4.7 Article

Reproducible Dendronized PEG Hydrogels via SPAAC Cross-Linking

Journal

BIOMACROMOLECULES
Volume 18, Issue 12, Pages 4054-4059

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.7b01115

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Funding

  1. National Science and Engineering Research Council of Canada (NSERC)
  2. Ontario Graduate Scholarships (OGS) program

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A common issue with hydrogel formulations is batch-to-batch irreproducibility originating from poorly defined polymer precursors. Here, we report the use of dendritic polymer end-groups to address this issue and maintain reproducibility between batches of poly(ethylene glycol) (PEG) hydrogels. Specifically, we synthesized two end-functionalized PEG chains: one with azide-terminated first- and second-generation dendrons and the other with strained cyclooctynes. The two complementary azide and alkyne polymers react via strain-promoted alkyne-azide cycloaddition (SPAAC) to produce hydrogels quickly in the absence of additional reagents or catalyst at low polymer concentrations. Hydrogels made with first-generation dendrons gelled in minutes and exhibited a small degree of swelling when incubated in PBS buffer at 37 degrees C, whereas hydrogels made from second-generation dendrons gelled in seconds with almost no swelling upon incubation at 37 degrees C. In both cases, the hydrogels proved reproducible, resulting in identical Youngs modulus values from different batches. The hydrogels prepared with second-generation dendrons were seeded with human mesenchymal stem cells and showed high cell viability as well as cell spreading over a two-week time frame. These studies show that the SPAAC hydrogels are noncytotoxic and are capable of supporting cell growth.

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