Interaction between phospholipid vesicular structures with long chain zwitterionic surfactants

Pankaj Sehgal*, Hidekazu Doe, Manu Sharma, Daniel E. Otzen

*Corresponding author for this work

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

5 Citations (Scopus)

Abstract

Solubilization of different zwitterionic phospholipid vesicles structures such as L-α-phosphatidyl-choline (PC) and 1,2-didecanoyl-snglycero-3-phosphocholine (DPC) have been studied in aqueous bulk by using zwitterionic surfactant dimethylhexadecylammoniopropanesulfonate (HPS). This has been done by studying the aggregation of HPS in pure water and in the presence of 7-36 μM of fixed concentrations of each lipid with the help of pyrene fluorescence intensity (I1/I3) measurements. The fluorescence measurements showed that HPS monomers undergo two kinds of aggregation process, which were identified by the three breaks in a plot of pyrene fluorescence versus HPS concentration. The first two breaks, C1 and C2, indicate the onset and completion of vesicle solubilization respectively, upon incorporation of HPS monomers into the vesicles and led to solubilization in the form of mixed micelles. This process was not clearly visible at low lipid concentration. We evaluated the partition coefficient (K), which defines the degree of partitioning of surfactant monomers into the vesicles with respect to the aqueous medium. A high K value of HPS-lipid aggregates indicates the stronger interactions between surfactant and lipid vesicles. The K values evaluated for PC and DPC are quite close to each other, which indicates that K values were independent of phospholipid chain length.

Original languageEnglish
Book seriesColloid and Polymer Science
Volume282
Issue7
Pages (from-to)677-683
Number of pages7
ISSN0303-402X
DOIs
Publication statusPublished - 1 May 2004

Keywords

  • Bulk properties
  • Critical micellar concentration
  • Mixed micelles
  • Surfactant-lipid interaction
  • Vesicles

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