png"  xlink:type="simple"/></disp-formula></sec><sec id="s2_4"><title>2.4. Data Analysis</title><p>Comparisons were based on simple percentages.</p></sec></sec><sec id="s3"><title>3. Results</title><p>The leaves had high flavonoids content (6477.706 g/kg) (<xref ref-type="table" rid="table1">Table 1</xref>). Twenty three known flavonoids were detected in the leaves. This consisted of 17.593% kaempferol, 12.538% (−)-epicatechin, 8.202% biochanin, 7.968% (+)-catechin, 7.875% apigenin, 6.254% naringenin, 6.124% daidzein, 4.418% quercetin, 4.376% butein, 3.895% robinetin, 3.047% baicalein, 2.986% nobiletin, 2.806% (−)-epigallocatechin, 2.444% genistein, 2.338% (+)- gallocatechin, 1.818% ellagic acid, 1.707% luteolin, 1.406% myricetin, 0.735% baicalin, 0.498% isorhamnetin, 0.404% (−)-epigallocatechin-3-gallate, 0.359% silymarin and 0.207% (−)-epicatechin-3-gallate.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Flavonoids composition of Tridax procumbens leaves</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Compounds</th><th align="center" valign="middle"  rowspan="2"  >Retention time (min)</th><th align="center" valign="middle"  colspan="2"  >Composition (mg/kg)</th></tr></thead><tr><td align="center" valign="middle" >/dry weight</td><td align="center" valign="middle" >/wet weight</td></tr><tr><td align="center" valign="middle" >(+)-Catechin</td><td align="center" valign="middle" >13.749</td><td align="center" valign="middle" >5187.515</td><td align="center" valign="middle" >516.158</td></tr><tr><td align="center" valign="middle" >(+)-Gallocatechin</td><td align="center" valign="middle" >15.043</td><td align="center" valign="middle" >1522.281</td><td align="center" valign="middle" >151.467</td></tr><tr><td align="center" valign="middle" >Genistein</td><td align="center" valign="middle" >15.626</td><td align="center" valign="middle" >1590.816</td><td align="center" valign="middle" >158.286</td></tr><tr><td align="center" valign="middle" >Daidzein</td><td align="center" valign="middle" >16.047</td><td align="center" valign="middle" >3986.855</td><td align="center" valign="middle" >396.692</td></tr><tr><td align="center" valign="middle" >Apigenin</td><td align="center" valign="middle" >16.380</td><td align="center" valign="middle" >5127.089</td><td align="center" valign="middle" >510.145</td></tr><tr><td align="center" valign="middle" >Butein</td><td align="center" valign="middle" >16.680</td><td align="center" valign="middle" >2849.149</td><td align="center" valign="middle" >283.490</td></tr><tr><td align="center" valign="middle" >Naringenin</td><td align="center" valign="middle" >16.792</td><td align="center" valign="middle" >4071.731</td><td align="center" valign="middle" >405.137</td></tr><tr><td align="center" valign="middle" >Biochanin</td><td align="center" valign="middle" >17.101</td><td align="center" valign="middle" >5339.931</td><td align="center" valign="middle" >531.323</td></tr><tr><td align="center" valign="middle" >Luteolin</td><td align="center" valign="middle" >17.371</td><td align="center" valign="middle" >1111.266</td><td align="center" valign="middle" >110.571</td></tr><tr><td align="center" valign="middle" >Kaempferol</td><td align="center" valign="middle" >18.503</td><td align="center" valign="middle" >11,453.533</td><td align="center" valign="middle" >1139.627</td></tr><tr><td align="center" valign="middle" >(−)-Epicatechin</td><td align="center" valign="middle" >19.530</td><td align="center" valign="middle" >8162.805</td><td align="center" valign="middle" >812.199</td></tr><tr><td align="center" valign="middle" >(−)-Epigallocatechin</td><td align="center" valign="middle" >20.478</td><td align="center" valign="middle" >1826.631</td><td align="center" valign="middle" >181.750</td></tr><tr><td align="center" valign="middle" >Quercetin</td><td align="center" valign="middle" >21.445</td><td align="center" valign="middle" >2875.972</td><td align="center" valign="middle" >286.159</td></tr><tr><td align="center" valign="middle" >(−)-Epicatechin-3-gallate</td><td align="center" valign="middle" >22.610</td><td align="center" valign="middle" >134.977</td><td align="center" valign="middle" >13.430</td></tr><tr><td align="center" valign="middle" >(−)-Epigallocatechin-3-gallate</td><td align="center" valign="middle" >23.238</td><td align="center" valign="middle" >263.286</td><td align="center" valign="middle" >26.197</td></tr><tr><td align="center" valign="middle" >Isorhamnetin</td><td align="center" valign="middle" >24.104</td><td align="center" valign="middle" >324.132</td><td align="center" valign="middle" >32.251</td></tr><tr><td align="center" valign="middle" >Robinetin</td><td align="center" valign="middle" >24.193</td><td align="center" valign="middle" >2535.979</td><td align="center" valign="middle" >252.330</td></tr><tr><td