Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments

Bibliographic Details
Main Author: Azenha, Ivo S.
Publication Date: 2021
Other Authors: Aniceto, José P. S., Ribeiro, Diogo P., Mendes, Adélio, Silva, Carlos M.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10773/37728
Summary: The reversed-phase chromatographic separation of two triterpenic acids (TTAs), betulinic and oleanolic acids, using a triacontyl (C30) stationary phase was addressed in this work. Methanol, water, acetonitrile, ethanol, isopropanol, ethyl acetate, acetone and mixtures thereof were tested, and the best mobile phase to conduct the separation was found to be methanol/acetonitrile 50/50 (%, v/v) at 23 °C, taking into account parameters like selectivity, resolution and TTAs solubility. The method of moments was used to determine the equilibrium constants of isotherms, the axial dispersion coefficients and the global linear driving force coefficients of pure betulinic and pure oleanolic acids. These parameters were then successfully validated by modeling unary and binary breakthrough curves. Simulated moving bed calculations showed that betulinic and oleanolic acids can be both obtained with purity of 99.2 % and productivity of 56.2 kg/(m3adsorbent day) using the packing material of an Acclaim C30 column with a 1-1-1-1 configuration with columns of 7.5 cm long. Finally, in order to recover the two TTAs from the SMB extract and raffinate streams, water was envisioned as a precipitation agent. Accordingly, the solubility of each TTA was measured in methanol/acetonitrile 70/30, 50/50, and 30/70 (%, v/v) modified with water. The obtained results showed that adding 65 % (%, v/v) of water it is possible to precipitate 98 % of the dissolved TTAs in all the tested methanol/acetonitrile mixtures.
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spelling Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of momentsBetulinic acidOleanolic acidTriterpenoidsTriacontyl (C30)Simulated moving bed chromatographyThe reversed-phase chromatographic separation of two triterpenic acids (TTAs), betulinic and oleanolic acids, using a triacontyl (C30) stationary phase was addressed in this work. Methanol, water, acetonitrile, ethanol, isopropanol, ethyl acetate, acetone and mixtures thereof were tested, and the best mobile phase to conduct the separation was found to be methanol/acetonitrile 50/50 (%, v/v) at 23 °C, taking into account parameters like selectivity, resolution and TTAs solubility. The method of moments was used to determine the equilibrium constants of isotherms, the axial dispersion coefficients and the global linear driving force coefficients of pure betulinic and pure oleanolic acids. These parameters were then successfully validated by modeling unary and binary breakthrough curves. Simulated moving bed calculations showed that betulinic and oleanolic acids can be both obtained with purity of 99.2 % and productivity of 56.2 kg/(m3adsorbent day) using the packing material of an Acclaim C30 column with a 1-1-1-1 configuration with columns of 7.5 cm long. Finally, in order to recover the two TTAs from the SMB extract and raffinate streams, water was envisioned as a precipitation agent. Accordingly, the solubility of each TTA was measured in methanol/acetonitrile 70/30, 50/50, and 30/70 (%, v/v) modified with water. The obtained results showed that adding 65 % (%, v/v) of water it is possible to precipitate 98 % of the dissolved TTAs in all the tested methanol/acetonitrile mixtures.Elsevier2023-05-15T14:14:15Z2021-04-01T00:00:00Z2021-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/37728eng1383-586610.1016/j.seppur.2020.118208Azenha, Ivo S.Aniceto, José P. S.Ribeiro, Diogo P.Mendes, AdélioSilva, Carlos M.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-11-11T01:46:52Zoai:ria.ua.pt:10773/37728Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:19:32.845604Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments
title Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments
spellingShingle Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments
Azenha, Ivo S.
Betulinic acid
Oleanolic acid
Triterpenoids
Triacontyl (C30)
Simulated moving bed chromatography
title_short Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments
title_full Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments
title_fullStr Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments
title_full_unstemmed Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments
title_sort Reversed-phase chromatographic separation and downstream precipitation of lupane- and oleanane-type triterpenoids: experiments and modeling based on the method of moments
author Azenha, Ivo S.
author_facet Azenha, Ivo S.
Aniceto, José P. S.
Ribeiro, Diogo P.
Mendes, Adélio
Silva, Carlos M.
author_role author
author2 Aniceto, José P. S.
Ribeiro, Diogo P.
Mendes, Adélio
Silva, Carlos M.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Azenha, Ivo S.
Aniceto, José P. S.
Ribeiro, Diogo P.
Mendes, Adélio
Silva, Carlos M.
dc.subject.por.fl_str_mv Betulinic acid
Oleanolic acid
Triterpenoids
Triacontyl (C30)
Simulated moving bed chromatography
topic Betulinic acid
Oleanolic acid
Triterpenoids
Triacontyl (C30)
Simulated moving bed chromatography
description The reversed-phase chromatographic separation of two triterpenic acids (TTAs), betulinic and oleanolic acids, using a triacontyl (C30) stationary phase was addressed in this work. Methanol, water, acetonitrile, ethanol, isopropanol, ethyl acetate, acetone and mixtures thereof were tested, and the best mobile phase to conduct the separation was found to be methanol/acetonitrile 50/50 (%, v/v) at 23 °C, taking into account parameters like selectivity, resolution and TTAs solubility. The method of moments was used to determine the equilibrium constants of isotherms, the axial dispersion coefficients and the global linear driving force coefficients of pure betulinic and pure oleanolic acids. These parameters were then successfully validated by modeling unary and binary breakthrough curves. Simulated moving bed calculations showed that betulinic and oleanolic acids can be both obtained with purity of 99.2 % and productivity of 56.2 kg/(m3adsorbent day) using the packing material of an Acclaim C30 column with a 1-1-1-1 configuration with columns of 7.5 cm long. Finally, in order to recover the two TTAs from the SMB extract and raffinate streams, water was envisioned as a precipitation agent. Accordingly, the solubility of each TTA was measured in methanol/acetonitrile 70/30, 50/50, and 30/70 (%, v/v) modified with water. The obtained results showed that adding 65 % (%, v/v) of water it is possible to precipitate 98 % of the dissolved TTAs in all the tested methanol/acetonitrile mixtures.
publishDate 2021
dc.date.none.fl_str_mv 2021-04-01T00:00:00Z
2021-04-01
2023-05-15T14:14:15Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/37728
url http://hdl.handle.net/10773/37728
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1383-5866
10.1016/j.seppur.2020.118208
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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institution RCAAP
reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
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