Cationic surfactants: self-assembly, structure-activity correlation and their biological applications

Detalhes bibliográficos
Autor(a) principal: Zakharova, Lucia Ya.
Data de Publicação: 2019
Outros Autores: Pashirova, Tatiana N., Doktorovova, Slavomira, Fernandes, Ana R., Sanchez-Lopez, Elena, Silva, Amélia M., Souto, Selma B., Souto, Eliana B.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/61960
Resumo: The development of biotechnological protocols based on cationic surfactants is a modern trend focusing on the fabrication of antimicrobial and bioimaging agents, supramolecular catalysts, stabilizers of nanoparticles, and especially drug and gene nanocarriers. The main emphasis given to the design of novel ecologically friendly and biocompatible cationic surfactants makes it possible to avoid the drawbacks of nanoformulations preventing their entry to clinical trials. To solve the problem of toxicity various ways are proposed, including the use of mixed composition with nontoxic nonionic surfactants and/or hydrotropic agents, design of amphiphilic compounds bearing natural or cleavable fragments. Essential advantages of cationic surfactants are the structural diversity of their head groups allowing of chemical modification and introduction of desirable moiety to answer the green chemistry criteria. The latter can be exemplified by the design of novel families of ecological friendly cleavable surfactants, with improved biodegradability, amphiphiles with natural fragments, and geminis with low aggregation threshold. Importantly, the development of amphiphilic nanocarriers for drug delivery allows understanding the correlation between the chemical structure of surfactants, their aggregation behavior, and their functional activity. This review focuses on several aspects related to the synthesis of innovative cationic surfactants and their broad biological applications including antimicrobial activity, solubilization of hydrophobic drugs, complexation with DNA, and catalytic effect toward important biochemical reaction.
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spelling Cationic surfactants: self-assembly, structure-activity correlation and their biological applicationsCationic surfactants1,4-diazabicyclo[2.2.2]octaneSelf-assemblySolubilizationdrug delivery systemsAntimicrobial nanocarriersEngenharia e Tecnologia::Biotecnologia IndustrialScience & TechnologyThe development of biotechnological protocols based on cationic surfactants is a modern trend focusing on the fabrication of antimicrobial and bioimaging agents, supramolecular catalysts, stabilizers of nanoparticles, and especially drug and gene nanocarriers. The main emphasis given to the design of novel ecologically friendly and biocompatible cationic surfactants makes it possible to avoid the drawbacks of nanoformulations preventing their entry to clinical trials. To solve the problem of toxicity various ways are proposed, including the use of mixed composition with nontoxic nonionic surfactants and/or hydrotropic agents, design of amphiphilic compounds bearing natural or cleavable fragments. Essential advantages of cationic surfactants are the structural diversity of their head groups allowing of chemical modification and introduction of desirable moiety to answer the green chemistry criteria. The latter can be exemplified by the design of novel families of ecological friendly cleavable surfactants, with improved biodegradability, amphiphiles with natural fragments, and geminis with low aggregation threshold. Importantly, the development of amphiphilic nanocarriers for drug delivery allows understanding the correlation between the chemical structure of surfactants, their aggregation behavior, and their functional activity. This review focuses on several aspects related to the synthesis of innovative cationic surfactants and their broad biological applications including antimicrobial activity, solubilization of hydrophobic drugs, complexation with DNA, and catalytic effect toward important biochemical reaction.Russian Science Foundation; grant No. 19-73-30012, and from the Portuguese Science and Technology Foundation (FCT) no. SFRH/BPD/101650/2014 granted to SD, SFRH/BD/130555/2017 granted to ARF, and project reference M-ERA-NET/0004/2015 (PAIRED)info:eu-repo/semantics/publishedVersionMDPIUniversidade do MinhoZakharova, Lucia Ya.Pashirova, Tatiana N.Doktorovova, SlavomiraFernandes, Ana R.Sanchez-Lopez, ElenaSilva, Amélia M.Souto, Selma B.Souto, Eliana B.2019-11-062019-11-06T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/61960engZakharova, Lucia Ya.; Pashirova, Tatiana N.; Doktorovova, Slavomira; Fernandes, Ana R.; Sanchez-Lopez, Elena; Silva, Amélia M.; Souto, Selma B.; Souto, Eliana, Cationic surfactants: self-assembly, structure-activity correlation and their biological applications. International Journal of Molecular Sciences, 20(22), 5534, 20191424-67831422-00671661-659610.3390/ijms2022553431698783http://www.mdpi.com/journal/ijmsinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:42:32Zoai:repositorium.sdum.uminho.pt:1822/61960Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:39:48.557523Repositório 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 Cationic surfactants: self-assembly, structure-activity correlation and their biological applications
title Cationic surfactants: self-assembly, structure-activity correlation and their biological applications
spellingShingle Cationic surfactants: self-assembly, structure-activity correlation and their biological applications
Zakharova, Lucia Ya.
