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Journal of Chromatography A
Volume 1125, Issue 1, 25 August 2006, Pages 89-94
 
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doi:10.1016/j.chroma.2006.05.031    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2006 Elsevier B.V. All rights reserved.

A high-performance liquid chromatography method for determination 2-(n-(N,N,N-trimethyl)-n-alkyl)-5-alkylfuryl halides in dipalmitoylphosphatidilcholine liposome solutions

Javier Moralesa, Antonio L. Zanoccoa, Germán Günthera and Else LempCorresponding Author Contact Information, a, E-mail The Corresponding Author

aUniversidad de Chile, Facultad de Ciencias Químicas y Farmacéuticas, Departamento de Química Orgánica y Fisicoquímica, Olivos 1007, Casilla 233, Santiago, Chile

Received 8 March 2006; 
revised 11 May 2006; 
accepted 12 May 2006. 
Available online 13 June 2006.

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Abstract

A high-performance liquid chromatography (HPLC) method for the determination of 2-(4-(N,N,N-trimethyl)-butyl)-5-dodecylfuryl bromide (DFTA) in dipalmitoylphophatidil-choline (DPPC) liposome solutions has been developed. Lipid-soluble furan derivatives, 2,5-disubstituted with different n-alkyl chains and a terminal trimethylammonium group are useful probes for studying singlet oxygen dynamics and equilibria in microcompartmentalized systems. The actual HPLC method uses a gradient elution and DAD detection. The chromatographic separation of these components is achieved using a C18 analytical column with a 10 mM solution of 1-heptanesulfonic acid (PIC-7)–methanol (10:90, v/v) as initial mobile phase. Both DFTA peaks are well resolved and free of interference from matrix components and reaction products. The method has been found to be linear (r > 0.999) over a wide concentration range and reliable to perform kinetic experiments in which the time dependent consumption of a tetraalkylammonium surfactant in a microorganized systems composed by lipidic surfactants is followed.

Keywords: HPLC; Tetraalkylammonium-derivatives; Liposomes; Singlet oxygen; Furane-derivatives; Phospholipids

Article Outline

1. Introduction
2. Experimental details
2.1. Chemicals
2.2. Liposome preparation [18] and [19]
2.3. Preparation of reagents
2.4. High-performance liquid chromatography (HPLC)
2.5. Preparation of DFTA loaded liposome samples for HPLC analysis
3. Results and discussion
3.1. Linearity and range
3.2. Accuracy
3.3. Precision
3.4. Quantitation limit
3.5. A kinetic experiment
4. Conclusions
Acknowledgements
References






 
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