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Author Notes:

Author to whom correspondence should be addressed: todd.mcdevitt@gladstone.ucsf.edu

M. H. Hettiaratchi and A. Schudel contributed equally to this work.

The authors would like to thank Dr. Devon Headen for his assistance in making PEG-MAL hydrogels, Dr. Ariel Kniss for her assistance in developing the MATLAB code for analysis of fluorescence intensity profiles, and Dr. Brandon Dixon for the use of his microscope.

Subjects:

Research Funding:

This work was supported by funding from the National Institutes of Health (R01 AR062006 to T.C.M.) and the Armed Forces Institute of Regenerative Medicine (Award No. W81XWH-14-2-0003 to R.E.G.).

M.H.H. was supported by a Natural Sciences and Engineering Research Council of Canada (NSERC) post-graduate scholarship and Philanthropic Educational Organization (P.E.O.) Scholar Award.

A.S. was supported by an American Heart Association Pre-Doctoral Fellowship.

Keywords:

  • Immune system
  • Proteins
  • Computational models
  • Tissue engineering
  • Biomaterials
  • Capillary flows
  • Chemical elements
  • Fluorescein
  • Therapeutics
  • Diffusion rate

A rapid method for determining protein diffusion through hydrogels for regenerative medicine applications.

Tools:

Journal Title:

APL Bioengineering

Volume:

Volume 2, Number 2

Publisher:

, Pages 026110-026110

Type of Work:

Article | Final Publisher PDF

Abstract:

Hydrogels present versatile platforms for the encapsulation and delivery of proteins and cells for regenerative medicine applications. However, differences in hydrogel cross-linking density, polymer weight content, and affinity for proteins all contribute to diverse diffusion rates of proteins through hydrogel networks. Here, we describe a simple method to accurately measure protein diffusion through hydrogels, within a few hours and without the use of large amounts of protein. We tracked the diffusion of several proteins of varying molecular weights along the axial direction of capillary tubes filled with alginate, collagen, or poly(ethylene glycol) hydrogels. The rate of protein diffusion decreased with increasing molecular weight. A computational model of protein diffusion through capillary tubes was also created to predict and verify experimental protein diffusion coefficients. This in vitro capillary tube-based method of measuring protein diffusion represents a simple strategy to interrogate protein diffusion through natural and synthetic hydrogels and aid in the design of better biomaterial-based delivery vehicles that can effectively modulate protein release.

Copyright information:

© 2018 Author(s).

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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