align="center" valign="middle" >Ellagic acid</td><td align="center" valign="middle" >24.546</td><td align="center" valign="middle" >1183.313</td><td align="center" valign="middle" >117.740</td></tr><tr><td align="center" valign="middle" >Myricetin</td><td align="center" valign="middle" >24.796</td><td align="center" valign="middle" >915.467</td><td align="center" valign="middle" >91.089</td></tr><tr><td align="center" valign="middle" >Baicalein</td><td align="center" valign="middle" >25.701</td><td align="center" valign="middle" >1983.819</td><td align="center" valign="middle" >197.390</td></tr><tr><td align="center" valign="middle" >Nobiletin</td><td align="center" valign="middle" >26.356</td><td align="center" valign="middle" >1944.091</td><td align="center" valign="middle" >193.437</td></tr><tr><td align="center" valign="middle" >Baicalin</td><td align="center" valign="middle" >26.956</td><td align="center" valign="middle" >478.418</td><td align="center" valign="middle" >47.603</td></tr><tr><td align="center" valign="middle" >Silymarin</td><td align="center" valign="middle" >27.813</td><td align="center" valign="middle" >233.524</td><td align="center" valign="middle" >23.236</td></tr><tr><td align="center" valign="middle" >Total flavonoids</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >65,102.577</td><td align="center" valign="middle" >6477.706</td></tr></tbody></table></table-wrap><p>The leaves had high hydroxycinnamates (0.580 g/kg), tannins (0.813 g/kg) and phytosterols (0.250 g/kg), moderate benzoic acid derivatives (0.032 g/kg) and lignans (0.077 g/kg), and low carotenoids (0.001 g/kg) contents (<xref ref-type="table" rid="table2">Table 2</xref>). Five known carotenoids were detected in the leaves. This consisted of 62.608% lutein, 13.989% carotene, 11.328% antheraxanthin, 8.532% neoxanthin and 3.542% violaxanthin. Four known benzoic acid derivatives were detected in the leaves. This consisted of 46.091% ferulic acid, 22.624% 4-hydroxybenzaldehyde, 16.441% vanillic acid and 14.843% 4-hydroxybenzoic acid. The hydroxycinnamates fraction consisted 100% of caffeic acid, the tannins fraction consisted 100% of tannic acid, while the phytosterols fraction consisted of stigmasterol (80.853%) and sitosterol (19.146%). The leaves had moderate lignans (0.077 g/kg) contents (<xref ref-type="table" rid="table3">Table 3</xref>). Six known lignans were detected in the leaves. This consisted of 77.326% galgravin, 12.221% dehydroabietic acid, 7.837% retusin, 2.612% epieudesmin, 0.003% apigenin-4’, 7-dimethyl ether and 0.00002% (9E,12E, 15E)-9,12,15-octadecatrien-1-ol.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Benzoic acid derivatives, carotenoids, phytosterols, hydroxycinnamates and tannins compositions of Tridax procumbens leaves</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Compounds</th><th align="center" valign="middle"  rowspan="2"  >Retention time (min)</th><th align="center" valign="middle"  colspan="2"  >Composition (mg/kg)</th></tr></thead><tr><td align="center" valign="middle" >/dry weight</td><td align="center" valign="middle" >/wet weight</td></tr><tr><td align="center" valign="middle" >Benzoic acid derivatives</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >4-Hydroxybenzaldehyde</td><td align="center" valign="middle" >8.947</td><td align="center" valign="middle" >73.708</td><td align="center" valign="middle" >7.334</td></tr><tr><td align="center" valign="middle" >4-Hydroxybenzoic acid</td><td align="center" valign="middle" >12.363</td><td align="center" valign="middle" >48.358</td><td align="center" valign="middle" >4.812</td></tr><tr><td align="center" valign="middle" >Vanillic acid</td><td align="center" valign="middle" >15.234</td><td align="center" valign="middle" >53.564</td><td align="center" valign="middle" >5.330</td></tr><tr><td align="center" valign="middle" >Ferulic acid</td><td align="center" valign="middle" >18.052</td><td align="center" valign="middle" >150.161</td><td align="center" valign="middle" >14.941</td></tr><tr><td align="center" valign="middle" >Total benzoic acid derivatives</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >325.792</td><td align="center" valign="middle" >32.416</td></tr><tr><td align="center" valign="middle" >Carotenoids</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Neoxanthin</td><td align="center" valign="middle" >19.525</td><td align="center" valign="middle" >1.2112</td><td align="center" valign="middle" >0.1205</td></tr><tr><td align="center" valign="middle" >Viola-xanthin</td><td align="center" valign="middle" >20.542</td><td align="center" valign="middle" >0.5028</td><td align="center" valign="middle" >0.0500</td></tr><tr><td align="center" valign="middle" >Anthera-xanthin</td><td