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Mixed Antimony(V) Complexes with Different Sugars to Modulate the Oral Bioavailability of Pentavalent Antimonial Drugs

Previous studies have shown that the association of the drug meglumine antimoniate (MA) with β-cyclodextrin can improve its bioavailability by the oral route. In this work, ribose and maltose were investigated for their ability to form mixed or association complexes with MA, release MA and modulate...

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Autores principales: Ferreira, Weverson A., Islam, Arshad, Andrade, Aretha Priscilla S., Fernandes, Flaviana R., Frézard, Frédéric, Demicheli, Cynthia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270655/
https://www.ncbi.nlm.nih.gov/pubmed/24786687
http://dx.doi.org/10.3390/molecules19055478
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author Ferreira, Weverson A.
Islam, Arshad
Andrade, Aretha Priscilla S.
Fernandes, Flaviana R.
Frézard, Frédéric
Demicheli, Cynthia
author_facet Ferreira, Weverson A.
Islam, Arshad
Andrade, Aretha Priscilla S.
Fernandes, Flaviana R.
Frézard, Frédéric
Demicheli, Cynthia
author_sort Ferreira, Weverson A.
collection PubMed
description Previous studies have shown that the association of the drug meglumine antimoniate (MA) with β-cyclodextrin can improve its bioavailability by the oral route. In this work, ribose and maltose were investigated for their ability to form mixed or association complexes with MA, release MA and modulate the serum levels of Sb after oral administration in mice. Analysis of the MA/ribose composition by high performance liquid chromatography coupled to mass spectrometry (LCMS-IT-TOF) revealed the presence of mixed meglumine-Sb-ribose and Sb-ribose complexes. Analysis of the MA/maltose composition suggested the formation of MA-maltose association compounds. Circular dichroism characterization of these compositions following dilution in water at 37 °C suggested a partial and slow dissociation of the association compounds. When the MA/ribose composition was administered orally and compared to MA, the serum concentration of Sb was significantly lower after 1 h and greater after 3 h. On the other hand, the MA/maltose composition showed similar serum Sb concentration after 1 h and higher level of Sb after 3 h, when compared to MA. In conclusion, the present study has demonstrated the formation of mixed or association complexes of MA with sugars, such as maltose and ribose, which promoted sustained serum level of Sb after oral administration.
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spelling pubmed-62706552018-12-21 Mixed Antimony(V) Complexes with Different Sugars to Modulate the Oral Bioavailability of Pentavalent Antimonial Drugs Ferreira, Weverson A. Islam, Arshad Andrade, Aretha Priscilla S. Fernandes, Flaviana R. Frézard, Frédéric Demicheli, Cynthia Molecules Article Previous studies have shown that the association of the drug meglumine antimoniate (MA) with β-cyclodextrin can improve its bioavailability by the oral route. In this work, ribose and maltose were investigated for their ability to form mixed or association complexes with MA, release MA and modulate the serum levels of Sb after oral administration in mice. Analysis of the MA/ribose composition by high performance liquid chromatography coupled to mass spectrometry (LCMS-IT-TOF) revealed the presence of mixed meglumine-Sb-ribose and Sb-ribose complexes. Analysis of the MA/maltose composition suggested the formation of MA-maltose association compounds. Circular dichroism characterization of these compositions following dilution in water at 37 °C suggested a partial and slow dissociation of the association compounds. When the MA/ribose composition was administered orally and compared to MA, the serum concentration of Sb was significantly lower after 1 h and greater after 3 h. On the other hand, the MA/maltose composition showed similar serum Sb concentration after 1 h and higher level of Sb after 3 h, when compared to MA. In conclusion, the present study has demonstrated the formation of mixed or association complexes of MA with sugars, such as maltose and ribose, which promoted sustained serum level of Sb after oral administration. MDPI 2014-04-28 /pmc/articles/PMC6270655/ /pubmed/24786687 http://dx.doi.org/10.3390/molecules19055478 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Ferreira, Weverson A.
Islam, Arshad
Andrade, Aretha Priscilla S.
Fernandes, Flaviana R.
Frézard, Frédéric
Demicheli, Cynthia
Mixed Antimony(V) Complexes with Different Sugars to Modulate the Oral Bioavailability of Pentavalent Antimonial Drugs
title Mixed Antimony(V) Complexes with Different Sugars to Modulate the Oral Bioavailability of Pentavalent Antimonial Drugs
title_full Mixed Antimony(V) Complexes with Different Sugars to Modulate the Oral Bioavailability of Pentavalent Antimonial Drugs
title_fullStr Mixed Antimony(V) Complexes with Different Sugars to Modulate the Oral Bioavailability of Pentavalent Antimonial Drugs
title_full_unstemmed Mixed Antimony(V) Complexes with Different Sugars to Modulate the Oral Bioavailability of Pentavalent Antimonial Drugs
title_short Mixed Antimony(V) Complexes with Different Sugars to Modulate the Oral Bioavailability of Pentavalent Antimonial Drugs
title_sort mixed antimony(v) complexes with different sugars to modulate the oral bioavailability of pentavalent antimonial drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270655/
https://www.ncbi.nlm.nih.gov/pubmed/24786687
http://dx.doi.org/10.3390/molecules19055478
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