<?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>0120-0488</journal-id>
<journal-title><![CDATA[Revista Colombiana de Entomología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Colomb. Entomol.]]></abbrev-journal-title>
<issn>0120-0488</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Colombiana de Entomología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-04882015000200019</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Polymers nanofibers as vehicles for the release of the synthetic sex pheromone of Grapholita molesta (Lepidoptera, Tortricidae)]]></article-title>
<article-title xml:lang="es"><![CDATA[Nanofibras poliméricas como vehículos de eliminación de feromona sexual sintética de Grapholita molesta (Lepidoptera, Tortricidae)]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[BISOTTO-DE-OLIVEIRA]]></surname>
<given-names><![CDATA[RICARDO]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[MORAIS]]></surname>
<given-names><![CDATA[ROSANA M.]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[ROGGIA]]></surname>
<given-names><![CDATA[ISABEL]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[SILVA]]></surname>
<given-names><![CDATA[SANDRA J. N.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[SANT&#8217;ANA]]></surname>
<given-names><![CDATA[JOSUÉ]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[PEREIRA]]></surname>
<given-names><![CDATA[CLÁUDIO N.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidade Federal do Rio Grande do Su Faculdade de Agronomia Departamento de Fitossanidade]]></institution>
<addr-line><![CDATA[Porto Alegre RS]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Tecnano Pesquisas e Servias Ltda.  ]]></institution>
<addr-line><![CDATA[Porto Alegre RS]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="A03">
<institution><![CDATA[,FEPAGRO Centro de Pesquisa em Florestas ]]></institution>
<addr-line><![CDATA[Rio Grande do Sul RS]]></addr-line>
<country>Brazil</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2015</year>
</pub-date>
<volume>41</volume>
<numero>2</numero>
<fpage>262</fpage>
<lpage>269</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-04882015000200019&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-04882015000200019&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-04882015000200019&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[The use of pheromones is a promising alternative in insect management and control. Recently, the incorporation and release of active ingredients from nanofibers has been of interest for agricultural purposes due to their higher surface area to volume ratios. The objective of this study was to produce nanofibers incorporating synthetic sex pheromones from the oriental fruit moth, Grapholita molesta (OFM), using different polymers. The nanofibers with pheromones were produced by electrospinning and were evaluated for: i) homogeneous distribution of OFM pheromone in nanofibers by electroantennography (EAG) tests; ii) dose-responses of OFM males to acetate cellulose nanofibers; iii) EAG responses of OFM males to different polymer nanofibers exposed under controled conditions for up to 5 weeks; iv) attractiveness of G. molesta to nanofibers containing synthetic OFM in field conditions; v) quantification of incorporated pheromone in PCL and PVAc nanofibers using gas chromatography and vi) morphology using scanning electron microscopy. The best field results were achieved in smoother fibers with higher impregnation. Pheromone incorporating nanofiber vehicles were tested that achieved the controlled release of the pheromone for up to three weeks in nanoscale and microscale. The polymer, solvent, and dosage incorporated in the nanofibers were important for controlled delivery. Understanding these factors is important for the development of better pheromone dispensers.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[El uso de feromonas es una alternativa promisora en el manejo y el control de plagas. Recientemente, la incorporación y eliminación de ingredientes activos de las nanofibras han despertado el interés para objetivos agrícolas debido a su elevada área en comparación a la superficie de proporción de volumen. El objetivo de este estudio fue producir nanofibras incorporando la feromona sexual sintética de la mariposa oriental Grapholita molesta (OFM) utilizando diferentes polímeros. Las nanofibras con feromona producidas por la técnica de electrohilado fueran evaluadas por: i) distribución homogénea de feromona de OFM en nanofibras por testes de electroantenografía (EAG); ii) dosis-respuestas de machos de OFM a nanofibras de acetato de celulosa; iii) respuestas EAG de machos de OFM a diferentes nanofibras de polímeros expuestos a condiciones controladas por hasta 5 semanas; iv) atracción de G. molesta a nanofibras conteniendo feromona sintética en condiciones de campo; v) cualificación de feromonas incorporadas de nanofibras de PCL y PVAc por cromatografía de gas y; vi) su morfología utilizando microscopio electrónico de exploración. Los mejores resultados de campo fueron conseguidos en fibras más blandas con mayor impregnación. Diferentes vehículos de nanofibras incorporando feromona fueron analizadas que consiguieron eliminación controlada de feromona hasta tres semanas, en nano y micro escalas. El polímero, solvente y dosis incorporadas en las nanofibras son importantes para la liberación controlada. Entender estos factores es importante para desarrollar mejores distribuidores de feromonas.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Polymer]]></kwd>
<kwd lng="en"><![CDATA[Electrospinning]]></kwd>
<kwd lng="en"><![CDATA[Nanofibers]]></kwd>
<kwd lng="en"><![CDATA[Electroantennography]]></kwd>
<kwd lng="en"><![CDATA[Pheromone]]></kwd>
<kwd lng="es"><![CDATA[Polímero]]></kwd>
<kwd lng="es"><![CDATA[Electrohilado]]></kwd>
<kwd lng="es"><![CDATA[Nanofibras]]></kwd>
<kwd lng="es"><![CDATA[Electroantenografía]]></kwd>
