<?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>0034-7418</journal-id>
<journal-title><![CDATA[Revista Colombiana de Ciencias Químico - Farmacéuticas]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. colomb. cienc. quim. farm.]]></abbrev-journal-title>
<issn>0034-7418</issn>
<publisher>
<publisher-name><![CDATA[Departamento de Farmácia, Facultad de Ciencias, Universidade Nacional da Colombia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-74182020000300675</article-id>
<article-id pub-id-type="doi">10.15446/rcciquifa.v49n3.91337</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Thermodynamic analysis and preferential solvation of gatifloxacin in DMF + methanol cosolvent mixtures]]></article-title>
<article-title xml:lang="es"><![CDATA[Análisis termodinâmico y solvatación preferencial de gatifloxacina en mezclas cosolventes DMF + metanol]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rojas-Motta]]></surname>
<given-names><![CDATA[Mónica]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rojas-Motta]]></surname>
<given-names><![CDATA[Jhon Edinson]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Diaz-Jimenez]]></surname>
<given-names><![CDATA[Jorge Luis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bahos-Narváez]]></surname>
<given-names><![CDATA[Fabio Andrés]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Blanco-Márquez]]></surname>
<given-names><![CDATA[Joaquín H.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ortiz]]></surname>
<given-names><![CDATA[Claudia Patricia]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[Daniel Ricardo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Cooperativa de Colombia Department of Engineering ]]></institution>
<addr-line><![CDATA[Neiva Huila]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Centro de Industria la Empresa y los Servicios, Tecnoparque Nodo Neiva  ]]></institution>
<addr-line><![CDATA[Neiva Huila]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Grupo de investigación Ciencia  ]]></institution>
<addr-line><![CDATA[Palermo ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Corporación Universitaria Minuto de Dios-UNIMINUTO  ]]></institution>
<addr-line><![CDATA[Neiva ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,Universidad Cooperativa de Colombia  ]]></institution>
<addr-line><![CDATA[Neiva Huila]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2020</year>
</pub-date>
<volume>49</volume>
<numero>3</numero>
<fpage>675</fpage>
<lpage>698</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0034-74182020000300675&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0034-74182020000300675&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0034-74182020000300675&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[SUMMARY This paper presents the thermodynamic analysis of solubility of gatifloxacin in the N,N-Dimethylformamide (DMF) + methanol (MeOH) cosolvent system at 10 temperatures. From the solubility data, the thermodynamic functions of solution, mixing, and transfers are calculated and analyzed using the Perlovich graphical method. On the other hand, an enthalpy-entropy compensation analysis is performed and the preferential solvation parameters are calculated using the inverse Kirkwood-Buff integral (IKBI) method. The result of the performed calculations indicates that the gatifloxacin solution process is endothermic with entropic favor, where the addition of DMF has a positive cosolvent effect in all cases. Regarding preferential solvation, the results are not entirely conclusive, since in all cases the values of the preferential solvation parameter are less than 0.01, so that, negligible preferential solvation takes place.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN Este artículo presenta el análisis termodinâmico de la solubilidad de gatifloxacina en el sistema cosolvente de A,A-Dimetilformamida (DMF) + metanol (MeOH) a 10 temperaturas. A partir de los datos de solubilidad se calculan las funciones termodinámicas de solución, mezcla y transferencia. Para el análisis además se utiliza el método gráfico Perlovich. Por otro lado, se realiza un análisis de compensación entalpía-entropía y se calculan los parámetros de solvatación preferencial utilizando el método de las integrales inversas de Kirkwood-BufF (IIKB). Los resultados del análisis termodinámico indican que el proceso de solución de gatifloxacina es endotérmica con favorecimiento entrópico, donde la adición de DMF tiene un efecto cosolvente positivo en todos los casos. En cuanto a la solvatación preferencial, los resultados no son del todo concluyentes, debido a que en todos los casos los valores del parámetro de solvatación preferencial son menores a 0,01 indicando una solvatación insignificante.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[gatifloxacin]]></kwd>
<kwd lng="en"><![CDATA[solubility]]></kwd>
<kwd lng="en"><![CDATA[N,N-dimethylformamide]]></kwd>
<kwd lng="en"><![CDATA[IKBI]]></kwd>
<kwd lng="en"><![CDATA[preferential solvation]]></kwd>
<kwd lng="es"><![CDATA[gatifloxacina]]></kwd>
<kwd lng="es"><![CDATA[solubilidad]]></kwd>
<kwd lng="es"><![CDATA[N,N-dimetilformamida]]></kwd>
<kwd lng="es"><![CDATA[IIKBI]]></kwd>
<kwd lng="es"><![CDATA[solvatación preferencial]]></kwd>
</kwd-group>
</article-meta>
</front><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Schultz]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[gatifloxacin ophthalmic solution for treatment of bacterial conjunctivitis: Safety, efficacy and patient perspective]]></article-title>
<source><![CDATA[Ophthalmol. Eye Dis]]></source>
<year>2012</year>
<volume>4</volume>
<page-range>65-70</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Deshpande]]></surname>
<given-names><![CDATA[D.]]></given-names>
</name>
<name>
<surname><![CDATA[Pasipanodya]]></surname>
