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Unusual behaviour induced by phase separation in hydrogel microspheres.

Clare L Heaysman1, Gary J Philips2, Andrew W Lloyd2

  • 1School of Pharmacy and Biomolecular Sciences, University of Brighton, Moulsecoomb, Brighton BN2 4GJ, UK; Biocompatibles UK Ltd, Farnham Business Park, Weydon Lane, Farnham, Surrey GU9 8QL, UK.

Acta Biomaterialia
|February 15, 2017
PubMed
Summary

Researchers developed novel cationic hydrogel microspheres exhibiting unique phase-separation during synthesis. This controlled phase-separation leads to distinct core-shell structures with potential for advanced drug delivery applications.

Keywords:
Hydrogel microspheresIon-exchangePhase-separation

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Area of Science:

  • Biomaterials Science
  • Polymer Chemistry
  • Drug Delivery Systems

Background:

  • Hydrogel microspheres are vital for biomedical applications, particularly in drug delivery via ion-exchange.
  • Existing systems primarily use anionic hydrogels for cationically charged drugs in treatments like drug-eluting bead chemoembolization (DEB-TACE).

Purpose of the Study:

  • To investigate the synthesis and properties of novel cationic hydrogel microspheres.
  • To explore the unusual behavior induced by phase-separation during microsphere synthesis.

Main Methods:

  • Synthesis of cationic hydrogel microspheres.
  • Induction of phase-separation during synthesis, leading to core-shell structures.
  • Swelling studies in aqueous environments and ion-exchange interactions with anionic compounds.

Main Results:

  • Phase-separation during synthesis resulted in a cationic polymer-enriched core and a polyvinyl alcohol (PVA)-based outer phase.
  • Swelling in water caused separation of the PVA-rich skin from the charged core in some formulations.
  • Ion-exchange with multi-anionic compounds induced differential contraction, creating a "golf-ball" surface morphology.

Conclusions:

  • The observed phase-separation and subsequent structural changes represent a novel phenomenon in hydrogel microsphere synthesis.
  • These findings suggest potential for new drug delivery systems that respond to drug loading by altering their structure or surface area.