<kwd lng="es"><![CDATA[Feromona]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  	    <p align="center"><font face="verdana" size="4"><b>Polymers nanofibers as vehicles for the release of the synthetic sex pheromone of <i>Grapholita molesta</i> (Lepidoptera, Tortricidae)</b></font></p>  	    <p align="center"><b><font face="verdana" size="3">Nanofibras polim&eacute;ricas como veh&iacute;culos de eliminaci&oacute;n de feromona sexual sint&eacute;tica de <i>Grapholita molesta</i> (Lepidoptera, Tortricidae)</font></b></p>      <p><b><font face="verdana" size="2">RICARDO BISOTTO-DE-OLIVEIRA<sup>1,2</sup>, ROSANA M. MORAIS<sup>3</sup>, ISABEL ROGGIA<sup>2</sup>,</font> <font face="verdana" size="2">SANDRA J. N. SILVA<sup>2</sup>, JOSU&Eacute; SANT&rsquo;ANA<sup>1</sup> and CL&Aacute;UDIO N. PEREIRA<sup>2</sup><sup></sup></font></b></p>     <p><sup>1 </sup><font face="verdana" size="2">Ph. D. PPG-Fitotecnia, Departamento de Fitossanidade, Faculdade de Agronomia Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.</font> <font face="verdana" size="2"><a href="mailto:ricardo.bisotto@ufrgs.br">ricardo.bisotto@ufrgs.br</a>, <a href="mailto:josue.santana@ufrgs.br">josue.santana@ufrgs.br</a>. Corresponding author.     <br> <sup>2</sup> Tecnano Pesquisas e Servias Ltda. Porto Alegre - RS - Brazil.</font>     <font face="verdana" size="2">com.br, <a href="mailto:sandrajussara@tecnano.com.br">sandrajussara@tecnano.com.br</a>, <a href="mailto:claudio@tecnano.com.br">claudio@tecnano.com.br</a>.     <br>     <sup>3</sup> Ph. D. FEPAGRO, Centro de Pesquisa em Florestas - Rio Grande do Sul, RS, Brazil.<a href="mailto:rosana-morais@fepagro.rs.gov.br">rosana-morais@fepagro.rs.gov.br</a>.</font> 	<hr>  	    <p><font face="verdana" size="2"><b>Abstract:</b> The use of pheromones is a promising alternative in insect management and control. Recently, the incorporation and release of active ingredients from nanofibers has been of interest for agricultural purposes due to their&nbsp;higher surface area to volume ratios. The objective of this study was to produce nanofibers incorporating synthetic sex&nbsp;pheromones from the oriental fruit moth, <i>Grapholita molesta</i> (OFM), using different polymers. The nanofibers with&nbsp;pheromones were produced by electrospinning and were evaluated for: i) homogeneous distribution of OFM pheromone&nbsp;in nanofibers by electroantennography (EAG) tests; ii) dose-responses of OFM males to acetate cellulose nanofibers;&nbsp;iii) EAG responses of OFM males to different polymer nanofibers exposed under controled conditions for up to 5&nbsp;weeks; iv) attractiveness of G. molesta to nanofibers containing synthetic OFM in field conditions; v) quantification of&nbsp;incorporated pheromone in PCL and PVAc nanofibers using gas chromatography and vi) morphology using scanning&nbsp;electron microscopy. The best field results were achieved in smoother fibers with higher impregnation. Pheromone&nbsp;incorporating nanofiber vehicles were tested that achieved the controlled release of the pheromone for up to three&nbsp;weeks in nanoscale and microscale. The polymer, solvent, and dosage incorporated in the nanofibers were important&nbsp;for controlled delivery. Understanding these factors is important for the development of better pheromone dispensers.</font></p>  	    <p><font face="verdana" size="2"><b>Key words:</b> Polymer. Electrospinning. Nanofibers. Electroantennography. Pheromone.</font></p> 	<hr>  	    <p><font face="verdana" size="2"><b>Resumen: </b>El uso de feromonas es una alternativa promisora en el manejo y el control de plagas. Recientemente, la incorporaci&oacute;n y eliminaci&oacute;n de ingredientes activos de las nanofibras han despertado el inter&eacute;s para objetivos&nbsp;agr&iacute;colas debido a su elevada &aacute;rea en comparaci&oacute;n a la superficie de proporci&oacute;n de volumen. El objetivo de este&nbsp;estudio fue producir nanofibras incorporando la feromona sexual sint&eacute;tica de la mariposa oriental <i>Grapholita molesta</i>&nbsp; (OFM) utilizando diferentes pol&iacute;meros. Las nanofibras con feromona producidas por la t&eacute;cnica de electrohilado fueran&nbsp;evaluadas por: i) distribuci&oacute;n homog&eacute;nea de feromona de OFM en nanofibras por testes de electroantenograf&iacute;a (EAG);&nbsp;ii) dosis-respuestas de machos de OFM a nanofibras de acetato de celulosa; iii) respuestas EAG de machos de OFM a&nbsp;diferentes nanofibras de pol&iacute;meros expuestos a condiciones controladas por hasta 5 semanas; iv) atracci&oacute;n de G. molesta&nbsp; a nanofibras conteniendo feromona sint&eacute;tica en condiciones de campo; v) cualificaci&oacute;n de feromonas incorporadas&nbsp;de nanofibras de PCL y PVAc por cromatograf&iacute;a de gas y; vi) su morfolog&iacute;a utilizando microscopio electr&oacute;nico de&nbsp;exploraci&oacute;n. Los mejores resultados de campo fueron conseguidos en fibras m&aacute;s blandas con mayor impregnaci&oacute;n.&nbsp;Diferentes veh&iacute;culos de nanofibras incorporando feromona fueron analizadas que consiguieron eliminaci&oacute;n controlada&nbsp;de feromona hasta tres semanas, en nano y micro escalas. El pol&iacute;mero, solvente y dosis incorporadas en las nanofibras son&nbsp;importantes para la liberaci&oacute;n controlada. Entender estos factores es importante para desarrollar mejores distribuidores&nbsp;de feromonas.</font></p>  	    ]]></body>