<given-names><![CDATA[J.G.]]></given-names>
</name>
<name>
<surname><![CDATA[Srivastava]]></surname>
<given-names><![CDATA[S.]]></given-names>
</name>
<name>
<surname><![CDATA[Bendet]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Koeuth]]></surname>
<given-names><![CDATA[T.]]></given-names>
</name>
<name>
<surname><![CDATA[Bhavnani]]></surname>
<given-names><![CDATA[S.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Ambrose]]></surname>
<given-names><![CDATA[P.G.]]></given-names>
</name>
<name>
<surname><![CDATA[Smythe]]></surname>
<given-names><![CDATA[W.]]></given-names>
</name>
<name>
<surname><![CDATA[Mcilleron]]></surname>
<given-names><![CDATA[H.]]></given-names>
</name>
<name>
<surname><![CDATA[Thwaites]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<name>
<surname><![CDATA[Gumusboga]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Van Deun]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Gumbo]]></surname>
<given-names><![CDATA[T.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[gatifloxacin pharmacokinetics/pharmacodynamics-based optimal dosing for pulmonary and meningeal multidrug-resistant tuberculosis]]></article-title>
<source><![CDATA[Clin. Infect. Dis]]></source>
<year>2018</year>
<volume>67</volume>
<page-range>274-83</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Coburn]]></surname>
<given-names><![CDATA[P.S.]]></given-names>
</name>
<name>
<surname><![CDATA[Miller]]></surname>
<given-names><![CDATA[F.C.]]></given-names>
</name>
<name>
<surname><![CDATA[LaGrow]]></surname>
<given-names><![CDATA[A.L.]]></given-names>
</name>
<name>
<surname><![CDATA[Land]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
<name>
<surname><![CDATA[Mursalin]]></surname>
<given-names><![CDATA[H.]]></given-names>
</name>
<name>
<surname><![CDATA[Livingston]]></surname>
<given-names><![CDATA[E.]]></given-names>
</name>
<name>
<surname><![CDATA[Amayem]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Chen]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<name>
<surname><![CDATA[Gao]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
<name>
<surname><![CDATA[Zhang]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Callegan]]></surname>
<given-names><![CDATA[M.C.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Disarming pore-forming toxins with biomimetic nanosponges in intraocular infections]]></article-title>
<source><![CDATA[mSphere]]></source>
<year>2019</year>
<volume>4</volume>
<page-range>e00262-19</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Romero-Nieto]]></surname>
<given-names><![CDATA[A.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Cerquera]]></surname>
<given-names><![CDATA[N.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic study of the solubility of ethylparaben in acetonitrile + water cosolvent mixtures at different temperatures]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2019</year>
<volume>287</volume>
<page-range>110894</page-range></nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Caviedes-Rubio]]></surname>
<given-names><![CDATA[D.I.]]></given-names>
</name>
<name>
<surname><![CDATA[Ortiz]]></surname>
<given-names><![CDATA[C.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Parra-Pava]]></surname>
<given-names><![CDATA[Y.L.]]></given-names>
</name>
<name>
<surname><![CDATA[Peña]]></surname>
<given-names><![CDATA[M.Á.]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Mirheydari]]></surname>
<given-names><![CDATA[S.N.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Acree, Jr.]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility of sulphadiazine in (acetonitrile + water) mixtures: Measurement, correlation, thermodynamics and preferential solvation]]></article-title>
<source><![CDATA[Phys. Chem. Liq]]></source>
<year>2020</year>
<volume>58</volume>
<page-range>381-96</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Oliveira]]></surname>
<given-names><![CDATA[J.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Oliveira]]></surname>
<given-names><![CDATA[O.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Ometto]]></surname>
<given-names><![CDATA[A.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Ferraudo]]></surname>
<given-names><![CDATA[A.S.]]></given-names>
</name>
<name>
<surname><![CDATA[Salgado]]></surname>
<given-names><![CDATA[M.H.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Environmental management system ISO 14001 factors for promoting the adoption of cleaner production practices]]></article-title>
<source><![CDATA[J. Clean Prod]]></source>
<year>2016</year>
<volume>133</volume>
<page-range>1384-94</page-range></nlm-citation>
</ref>
<ref id="B7">
<label>7</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Caviedes-Rubio]]></surname>
<given-names><![CDATA[D.I.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Olaya-Amaya]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Normatividad ambiental dirigida a regular la presencia de los productos farmacéuticos residuales en ambientes acuáticos]]></article-title>
<source><![CDATA[Rev. Jurídica Piélagus]]></source>
<year>2017</year>
<volume>16</volume>
<page-range>121-30</page-range></nlm-citation>
</ref>
<ref id="B8">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Yue]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Acree]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Abraham]]></surname>
<given-names><![CDATA[M.H.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Applications of Abraham solvation parameter model: estimation of the lethal median molar concentration of the antiepileptic drug levetiracetam towards aquatic organisms from measured solubility data]]></article-title>
<source><![CDATA[Phys. Chem. Liq]]></source>
<year>2020</year>
<volume>58</volume>
<page-range>302-8</page-range></nlm-citation>
</ref>
