AI Article Synopsis

  • - The study focuses on the phase behavior of crosslinked hydrogels, highlighting their ability to switch between dehydrated and hydrated states based on temperature changes, which affects water absorption and release.
  • - A novel hydrogel system is introduced that can change its volume in response to carbon dioxide (CO) exposure, allowing for significant swelling (up to fivefold) and temperature shifts of up to 8.6 °C.
  • - The findings suggest potential applications in drug delivery, as the hydrogel's phase transitions can be precisely tuned through its composition to suit specific uses, promoting further exploration in smart material development.

Article Abstract

Macromolecules exhibit rich phase behavior that may be exploited for advanced material design. In particular, the volume phase transition in certain crosslinked hydrogels is a key property controlling the transition between a collapsed/dehydrated and a swollen/hydrated state, thereby regulating the release and absorption of water via a temperature change. In this work, a simple and tunable system exhibiting a carbon dioxide (CO)-switchable volume phase transition is introduced, which displays isothermal swelling-shrinking behavior that is activated by addition and removal of CO respectively. Through systematic compositional studies, shifts in phase transition temperatures of up to 8.6 °C are measured upon CO exposure, which enables pronounced isothermal swelling in response to CO, reaching up to a fivefold increase in mass. The shift in transition temperature and the extent of swelling are controlled by the hydrogel composition, thus enabling the transition temperature and swelling degree to be tuned a priori for a particular application. Controlled release experiments from these gels upon a CO-induced phase transition suggest viability for drug delivery applications. It is anticipated that this work will motivate and expand efforts to exploit phase behavior for smart material development.

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Source
http://dx.doi.org/10.1002/marc.202400772DOI Listing

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