<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0366-1644</journal-id>
<journal-title><![CDATA[Boletín de la Sociedad Chilena de Química]]></journal-title>
<abbrev-journal-title><![CDATA[Bol. Soc. Chil. Quím.]]></abbrev-journal-title>
<issn>0366-1644</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Chilena de Química]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0366-16442002000400030</article-id>
<article-id pub-id-type="doi">10.4067/S0366-16442002000400030</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[VOLATILE COMPOUNDS OF LITHRAEA CAUSTICA (LITRE) DETERMINATED BY SOLID PHASE MICRO-EXTRACTION (SPME)]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[GARBARINO]]></surname>
<given-names><![CDATA[JUAN A]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[SALVATORE]]></surname>
<given-names><![CDATA[GIUSEPPE]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[PIVANOVO]]></surname>
<given-names><![CDATA[MARISA]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[CHAMY]]></surname>
<given-names><![CDATA[MARÍA CRISTINA]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[NICOLETTI]]></surname>
<given-names><![CDATA[MARCELLO]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[DE IOANNES]]></surname>
<given-names><![CDATA[ALFREDO]]></given-names>
</name>
<xref ref-type="aff" rid="A04"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Técnica Federico Santa María Departamento de Química ]]></institution>
<addr-line><![CDATA[Valparaíso ]]></addr-line>
<country>Chile</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Istituto Superiore di Sanità Laboratorio di Tossicologia Comparata ed Ecotossicologia ]]></institution>
<addr-line><![CDATA[Rome ]]></addr-line>
<country>Italy</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Università La Sapienza Dipto. Biologia Vegetale ]]></institution>
<addr-line><![CDATA[Rome ]]></addr-line>
<country>Italy</country>
</aff>
<aff id="A04">
<institution><![CDATA[,P. Universidad Católica Facultad de Ciencias Biológicas ]]></institution>
<addr-line><![CDATA[Santiago ]]></addr-line>
<country>Chile</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2002</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2002</year>
</pub-date>
<volume>47</volume>
<numero>4</numero>
<fpage>567</fpage>
<lpage>569</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.cl/scielo.php?script=sci_arttext&amp;pid=S0366-16442002000400030&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.cl/scielo.php?script=sci_abstract&amp;pid=S0366-16442002000400030&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.cl/scielo.php?script=sci_pdf&amp;pid=S0366-16442002000400030&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[The head space of the aerial parts of Lithraea caustica was analyzed by Solid Phase Micro-Extraction (SPME) technique, obtaining as main volatile compounds the monoterpenes, myrcene, a -pinene, , p-cymene and limonene, as well as the sesquiterpene caryophylene.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[De las partes áereas de Lithraea caustica y usando la técnica de Micro-Extracción en Fase Sólida (MEFS), fueron identificados y cuantificados los principales compuestos volátiles: los monoterpenos, mirceno, a -pineno, p-cimeno y limoneno, y el sesquiterpeno cariofileno.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Lithraea caustica]]></kwd>
<kwd lng="en"><![CDATA[Anacardiaceae]]></kwd>
<kwd lng="en"><![CDATA[Solid Phase Micro-Extraction]]></kwd>
<kwd lng="en"><![CDATA[head space components]]></kwd>
<kwd lng="en"><![CDATA[monoterpenes, sesquiterpenes]]></kwd>
<kwd lng="es"><![CDATA[Lithraea caustica]]></kwd>
<kwd lng="es"><![CDATA[Anacardiaceae]]></kwd>
<kwd lng="es"><![CDATA[Micro-Extracción en Fase Sólida]]></kwd>
