The bending rigidity kc of bilayer vesicles self-assembled from
amphiphilic diblock copolymers has been measured using single and
dual-micropipet techniques. These copolymers are nearly a factor of 5 greater
in hydrophobic membrane thickness d than their lipid counterparts, and an
order of magnitude larger in molecular weight Mˉn. The macromolecular
structure of these amphiphiles lends insight into and extends relationships for
traditional surfactant behavior. We find the scaling of kc with thickness to
be nearly quadratic, in agreement with existing theories for bilayer membranes.
The results here are key to understanding and designing soft interfaces such as
biomembrane mimetics