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Published on: April 5, 2018
Partition and Solubilization of Phospholipid Vesicles by Noncovalently Constructed Oligomeric-like Surfactants
Zhidi Chen1,2, Yao Chen1, Linyi Zhu1
1CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
Abstract:
This work has investigated the interaction of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) vesicles with oligomeric surfactants noncovalently formed by sodium dodecyl sulfate (SDS) and a series of polyamines, 1,3-diaminopropane (PDA), triamine, spermidine, and spermine. The partition coefficients (P) of these surfactants between lipid bilayers and the aqueous phase are measured by isothermal titration microcalorimetry (ITC), showing that the P value increases and the Gibbs free energy of the partition becomes more negative with increasing oligomerization degree of the surfactants. This changing trend is similar to that of synthetic oligomeric surfactants regardless of the charge properties, suggesting that the polyamine and SDS molecules interact with the DOPC bilayer simultaneously. Meanwhile, the DOPC solubilization by these surfactants is evaluated by the effective surfactant-to-lipid molar ratios for the onset (Resat) and end (Resol) of the solubilization process, which are determined from the phase boundaries obtained by ITC, turbidity, and dynamic light scattering measurements. With the increment of oligomerization degree, the Resat and Resol values increase anomalously and are much larger than those of the synthetic surfactants with the same oligomerization degree, suggesting that noncovalently constructed oligomeric surfactants exhibit lower solubilization ability to phospholipid vesicles than the corresponding covalent oligomeric surfactants. Therefore, the noncovalently constructed oligomeric-like surfactants facilitate strong partition but weak solubilization to phospholipid vesicles, which may provide a useful strategy to mildly adjust the permeation and fluidity of phospholipid vesicles with solubilization delay.
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