| Literature DB >> 27341012 |
Cynthia X Wang1, Stefanie Utech2, Jeffrey D Gopez1, Mathijs F J Mabesoone3, Craig J Hawker1, Daniel Klinger1,4.
Abstract
Well-defined microgel particles were prepared by combining coacervate-driven cross-linking of ionic triblock copolymers with the ability to control particle size and encapsulate functional cargos inherent in microfluidic devices. In this approach, the efficient assembly of PEO-based triblock copolymers with oppositely charged end-blocks allows for bioinspired cross-linking under mild conditions in dispersed aqueous droplets. This strategy enables the integration of charged cargos into the coacervate domains (e.g., the loading of anionic model compounds through electrostatic association with cationic end-blocks). Distinct release profiles can be realized by systematically varying the chemical nature of the payload and the microgel dimensions. This mild and noncovalent assembly method represents a promising new approach to tunable microgels as scaffolds for colloidal biomaterials in therapeutics and regenerative medicine.Entities:
Keywords: coacervates; droplet microfluidics; microgels; physical cross-links; polyelectrolytes; triblock copolymers
Year: 2016 PMID: 27341012 DOI: 10.1021/acsami.6b03356
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229