Interfacial and emulsion stabilising properties of amphiphilic water-soluble poly(ethylene glycol)poly(lactic acid) copolymers for the fabrication of biocompatible nanoparticles

被引:29
作者
Gref, R
Babak, V
Bouillot, P
Lukina, I
Bodorev, M
Dellacherie, E
机构
[1] Ecole Natl Super Ind Chim, Lab Chim Phys Macromol, F-54001 Nancy, France
[2] INEOS RAN, Physicochem Interfacial Phenomena Lab, Moscow 117813, Russia
[3] ENSAIA, Lab Biochim Appl, F-54505 Vandoeuvre Nancy, France
关键词
biocompatible surfactants; microscopic emulsion films; nanoemulsions; poly(ethylene glycol); poly(lactic acid); steric stabilisation;
D O I
10.1016/S0927-7757(98)00524-X
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The steric stabilisation of microscopic decane-water-decane films (with a diameter of about 100 mu m) and decane-in-water nanoemulsions (with mean droplet size of about 200 nm) by the adsorption layers of biocompatible and biodegradable water-soluble surface-active poly(ethylene glycol)-poly(lactic acid) (PEG-PLA) diblock copolymers with different HLB was studied as a function of both PEG and PLA molecular weights (MW), varying from 0.5 to 10 kg/mol. In the MW range studied, it was shown that the stability or the lifetime of the microscopic emulsion films (MEF) and of the nanoemulsions depends mainly on the length (l(PLA))of the hydrophobic PLA blocks (it increases with increase of l(PLA)), and is characterised by a stepwise dependence on the surfactant concentration. A sharp transition, from very stable to unstable MEF and emulsions: occurred at a well-defined critical surfactant concentration C*. The PLA blocks, insoluble in both decane and water, adopt the most energetically favourable "side-on" orientation at the decane-water interface, whereas the PEG blocks are oriented towards the water phase in a "mushroom" or "brush" conformation. The length of the PLA blocks determines the minimal area per adsorbed surfactant molecule at the interface and consequently the critical concentration C*. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:413 / 420
页数:8
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