Web Release Date: June 29,
Self-Assembling Biomaterials: L-Lysine-Dendron-Substituted
Cholesteryl-(L-lactic acid)
Department of Materials Science and Engineering, Department of Chemistry, Medical School, Northwestern University, Evanston, Illinois 60208
Received November 13, 2001
Revised Manuscript Received April 4, 2002
Abstract:
This report describes the synthesis and supramolecular organization of a novel class
of linear-dendritic block copolymers. The molecules, which are termed rodcoil dendrons, consist
of a cholesterol moiety that is attached to L-lysine dendrons of three different generations via a
biodegradable oligo(L-lactic acid)
spacer. Whereas the molecules exhibit very poor ordering in the
dry state, different supramolecular morphologies were observed in the hydrated state. Cholesteryl-(L-lactic acid)
-(L-lysine)G1 and cholesteryl-(L-lactic acid)
-(L-lysine)G2 self-assemble into lamellar structures with periodicities that depend on degree of hydration. At low degrees of hydration, lamellar ordering
was also observed for cholesteryl-(L-lactic acid)
-(L-lysine)G3. However, at 50 wt %, water steric
hindrance in the highly hydrated L-lysine dendrons no longer allows lamellar ordering, and discrete
nanosized aggregates are formed. Evidence for the formation of such nanoaggregates was obtained from
dynamic light scattering, electron microscopy, and atomic force microscopy. These rodcoil dendron
biomaterials could be of potential interest as temporary molecular scaffolds for cell and tissue engineering.
Download the full text: PDF | HTML