<body><![CDATA[<p><font face="verdana" size="2"><b>Palabras clave: </b>Pol&iacute;mero. Electrohilado. Nanofibras. Electroantenograf&iacute;a. Feromona.</font></p> 	<hr>  	    <p><font face="verdana" size="3"><b>Introduction</b></font></p>  	    <p><font face="verdana" size="2">The use of pheromones is a promising alternative in the management and control of agricultural pests. These&nbsp;substances have the advantage of high specificity and its&nbsp;use does not harm the environment, compared to traditional&nbsp;methods based on the use of insecticides (Vilela and Mafra-Neto 2001). These attractive compounds can be used in&nbsp;agricultural systems in order to monitor or control insects.&nbsp;The control can be obtained by collecting mass of males, as&nbsp;well as confounding by sexual mating disruption or when the&nbsp;male confusion is caused due to the excess chemical stimulus&nbsp;in the field, preventing mating (Degen <i><i>et al</i></i>. 2005; Kovanci et&nbsp;al. 2005; Charmillot <i><i>et al</i></i>. 1997).</font></p>  	    <p><font face="verdana" size="2">In Brazil, the semiochemicals market has increased considerably, bringing the use of pheromones in many </font><font face="verdana" size="2">cultures as an alternative to control pests important species, such as pink worm <i>Pectinophora gossypiella</i> (Saunders,&nbsp;1843) (Lepidoptera, Gelechiidae), tomato borer <i>Tuta&nbsp;absoluta</i> (Meyrick, 1917) (Lepidoptera, Gelechiidae),&nbsp;cotton boll weevils <i>Antonomus grandis</i> Boheman, 1843&nbsp;(Coleoptera, Curculionidae), sand fly <i>Lutzomyia longipalpis</i>&nbsp;Lutz and Neiva, 1912 (Diptera, Psychodidae), sugar cane&nbsp;borer <i>Diatraea saccharalis</i> (Fabricius, 1794) (Lepidoptera,&nbsp;Pyralidae) among others (ISCA 2013).</font></p>  	    <p><font face="verdana" size="2">Numerous forms of dispersal have been developed for capturing <i>Grapholita molesta</i> (Busk, 1916) (Lepidoptera,&nbsp;Tortricidae), especially pastes, polymer sachets and&nbsp;microencapsulated formulations (ISCA 2013). Recently,&nbsp;the incorporation and release of active ingredients from&nbsp;nanofibers has been of great interest for pharmaceutical and&nbsp;agricultural purposes. Due to their higher surface area to&nbsp;volume ratio, nanofibers have been studied for applications&nbsp;such as drug delivery carriers (Ramakrishna 2005). There is&nbsp;increasing interest in better dispersal of agricultural inputs&nbsp;in crops aiming to increase productivity and lower costs.&nbsp;Electrospinning (ES) is one of the most interesting new&nbsp;methods for drug delivery (Liao <i><i>et al</i></i>. 2008; Xu <i><i>et al</i></i>. 2008;&nbsp;Chakraborty <i><i>et al</i></i>. 2009; Tamaro <i><i>et al</i></i>. 2009; Cui <i><i>et al</i></i>. 2006)&nbsp;and the nanofibers produced can also bring benefits to the&nbsp;agriculture area.</font></p> 	    <p><font face="verdana" size="2">The novel application of nanotechnology, specifically polymeric nanofiber as vehicles for semiochemicals&nbsp;dispensing in agriculture was based on a pioneering study&nbsp;conducted in Germany by Hellmann <i><i>et al</i></i>. (2009). In this&nbsp;study, the authors used the electrospinning technique for&nbsp;producing cellulose acetate nanofibers containing the grape&nbsp;berry moth Lobesia botrana (Denis &amp; Schiffermuller,&nbsp;1775) (Lepidoptera, Tortricidae) synthetic sex pheromone.&nbsp;The authors examined the possibility of incorporating the&nbsp;pheromone of this species within the nanofibers for their use&nbsp;in mating disruption in grapevine orchards.</font></p>  	    <p><font face="verdana" size="2">Subsequently, Lindner <i><i>et al</i></i>. (2011) realized laboratory tests to characterize the nanofibers containing the L. botrana&nbsp;pheromone. Hummel <i><i>et al</i></i>. (2011) performed bioassays in&nbsp;the wind tunnel, also quantifying the mass loss of nanofibers&nbsp;with the aid of analytical balances and by conducting&nbsp;thermogravimetric analysis (TGA). According to Hummel et&nbsp;al. (2011), in the future, these nanofibers vehicles containing&nbsp;pheromone could be deposited directly on the plants, with&nbsp;the aid of portable electrospinning machine, which would&nbsp;allow the coverage of orchard large areas, while increasing&nbsp;the efficiency of the sexual confusion technique. Thus, in&nbsp;theory, it would be possible to produce nanofibers containing&nbsp;an emulsion encapsulating pheromone molecules. These&nbsp;small scale capsules dispersed in continuous polymer phase&nbsp;produced by electrospininng method would have a large area&nbsp;relative to the total, lowering cost and increasing efficiency&nbsp;of the mating disruption strategy.</font></p>  	    <p><font face="verdana" size="2">To date, information about the use of nanofibers as vehicles for dispersing insect pheromones are scarce and&nbsp;largely based on the results obtained by Hellmann <i><i>et al</i></i>.&nbsp;(2009), Hummel <i><i>et al</i></i>. (2011) and Lindner <i><i>et al</i></i>. (2011),&nbsp;which served as parameters in the selection and polymer&nbsp;concentrations pheromones to be investigated. The OFM&nbsp;synthetic pheromone was chosen as a model compound&nbsp;for the study of a nanofibers vehicle because of its known&nbsp;efficiency in the pest management when used in other&nbsp;formulations. Thus, the objectives of this study were: i)&nbsp;evaluate the distribution of OFM pheromone in nanofibers&nbsp;through electroantennographic bioassays; ii) estimate the&nbsp;dose-responses of the oFm males to acetate cellulose&nbsp;nanofibers; iii) measure the EAG responses of OFM males&nbsp;to nanofibers exposed at controled conditions for until 5&nbsp;weeks; iv) evaluate the attractiveness of adult G. molesta&nbsp;to nanofibers containing synthetic sex pheromone in field&nbsp;conditions; v) quantify the pheromone in PVAc and PCL&nbsp;nanofibers by gas chromatography and; vi) determine&nbsp;the morphology of the nanofibers produced by scanning&nbsp;electron microscopy (SEM).</font></p>  	    <p><font face="verdana" size="3"><b>Materials and methods</b></font></p>  	    <p><font face="verdana" size="2"><b>Insects rearing.</b> The G. molesta individuals used in the bioassays were obtained from rearing in BIOECOLAB-</font><font face="verdana" size="2">UFRGS, Department of Crop Protection, Faculty of Agronomy, Federal University of Rio Grande do Sul, kept&nbsp;under controlled conditions (25 &plusmn; 1 &deg;C, 60 &plusmn; 10% relative&nbsp;humidity, and a 16-8 L-D hour photoperiod). The larvae were&nbsp;artificial diet fed, following the methodology of Arioli <i><i>et al</i></i>.&nbsp;(2007) and the adults were fed with water honey solution&nbsp;(15% honey and 5% methylparaben). Only male insects were&nbsp;used in the bioassays.</font></p>  	    ]]></body>
