Cationic Surfactants: Self-Assembly, Structure-Activity Correlation and Their Biological Applications.
1,4-diazabicyclo[2.2.2]octane
antimicrobial nanocarriers
cationic surfactants
drug delivery systems
self-assembly
solubilization
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
06 Nov 2019
06 Nov 2019
Historique:
received:
09
09
2019
revised:
31
10
2019
accepted:
04
11
2019
entrez:
9
11
2019
pubmed:
9
11
2019
medline:
14
4
2020
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 31698783
pii: ijms20225534
doi: 10.3390/ijms20225534
pmc: PMC6888607
pii:
doi:
Substances chimiques
Cations
0
Surface-Active Agents
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Russian Scientific Foundation
ID : Grant no. 19-73-30012
Organisme : Portuguese Science and Technology Foundation (FCT)
ID : Grants no. SFRH/BPD/101650/2014, SFRH/BD/130555/2017, M-ERA-NET/0004/2015 (PAIRED)
Déclaration de conflit d'intérêts
The authors declare no conflict of interest.
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