posted on 2016-09-07, 00:00authored byElias Sideris, Donald
R. Griffin, Yichen Ding, Shuoran Li, Westbrook
M. Weaver, Dino Di Carlo, Tzung Hsiai, Tatiana Segura
The extracellular matrix (ECM) provides
tissues with the mechanical
support, space, and bioactive signals needed for homeostasis or tissue
repair after wounding or disease. Hydrogel based scaffolds that can
match the bulk mechanical properties of the target tissue have been
extensively explored as ECM mimics. Although the addition of microporosity
to hydrogel scaffolds has been shown to enhance cell/tissue–material
integration, the introduction of microporosity often involves harsh
chemical methods, which limit bioactive signal incorporation and injectability.
Particle hydrogels are an emerging platform to generate in situ forming
microporous scaffolds. In this approach, μgel particles are
annealed to each other to form a bulk scaffold that is porous because
of the void space left by the packed microgels. In the present work,
we discuss the formation of hyaluronic acid-based microfluidic generated
microgels for the generation of a completely biodegradable material.
The generation of particle scaffolds requires two orthogonal chemistries,
one for microgel generation and one for microgel annealing and scaffold
formation. Here we explore three orthogonal annealing chemistries
based on an enzymatic reaction, light based radical polymerization,
and amine/carboxylic acid based cross-linking to demonstrate the versatility
of our particle hydrogels and explore potential physical differences
between the approaches. We explore the connectivity of the generated
pores, the pore area/void fraction of the resulting scaffold, the
mechanical properties of the scaffold, and cell spreading within scaffolds
formed with the three different annealing mechanisms.