<kwd lng="es"><![CDATA[componentes volátiles]]></kwd>
<kwd lng="es"><![CDATA[monoterpenos]]></kwd>
<kwd lng="es"><![CDATA[sesquiterpenos]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="center"> <B>VOLATILE COMPOUNDS OF <I>LITHRAEA CAUSTICA</I> (LITRE)    <br>   DETERMINATED BY SOLID PHASE MICRO-EXTRACTION (SPME).</b></p>     <p align="center"></p>     <p align="center"><i>JUAN A. GARBARINO<SUP><a href="#a1">1</a><a href="#z">*</a></SUP>,    GIUSEPPE SALVATORE<SUP><a href="#a2">2</a></SUP>, MARISA PIVANOVO<SUP><a href="#a1">1</a></SUP>,    <br>   MAR&Iacute;A CRISTINA CHAMY<SUP><a href="#a1">1</a></SUP>, MARCELLO NICOLETTI<SUP><a href="#a3">3</a></SUP>    AND ALFREDO DE IOANNES<SUP><a href="#a4">4</a></SUP>.</i></p>     <p align="center"><small><a name="a1"></a><SUP>1</sup> Departamento de Qu&iacute;mica,    Universidad T&eacute;cnica Federico Santa Mar&iacute;a,    <br>   Casilla 110-V, Valpara&iacute;so, Chile. E-mail: <A HREF="mailto:juan.garbarino@qui.utfsm.cl">juan.garbarino@qui.utfsm.cl    <br>   </A><a name="a2"></a><A HREF="mailto:juan.garbarino@qui.utfsm.cl"> </A><SUP>2    </sup>Laboratorio di Tossicologia Comparata ed Ecotossicologia,    <br>   Istituto Superiore di Sanit&agrave;, Viale Regina Elena, 299, Rome, Italy. E-mail:    <A HREF="mailto:pino@iss.it">pino@iss.it    <br>   </A><a name="a3"></a><A HREF="mailto:pino@iss.it"> </A><SUP>3 </sup>Dipto. Biologia    Vegetale, Universit&agrave; &quot;La Sapienza&quot;,     ]]></body>
<body><![CDATA[<br>   Ple. Aldo Moro, 5, Rome, Italy. E-mail: <A HREF="mailto:marcello.nicoletti@uniroma1.it">marcello.nicoletti@uniroma1.it</A>    <br>   <SUP><a name="a4"></a>4</sup>Facultad de Ciencias Biol&oacute;gicas, P. Universidad    Cat&oacute;lica,     <br>   Av. Bernardo O’Higgins 340, Santiago. E-mail: <A HREF="mailto:aioannes@biosonda.com">aioannes@biosonda.com</A></small></p>     <p align="center">(Received: May 16, 2002 - Accepted: August 9, 2002)</p>      <p align="center"><b>ABSTRACT</b></p> <dir>       <p>The head space of the aerial parts of <I>Lithraea caustica </I>was analyzed      by Solid Phase Micro-Extraction (SPME) technique, obtaining as main volatile      compounds the monoterpenes, myrcene, &#97; -pinene, , <I>p-</I>cymene and      limonene, as well as the sesquiterpene caryophylene. </p>       <p><B><i>KEY WORDS</i></b>: <I>Lithraea caustica</I>, Anacardiaceae, Solid Phase      Micro-Extraction, head space components, monoterpenes, sesquiterpenes.</p> </dir>      <p align="center"><b>RESUMEN</b></p> <dir>       <p>De las partes &aacute;ereas de <I>Lithraea caustica</I> y usando la t&eacute;cnica      de Micro-Extracci&oacute;n en Fase S&oacute;lida (MEFS), fueron identificados      y cuantificados los principales compuestos vol&aacute;tiles: los monoterpenos,      mirceno, &#97; -pineno, <I>p</I>-cimeno y limoneno, y el sesquiterpeno cariofileno.</p>       <p><i><B>PALABRAS CLAVES</b></i><B>: </b><I>Lithraea caustica</I>, Anacardiaceae,      Micro-Extracci&oacute;n en Fase S&oacute;lida, componentes vol&aacute;tiles,      monoterpenos, sesquiterpenos.</p> </dir>     ]]></body>
<body><![CDATA[<p ALIGN="CENTER"><b>INTRODUCTION</b></p>     <p ALIGN="CENTER"></p>     <p><I>Lithraea caustica</i> (Anacardiaceae) known as <I>litre</I> is an evergreen    tree or shrub endemic in Chile, distributed from Coquimbo (IV Region) to Cautin    (IX Region). Due to the hardness, its wood is very appreciated for the construction    of small crafts(<a href="#1">1</a>,<a href="#2">2</a>).</p>      <p>No application is known in popular medicine; on the contrary, and specially    during flowering time (September-December), it produces a strong dermatitis    in sensitive individuals(<a href="#3">3</a>).