<body><![CDATA[<p><font face="verdana" size="2"><b>Electroantennography (EAG). </b>Insects used in the bioassays had the antennas sectioned at the pedicel and were connected&nbsp;to a bifurcated silver electrode. The antenna&rsquo;s apical and basal&nbsp;ends were attached between the registration and the neutral&nbsp;electrode, respectively. Both were immersed in Spectra&nbsp;360&reg; salt-free gels to enhance the electrical conductivity&nbsp;of the sample. The analogical signal response, measured in&nbsp;millivolts, was captured, amplified and processed with a data&nbsp;acquisition controller (IDAC -4 Syntech&reg;) and subsequently&nbsp;recorded by software (EAG2000, Syntech).</font></p>  	    <p><font face="verdana" size="2">All treatments were individually inserted into Pasteur pipettes. The front end of the pipette was placed into a hole&nbsp;in a metal tube (1cm diameter x 18 cm in length) oriented&nbsp;toward the antenna, having an approximated 1 cm distance.&nbsp;The antennas were subjected to air pulses generated by a flow&nbsp;controller (CS -02, Syntech&reg;) in a volume of 2.5 mL/ 0.5 s with&nbsp;different treatments. It has been stipulated time of one minute&nbsp;between successive stimuli so that the antenna regained&nbsp;their capacity to perceive odorant. The electrophysiological&nbsp;responses of each treatment were recorded in millivolts and&nbsp;the EAG average responses were compared by ANOVA&nbsp;(Tukey test; a = 0.05) using the BioEstat 5.0 statistics program&nbsp;(Ayres <i><i>et al</i></i>. 2007). The antennas were used only once in each&nbsp;repetition. For each EAG response test, 15 virgin males aged&nbsp;between three to seven days were used.</font></p>  	    <p><font face="verdana" size="2"><b>Production of electrospinning nanofibers containing the OFM synthetic sex pheromone. </b>The polymer nanofibers&nbsp;were produced at Tecnano Research and Services Ltd., using&nbsp;a custom made electrospinning machine with a 60 kV HV&nbsp;supply. The syringe pump consisted of 3 ml syringe and a&nbsp;rotary aluminum collector was adjusted to about 60 rpm. In&nbsp;this process, polymer dispersions were prepared dissolved&nbsp;in specific solvents, with and without the synthetic sex&nbsp;pheromone of G. molesta (P9000 - 90 Bedoukian OFM&nbsp;Technical Pheromone). The polymers used were cellulose&nbsp;acetate (CA), polyvinyl acetate (PVAc), polycaprolactone&nbsp;(PCL), polyvinyl pyrrolidone (PVP) and styrene-butadiene-styrene (SBS) copolymer, and its blends. The solvents used&nbsp;were dichloromethane (DCM), dimethylformamide (DMF),&nbsp;ethanol (EtOH), tetrahydrofuran (THF) and water, either&nbsp;alone or in solvent blends. The polymer, or polymer blend,&nbsp;was dissolved using the solvent mix in order to obtain a final&nbsp;polymer concentration ranging from 0.02 to 10% (w/v) of&nbsp;OFM synthetic pheromone that was fed into the ES machine&nbsp;with a syringe pump at a rate of 0.05 ml/min using a 3 ml&nbsp;syringe with a blunted needle. A voltage of 1.81 kV/cm was&nbsp;applied between the needle and the earthed collector. The&nbsp;nanofiber films were deposited onto the glass slides and&nbsp;directly onto the metal stub for microscope analysis. The&nbsp;produced nanofibers were isolated and placed at -10 &deg;C until&nbsp;the time of the bioassays.</font></p>  	    <p><font face="verdana" size="2">Bioassays were conducted in laboratory (EAG) and in field conditions. Initially, based on Hellmann&rsquo;s work (2009),&nbsp;cellulose acetate nanofibers were produced and tested to&nbsp;verify the possibility of incorporating the G. molesta synthetic&nbsp;sex pheromone in these nanoscale matrixes.</font></p> 	    <p><font face="verdana" size="2"><b>Bioassays</b></font></p>  	    <p><font face="verdana" size="2"><b>i) Distribution of OFM pheromone in cellulose acetate&nbsp;nanofibers through electroantennographic tests.</b> Cellulose&nbsp;acetate nanofibers having dimensions of 100 cm<sup>2</sup> were&nbsp;produced containing about 10% OFM pheromone based on&nbsp;polymer concentration. To check the homogeneity of the&nbsp;distribution of the pheromone within the matrixes, each&nbsp;nanofiber was divided into 25 quadrants measuring 4 cm<sup>2</sup> and&nbsp;identified for use in electroantennographic bioassays. The G.&nbsp;molesta male antennal stimuli from each of the quadrants&nbsp;removed from nanofibers was evaluated by the bioactivity&nbsp;test and subjected to ANOVA determinations by Tukey test&nbsp;(a = 0.05).</font></p>  	    <p><font face="verdana" size="2"><b>ii)&nbsp;Dose-responses of the OFM males to cellulose acetate&nbsp;nanofibers. </b>EAG responses of G. molesta males were&nbsp;evaluated after stimuli of CA nanofibers containing 0.02,&nbsp;0.2, 1, 2, 5 and 10% (w/v) synthetic sex pheromone. The&nbsp;EAG dose-response effect was observed after stimuli of the&nbsp;antennae by 2 cm<sup>2</sup> cut pieces nanofibers having different&nbsp;concentrations and offered separately from the lowest to the&nbsp;highest dose. The bioassays data were subjected to ANOVA&nbsp;determinations by Tukey test (a = 0.05).</font></p>  	    <p><font face="verdana" size="2"><b>iii) EAG responses of OFM males to different polymer&nbsp;nanofibers exposed at controled conditions for until 5&nbsp;weeks. </b>The different polymers nanofibers containing 0.2%&nbsp;OFM pheromone and without pheromone were exposed in a&nbsp;controlled environment (25 &deg;C , 14 h photoperiod , 70% RH )&nbsp;for up to five weeks nanofibers: 1) Cellulose acetate; 2) PVAc/&nbsp;PVP; 3) PCL + THF; 4) PCL + DCM. The electrophysiological&nbsp;responses of G. molesta males were compared in the same&nbsp;polymer nanofibers containing pheromone between different&nbsp;exposure times and control (not exposed). The bioassays data&nbsp;were subjected to ANOVA determinations by Tukey test (a&nbsp;= 0.05).