Interactions of doxorubicin with organized interfacial assemblies. 2. Spectroscopic characterization

Doxorubicin is an anthracycline that has found wide use as a chemotherapeutic agent, with the primary limitation to its use being cardiotoxicity. Depending on the identity and location of pendent side groups, the anthracyclines exhibit varying degrees of chemotherapeutic activity and toxicity, and a...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 29(2013), 47 vom: 26. Nov., Seite 14570-9
1. Verfasser: Nieciecka, Dorota (VerfasserIn)
Weitere Verfasser: Królikowska, Agata, Setiawan, Iwan, Krysinski, Pawel, Blanchard, G J
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Amines Antibiotics, Antineoplastic Lipid Bilayers Organophosphates Doxorubicin 80168379AG stearylamine mehr... FFV58UNY7O Dimyristoylphosphatidylcholine U86ZGC74V5
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520 |a Doxorubicin is an anthracycline that has found wide use as a chemotherapeutic agent, with the primary limitation to its use being cardiotoxicity. Depending on the identity and location of pendent side groups, the anthracyclines exhibit varying degrees of chemotherapeutic activity and toxicity, and a key area of research activity lies in understanding how the structure of the anthracycline influences its interactions with amphiphilic interfaces. We have studied interactions between doxorubicin and interfacial adlayers of octadecylamine (C18NH2), dihexadecylphosphate (DHP), and both monolayers and bilayers of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) on mica using time- and frequency-resolved spectroscopic measurements. We report surface-enhanced resonance Raman data and fluorescence lifetime and anisotropy imaging data for doxorubicin at these interfaces. For all monolayers, there is a substantial interaction between doxorubicin and the interface. For DMPC bilayers, the extent of the interaction between doxorubicin and the interface depends on how the interface was formed 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Research Support, U.S. Gov't, Non-P.H.S. 
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650 7 |a Antibiotics, Antineoplastic  |2 NLM 
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650 7 |a Organophosphates  |2 NLM 
650 7 |a Doxorubicin  |2 NLM 
650 7 |a 80168379AG  |2 NLM 
650 7 |a stearylamine  |2 NLM 
650 7 |a FFV58UNY7O  |2 NLM 
650 7 |a Dimyristoylphosphatidylcholine  |2 NLM 
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700 1 |a Królikowska, Agata  |e verfasserin  |4 aut 
700 1 |a Setiawan, Iwan  |e verfasserin  |4 aut 
700 1 |a Krysinski, Pawel  |e verfasserin  |4 aut 
700 1 |a Blanchard, G J  |e verfasserin  |4 aut 
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