4.5 Review

PEG Hydrogels for the Controlled Release of Biomolecules in Regenerative Medicine

Journal

PHARMACEUTICAL RESEARCH
Volume 26, Issue 3, Pages 631-643

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-008-9801-2

Keywords

controlled release; hydrogel; PEG; regenerative medicine

Funding

  1. Howard Hughes Medical Institute
  2. NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH [R01DE016523] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF DENTAL &CRANIOFACIAL RESEARCH [R01DE012998] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK076084] Funding Source: NIH RePORTER

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Polyethylene glycol (PEG) hydrogels are widely used in a variety of biomedical applications, including matrices for controlled release of biomolecules and scaffolds for regenerative medicine. The design, fabrication, and characterization of PEG hydrogels rely on the understanding of fundamental gelation kinetics as well as the purpose of the application. This review article will focus on different polymerization mechanisms of PEG-based hydrogels and the importance of these biocompatible hydrogels in regenerative medicine applications. Furthermore, the design criteria that are important in maintaining the availability and stability of the biomolecules as well as the mechanisms for loading of biomolecules within PEG hydrogels will also be discussed. Finally, we overview and provide a perspective on some of the emerging novel design and applications of PEG hydrogel systems, including the spatiotemporal-controlled delivery of biomolecules, hybrid hydrogels, and PEG hydrogels designed for controlled stem cell differentiation.

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