</font></p>  	    <p><font face="verdana" size="2"><b>iv) Attractiveness of G. molesta to PVAc/PVP blend and&nbsp;PCL nanofibers containing synthetic sex pheromone in&nbsp;field conditions.</b> The nanofibers containing the OFM sex&nbsp;pheromone attractiveness was evaluated in peach and plum&nbsp;orchards located in the district of Charqueadas and Eldorado&nbsp;do Sul, (RS - Brazil). Delta traps were baited with PVAc/ PVP&nbsp;blend and PCL nanofibers, produced with 2 different solvents,&nbsp;measuring 4 cm<sup>2</sup>, both made in the electrospinning with&nbsp;containing 10% OFM synthetic sex pheromone additivated&nbsp;with antioxidant and UV protector. Delta traps were also&nbsp;for means of comparison, baited with 2 different controls:&nbsp;nanofibers without pheromone, as negative controls; and&nbsp;commercial bait (Isca Lure Grafolita<sup>&reg;</sup>), as positive control in&nbsp;order to evaluate the presence of the oriental fruit moth inner&nbsp;the orchards. The nanofibers were placed inside screened&nbsp;sachets and hanged on the inside top of the traps. These were&nbsp;installed in the plants branches at an approximate height&nbsp;of 1.70 m above the ground and spaced 30 meters apart.&nbsp;The five treatments were arranged in randomized blocks&nbsp;within areas of approximately 0.5 hectares, and had eight&nbsp;repetitions. There were two periods of installation (11/01/11&nbsp;and 01/03/12), from which the attractive field remained for&nbsp;30 days, and weekly number of registered individuals of&nbsp; G. molesta captured. The bioassays data were subjected to&nbsp;Kruskal-Wallis test (Student-Newman; a = 0.05) using the&nbsp;BioEstat 5.0 statistics program (Ayres <i><i>et al</i></i>. 2007).</font></p>  	    <p><font face="verdana" size="2"><b>v) Quantify the pheromone in PVAc and PCL nanofibers&nbsp;by gas chromatography.</b> Oriental fruit moth (OFM)&nbsp;pheromone (Bedoukian Research, Danbury, CT) was used for&nbsp;most of the lab and field tests in this research. This pheromone&nbsp;was chosen because synthetic OFM pheromone is readily&nbsp;available. Synthetic OFM pheromone is a mixture of (Z)-8-dodecen-1-yl acetate, (E)-8-dodecen-1-yl acetate, and (Z)-8-dodecen-1-ol, in a 93:6:1 ratio. The amount of pheromone&nbsp;in the samples was calculated by gas chromatography (GC)&nbsp;Dani model Master A, equipped with a flame photo-ionization&nbsp;detector (PID) and a megabore capillary column (DB-1. 30&nbsp;m x 0.25 mm, 0.53 mm diameter, Agilent Technologies).&nbsp;The initial temperature of the injector was 250 &deg;C and the&nbsp;detector was heated to 200 &deg;C. After the injection of the&nbsp;sample, the temperature of the oven was maintained at 135&nbsp;&deg;C for 2 minutes and then heated to 200 &deg;C with a margin of&nbsp;10&deg; C.min-1. The samples were analised in triplicate and the&nbsp;quantity of volume injected was 1 pL.</font></p>  	    ]]></body>
<body><![CDATA[<p><font face="verdana" size="2"><b>vi) Morphology of the nanofibers produced by scanning&nbsp;electron microscopy (SEM).</b> Images from sEm of the</font> <font face="verdana" size="2">electrospun samples of PCL and PVAc nanofibers were performed on a JEOL - JSM 6060 (JEOL Ltd.) electron&nbsp;microscope. The piece of aluminum foil containing the fibers&nbsp;was mounted on an aluminum stub and sputter-coated with 15&nbsp;nm of gold for analysis. Three SEM photographs from every&nbsp;sample were used for analysis. The analysis was performed&nbsp;by measuring the diameter in every photograph 30 times. The&nbsp;software used for the measurements and statistical analysis&nbsp;was ImageJ 1.47x.</font></p>  	    <p><font face="verdana" size="2">The all data were submitted to normality and homoscedasticity tests.</font></p>  	    <p><font face="verdana" size="3"><b>Results</b></font></p> 	    <p><font face="verdana" size="2"><b>i)&nbsp;Distribution of OFM pheromone in cellulose acetate&nbsp;nanofibers through electroantennographic bioassays.</b></font> <font face="verdana" size="2">There was no significant difference (P &gt; 0.05) between the electrophysiological responses of G. molesta antennae male&nbsp;within the different portions coming from the different&nbsp;quadrants of the nanofibers. This result indicates that&nbsp;the synthetic sex pheromone of G. molesta was evenly&nbsp;distributed in all parts of the cellulose acetate nanofiber. That&nbsp;is an important find since the electrospinning is a random mat&nbsp;of nanofibers and validate the fact that we are using cut pieces&nbsp;of an entire mat.</font></p>  	    <p><font face="verdana" size="2"><b>ii) Dose-responses of the OFM males to cellulose&nbsp;acetate nanofibers. </b>The electrophysiological responses&nbsp;of G. molesta males subjected to stimuli with nanofibers&nbsp;containing different percentages of pheromone were&nbsp;statistically significant (F = 24.27, df = 6, P &lt; 0.0001)&nbsp;(<a href="#(fig1)">Fig. 1</a>). The sizes of electrophysiological responses were&nbsp;similar among treatments nanofibers containing 0.02,&nbsp;0.2 and 1% and between treatments containing 2, 5 and&nbsp;10% pheromone. This result demonstrates the presence of&nbsp;pheromone in the nanofiber, whereas the antennae of G.</font> <font face="verdana" size="2">molesta males demonstrated bioactivity to stimuli, increasing the size of EAG response as a function of the concentration&nbsp;of pheromone in the nanofiber.</font></p>    <p align="center"><a name="(fig1)"><img src="img/revistas/rcen/v41n2/v41n2a19fig1.gif"></a></p>  	    <p><font face="verdana" size="2"><b>iii) EAG responses of OFM males to different polymer&nbsp;nanofibers exposed at controled conditions for until 5&nbsp;weeks.