Abstract

Optimization of micellar molecular encapsulation systems, such as drug delivery vehicles, can be achieved through fundamental understanding of block copolymer micelle structure and dynamics. Herein, we present a study of PEO–PCL block copolymer spherical micelles that self-assemble at 1% wt/vol in D2O–THF-d8 mixtures. Varying solvent composition as a function of cosolvent THF-d8 at constant polymer concentration (1% wt/vol) allows sensitive study of how small molecule additives influence micelle structure and dynamics. We conduct nuclear magnetic resonance spectroscopy and diffusometry on two block copolymer (2k series: PEO2k–PCL3k; 5k series: PEO5k–PCL8k) spherical micelles that show drastically different behaviors. Unimers and micelles coexist in solution from 10–60 vol % THF-d8 for the 2k series but only coexist at 60 vol % THF-d8 for the 5k series. At ≥ 60 vol % THF-d8 micelles disassemble into free unimers for both series. We observe relatively flat micelle diffusion coefficients (∼1 × 10–10 m2/s) wi...

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