align="center" valign="middle" >21.441</td><td align="center" valign="middle" >1.6080</td><td align="center" valign="middle" >0.1600</td></tr><tr><td align="center" valign="middle" >Carotene</td><td align="center" valign="middle" >23.191</td><td align="center" valign="middle" >1.9856</td><td align="center" valign="middle" >0.1980</td></tr><tr><td align="center" valign="middle" >Lutein</td><td align="center" valign="middle" >24.796</td><td align="center" valign="middle" >8.8870</td><td align="center" valign="middle" >0.8843</td></tr><tr><td align="center" valign="middle" >Total carotenoids</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >14.1947</td><td align="center" valign="middle" >1.4124</td></tr><tr><td align="center" valign="middle" >Phytosterols</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Stigmasterol</td><td align="center" valign="middle" >23.264</td><td align="center" valign="middle" >2032.970</td><td align="center" valign="middle" >202.281</td></tr><tr><td align="center" valign="middle" >Sitosterol</td><td align="center" valign="middle" >24.802</td><td align="center" valign="middle" >481.414</td><td align="center" valign="middle" >47.901</td></tr><tr><td align="center" valign="middle" >Total phytosterols</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >2514.390</td><td align="center" valign="middle" >250.182</td></tr><tr><td align="center" valign="middle" >Tannins</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Tannic acid</td><td align="center" valign="middle" >19.223</td><td align="center" valign="middle" >8175.408</td><td align="center" valign="middle" >813.453</td></tr><tr><td align="center" valign="middle" >Total tannins</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >8175.408</td><td align="center" valign="middle" >813.453</td></tr><tr><td align="center" valign="middle" >Hydroxycinnamates</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Caffeic acid</td><td align="center" valign="middle" >14.096</td><td align="center" valign="middle" >5830.871</td><td align="center" valign="middle" >580.172</td></tr><tr><td align="center" valign="middle" >Total hydroxycinnamates</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >5830.871</td><td align="center" valign="middle" >580.172</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Lignans composition of Tridax procumbens leaves</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Compounds</th><th align="center" valign="middle"  rowspan="2"  >Retention time (min)</th><th align="center" valign="middle"  colspan="2"  >Composition (mg/kg)</th></tr></thead><tr><td align="center" valign="middle" >/dry weight</td><td align="center" valign="middle" >/wet weight</td></tr><tr><td align="center" valign="middle" >(9E,12E,15E)-9,12,15-Octadecatrien-1-ol</td><td align="center" valign="middle" >14.095</td><td align="center" valign="middle" >0.00014</td><td align="center" valign="middle" >0.000,01</td></tr><tr><td align="center" valign="middle" >Apigenin-4’,7-dimethyl ether</td><td align="center" valign="middle" >16.270</td><td align="center" valign="middle" >0.02540</td><td align="center" valign="middle" >0.002,53</td></tr><tr><td align="center" valign="middle" >Dehydroabietic acid</td><td align="center" valign="middle" >18.618</td><td align="center" valign="middle" >94.933,90</td><td align="center" valign="middle" >9.445,92</td></tr><tr><td align="center" valign="middle" >Retusin</td><td align="center" valign="middle" >19.625</td><td align="center" valign="middle" >60.875,60</td><td align="center" valign="middle" >6.057,12</td></tr><tr><td align="center" valign="middle" >Galgravin</td><td align="center" valign="middle" >20.444</td><td align="center" valign="middle" >600.666,70</td><td align="center" valign="middle" >59.766,34</td></tr><tr><td align="center" valign="middle" >Epieudesmin</td><td align="center" valign="middle" >22.324</td><td align="center" valign="middle" >20.293,10</td><td align="center" valign="middle" >2.019,16</td></tr><tr><td align="center" valign="middle" >Total lignans</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >776.794,70</td><td align="center" valign="middle" >77.291,07</td></tr></tbody></table></table-wrap><p>The leaves had very high alkaloids content (10.191 g/kg) (<xref ref-type="table" rid="table4">Table 4</xref>). Thirty nine known alkaloids were detected in the leaves. This consisted of 68.756% akuammidine, 16.508% voacangine, 4.944% echitamine, 2.3167% lupanine, 2.253% angustifoline, 1.902% augustamine, 0.549% crinamidine, 0.477% echitamidine, 0.327% cinchonidine, 0.324% oxoassoanine, 0.317% trigonelline, 0.178% crinane-3α-ol, 0.177% choline, 0.141% cinchonine, 0.117% indicine-N-oxide, 0.093% monocrotaline, 0.079% nitidine, 0.064% 6-hydroxypowelline, 0.050% 13-α-hydrorhombifoline, 0.043% acronycine, 0.041% powelline, 0.041% ambelline, 0.040% 6-hydroxyundula- tine, 0.040% dihydro-oxo-demethoxyhaemanthamine, 0.039% 9-octadecenamide, 0.037% ellipcine, 0.030% 1β,2β-epoxyambelline, 0.028% buphanidrine, 0.026% undulatine, 0.020% 6-hydroxybuphanidrine, 0.016% sparteine, etc.