Synthesis and Phase Behavior of New Amphiphilic PEG-Based Triblock Copolymers as Gelling Agents for Lamellar Liquid Crystalline Phases
Author(s) -
Nelle L. Slack,
Mathias Schellhorn,
Petra Eiselt,
Michael A. Chibbaro,
Uwe Schulze,
Heidi E. Warriner,
Patrick Davidson,
HansWerner Schmidt,
Cyrus R. Safinya
Publication year - 1998
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/ma980901g
Subject(s) - lamellar structure , copolymer , amphiphile , ethylene glycol , polymer chemistry , lamellar phase , self healing hydrogels , polymer , pulmonary surfactant , materials science , chemical engineering , peg ratio , phase (matter) , self assembly , chemistry , organic chemistry , crystallography , nanotechnology , finance , economics , engineering
We report the first evidence of the potential of new amphiphilic ABA-triblock copolymers as gelling agents for lamellar liquid crystalline LR 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 LR 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.
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