The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems

Detalhes bibliográficos
Autor(a) principal: Basaiahgari, Anusha
Data de Publicação: 2020
Outros Autores: Passos, Helena, Coutinho, João A. P., Gardas, Ramesh L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/33187
Resumo: The use of hydrophilic zwitterionic compounds (ZI) to act as phase forming components of aqueous biphasic systems (ABS) has been attracting increased interest. Although previous works studied the phase behavior of ZI, there is still a lack of knowledge on the partition behavior of compounds in ZI-based ABS. This work reports a study on the influence of ZI structure for the extraction of 7 different biomolecules selected as molecular probes – 2 alkaloids (nicotine and caffeine), 2 phenolic compounds (gallic acid and vanillic acid) and 3 amino acids (L-tryptophan, L-tyrosine and L-phenylalanine). The partition and extraction efficiencies of these biomolecules were evaluated in ternary systems composed of hydrophilic ZI constituted by ammonium, imidazolium, pyridinium and piperidinium cationic and SO3− anionic groups, K2CO3 and water. The obtained results show that all the biomolecules preferentially partition to the ZI-rich phase, and the extent of their partition was closely related with the octanol–water partition coefficients of both biomolecules and ZI. It was demonstrated that the partition of biomolecules in ZI-based ABS is firstly ruled by hydrophobic/hydrophilic effects and only in some particular cases specific interactions between the biomolecule and the ZI affect their partition. Furthermore, despite the similarity between ZI and ionic liquids behavior as phase forming compounds of ABS for the extraction of biomolecules, ZI-based ABS presented a better performance in the extraction of phenolic compounds in alkaline environment.
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spelling The influence of zwitterions on the partition of biomolecules in aqueous biphasic systemsAqueous biphasic systemsZwitterionic compoundsAlkaloidsPhenolic compoundsAmino acidsPartition coefficientHydrophobic/hydrophilic effectsThe use of hydrophilic zwitterionic compounds (ZI) to act as phase forming components of aqueous biphasic systems (ABS) has been attracting increased interest. Although previous works studied the phase behavior of ZI, there is still a lack of knowledge on the partition behavior of compounds in ZI-based ABS. This work reports a study on the influence of ZI structure for the extraction of 7 different biomolecules selected as molecular probes – 2 alkaloids (nicotine and caffeine), 2 phenolic compounds (gallic acid and vanillic acid) and 3 amino acids (L-tryptophan, L-tyrosine and L-phenylalanine). The partition and extraction efficiencies of these biomolecules were evaluated in ternary systems composed of hydrophilic ZI constituted by ammonium, imidazolium, pyridinium and piperidinium cationic and SO3− anionic groups, K2CO3 and water. The obtained results show that all the biomolecules preferentially partition to the ZI-rich phase, and the extent of their partition was closely related with the octanol–water partition coefficients of both biomolecules and ZI. It was demonstrated that the partition of biomolecules in ZI-based ABS is firstly ruled by hydrophobic/hydrophilic effects and only in some particular cases specific interactions between the biomolecule and the ZI affect their partition. Furthermore, despite the similarity between ZI and ionic liquids behavior as phase forming compounds of ABS for the extraction of biomolecules, ZI-based ABS presented a better performance in the extraction of phenolic compounds in alkaline environment.Elsevier2022-12-15T00:00:00Z2020-12-15T00:00:00Z2020-12-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/33187eng1383-586610.1016/j.seppur.2020.117537Basaiahgari, AnushaPassos, HelenaCoutinho, João A. P.Gardas, Ramesh L.info:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:03:42Zoai:ria.ua.pt:10773/33187Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:04:36.728787Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems
title The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems
spellingShingle The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems
Basaiahgari, Anusha
Aqueous biphasic systems
Zwitterionic compounds
Alkaloids
Phenolic compounds
Amino acids
Partition coefficient
Hydrophobic/hydrophilic effects
title_short The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems
title_full The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems
title_fullStr The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems
title_full_unstemmed The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems
title_sort The influence of zwitterions on the partition of biomolecules in aqueous biphasic systems
author Basaiahgari, Anusha
author_facet Basaiahgari, Anusha
Passos, Helena
Coutinho, João A. P.
Gardas, Ramesh L.
author_role author
author2 Passos, Helena
Coutinho, João A. P.
Gardas, Ramesh L.
author2_role author
author
author
dc.contributor.author.fl_str_mv Basaiahgari, Anusha
Passos, Helena
Coutinho, João A. P.
Gardas, Ramesh L.
dc.subject.por.fl_str_mv Aqueous biphasic systems
Zwitterionic compounds
Alkaloids
Phenolic compounds
Amino acids
Partition coefficient
Hydrophobic/hydrophilic effects
topic Aqueous biphasic systems
Zwitterionic compounds
Alkaloids
Phenolic compounds
Amino acids
Partition coefficient
Hydrophobic/hydrophilic effects
description The use of hydrophilic zwitterionic compounds (ZI) to act as phase forming components of aqueous biphasic systems (ABS) has been attracting increased interest. Although previous works studied the phase behavior of ZI, there is still a lack of knowledge on the partition behavior of compounds in ZI-based ABS. This work reports a study on the influence of ZI structure for the extraction of 7 different biomolecules selected as molecular probes – 2 alkaloids (nicotine and caffeine), 2 phenolic compounds (gallic acid and vanillic acid) and 3 amino acids (L-tryptophan, L-tyrosine and L-phenylalanine). The partition and extraction efficiencies of these biomolecules were evaluated in ternary systems composed of hydrophilic ZI constituted by ammonium, imidazolium, pyridinium and piperidinium cationic and SO3− anionic groups, K2CO3 and water. The obtained results show that all the biomolecules preferentially partition to the ZI-rich phase, and the extent of their partition was closely related with the octanol–water partition coefficients of both biomolecules and ZI. It was demonstrated that the partition of biomolecules in ZI-based ABS is firstly ruled by hydrophobic/hydrophilic effects and only in some particular cases specific interactions between the biomolecule and the ZI affect their partition. Furthermore, despite the similarity between ZI and ionic liquids behavior as phase forming compounds of ABS for the extraction of biomolecules, ZI-based ABS presented a better performance in the extraction of phenolic compounds in alkaline environment.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-15T00:00:00Z
2020-12-15
2022-12-15T00:00:00Z
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/10773/33187
url http://hdl.handle.net/10773/33187
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1383-5866
10.1016/j.seppur.2020.117537
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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