</p></sec><sec id="s4"><title>4. Discussion</title><p>The leaves had higher catechin, gallocatechin, epicatechin, epigallocatechin, epicatechin gallate, epigallocatechin gallate, naringenin, apigenin, luteolin, kaempferol, myricetin and quercetin contents than lettuce and onions [<xref ref-type="bibr" rid="scirp.58815-ref33">33</xref>] . Amongst the biological activities of flavonoids are actions against free radicals, free radical mediated cellular signaling, inflammation, allergies, platelet aggregation, microbes, ulcers, viruses, tumors and hepatotoxins [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] . Luteolin has antibacterial, anti-inflammatory, anti-mutagenic, antioxidant [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , anti-allergic, anti-andro- genic, anticancer, anti-diabetic, anti-estrogenic, antimicrobial, hypocholesterolemic, hypotensive, neuroprotective and radio-protective [<xref ref-type="bibr" rid="scirp.58815-ref35">35</xref>] activities. Kaempferol is known for its antibacterial, anti-inflammatory, antioxidant [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , analgesic, anti-allergic, anticancer, anti-diabetic, antifungal, antiprotozoal, anti-osteoporotic, anti- thrombogenic, antiviral, cardioprotective, hepatoprotective, hypocholesterolemic, hypotriglyceridemic and neuroprotective [<xref ref-type="bibr" rid="scirp.58815-ref36">36</xref>] activities. Kaempferol-3-O-rutinoside has hypotensive activity [<xref ref-type="bibr" rid="scirp.58815-ref37">37</xref>] .</p><p>Apigenin has antibacterial, anti-inflammatory, diuretic, hypotensive, smooth muscle relaxation enhancing [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , antioxidant, anti-carcinogenic, antidepressant, cardioprotective, hepatoprotective, anti-peroxidative [<xref ref-type="bibr" rid="scirp.58815-ref38">38</xref>] , anti-tumor, anti-proliferative, oxygenase inhibitory and apoptosis inducing [<xref ref-type="bibr" rid="scirp.58815-ref39">39</xref>] activities. Naringenin has anti- atherogenic, anticancer, anti-fibrogenic, anti-inflammatory, anti-mutagenic, antioxidant, hepatoprotective, hypocholesterolemic [<xref ref-type="bibr" rid="scirp.58815-ref40">40</xref>] , anti-ulcer and cardioprotective [<xref ref-type="bibr" rid="scirp.58815-ref41">41</xref>] properties.</p><p>Catechins are antimicrobial [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , anti-allergic, anti-carcinogenic, anti-diabetic, antihypertensive, anti-in- flammatory, anti-mutagenic, anti-obesity, antioxidant, anti-platelet, anti-proliferative, anti-tumorigenic, anti- ulcer, chemo-preventive, hypocholesterolemic and neuroprotective [<xref ref-type="bibr" rid="scirp.58815-ref42">42</xref>] agents. (+)-Catechin has been reported to have cardioprotective [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , antispasmodic, bronchodilator and vasodilator [<xref ref-type="bibr" rid="scirp.58815-ref43">43</xref>] activities. Epicatechin, epicatechin gallate and epigallocatechin gallate provide protective benefits by their free radical scavenging ability and their inhibition of eicosanoid synthesis and platelet aggregation [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] . In addition, epicatechin has antioxidant [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] and hypoglycemic activities [<xref ref-type="bibr" rid="scirp.58815-ref44">44</xref>] .</p><p>Diadzein and genistein have antithrombotic, hypocholesterolemic, hypotensive [<xref ref-type="bibr" rid="scirp.58815-ref45">45</xref>] , anticancer and estrogen- like properties [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] . Genistein also has anti-diabetic, anti-inflammatory, anti-obesity, antioxidant and cardio- protective [<xref ref-type="bibr" rid="scirp.58815-ref46">46</xref>] activities. Nobiletin has anti-atherosclerotic, anti-dyslipidemic, antihypertensive, anti-inflam- matory, antioxidant, anti-resorptive, antithrombotic [<xref ref-type="bibr" rid="scirp.58815-ref47">47</xref>] , anti-angiogenic, anti-carcinogenic, anti-dementia, cognitive impairment improving [<xref ref-type="bibr" rid="scirp.58815-ref48">48</xref>] and antitumor properties, and enhances adiponectin secretion [<xref ref-type="bibr" rid="scirp.58815-ref49">49</xref>] .