Synthesis and phase behavior of new amphiphilic PEG-based triblock copolymers as gelling agents for lamellar liquid crystalline phases

被引:18
|
作者
Slack, NL
Schellhorn, M
Eiselt, P
Chibbaro, MA
Schulze, U
Warriner, HE
Davidson, P
Schmidt, HW
Safinya, CR
机构
[1] Univ Bayreuth, Bayreuther Inst Makromol Forsch, D-95440 Bayreuth, Germany
[2] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA
[4] Univ Calif Santa Barbara, Biochem & Mol Biol Program, Santa Barbara, CA 93106 USA
[5] Boehringer Ingelheim KG, D-55216 Ingelheim, Germany
[6] Univ Paris Sud, Phys Solides Lab, CNRS, F-91405 Orsay, France
关键词
D O I
10.1021/ma980901g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report the first evidence of the potential of new amphiphilic ABA-triblock copolymers as gelling agents for lamellar liquid crystalline L-alpha phases. Recently, we described a new type of lamellar hydrogels which are not based on a polymer network swollen in water but are obtained by the addition of small amounts of a nonionic polymer surfactant to the fluid lamellar L-alpha phase of the dimyristoyl-phosphatidyl-choline(DMPC)/pentanol/water system. In contrast with these previously reported gelling agents which were all AB-diblock copolymers, the novel ABA-triblock copolymers consist of double chain hydrophobic moieties (A) attached to each end of a poly(ethylene glycol) chain (B). The synthesis of these new macromolecules and their gelation properties are described. The comparison of these novel lamellar hydrogels with those based on the AB-diblock copolymers provides direct evidence for the existence of cross-bridging conformations of the ABA-triblock copolymers between adjacent membranes.
引用
收藏
页码:8503 / 8508
页数:6
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