Enhancement of solubility of albendazole by complexation with β-cyclodextrin

Detalhes bibliográficos
Autor(a) principal: Moriwaki,C.
Data de Publicação: 2008
Outros Autores: Costa,G. L., Ferracini,C. N., Moraes,F. F. de, Zanin,G. M., Pineda,E. A. G., Matioli,G.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Chemical Engineering
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322008000200005
Resumo: A high dosage of albendazole (ABZ) is required for treating systemic helminthe infections because of its low solubility. Aiming at increasing ABZ solubility, complexation with beta-cyclodextrin (β-CD) using aqueous and acetic acid solutions as ABZ solubilizer was studied. In aqueous β-CD, complexation increased solubility 53.4 times, giving a complex equilibrium constant of 1266 L mol-1 with a maximum ABZ concentration of 276 µmol L-1 for 16.3 mmol L-1 β-CD. For complexation in 1.05 mol L-1 acetic acid, UV absorbance spectra and ¹H-NMR analysis confirmed complex formation. The UV absorbance of ABZ/acid acetic/β-CD solutions was modeled by the formation of two complexes with molar ratios 1:1 and 1:2 ABZ:β-CD. When neutralized with NaOH these solutions did not form precipitates only for the ABZ:β-CD molar ratios of 1:8 and 1:10, showing that ABZ solubility could be increased 306 times. Results show that high β-CD molar ratios hold ABZ in solution by complexation enhanced by the acetate anion.
id ABEQ-1_d93b9e76cc4e71278f452584f8c704af
oai_identifier_str oai:scielo:S0104-66322008000200005
network_acronym_str ABEQ-1
network_name_str Brazilian Journal of Chemical Engineering
repository_id_str
spelling Enhancement of solubility of albendazole by complexation with β-cyclodextrinAlbendazoleCyclodextrinsβ-cyclodextrinComplexationSolubilityA high dosage of albendazole (ABZ) is required for treating systemic helminthe infections because of its low solubility. Aiming at increasing ABZ solubility, complexation with beta-cyclodextrin (β-CD) using aqueous and acetic acid solutions as ABZ solubilizer was studied. In aqueous β-CD, complexation increased solubility 53.4 times, giving a complex equilibrium constant of 1266 L mol-1 with a maximum ABZ concentration of 276 µmol L-1 for 16.3 mmol L-1 β-CD. For complexation in 1.05 mol L-1 acetic acid, UV absorbance spectra and ¹H-NMR analysis confirmed complex formation. The UV absorbance of ABZ/acid acetic/β-CD solutions was modeled by the formation of two complexes with molar ratios 1:1 and 1:2 ABZ:β-CD. When neutralized with NaOH these solutions did not form precipitates only for the ABZ:β-CD molar ratios of 1:8 and 1:10, showing that ABZ solubility could be increased 306 times. Results show that high β-CD molar ratios hold ABZ in solution by complexation enhanced by the acetate anion.Brazilian Society of Chemical Engineering2008-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322008000200005Brazilian Journal of Chemical Engineering v.25 n.2 2008reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/S0104-66322008000200005info:eu-repo/semantics/openAccessMoriwaki,C.Costa,G. L.Ferracini,C. N.Moraes,F. F. deZanin,G. M.Pineda,E. A. G.Matioli,G.eng2008-07-03T00:00:00Zoai:scielo:S0104-66322008000200005Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2008-07-03T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false
dc.title.none.fl_str_mv Enhancement of solubility of albendazole by complexation with β-cyclodextrin
title Enhancement of solubility of albendazole by complexation with β-cyclodextrin
spellingShingle Enhancement of solubility of albendazole by complexation with β-cyclodextrin
Moriwaki,C.
Albendazole
Cyclodextrins
β-cyclodextrin
Complexation
Solubility
title_short Enhancement of solubility of albendazole by complexation with β-cyclodextrin
title_full Enhancement of solubility of albendazole by complexation with β-cyclodextrin
title_fullStr Enhancement of solubility of albendazole by complexation with β-cyclodextrin
title_full_unstemmed Enhancement of solubility of albendazole by complexation with β-cyclodextrin
title_sort Enhancement of solubility of albendazole by complexation with β-cyclodextrin
author Moriwaki,C.
author_facet Moriwaki,C.
Costa,G. L.
Ferracini,C. N.
Moraes,F. F. de
Zanin,G. M.
Pineda,E. A. G.
Matioli,G.
author_role author
author2 Costa,G. L.
Ferracini,C. N.
Moraes,F. F. de
Zanin,G. M.
Pineda,E. A. G.
Matioli,G.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Moriwaki,C.
Costa,G. L.
Ferracini,C. N.
Moraes,F. F. de
Zanin,G. M.
Pineda,E. A. G.
Matioli,G.
dc.subject.por.fl_str_mv Albendazole
Cyclodextrins
β-cyclodextrin
Complexation
Solubility
topic Albendazole
Cyclodextrins
β-cyclodextrin
Complexation
Solubility
description A high dosage of albendazole (ABZ) is required for treating systemic helminthe infections because of its low solubility. Aiming at increasing ABZ solubility, complexation with beta-cyclodextrin (β-CD) using aqueous and acetic acid solutions as ABZ solubilizer was studied. In aqueous β-CD, complexation increased solubility 53.4 times, giving a complex equilibrium constant of 1266 L mol-1 with a maximum ABZ concentration of 276 µmol L-1 for 16.3 mmol L-1 β-CD. For complexation in 1.05 mol L-1 acetic acid, UV absorbance spectra and ¹H-NMR analysis confirmed complex formation. The UV absorbance of ABZ/acid acetic/β-CD solutions was modeled by the formation of two complexes with molar ratios 1:1 and 1:2 ABZ:β-CD. When neutralized with NaOH these solutions did not form precipitates only for the ABZ:β-CD molar ratios of 1:8 and 1:10, showing that ABZ solubility could be increased 306 times. Results show that high β-CD molar ratios hold ABZ in solution by complexation enhanced by the acetate anion.
publishDate 2008
dc.date.none.fl_str_mv 2008-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322008000200005
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322008000200005
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0104-66322008000200005
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Brazilian Society of Chemical Engineering
publisher.none.fl_str_mv Brazilian Society of Chemical Engineering
dc.source.none.fl_str_mv Brazilian Journal of Chemical Engineering v.25 n.2 2008
reponame:Brazilian Journal of Chemical Engineering
instname:Associação Brasileira de Engenharia Química (ABEQ)
instacron:ABEQ
instname_str Associação Brasileira de Engenharia Química (ABEQ)
instacron_str ABEQ
institution ABEQ
reponame_str Brazilian Journal of Chemical Engineering
collection Brazilian Journal of Chemical Engineering
repository.name.fl_str_mv Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)
repository.mail.fl_str_mv rgiudici@usp.br||rgiudici@usp.br
_version_ 1754213172639694848