</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Alkaloids composition of Tridax procumbens leaves</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Compounds</th><th align="center" valign="middle"  rowspan="2"  >Retention time (min)</th><th align="center" valign="middle"  colspan="2"  >Composition (mg/kg)</th></tr></thead><tr><td align="center" valign="middle" >/dry weight</td><td align="center" valign="middle" >/wet weight</td></tr><tr><td align="center" valign="middle" >Choline</td><td align="center" valign="middle" >7.085</td><td align="center" valign="middle" >181.122</td><td align="center" valign="middle" >18.022</td></tr><tr><td align="center" valign="middle" >Trigonelline</td><td align="center" valign="middle" >7.642</td><td align="center" valign="middle" >324.271</td><td align="center" valign="middle" >32.265</td></tr><tr><td align="center" valign="middle" >Angustifoline</td><td align="center" valign="middle" >8.073</td><td align="center" valign="middle" >2307.790</td><td align="center" valign="middle" >229.625</td></tr><tr><td align="center" valign="middle" >Sparteine</td><td align="center" valign="middle" >9.035</td><td align="center" valign="middle" >16.494</td><td align="center" valign="middle" >1.641</td></tr><tr><td align="center" valign="middle" >Ellipcine</td><td align="center" valign="middle" >9.785</td><td align="center" valign="middle" >38.235</td><td align="center" valign="middle" >3.804</td></tr><tr><td align="center" valign="middle" >Lupanine</td><td align="center" valign="middle" >11.178</td><td align="center" valign="middle" >2372.643</td><td align="center" valign="middle" >236.078</td></tr><tr><td align="center" valign="middle" >13-α-Hydrorhombifoline</td><td align="center" valign="middle" >11.296</td><td align="center" valign="middle" >51.108</td><td align="center" valign="middle" >5.085</td></tr><tr><td align="center" valign="middle" >9-Octadecenamide</td><td align="center" valign="middle" >12.810</td><td align="center" valign="middle" >40.003</td><td align="center" valign="middle" >3.980</td></tr><tr><td align="center" valign="middle" >Dihydro-oxo-demethoxyhaemanthamine</td><td align="center" valign="middle" >14.126</td><td align="center" valign="middle" >40.477</td><td align="center" valign="middle" >4.028</td></tr><tr><td align="center" valign="middle" >Augustamine</td><td align="center" valign="middle" >14.915</td><td align="center" valign="middle" >1948.528</td><td align="center" valign="middle" >193.879</td></tr><tr><td align="center" valign="middle" >Oxoassoanine</td><td align="center" valign="middle" >15.375</td><td align="center" valign="middle" >331.419</td><td align="center" valign="middle" >32.976</td></tr><tr><td align="center" valign="middle" >Cinchonidine</td><td align="center" valign="middle" >16.646</td><td align="center" valign="middle" >335.341</td><td align="center" valign="middle" >33.366</td></tr><tr><td align="center" valign="middle" >Cinchonine</td><td align="center" valign="middle" >16.347</td><td align="center" valign="middle" >144.085</td><td align="center" valign="middle" >14.337</td></tr><tr><td align="center" valign="middle" >Crinane-3α-ol</td><td align="center" valign="middle" >16.428</td><td align="center" valign="middle" >182.460</td><td align="center" valign="middle" >18.155</td></tr><tr><td align="center" valign="middle" >Buphanidrine</td><td align="center" valign="middle" >16.544</td><td align="center" valign="middle" >28.978</td><td align="center" valign="middle" >2.883</td></tr><tr><td align="center" valign="middle" >Indicine-N-oxide</td><td align="center" valign="middle" >17.472</td><td align="center" valign="middle" >119.855</td><td align="center" valign="middle" >11.926</td></tr><tr><td align="center" valign="middle" >Powelline</td><td align="center" valign="middle" >18.669</td><td align="center" valign="middle" >41.741</td><td align="center" valign="middle" >4.153</td></tr><tr><td align="center" valign="middle" >Undulatine</td><td align="center" valign="middle" >18.763</td><td align="center" valign="middle" >26.893</td><td align="center" valign="middle" >2.676</td></tr><tr><td align="center" valign="middle" >Ambelline</td><td align="center" valign="middle" >19.669</td><td align="center" valign="middle" >41.741</td><td align="center" valign="middle" >4.153</td></tr><tr><td align="center" valign="middle" >6-Hydroxybuphanidrine</td><td align="center" valign="middle" >20.552</td><td align="center" valign="middle" >20.539</td><td align="center" valign="middle" >2.044</td></tr><tr><td align="center" valign="middle" >Acronycine</td><td align="center" valign="middle" >21.239</td><td align="center" valign="middle" >43.732</td><td align="center" valign="middle" >4.351</td></tr><tr><td align="center" valign="middle" >Monocrotaline</td><td align="center" valign="middle" >21.388</td><td align="center" valign="middle" >95.111</td><td align="center" valign="middle" >9.464</td></tr><tr><td align="center" valign="middle" >6-Hydroxypowelline</td><td align="center" valign="middle" >21.734</td><td align="center" valign="middle" >65.350</td><td