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Shear-thinning and self-healing hydrogels as injectable therapeutics and for 3D-printing
Journal article   Open access   Peer reviewed

Shear-thinning and self-healing hydrogels as injectable therapeutics and for 3D-printing

Claudia Loebel, Christopher B Rodell, Minna H Chen and Jason A Burdick
Nature protocols, v 12(8), pp 1521-1541
Aug 2017
PMID: 28683063
url
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546336View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

Adamantane - metabolism Animals beta-Cyclodextrins - metabolism Drug Carriers - administration & dosage Hyaluronic Acid - administration & dosage Hydrogels - administration & dosage Hydrogels - chemistry Injections Mice Printing, Three-Dimensional ESI Highly Cited Paper (Incites)
The design of injectable hydrogel systems addresses the growing demand for minimally invasive approaches for local and sustained delivery of therapeutics. We developed a class of hyaluronic acid (HA) hydrogels that form through noncovalent guest-host interactions, undergo disassembly (shear-thinning) when injected through a syringe and then reassemble within seconds (self-healing) when shear forces are removed. Its unique properties enable the use of this hydrogel system for numerous applications, such as injection in vivo (including with cells and therapeutic molecules) or as a 'bioink' in 3D-printing applications. Here, we describe the functionalization of HA either with adamantanes (guest moieties) via controlled esterification or with β-cyclodextrins (host moieties) through amidation. We also describe how to modify the HA derivatives with methacrylates for secondary covalent cross-linking and for reaction with fluorophores for in vitro and in vivo imaging. HA polymers are rationally designed from relatively low-molecular-weight starting materials, with the degree of modification controlled, and have matched guest-to-host stoichiometry, allowing the preparation of hydrogels with tailored properties. This procedure takes 3-4 weeks to complete. We detail the preparation and characterization of the guest-host hydrogels, including assessment of their rheological properties, erosion and biomolecule release in vitro. We furthermore demonstrate how to encapsulate cells in vitro and provide procedures for quantitative assessment of in vivo hydrogel degradation by imaging of fluorescently derivatized materials.

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Collaboration types
Domestic collaboration
Web of Science research areas
Biochemical Research Methods
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