Self-Assembly of Amorphous, pH-Degradable Polymer Nanodiscs of Controllable Size and Functionality

03 October 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Amphiphilic bottlebrush block copolymers (BBC) with tadpole-like, coil-rod architecture can be used to self-assemble into functional polymer nanodiscs directly in water. The hydrophobic segments of the BBC were tuned via the ratio of ethoxy-ethyl glycidyl ether (EE) to tetrahydropyranyl glycidyl ether (TP) within the grafted polymer sidechains. In turn, this variation controlled the sizes, pH-responsiveness, and drug loading capacity of the self-assembled nanodiscs. Notably, as EE exhibited faster hydrolysis than TP, the nanodiscs featured variable degradation rates under mild acidic conditions, aiding small molecule release and time-dependent and complete degradation of discs into fully water-soluble copolymers.

Keywords

self-assembly
2D
platelets
bottlebrush copolymer
core-shell
stimuli-response

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