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doi:10.1016/j.jcis.2007.08.014    
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Copyright © 2007 Elsevier Inc. All rights reserved.

Memory effects of monolayers and vesicles formed by the non-ionic surfactant, 2C18E12

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D.J. Barlowa, C.M. Hollinsheada, R.D. Harveya, L. Kudsiovaa and M.J. LawrenceCorresponding Author Contact Information, a, E-mail The Corresponding Author, E-mail The Corresponding Author

aDepartment of Pharmacy, Franklin Wilkins Building, King's College London, 150 Stamford Street, London SE1 9NH, UK


Received 20 April 2007; 
accepted 6 August 2007. 
Available online 11 August 2007.

Abstract

The behaviour of monolayers and bilayers formed by the dialkyl chain non-ionic surfactant, 1,2-di-O-octadecyl-rac-glycerol-3-ω-methoxydodecaethylene glycol (2C18E12) in water at 297 K has been investigated. Using a surface film balance (or Langmuir trough) the compression–expansion cycle of the 2C18E12 monolayer was found to be reversible when compressed to surface pressures (π) less than 42 mN m−1. Compression of 2C18E12 monolayer to π greater than 42 mN m−1 above this resulted in a considerable hysteresis upon expansion with the π remaining high relative to that obtained upon compression, suggesting a time/pressure dependent re-arrangement of 2C18E12 molecules in the film. Morphology of the 2C18E12 monolayer, investigated using Brewster angle microscopy, was also found to depend upon monolayer history. Bright, randomly dispersed domains of 2C18E12 of approximately 5 μm in size were observed during compression of the monolayer to π less than 42 mN m−1. At π of 42 mN m−1 and above, the surfactant film appeared to be almost completely ‘solid-like.’ Regardless of the extent of compression of the monolayer film, expansion of the film caused formation of chains or ‘necklaces’ of individual surfactant domains, with the extent of chain formation dependent upon pressure of compression of the monolayer and the length of time held at that pressure. Irreversible effects on 2C18E12 vesicle size were also seen upon temperature cycling the vesicles through their liquid–crystalline phase transition temperature with vesicles shrinking in size and not returning to their original size upon standing at 298 K for periods of more than 24 h. No comparable hysteresis, time, pressure or temperature effects were observed with the monolayer or vesicles formed by the corresponding phospholipid, disteaorylphosphatidylcholine, under identical conditions. The effects observed with 2C18E12 are attributed to the ability of the polyoxyethylene head group to dehydrate and intrude into the hydrophobic chain region of the mono- and bilayers. These studies have important implications for the use of the vesicles formed by 2C18E12 as drug delivery vehicles.

Graphical abstract

The anomalous behaviour of monolayers and vesicles produced by a non-ionic dichain surfactant has been investigated using a combination of Langmuir trough, Brewster angle and variable temperature turbidity measurements.


Keywords: Non-ionic surfactant; Monolayers; Vesicles; Langmuir isotherm; Brewster angle microscopy; Variable temperature turbidity measurements

Article Outline

1. Introduction
2. Experimental
2.1. Materials
2.2. Langmuir film
2.3. Brewster angle microscopy (BAM)
2.4. Vesicle preparation
2.5. Turbidity studies
3. Results
3.1. Monolayer studies
3.1.1. πA isotherms
3.1.2. BAM images
3.2. Vesicles
3.2.1. Turbidity studies
4. Discussion
5. Conclusion
References











Corresponding Author Contact InformationCorresponding author.

 
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