Open AccessInjectable Microporous Annealed Particle Hydrogel Based on Guest–Host‐Interlinked Polyethylene Glycol Maleimide Microgels
Author(s) -
Widener Adrienne E.,
Duraivel Senthilkumar,
Angelini Thomas E.,
Phelps Edward A.
Publication year - 2022
Publication title -
advanced nanobiomed research
Language(s) - English
Resource type - Journals
ISSN - 2699-9307
DOI - 10.1002/anbr.202200030
Subject(s) - self healing hydrogels , materials science , cell encapsulation , polyethylene glycol , chemical engineering , microporous material , tissue engineering , nanotechnology , peg ratio , emulsion , polymer chemistry , composite material , biomedical engineering , medicine , finance , engineering , economics
Microporous annealed particle (MAP) hydrogels have emerged as a versatile biomaterial platform for regenerative medicine. MAP hydrogels have been used for the delivery of cells and organoids but often require annealing post‐injection by an external source. An injectable, self‐annealing MAP hydrogel with reversible interparticle linkages based on guest–host functionalized polyethylene glycol‐maleimide (PEG‐MAL) microgels is engineered. The effect of guest–host linkages is evaluated on different types of microgels fabricated by either batch emulsion or mechanical fragmentation methods. Batch emulsion generates small spherical microgels with controllable (10–100 μm) diameters and mechanical fragmentation generates irregular microgels with larger diameters (100–200 μm). Spherical microgels (15 μm) show self‐healing behavior and have completely recovered from high strain while fragmented microgels (133 μm) do not recover. Guest–host interactions significantly contribute to the mechanical properties of spherical microgels but have no effect on fragmented microgels. Spherical microgels are superior to the fragmented microgels for co‐injection of immune cells and pancreatic islets due to their lower force of injection, demonstrating more homogeneously distributed cells and greater cell viability after injection. Based on these studies, the spherical guest–host MAP hydrogels provide a controllable, injectable scaffold for engineered microenvironments and cell delivery applications.