# Viscoelastic Response of Double Hydrophilic Block Copolymers for Drug Delivery Applications

## TL;DR

This study explores how the mechanical properties of double hydrophilic block copolymers can be tuned for drug delivery by adjusting their composition and structure.

## Contribution

The study reveals how the viscoelastic behavior of DHBCs can be tailored for drug delivery by altering block composition and arrangement.

## Key findings

- Increasing VBTMAC content leads to a transition from liquid-like to elastic-like viscoelastic behavior.
- Changing block arrangement affects the presence of bulk-like regions, altering viscoelastic response.
- Copolymers show reduced free volume and increased activation energy with higher VBTMAC content.

## Abstract

This study investigates the mechanical properties of double hydrophilic block copolymers (DHBCs) based on poly[oligo(ethylene glycol) methacrylate] (POEGMA) and poly(vinyl benzyl trimethylammonium chloride) (PVBTMAC) blocks by employing small amplitude oscillatory shear (SAOS) rheological measurements. We report that the mechanical properties of DHBCs are governed by the interfacial glass transition temperature (Tginter), verifying the disordered state of these copolymers. An increase in zero shear viscosity can be observed by increasing the VBTMAC content, yielding a transition from liquid-like to gel-like and finally to an elastic-like response for the PVBTMAC homopolymer. By changing the block arrangement along the backbone from statistical to sequential, a distinct change in the viscoelastic response is obvious, indicating the presence/absence of bulk-like regions. The tunable viscosity values and shear-thinning behavior achieved through alteration of the copolymer composition and block arrangement along the backbone render the studied DHBCs promising candidates for drug delivery applications. In the second part, the rheological data are analyzed within the framework of the classical free volume theories of glass formation. Specifically, the copolymers exhibit reduced fractional free volume and similar fragility values compared to the PVBTMAC homopolymer. On the contrary, the activation energy increases by increasing the VBTMAC content, reflecting the required higher energy for the relaxation of the glassy VBTMAC segments. Overall, this study provides information about the viscoelastic properties of DHBCs with densely grafted macromolecular architecture and shows how the mechanical and dynamical properties can be tailored for different drug delivery applications by simply altering the ratio between the two homopolymers.