align="center" valign="middle" >6.502</td></tr><tr><td align="center" valign="middle" >Nitidine</td><td align="center" valign="middle" >22.347</td><td align="center" valign="middle" >80.852</td><td align="center" valign="middle" >8.045</td></tr><tr><td align="center" valign="middle" >Crinamidine</td><td align="center" valign="middle" >23.960</td><td align="center" valign="middle" >562.134</td><td align="center" valign="middle" >55.932</td></tr><tr><td align="center" valign="middle" >1β,2β-Epoxyambelline</td><td align="center" valign="middle" >24.729</td><td align="center" valign="middle" >30.717</td><td align="center" valign="middle" >3.056</td></tr><tr><td align="center" valign="middle" >6-Hydroxyundulatine</td><td align="center" valign="middle" >24.842</td><td align="center" valign="middle" >40.889</td><td align="center" valign="middle" >4.069</td></tr><tr><td align="center" valign="middle" >Epoxy-3,7-dimethoxycrinane-11-one</td><td align="center" valign="middle" >25.615</td><td align="center" valign="middle" >7.0315</td><td align="center" valign="middle" >0.700</td></tr><tr><td align="center" valign="middle" >Akuammidine</td><td align="center" valign="middle" >26.919</td><td align="center" valign="middle" >70,420.759</td><td align="center" valign="middle" >7006.866</td></tr><tr><td align="center" valign="middle" >Echitamidine</td><td align="center" valign="middle" >26.786</td><td align="center" valign="middle" >488.511</td><td align="center" valign="middle" >48.607</td></tr><tr><td align="center" valign="middle" >Voacangine</td><td align="center" valign="middle" >27.072</td><td align="center" valign="middle" >16,907.728</td><td align="center" valign="middle" >1682.319</td></tr><tr><td align="center" valign="middle" >Mitraphylin</td><td align="center" valign="middle" >27.624</td><td align="center" valign="middle" >0.010</td><td align="center" valign="middle" >0.001</td></tr><tr><td align="center" valign="middle" >Camptothecin</td><td align="center" valign="middle" >28.229</td><td align="center" valign="middle" >5.434</td><td align="center" valign="middle" >0.541</td></tr><tr><td align="center" valign="middle" >Echitamine</td><td align="center" valign="middle" >28.451</td><td align="center" valign="middle" >5063.374</td><td align="center" valign="middle" >503.806</td></tr><tr><td align="center" valign="middle" >Colchicine</td><td align="center" valign="middle" >29.036</td><td align="center" valign="middle" >1.322</td><td align="center" valign="middle" >0.132</td></tr><tr><td align="center" valign="middle" >Emetine</td><td align="center" valign="middle" >29.462</td><td align="center" valign="middle" >8.172</td><td align="center" valign="middle" >0.813</td></tr><tr><td align="center" valign="middle" >Tetrandrine</td><td align="center" valign="middle" >30.153</td><td align="center" valign="middle" >1.786</td><td align="center" valign="middle" >0.178</td></tr><tr><td align="center" valign="middle" >Thalicarpin</td><td align="center" valign="middle" >30.050</td><td align="center" valign="middle" >2.639</td><td align="center" valign="middle" >0.263</td></tr><tr><td align="center" valign="middle" >Paclitaxel</td><td align="center" valign="middle" >32.211</td><td align="center" valign="middle" >3.238</td><td align="center" valign="middle" >0.322</td></tr><tr><td align="center" valign="middle" >Total alkaloids</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >102,421.000</td><td align="center" valign="middle" >10,190.890</td></tr></tbody></table></table-wrap><p>Studies have shown that ellagic acid has anti-allergic, anticancer, anti-depressant, anti-diabetic, anti-inflam- matory, antimalarial, antioxidant, anti-wrinkle, neuroprotective [<xref ref-type="bibr" rid="scirp.58815-ref50">50</xref>] , anti-apoptotic, anti-atherogenic, anti-pro- liferative and chemo-preventive [<xref ref-type="bibr" rid="scirp.58815-ref51">51</xref>] activities. Silymarin is an anti-arthritic, anti-carcinogenic, anti-diabetic, anti-hypercholesterolemic, anti-inflammatory, anti-obesity, antioxidant, cardioprotective, gastroprotective, hepatoprotective, immunomodulatory, neuroprotective and neurotropic [<xref ref-type="bibr" rid="scirp.58815-ref52">52</xref>] agent.</p><p>Myricetin exhibits antibacterial, anti-gonadotropic, antioxidant [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , anti-carcinogenic, anti-diabetic, anti- hyperlipidemic, anti-inflammatory, antimicrobial, antioxidant, anti-platelet, antiviral and cytoprotective [<xref ref-type="bibr" rid="scirp.58815-ref53">53</xref>] activities. Biochanin A has been reported to have anticancer, anti-inflammatory, antimicrobial, antioxidant, immunomodulatory and hepatoprotective [<xref ref-type="bibr" rid="scirp.58815-ref54">54</xref>] activities. Robinetin is a chemopreventive [<xref ref-type="bibr" rid="scirp.58815-ref55">55</xref>] agent; while butein is an antioxidant, pro-apoptotic and hepatoprotective [<xref ref-type="bibr" rid="scirp.58815-ref56">56</xref>] agent.