</p>      <p>In a previous phytochemical study of the constituents of leaves and twigs,    a new alkyl catechol was isolated, the litreol (3-[pentadecyl-10-enyl-catechol])    which demostrated to be a powerful allergenic vehicle (<a href="#4">4</a>).    Nevertheless literature(<a href="#3">3</a>) and oral informations, collected    by conversations with countrymen and forest rangers who suffered strong dermatitis    without physical contacts with the plants, indicate that the disease can be    induced not only by contact, but also at distance. Therefore, we studied the    composition of the volatile compounds produced by <I>litre</I> in order to verifiy    the presence of allergenic substances.</p>      <p>The major components of the head space of <I>litre</I> were established by    means of the Solid Phase Micro-Extraction (SPME)(<a href="#5">5</a>,<a href="#6">6</a>,<a href="#7">7</a>).    SPME is a clean fast technique, which allows, without the use of solvents, to    perform the direct analysis of volatile substances stored in the head space    (HS) created in a closed system which contains the plant material. </p>     <p>The aerial parts of <I>Lithraea caustica</I> (Mol.) H. et Arn. were collected    in Laguna Verde, Valparaiso (V Region), Chile, in September 2001. One sample    was deposited in the herbarium of the Universidad Federico Santa Maria.</p>      <p>Manual SPME holder with fused silica fiber covered with polydimethylsiloxane,    100 &#109; m (Supelco<sup><font size="2">TM</font></sup>). PE Autosystem Gas    Chromatograph with two capillar columns of SBP5 fused silica (60 m x 0.25 mm,    film thickness 0.25 <font face="Symbol">&#109;</font>m) paralelly mounted, with    flame ionization detector (FID, maintained at 270 ºC); and Turbomass 4.1.1 Mass    Spectrometer (70 ev, transfer line 220 ºC); helium as carrier gas (1 ml / min)    oxygen and moisture free, using Supelco<sup><font size="2">TM</font></sup>High    Capacity Heated Carrier Gas Purifier arranged with OMI-2 Indicating Tube. Inyector    temp. 270 ºC. Two different softwares linked to the CG/FID and CG/EM, respectively.    Turbochrom and Turbomass Analytical Workstation with NIST/EPA/MSDC Mass Spectral    Database.</p>      <p>The clean fresh plant material was stored in paper bags for its quickly translate    to Italy. The analysis was carried out in the Istituto Superiore di Sanit&agrave;    in Rome. The sample (81 g) was deposited in a Schott Duran 1 l flask. A Thermolite<font face="Symbol">&#226;</font>    Shimadzu Plug Septum was inserted in the cover through which the holder was    introduced during 30 min. The sample adsorbed in this way was deadsorbed in    a CG-mass apparatus. The components of the mixture were identified determining    their retention times, Kovat Index (<a href="#8">8</a>) and mass spectra, and    comparing these data with those of standard samples. The procedure was repetead    six times, always resulting the same chromatographic pattern.</p>      <p>The composition of the head space of <I>litre</I> (<a href="#t1">Table 1</a>)    is mainly characterized by the presence of monoterpenes, being myrcene (50%),    <font face="Symbol">&#97;</font> -pinene (16%), <I>p</I>-cymene (12%), and limonene    (11%) the most abundant ones. Also a sesquiterpene, caryophyllene (6%), and    the monoterpenes &#98; -pinene and &#97; -phellandrene are present as minor    components.</p>     ]]></body>
