<?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>0120-100X</journal-id>
<journal-title><![CDATA[Revista ION]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. ion]]></abbrev-journal-title>
<issn>0120-100X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Industrial de Santander]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-100X2020000100079</article-id>
<article-id pub-id-type="doi">10.18273/revion.v33n1-2020008</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Nanopartículas de plata funcionalizadas in situ con D-limoneno: efecto en la actividad antibacteriana]]></article-title>
<article-title xml:lang="en"><![CDATA[Silver nanoparticles functionalized in situ with D-Limonene: effect on antibacterial activity]]></article-title>
<article-title xml:lang="pt"><![CDATA[Nanopartículas de prata funcionalizadas in situ com D-Limoneno: efeitona atividade antibacteriana]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Echeverry-Chica]]></surname>
<given-names><![CDATA[Julián]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Naranjo-Díaz]]></surname>
<given-names><![CDATA[Andrea]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Araque-Marín]]></surname>
<given-names><![CDATA[Pedronel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad EIA  ]]></institution>
<addr-line><![CDATA[Envigado ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Laboratorio Clínico Hematológico  ]]></institution>
<addr-line><![CDATA[Medellín ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2020</year>
</pub-date>
<volume>33</volume>
<numero>1</numero>
<fpage>79</fpage>
<lpage>92</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-100X2020000100079&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-100X2020000100079&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-100X2020000100079&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Este estudio se centró en la formulación y caracterización de nanopartículas de plata (AgNP) funcionalizadas con d-limoneno. Las nanopartículas se funcionalizaron por inversión de fase y la síntesis de las nanopartículas se realizó in situ; se determinó el tamaño de partícula por difracción laser, potencial zeta y estabilidad coloidal óptica utilizando Multiscan 20 por un periodo de 24 horas a 37 °C; se determinó la concentración mínima inhibitorio (CMI) y la concentración mínima bactericida (CMB) del material formulado sobre las bacterias Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 29213, Klebsiella oxytoca ATCC 700324, Enterococcus casseliflavus ATCC 700327, Escherichia coli BLEE+, Pseudomona aeruginosa resistente a carbapenémicos. Las nanopartículas presentaron estabilidad coloidal a una concentración de d-limoneno del 3,93 %, iones plata al 1,61x0-3 %, coadyuvante no iónico al 24 % y ácido ascórbico al 5,88 %; cómo sistema regulador se utilizó ácido cítrico/citrato (1:1) 0,48M para un pH de 4,5. La formulación se clasificó como un sistema polidisperso (PD = 0,0851), con una potencial zeta de -11,6 mV y tamaño promedio de partícula de 81,5 ± 0,9 nm. Se evidenció una velocidad de migración de partícula de -0,199 ± 0,006 mm h-1, un perfil de transmisión constante y perfil de retrodispersión con variaciones del 10 %, lo que representa una formulación estable. Las nanopartículas presentaron una CMI y una CMB de 28 &#956;g mL-1 (5,6x10-2 % d-limoneno y 4,7x10-5 % AgNP) contra todas las bacterias probadas.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract This study focused on the formulation and characterization of silver nanoparticles (AgNP) functionalized with d-limonene. The nanoparticles were functionalized by phase inversion and the synthesis of the nanoparticles was performed in situ; the particle size was determined by laser diffraction, zeta potential and colloidal optical stability using Multiscan 20 for a period of 24 hours at 37 °C; the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (CMB) of the formulated material on the bacterias Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 29213, Klebsiella oxytoca ATCC 700324, Enterococcus casseliflavus ATCC 700327, Escherichia coli BLEE, Pseudomona aeruginosa resistant to carbapenems. The nanoparticles showed colloidal stability at a concentration of 3.93 % d-limonene, 1.6x10-3 % silver ions, 24 % non-ionic adjuvant and 5.88 % ascorbic acid, citric acid/citrate was used as a regulatory system (1:1) 0.48 M for a pH of 4.5. The formulation was classified as a polydispersed system (PD = 0.0851), with a zeta potential of -11.6 mV and average particle size of 81.5 ± 0.9 nm. A particle migration rate of -0.199 ± 0.006 mm h-1 was evidenced, a constant transmission profile, a backscatter profile with variations of 10 %, which represents a stable formulation. The nanoparticles presented an MIC and an MIB of 28 &#956;g mL-1 (5.6x10-2 % limonene, 4.7x10-5 % AgNP) against all the bacteria tested.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo Este estudo focou na formulação e caracterização de nanopartículas de prata AgNP funcionalizadas com d-limoneno. As nanopartículas foram funcionalizadas por inversão de fase e a síntese das nanopartículas foi realizada in situ; o tamanho das partículas foi determinado por difração a laser, potencial zeta e estabilidade óptica coloidal usando o Multiscan 20 por um período de 24 horas a 37 °C; a concentração inibitória mínima (CMI) e a concentração bactericida mínima (CMB) do material formulado na bactéria Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 29213, Klebsiella oxytoca ATCC 700324, Enterococcus casseliflavus ATCC 700327, Escherichia coli BLEE, Pseudomona aeres. As nanopartículas apresentaram estabilidade coloidal na concentração de 3,93 % de d-limoneno, 1,6x10-3 % de íons de prata, 24 % de adjuvante não iônico e 5,88 % de ácido ascórbico, ácido cítrico/ citrato (1:1) 0,48 M foi usado como sistema regulador para um pH de 4,5. A formulação foi classificada como um sistema polidisperso (PD = 0,0851), com um potencial zeta de -11,6 mV e tamanho médio de partícula de 81,5 ± 0,9 nm. Era evidente uma taxa de migração de partículas de -0,199 ± 0,006 mm h-1, um perfil de transmissão constante, um perfil de retroespalhamento com variações de 10 %, o que representa uma formulação estável. A nanopartículas apresentou CIM e MIB de 28 &#956;g mL-1 (d-limoneno 5,6x10-2 %, AgNP 4,7x10-5 %) contra todas as bactérias testadas.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Nanopartículas de Plata]]></kwd>
<kwd lng="es"><![CDATA[Inversión de Fases]]></kwd>
<kwd lng="es"><![CDATA[Resistencia Bacteriana]]></kwd>
<kwd lng="es"><![CDATA[Concentración Mínima Inhibitoria]]></kwd>
<kwd lng="en"><![CDATA[Silver Nanoparticles]]></kwd>
<kwd lng="en"><![CDATA[Phase Inversion]]></kwd>
<kwd lng="en"><![CDATA[Bacterial Resistance]]></kwd>
<kwd lng="en"><![CDATA[Minimal Inhibitory Concentration]]></kwd>
<kwd lng="pt"><![CDATA[Nanopartículas de Prata]]></kwd>
<kwd lng="pt"><![CDATA[Inversão de Fase]]></kwd>
<kwd lng="pt"><![CDATA[Resistência Bacteriana]]></kwd>
<kwd lng="pt"><![CDATA[Concentração Inibitória Mínima]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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<label>44</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Katz]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Baltz]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Natural product discovery: past, present, and future]]></article-title>
<source><![CDATA[J Ind Microbiol Biotechnol]]></source>
<year>2016</year>
<volume>43</volume>
<numero>2-3</numero>
<issue>2-3</issue>
<page-range>155-76</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