</p><p>Baicalein is a potent free radical scavenger and xanthine oxidase inhibitor, thus improving endothelial function and conferring cardiovascular protective actions against oxidative stress-induced cell injury. Baicalein has anti-arteriosclerotic, antibacterial, antihypertensive, anti-inflammatory, anti-mitogenic, antioxidant, anti-proli- ferative, anti-thrombotic, antitumor, antiviral and cardio-protective [<xref ref-type="bibr" rid="scirp.58815-ref57">57</xref>] activities. Quercetin has been reported to have anti-allergic, anti-arthritic, antibacterial, anti-carcinogenic, anti-cancer, anti-cataractogenic, anti-diabetic, antihypertensive, anti-inflammatory, antioxidant, antiviral, cardio-protective, gastro-protective, hepatoprotective and hypocholesterolemic [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref58">58</xref>] activities.</p><p>The carotene and lutein contents of the leaves were higher than those of cabbage, but lower than those of amaranth [<xref ref-type="bibr" rid="scirp.58815-ref59">59</xref>] . Carotenoids have been widely accepted as safe chemicals for food supplementation and neutraceutical purposes due to their intense coloring abilities, their role as precursors of vitamin A, and their antioxidant activity in animals [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref60">60</xref>] . They have been shown to be beneficial in preventing major health problems in developing and developed countries, including cancers, cardiovascular and coronary heart diseases, photosensitivity disorders, age-related macular degeneration and cataract [<xref ref-type="bibr" rid="scirp.58815-ref60">60</xref>] . Carotenes and lutein protect against uterine, prostate, breast, colorectal and lung cancers [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] . Carotenes, in addition, have pro-vitamin A and antioxidant [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] activities.</p><p>The leaves had higher caffeic, vanilic and 4-hydroxybenzoic acids, but lower ferulic acid contents than red cabbage [<xref ref-type="bibr" rid="scirp.58815-ref61">61</xref>] . Phenolic acids are powerful antioxidants and have been reported to demonstrate antibacterial, antiviral, anti-carcinogenic, anti-inflammatory and vasodilatory actions [<xref ref-type="bibr" rid="scirp.58815-ref61">61</xref>] . 4-Hydroxybenzaldehyde is used as a flavor and fragrance agent. Caffeic acid has anti-diabetic [<xref ref-type="bibr" rid="scirp.58815-ref50">50</xref>] , antioxidant [<xref ref-type="bibr" rid="scirp.58815-ref62">62</xref>] , anti-inflammatory and photo-protective [<xref ref-type="bibr" rid="scirp.58815-ref63">63</xref>] activities. 4-Hydroxybenzoic acid esters (also called parabens), are widely used as antimicrobial agents in a large variety of food, pharmaceutical, and cosmetic products due to their excellent antimicrobial activities, low toxicity and stability over a wide pH range [<xref ref-type="bibr" rid="scirp.58815-ref64">64</xref>] . 4-Hydroxybenzoic acid has antifungal, anti-mutagenic, anti-sickling, estrogenic and antimicrobial [<xref ref-type="bibr" rid="scirp.58815-ref62">62</xref>] activities. Vanillic acid (4-hydroxy-3-methox- ybenzoic acid) is used as a flavoring agent. It has anti-sickling, anthelmintic, hepatoprotective, immune-mod- ulating, anti-inflammatory, antifungal, anti-mutagenic, estrogenic and antimicrobial [<xref ref-type="bibr" rid="scirp.58815-ref62">62</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref65">65</xref>] activities. It also inhibits snake venom 5’-nucleotidase [<xref ref-type="bibr" rid="scirp.58815-ref62">62</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref65">65</xref>] . Ferulic acid has antioxidant, hypocholesterolemic, anti-inflam- matory, photo-protective, cardio-protective and sperm viability boosting activities [<xref ref-type="bibr" rid="scirp.58815-ref62">62</xref>] .</p><p>The leaves had higher total phytosterols, stigmasterol and sitosterol contents than those of white cabbage and onions [<xref ref-type="bibr" rid="scirp.58815-ref66">66</xref>] . Phytosterols have anti-inflammatory [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , hypocholesterolemic, anti-cancer [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.58815-ref66">66</xref>] , anti-ulcer, anti-fungal, anti-atherogenic, antioxidant [<xref ref-type="bibr" rid="scirp.58815-ref67">67</xref>] and estrogenic [<xref ref-type="bibr" rid="scirp.58815-ref68">68</xref>] activities. Stigmasterol has anti-osteoarthritic, anti-hypercholestrolemic, cytotoxicity, antitumor, thyroid inhibiting, hypoglycemic, anti-mutagenic, antioxidant, anti-inflammatory, anticonvulsant