Korea Polymer Journal, Vol.6, No.1, 34-40, March, 1998
Self-Assembly of Rigid Polypeptides
the amphiphilic block copolymers, consisting of polypeptides [poly(γ-benzyl L-glutamate) or poly(L-ieucinel)]as the hydrophobic component and polyether [or poly(N-isopropylacrylamide) (PNIPAAm)] as the hydrophilic one were prepared by the ring-opening polymerization of the corresponding N-carboxyanhydrides, initiated by the amino-terminated poly(ethylene oxide) (PEO) (or PNIPAAm). These amphiphilic copolymers in water can self-assemble to form stable micelles that are presumed to compose of the hydrophilic shell and the rigid rod-like and hydrophobic core. The micellar properties such as CMC, micelle size, and micelle shape were studied by fluorescent probe techniques, dynamic light scattering, and transmission electron microscopy. respectivwly From application of self-assembled micelles it was found that release characteristics of the hydrophobic drugs (clonazepam or indomethacin) loaded into the core part of these micelles was dependent on the drug loading contents and chain length of the hydrophobic part of the copolymers. The higher the hydrophobic portion in the block copolymer, the smaller the CMC of the copolymer. For the polymeric micelles with PNIPAAm outershell, their CMCs are less affected by temperature than the other polymeric micelles. this property strongly affects the behavior of the drug release from polymeric micelle with PNIPAAm outershell with temperature.
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