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University of Illinois at Urbana-Champaign

Control of covalent and non-covalent presentation of biomolecules within collagen GAG scaffolds

Abstract

dc:description

Mass transport continues to be a major bottleneck in the development of biomaterials. The diffusive limitation of biomaterials restricts cell viability to regions where nutrients are readily available. To overcome this transport limitation, angiogenic biomaterials that utilize biomolecular cues such as Vascular Endothelial Growth Factor to drive vascularization are being explored. To develop these biomaterials, techniques to present these factors must first be investigated. Experiments were conducted with collagen glycosaminoglycan (CG) scaffolds to determine optimal conditions to control the levels of covalent and non-specific attachment of biotinylated Concanavalin A (ConA) via two distinct covalent patterning techniques: 1-ethyl-3-3-dimethylaminopropylcarbodiimide hydrochloride (EDC) crosslinking and benzophenone (BP) biophotolithography. The results indicated that longer contact time of ConA with the CG scaffold independent of covalent attachment methods led to significantly higher amounts of fouling (non-specific attachment). The fouling was best minimized using a 1 hour wash followed by an overnight wash in a solution of 5% sucrose in PBS compared to no wash, PBS, 5% BSA in PBS, and 1% Tween in PBS. The total ConA immobilized by EDC chemistry was found to be strongly correlated to the amount of protein loading and was higher for an EDC:N-hydroxysuccinimide:Carboxyl ratio of 5:12.5:1 compared to 2.5:6.25:1 and 10:25:1. For BP chemistry, the UV exposure time was found to be significantly correlated to the total amount of ConA immobilized. Components of the scaffolds were also tested to determine their impact on covalent patterning and fouling. It was found that the Collagen Matrix yielded BP patterns with better resolution and less background noise caused by non-specific attachment. The use of Chondroitin Sulfate was found to have significantly less fouling than Hyaluronic Acid within scaffolds, which was unexpected. Further, the Hyaluronic Acid yielded significantly higher total ConA immobilization.

Degree

thesis:*
Name thesis:degree_name
M.S.
Level thesis:degree_level
Thesis
Discipline thesis:degree_discipline
Chemical Engineering
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2013

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Pence, Jacquelyn
Contributors dc:contributor
  • Harley, Brendan A.

Subjects

dc:subject × 6

Rights

dc:rights
Statement dc:rights
  • Copyright 2012 Jacquelyn C. Pence
Language dc:language
en

Identifiers

dc:identifier.*
Handle dc:identifier
http://hdl.handle.net/2142/42307
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/42307

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Pence, Jacquelyn. Control of covalent and non-covalent presentation of biomolecules within collagen GAG scaffolds. Thesis thesis, University of Illinois at Urbana-Champaign, 2013. http://hdl.handle.net/2142/42307