and sedative [<xref ref-type="bibr" rid="scirp.58815-ref69">69</xref>] , chemopreventive, anticancer, estrogenic [<xref ref-type="bibr" rid="scirp.58815-ref70">70</xref>] activities. β-Sitosterol has been reported to have anti-inflammatory, anti-neoplastic, immune-modulating, antipyretic [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , cholesterol-lowering, antipyretic, antineoplastic, anti-diabetic, cardio-protective, estrogenic [<xref ref-type="bibr" rid="scirp.58815-ref68">68</xref>] , antimicrobial, antioxidant, chemopreventive, anticancer and antipyretic [<xref ref-type="bibr" rid="scirp.58815-ref71">71</xref>] activities. It is used in the treatment of benign prostate hyperplasia [<xref ref-type="bibr" rid="scirp.58815-ref71">71</xref>] , and alters sex steroid levels [<xref ref-type="bibr" rid="scirp.58815-ref68">68</xref>] . Sitosterylglucoside has been identified as an “adaptogens” [<xref ref-type="bibr" rid="scirp.58815-ref67">67</xref>] . According to Berger and colleagues [<xref ref-type="bibr" rid="scirp.58815-ref67">67</xref>] , adaptogens are a group of natural plant products which promote overall health without the rapid response normally elicited by a drug and without the side effects associated with any drug used.</p><p>The leaves had higher total tannin content than red pepper [<xref ref-type="bibr" rid="scirp.58815-ref72">72</xref>] , but lower tannic acid content than cabbage [<xref ref-type="bibr" rid="scirp.58815-ref73">73</xref>] . Tannins have antioxidant, antimicrobial [<xref ref-type="bibr" rid="scirp.58815-ref34">34</xref>] , anticancer [<xref ref-type="bibr" rid="scirp.58815-ref74">74</xref>] activities. Tannic acid has antihypertensive, anti-diarrheal, anti-cancer, anti-asthmatic, cardioprotective, anti-diabetic, anti-cataractogenic, tumor inhibition, anti-inflammatory, anti-adipogenic [<xref ref-type="bibr" rid="scirp.58815-ref74">74</xref>] and hepatoprotective [<xref ref-type="bibr" rid="scirp.58815-ref75">75</xref>] activities.</p><p>The leaves had higher total lignans contents than garlic and lettuce [<xref ref-type="bibr" rid="scirp.58815-ref76">76</xref>] . Lignans have antioxidant, anticancer, anti-diabetic, antiviral, bactericidal, anti-inflammatory, anti-atherosclerotic, cardio-protective [<xref ref-type="bibr" rid="scirp.58815-ref77">77</xref>] , anti-hepato- toxic, antitumor, antiplatelet aggregation [<xref ref-type="bibr" rid="scirp.58815-ref78">78</xref>] and estrogen-like [<xref ref-type="bibr" rid="scirp.58815-ref76">76</xref>] activities. Galgravin has been reported to exhibit anti-inflammatory, anti-malarial, anti-platelet, anti-resorptive [<xref ref-type="bibr" rid="scirp.58815-ref79">79</xref>] , anti-rheumatoid, neurotrophic and neuroprotective [<xref ref-type="bibr" rid="scirp.58815-ref28">28</xref>] activities.</p><p>Akuammidine has antibacterial, antifungal [<xref ref-type="bibr" rid="scirp.58815-ref80">80</xref>] , antimalarial, anti-inflammatory, hypotensive, skeletal muscle relaxant, local analgesic and anti-depressant [<xref ref-type="bibr" rid="scirp.58815-ref81">81</xref>] activities. Voacangine has been reported to have cardiovascular toning, central nervous system depressant, anti-convulsive, anti-pyretic, analgesic, local anesthetic, acetyl cholinesterase inhibitory [<xref ref-type="bibr" rid="scirp.58815-ref82">82</xref>] , anti-angiogenic [<xref ref-type="bibr" rid="scirp.58815-ref83">83</xref>] and anti-mycobacterial [<xref ref-type="bibr" rid="scirp.58815-ref84">84</xref>] activities. Studies have shown that echitamine has diuretic, hypotensive [<xref ref-type="bibr" rid="scirp.58815-ref85">85</xref>] , central nervous system depressant and antiepileptic [<xref ref-type="bibr" rid="scirp.58815-ref86">86</xref>] properties. Augustifoline is a bacteriostatic agent [<xref ref-type="bibr" rid="scirp.58815-ref87">87</xref>] while lupanine is an anti-arrhythmic, hypotensive, hypoglycemic, β-glucosidase inhibitory, bacteriostatic [<xref ref-type="bibr" rid="scirp.58815-ref87">87</xref>] , oxytocic and central nervous system depressant [<xref ref-type="bibr" rid="scirp.58815-ref88">88</xref>] agent.</p><p>Finally, the present study showed that the leaves of Tridax procumbens contain a variety of biologically active phytochemicals. The beneficial roles of these bioactive phytochemical constituents can be harnessed in the diet, making them veritable tools for nutritional therapy. This, therefore, emphasizes the potential of these leaves as a functional food.</p></sec><sec id="s5"><title>Cite this paper</title><p>Catherine C.Ikewuchi,Jude C.Ikewuchi,Mercy O.Ifeanacho, (2015) Phytochemical Composition of Tridax procumbens Linn Leaves: Potential as a Functional Food. 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