A. Kasselouri et al., MIXED MONOLAYERS OF AMPHIPHILIC CYCLODEXTRINS AND PHOSPHOLIPIDS .1. MISCIBILITY UNDER DYNAMIC CONDITIONS OF COMPRESSION, Journal of colloid and interface science, 180(2), 1996, pp. 384-397
The miscibility of per-(6-amino-2,3-di-O-hexyl) beta-CD hydrochloride
salt abbreviated NH3-(beta)-CD-OC6 with 1,2 dipalmitoyl, 3-sn-phosphat
idyl choline (DPPC) and 1,2 dipalmitoyl, 3-sn-phosphatidic acid (DPPA)
and of per-(6-dodecanoylamino-6-deoxy) beta-CD abbreviated C11CONH-be
ta-CD with DPPC has been assessed by surface pressure-area experiments
under dynamic conditions. The determination of their mixing behavior
has been approached by thermodynamic characterization derived from a c
omparison of the composition dependence of collapse pressure, for vari
ous contents of two components in monolayers, with that predicted from
a model of ideal mixing. Component miscibility has additionally been
addressed by the use of the Smaby-Brockman state equation for liquid-e
xpanded monolayers which characterizes interaction between monolayer c
omponents using the water activity coefficient, While for both NH3-bet
a-CD-OC6-DPPC and NH3-beta CD-OC6-DPPA systems the average surface are
as followed the additivity rule, for the latter system surface pressur
es at collapse significantly deviated from ideality, The occurrence of
an interaction at the level of oppositely charged polar groups of NH3
-beta-CDOC6 and DPPA was also demonstrated by the nonideal composition
dependence of the water activity coefficient (f(1)) characterizing th
e interfacial water. The mixing energies and interaction parameters at
collapse pressures were calculated using the Joos approach. Positive
values of these factors indicated that NH3-beta-CD-OC6 and DPPA mixed
films were thermodynamically less stable than the films in which ideal
mixing of components occurred. The mixing of NH3-beta-CD-OC6 with DPP
C appeared to be almost ideal, In the case of the C11CONH-beta-CD-DPPC
system, analysis according to both the Joos and Goodrich approaches s
howed the occurrence of an important interaction which resulted in neg
ative mixing energies characteristic of thermodynamically stable mixed
films. (C) 1996 Academic Press, Inc.