<ref id="B9">
<label>9</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Peña]]></surname>
<given-names><![CDATA[M.A]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Acree]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Further numerical analyses on the solubility of sulfapyridine in ethanol + water mixtures]]></article-title>
<source><![CDATA[Pharm. Sci]]></source>
<year>2016</year>
<volume>22</volume>
<page-range>143-52</page-range></nlm-citation>
</ref>
<ref id="B10">
<label>10</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Marcus]]></surname>
<given-names><![CDATA[Y.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[On the preferential solvation of drugs and PAHs in binary solvent mixtures]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2008</year>
<volume>140</volume>
<page-range>61-7</page-range></nlm-citation>
</ref>
<ref id="B11">
<label>11</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Samanta]]></surname>
<given-names><![CDATA[S.K.]]></given-names>
</name>
<name>
<surname><![CDATA[Singh]]></surname>
<given-names><![CDATA[O.V.]]></given-names>
</name>
<name>
<surname><![CDATA[Jain]]></surname>
<given-names><![CDATA[R.K.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Polycyclic aromatic hydrocarbons: Environmental pollution and bioremediation]]></article-title>
<source><![CDATA[Trends Biotechnol]]></source>
<year>2002</year>
<volume>20</volume>
<page-range>243-8</page-range></nlm-citation>
</ref>
<ref id="B12">
<label>12</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Edwards]]></surname>
<given-names><![CDATA[N.T.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Polycyclic aromatic hydrocarbons (PAH's) in the terrestrial environment-A Review]]></article-title>
<source><![CDATA[J. Environ. Quality]]></source>
<year>1983</year>
<volume>12</volume>
<page-range>427-41</page-range></nlm-citation>
</ref>
<ref id="B13">
<label>13</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Acree, Jr]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Rytting]]></surname>
<given-names><![CDATA[J.H.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility in binary solvent systems I: Specific versus nonspecific interactions]]></article-title>
<source><![CDATA[J. Pharm. Sci]]></source>
<year>1982</year>
<volume>71</volume>
<page-range>201-5</page-range></nlm-citation>
</ref>
<ref id="B14">
<label>14</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Jouyban-Gharamaleki]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Valaee]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Barzegar-Jalali]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Clark]]></surname>
<given-names><![CDATA[B.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Acree, Jr]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Comparison of various cosolvency models for calculating solute solubility in water-cosolvent mixtures]]></article-title>
<source><![CDATA[Int. J. Pharm]]></source>
<year>1999</year>
<volume>177</volume>
<page-range>93-101</page-range></nlm-citation>
</ref>
<ref id="B15">
<label>15</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility prediction of drugs in water-polyethylene glycol 400 mixtures using Jouyban-Acree model]]></article-title>
<source><![CDATA[Chem. Pharm. Bull]]></source>
<year>2006</year>
<volume>54</volume>
<page-range>1561-6</page-range></nlm-citation>
</ref>
<ref id="B16">
<label>16</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cárdenas]]></surname>
<given-names><![CDATA[Z.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Jiménez]]></surname>
<given-names><![CDATA[D.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Rodríguez]]></surname>
<given-names><![CDATA[G.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Khoubnasabjafari]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility of methocarbamol in some cosolvent + water mixtures at 298.15 K and correlation with the Jouyban-Acree model]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2013</year>
<volume>188</volume>
<page-range>162-6</page-range></nlm-citation>
</ref>
<ref id="B17">
<label>17</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Acree, Jr.]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Rytting]]></surname>
<given-names><![CDATA[J.H.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility in binary solvent systems. IV. Prediction of naphthalene solubilities using the UNIFAC group contribution model]]></article-title>
<source><![CDATA[Int. J. Pharm]]></source>
<year>1983</year>
<volume>13</volume>
<page-range>197-204</page-range></nlm-citation>
</ref>
<ref id="B18">
<label>18</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Martin]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Newburger]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Adjei]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Extended Hildebrand solubility approach: Solubility of theophylline in polar binary solvents]]></article-title>
<source><![CDATA[J. Pharm. Sci]]></source>
<year>1980</year>
<volume>69</volume>
<page-range>487-91</page-range></nlm-citation>
</ref>
<ref id="B19">
<label>19</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Acree, Jr.]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Tucker]]></surname>
<given-names><![CDATA[S.A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermochemical investigations of hydrogen-bonded solutions Part 6. Comparison of mobile order theory versus Kretschmer-Wiebe association model for describing anthracene solubilities in binary hydrocarbon + alcohol solvent mixtures]]></article-title>
<source><![CDATA[Fluid Phase Equilib]]></source>
<year>1994</year>
<volume>102</volume>
<page-range>17-29</page-range></nlm-citation>
</ref>
<ref id="B20">
