Source abstract
Abstract
Ultrasound-induced degradation of soft polymeric colloids, like microgels, as well as a controlled drug release enabled by mechanoresponsive bonds, has recently attracted considerable attention. However, most examples in the literature focus primarily on the applications rather than examining the underlying mechanisms of the structural changes occurring in microgels due to cavitation─changes that are crucial for developing effective drug delivery systems. In this work, we provide a comprehensive view of how microgel structure governs the susceptibility to rupture and mass loss upon cavitation, investigating both conventional microgels containing mechanoresponsive disulfide bonds and more complex asymmetrically cross-linked core-shell microgels. By combining dynamic and static light scattering, small-angle X-ray scattering, and atomic force microscopy, we demonstrate that an interplay between mechanoresponsive cross-links and the swelling degree determines the microgels' susceptibility to ultrasound-induced damage. Our findings indicate that local stress from cavitation bubbles varies strongly within the microgel dispersion. The majority of microgels undergo gradual erosion at their periphery, resulting in smaller yet structurally intact particles over time, observable by light scattering and AFM. In contrast, microgels closer to a cavitation bubble can experience partial rupture or complete disintegration, producing smaller, more polydisperse fragments, which contribute substantially to the overall mass loss observed. In the core-shell microgels with different cross-linkers in the core and shell, degradation occurs nearly uniformly across both regions, instead of selectively targeting the weaker part. These observations highlight the complexity of the degradation dynamics as well as the similarity to processes seen in linear polymers and bulk hydrogels.
Affiliations
Institute of Experimental Physics of Condensed Matter, Heinrich-Heine University, Universitätsstr. 1, Düsseldorf 40225, Germany, EU
Institute of Physical Chemistry, RWTH Aachen University, Landoltweg 2, Aachen 52074, Germany, EU
DWI − Leibniz Institute for Interactive Materials, Forckenbeckstr. 50, Aachen 52074, Germany, EU
Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry (ITMC), RWTH Aachen University, Worringerweg 2, Aachen 52074, Germany, EU
Australian Synchrotron, ANSTO, 800 Blackburn Rd, Clayton, Victoria 3168, Australia
MAX IV Laboratory, Lund University, P.O. Box 118, Lund 22100, Sweden, EU
Division of Physical Chemistry, Lund University, P.O. Box 124, Lund 22100, Sweden
Aachen Maastricht Institute for Biobased Materials (AMIBM), Maastricht University, Brightlands Chemelot Campus, Urmonderbaan 22, Sittard-Geleen 6167 RD, The Netherlands, EU
Funding
Vetenskapsr?det · Deutsche Forschungsgemeinschaft · Knut och Alice Wallenbergs Stiftelse