Cationic surfactants
1,4-diazabicyclo[2.2.2]octane
Self-assembly
Solubilization
drug delivery systems
Antimicrobial nanocarriers
Engenharia e Tecnologia::Biotecnologia Industrial
Science & Technology
title_short Cationic surfactants: self-assembly, structure-activity correlation and their biological applications
title_full Cationic surfactants: self-assembly, structure-activity correlation and their biological applications
title_fullStr Cationic surfactants: self-assembly, structure-activity correlation and their biological applications
title_full_unstemmed Cationic surfactants: self-assembly, structure-activity correlation and their biological applications
title_sort Cationic surfactants: self-assembly, structure-activity correlation and their biological applications
author Zakharova, Lucia Ya.
author_facet Zakharova, Lucia Ya.
Pashirova, Tatiana N.
Doktorovova, Slavomira
Fernandes, Ana R.
Sanchez-Lopez, Elena
Silva, Amélia M.
Souto, Selma B.
Souto, Eliana B.
author_role author
author2 Pashirova, Tatiana N.
Doktorovova, Slavomira
Fernandes, Ana R.
Sanchez-Lopez, Elena
Silva, Amélia M.
Souto, Selma B.
Souto, Eliana B.
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Zakharova, Lucia Ya.
Pashirova, Tatiana N.
Doktorovova, Slavomira
Fernandes, Ana R.
Sanchez-Lopez, Elena
Silva, Amélia M.
Souto, Selma B.
Souto, Eliana B.
dc.subject.por.fl_str_mv Cationic surfactants
1,4-diazabicyclo[2.2.2]octane
Self-assembly
Solubilization
drug delivery systems
Antimicrobial nanocarriers
Engenharia e Tecnologia::Biotecnologia Industrial
Science & Technology
topic Cationic surfactants
1,4-diazabicyclo[2.2.2]octane
Self-assembly
Solubilization
drug delivery systems
Antimicrobial nanocarriers
Engenharia e Tecnologia::Biotecnologia Industrial
Science & Technology
description The development of biotechnological protocols based on cationic surfactants is a modern trend focusing on the fabrication of antimicrobial and bioimaging agents, supramolecular catalysts, stabilizers of nanoparticles, and especially drug and gene nanocarriers. The main emphasis given to the design of novel ecologically friendly and biocompatible cationic surfactants makes it possible to avoid the drawbacks of nanoformulations preventing their entry to clinical trials. To solve the problem of toxicity various ways are proposed, including the use of mixed composition with nontoxic nonionic surfactants and/or hydrotropic agents, design of amphiphilic compounds bearing natural or cleavable fragments. Essential advantages of cationic surfactants are the structural diversity of their head groups allowing of chemical modification and introduction of desirable moiety to answer the green chemistry criteria. The latter can be exemplified by the design of novel families of ecological friendly cleavable surfactants, with improved biodegradability, amphiphiles with natural fragments, and geminis with low aggregation threshold. Importantly, the development of amphiphilic nanocarriers for drug delivery allows understanding the correlation between the chemical structure of surfactants, their aggregation behavior, and their functional activity. This review focuses on several aspects related to the synthesis of innovative cationic surfactants and their broad biological applications including antimicrobial activity, solubilization of hydrophobic drugs, complexation with DNA, and catalytic effect toward important biochemical reaction.
publishDate 2019
dc.date.none.fl_str_mv 2019-11-06
2019-11-06T00:00:00Z
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/1822/61960
url http://hdl.handle.net/1822/61960
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Zakharova, Lucia Ya.; Pashirova, Tatiana N.; Doktorovova, Slavomira; Fernandes, Ana R.; Sanchez-Lopez, Elena; Silva, Amélia M.; Souto, Selma B.; Souto, Eliana, Cationic surfactants: self-assembly, structure-activity correlation and their biological applications. International Journal of Molecular Sciences, 20(22), 5534, 2019
1424-6783
1422-0067
1661-6596
10.3390/ijms20225534
31698783
http://www.mdpi.com/journal/ijms
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 MDPI
publisher.none.fl_str_mv MDPI
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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