<label>20</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ruckenstein]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Shulgin]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility of drugs in aqueous solutions: Part 1. Ideal mixed solvent approximation]]></article-title>
<source><![CDATA[Int. J. Pharm]]></source>
<year>2003</year>
<volume>258</volume>
<page-range>193-201</page-range></nlm-citation>
</ref>
<ref id="B21">
<label>21</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Wu]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<name>
<surname><![CDATA[Xu]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<name>
<surname><![CDATA[Zhao]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic solubility of gatifloxacin in nonaqueous solvent mixtures of AiV-dimethylformamide plus isopropanol/methanol/ n-propanol/ethanol]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>2019</year>
<volume>64</volume>
<page-range>6071-7</page-range></nlm-citation>
</ref>
<ref id="B22">
<label>22</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Shi]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Feng]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[He]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Li]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility determination and correlation of gatifloxacin, enrofloxacin, and ciprofloxacin in supercritical CO2]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>2017</year>
<volume>62</volume>
<page-range>4235-43</page-range></nlm-citation>
</ref>
<ref id="B23">
<label>23</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Blanco-Márquez]]></surname>
<given-names><![CDATA[J.H.]]></given-names>
</name>
<name>
<surname><![CDATA[Quigua-Medina]]></surname>
<given-names><![CDATA[Y.A.]]></given-names>
</name>
<name>
<surname><![CDATA[García-Murillo]]></surname>
<given-names><![CDATA[J.D.]]></given-names>
</name>
<name>
<surname><![CDATA[Castro-Camacho]]></surname>
<given-names><![CDATA[J.K.]]></given-names>
</name>
<name>
<surname><![CDATA[Ortiz]]></surname>
<given-names><![CDATA[C.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Cerquera]]></surname>
<given-names><![CDATA[N.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic analysis and applications of the Abraham solvation parameter model in the study of the solubility of some sulfonamides]]></article-title>
<source><![CDATA[Rev. Colomb. Cienc. Quím. Farm]]></source>
<year>2020</year>
<volume>49</volume>
<page-range>234-55</page-range></nlm-citation>
</ref>
<ref id="B24">
<label>24</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Osorio]]></surname>
<given-names><![CDATA[I.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Acree, Jr.]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility of sulfacetamide in aqueous propylene glycol mixtures: Measurement, correlation, dissolution thermodynamics, preferential solvation and solute volumetric contribution at saturation]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2020</year>
<volume>297</volume>
<page-range>111889</page-range></nlm-citation>
</ref>
<ref id="B25">
<label>25</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Barton]]></surname>
<given-names><![CDATA[A.F.M.]]></given-names>
</name>
</person-group>
<source><![CDATA[Handbook of solubility parameters and other cohesion parameters]]></source>
<year>1991</year>
<edition>2nd</edition>
<publisher-name><![CDATA[CRC Press]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B26">
<label>26</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Fedors]]></surname>
<given-names><![CDATA[R.F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[A method for estimating both the solubility parameters and molar volumes of liquids]]></article-title>
<source><![CDATA[Polym. Eng. Sci]]></source>
<year>1974</year>
<volume>14</volume>
<page-range>147-54</page-range></nlm-citation>
</ref>
<ref id="B27">
<label>27</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Blanco-Márquez]]></surname>
<given-names><![CDATA[J.H.]]></given-names>
</name>
<name>
<surname><![CDATA[Ortiz]]></surname>
<given-names><![CDATA[C.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Cerquera]]></surname>
<given-names><![CDATA[N.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic analysis of the solubility and preferential solvation of sulfamerazine in (acetonitrile + water) cosolvent mixtures at different temperatures]]></article-title>
<source><![CDATA[J Mol. Liq]]></source>
<year>2019</year>
<volume>293</volume>
<page-range>111507</page-range></nlm-citation>
</ref>
<ref id="B28">
<label>28</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Blanco-Márquez]]></surname>
<given-names><![CDATA[J.H.]]></given-names>
</name>
<name>
<surname><![CDATA[Caviedes Rubio]]></surname>
<given-names><![CDATA[D.I.]]></given-names>
</name>
<name>
<surname><![CDATA[Ortiz]]></surname>
<given-names><![CDATA[C.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Cerquera]]></surname>
<given-names><![CDATA[N.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic analysis and preferential solvation of sulfamethazine in acetonitrile + water cosolvent mixtures]]></article-title>
<source><![CDATA[Fluid Phase Equilib]]></source>
<year>2020</year>
<volume>505</volume>
<page-range>112361</page-range></nlm-citation>
</ref>
<ref id="B29">
<label>29</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Yalkowsky]]></surname>
<given-names><![CDATA[S.H.]]></given-names>
</name>
<name>
<surname><![CDATA[Wu]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Estimation of the ideal solubility (crystal-liquid fugacity ratio) of organic compounds]]></article-title>
<source><![CDATA[J. Pharm. Sci]]></source>
<year>2010</year>
<volume>99</volume>
<page-range>1100-6</page-range></nlm-citation>
</ref>
<ref id="B30">
<label>30</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Romero-Nieto]]></surname>
