Clinical percutaneous delivery of synthetically engineered hydrogels remains limited due to challenges posed by crosslinking kineticstoo fast leads to delivery failure, too slow limits material retention. To overcome this challenge, supramolecular assembly is exploited to localize hydrogels at the injection site and introduce subsequent covalent crosslinking to control final material properties. Supramolecular gels are designed through the separate pendant modifications of hyaluronic acid (HA) by the guest-host pair cyclodextrin and adamantane, enabling shear-thinning injection and high target site retention (>98%). Secondary covalent crosslinking occurs via addition of thiols and Michael-acceptors (i.e., methacrylates, acrylates, vinyl sulfones) on HA and increases hydrogel moduli (E = 25.0 +/- 4.5 kPa) and stability (>3.5 fold in vivo at 28 d). Application of the dual-crosslinking hydrogel to a myocardial infarct model shows improved outcomes relative to untreated and supramolecular hydrogel alone controls, demonstrating its potential in a range of applications where the precise delivery of hydrogels with tunable properties is desired.
Shear-Thinning Supramolecular Hydrogels with Secondary Autonomous Covalent Crosslinking to Modulate Viscoelastic Properties In Vivo
Creators
Christopher B. Rodell - University of Pennsylvania
John W. MacArthur - University of Pennsylvania
Shauna M. Dorsey - University of Pennsylvania
Ryan J. Wade - University of Pennsylvania
Leo L. Wang - University of Pennsylvania
Y. Joseph Woo - Stanford University
Jason A. Burdick - University of Pennsylvania
Publication Details
Advanced functional materials, v 25(4), pp 636-644
Publisher
Wiley
Number of pages
9
Grant note
American Heart Association
R01HL089315 / NATIONAL HEART, LUNG, AND BLOOD INSTITUTE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Heart Lung & Blood Institute (NHLBI)
R01 HL111090; R01 HL089315 / National Institutes of Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA
Resource Type
Journal article
Language
English
Academic Unit
School of Biomedical Engineering, Science, and Health Systems
Web of Science ID
WOS:000348856500015
Scopus ID
2-s2.0-85027954602
Other Identifier
991019176646904721
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