<?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>2007-3380</journal-id>
<journal-title><![CDATA[Revista bio ciencias]]></journal-title>
<abbrev-journal-title><![CDATA[Revista bio ciencias]]></abbrev-journal-title>
<issn>2007-3380</issn>
<publisher>
<publisher-name><![CDATA[Universidad Autónoma de Nayarit]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2007-33802023000100408</article-id>
<article-id pub-id-type="doi">10.15741/revbio.10.e1410</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[High Performance Liquid Chromatography coupled Diode Array Detector (HPLC-DAD) method development and validation for the quantification of triclosan in toothpaste.]]></article-title>
<article-title xml:lang="es"><![CDATA[Desarrollo de un método mediante Cromatografía de Líquidos de Alta Eficiencia acoplado a un detector de arreglo de diodos (HPLC-DAD) y su validación para la cuantificación de triclosán en pasta de dientes.]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Muñiz-Valencia]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez-Pérez]]></surname>
<given-names><![CDATA[M. A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Barragan-Mendoza]]></surname>
<given-names><![CDATA[L.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cruz-Torres]]></surname>
<given-names><![CDATA[L.F. De la]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Macias-López]]></surname>
<given-names><![CDATA[E.G.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Maldonado-Michel]]></surname>
<given-names><![CDATA[M.A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez-Aguilar]]></surname>
<given-names><![CDATA[B.A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ceballos-Magaña]]></surname>
<given-names><![CDATA[S.G.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Colima Facultad de Ciencias Químicas ]]></institution>
<addr-line><![CDATA[Colima ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad de Colima Facultad de Ciencias ]]></institution>
<addr-line><![CDATA[Colima ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2023</year>
</pub-date>
<volume>10</volume>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2007-33802023000100408&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2007-33802023000100408&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2007-33802023000100408&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Triclosan is used in many healthcare products as a broad-spectrum antimicrobial and disinfectant agent; however, it is currently considered an emerging pollutant. The present study aimed to develop an analytical method using liquid chromatography coupled to a Diode Array Detector for triclosan determination in toothpaste. Method development involved the optimization of separation and sample preparation. For chromatographic separation optimization, different Reverse Phase columns and elution systems were tested. After different experiments, chromatographic separation was optimized employing the following conditions: a Symmetry C18 column at 30 °C, 0.6 mL/min flow-rate, running time of about 3 minutes, and wavelength detection at 225 nm. To optimize toothpaste sample preparation, a response surface methodology using a Box-Behnken fractional factorial design was chosen. The sample preparation consisted of extracting 0.2 g of the sample by sonication for 7 minutes using 2 mL of methanol. According to the International Conference on Harmonization and European Commission Decision 200/657/EC guidelines, the developed method was validated. The developed analytical method was found fast, economic, linear, sensitive, precise, and robust and allowed to quantify triclosan in different healthcare products.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN El triclosán se utiliza en muchos productos para el cuidado de la salud como agente antimicrobiano y desinfectante de amplio espectro; sin embargo, actualmente se considera un contaminante emergente. El presente estudio tuvo como objetivo desarrollar un método de cromatografía de líquidos acoplada a un detector de arreglo de diodos para la determinación de triclosán en pasta de dientes. El desarrollo del método implicó la optimización de la separación y la preparación de muestras. Para la optimización de la separación cromatográfica, se probaron diferentes columnas de Fase Inversa y sistemas de elución. Después de diferentes experimentos, se optimizó la separación cromatográfica empleando las siguientes condiciones: una columna Symmetry C18 a 30 °C, velocidad de flujo de 0.6 mL/min, tiempo de análisis de aproximadamente 3 minutos y detección de longitud de onda a 225 nm. Para optimizar la preparación de la muestra de pasta de dientes, se eligió una metodología de superficie de respuesta que utiliza un diseño factorial fraccional Box-Behnken. La preparación de la muestra consistió en extraer 0.2 g de muestra mediante sonicación durante 7 minutos utilizando 2 mL de metanol. El método desarrollado fue validado de acuerdo con la Conferencia Internacional sobre Armonización y las directrices de la Decisión de la Comisión Europea 200/657/CE. El método analítico desarrollado se determinó como rápido, económico, lineal, sensible, preciso y robusto y permitió cuantificar triclosán en diferentes productos de salud.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Contaminantes emergentes]]></kwd>
<kwd lng="en"><![CDATA[alterador endocrino]]></kwd>
<kwd lng="en"><![CDATA[HPLC-DAD]]></kwd>
<kwd lng="en"><![CDATA[triclosan]]></kwd>
<kwd lng="en"><![CDATA[productos de cuidado personal]]></kwd>
<kwd lng="es"><![CDATA[Emerging pollutants]]></kwd>
<kwd lng="es"><![CDATA[endocrine disruptor]]></kwd>
<kwd lng="es"><![CDATA[HPLC-DAD]]></kwd>
<kwd lng="es"><![CDATA[triclosán]]></kwd>
<kwd lng="es"><![CDATA[personal care products.]]></kwd>
</kwd-group>
</article-meta>
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