<given-names><![CDATA[A.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Caviedes-Rubio]]></surname>
<given-names><![CDATA[D.I.]]></given-names>
</name>
<name>
<surname><![CDATA[Polania-Orozco]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<name>
<surname><![CDATA[Cerquera]]></surname>
<given-names><![CDATA[N.E.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Temperature and cosolvent composition effects in the solubility of methylparaben in acetonitrile + water mixtures]]></article-title>
<source><![CDATA[Phys. Chem. Liq]]></source>
<year>2020</year>
<publisher-name><![CDATA[Forthcomming]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B31">
<label>31</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Mirmehrabi]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<name>
<surname><![CDATA[Rohani]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Perry]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic modeling of activity coefficient and prediction of solubility: Part 1 predictive models]]></article-title>
<source><![CDATA[J. Pharm. Sci]]></source>
<year>2006</year>
<volume>95</volume>
<page-range>790-7</page-range></nlm-citation>
</ref>
<ref id="B32">
<label>32</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility and preferential solvation of meloxicam in methanol+ water mixtures at 298.15 K]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2014</year>
<volume>197</volume>
<page-range>368-76</page-range></nlm-citation>
</ref>
<ref id="B33">
<label>33</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solution thermodynamics of sulfadiazine in ethanol + water mixtures]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2013</year>
<volume>187</volume>
<page-range>99-105</page-range></nlm-citation>
</ref>
<ref id="B34">
<label>34</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Krug]]></surname>
<given-names><![CDATA[R.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Hunter]]></surname>
<given-names><![CDATA[W.G.]]></given-names>
</name>
<name>
<surname><![CDATA[Grieger]]></surname>
<given-names><![CDATA[R.A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpy-entropy compensation. 1. Some fundamental statistical problems associated with the analysis of van't Hoff and arrhenius data]]></article-title>
<source><![CDATA[J. Phys. Chem]]></source>
<year>1976</year>
<volume>80</volume>
<page-range>2335-41</page-range></nlm-citation>
</ref>
<ref id="B35">
<label>35</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Krug]]></surname>
<given-names><![CDATA[R.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Hunter]]></surname>
<given-names><![CDATA[W.G.]]></given-names>
</name>
<name>
<surname><![CDATA[Grieger]]></surname>
<given-names><![CDATA[R.A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpy-entropy compensation. 2. Separation of the chemical from the statistical effect]]></article-title>
<source><![CDATA[J. Phys. Chem]]></source>
<year>1976</year>
<volume>80</volume>
<page-range>2341-51</page-range></nlm-citation>
</ref>
<ref id="B36">
<label>36</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Romdhani]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility of sulfamethizole in some propylene glycol+water mixtures at several temperatures]]></article-title>
<source><![CDATA[Fluid Phase Equilib]]></source>
<year>2012</year>
<volume>322</volume>
<page-range>113-9</page-range></nlm-citation>
</ref>
<ref id="B37">
<label>37</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Rodríguez]]></surname>
<given-names><![CDATA[G.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic study of the solubility of sulfapyridine in some ethanol + water mixtures]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2013</year>
<volume>177</volume>
<page-range>156161</page-range></nlm-citation>
</ref>
<ref id="B38">
<label>38</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Perlovich]]></surname>
<given-names><![CDATA[G.L.]]></given-names>
</name>
<name>
<surname><![CDATA[Ryzhakov]]></surname>
<given-names><![CDATA[A.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Strakhova]]></surname>
<given-names><![CDATA[N.N.]]></given-names>
</name>
<name>
<surname><![CDATA[Kazachenko]]></surname>
<given-names><![CDATA[V.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Schaper]]></surname>
<given-names><![CDATA[K.-J.]]></given-names>
</name>
<name>
<surname><![CDATA[Raevsky]]></surname>
<given-names><![CDATA[O.A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic aspects of solubility and partitioning processes of some sulfonamides in the solvents modeling biological media]]></article-title>
<source><![CDATA[J. Chem. Thermodyn]]></source>
<year>2014</year>
<volume>69</volume>
<page-range>56-65</page-range></nlm-citation>
</ref>
<ref id="B39">
<label>39</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Perlovich]]></surname>
<given-names><![CDATA[G.L.]]></given-names>
</name>
<name>
<surname><![CDATA[Strakhova]]></surname>
<given-names><![CDATA[N.N.]]></given-names>
</name>
<name>
<surname><![CDATA[Kazachenko]]></surname>
<given-names><![CDATA[V.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Volkova]]></surname>
<given-names><![CDATA[T.V.]]></given-names>
</name>
<name>
<surname><![CDATA[Tkachev]]></surname>
<given-names><![CDATA[V.V.]]></given-names>
</name>
<name>
<surname><![CDATA[Schaper]]></surname>
<given-names><![CDATA[K.-J.]]></given-names>
</name>
<name>
<surname><![CDATA[Raevsky]]></surname>
<given-names><![CDATA[O.A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Sulfonamides as a subject to study molecular interactions in crystals and solutions: Sublimation, solubility, solvation, distribution and crystal structure]]></article-title>
<source><![CDATA[Int. J. Pharm]]></source>
<year>2008</year>
<volume>349</volume>
<page-range>300-13</page-range></nlm-citation>
</ref>
<ref id="B40">
