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dc.contributor.author
de Paula, Karina  
dc.contributor.author
Camí, Gerardo Enrique  
dc.contributor.author
Brusau, Elena Virginia  
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Narda, Griselda Edith  
dc.contributor.author
Ellena, Javier  
dc.date.available
2015-09-30T15:54:17Z  
dc.date.issued
2013-07-29  
dc.identifier.citation
de Paula, Karina; Camí, Gerardo Enrique; Brusau, Elena Virginia; Narda, Griselda Edith; Ellena, Javier; Mebendazole Mesylate Monohydrate: A New Route to Improve the Solubility of Mebendazole Polymorphs; John Wiley & Sons; Journal of Pharmaceutical Sciences; 102; 10; 29-7-2013; 3528-3538  
dc.identifier.issn
1520-6017  
dc.identifier.uri
http://hdl.handle.net/11336/2209  
dc.description.abstract
Mebendazole mesylate monohydrate, a new stable salt of mebendazole (MBZ), has been synthesized and fully characterized. It was obtained from recrystallization of MBZ forms A, B, or C in diverse solvents with the addition of methyl sulfonic acid solution. The crystal packing is first organized as a two-dimensional array consisting of rows of alternating MBZ molecules linked to columns of mesylate ions by hydrogen bonds. The three-dimensional structure is further developed by classical intermolecular interactions involving water molecules. In addition, nonclassical contacts are also found. The vibrational behavior is consistent with the crystal structure, the most important functional groups showing shifts to lower or higher frequencies in relation to the MBZ polymorphs. Thermal analysis indicates that the compound is stable up to 50◦C. Decomposition occurs in five steps. Solubility studies show that the title compound presents a significant higher performance than polymorph C.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
John Wiley & Sons  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
CRYSTAL STRUCTURE  
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DISSOLUTION  
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FTIR-RAMAN SPECTROSCOPY  
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MEBENDAZOLE MESYLATE  
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SOLID STATE  
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THERMAL STABILITY  
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Físico-Química, Ciencia de los Polímeros, Electroquímica  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Mebendazole Mesylate Monohydrate: A New Route to Improve the Solubility of Mebendazole Polymorphs  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2016-03-30 10:35:44.97925-03  
dc.journal.volume
102  
dc.journal.number
10  
dc.journal.pagination
3528-3538  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Hoboken  
dc.description.fil
Fil: de Paula, Karina. Universidade de Sao Paulo; Brasil  
dc.description.fil
Fil: Camí, Gerardo Enrique. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Laboratorio de Química Inorgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Investigaciones en Tecnología Química; Argentina  
dc.description.fil
Fil: Brusau, Elena Virginia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Investigaciones en Tecnología Química; Argentina  
dc.description.fil
Fil: Narda, Griselda Edith. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Investigaciones en Tecnología Química; Argentina  
dc.description.fil
Fil: Ellena, Javier. Universidade de Sao Paulo; Brasil  
dc.journal.title
Journal of Pharmaceutical Sciences  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/jps.23658/abstract  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/DOI:10.1002/jps.23658