<body><![CDATA[<p><small><a name="t1"></a><b>Table 1. </b>Volatile compounds of <i>Lithraea caustica.</i></small></p> <table BORDER =0 cellpadding=4 width=100%>   <tr>      <td colspan="4" valign="TOP" height="17">        <hr size="1">     </td>   </tr>   <tr>      <td width="12%" valign="TOP" height="43">            <p align="center">Peak      </td>     <td width="23%" valign="TOP" height="43" align="center">            <p align="CENTER">Retention time    <br>         (min) </p>     </td>     <td width="25%" valign="TOP" height="43" align="center">            <p align="CENTER">Percent    <br>         (%) </p>     </td>     <td width="15%" valign="TOP" height="43">            <p align="left">Compound      </td>   </tr>   <tr>      <td colspan="4" valign="TOP">        <hr size="1">     </td>   </tr>   <tr>      <td width="12%" valign="TOP">            <p align="center">1      </td>     <td width="23%" valign="TOP" align="center">            <p>13.10      </td>     <td width="25%" valign="TOP" align="center">            <p>16.0      </td>     <td width="15%" valign="TOP">            ]]></body>
<body><![CDATA[<p><font face="Symbol">&#97;</font> -pinene      </td>   </tr>   <tr>      <td width="12%" valign="TOP">            <p align="center">2      </td>     <td width="23%" valign="TOP" align="center">            <p>15.65      </td>     <td width="25%" valign="TOP" align="center">            <p>4.1      </td>     <td width="15%" valign="TOP">            <p><font face="Symbol">&#98;</font> -pinene      </td>   </tr>   <tr>      <td width="12%" valign="TOP">            <p align="center">3      </td>     <td width="23%" valign="TOP" align="center">            <p>16.36      </td>     <td width="25%" valign="TOP" align="center">            <p>50.0      </td>     <td width="15%" valign="TOP">            <p>Myrcene      </td>   </tr>   <tr>      <td width="12%" valign="TOP">            <p align="center">4      </td>     <td width="23%" valign="TOP" align="center">            ]]></body>
<body><![CDATA[<p>17.32      </td>     <td width="25%" valign="TOP" align="center">            <p>1.9      </td>     <td width="15%" valign="TOP">            <p><font face="Symbol">&#97;</font> -phellandrene      </td>   </tr>   <tr>      <td width="12%" valign="TOP">            <p align="center">5      </td>     <td width="23%" valign="TOP" align="center">            <p>18.64      </td>     <td width="25%" valign="TOP" align="center">            <p>11.6      </td>     <td width="15%" valign="TOP">            <p><i>p</i>-cymene      </td>   </tr>   <tr>      <td width="12%" valign="TOP">            <p align="center">6      </td>     <td width="23%" valign="TOP" align="center">            <p>18.90      </td>     <td width="25%" valign="TOP" align="center">            <p>10.7      </td>     <td width="15%" valign="TOP">            ]]></body>
<body><![CDATA[<p>Limonene      </td>   </tr>   <tr>      <td width="12%" valign="TOP">            <p align="center">7      </td>     <td width="23%" valign="TOP" align="center">            <p>49.15      </td>     <td width="25%" valign="TOP" align="center">            <p>5.7      </td>     <td width="15%" valign="TOP">            <p>Caryophyllene      </td>   </tr>   <tr>      <td colspan="4" valign="TOP">       <hr size="1">     </td>   </tr> </table>      <p>However no one of these substances has known allergenic properties    and therefore the idea of considering some of the volatiles as responsible of    such allergies is not probable, although the presence of undetectable active    compounds can not be excluded. </p>      <p>Research will be continued to obtain informations about possible    variations of the volatile content in accordance with the vegative cycle of    the plant, as well as its habitats.</p>     <p align="center"><b>ACKNOWLEDGMENTS</b></p>     <p ALIGN="CENTER"></p>     <p>The authors thank the CONICYT (Chile) <font face="Symbol">&frac34;</font> CNR    (Italy) Scientific Cooperation Programme for Financial Support for Academic    Interchange (MP and GS), and L. Farina and S. Maurizi (ISS) for their collaboration.</p>      ]]></body>
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