<label>40</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Holguín]]></surname>
<given-names><![CDATA[A.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic study of the solubility of triclocarban in ethanol + propylene glycol mixtures]]></article-title>
<source><![CDATA[Quim. Nova]]></source>
<year>2012</year>
<volume>35</volume>
<page-range>280285</page-range></nlm-citation>
</ref>
<ref id="B41">
<label>41</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Perlovich]]></surname>
<given-names><![CDATA[G.L.]]></given-names>
</name>
<name>
<surname><![CDATA[Tkachev]]></surname>
<given-names><![CDATA[V.V.]]></given-names>
</name>
<name>
<surname><![CDATA[Strakhova]]></surname>
<given-names><![CDATA[N.N.]]></given-names>
</name>
<name>
<surname><![CDATA[Kazachenko]]></surname>
<given-names><![CDATA[V.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Volkova]]></surname>
<given-names><![CDATA[T.V.]]></given-names>
</name>
<name>
<surname><![CDATA[Surov]]></surname>
<given-names><![CDATA[O.V.]]></given-names>
</name>
<name>
<surname><![CDATA[Schaper]]></surname>
<given-names><![CDATA[K.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Raevsky]]></surname>
<given-names><![CDATA[O.A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic and structural aspects of sulfonamide crystals and solutions]]></article-title>
<source><![CDATA[J. Pharm. Sci]]></source>
<year>2009</year>
<volume>98</volume>
<page-range>4738-55</page-range></nlm-citation>
</ref>
<ref id="B42">
<label>42</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Mogollon-Waltero]]></surname>
<given-names><![CDATA[E.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Ortiz]]></surname>
<given-names><![CDATA[C.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Peña]]></surname>
<given-names><![CDATA[M.Á.]]></given-names>
</name>
<name>
<surname><![CDATA[Almanza]]></surname>
<given-names><![CDATA[O.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpy-entropy compensation analysis of the triclocarban dissolution process in some {1,4-dioxane (1) + water (2)} mixtures]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2018</year>
<volume>271</volume>
<page-range>522-9</page-range></nlm-citation>
</ref>
<ref id="B43">
<label>43</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ruidiaz]]></surname>
<given-names><![CDATA[M.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Marcus]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility and preferential solvation of indomethacin in 1,4-dioxane+water solvent mixtures]]></article-title>
<source><![CDATA[Fluid Phase Equilib]]></source>
<year>2010</year>
<volume>299</volume>
<page-range>259-65</page-range></nlm-citation>
</ref>
<ref id="B44">
<label>44</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Gutiérrez]]></surname>
<given-names><![CDATA[R.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solution thermodynamics of lysine clonixinate in some ethanol + water mixtures]]></article-title>
<source><![CDATA[Lat. Am. J. Pharm]]></source>
<year>2012</year>
<volume>31</volume>
<page-range>226-34</page-range></nlm-citation>
</ref>
<ref id="B45">
<label>45</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Vargas]]></surname>
<given-names><![CDATA[E.F.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamics of the mixing process of several sodium sulfonamides in ethanol + water cosolvent mixtures]]></article-title>
<source><![CDATA[Vitae, Rev. Fac. Quim. Farm]]></source>
<year>2011</year>
<volume>18</volume>
<page-range>192-200</page-range></nlm-citation>
</ref>
<ref id="B46">
<label>46</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cristancho]]></surname>
<given-names><![CDATA[D.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Sotomayor]]></surname>
<given-names><![CDATA[R.G.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Romdhani]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamics of mixing of the &#946;-adrenergic blocker propranolol-HCl in ethanol + water mixtures]]></article-title>
<source><![CDATA[Rev. Colomb. Cienc. Quim. Farm]]></source>
<year>2011</year>
<volume>40</volume>
<page-range>261-71</page-range></nlm-citation>
</ref>
<ref id="B47">
<label>47</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bustamante]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Escalera]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpy and entropy contributions to the solubility of sulphamethoxypyridazine in solvent mixtures showing two solubility maxima]]></article-title>
<source><![CDATA[J. Pharm. Pharmacol]]></source>
<year>1995</year>
<volume>47</volume>
<page-range>550-5</page-range></nlm-citation>
</ref>
<ref id="B48">
<label>48</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Holguín]]></surname>
<given-names><![CDATA[A.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Almanza]]></surname>
<given-names><![CDATA[O.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Marcus]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility and preferential solvation of meloxicam in ethanol+water mixtures]]></article-title>
<source><![CDATA[Fluid Phase Equilib]]></source>
<year>2011</year>
<volume>305</volume>
<page-range>88-95</page-range></nlm-citation>
</ref>
<ref id="B49">
<label>49</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Mauger]]></surname>
<given-names><![CDATA[J.W.]]></given-names>
</name>
<name>
<surname><![CDATA[Paruta]]></surname>
<given-names><![CDATA[A.N.]]></given-names>
</name>
<name>
<surname><![CDATA[Gerraughty]]></surname>
<given-names><![CDATA[R.J.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubilities of sulfadiazine, sulfisomidine, and sulfadimethoxine in several normal alcohols]]></article-title>
<source><![CDATA[J. Pharm. Sci]]></source>
<year>1972</year>
<volume>61</volume>
<page-range>94-7</page-range></nlm-citation>
</ref>
<ref id="B50">