</b> The EAG responses of G. molesta males showed a&nbsp;significant difference only between 10% CA polymer in&nbsp;contrast with (8:2% PVAc/PVP polymers) and 10% PCL&nbsp;from DCM polymer, while the other had no difference (F&nbsp;= 3.05, df = 4, P &gt; 0.05) (<a href="#(fig2)">Fig. 2</a>). When compared to their&nbsp;respective controls, the treatments containing pheromone&nbsp;produced significantly greater EAG responses, except for&nbsp;treatment 5 (6:4% SBS/ PVAc).</font></p>    <p align="center"><a name="(fig1)"><img src="img/revistas/rcen/v41n2/v41n2a19fig2.gif"></a></p>  	    <p><font face="verdana" size="2">The formulation with the polymer 10% PCL with THF (Polymer 3) showed the greater retention of the pheromone&nbsp;producing electrophysiological responses equal to the new&nbsp;fiber until the third week of exposure, after being significantly&nbsp;equal to the control matrix. Thus, this formulation was one of&nbsp;those chosen for the preparation of nanofibers that were used in&nbsp;the experiments under field conditions. The formulation 10%&nbsp;PCL with DCM (Polymer 4) triggered electrophysiological&nbsp;responses similar to the new fiber only in the first week,&nbsp;decreased in relation to this, the other exposure times.&nbsp;With respect to 8:2% PVAc/ PVP (Polymer 2), although all&nbsp;treatments exhibited have lower response than the new fiber,&nbsp;these were stable and did not differ between itself from the&nbsp;first to the fifth week (<a href="#(fig3)">Fig. 3</a>). Furthermore, this was the only&nbsp;polymer which triggered electrophysiological responses were&nbsp;significantly higher after the fifth week of exposure compared&nbsp;to its control (no addition of pheromone in the fiber).</font></p>    <p align="center"><a name="(fig3)"><img src="img/revistas/rcen/v41n2/v41n2a19fig3.gif"></a></p>  	    ]]></body>
<body><![CDATA[<p><font face="verdana" size="2">For field conditions bioassays, only the nanofibers that showed the best characteristics of homogeneity, retention and&nbsp;gradual release of pheromone, under laboratory conditions,&nbsp;were selected (PVAc and PCL), while the others made from&nbsp;cellulose acetate and SBS/ PVAc were eliminated for these&nbsp;experiments.</font></p>  	    <p><font face="verdana" size="2"><b>iv) Attractiveness of adult G. molesta to PVAc and PCL&nbsp;nanofibers containing synthetic OFM sex pheromone&nbsp;in field conditions.</b> The Delta traps baited with nanofibers&nbsp;made of 8:2% PVAc/ PVP and 10% PCL with THF captured&nbsp;13.75 &plusmn; 0.38 males and 9.78 &plusmn; 0.32 on average, respectively,&nbsp;did not differ from each other (P &gt; 0.05). These averages&nbsp;were significantly higher than their respective controls (2.12&nbsp;and 2.75 males on average), however, were lower than the&nbsp;average obtained with the commercially available bait (Isca&nbsp;Lure Grafolita&reg;) (39.75 &plusmn; 0.51) (P &lt; 0.05, H = 26.75, df =&nbsp;4) (<a href="#(fig4)">Fig. 4</a>).</font></p>    <p align="center"><a name="(fig4)"><img src="img/revistas/rcen/v41n2/v41n2a19fig4.gif"></a></p> 	    <p><b><font face="verdana" size="2">v) Quantify the pheromone in PVAc and PCL nanofibers.</font></b> <font face="verdana" size="2">Pheromone content in the tested nanofibers. The calibration curve showed a good repetition of the method (R<sup>2</sup> = 0.99).&nbsp;After validating the GC measurement for measuring the&nbsp;pheromone content in nanofibers, the following nanofibers&nbsp;were evaluated: PVAc/ PVP, PCL with THF and PCL with&nbsp;DCM.</font></p>  	    <p><font face="verdana" size="2">The three nanofibers samples with impregnated dodecenyl acetate were evaluated by GC analysis (<a href="#(tab2)">Table 2</a>). The PCL&nbsp;nanofibers produced using the solvent THF had the higher&nbsp;pheromone content. The different percentage of pheromone&nbsp;based on polymer mass found using the same polymer&nbsp;blend suggests that the solvent and co-solvent selection had&nbsp;importance to the encapsulation efficiency.</font></p>    <p align="center"><a name="(tab2)"><img src="img/revistas/rcen/v41n2/v41n2a19tab2.gif"></a></p>  	    <p><b><font face="verdana" size="2">vi) Morphology of the nanofibers produced by scanning&nbsp;electron microscopy (SEM) and through this morphology.</font></b> <font face="verdana" size="2">Following are presented the images obtained for the samples analyzed in scanning electron microscopy. The <a href="#(fig5)">figure 5</a> shows&nbsp;that the electronic microscope images of PCL nanofibers&nbsp;produced using the THF solvent had the format of beads-on-strings (A), while smoother fibers (B) were obtained with the&nbsp;pheromone addiction. The nanofibers containing the active&nbsp;(0.835 &plusmn; 0.4 mM), had higher mean diameter greater than&nbsp;the control (0.370 &plusmn; 0.2 mM) (<a href="#(tab1)">Table 1</a>). The increase in the&nbsp;average diameter of the nanofibers was statistically significant&nbsp;P &lt; 0.05. <a href="#(fig5)">Figures 5</a> and 6 show photomicrographs of fibers&nbsp;from polycaprolactone dissolved in organic solvent mixture.&nbsp;The same features were seen in <a href="#(fig6)">figure 6</a> for the fibers made&nbsp;using the solvent DCM. In that second case, there were more&nbsp;beads than the first. The nanofibers containing the active&nbsp;(0.681 &plusmn;0.3 mM), showed larger diameter compared to&nbsp;control (0.442 &plusmn; 0.1 mM). The increase of average diameter&nbsp;of nanofibers showed at <a href="#(tab1)">table 1</a> was statistically significant&nbsp;(P &lt; 0.05).</font></p>    <p align="center"><a name="(fig5)"><img src="img/revistas/rcen/v41n2/v41n2a19fig5.gif"></a></p>    <p align="center"><a name="(fig6)"><img src="img/revistas/rcen/v41n2/v41n2a19fig6.gif"></a></p>    <p align="center"><a name="(tab1)"><img src="img/revistas/rcen/v41n2/v41n2a19tab1.gif"></a></p>  	    ]]></body>
