Effects of alcohols and diols on the phase behaviour of quaternary systems

被引:122
作者
Alany, RG [1 ]
Rades, T
Agatonovic-Kustrin, S
Davies, NM
Tucker, IG
机构
[1] Univ Otago, Sch Pharm, Dunedin, New Zealand
[2] F Hoffmann La Roche & Co Ltd, PRNF, CH-4070 Basel, Switzerland
关键词
microemulsions; cosurfactants; alcohols; diols; phase diagrams;
D O I
10.1016/S0378-5173(99)00408-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the current study was to investigate the effect of different co-surfactants on the phase behaviour of the pseudoternary system water:ethyl oleate:nonionic surfactant blend (sorbitan monolaurate/polyoxyethylene 20 sorbitan mono-oleate). Four aliphatic alcohols (1-propanol, 1-butanol, 1-hexanol and 1-octanol) and four 1,2-alkanediols (1,2-propanediol. 1,2-pentanediol, 1,2-hexanediol and 1,2-octanediol) were used. The co-surfactant-free system forms two different colloidal structures, a water-in-oil microemulsion (w/o ME) and lamellar liquid crystals (LC) and two coarse dispersions, water-in-oil (w/o EM) and oil-in-water (o/w EM) emulsions. Microemulsion region area (%ME), liquid crystalline region area (%LC), amount of amphiphile blend required to produce a balanced microemulsion (%AMPH) and amount of water solubilised (%W)were used as assessment criteria to evaluate the co-surfactants. Seven calculated physico-chemical descriptors were used to represent the different co-surfactants. 1-butanol, 1,2-hexanediol and 1,2-octanediol produced balanced MEs capable of solubilising a high percentage of both oil and water. A similarity was observed between the descriptors attributed to I-butanol and 1,2-hexanediol. The requirements of a co-surfactant molecule to produce a balanced microemulsion were: HLB Value 7.0-8.0, a carbon backbone of 4-6 atoms, percentage carbon of 60-65%, percentage oxygen of 20-30%, log P value 0.2-0.9 and log 1/S (S: aqueous solubility) close to zero. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:141 / 145
页数:5
相关论文
共 7 条
[1]   Use of artificial neural networks to predict quaternery phase systems from limited experimental data [J].
Alany, RG ;
Agatonovic-Kustrin, S ;
Rades, T ;
Tucker, IG .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1999, 19 (3-4) :443-452
[2]  
BOURREL M, 1988, MICROEMULSIONS RELAT, P15
[3]   The effect of alcohols with different structures on the formation of warm O/W microemulsions [J].
Cavalli, R ;
Marengo, E ;
Caputo, O ;
Ugazio, E ;
Gasco, MR .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 1996, 17 (07) :717-734
[4]   PREPARING NONTOXIC MICROEMULSIONS [J].
KAHLWEIT, M ;
BUSSE, G ;
FAULHABER, B ;
EIBL, H .
LANGMUIR, 1995, 11 (11) :4185-4187
[5]   Preparing nontoxic microemulsions with alkyl monoglucosides and the role of alkanediols as cosolvents [J].
Kahlweit, M ;
Busse, G ;
Faulhaber, B .
LANGMUIR, 1996, 12 (04) :861-862
[6]  
Prince L., 1977, MICROEMULSIONS THEOR, P1, DOI 10.1016/B978-0-12-565750-1.50006-0
[7]   LECITHIN-BASED MICROEMULSIONS - PHASE-BEHAVIOR AND MICROSTRUCTURE [J].
SHINODA, K ;
ARAKI, M ;
SADAGHIANI, A ;
KHAN, A ;
LINDMAN, B .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (02) :989-993