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Covalent stabilization of alginate hydrogel beads via Staudinger ligation: Assessment of poly(ethylene glycol) and alginate cross‐linkers
Author(s) -
GattásAsfura Kerim M.,
Fraker Christopher A.,
Stabler Cherie L.
Publication year - 2011
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.33162
Subject(s) - self healing hydrogels , ethylene glycol , materials science , covalent bond , peg ratio , polymer , swelling , glucuronic acid , tissue engineering , cell encapsulation , linker , polymer chemistry , chemical engineering , chemistry , biomedical engineering , organic chemistry , composite material , polysaccharide , medicine , finance , computer science , engineering , economics , operating system
Cellular encapsulation within alginate hydrogel capsules has broad applications in tissue engineering. In seeking to improve the inherent instability of ionically cross‐linked alginate hydrogels, we previously demonstrated the covalent stabilization of Ba 2+ cross‐linked alginate‐azide beads via chemoselective Staudinger ligation using a 1‐methyl‐2‐diphenylphosphino‐terephthalate (MDT) terminated poly(ethylene glycol) (PEG) linker. In this study, we functionalized variant PEG, linear and branched, and alginate polymers with MDT groups to evaluate the effect of size, structural design, number of functional groups, and charge on the resulting hydrogel bead. All cross‐linkers resulted in enhanced covalent stabilization of alginate beads, with significant decreases in swelling and resistance to dissolution via Ba 2+ chelation. The MDT‐functionalized alginate resulted in the most stable and homogeneous bead, with the most restrictive permeability even after EDTA exposure. Co‐encapsulation of MIN6 cells within the cross‐linked alginate hydrogel beads resulted in minimal effects on viability, whereas the degree of proliferation following culture varied with cross‐linker type. Altogether, the results illustrate that manipulating the cross‐linker structural design permits flexibility in resulting alginate beads characteristics. Covalent stabilization of alginate hydrogel beads with these chemoselective alginate and PEG‐based cross‐linkers provides a unique platform for cellular encapsulation. © 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 99A: 47–57, 2011.