Imidazolium Salts Mimicking the Structure of Natural Lipids Exploit Remarkable Properties Forming Lamellar Phases and Giant Vesicles

Tailor-made ionic liquids based on imidazolium salts have recently attracted a large amount of attention because of their extraordinary properties and versatile functionality. An intriguing ability to interact with and stabilize membranes has already been reported for 1,3-dialkylimidazolium compound...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 33(2017), 6 vom: 14. Feb., Seite 1333-1342
1. Verfasser: Drücker, Patrick (VerfasserIn)
Weitere Verfasser: Rühling, Andreas, Grill, David, Wang, Da, Draeger, Annette, Gerke, Volker, Glorius, Frank, Galla, Hans-Joachim
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2017
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Fluorescent Dyes Imidazoles Ionic Liquids Laurates Lipid Bilayers Phosphatidylcholines Phosphatidylserines Unilamellar Liposomes mehr... Viscoelastic Substances Diphenylhexatriene 1720-32-7 1-palmitoyl-2-oleoylglycero-3-phosphoserine 40290-44-6 2-Naphthylamine CKR7XL41N4 1-palmitoyl-2-oleoylphosphatidylcholine TE895536Y5 laurdan Y97FBL93VW
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520 |a Tailor-made ionic liquids based on imidazolium salts have recently attracted a large amount of attention because of their extraordinary properties and versatile functionality. An intriguing ability to interact with and stabilize membranes has already been reported for 1,3-dialkylimidazolium compounds. We now reveal further insights into the field by investigating 1,3-dimethyl-4,5-dialkylimidazolium (Cn-IMe·HI, n = 7, 11, 15) and 1,3-dibenzyl-4,5-dialkylimidazolium (Cn-IBn·HBr, n = 7, 11, 15) salts. Diverse alkyl chain lengths and headgroups differing in their steric demand were employed for the membrane interface interaction with bilayer membranes imitating the cellular plasma membrane. Membrane hydration properties and domain fluidization were analyzed by fluorescent bilayer probes in direct comparison to established model membranes in a buffered aqueous environment, which resembles the salt content and pH of the cytosol of living cells. Membrane binding and insertion was analyzed via a quartz crystal microbalance and confocal laser scanning microscopy. We show that short-chain 4,5-dialkylimidazolium salts with a bulky headgroup were able to disintegrate membranes. Long-chain imidazolium salts form bilayer membrane vesicles spontaneously and autonomously without the addition of other lipids. These 4,5-dialkylimidazolium salts are highly eligible for further biochemical engineering and drug delivery 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Imidazoles  |2 NLM 
650 7 |a Ionic Liquids  |2 NLM 
650 7 |a Laurates  |2 NLM 
650 7 |a Lipid Bilayers  |2 NLM 
650 7 |a Phosphatidylcholines  |2 NLM 
650 7 |a Phosphatidylserines  |2 NLM 
650 7 |a Unilamellar Liposomes  |2 NLM 
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650 7 |a Diphenylhexatriene  |2 NLM 
650 7 |a 1720-32-7  |2 NLM 
650 7 |a 1-palmitoyl-2-oleoylglycero-3-phosphoserine  |2 NLM 
650 7 |a 40290-44-6  |2 NLM 
650 7 |a 2-Naphthylamine  |2 NLM 
650 7 |a CKR7XL41N4  |2 NLM 
650 7 |a 1-palmitoyl-2-oleoylphosphatidylcholine  |2 NLM 
650 7 |a TE895536Y5  |2 NLM 
650 7 |a laurdan  |2 NLM 
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700 1 |a Rühling, Andreas  |e verfasserin  |4 aut 
700 1 |a Grill, David  |e verfasserin  |4 aut 
700 1 |a Wang, Da  |e verfasserin  |4 aut 
700 1 |a Draeger, Annette  |e verfasserin  |4 aut 
700 1 |a Gerke, Volker  |e verfasserin  |4 aut 
700 1 |a Glorius, Frank  |e verfasserin  |4 aut 
700 1 |a Galla, Hans-Joachim  |e verfasserin  |4 aut 
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