<body><![CDATA[<p><font face="verdana" size="2">On the other side, the nanofibers produced with PVAc/ PVP were smoother (<a href="#(fig7)">Fig. 7</a>). The fibers containing the active&nbsp;(1.217 &plusmn; 0.5 mM) had greater average diameter compared to&nbsp;control (1.630 &plusmn; 0.7 mM). This increase in diameter was also&nbsp;statistically significant (P &lt; 0.05) (<a href="#(tab1)">Table 1</a>).</font></p>    <p align="center"><a name="(fig7)"><img src="img/revistas/rcen/v41n2/v41n2a19fig7.gif"></a></p>  	    <p><b><font face="verdana" size="3">Discussion</font></b></p>  	    <p><font face="verdana" size="2">The present study was based upon the few papers using nanofiber as pheromone vehicles from the literature. The&nbsp;nanofibers polymer selection was firstly based on study&nbsp;carried out by Hellmann <i><i>et al</i></i>. (2009), where cellulose&nbsp;acetate film were tested in vitro and found to be an excellent&nbsp;vehicle for the transport of European grape berry moth&nbsp;pheromone Lobesia botrana due to features such as the&nbsp;ability to incorporate pheromone molecules and its rate of </font><font face="verdana" size="2">release for weeks straight. In the present study, the efficacy of incorporation and release of pheromone from nanofiber mats&nbsp;and its even distribution inside the matrixes was evaluated by&nbsp;the bioassays proposed. Pheromones impregnation dosages&nbsp;that caused major electrophysiological responses of G.&nbsp;molesta males concentrations were 2 to 10%.</font></p>  	    <p><font face="verdana" size="2">Because of the short duration of the cellulose acetate nanofiber in the initial tests, new polymers and its blends&nbsp;were also tested. Because of the chemical similarity between&nbsp;PVAc and PCL, both esters, with the major G. molesta&nbsp;component pheromone, dodecenyl acetate, those polymers&nbsp;were chosen. Styrene-butadiene-styrene was selected&nbsp;because rubber septa are known dispenser for pheromones&nbsp;and that the longer carbon chain of the principal component-dodecenyl acetate- is non polar. Polyvinyl pyrrolidone was&nbsp;preferred for blending with PVAc to add polar group and&nbsp;an amphyphilic character for increase the solubilization&nbsp;of the dodecenol molecule, other pheromone component.&nbsp;Cellulose acetate polymer was less efficient than PVAc and&nbsp;PCL the bioassays performed in this study, when assessed&nbsp;in vivo by electrophysiological responses of insects, in&nbsp;respect to pheromonal retention, and also for environment&nbsp;exposed durability. So these polymers were selected for the&nbsp;following testing.</font></p>  	    <p><font face="verdana" size="2">The polyvinyl acetate blend (PVAc/ PVP), despite a drop in electrophysiological responses when the fibers were&nbsp;exposed to environment, the response remained throughout&nbsp;the five weeks at the same rate of release. The blend PVAc/&nbsp;PVP is extensively studied in the pharmaceutical industry&nbsp;due to the efficiency of drug release, are ideal for this reason&nbsp;the healing drug delivery, requiring a release and prolonged&nbsp;linear (Jannesari <i><i>et al</i></i>. 2011). Such behavior is regarded as&nbsp;one of the properties assigned to this amphiphilic blend.&nbsp;Since the (Z)-8-dodecenyl acetate molecule has polar and&nbsp;non-polar groups, the amphiphilic character match each of&nbsp;these groups, and this could be one of the reasons of the&nbsp;controlled release achieved.</font></p>  	    <p><font face="verdana" size="2">The polymer PCL showed the longest pheromone retention period even after exposure to environment, which is&nbsp;an important feature for agricultural purposes. This polymer&nbsp;is biodegradable polyester, aliphatic, what is also a desirable&nbsp;feature when applications to agriculture are in concern.&nbsp;Aliphatic polyesters have been employed as slow-release&nbsp;agents in agriculture for a long time (Sinclair 1973). They&nbsp;degrade into natural materials harmless to the environment&nbsp;while slowly releasing the encapsulated herbicides or&nbsp;pesticides. Because of these properties, two different&nbsp;formulations were tested, having two different solvent&nbsp;mixes, DCM or THF blended with DMF solvent. These two&nbsp;formulations have different impregnating efficiency when&nbsp;GC measured, as will be discussed below.</font></p>  	    <p><font face="verdana" size="2">Analyzing the electronic microscope images, the PCL nanofibers were all beads-on-strings, although the fibers&nbsp;became smoother with the pheromone addiction. In the images&nbsp;6A and 6B, it is observed that change. The reduction of the&nbsp;beads and reduction of fiber diameter are two morphologic&nbsp;characteristics that result from the increased polarity of the&nbsp;electrospinning solution (Tungprapa <i><i>et al</i></i>. 2007). The solvent&nbsp;used was tetrahydrofuran, an aprotic solvent with dielectric&nbsp;constant (e) 7.58 to 20 <sup>o</sup>C. The nanofibers containing the&nbsp;active (0.835 &plusmn; 0.4 mM), had higher mean diameter greater&nbsp;than the control (0.370 &plusmn; 0.2 mM). The increase in the average&nbsp;diameter of the nanofibers was statistically significant P&nbsp;&lt; 0.05. The nanofibers in the form of bead-in-strings were&nbsp;becoming flat with the incorporation of the active ingredient&nbsp;(<a href="#(fig5)">Fig. 5</a>).</font></p>  	    <p><font face="verdana" size="2">The same features were seen in <a href="#(fig6)">figure 6</a> for the fiber made from polycaprolactone dissolved in DCM, although with more&nbsp;beads than the based on THF. The solvent dichloromethane&nbsp;is an aprotic solvent with a higher dielectric constant (e) 9.08&nbsp;to 20 &deg;C. The nanofibers containing the active (0.681 &plusmn; 0.3&nbsp;mM), showed larger diameter compared to control (0.442&nbsp;&plusmn; 0.1 mM) (<a href="#(tab1)">Table 1</a>). The increase of average diameter of&nbsp;nanofibers was statistically significant (P &lt; 0.05).</font></p>  	    <p><font face="verdana" size="2">In the third case, the nanofibers produced with PVAc/ PVP were smoother. The fibers containing the active&nbsp;(1.217 &plusmn; 0.5 mM) had greater average diameter compared&nbsp;to control (1.630 &plusmn; 0.7 mM). This increase in diameter&nbsp;was also statistically significant (P &lt; 0.05). Smoother, or&nbsp;uniform, fibers with fewer beads are desirable, since they&nbsp;indicate that they are more resistant and more compatible&nbsp;(Doshi and Reneker 1995). One way to reduce the amount&nbsp;of beads is to increase solution conductivity (Ramakrishna&nbsp; <i><i>et al</i></i>. 2005), which is obtained by selection of more polar&nbsp;solvents by the addition of salts to the solution, or by adding&nbsp;an active ingredient with polarity, which seems to have been&nbsp;the case under discussion. The smoother fiber should have&nbsp;occurred due to the high dielectric constant of the solution,&nbsp;higher than in the previous cases cited solvents (dielectric&nbsp;constant of 80 and 24, at 20 <sup>o</sup>C, for the cases of water and&nbsp;ethanol).</font>	</p> 	    ]]></body>