<label>50</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Lumry]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Rajender]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpy-entropy compensation phenomena in water solutions of proteins and small molecules: A ubiquitous properly of water]]></article-title>
<source><![CDATA[Biopolymers]]></source>
<year>1970</year>
<volume>9</volume>
<page-range>1125-227</page-range></nlm-citation>
</ref>
<ref id="B51">
<label>51</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ben-Naim]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Theory of preferential solvation of nonelectrolytes]]></article-title>
<source><![CDATA[Cell Biophys]]></source>
<year>1988</year>
<volume>12</volume>
<page-range>255-69</page-range></nlm-citation>
</ref>
<ref id="B52">
<label>52</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ben-Naim]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Navarro]]></surname>
<given-names><![CDATA[A.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Leal]]></surname>
<given-names><![CDATA[J.M.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Kirkwood-Buff analysis of local properties of solutions]]></article-title>
<source><![CDATA[Phys. Chem. Chem. Phys]]></source>
<year>2008</year>
<volume>10</volume>
<page-range>2451-60</page-range></nlm-citation>
</ref>
<ref id="B53">
<label>53</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ben-Naim]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Inversion of the Kirkwood-Buff theory of solutions: Application to the water-ethanol system]]></article-title>
<source><![CDATA[J. Chem. Phys]]></source>
<year>1977</year>
<volume>67</volume>
<page-range>4884-90</page-range></nlm-citation>
</ref>
<ref id="B54">
<label>54</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Marcus]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
</person-group>
<source><![CDATA[Solvent mixtures: Properties and selective solvation]]></source>
<year>2002</year>
<publisher-loc><![CDATA[New York ]]></publisher-loc>
<publisher-name><![CDATA[Marcel Dekker, Inc]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B55">
<label>55</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Almanza]]></surname>
<given-names><![CDATA[O.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Peña]]></surname>
<given-names><![CDATA[M.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Acree, Jr]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solution thermodynamics and preferential solvation of sulfamethazine in (methanol + water) mixtures]]></article-title>
<source><![CDATA[J. Chem. Thermodyn]]></source>
<year>2016</year>
<volume>97</volume>
<page-range>264-76</page-range></nlm-citation>
</ref>
<ref id="B56">
<label>56</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ben-Naim]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Preferential solvation in two- and in three-component systems]]></article-title>
<source><![CDATA[Pure Appl. Chem]]></source>
<year>1990</year>
<volume>62</volume>
<page-range>25-34</page-range></nlm-citation>
</ref>
<ref id="B57">
<label>57</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Sandoval-Castro]]></surname>
<given-names><![CDATA[J.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Ortiz]]></surname>
<given-names><![CDATA[C.P.]]></given-names>
</name>
<name>
<surname><![CDATA[Rodríguez-Rubiano]]></surname>
<given-names><![CDATA[J.D]]></given-names>
</name>
<name>
<surname><![CDATA[Rodríguez-Rodríguez]]></surname>
<given-names><![CDATA[G.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Preferential solvation of tricin in {ethanol (1) + water (2)} mixtures at several temperatures]]></article-title>
<source><![CDATA[Rev. Colomb. Cienc. Quim. Farm]]></source>
<year>2018</year>
<volume>47</volume>
<page-range>135-48</page-range></nlm-citation>
</ref>
<ref id="B58">
<label>58</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Gaviria-Castillo]]></surname>
<given-names><![CDATA[A.C.]]></given-names>
</name>
<name>
<surname><![CDATA[Artunduaga-Tole]]></surname>
<given-names><![CDATA[J.D.]]></given-names>
</name>
<name>
<surname><![CDATA[Rodríguez-Rubiano]]></surname>
<given-names><![CDATA[J.D.]]></given-names>
</name>
<name>
<surname><![CDATA[Zuñiga-Andrade]]></surname>
<given-names><![CDATA[J.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solution thermodynamics and preferential solvation of triclocarban in {1,4-dioxane (1) + water (2)} mixtures at 298.15 K]]></article-title>
<source><![CDATA[Phys. Chem. Liq]]></source>
<year>2019</year>
<volume>57</volume>
<page-range>55-66</page-range></nlm-citation>
</ref>
<ref id="B59">
<label>59</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Preferential solvation of sulfadiazine, sulfamerazine and sulfamethazine in ethanol + water solvent mixtures according to the IKBI method]]></article-title>
<source><![CDATA[J. Mol. Liq]]></source>
<year>2014</year>
<volume>193</volume>
<page-range>152-9</page-range></nlm-citation>
</ref>
<ref id="B60">
<label>60</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cárdenas]]></surname>
<given-names><![CDATA[Z.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Jiménez]]></surname>
<given-names><![CDATA[D.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Almanza]]></surname>
<given-names><![CDATA[O.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Jouyban]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Acree, Jr.]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility and preferential solvation of some n-alkyl-parabens in methanol + water mixtures at 298.15 K]]></article-title>
<source><![CDATA[J. Chem. Thermodyn]]></source>
<year>2017</year>
<volume>108</volume>
<page-range>26-37</page-range></nlm-citation>
</ref>
<ref id="B61">
