Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , |
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=S0104-66322013000100006 |
Resumo: | The enzymatic synthesis of amoxicillin is catalyzed by Penicillin G Acylase (PGA). As byproducts, hydroxyphenylglycine and alcohol are also formed from hydrolytic reactions and antibiotic synthesis, respectively. The design of this process should be directed to promote the synthesis reaction. At the same time, it is necessary to reduce the hydrolytic reaction of amoxicillin through its crystallization or separation from the reaction medium. This work presents measurements of solid-liquid equilibrium data for amoxicillin and hydroxyphenylglycine in water at different temperatures (283.15 - 298.15 K), pH (5.5 - 7.5) and ethanol composition (0 - 70 wt.%). This information is relevant to determine the conditions that offer the lowest solubility for the antibiotic, favoring its separation and purification. All solubility data were obtained using an analytical method with indirect determination by UV spectroscopy. Ideal thermodynamic modeling was applied to describe the experimental solubility data sets. |
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Brazilian Journal of Chemical Engineering |
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Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous mediaAmoxicillinHydroxyphenylglycineSolubilityCrystallizationEnzymatic synthesisThe enzymatic synthesis of amoxicillin is catalyzed by Penicillin G Acylase (PGA). As byproducts, hydroxyphenylglycine and alcohol are also formed from hydrolytic reactions and antibiotic synthesis, respectively. The design of this process should be directed to promote the synthesis reaction. At the same time, it is necessary to reduce the hydrolytic reaction of amoxicillin through its crystallization or separation from the reaction medium. This work presents measurements of solid-liquid equilibrium data for amoxicillin and hydroxyphenylglycine in water at different temperatures (283.15 - 298.15 K), pH (5.5 - 7.5) and ethanol composition (0 - 70 wt.%). This information is relevant to determine the conditions that offer the lowest solubility for the antibiotic, favoring its separation and purification. All solubility data were obtained using an analytical method with indirect determination by UV spectroscopy. Ideal thermodynamic modeling was applied to describe the experimental solubility data sets.Brazilian Society of Chemical Engineering2013-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322013000100006Brazilian Journal of Chemical Engineering v.30 n.1 2013reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/S0104-66322013000100006info:eu-repo/semantics/openAccessBezerra,I. M.Chiavone-Filho,O.Mattedi,S.eng2013-03-01T00:00:00Zoai:scielo:S0104-66322013000100006Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2013-03-01T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false |
dc.title.none.fl_str_mv |
Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media |
title |
Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media |
spellingShingle |
Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media Bezerra,I. M. Amoxicillin Hydroxyphenylglycine Solubility Crystallization Enzymatic synthesis |
title_short |
Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media |
title_full |
Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media |
title_fullStr |
Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media |
title_full_unstemmed |
Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media |
title_sort |
Solid-liquid equilibrium data of amoxicillin and hydroxyphenylglycine in aqueous media |
author |
Bezerra,I. M. |
author_facet |
Bezerra,I. M. Chiavone-Filho,O. Mattedi,S. |
author_role |
author |
author2 |
Chiavone-Filho,O. Mattedi,S. |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Bezerra,I. M. Chiavone-Filho,O. Mattedi,S. |
dc.subject.por.fl_str_mv |
Amoxicillin Hydroxyphenylglycine Solubility Crystallization Enzymatic synthesis |
topic |
Amoxicillin Hydroxyphenylglycine Solubility Crystallization Enzymatic synthesis |
description |
The enzymatic synthesis of amoxicillin is catalyzed by Penicillin G Acylase (PGA). As byproducts, hydroxyphenylglycine and alcohol are also formed from hydrolytic reactions and antibiotic synthesis, respectively. The design of this process should be directed to promote the synthesis reaction. At the same time, it is necessary to reduce the hydrolytic reaction of amoxicillin through its crystallization or separation from the reaction medium. This work presents measurements of solid-liquid equilibrium data for amoxicillin and hydroxyphenylglycine in water at different temperatures (283.15 - 298.15 K), pH (5.5 - 7.5) and ethanol composition (0 - 70 wt.%). This information is relevant to determine the conditions that offer the lowest solubility for the antibiotic, favoring its separation and purification. All solubility data were obtained using an analytical method with indirect determination by UV spectroscopy. Ideal thermodynamic modeling was applied to describe the experimental solubility data sets. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-03-01 |
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=S0104-66322013000100006 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322013000100006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0104-66322013000100006 |
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.30 n.1 2013 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_ |
1754213173880160256 |