<body><![CDATA[<p><font face="verdana" size="2">In the PVAc/ PVP fibers, there was also interweaving of the fibers, which is desirable because the increased resistance&nbsp;of the resulting film, but it is noted fusion of the fibers, which&nbsp;may indicate a case of wet-spinning, when the solvent is not&nbsp;evaporated completely in route to the collector metal (Tang&nbsp; <i><i>et al</i></i>. 2009). That signifies that the solvent has boiling point&nbsp;higher than other solvents used and not evaporated completely&nbsp;until reaching the metal collector. This high boiling point of&nbsp;the solvent used is the reason for the case of wet-spinning.&nbsp;In this case, increasing the distance collector or a change in&nbsp;concentration of each solvent can optimize the solution. This&nbsp;was not done because it standardized the distance between&nbsp;the needle and collector for 3 samples and their respective&nbsp;controls.</font></p>  	    <p><font face="verdana" size="2">Yang <i><i>et al</i></i>. (2004) investigated the effects of solvents, including DCM, EtOH, DMF and mixtures of solvents,&nbsp;the morphology and diameter of PVP nanofibers obtained&nbsp;by ES. In solvent systems simple to 4% by weight of PVP,&nbsp;the nanofibers electrospining from ethanol were smooth,&nbsp;whereas the nanofibers from DMF and DCM exhibited&nbsp;beads-on-strings structure. In systems solvent mixtures, a&nbsp;mixture of ethanol/ DMF, with a mass ratio of 50/50 was&nbsp;obtained as a good solvent for PVP producing nanofibers&nbsp;with diameters as small as 20 nm. In a solvent mixture such&nbsp;as PVP concentration was increased from 4 to 8% by weight,&nbsp;the fiber diameter increased from 20 to 50 nm, no significant&nbsp;change in size distribution.</font></p>  	    <p><font face="verdana" size="2">It is well known that physicochemical properties such as dielectric constant, boiling point, surface tension and&nbsp;viscosity of the polymer solution are important factors to&nbsp;define the morphological characteristics of the nanofibers&nbsp;generated. The polymer concentration and molecular weight&nbsp;of the polymer is also related to the latter property. Thin&nbsp;and uniform nanofibers were produced by electrospinning&nbsp;by authors from PVP solutions in solvents with a dielectric&nbsp;constant significantly high, low surface tension and low&nbsp;viscosity (Chuangchote <i><i>et al</i></i>. 2009).</font></p> 	    <p><font face="verdana" size="2">The field exposure experiment demonstrated that although the PVAc/ PVP and tested polyester 10% PCL with THF had&nbsp;statistically superior capture than their respective controls,&nbsp;it was lower than that obtained with the commercial rubber&nbsp;septum. The results also showed that higher pheromone&nbsp;content is related to higher capture. The reason may be that&nbsp;the mass of the commercial septum is much higher than the&nbsp;nanofiber.</font></p>  	    <p><font face="verdana" size="2">Thus, these results indicate that adjustments are needed to maximize the ability to capture the field with the use of these&nbsp;polymers, as well as further investigation of other polymers&nbsp;capable of use in the manufacture of nanofibers used as&nbsp;dispersing pheromones.</font></p>  	    <p><font face="verdana" size="2">The results of chromatographic analysis showed a greater pheromone impregnation of PCL with THF nanofibers (<a href="#(tab1)">Table&nbsp;1</a>). These nanofibers had the greater pheromone persistence&nbsp;in the environment. The pheromone content was also higher&nbsp;than that found in PVAc/ PVP blend. The validation of the&nbsp;technique for pheromone dosage in nanofibers was obtained&nbsp;after the field trials that was the reason we could not use&nbsp;fibers with similar content of pheromone. For future studies&nbsp;the pheromone content should be normalized in order to&nbsp;determine what are the predominant factors involved in the&nbsp;controlled release of pheromone.</font></p>  	    <p><font face="verdana" size="2">The results of <a href="#(tab1)">table 1</a> and SEM images shows that there is a relationship between the appearance of the nanofibers, the&nbsp;pheromone content in each fiber and the controlled delivery&nbsp;of the nanofibers. Other studies should be done to assess&nbsp;the relationship between the morphology of the fibers, the&nbsp;polymer utilized and the pheromone release. The polymer,&nbsp;solvent and dosage incorporated in the nanofibers are&nbsp;important to the controlled delivery. Understand these factors&nbsp;is important in order to develop better pheromone dispensers.</font></p>  	    <p><font face="verdana" size="3"><b>Acknowledgements</b></font></p>  	    <p><font face="verdana" size="2">The authors are grateful for the financial support provided by Brazil&rsquo;s National Council for Scientific and Technological&nbsp;Development (CNPq), FAPERGS (Fundagao de Amparo&nbsp;&agrave; Pesquisa do Estado do Rio Grande do Sul) and FINEP&nbsp;(Financiadora de Estudo e Projetos).</font></p>  	    <p><b><font face="verdana" size="3">Literature cited</font></b></p>  	    ]]></body>
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