<label>61</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Preferential solvation of some structurally related sulfonamides in 1-propanol + water co-solvent mixtures]]></article-title>
<source><![CDATA[Phys. Chem. Liq]]></source>
<year>2015</year>
<volume>53</volume>
<page-range>293306</page-range></nlm-citation>
</ref>
<ref id="B62">
<label>62</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[García-Giménez]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez-López]]></surname>
<given-names><![CDATA[J.F.]]></given-names>
</name>
<name>
<surname><![CDATA[Blanco]]></surname>
<given-names><![CDATA[S.T.]]></given-names>
</name>
<name>
<surname><![CDATA[Velasco]]></surname>
<given-names><![CDATA[I.]]></given-names>
</name>
<name>
<surname><![CDATA[Otín]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Densities and isothermal compressibilities at pressures up to 20 MPa of the systems N,N-dimethylformamide or N,N-dimethylacetamide + &#945;,&#969;- dichloroalkane]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>2007</year>
<volume>52</volume>
<page-range>2368-74</page-range></nlm-citation>
</ref>
<ref id="B63">
<label>63</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Marcus]]></surname>
<given-names><![CDATA[Y.]]></given-names>
</name>
</person-group>
<source><![CDATA[The Properties of Solvents]]></source>
<year>1999</year>
<publisher-loc><![CDATA[New York ]]></publisher-loc>
<publisher-name><![CDATA[John Wiley &amp; Sons, Ltd]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B64">
<label>64</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Gad&#382;uri&#263;]]></surname>
<given-names><![CDATA[S.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Volumetric properties ofbinary mixtures of 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophos-phate with N-methylformamide, N-ethylformamide, N,N-dimethylformamide, N,N-dibutylformamide, and &#945;,&#969; -dimethylacetamide from (293.15 to 323]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>2014</year>
<volume>59</volume>
<page-range>1225-31</page-range></nlm-citation>
</ref>
<ref id="B65">
<label>65</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[kijev&#269;anin]]></surname>
<given-names><![CDATA[M.L.]]></given-names>
</name>
<name>
<surname><![CDATA[Djuri&#353;]]></surname>
<given-names><![CDATA[M.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Radovi&#263;]]></surname>
<given-names><![CDATA[I.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Djordjevi&#263;]]></surname>
<given-names><![CDATA[B.D.]]></given-names>
</name>
<name>
<surname><![CDATA[&#352;erbanovi&#263;]]></surname>
<given-names><![CDATA[S.P.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Volumetric properties of the binary methanol + chloroform and ternary methanol + chloroform + benzene mixtures at (288.15, 293.15, 298.15, 303.15, 308.15, and 313.15) K]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>2007</year>
<volume>52</volume>
<page-range>1136-40</page-range></nlm-citation>
</ref>
<ref id="B66">
<label>66</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Peña]]></surname>
<given-names><![CDATA[M.Á.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Preferential solvation of indomethacin in 1,4-dioxane + water mixtures according to the inverse Kirkwood-Buff integrals method]]></article-title>
<source><![CDATA[Phys. Chem. Liq]]></source>
<year>2016</year>
<volume>54</volume>
<page-range>462-74</page-range></nlm-citation>
</ref>
<ref id="B67">
<label>67</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Jiménez]]></surname>
<given-names><![CDATA[D.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Cárdenas]]></surname>
<given-names><![CDATA[Z.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Peña]]></surname>
<given-names><![CDATA[M.A.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solubility temperature dependence and preferential solvation of sulfadiazine in 1,4-dioxane+water co-solvent mixtures]]></article-title>
<source><![CDATA[Fluid Phase Equilib]]></source>
<year>2015</year>
<volume>397</volume>
<page-range>26-36</page-range></nlm-citation>
</ref>
<ref id="B68">
<label>68</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Peña]]></surname>
<given-names><![CDATA[M.Á.]]></given-names>
</name>
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[D.R.]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Preferential solvation of some n-alkyl p-substituted benzoates in propylene glycol + water cosolvent mixtures]]></article-title>
<source><![CDATA[Phys. Chem. Liq]]></source>
<year>2015</year>
<volume>53</volume>
<page-range>455-66</page-range></nlm-citation>
</ref>
<ref id="B69">
<label>69</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Kamlet]]></surname>
<given-names><![CDATA[M.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Taft]]></surname>
<given-names><![CDATA[R.W.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[The solvatochromic comparison method. I. The (3-scale of solvent hydrogen-bond acceptor (HBA) basicities]]></article-title>
<source><![CDATA[J. Am. Chem. Soc]]></source>
<year>1976</year>
<volume>98</volume>
<page-range>377383</page-range></nlm-citation>
</ref>
<ref id="B70">
<label>70</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Laurence]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Legros]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Nicolet]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Vuluga]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Chantzis]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Jacquemin]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Solvatomagnetic comparison method: A proper quantification of solvent hydrogen-bond basicity]]></article-title>
<source><![CDATA[J. Phys. Chem. B]]></source>
<year>2014</year>
<volume>118</volume>
<page-range>7594-608</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
