4.6 Article

Composite Bijel-Templated Hydrogels for Cell Delivery

Journal

ACS BIOMATERIALS SCIENCE & ENGINEERING
Volume 4, Issue 2, Pages 587-594

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.7b00809

Keywords

bijel; self-assembly; cell delivery; composite; microstructure

Funding

  1. NASA Research Opportunities in Complex Fluids and Macromolecular Biophysics Program [NNX13AQ69G]
  2. National Institutes of Health Laser Microbeam and Medical Program [P41EB015890]
  3. National Science Foundation Interdisciplinary Graduate Education and Research Traineeship (IGERT) Biophotonics across Energy, Space, and Time (BEST) program [NSF-DGE-1144901]
  4. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [P41EB015890] Funding Source: NIH RePORTER

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Numerous processing techniques aim to impart interconnected, porous structures within regenerative medicine materials to support cell delivery and direct tissue growth. Many of these techniques lack predictable control of scaffold architecture, and rapid prototyping methods are often limited by time-consuming, layer-by-layer fabrication of microfeatures. Bicontinuous interfacially jammed emulsion gels (bijels) offer a robust, self-assembly based platform for synthesizing a new class of morphologically unique cell delivery biomaterials. Bijels form via kinetic arrest of temperature-driven spinodal decomposition in partially miscible binary liquid systems. These nonequilibrium soft materials comprise cocontinuous, fully interpenetrating, nonconstricting liquid domains separated by a nanoparticle monolayer. Through the selective introduction of biocompatible precursors, hydrogel scaffolds displaying the morphological characteristics of the parent bijel can be formed. We report using bijel templating to generate structurally unique, fibrin-loaded polyethylene glycol hydrogel composites. Demonstration of composite bijel-templated hydrogels (CBiTHs) as a new cell delivery system was carried out in vitro using fluorescence-based tracking of cells delivered to previously acellular fibrin gels. Imaging analysis confirmed repeatable delivery of normal human dermal fibroblasts to acellular fibrin gels.

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