Surface properties of unsaturated non-oxidized and oxidized free fatty acids spread as monomolecular films at an argon/water interface

被引:20
作者
Abousalham, A
Fotiadu, F
Buono, G
Verger, R
机构
[1] CNRS, UPR 9025, Lab Lipolyse Enzymat, F-13402 Marseille 20, France
[2] Univ Aix Marseille 3, ENSSPICAM, F-133997 Marseille, France
关键词
area per molecule; beta-cyclodextrin; dipole moment; monomolecular film desorption; oxidized free fatty acid; surface pressure;
D O I
10.1016/S0009-3084(99)00109-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interfacial properties of monomolecular films of stearic acid (SA) oleic acid (OA), linoleic acid (LA), ricinoleic acid (RA), 13(S)-hydroperoxyoctadeca-9Z, 11E-dienoic acid (13-HPODE) and 13(S)-hydroxyoctadeca-9Z, 11E-dienoic acid (13-HODE) were studied by recording the changes occurring in response to monomolecular film compression in their surface pressure and surface potential at the argon/water interface. The oxidized free fatty acids are more expanded than the parent non-oxidized free fatty acids, reflecting a higher hydrophilic-lipophilic balance. The lift-off values of the molecular area of 13-HODE, 13-HPODE and RA were 68, 74 and 106 Angstrom(2) molecule(-1), respectively, as compared to 47 and 40 Angstrom(2) molecule(-1) in the case of LA and OA, respectively. Variations in the molecular orientation of free fatty acids can result in large changes in the dipole moment which are not accompanied by appreciable changes in the surface pressure. In the case of the oxidized free fatty acids, the spontaneous desorption into the aqueous phase was found to increase at increasing surface pressures. The desorption rates of OA and LA increased dramatically in the presence of P-cyclodextrin (P-CD); whereas the presence of P-CD only slightly increased the desorption rates of the oxidized free fatty acids. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:93 / 99
页数:7
相关论文
共 38 条
[1]  
ADAM NK, 1968, PHYSICS CHEM SURFACE, P74
[2]  
ASGHARIAN B, 1988, COLLOID SURFACE, V34, P143
[3]   THE DIFFERENT TYPES OF ISOTHERM EXHIBITED BY INSOLUBLE FATTY-ACID MONOLAYERS - A THEORETICAL INTERPRETATION OF PHASE-TRANSITIONS IN THE CONDENSED STATE [J].
BARET, JF ;
HASMONAY, H ;
FIRPO, JL ;
DUPIN, JJ ;
DUPEYRAT, M .
CHEMISTRY AND PHYSICS OF LIPIDS, 1982, 30 (2-3) :177-187
[4]   CENTRAL NERVOUS-SYSTEM TRAUMA AND STROKE .1. BIOCHEMICAL CONSIDERATIONS FOR OXYGEN RADICAL FORMATION AND LIPID-PEROXIDATION [J].
BRAUGHLER, JM ;
HALL, ED .
FREE RADICAL BIOLOGY AND MEDICINE, 1989, 6 (03) :289-301
[5]   DIPOLE POTENTIAL OF LIPID-MEMBRANES [J].
BROCKMAN, H .
CHEMISTRY AND PHYSICS OF LIPIDS, 1994, 73 (1-2) :57-79
[6]   Direct imaging by cryo-TEM shows membrane break-up by phospholipase A2 enzymatic activity [J].
Callisen, TH ;
Talmon, Y .
BIOCHEMISTRY, 1998, 37 (31) :10987-10993
[7]   PHASE-BEHAVIOR AND BILAYER PROPERTIES OF FATTY-ACIDS - HYDRATED 1-1 ACID SOAPS [J].
CISTOLA, DP ;
ATKINSON, D ;
HAMILTON, JA ;
SMALL, DM .
BIOCHEMISTRY, 1986, 25 (10) :2804-2812
[8]  
Davies JT., 1963, INTERFACIAL PHENOMEN, P480
[9]  
GAINES GL, 1966, INSOLUBLE MONOLAYERS, P188
[10]   DECOMPOSITION OF LINOLEIC-ACID HYDROPEROXIDES - ENZYMIC REACTIONS COMPARED WITH NONENZYMIC [J].
GARDNER, HW .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1975, 23 (02) :129-136