Design of multi-functional hydrogel for cell therapies

Cha, Chaenyung

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https://hdl.handle.net/2142/29621 Copy

Description

Title

Design of multi-functional hydrogel for cell therapies

Author(s)

Cha, Chaenyung

Issue Date

2012-02-06T20:07:20Z

Director of Research (if dissertation) or Advisor (if thesis)

Kong, Hyun Joon

Committee Member(s)

• Bashir, Rashid
• Gillette, Martha U.
• Leckband, Deborah E.

Department of Study

Chemistry

Discipline

Chemistry

Degree Granting Institution

University of Illinois at Urbana-Champaign

Degree Name

Ph.D.

Degree Level

Dissertation

Keyword(s)

• Hydrogel
• Cell Therapy
• Methacrylic Alginate
• Hydrophilic Pendant Chains
• Decoupled Control
• Stiffness
• Permeability
• Polyaspartamide Protein Linker
• Biomineralization

Abstract

Hydrogels are being actively investigated as encapsulation devices for cell transplantation therapies, as they provide structural stability and protection against harsh chemical and mechanical stimuli, and host immune system. In addition, chemical moieties, mechanical stiffness, and minerals presented in hydrogels act as insoluble signals to regulate a variety of cellular function. However, the conventional hydrogel design is plagued by complex dependencies between hydrogel properties; stiffness, permeability, density of cell adhesion molecules, and mineralization capacity. The objective of this research is to decouple or tune the intricate dependencies between these hydrogel properties, in order to better understand and regulate cellular activities in a 3D matrix. The hydrogel system is created by the assembly of three functional modules that contribute to the overall hydrogel properties: (1) The dependency between stiffness and permeability was tuned by incorporating pendant polymeric chains into a poly(ethylene glycol)-based hydrogel system; (2) Incorporation of alginate into a hydrogel system by co-polymerization allowed the control of hydrogel stiffness without affecting permeability; (3) The hydrogel was modified with cell adhesion proteins independent of other hydrogel properties using an amine-reactive polyaspartamide linker enabling single-step protein conjugation. Furthermore, mineralization capacity of the hydrogel was controlled independently by modulating hydrophobicity, charge density, and porosity. The efficacy of the hydrogel system developed in this research was evaluated by encapsulating two different cell types, fibroblasts and mesenchymal stem cells, and exploring the effects of hydrogel properties on the viability and growth factor expression of the encapsulated cells.

Graduation Semester

2011-12

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http://hdl.handle.net/2142/29621

Copyright and License Information

Copyright © 2011 Chaenyung Cha. All rights reserved.

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